-
1
-
-
0036783078
-
History of human parasitology
-
CrossRef PubMed
-
Cox, F. E. G. (2002) History of human parasitology. Clin. Microbiol. Rev. 15, 595-612 CrossRef PubMed
-
(2002)
Clin. Microbiol. Rev.
, vol.15
, pp. 595-612
-
-
Cox, F.E.G.1
-
2
-
-
21044443813
-
Plasmodium dominicana n. Sp. (Plasmodiidae: Haemospororida) from Tertiary Dominican amber
-
CrossRef PubMed
-
Poinar, G. (2005) Plasmodium dominicana n. sp. (Plasmodiidae: Haemospororida) from Tertiary Dominican amber. Syst. Parasitol. 61, 47-52 CrossRef PubMed
-
(2005)
Syst. Parasitol.
, vol.61
, pp. 47-52
-
-
Poinar, G.1
-
3
-
-
8744257799
-
Traditional herbal medicines for malaria
-
Willcox, M. L. and Bodeker, G. (2004) Traditional herbal medicines for malaria. BMJ 329, 1156-1159 CrossRef PubMed (Pubitemid 39524776)
-
(2004)
British Medical Journal
, vol.329
, Issue.7475
, pp. 1156-1159
-
-
Willcox, M.L.1
Bodeker, G.2
-
4
-
-
33646942669
-
Reflections on the 'discovery' of the antimalarial qinghao
-
CrossRef PubMed
-
Hsu, E. (2006) Reflections on the 'discovery' of the antimalarial qinghao. Br. J. Clin. Pharmacol. 61, 666-670 CrossRef PubMed
-
(2006)
Br. J. Clin. Pharmacol.
, vol.61
, pp. 666-670
-
-
Hsu, E.1
-
5
-
-
77649196518
-
Ancient Chinese methods are remarkably effective for the preparation of artemisinin-rich extracts of qing hao with potent antimalarial activity
-
CrossRef PubMed
-
Wright, C. W., Linley, P. A., Brun, R., Wittlin, S. and Hsu, E. (2010) Ancient Chinese methods are remarkably effective for the preparation of artemisinin-rich extracts of qing hao with potent antimalarial activity. Molecules 15, 804-812 CrossRef PubMed
-
(2010)
Molecules
, vol.15
, pp. 804-812
-
-
Wright, C.W.1
Linley, P.A.2
Brun, R.3
Wittlin, S.4
Hsu, E.5
-
6
-
-
78650265020
-
Malaria, a journey in time: In search of the lost myths and forgotten stories
-
CrossRef PubMed
-
Neghina, R., Neghina, A. M., Marincu, I. and Iacobiciu, I. (2010) Malaria, a journey in time: in search of the lost myths and forgotten stories. Am. J. Med. Sci. 340, 492-498 CrossRef PubMed
-
(2010)
Am. J. Med. Sci.
, vol.340
, pp. 492-498
-
-
Neghina, R.1
Neghina, A.M.2
Marincu, I.3
Iacobiciu, I.4
-
8
-
-
68049123592
-
Artemisinin resistance in Plasmodium falciparum malaria
-
CrossRef PubMed
-
Dondorp, A. M., Nosten, F., Yi, P., Das, D., Phyo, A. P., Tarning, J., Lwin, K. M., Ariey, F., Hanpithakpong, W., Lee, S. J. et al. (2009) Artemisinin resistance in Plasmodium falciparum malaria. N. Engl. J. Med. 361, 455-467 CrossRef PubMed
-
(2009)
N. Engl. J. Med.
, vol.361
, pp. 455-467
-
-
Dondorp, A.M.1
Nosten, F.2
Yi, P.3
Das, D.4
Phyo, A.P.5
Tarning, J.6
Lwin, K.M.7
Ariey, F.8
Hanpithakpong, W.9
Lee, S.J.10
-
9
-
-
57749099137
-
Evidence of artemisinin-resistant malaria in western Cambodia
-
CrossRef PubMed
-
Noedl, H., Se, Y., Schaecher, K., Smith, B. L., Socheat, D. and Fukuda, M. M. (2008) Evidence of artemisinin-resistant malaria in western Cambodia. N. Engl. J. Med. 359, 2619-2620 CrossRef PubMed
-
(2008)
N. Engl. J. Med.
, vol.359
, pp. 2619-2620
-
-
Noedl, H.1
Se, Y.2
Schaecher, K.3
Smith, B.L.4
Socheat, D.5
Fukuda, M.M.6
-
10
-
-
68049146050
-
Artemisinin-resistant malaria in Asia
-
CrossRef PubMed
-
Noedl, H., Socheat, D. and Satimai, W. (2009) Artemisinin-resistant malaria in Asia. N. Engl. J. Med. 361, 540-541 CrossRef PubMed
-
(2009)
N. Engl. J. Med.
, vol.361
, pp. 540-541
-
-
Noedl, H.1
Socheat, D.2
Satimai, W.3
-
11
-
-
84859506329
-
A major genome region underlying artemisinin resistance in malaria
-
CrossRef PubMed
-
Cheeseman, I. H., Miller, B. A., Nair, S., Nkhoma, S., Tan, A., Tan, J. C., Al Saai, S., Phyo, A. P., Moo, C. L., Lwin, K. M. et al. (2012) A major genome region underlying artemisinin resistance in malaria. Science 336, 79-82 CrossRef PubMed
-
(2012)
Science
, vol.336
, pp. 79-82
-
-
Cheeseman, I.H.1
Miller, B.A.2
Nair, S.3
Nkhoma, S.4
Tan, A.5
Tan, J.C.6
Al Saai, S.7
Phyo, A.P.8
Moo, C.L.9
Lwin, K.M.10
-
12
-
-
84886638407
-
Novel approaches in antimalarial drug discovery
-
CrossRef PubMed
-
Held, J., Kreidenweiss, A. and Mordmuller, B. (2013) Novel approaches in antimalarial drug discovery. Expert Opin. Drug Discov. 8, 1325-1337 CrossRef PubMed
-
(2013)
Expert Opin. Drug Discov.
, vol.8
, pp. 1325-1337
-
-
Held, J.1
Kreidenweiss, A.2
Mordmuller, B.3
-
13
-
-
84887989421
-
Antimalarial drug discovery: Approaches and progress towards new medicines
-
CrossRef PubMed
-
Flannery, E. L., Chatterjee, A. K. and Winzeler, E. A. (2013) Antimalarial drug discovery: approaches and progress towards new medicines. Nat. Rev. Microbiol. 11, 849-862 CrossRef PubMed
-
(2013)
Nat. Rev. Microbiol.
, vol.11
, pp. 849-862
-
-
Flannery, E.L.1
Chatterjee, A.K.2
Winzeler, E.A.3
-
14
-
-
5444247213
-
Combating susceptibility to drug resistance: Lessons from HIV-1 protease
-
DOI 10.1016/j.chembiol.2004.08.010, PII S1074552104002431
-
King, N. M., Prabu-Jeyabalan, M. M., Nalivaika, E. A. and Schiffer, C. A. (2004) Combating susceptibility to drug resistance: lessons from HIV-1 protease. Chem. Biol. 11, 1333-1338 PubMed (Pubitemid 39351371)
-
(2004)
Chemistry and Biology
, vol.11
, Issue.10
, pp. 1333-1338
-
-
King, N.M.1
Prabu-Jeyabalan, M.2
Nalivaika, E.A.3
Schiffer, C.A.4
-
15
-
-
79952171610
-
Molecular basis for drug resistance in HIV-1 protease
-
CrossRef PubMed
-
Ali, A., Bandaranayake, R. M., Cai, Y. F., King, N. M., Kolli, M., Mittal, S., Murzycki, J. F., Nalam, M. N. L., Nalivaika, E. A., Ozen, A. et al. (2010) Molecular basis for drug resistance in HIV-1 protease. Viruses 2, 2509-2535 CrossRef PubMed
-
(2010)
Viruses
, vol.2
, pp. 2509-2535
-
-
Ali, A.1
Bandaranayake, R.M.2
Cai, Y.F.3
King, N.M.4
Kolli, M.5
Mittal, S.6
Murzycki, J.F.7
Nalam, M.N.L.8
Nalivaika, E.A.9
Ozen, A.10
-
16
-
-
78650481557
-
Drug resistance against HCV NS3/4A inhibitors is defined by the balance of substrate recognition versus inhibitor binding
-
CrossRef PubMed
-
Romano, K. P., Ali, A., Royer, W. E. and Schiffer, C. A. (2010) Drug resistance against HCV NS3/4A inhibitors is defined by the balance of substrate recognition versus inhibitor binding. Proc. Natl. Acad. Sci. U.S.A. 107, 20986-20991 CrossRef PubMed
-
(2010)
Proc. Natl. Acad. Sci. U.S.A.
, vol.107
, pp. 20986-20991
-
-
Romano, K.P.1
Ali, A.2
Royer, W.E.3
Schiffer, C.A.4
-
17
-
-
84867653932
-
Malarial dihydrofolate reductase as a paradigm for drug development against a resistance-compromised target
-
CrossRef PubMed
-
Yuthavong, Y., Tarnchompoo, B., Vilaivan, T., Chitnumsub, P., Kamchonwongpaisan, S., Charman, S. A., McLennan, D. N., White, K. L., Vivas, L., Bongard, E. et al. (2012) Malarial dihydrofolate reductase as a paradigm for drug development against a resistance-compromised target. Proc. Natl. Acad. Sci. U.S.A. 109, 16823-16828 CrossRef PubMed
-
(2012)
Proc. Natl. Acad. Sci. U.S.A.
, vol.109
, pp. 16823-16828
-
-
Yuthavong, Y.1
Tarnchompoo, B.2
Vilaivan, T.3
Chitnumsub, P.4
Kamchonwongpaisan, S.5
Charman, S.A.6
McLennan, D.N.7
White, K.L.8
Vivas, L.9
Bongard, E.10
-
18
-
-
84857852709
-
New targets, new hope: Novel drug targets for curbing malaria
-
CrossRef
-
Arora, N. and Banerjee, A. K. (2012) New targets, new hope: novel drug targets for curbing malaria. Mini Rev. Med. Chem. 2012, 210-226 CrossRef
-
(2012)
Mini Rev. Med. Chem.
, vol.2012
, pp. 210-226
-
-
Arora, N.1
Banerjee, A.K.2
-
19
-
-
79961240592
-
Chemical genomic profiling for antimalarial therapies, response signatures, and molecular targets
-
CrossRef PubMed
-
Yuan, J., Cheng, K. C., Johnson, R. L., Huang, R., Pattaradilokrat, S., Liu, A., Guha, R., Fidock, D. A., Inglese, J., Wellems, T. E. et al. (2011) Chemical genomic profiling for antimalarial therapies, response signatures, and molecular targets. Science 333, 724-729 CrossRef PubMed
-
(2011)
Science
, vol.333
, pp. 724-729
-
-
Yuan, J.1
Cheng, K.C.2
Johnson, R.L.3
Huang, R.4
Pattaradilokrat, S.5
Liu, A.6
Guha, R.7
Fidock, D.A.8
Inglese, J.9
Wellems, T.E.10
-
20
-
-
79959959354
-
The state of the art in anti-malaria drug discovery and development
-
CrossRef PubMed
-
Burrows, J. N., Chibale, K. and Wells, T. N. (2011) The state of the art in anti-malaria drug discovery and development. Curr. Top. Med. Chem. 11, 1226-1254 CrossRef PubMed
-
(2011)
Curr. Top. Med. Chem.
, vol.11
, pp. 1226-1254
-
-
Burrows, J.N.1
Chibale, K.2
Wells, T.N.3
-
21
-
-
77952704258
-
Thousands of chemical starting points for antimalarial lead identification
-
CrossRef PubMed
-
Gamo, F. J., Sanz, L. M., Vidal, J., de Cozar, C., Alvarez, E., Lavandera, J. L., Vanderwall, D. E., Green, D. V. S., Kumar, V., Hasan, S. et al. (2010) Thousands of chemical starting points for antimalarial lead identification. Nature 465, 305-310 CrossRef PubMed
-
(2010)
Nature
, vol.465
, pp. 305-310
-
-
Gamo, F.J.1
Sanz, L.M.2
Vidal, J.3
De Cozar, C.4
Alvarez, E.5
Lavandera, J.L.6
Vanderwall, D.E.7
Green, D.V.S.8
Kumar, V.9
Hasan, S.10
-
22
-
-
77952718950
-
Chemical genetics of Plasmodium falciparum
-
CrossRef PubMed
-
Guiguemde, W. A., Shelat, A. A., Bouck, D., Duffy, S., Crowther, G. J., Davis, P. H., Smithson, D. C., Connelly, M., Clark, J., Zhu, F. Y. et al. (2010) Chemical genetics of Plasmodium falciparum. Nature 465, 311-315 CrossRef PubMed
-
(2010)
Nature
, vol.465
, pp. 311-315
-
-
Guiguemde, W.A.1
Shelat, A.A.2
Bouck, D.3
Duffy, S.4
Crowther, G.J.5
Davis, P.H.6
Smithson, D.C.7
Connelly, M.8
Clark, J.9
Zhu, F.Y.10
-
23
-
-
77956280420
-
Spiroindolones, a potent compound class for the treatment of malaria
-
CrossRef PubMed
-
Rottmann, M., McNamara, C., Yeung, B. K. S., Lee, M. C. S., Zou, B., Russell, B., Seitz, P., Plouffe, D. M., Dharia, N. V., Tan, J. et al. (2010) Spiroindolones, a potent compound class for the treatment of malaria. Science 329, 1175-1180 CrossRef PubMed
-
(2010)
Science
, vol.329
, pp. 1175-1180
-
-
Rottmann, M.1
McNamara, C.2
Yeung, B.K.S.3
Lee, M.C.S.4
Zou, B.5
Russell, B.6
Seitz, P.7
Plouffe, D.M.8
Dharia, N.V.9
Tan, J.10
-
24
-
-
7644226738
-
Primaquine therapy for malaria
-
DOI 10.1086/424663
-
Baird, J. K. and Hoffman, S. L. (2004) Primaquine therapy for malaria. Clin. Infect. Dis. 39, 1336-1345 CrossRef PubMed (Pubitemid 39458520)
-
(2004)
Clinical Infectious Diseases
, vol.39
, Issue.9
, pp. 1336-1345
-
-
Baird, J.K.1
Hoffman, S.L.2
-
25
-
-
70350784153
-
A pre-emptive strike against malaria's stealthy hepatic forms
-
CrossRef PubMed
-
Mazier, D., Renia, L. and Snounou, G. (2009) A pre-emptive strike against malaria's stealthy hepatic forms. Nat. Rev. Drug Discov. 8, 854-864 CrossRef PubMed
-
(2009)
Nat. Rev. Drug Discov.
, vol.8
, pp. 854-864
-
-
Mazier, D.1
Renia, L.2
Snounou, G.3
-
26
-
-
80053494971
-
The next opportunity in anti-malaria drug discovery: The liver stage
-
CrossRef PubMed
-
Derbyshire, E. R., Mota, M. M. and Clardy, J. (2011) The next opportunity in anti-malaria drug discovery: the liver stage. PLoS Pathog. 7, e1002178 CrossRef PubMed
-
(2011)
PLoS Pathog.
, vol.7
-
-
Derbyshire, E.R.1
Mota, M.M.2
Clardy, J.3
-
27
-
-
70449100668
-
Redefining the role of de novo fatty acid synthesis in Plasmodium parasites
-
CrossRef PubMed
-
Tarun, A. S., Vaughan, A. M. and Kappe, S. H. I. (2009) Redefining the role of de novo fatty acid synthesis in Plasmodium parasites. Trends Parasitol. 25, 545-550 CrossRef PubMed
-
(2009)
Trends Parasitol.
, vol.25
, pp. 545-550
-
-
Tarun, A.S.1
Vaughan, A.M.2
Kappe, S.H.I.3
-
28
-
-
59849125892
-
Type II fatty acid synthesis is essential only for malaria parasite late liver stage development
-
CrossRef PubMed
-
Vaughan, A. M., O'Neill, M. T., Tarun, A. S., Camargo, N., Phuong, T. M., Aly, A. S. I., Cowman, A. F. and Kappe, S. H. I. (2009) Type II fatty acid synthesis is essential only for malaria parasite late liver stage development. Cell. Microbiol. 11, 506-520 CrossRef PubMed
-
(2009)
Cell. Microbiol.
, vol.11
, pp. 506-520
-
-
Vaughan, A.M.1
O'Neill, M.T.2
Tarun, A.S.3
Camargo, N.4
Phuong, T.M.5
Aly, A.S.I.6
Cowman, A.F.7
Kappe, S.H.I.8
-
29
-
-
50849119416
-
The caspase-1 inflammasome: A pilot of innate immune responses
-
CrossRef PubMed
-
Yu, H. B. and Finlay, B. B. (2008) The caspase-1 inflammasome: a pilot of innate immune responses. Cell Host Microbe 4, 198-208 CrossRef PubMed
-
(2008)
Cell Host Microbe
, vol.4
, pp. 198-208
-
-
Yu, H.B.1
Finlay, B.B.2
-
30
-
-
58149114916
-
Mechanical features of Plasmodium falciparum acyl carrier protein in the delivery of substrates
-
CrossRef PubMed
-
Colizzi, F., Recanatini, M. and Cavalli, A. (2008) Mechanical features of Plasmodium falciparum acyl carrier protein in the delivery of substrates. J. Chem. Inf. Model. 48, 2289-2293 CrossRef PubMed
-
(2008)
J. Chem. Inf. Model.
, vol.48
, pp. 2289-2293
-
-
Colizzi, F.1
Recanatini, M.2
Cavalli, A.3
-
31
-
-
57049083416
-
The multienzyme architecture of eukaryotic fatty acid synthases
-
CrossRef PubMed
-
Leibundgut, M., Maier, T., Jenni, S. and Ban, N. (2008) The multienzyme architecture of eukaryotic fatty acid synthases. Curr. Opin. Struct. Biol. 18, 714-725 CrossRef PubMed
-
(2008)
Curr. Opin. Struct. Biol.
, vol.18
, pp. 714-725
-
-
Leibundgut, M.1
Maier, T.2
Jenni, S.3
Ban, N.4
-
32
-
-
0030581109
-
Escherichia coli as a model for the regulation of dissociable (type II) fatty acid biosynthesis
-
DOI 10.1016/0005-2760(96)00056-2
-
Rock, C. O. and Cronan, J. E. (1996) Escherichia coli as a model for the regulation of dissociable (type II) fatty acid biosynthesis. Biochim. Biophys. Acta 1302, 1-16 CrossRef PubMed (Pubitemid 26267038)
-
(1996)
Biochimica et Biophysica Acta - Lipids and Lipid Metabolism
, vol.1302
, Issue.1
, pp. 1-16
-
-
Rock, C.O.1
Cronan, J.E.2
-
33
-
-
9144226932
-
FAS't inhibition of malaria
-
CrossRef PubMed
-
Surolia, A., Ramya, T. N. C., Ramya, V. and Surolia, N. (2004) FAS't inhibition of malaria. Biochem. J. 383, 401-412 CrossRef PubMed
-
(2004)
Biochem. J.
, vol.383
, pp. 401-412
-
-
Surolia, A.1
Ramya, T.N.C.2
Ramya, V.3
Surolia, N.4
-
34
-
-
41949086428
-
Structural basis for catalytic and inhibitory mechanisms of β-hydroxyacyl-acyl carrier protein dehydratase (FabZ)
-
CrossRef PubMed
-
Zhang, L., Liu, W. Z., Hu, T. C., Du, L., Luo, C., Chen, K. X., Shen, X. and Jiang, H. L. (2008) Structural basis for catalytic and inhibitory mechanisms of β-hydroxyacyl-acyl carrier protein dehydratase (FabZ). J. Biol. Chem. 283, 5370-5379 CrossRef PubMed
-
(2008)
J. Biol. Chem.
, vol.283
, pp. 5370-5379
-
-
Zhang, L.1
Liu, W.Z.2
Hu, T.C.3
Du, L.4
Luo, C.5
Chen, K.X.6
Shen, X.7
Jiang, H.L.8
-
35
-
-
22544476228
-
The crystal structure of PfFabZ, the unique β-hydroxyacyl-ACP dehydratase involved in fatty acid biosynthesis of Plasmodium falciparum
-
DOI 10.1110/ps.051373005
-
Kostrewa, D., Winkler, F. K., Folkers, G., Scapozza, L. and Perozzo, R. (2005) The crystal structure of PfFabZ, the unique β-hydroxyacyl-ACP dehydratase involved in fatty acid biosynthesis of Plasmodium falciparum. Protein Sci. 14, 1570-1580 CrossRef PubMed (Pubitemid 41014815)
-
(2005)
Protein Science
, vol.14
, Issue.6
, pp. 1570-1580
-
-
Kostrewa, D.1
Winkler, F.K.2
Folkers, G.3
Scapozza, L.4
Perozzo, R.5
-
36
-
-
33646203969
-
Crystal structure of dimeric FabZ of Plasmodium falciparum reveals conformational switching to active hexamers by peptide flips
-
CrossRef PubMed
-
Swarnamukhi, P. L., Sharma, S. K., Bajaj, P., Surolia, N., Surolia, A. and Suguna, K. (2006) Crystal structure of dimeric FabZ of Plasmodium falciparum reveals conformational switching to active hexamers by peptide flips. FEBS Lett. 580, 2653-2660 CrossRef PubMed
-
(2006)
FEBS Lett.
, vol.580
, pp. 2653-2660
-
-
Swarnamukhi, P.L.1
Sharma, S.K.2
Bajaj, P.3
Surolia, N.4
Surolia, A.5
Suguna, K.6
-
37
-
-
0242580787
-
Identification, Characterization, and Inhibition of Plasmodium falciparum β-Hydroxyacyl-Acyl Carrier Protein Dehydratase (FabZ)
-
DOI 10.1074/jbc.M304283200
-
Sharma, S. K., Kapoor, M., Ramya, T. N. C., Kumar, S., Kumar, G., Modak, R., Sharma, S., Surolia, N. and Surolia, A. (2003) Identification, characterization, and inhibition of Plasmodium falciparum β-hydroxyacyl- acyl carrier protein dehydratase (FabZ). J. Biol. Chem. 278, 45661-45671 CrossRef PubMed (Pubitemid 37432708)
-
(2003)
Journal of Biological Chemistry
, vol.278
, Issue.46
, pp. 45661-45671
-
-
Sharma, S.K.1
Kapoor, M.2
Ramya, T.N.C.3
Kumar, S.4
Kumar, G.5
Modak, R.6
Sharma, S.7
Surolia, N.8
Surolia, A.9
-
38
-
-
51149120354
-
Synthesis and biological evaluation of NAS-21 and NAS-91 analogues as potential inhibitors of the mycobacterial FAS-II dehydratase enzyme Rv0636
-
CrossRef PubMed
-
Bhowruth, V., Brown, A. K. and Besra, G. S. (2008) Synthesis and biological evaluation of NAS-21 and NAS-91 analogues as potential inhibitors of the mycobacterial FAS-II dehydratase enzyme Rv0636. Microbiology 154, 1866-1875 CrossRef PubMed
-
(2008)
Microbiology
, vol.154
, pp. 1866-1875
-
-
Bhowruth, V.1
Brown, A.K.2
Besra, G.S.3
-
39
-
-
40549088222
-
Antimycobacterial activity and mechanism of action of NAS-91
-
DOI 10.1128/AAC.00968-07
-
Gratraud, P., Surolia, N., Besra, G. S., Surolia, A. and Kremer, L. (2008) Antimycobacterial activity and mechanism of action of NAS-91. Antimicrob. Agents Chemother. 52, 1162-1166 CrossRef PubMed (Pubitemid 351358407)
-
(2008)
Antimicrobial Agents and Chemotherapy
, vol.52
, Issue.3
, pp. 1162-1166
-
-
Gratraud, P.1
Surolia, N.2
Besra, G.S.3
Surolia, A.4
Kremer, L.5
-
40
-
-
84860390428
-
Structural basis for the functional and inhibitory mechanisms of β-hydroxyacyl-acyl carrier protein dehydratase (FabZ) of Plasmodium falciparum
-
CrossRef PubMed
-
Maity, K., Venkata, B. S., Kapoor, N., Surolia, N., Surolia, A. and Suguna, K. (2011) Structural basis for the functional and inhibitory mechanisms of β-hydroxyacyl-acyl carrier protein dehydratase (FabZ) of Plasmodium falciparum. J. Struct. Biol. 176, 238-249 CrossRef PubMed
-
(2011)
J. Struct. Biol.
, vol.176
, pp. 238-249
-
-
Maity, K.1
Venkata, B.S.2
Kapoor, N.3
Surolia, N.4
Surolia, A.5
Suguna, K.6
-
41
-
-
33744819176
-
Inhibition of Plasmodium falciparum fatty acid biosynthesis: Evaluation of FabG, FabZ, and FabI as drug targets for flavonoids
-
DOI 10.1021/jm0600545
-
Tasdemir, D., Lack, G., Brun, R., Ruedi, P., Scapozza, L. and Perozzo, R. (2006) Inhibition of Plasmodium falciparum fatty acid biosynthesis: evaluation of FabG, FabZ, and FabI as drug targets for flavonoids. J. Med. Chem. 49, 3345-3353 CrossRef PubMed (Pubitemid 43830532)
-
(2006)
Journal of Medicinal Chemistry
, vol.49
, Issue.11
, pp. 3345-3353
-
-
Tasdemir, D.1
Lack, G.2
Brun, R.3
Ruedi, P.4
Scapozza, L.5
Perozzo, R.6
-
42
-
-
0035126479
-
Triclosan offers protection against blood stages of malaria by inhibiting enoyl-ACP reductase of Plasmodium falciparum
-
DOI 10.1038/84612
-
Surolia, N. and Surolia, A. (2001) Triclosan offers protection against blood stages of malaria by inhibiting enoyl-ACP reductase of Plasmodium falciparum. Nat. Med. 7, 167-173 CrossRef PubMed (Pubitemid 32148482)
-
(2001)
Nature Medicine
, vol.7
, Issue.2
, pp. 167-173
-
-
Surolia, N.1
Surolia, A.2
-
43
-
-
0037066782
-
Structural elucidation of the specificity of the antibacterial agent triclosan for malarial enoyl acyl carrier protein reductase
-
DOI 10.1074/jbc.M112000200
-
Perozzo, R., Kuo, M., Sidhu, A. B. S., Valiyaveettil, J. T., Bittman, R., Jacobs, W. R., Fidock, D. A. and Sacchettini, J. C. (2002) Structural elucidation of the specificity of the antibacterial agent triclosan for malarial enoyl acyl carrier protein reductase. J. Biol. Chem. 277, 13106-13114 CrossRef PubMed (Pubitemid 34952681)
-
(2002)
Journal of Biological Chemistry
, vol.277
, Issue.15
, pp. 13106-13114
-
-
Perozzo, R.1
Kuo, M.2
Sidhu, A.B.S.3
Valiyaveettil, J.T.4
Bittman, R.5
Jacobs Jr., W.R.6
Fidock, D.A.7
Sacchettini, J.C.8
-
44
-
-
33750036420
-
Novel diphenyl ethers: Design, docking studies, synthesis and inhibition of enoyl ACP reductase of Plasmodium falciparum and Escherichia coli
-
DOI 10.1016/j.bmc.2006.07.034, PII S0968089606005888
-
Chhibber, M., Kurnara, G., Parasuraman, P., Ramya, T. N. C., Surolia, N. and Surolia, A. (2006) Novel diphenyl ethers: design, docking studies, synthesis and inhibition of enoyl ACP reductase of Plasmodium falciparum and Escherichia coli. Bioorg. Med. Chem. 14, 8086-8098 CrossRef PubMed (Pubitemid 44584690)
-
(2006)
Bioorganic and Medicinal Chemistry
, vol.14
, Issue.23
, pp. 8086-8098
-
-
Chhibber, M.1
Kumar, G.2
Parasuraman, P.3
Ramya, T.N.C.4
Surolia, N.5
Surolia, A.6
-
45
-
-
26844461350
-
Synthesis, biological activity, and X-ray crystal structural analysis of diaryl ether inhibitors of malarial enoyl acyl carrier protein reductase. Part 1: 4′-Substituted triclosan derivatives
-
DOI 10.1016/j.bmcl.2005.08.044, PII S0960894X05010796
-
Freundlich, J. S., Anderson, J. W., Sarantakis, D., Shieh, H. M., Yu, M., Valderramos, J. C., Lucumi, E., Kuo, M., Jacobs, W. R., Fidock, D. A. et al. (2005) Synthesis, biological activity, and X-ray crystal structural analysis of diaryl ether inhibitors of malarial enoyl acyl carrier protein reductase. Part 1: 4′-substituted triclosan derivatives. Bioorg. Med. Chem. Lett. 15, 5247-5252 CrossRef PubMed (Pubitemid 41463657)
-
(2005)
Bioorganic and Medicinal Chemistry Letters
, vol.15
, Issue.23
, pp. 5247-5252
-
-
Freundlich, J.S.1
Anderson, J.W.2
Sarantakis, D.3
Shieh, H.-M.4
Yu, M.5
Valderramos, J.-C.6
Lucumi, E.7
Kuo, M.8
Jacobs Jr., W.R.9
Fidock, D.A.10
Schiehser, G.A.11
Jacobus, D.P.12
Sacchettini, J.C.13
-
46
-
-
33644802299
-
Synthesis and biological activity of diaryl ether inhibitors of malarial enoyl acyl carrier protein reductase. Part 2: 2′-Substituted triclosan derivatives
-
DOI 10.1016/j.bmcl.2006.01.051, PII S0960894X06000941
-
Freundlich, J. S., Yu, M., Lucumi, E., Kuo, M., Tsai, H. C., Valderramos, J. C., Karagyozov, L., Jacobs, W. R., Schiehser, G. A., Fidock, D. A. et al. (2006) Synthesis and biological activity of diaryl ether inhibitors of malarial enoyl acyl carrier protein reductase. Part 2: 2′-substituted triclosan derivatives. Bioorg. Med. Chem. Lett. 16, 2163-2169 CrossRef PubMed (Pubitemid 43351071)
-
(2006)
Bioorganic and Medicinal Chemistry Letters
, vol.16
, Issue.8
, pp. 2163-2169
-
-
Freundlich, J.S.1
Yu, M.2
Lucumi, E.3
Kuo, M.4
Tsai, H.-C.5
Valderramos, J.-C.6
Karagyozov, L.7
Jacobs Jr., W.R.8
Schiehser, G.A.9
Fidock, D.A.10
Jacobus, D.P.11
Sacchettini, J.C.12
-
47
-
-
77953581267
-
X-ray crystallographic analysis of the complexes of enoyl acyl carrier protein reductase of Plasmodium falciparum with triclosan variants to elucidate the importance of different functional groups in enzyme inhibition
-
PubMed
-
Maity, K., Bhargav, S. P., Sankaran, B., Surolia, N., Surolia, A. and Suguna, K. (2010) X-ray crystallographic analysis of the complexes of enoyl acyl carrier protein reductase of Plasmodium falciparum with triclosan variants to elucidate the importance of different functional groups in enzyme inhibition. IUBMB Life 62, 467-476 PubMed
-
(2010)
IUBMB Life
, vol.62
, pp. 467-476
-
-
Maity, K.1
Bhargav, S.P.2
Sankaran, B.3
Surolia, N.4
Surolia, A.5
Suguna, K.6
-
48
-
-
84885671430
-
Design, synthesis, and biological and crystallographic evaluation of novel inhibitors of Plasmodium falciparum enoyl-ACP-reductase (PfFabl)
-
CrossRef PubMed
-
Belluti, F., Perozzo, R., Lauciello, L., Colizzi, F., Kostrewa, D., Bisi, A., Gobbi, S., Rampa, A., Bolognesi, M. L., Recanatini, M. et al. (2013) Design, synthesis, and biological and crystallographic evaluation of novel inhibitors of Plasmodium falciparum enoyl-ACP-reductase (PfFabl). J. Med. Chem. 56, 7516-7526 CrossRef PubMed
-
(2013)
J. Med. Chem.
, vol.56
, pp. 7516-7526
-
-
Belluti, F.1
Perozzo, R.2
Lauciello, L.3
Colizzi, F.4
Kostrewa, D.5
Bisi, A.6
Gobbi, S.7
Rampa, A.8
Bolognesi, M.L.9
Recanatini, M.10
-
49
-
-
4243159924
-
Privileged structures: Applications in drug discovery
-
DeSimone, R. W., Currie, K. S., Mitchell, S. A., Darrow, J. W. and Pippin, D. A. (2004) Privileged structures: applications in drug discovery. Comb. Chem. High Throughput Screen. 7, 473-493 CrossRef PubMed (Pubitemid 39108267)
-
(2004)
Combinatorial Chemistry and High Throughput Screening
, vol.7
, Issue.5
, pp. 473-493
-
-
DeSimone, R.W.1
Currie, K.S.2
Mitchell, S.A.3
Darrow, J.W.4
Pippin, D.A.5
-
50
-
-
0037076321
-
Structure of 2C-methyl-D-erythritol 2,4-cyclodiphosphate synthase: An essential enzyme for isoprenoid biosynthesis and target for antimicrobial drug development
-
DOI 10.1073/pnas.102679799
-
Kemp, L. E., Bond, C. S. and Hunter, W. N. (2002) Structure of 2C-methyl-D-erythritol 2,4-cyclodiphosphate synthase: an essential enzyme for isoprenoid biosynthesis and target for antimicrobial drug development. Proc. Natl. Acad. Sci. U.S.A. 99, 6591-6596 CrossRef PubMed (Pubitemid 34526177)
-
(2002)
Proceedings of the National Academy of Sciences of the United States of America
, vol.99
, Issue.10
, pp. 6591-6596
-
-
Kemp, L.E.1
Bond, C.S.2
Hunter, W.N.3
-
51
-
-
0026639957
-
Sterol molecule: Structure, biosynthesis, and function
-
CrossRef PubMed
-
Bloch, K. (1992) Sterol molecule: structure, biosynthesis, and function. Steroids 57, 378-383 CrossRef PubMed
-
(1992)
Steroids
, vol.57
, pp. 378-383
-
-
Bloch, K.1
-
52
-
-
0027368126
-
Isoprenoid biosynthesis in bacteria: A novel pathway for the early steps leading to isopentenyl diphosphate
-
Rohmer, M., Knani, M., Simonin, P., Sutter, B. and Sahm, H. (1993) Isoprenoid biosynthesis in bacteria: a novel pathway for the early steps leading to isopentenyl diphosphate. Biochem. J. 295, 517-524 PubMed (Pubitemid 23315192)
-
(1993)
Biochemical Journal
, vol.295
, Issue.2
, pp. 517-524
-
-
Rohmer, M.1
Knani, M.2
Simonin, P.3
Sutter, B.4
Sahm, H.5
-
53
-
-
0032170425
-
The deoxyxylulose phosphate pathway of terpenoid biosynthesis in plants and microorganisms
-
Eisenreich, W., Schwarz, M., Cartayrade, A., Arigoni, D., Zenk, M. H. and Bacher, A. (1998) The deoxyxylulose phosphate pathway of terpenoid biosynthesis in plants and microorganisms. Chem. Biol. 5, R221-R233 CrossRef PubMed (Pubitemid 28436724)
-
(1998)
Chemistry and Biology
, vol.5
, Issue.9
-
-
Eisenreich, W.1
Schwarz, M.2
Cartayrade, A.3
Arigoni, D.4
Zenk, M.H.5
Bacher, A.6
-
54
-
-
74849090103
-
Functional genetic analysis of the Plasmodium falciparum deoxyxylulose 5-phosphate reductoisomerase gene
-
CrossRef PubMed
-
Odom, A. R. and Van Voorhis, W. C. (2010) Functional genetic analysis of the Plasmodium falciparum deoxyxylulose 5-phosphate reductoisomerase gene. Mol. Biochem. Parasitol. 170, 108-111 CrossRef PubMed
-
(2010)
Mol. Biochem. Parasitol.
, vol.170
, pp. 108-111
-
-
Odom, A.R.1
Van Voorhis, W.C.2
-
55
-
-
0033520336
-
Inhibitors of the nonmevalonate pathway of isoprenoid biosynthesis as antimalarial drugs
-
DOI 10.1126/science.285.5433.1573
-
Jomaa, H., Wiesner, J., Sanderbrand, S., Altincicek, B., Weidemeyer, C., Hintz, M., Turbachova, I., Eberl, M., Zeidler, J., Lichtenthaler, H. K. et al. (1999) Inhibitors of the nonmevalonate pathway of isoprenoid biosynthesis as antimalarial drugs. Science 285, 1573-1576 CrossRef PubMed (Pubitemid 29420582)
-
(1999)
Science
, vol.285
, Issue.5433
, pp. 1573-1576
-
-
Jomaa, H.1
Wiesner, J.2
Sanderbrand, S.3
Altincicek, B.4
Weidemeyer, C.5
Hintz, M.6
Turbachova, I.7
Eberl, M.8
Zeidler, J.9
Lichtenthaler, H.K.10
Soldati, D.11
Beck, E.12
-
56
-
-
0033179512
-
Active isoprenoid pathway in the intra-erythrocytic stages of Plasmodium falciparum: Presence of dolichols of 11 and 12 isoprene units
-
DOI 10.1042/0264-6021:3410629
-
Couto, A. S., Kimura, E. A., Peres, V. J., Uhrig, M. L. and Katzin, A. M. (1999) Active isoprenoid pathway in the intra-erythrocytic stages of Plasmodium falciparum: presence of dolichols of 11 and 12 isoprene units. Biochem. J. 341, 629-637 CrossRef PubMed (Pubitemid 29389193)
-
(1999)
Biochemical Journal
, vol.341
, Issue.3
, pp. 629-637
-
-
Couto, A.S.1
Kimura, E.A.2
Peres, V.J.3
Uhrig, M.L.4
Katzin, A.M.5
-
57
-
-
0019257557
-
Studies on new phosphonic acid antibiotics. II. Taxonomic studies on producing organisms of the phosphonic acid and related compounds
-
Iguchi, E., Okuhara, M., Kohsaka, M., Aoki, H. and Imanaka, H. (1980) Studies on new phosphonic acid antibiotics. 2. Taxonomic studies on producing organisms of the phosphonic acid and related-compounds. J. Antibiot. 33, 18-23 CrossRef (Pubitemid 11135303)
-
(1980)
Journal of Antibiotics
, vol.33
, Issue.1
, pp. 18-23
-
-
Iguchi, E.1
Okuhara, M.2
Kohsaka, M.3
-
58
-
-
0037079323
-
Fosmidomycin for malaria
-
DOI 10.1016/S0140-6736(02)11860-5
-
Missinou, M. A., Borrmann, S., Schindler, A., Issifou, S., Adegnika, A. A., Matsiegui, P. B., Binder, R., Lell, B., Wiesner, J., Baranek, T. et al. (2002) Fosmidomycin for malaria. Lancet 360, 1941-1942 CrossRef PubMed (Pubitemid 35472137)
-
(2002)
Lancet
, vol.360
, Issue.9349
, pp. 1941-1942
-
-
Missinou, M.A.1
Borrmann, S.2
Schindler, A.3
Issifou, S.4
Adegnika, A.A.5
Matsiegui, P.-B.6
Binder, R.7
Lell, B.8
Wiesner, J.9
Baranek, T.10
Jomaa, H.11
Kremsner, P.G.12
-
59
-
-
0037308581
-
Fosmidomycin, a novel chemotherapeutic agent for malaria
-
DOI 10.1128/AAC.47.2.735-738.2003
-
Lell, B., Ruangweerayut, R., Wiesner, J., Missinou, M. A., Schindler, A., Baranek, T., Hintz, M., Hutchinson, D., Jomaa, H. and Kremsner, P. G. (2003) Fosmidomycin, a novel chemotherapeutic agent for malaria. Antimicrob. Agents Chemother. 47, 735-738 CrossRef PubMed (Pubitemid 36158108)
-
(2003)
Antimicrobial Agents and Chemotherapy
, vol.47
, Issue.2
, pp. 735-738
-
-
Lell, B.1
Ruangweerayut, R.2
Wiesner, J.3
Missinou, M.A.4
Schindler, A.5
Baranek, T.6
Hintz, M.7
Hutchinson, D.8
Jomaa, H.9
Kremsner, P.G.10
-
60
-
-
6944247618
-
Fosmidomycin-clindamycin for the treatment of Plasmodium falciparum malaria
-
DOI 10.1086/424603
-
Borrmann, S., Issifou, S., Esser, G., Adegnika, A. A., Ramharter, M., Matsiegui, P. B., Oyakhirome, S., Mawili-Mboumba, D. P., Missinou, M. A., Kun, J. F. J. et al. (2004) Fosmidomycin-clindamycin for the treatment of Plasmodium falciparum malaria. J. Infect. Dis. 190, 1534-1540 CrossRef PubMed (Pubitemid 39411000)
-
(2004)
Journal of Infectious Diseases
, vol.190
, Issue.9
, pp. 1534-1540
-
-
Borrmann, S.1
Issifou, S.2
Esser, G.3
Adegnika, A.A.4
Ramharter, M.5
Matsiegui, P.-B.6
Oyakhirome, S.7
Mawili-Mboumba, D.P.8
Missinou, M.A.9
Kun, J.F.J.10
Jomaa, H.11
Kremsner, P.G.12
-
61
-
-
40949137369
-
Synthesis of β- and γ-oxa isosteres of fosmidomycin and FR900098 as antimalarial candidates
-
DOI 10.1016/j.bmc.2007.12.001, PII S0968089607010516
-
Haemers, T., Wiesner, J., Giessmann, D., Verbrugghen, T., Hillaert, U., Ortmann, R., Jomaa, H., Link, A., Schlitzer, M. and Van Calenbergh, S. (2008) Synthesis of β- and γ-oxa isosteres of fosmidomycin and FR900098 as antimalarial candidates. Bioorg. Med. Chem. 16, 3361-3371 CrossRef PubMed (Pubitemid 351418172)
-
(2008)
Bioorganic and Medicinal Chemistry
, vol.16
, Issue.6
, pp. 3361-3371
-
-
Haemers, T.1
Wiesner, J.2
Giessmann, D.3
Verbrugghen, T.4
Hillaert, U.5
Ortmann, R.6
Jomaa, H.7
Link, A.8
Schlitzer, M.9
Van Calenbergh, S.10
-
62
-
-
84873951765
-
Antimalarial and structural studies of pyridine-containing inhibitors of 1-deoxyxylulose-5-phosphate reductoisomerase
-
CrossRef PubMed
-
Xue, J., Diao, J. S., Cai, G. B., Deng, L. S., Zheng, B. S., Yao, Y. and Song, Y. C. (2013) Antimalarial and structural studies of pyridine-containing inhibitors of 1-deoxyxylulose-5-phosphate reductoisomerase. ACS Med. Chem. Lett. 4, 278-282 CrossRef PubMed
-
(2013)
ACS Med. Chem. Lett.
, vol.4
, pp. 278-282
-
-
Xue, J.1
Diao, J.S.2
Cai, G.B.3
Deng, L.S.4
Zheng, B.S.5
Yao, Y.6
Song, Y.C.7
-
63
-
-
84856430758
-
Molecular basis of fosmidomycin's action on the human malaria parasite Plasmodium falciparum
-
CrossRef PubMed
-
Umeda, T., Tanaka, N., Kusakabe, Y., Nakanishi, M., Kitade, Y. and Nakamura, K. T. (2011) Molecular basis of fosmidomycin's action on the human malaria parasite Plasmodium falciparum. Sci. Rep. 1, 9 CrossRef PubMed
-
(2011)
Sci. Rep.
, vol.1
, pp. 9
-
-
Umeda, T.1
Tanaka, N.2
Kusakabe, Y.3
Nakanishi, M.4
Kitade, Y.5
Nakamura, K.T.6
-
64
-
-
80053909858
-
Reverse fosmidomycin derivatives against the antimalarial drug target IspC (Dxr)
-
CrossRef PubMed
-
Behrendt, C. T., Kunfermann, A., Illarionova, V., Matheeussen, A., Pein, M. K., Grawert, T., Kaiser, J., Bacher, A., Eisenreich, W., Illarionov, B. et al. (2011) Reverse fosmidomycin derivatives against the antimalarial drug target IspC (Dxr). J. Med. Chem. 54, 6796-6802 CrossRef PubMed
-
(2011)
J. Med. Chem.
, vol.54
, pp. 6796-6802
-
-
Behrendt, C.T.1
Kunfermann, A.2
Illarionova, V.3
Matheeussen, A.4
Pein, M.K.5
Grawert, T.6
Kaiser, J.7
Bacher, A.8
Eisenreich, W.9
Illarionov, B.10
-
65
-
-
79951532785
-
Structures of 1-deoxy-D-xylulose-5-phosphate reductoisomerase/lipophilic phosphonate complexes
-
CrossRef PubMed
-
Deng, L. S., Endo, K., Kato, M., Cheng, G., Yajima, S. and Song, Y. C. (2011) Structures of 1-deoxy-D-xylulose-5-phosphate reductoisomerase/lipophilic phosphonate complexes. ACS Med. Chem. Lett. 2, 165-170 CrossRef PubMed
-
(2011)
ACS Med. Chem. Lett.
, vol.2
, pp. 165-170
-
-
Deng, L.S.1
Endo, K.2
Kato, M.3
Cheng, G.4
Yajima, S.5
Song, Y.C.6
-
66
-
-
84886539599
-
IspC as target for antiinfective drug discovery: Synthesis, enantiomeric separation, and structural biology of fosmidomycin thia isosters
-
CrossRef PubMed
-
Kunfermann, A., Lienau, C., Illarionov, B., Held, J., Grawert, T., Behrendt, C. T., Werner, P., Hahn, S., Eisenreich, W., Riederer, U. et al. (2013) IspC as target for antiinfective drug discovery: synthesis, enantiomeric separation, and structural biology of fosmidomycin thia isosters. J. Med. Chem. 56, 8151-8162 CrossRef PubMed
-
(2013)
J. Med. Chem.
, vol.56
, pp. 8151-8162
-
-
Kunfermann, A.1
Lienau, C.2
Illarionov, B.3
Held, J.4
Grawert, T.5
Behrendt, C.T.6
Werner, P.7
Hahn, S.8
Eisenreich, W.9
Riederer, U.10
-
67
-
-
0034628578
-
Antimalarial activity of compounds interfering with Plasmodium falciparum phospholipid metabolism: Comparison between mono- and bisquaternary ammonium salts
-
DOI 10.1021/jm9911027
-
Calas, M., Ancelin, M. L., Cordina, G., Portefaix, P., Piquet, G., Vidal-Sailhan, V. and Vial, H. (2000) Antimalarial activity of compounds interfering with Plasmodium falciparum phospholipid metabolism: comparison between mono- and bisquaternary ammonium salts. J. Med. Chem. 43, 505-516 CrossRef PubMed (Pubitemid 30102090)
-
(2000)
Journal of Medicinal Chemistry
, vol.43
, Issue.3
, pp. 505-516
-
-
Calas, M.1
Ancelin, M.L.2
Cordina, G.3
Portefaix, P.4
Piquet, G.5
Vidal-Sailhan, V.6
Vial, H.7
-
68
-
-
0037083529
-
A class of potent antimalarials and their specific accumulation in infected erythrocytes
-
DOI 10.1126/science.1067236
-
Wengelnik, K., Vidal, V., Ancelin, M. L., Cathiard, A. M., Morgat, J. L., Kocken, C. H., Calas, M., Herrera, S., Thomas, A. W. and Vial, H. J. (2002) A class of potent antimalarials and their specific accumulation in infected erythrocytes. Science 295, 1311-1314 CrossRef PubMed (Pubitemid 34157625)
-
(2002)
Science
, vol.295
, Issue.5558
, pp. 1311-1314
-
-
Wengelnik, K.1
Vidal, V.2
Ancelin, M.L.3
Cathiard, A.-M.4
Morgat, J.L.5
Kocken, C.H.6
Calas, M.7
Herrera, S.8
Thomas, A.W.9
Vial, H.J.10
-
69
-
-
55549143016
-
Disruption of the Plasmodium falciparum PfPMT gene results in a complete loss of phosphatidylcholine biosynthesis via the serine-decarboxylase- phosphoethanolamine-methyltransferase pathway and severe growth and survival defects
-
CrossRef PubMed
-
Witola, W. H., El Bissati, K., Pessi, G., Xie, C., Roepe, P. D. and Ben Mamoun, C. (2008) Disruption of the Plasmodium falciparum PfPMT gene results in a complete loss of phosphatidylcholine biosynthesis via the serine- decarboxylase-phosphoethanolamine-methyltransferase pathway and severe growth and survival defects. J. Biol. Chem. 283, 27636-27643 CrossRef PubMed
-
(2008)
J. Biol. Chem.
, vol.283
, pp. 27636-27643
-
-
Witola, W.H.1
El Bissati, K.2
Pessi, G.3
Xie, C.4
Roepe, P.D.5
Ben Mamoun, C.6
-
70
-
-
16844367110
-
In vivo evidence for the specificity of Plasmodium falciparum phosphoethanolamine methyltransferase and its coupling to the Kennedy pathway
-
CrossRef PubMed
-
Pessi, G., Choi, J. Y., Reynolds, J. M., Voelker, D. R. and Ben Mamoun, C. (2005) In vivo evidence for the specificity of Plasmodium falciparum phosphoethanolamine methyltransferase and its coupling to the Kennedy pathway. J. Biol. Chem. 280, 12461-12466 CrossRef PubMed
-
(2005)
J. Biol. Chem.
, vol.280
, pp. 12461-12466
-
-
Pessi, G.1
Choi, J.Y.2
Reynolds, J.M.3
Voelker, D.R.4
Ben Mamoun, C.5
-
71
-
-
43149112081
-
Biochemical and genetic analysis of the phosphoethanolamine methyltransferase of the human malaria parasite Plasmodium falciparum
-
CrossRef PubMed
-
Reynolds, J. M., Takebe, S., Choi, J. Y., El Bissati, K., Witola, W. H., Bobenchik, A. M., Hoch, J. C., Voelker, D. R. and Ben Mamoun, C. (2008) Biochemical and genetic analysis of the phosphoethanolamine methyltransferase of the human malaria parasite Plasmodium falciparum. J. Biol. Chem. 283, 7894-7900 CrossRef PubMed
-
(2008)
J. Biol. Chem.
, vol.283
, pp. 7894-7900
-
-
Reynolds, J.M.1
Takebe, S.2
Choi, J.Y.3
El Bissati, K.4
Witola, W.H.5
Bobenchik, A.M.6
Hoch, J.C.7
Voelker, D.R.8
Ben Mamoun, C.9
-
72
-
-
1942437433
-
A pathway for phosphatidylcholine biosynthesis in Plasmodium falciparum involving phosphoethanolamine methylation
-
DOI 10.1073/pnas.0307742101
-
Pessi, G., Kociubinski, G. and Ben Mamoun, C. (2004) A pathway for phosphatidylcholine biosynthesis in Plasmodium falciparum involving phosphoethanolamine methylation. Proc. Natl. Acad. Sci. U.S.A. 101, 6206-6211 CrossRef PubMed (Pubitemid 38520552)
-
(2004)
Proceedings of the National Academy of Sciences of the United States of America
, vol.101
, Issue.16
, pp. 6206-6211
-
-
Pessi, G.1
Kociubinski, G.2
Ben, M.C.3
-
73
-
-
79958025884
-
Phosphoethanolamine methyltransferases in phosphocholine biosynthesis: Functions and potential for antiparasite therapy
-
CrossRef
-
Bobenchik, A. M., Augagneur, Y., Hao, B., Hoch, J. C. and Ben Mamoun, C. (2011) Phosphoethanolamine methyltransferases in phosphocholine biosynthesis: functions and potential for antiparasite therapy. FEMS Microbiol. Immunol. 35, 609-619 CrossRef
-
(2011)
FEMS Microbiol. Immunol.
, vol.35
, pp. 609-619
-
-
Bobenchik, A.M.1
Augagneur, Y.2
Hao, B.3
Hoch, J.C.4
Ben Mamoun, C.5
-
74
-
-
77649288041
-
Identification of inhibitors of Plasmodium falciparum phosphoethanolamine methyltransferase using an enzyme-coupled transmethylation assay
-
CrossRef PubMed
-
Bobenchik, A. M., Choi, J. Y., Mishra, A., Rujan, I. N., Hao, B., Voelker, D. R., Hoch, J. C. and Ben Mamoun, C. (2010) Identification of inhibitors of Plasmodium falciparum phosphoethanolamine methyltransferase using an enzyme-coupled transmethylation assay. BMC Biochem. 11, 4 CrossRef PubMed
-
(2010)
BMC Biochem.
, vol.11
, pp. 4
-
-
Bobenchik, A.M.1
Choi, J.Y.2
Mishra, A.3
Rujan, I.N.4
Hao, B.5
Voelker, D.R.6
Hoch, J.C.7
Ben Mamoun, C.8
-
75
-
-
80055072963
-
Thermodynamic evaluation of ligand binding in the plant-like phosphoethanolamine methyltransferases of the parasitic nematode Haemonchus contortus
-
CrossRef PubMed
-
Lee, S. G., Haakenson, W., McCarter, J. P., Williams, D. J., Hresko, M. C. and Jez, J. M. (2011) Thermodynamic evaluation of ligand binding in the plant-like phosphoethanolamine methyltransferases of the parasitic nematode Haemonchus contortus. J. Biol. Chem. 286, 38060-38068 CrossRef PubMed
-
(2011)
J. Biol. Chem.
, vol.286
, pp. 38060-38068
-
-
Lee, S.G.1
Haakenson, W.2
McCarter, J.P.3
Williams, D.J.4
Hresko, M.C.5
Jez, J.M.6
-
76
-
-
0018935181
-
Plasmodium falciparum: Antimalarial activity in culture of sinefungin and other methylation inhibitors
-
DOI 10.1016/0014-4894(80)90010-7
-
Trager, W., Tershakovec, M., Chiang, P. K. and Cantoni, G. L. (1980) Plasmodium falciparum: antimalarial activity in culture of sinefungin and other methylation inhibitors. Exp. Parasitol. 50, 83-89 CrossRef PubMed (Pubitemid 10023944)
-
(1980)
Experimental Parasitology
, vol.50
, Issue.1
, pp. 83-89
-
-
Trager, W.1
Tershakovec, M.2
Chiang, P.K.3
Cantoni, G.L.4
-
77
-
-
84862974974
-
Structure and reaction mechanism of phosphoethanolamine methyltransferase from the malaria parasite Plasmodium falciparum: An antiparasitic drug target
-
CrossRef PubMed
-
Lee, S. G., Kim, Y., Alpert, T. D., Nagata, A. and Jez, J. M. (2012) Structure and reaction mechanism of phosphoethanolamine methyltransferase from the malaria parasite Plasmodium falciparum: an antiparasitic drug target. J. Biol. Chem. 287, 1426-1434 CrossRef PubMed
-
(2012)
J. Biol. Chem.
, vol.287
, pp. 1426-1434
-
-
Lee, S.G.1
Kim, Y.2
Alpert, T.D.3
Nagata, A.4
Jez, J.M.5
-
78
-
-
84863983632
-
Crystal structure of phosphoethanolamine methyltransferase from Plasmodium falciparum in complex with amodiaquine
-
CrossRef PubMed
-
Lee, S. G., Alpert, T. D. and Jez, J. M. (2012) Crystal structure of phosphoethanolamine methyltransferase from Plasmodium falciparum in complex with amodiaquine. Bioorg. Med. Chem. Lett. 22, 4990-4993 CrossRef PubMed
-
(2012)
Bioorg. Med. Chem. Lett.
, vol.22
, pp. 4990-4993
-
-
Lee, S.G.1
Alpert, T.D.2
Jez, J.M.3
-
79
-
-
84887302542
-
Plasmodium falciparum phosphoethanolamine methyltransferase is essential for malaria transmission
-
CrossRef PubMed
-
Bobenchik, A. M., Witola, W. H., Augagneur, Y., Lochlainn, L. N., Garg, A., Pachikara, N., Choi, J.-Y., Zhao, Y. O., Usmani-Brown, S., Lee, A. et al. (2013) Plasmodium falciparum phosphoethanolamine methyltransferase is essential for malaria transmission. Proc. Natl. Acad. Sci. U.S.A. 110, 18262-18267 CrossRef PubMed
-
(2013)
Proc. Natl. Acad. Sci. U.S.A.
, vol.110
, pp. 18262-18267
-
-
Bobenchik, A.M.1
Witola, W.H.2
Augagneur, Y.3
Lochlainn, L.N.4
Garg, A.5
Pachikara, N.6
Choi, J.-Y.7
Zhao, Y.O.8
Usmani-Brown, S.9
Lee, A.10
-
80
-
-
20144384735
-
Targeting a novel Plasmodium falciparum purine recycling pathway with specific immucillins
-
DOI 10.1074/jbc.M412693200
-
Ting, L. M., Shi, W. X., Lewandowicz, A., Singh, V., Mwakingwe, A., Birck, M. R., Ringia, E. A. T., Bench, G., Madrid, D. C., Tyler, P. C. et al. (2005) Targeting a novel Plasmodium falciparum purine recycling pathway with specific immucillins. J. Biol. Chem. 280, 9547-9554 CrossRef PubMed (Pubitemid 40409650)
-
(2005)
Journal of Biological Chemistry
, vol.280
, Issue.10
, pp. 9547-9554
-
-
Ting, L.-M.1
Shi, W.2
Lewandowicz, A.3
Singh, V.4
Mwakingwe, A.5
Birck, M.R.6
Taylor, R.E.A.7
Bench, G.8
Madrid, D.C.9
Tyler, P.C.10
Evans, G.B.11
Furneaux, R.H.12
Schramm, V.L.13
Kim, K.14
-
81
-
-
77955624880
-
Inhibitors of the purine salvage pathway: A valuable approach for antiprotozoal chemotherapy?
-
CrossRef PubMed
-
Berg, M., Van der Veken, P., Goeminne, A., Haemers, A. and Augustyns, K. (2010) Inhibitors of the purine salvage pathway: a valuable approach for antiprotozoal chemotherapy? Curr. Med. Chem. 17, 2456-2481 CrossRef PubMed
-
(2010)
Curr. Med. Chem.
, vol.17
, pp. 2456-2481
-
-
Berg, M.1
Van Der Veken, P.2
Goeminne, A.3
Haemers, A.4
Augustyns, K.5
-
82
-
-
0033017467
-
Transition-state analogs as inhibitors of human and malarial hypoxanthine-guanine phosphoribosyltransferases
-
DOI 10.1038/9367
-
Li, C. M., Tyler, P. C., Furneaux, R. H., Kicska, G., Xu, Y. M., Grubmeyer, C., Girvin, M. E. and Schramm, V. L. (1999) Transition-state analogs as inhibitors of human and malarial hypoxanthine-guanine phosphoribosyltransferases. Nat. Struct. Biol. 6, 582-587 CrossRef PubMed (Pubitemid 29252841)
-
(1999)
Nature Structural Biology
, vol.6
, Issue.6
, pp. 582-587
-
-
Li, C.M.1
Tyler, P.C.2
Furneaux, R.H.3
Kicska, G.4
Xu, Y.5
Grubmeyer, C.6
Girvin, M.E.7
Schramm, V.L.8
-
83
-
-
84862749642
-
Acyclic immucillin phosphonates: Second-generation inhibitors of Plasmodium falciparum hypoxanthine-guanine-xanthine phosphoribosyltransferase
-
CrossRef PubMed
-
Hazleton, K. Z., Ho, M. C., Cassera, M. B., Clinch, K., Crump, D. R., Rosario, I., Merino, E. F., Almo, S. C., Tyler, P. C. and Schramm, V. L. (2012) Acyclic immucillin phosphonates: second-generation inhibitors of Plasmodium falciparum hypoxanthine-guanine-xanthine phosphoribosyltransferase. Chem. Biol. 19, 721-730 CrossRef PubMed
-
(2012)
Chem. Biol.
, vol.19
, pp. 721-730
-
-
Hazleton, K.Z.1
Ho, M.C.2
Cassera, M.B.3
Clinch, K.4
Crump, D.R.5
Rosario, I.6
Merino, E.F.7
Almo, S.C.8
Tyler, P.C.9
Schramm, V.L.10
-
84
-
-
0033519996
-
The 2.0Å structure of malarial purine phosphoribosyltransferase in complex with a transition-state analogue inhibitor
-
CrossRef PubMed
-
Shi, W. X., Li, C. M., Tyler, P. C., Furneaux, R. H., Cahill, S. M., Girvin, M. E., Grubmeyer, C., Schramm, V. L. and Almo, S. C. (1999) The 2.0Å structure of malarial purine phosphoribosyltransferase in complex with a transition-state analogue inhibitor. Biochemistry 38, 9872-9880 CrossRef PubMed
-
(1999)
Biochemistry
, vol.38
, pp. 9872-9880
-
-
Shi, W.X.1
Li, C.M.2
Tyler, P.C.3
Furneaux, R.H.4
Cahill, S.M.5
Girvin, M.E.6
Grubmeyer, C.7
Schramm, V.L.8
Almo, S.C.9
-
85
-
-
0032587578
-
The 2.0 Å structure of human hypoxanthine-guanine phosphoribosyltransferase in complex with a transition-state analog inhibitor
-
DOI 10.1038/9376
-
Shi, W. X., Li, C. M., Tyler, P. C., Furneaux, R. H., Grubmeyer, C., Schramm, V. L. and Almo, S. C. (1999) The 2.0Å structure of human hypoxanthine-guanine phosphoribosyltransferase in complex with a transition-state analog inhibitor. Nat. Struct. Biol. 6, 588-593 CrossRef PubMed (Pubitemid 29252842)
-
(1999)
Nature Structural Biology
, vol.6
, Issue.6
, pp. 588-593
-
-
Shi, W.1
Li, C.M.2
Tyler, P.C.3
Furneaux, R.H.4
Grubmeyer, C.5
Schramm, V.L.6
Almo, S.C.7
-
86
-
-
67650745021
-
Inhibition of hypoxanthine-guanine phosphoribosyltransferase by acyclic nucleoside phosphonates: A new class of antimalarial therapeutics
-
CrossRef PubMed
-
Keough, D. T., Hockova, D., Holy, A., Naesens, L. M. J., Skinner-Adams, T. S., de Jersey, J. and Guddat, L. W. (2009) Inhibition of hypoxanthine-guanine phosphoribosyltransferase by acyclic nucleoside phosphonates: a new class of antimalarial therapeutics. J. Med. Chem. 52, 4391-4399 CrossRef PubMed
-
(2009)
J. Med. Chem.
, vol.52
, pp. 4391-4399
-
-
Keough, D.T.1
Hockova, D.2
Holy, A.3
Naesens, L.M.J.4
Skinner-Adams, T.S.5
De Jersey, J.6
Guddat, L.W.7
-
87
-
-
77954761602
-
Plasmodium vivax hypoxanthine-guanine phosphoribosyltransferase: A target for anti-malarial chemotherapy
-
CrossRef PubMed
-
Keough, D. T., Hockova, D., Krecmerova, M., Cesnek, M., Holy, A., Naesens, L., Brereton, I. M., Winzor, D. J., de Jersey, J. and Guddat, L. W. (2010) Plasmodium vivax hypoxanthine-guanine phosphoribosyltransferase: a target for anti-malarial chemotherapy. Mol. Biochem. Parasitol. 173, 165-169 CrossRef PubMed
-
(2010)
Mol. Biochem. Parasitol.
, vol.173
, pp. 165-169
-
-
Keough, D.T.1
Hockova, D.2
Krecmerova, M.3
Cesnek, M.4
Holy, A.5
Naesens, L.6
Brereton, I.M.7
Winzor, D.J.8
De Jersey, J.9
Guddat, L.W.10
-
88
-
-
84863826337
-
Synthesis of novel N-branched acyclic nucleoside phosphonates as potent and selective inhibitors of human, Plasmodium falciparum and Plasmodium vivax 6-oxopurine phosphoribosyltransferases
-
CrossRef PubMed
-
Hockova, D., Keough, D. T., Janeba, Z., Wang, T. H., de Jersey, J. and Guddat, L. W. (2012) Synthesis of novel N-branched acyclic nucleoside phosphonates as potent and selective inhibitors of human, Plasmodium falciparum and Plasmodium vivax 6-oxopurine phosphoribosyltransferases. J. Med. Chem. 55, 6209-6223 CrossRef PubMed
-
(2012)
J. Med. Chem.
, vol.55
, pp. 6209-6223
-
-
Hockova, D.1
Keough, D.T.2
Janeba, Z.3
Wang, T.H.4
De Jersey, J.5
Guddat, L.W.6
-
89
-
-
84875691966
-
Acyclic nucleoside phosphonates containing a second phosphonate group are potent inhibitors of 6-oxopurine phosphoribosyltransferases and have antimalarial activity
-
CrossRef PubMed
-
Keough, D. T., Spacek, P., Hockova, D., Tichy, T., Vrbkova, S., Slavetinska, L., Janeba, Z., Naesens, L., Edstein, M. D., Chavchich, M. et al. (2013) Acyclic nucleoside phosphonates containing a second phosphonate group are potent inhibitors of 6-oxopurine phosphoribosyltransferases and have antimalarial activity. J. Med. Chem. 56, 2513-2526 CrossRef PubMed
-
(2013)
J. Med. Chem.
, vol.56
, pp. 2513-2526
-
-
Keough, D.T.1
Spacek, P.2
Hockova, D.3
Tichy, T.4
Vrbkova, S.5
Slavetinska, L.6
Janeba, Z.7
Naesens, L.8
Edstein, M.D.9
Chavchich, M.10
-
90
-
-
43049112098
-
Prodrugs of phosphates and phosphonates
-
DOI 10.1021/jm701260b
-
Hecker, S. J. and Erion, M. D. (2008) Prodrugs of phosphates and phosphonates. J. Med. Chem. 51, 2328-2345 CrossRef PubMed (Pubitemid 351628494)
-
(2008)
Journal of Medicinal Chemistry
, vol.51
, Issue.8
, pp. 2328-2345
-
-
Hecker, S.J.1
Erion, M.D.2
-
91
-
-
80051692910
-
Purine and pyrimidine pathways as targets in Plasmodium falciparum
-
CrossRef PubMed
-
Cassera, M. B., Zhang, Y., Hazleton, K. Z. and Schramm, V. L. (2011) Purine and pyrimidine pathways as targets in Plasmodium falciparum. Curr. Top. Med. Chem. 11, 2103-2115 CrossRef PubMed
-
(2011)
Curr. Top. Med. Chem.
, vol.11
, pp. 2103-2115
-
-
Cassera, M.B.1
Zhang, Y.2
Hazleton, K.Z.3
Schramm, V.L.4
-
92
-
-
0036479245
-
Purine-less death in Plasmodium falciparum induced by immucillin-H, a transition state analogue of purine nucleoside phosphorylase
-
DOI 10.1074/jbc.M105906200
-
Kicska, G. A., Tyler, P. C., Evans, G. B., Furneaux, R. H., Schramm, V. L. and Kim, K. (2002) Purine-less death in Plasmodium falciparum induced by immucillin-H, a transition state analogue of purine nucleoside phosphorylase. J. Biol. Chem. 277, 3226-3231 CrossRef PubMed (Pubitemid 34953185)
-
(2002)
Journal of Biological Chemistry
, vol.277
, Issue.5
, pp. 3226-3231
-
-
Kicska, G.A.1
Tyler, P.C.2
Evans, G.B.3
Furneaux, R.H.4
Schramm, V.L.5
Kim, K.6
-
93
-
-
23944513862
-
Purine and pyrimidine transport in pathogenic protozoa: From biology to therapy
-
DOI 10.1016/j.femsre.2005.03.004, PII S0168644505000380
-
de Koning, H. P., Bridges, D. J. and Burchmore, R. J. S. (2005) Purine and pyrimidine transport in pathogenic protozoa: from biology to therapy. FEMS Microbiol. Immunol. 29, 987-1020 CrossRef (Pubitemid 41416847)
-
(2005)
FEMS Microbiology Reviews
, vol.29
, Issue.5
, pp. 987-1020
-
-
De Koning, H.P.1
Bridges, D.J.2
Burchmore, R.J.S.3
-
94
-
-
0020136030
-
Enzymes of purine and pyrimidine metabolism from the human malaria parasite, Plasmodium falciparum
-
CrossRef PubMed
-
Reyes, P., Rathod, P. K., Sanchez, D. J., Mrema, J. E. K., Rieckmann, K. H. and Heidrich, H. G. (1982) Enzymes of purine and pyrimidine metabolism from the human malaria parasite, Plasmodium falciparum. Mol. Biochem. Parasitol. 5, 275-290 CrossRef PubMed
-
(1982)
Mol. Biochem. Parasitol.
, vol.5
, pp. 275-290
-
-
Reyes, P.1
Rathod, P.K.2
Sanchez, D.J.3
Mrema, J.E.K.4
Rieckmann, K.H.5
Heidrich, H.G.6
-
95
-
-
2242437134
-
Atomic dissection of the hydrogen bond network for transition-state analogue binding to purine nucleoside phosphorylase
-
DOI 10.1021/bi026636f
-
Kicska, G. A., Tyler, P. C., Evans, G. B., Furneaux, R. H., Shi, W. X., Fedorov, A., Lewandowicz, A., Cahill, S. M., Almo, S. C. and Schramm, V. L. (2002) Atomic dissection of the hydrogen bond network for transition-state analogue binding to purine nucleoside phosphorylase. Biochemistry 41, 14489-14498 CrossRef PubMed (Pubitemid 35440260)
-
(2002)
Biochemistry
, vol.41
, Issue.49
, pp. 14489-14498
-
-
Kicska, G.A.1
Tyler, P.C.2
Evans, G.B.3
Furneaux, R.H.4
Shi, W.5
Fedorov, A.6
Lewandowicz, A.7
Cahill, S.M.8
Almo, S.C.9
Schramm, V.L.10
-
96
-
-
34247603923
-
Neighboring group participation in the transition state of human purine nucleoside phosphorylase
-
DOI 10.1021/bi700147b
-
Murkin, A. S., Birck, M. R., Rinaldo-Matthis, A., Shi, W. X., Taylor, E. A., Almo, S. C. and Schramm, V. L. (2007) Neighboring group participation in the transition state of purine nucleoside phosphorylase. Biochemistry 46, 5038-5049 CrossRef PubMed (Pubitemid 46683002)
-
(2007)
Biochemistry
, vol.46
, Issue.17
, pp. 5038-5049
-
-
Murkin, A.S.1
Birck, M.R.2
Rinaldo-Matthis, A.3
Shi, W.4
Taylor, E.A.5
Almo, S.C.6
Schramm, V.L.7
-
97
-
-
34247603923
-
Neighboring group participation in the transition state of human purine nucleoside phosphorylase
-
DOI 10.1021/bi700147b
-
Murkin, A. S., Birck, M. R., Rinaldo-Matthis, A., Shi, W. X., Taylor, E. A., Almo, S. C. and Schramm, V. L. (2007) Neighboring group participation in the transition state of human purine nucleoside phosphorylase. Biochemistry 46, 5038-5049 CrossRef PubMed (Pubitemid 46683002)
-
(2007)
Biochemistry
, vol.46
, Issue.17
, pp. 5038-5049
-
-
Murkin, A.S.1
Birck, M.R.2
Rinaldo-Matthis, A.3
Shi, W.4
Taylor, E.A.5
Almo, S.C.6
Schramm, V.L.7
-
98
-
-
39549099106
-
Transition-state interactions revealed in purine nucleoside phosphorylase by binding isotope effects
-
DOI 10.1021/ja7104398
-
Murkin, A. S., Tyler, P. C. and Schramm, V. L. (2008) Transition-state interactions revealed in purine nucleoside phosphorylase by binding isotope effects. J. Am. Chem. Soc. 130, 2166-2167 CrossRef PubMed (Pubitemid 351287987)
-
(2008)
Journal of the American Chemical Society
, vol.130
, Issue.7
, pp. 2166-2167
-
-
Murkin, A.S.1
Tyler, P.C.2
Schramm, V.L.3
-
99
-
-
38349138985
-
L-Enantiomers of transition state analogue inhibitors bound to human purine nucleoside phosphorylase
-
CrossRef PubMed
-
Rinaldo-Matthis, A., Murkin, A. S., Ramagopal, U. A., Clinch, K., Mee, S. P. H., Evans, G. B., Tyler, P. C., Furneaux, R. H., Almoj, S. C. and Schramm, V. L. (2008) L-Enantiomers of transition state analogue inhibitors bound to human purine nucleoside phosphorylase. J. Am. Chem. Soc. 130, 842-844 CrossRef PubMed
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 842-844
-
-
Rinaldo-Matthis, A.1
Murkin, A.S.2
Ramagopal, U.A.3
Clinch, K.4
Mee, S.P.H.5
Evans, G.B.6
Tyler, P.C.7
Furneaux, R.H.8
Almoj, S.C.9
Schramm, V.L.10
-
100
-
-
2442431653
-
Plasmodium falciparum purine nucleoside phosphorylase: Crystal structures, immucillin inhibitors, and dual catalytic function
-
DOI 10.1074/jbc.C400068200
-
Shi, W. X., Ting, L. M., Kicska, G. A., Lewandowicz, A., Tyler, P. C., Evans, G. B., Furneaux, R. H., Kim, K., Almo, S. C. and Schramm, V. L. (2004) Plasmodium falciparum purine nucleoside phosphorylase: crystal structures, immucillin inhibitors, and dual catalytic function. J. Biol. Chem. 279, 18103-18106 CrossRef PubMed (Pubitemid 38623220)
-
(2004)
Journal of Biological Chemistry
, vol.279
, Issue.18
, pp. 18103-18106
-
-
Shi, W.1
Ting, L.-M.2
Kicska, G.A.3
Lewandowicz, A.4
Tyler, P.C.5
Evans, G.B.6
Furneaux, R.H.7
Kim, K.8
Almo, S.C.9
Schramm, V.L.10
-
101
-
-
80855133585
-
Plasmodium falciparum parasites are killed by a transition state analogue of purine nucleoside phosphorylase in a primate animal model
-
CrossRef PubMed
-
Cassera, M. B., Hazleton, K. Z., Merino, E. F., Obaldia, N., Ho, M. C., Murkin, A. S., DePinto, R., Gutierrez, J. A., Almo, S. C., Evans, G. B. et al. (2011) Plasmodium falciparum parasites are killed by a transition state analogue of purine nucleoside phosphorylase in a primate animal model. PLoS ONE 6, e26916 CrossRef PubMed
-
(2011)
PLoS ONE
, vol.6
-
-
Cassera, M.B.1
Hazleton, K.Z.2
Merino, E.F.3
Obaldia, N.4
Ho, M.C.5
Murkin, A.S.6
DePinto, R.7
Gutierrez, J.A.8
Almo, S.C.9
Evans, G.B.10
-
102
-
-
37549009025
-
Structural basis for the decarboxylation of orotidine 5′- monophosphate (OMP) by Plasmodium falciparum OMP decarboxylase
-
DOI 10.1093/jb/mvm193
-
Tokuoka, K., Kusakari, Y., Krungkrai, S. R., Matsumura, H., Kai, Y., Krungkrai, J., Horii, T. and Inoue, T. (2008) Structural basis for the decarboxylation of orotidine 5′-monophosphate (OMP) by Plasmodium falciparum OMP decarboxylase. J. Biochem. (Tokyo) 143, 69-78 CrossRef (Pubitemid 351197713)
-
(2008)
Journal of Biochemistry
, vol.143
, Issue.1
, pp. 69-78
-
-
Tokuoka, K.1
Kusakari, Y.2
Krungkrai, S.R.3
Matsumura, H.4
Kai, Y.5
Krungkrai, J.6
Horii, T.7
Inoue, T.8
-
103
-
-
84864495634
-
The in silico screening and X-ray structure analysis of the inhibitor complex of Plasmodium falciparum orotidine 5′-monophosphate decarboxylase
-
CrossRef
-
Takashima, Y., Mizohata, E., Krungkrai, S. R., Fukunishi, Y., Kinoshita, T., Sakata, T., Matsumura, H., Krungkrai, J., Horii, T. and Inoue, T. (2012) The in silico screening and X-ray structure analysis of the inhibitor complex of Plasmodium falciparum orotidine 5′-monophosphate decarboxylase. J. Biochem. (Tokyo) 152, 133-138 CrossRef
-
(2012)
J. Biochem. (Tokyo)
, vol.152
, pp. 133-138
-
-
Takashima, Y.1
Mizohata, E.2
Krungkrai, S.R.3
Fukunishi, Y.4
Kinoshita, T.5
Sakata, T.6
Matsumura, H.7
Krungkrai, J.8
Horii, T.9
Inoue, T.10
-
104
-
-
33748594188
-
Multiple target screening method for robust and accurate in silico ligand screening
-
DOI 10.1016/j.jmgm.2005.11.006, PII S1093326305001658
-
Fukunishi, Y., Mikami, Y., Kubota, S. and Nakamura, H. (2006) Multiple target screening method for robust and accurate in silico ligand screening. J. Mol. Graph. Model. 25, 61-70 CrossRef PubMed (Pubitemid 44376445)
-
(2006)
Journal of Molecular Graphics and Modelling
, vol.25
, Issue.1
, pp. 61-70
-
-
Fukunishi, Y.1
Mikami, Y.2
Kubota, S.3
Nakamura, H.4
-
105
-
-
31544477769
-
Classification of chemical compounds by protein-compound docking for use in designing a focused library
-
DOI 10.1021/jm050480a
-
Fukunishi, Y., Mikami, Y., Takedomi, K., Yamanouchi, M., Shima, H. and Nakamura, H. (2006) Classification of chemical compounds by protein-compound docking for use in designing a focused library. J. Med. Chem. 49, 523-533 CrossRef PubMed (Pubitemid 43157486)
-
(2006)
Journal of Medicinal Chemistry
, vol.49
, Issue.2
, pp. 523-533
-
-
Fukunishi, Y.1
Mikami, Y.2
Takedomi, K.3
Yamimouehi, M.4
Shima, H.5
Nakamura, H.6
-
106
-
-
0346707194
-
Primary structure of the gene encoding the bifunctional dihydrofolate reductase-thymidylate synthase of Leishmania major
-
Beverley, S. M., Ellenberger, T. E. and Cordingley, J. S. (1986) Primary structure of the gene encoding the bifunctional dihydrofolate reductase-thymidylate synthase of Leishmania major . Proc. Natl. Acad. Sci. U.S.A. 83, 2584-2588 CrossRef PubMed (Pubitemid 16026927)
-
(1986)
Proceedings of the National Academy of Sciences of the United States of America
, vol.83
, Issue.8
, pp. 2584-2588
-
-
Beverley, S.M.1
Ellenberger, T.E.2
Cordingley, J.S.3
-
107
-
-
0021913821
-
Receptor-based design of dihydrofolate-reductase inhibitors: Comparison of crystallographically determined enzyme binding with enzyme affinity in a series of carboxy-substituted trimethoprime analogs
-
CrossRef PubMed
-
Kuyper, L. F., Roth, B., Baccanari, D. P., Ferone, R., Beddell, C. R., Champness, J. N., Stammers, D. K., Dann, J. G., Norrington, F. E., Baker, D. J. and Goodford, P. J. (1985) Receptor-based design of dihydrofolate-reductase inhibitors: comparison of crystallographically determined enzyme binding with enzyme affinity in a series of carboxy-substituted trimethoprime analogs. J. Med. Chem. 28, 303-311 CrossRef PubMed
-
(1985)
J. Med. Chem.
, vol.28
, pp. 303-311
-
-
Kuyper, L.F.1
Roth, B.2
Baccanari, D.P.3
Ferone, R.4
Beddell, C.R.5
Champness, J.N.6
Stammers, D.K.7
Dann, J.G.8
Norrington, F.E.9
Baker, D.J.10
Goodford, P.J.11
-
108
-
-
77952653707
-
Preclinical evaluation of the antifolate QN254, 5-chloro-N'6′-(2,5- dimethoxy-benzyl)-quinazoline-2,4,6-triamine, as an antimalarial drug candidate
-
CrossRef PubMed
-
Nzila, A., Rottmann, M., Chitnumsub, P., Kiara, S. M., Kamchonwongpaisan, S., Maneeruttanarungroj, C., Taweechai, S., Yeung, B. K. S., Goh, A., Lakshminarayana, S. B. et al. (2010) Preclinical evaluation of the antifolate QN254, 5-chloro-N'6′-(2,5-dimethoxy-benzyl)-quinazoline-2,4,6-triamine, as an antimalarial drug candidate. Antimicrob. Agents Chemother. 54, 2603-2610 CrossRef PubMed
-
(2010)
Antimicrob. Agents Chemother.
, vol.54
, pp. 2603-2610
-
-
Nzila, A.1
Rottmann, M.2
Chitnumsub, P.3
Kiara, S.M.4
Kamchonwongpaisan, S.5
Maneeruttanarungroj, C.6
Taweechai, S.7
Yeung, B.K.S.8
Goh, A.9
Lakshminarayana, S.B.10
-
109
-
-
0037666888
-
Implications of protein flexibility for drug discovery
-
CrossRef PubMed
-
Teague, S. J. (2003) Implications of protein flexibility for drug discovery. Nat. Rev. Drug Discov. 2, 527-541 CrossRef PubMed
-
(2003)
Nat. Rev. Drug Discov.
, vol.2
, pp. 527-541
-
-
Teague, S.J.1
-
110
-
-
67649628164
-
New approaches to HIV protease inhibitor drug design II: Testing the substrate envelope hypothesis to avoid drug resistance and discover robust inhibitors
-
CrossRef PubMed
-
Nalam, M. N. L. and Schiffer, C. A. (2008) New approaches to HIV protease inhibitor drug design II: testing the substrate envelope hypothesis to avoid drug resistance and discover robust inhibitors. Curr. Opin. HIV AIDS. 3, 642-646 CrossRef PubMed
-
(2008)
Curr. Opin. HIV AIDS.
, vol.3
, pp. 642-646
-
-
Nalam, M.N.L.1
Schiffer, C.A.2
-
111
-
-
58749102067
-
Mutational, inhibitory and microcalorimetric analyses of Plasmodium falciparum TMP kinase: Implications for drug discovery
-
CrossRef PubMed
-
Kandeel, M., Ando, T., Kitamura, Y., Abdel-Aziz, M. and Kitade, Y. (2009) Mutational, inhibitory and microcalorimetric analyses of Plasmodium falciparum TMP kinase: implications for drug discovery. Parasitology 136, 11-25 CrossRef PubMed
-
(2009)
Parasitology
, vol.136
, pp. 11-25
-
-
Kandeel, M.1
Ando, T.2
Kitamura, Y.3
Abdel-Aziz, M.4
Kitade, Y.5
-
112
-
-
77954911479
-
Structural basis for the efficient phosphorylation of AZT-MP (3′-azido-3′-deoxythymidine monophosphate) and dGMP by Plasmodium falciparum type I thymidylate kinase
-
CrossRef PubMed
-
Whittingham, J. L., Carrero-Lerida, J., Brannigan, J. A., Ruiz-Perez, L. M., Silva, A. P. G., Fogg, M. J., Wilkinson, A. J., Gilbert, I. H., Wilson, K. S. and Gonzalez-Pacanowska, D. (2010) Structural basis for the efficient phosphorylation of AZT-MP (3′-azido-3′-deoxythymidine monophosphate) and dGMP by Plasmodium falciparum type I thymidylate kinase. Biochem. J. 428, 499-509 CrossRef PubMed
-
(2010)
Biochem. J.
, vol.428
, pp. 499-509
-
-
Whittingham, J.L.1
Carrero-Lerida, J.2
Brannigan, J.A.3
Ruiz-Perez, L.M.4
Silva, A.P.G.5
Fogg, M.J.6
Wilkinson, A.J.7
Gilbert, I.H.8
Wilson, K.S.9
Gonzalez-Pacanowska, D.10
-
113
-
-
77957559686
-
Potential application of thymidylate kinase in nucleoside analogue activation in Plasmodium falciparum
-
CrossRef PubMed
-
Cui, H. Q., Ruiz-Perez, L. M., Gonzalez-Pacanowska, D. and Gilbert, I. H. (2010) Potential application of thymidylate kinase in nucleoside analogue activation in Plasmodium falciparum. Bioorg. Med. Chem. 18, 7302-7309 CrossRef PubMed
-
(2010)
Bioorg. Med. Chem.
, vol.18
, pp. 7302-7309
-
-
Cui, H.Q.1
Ruiz-Perez, L.M.2
Gonzalez-Pacanowska, D.3
Gilbert, I.H.4
-
114
-
-
84871654541
-
Synthesis and evaluation of α-thymidine analogues as novel antimalarials
-
CrossRef PubMed
-
Cui, H., Carrero-Lerida, J., Silva, A. P. G., Whittingham, J. L., Brannigan, J. A., Ruiz-Perez, L. M., Read, K. D., Wilson, K. S., Gonzalez-Pacanowska, D. and Gilbert, I. H. (2012) Synthesis and evaluation of α-thymidine analogues as novel antimalarials. J. Med. Chem. 55, 10948-10957 CrossRef PubMed
-
(2012)
J. Med. Chem.
, vol.55
, pp. 10948-10957
-
-
Cui, H.1
Carrero-Lerida, J.2
Silva, A.P.G.3
Whittingham, J.L.4
Brannigan, J.A.5
Ruiz-Perez, L.M.6
Read, K.D.7
Wilson, K.S.8
Gonzalez-Pacanowska, D.9
Gilbert, I.H.10
-
115
-
-
35848946837
-
Rational design of 5′-thiourea-substituted α-thymidine analogues as thymidine monophosphate kinase inhibitors capable of inhibiting mycobacterial growth
-
DOI 10.1021/jm0706158
-
Van Daele, I., Munier-Lehmann, H., Froeyen, M., Balzarini, J. and Van Calenbergh, S. (2007) Rational design of 5′-thiourea-substituted α-thymidine analogues as thymidine monophosphate kinase inhibitors capable of inhibiting mycobacterial growth. J. Med. Chem. 50, 5281-5292 CrossRef PubMed (Pubitemid 350057840)
-
(2007)
Journal of Medicinal Chemistry
, vol.50
, Issue.22
, pp. 5281-5292
-
-
Van Daele, I.1
Munier-Lehmann, H.2
Froeyen, M.3
Balzarini, J.4
Van Calenbergh, S.5
-
116
-
-
61849128423
-
Keeping uracil out of DNA: Physiological role, structure and catalytic mechanism of dUTPases
-
CrossRef PubMed
-
Vertessy, B. G. and Toth, J. (2009) Keeping uracil out of DNA: physiological role, structure and catalytic mechanism of dUTPases. Acc. Chem. Res. 42, 97-106 CrossRef PubMed
-
(2009)
Acc. Chem. Res.
, vol.42
, pp. 97-106
-
-
Vertessy, B.G.1
Toth, J.2
-
117
-
-
0034966740
-
Kinetic properties and inhibition of the dimeric dUTPase-dUDPase from Leishmania major
-
DOI 10.1110/ps.48801
-
Hidalgo-Zarco, F., Camacho, A. G., Bernier-Villamor, V., Nord, J., Ruiz-Perez, L. M. and Gonzalez-Pacanowska, D. (2001) Kinetic properties and inhibition of the dimeric dUTPase-dUDPase from Leishmania major . Protein Sci. 10, 1426-1433 CrossRef PubMed (Pubitemid 32568109)
-
(2001)
Protein Science
, vol.10
, Issue.7
, pp. 1426-1433
-
-
Hidalgo-Zarco, F.1
Camacho, A.G.2
Bernier-Villamor, V.3
Nord, J.4
Ruiz-Perez, L.M.5
Gonzalez-Pacanowska, D.6
-
118
-
-
0031308373
-
dUTP pyrophosphatase as a potential target for chemotherapeutic drug development
-
McIntosh, E. M. and Haynes, R. H. (1997) dUTP pyrophosphatase as a potential target for chemotherapeutic drug development. Acta Biochim. Polon. 44, 159-171
-
(1997)
Acta Biochim. Polon.
, vol.44
, pp. 159-171
-
-
McIntosh, E.M.1
Haynes, R.H.2
-
119
-
-
0023967987
-
Lethality of a dUT (deoxyuridine triphosphatase) mutation in Escherichia coli
-
PubMed
-
Elhajj, H. H., Zhang, H. and Weiss, B. (1988) Lethality of a dUT (deoxyuridine triphosphatase) mutation in Escherichia coli. J. Bacteriol. 170, 1069-1075 PubMed
-
(1988)
J. Bacteriol.
, vol.170
, pp. 1069-1075
-
-
Elhajj, H.H.1
Zhang, H.2
Weiss, B.3
-
120
-
-
0027426749
-
dUTP pyrophosphatase is an essential enzyme in Saccharomyces cerevisiae
-
Gadsden, M. H., McIntosh, E. M., Game, J. C., Wilson, P. J. and Haynes, R. H. (1993) dUTP pyrophosphatase is an essential enzyme in Saccharomyces cerevisiae. EMBO J. 12, 4425-4431 PubMed (Pubitemid 23302057)
-
(1993)
EMBO Journal
, vol.12
, Issue.11
, pp. 4425-4431
-
-
Gadsden, M.H.1
McIntosh, E.M.2
Game, J.C.3
Wilson, P.J.4
Haynes, R.H.5
-
121
-
-
24944499627
-
Deoxyuridine triphosphate nucleotidohydrolase as a potential antiparasitic drug target
-
DOI 10.1021/jm050111e
-
Nguyen, C., Kasinathan, G., Leal-Cortijo, I., Musso-Buendia, A., Kaiser, M., Brun, R., Ruiz-Perez, L. M., Johansson, N. G., Gonzalez-Pacanowska, D. and Gilbert, I. H. (2005) Deoxyuridine triphosphate nucleotidohydrolase as a potential antiparasitic drug target. J. Med. Chem. 48, 5942-5954 CrossRef PubMed (Pubitemid 41324605)
-
(2005)
Journal of Medicinal Chemistry
, vol.48
, Issue.19
, pp. 5942-5954
-
-
Nguyen, C.1
Kasinathan, G.2
Leal-Cortijo, I.3
Musso-Buendia, A.4
Kaiser, M.5
Brun, R.6
Ruiz-Perez, L.M.7
Johansson, N.G.8
Gonzalez-Pacanowska, D.9
Gilbert, I.H.10
-
122
-
-
33745832313
-
Acyclic nucleoside analogues as inhibitors of Plasmodium falciparum dUTPase
-
DOI 10.1021/jm060126s
-
Nguyen, C., Ruda, G. F., Schipani, A., Kasinathan, G., Leal, I., Musso-Buendia, A., Kaiser, M., Brun, R., Ruiz-Perez, L. M., Sahlberg, B. L. et al. (2006) Acyclic nucleoside analogues as inhibitors of Plasmodium falciparum dUTPase. J. Med. Chem. 49, 4183-4195 CrossRef PubMed (Pubitemid 44036662)
-
(2006)
Journal of Medicinal Chemistry
, vol.49
, Issue.14
, pp. 4183-4195
-
-
Nguyen, C.1
Ruda, G.F.2
Schipani, A.3
Kasinathan, G.4
Leal, I.5
Musso-Buendia, A.6
Kaiser, M.7
Brun, R.8
Ruiz-Perez, L.M.9
Sahlberg, B.-L.10
Johansson, N.G.11
Gonzalez-Pacanowska, D.12
Gilbert, I.H.13
-
123
-
-
13844296398
-
dUTPase as a platform for antimalarial drug design: Structural basis for the selectivity of a class of nucleoside inhibitors
-
DOI 10.1016/j.str.2004.11.015
-
Whittingham, J. L., Leal, I., Nguyen, C., Kasinathan, G., Bell, E., Jones, A. F., Berry, C., Benito, A., Turkenburg, J. P., Dodson, E. J. et al. (2005) dUTPase as a platform for antimalarial drug design: structural basis for the selectivity of a class of nucleoside inhibitors. Structure 13, 329-338 CrossRef PubMed (Pubitemid 40247708)
-
(2005)
Structure
, vol.13
, Issue.2
, pp. 329-338
-
-
Whittingham, J.L.1
Leal, I.2
Nguyen, C.3
Kasinathan, G.4
Bell, E.5
Jones, A.F.6
Berry, C.7
Benito, A.8
Turkenburg, J.P.9
Dodson, E.J.10
Ruiz, P.L.M.11
Wilkinson, A.J.12
Johansson, N.G.13
Brun, R.14
Gilbert, I.H.15
Pacanowska, D.G.16
Wilson, K.S.17
-
124
-
-
60149107206
-
Design, synthesis and evaluation of novel uracil acetamide derivatives as potential inhibitors of Plasmodium falciparum dUTP nucleotidohydrolase
-
CrossRef PubMed
-
McCarthy, O., Musso-Buendia, A., Kaiser, M., Brun, R., Ruiz-Perez, L. M., Johansson, N. G., Pacanowska, D. G. and Gilbert, I. H. (2009) Design, synthesis and evaluation of novel uracil acetamide derivatives as potential inhibitors of Plasmodium falciparum dUTP nucleotidohydrolase. Eur. J. Med. Chem. 44, 678-688 CrossRef PubMed
-
(2009)
Eur. J. Med. Chem.
, vol.44
, pp. 678-688
-
-
McCarthy, O.1
Musso-Buendia, A.2
Kaiser, M.3
Brun, R.4
Ruiz-Perez, L.M.5
Johansson, N.G.6
Pacanowska, D.G.7
Gilbert, I.H.8
-
125
-
-
79953202128
-
β-Branched acyclic nucleoside analogues as inhibitors of Plasmodium falciparum dUTPase
-
CrossRef PubMed
-
Baragana, B., McCarthy, O., Sanchez, P., Bosch-Navarrete, C., Kaiser, M., Brun, R., Whittingham, J. L., Roberts, S. M., Zhou, X. X., Wilson, K. S. et al. (2011) β-Branched acyclic nucleoside analogues as inhibitors of Plasmodium falciparum dUTPase. Bioorg. Med. Chem. 19, 2378-2391 CrossRef PubMed
-
(2011)
Bioorg. Med. Chem.
, vol.19
, pp. 2378-2391
-
-
Baragana, B.1
McCarthy, O.2
Sanchez, P.3
Bosch-Navarrete, C.4
Kaiser, M.5
Brun, R.6
Whittingham, J.L.7
Roberts, S.M.8
Zhou, X.X.9
Wilson, K.S.10
-
126
-
-
80053422180
-
Design, synthesis, and evaluation of 5′-diphenyl nucleoside analogues as inhibitors of the Plasmodium falciparum dUTPase
-
CrossRef PubMed
-
Hampton, S. E., Baragana, B., Schipani, A., Bosch-Navarrete, C., Musso-Buendia, J. A., Recio, E., Kaiser, M., Whittingham, J. L., Roberts, S. M., Shevtsov, M. et al. (2011) Design, synthesis, and evaluation of 5′-diphenyl nucleoside analogues as inhibitors of the Plasmodium falciparum dUTPase. ChemMedChem 6, 1816-1831 CrossRef PubMed
-
(2011)
ChemMedChem
, vol.6
, pp. 1816-1831
-
-
Hampton, S.E.1
Baragana, B.2
Schipani, A.3
Bosch-Navarrete, C.4
Musso-Buendia, J.A.5
Recio, E.6
Kaiser, M.7
Whittingham, J.L.8
Roberts, S.M.9
Shevtsov, M.10
-
127
-
-
79961223551
-
Structure-guided lead optimization of triazolopyrimidine-ring substituents identifies potent Plasmodium falciparum dihydroorotate dehydrogenase inhibitors with clinical candidate potential
-
CrossRef PubMed
-
Coteron, J. M., Marco, M., Esquivias, J., Deng, X. Y., White, K. L., White, J., Koltun, M., El Mazouni, F., Kokkonda, S., Katneni, K. et al. (2011) Structure-guided lead optimization of triazolopyrimidine-ring substituents identifies potent Plasmodium falciparum dihydroorotate dehydrogenase inhibitors with clinical candidate potential. J. Med. Chem. 54, 5540-5561 CrossRef PubMed
-
(2011)
J. Med. Chem.
, vol.54
, pp. 5540-5561
-
-
Coteron, J.M.1
Marco, M.2
Esquivias, J.3
Deng, X.Y.4
White, K.L.5
White, J.6
Koltun, M.7
El Mazouni, F.8
Kokkonda, S.9
Katneni, K.10
-
128
-
-
64549087994
-
Identification of a metabolically stable triazolopyrimidine-based dihydroorotate dehydrogenase inhibitor with antimalarial activity in mice
-
CrossRef PubMed
-
Gujjar, R., Marwaha, A., El Mazouni, F., White, J., White, K. L., Creason, S., Shackleford, D. M., Baldwin, J., Charman, W. N., Buckner, F. S. et al. (2009) Identification of a metabolically stable triazolopyrimidine-based dihydroorotate dehydrogenase inhibitor with antimalarial activity in mice. J. Med. Chem. 52, 1864-1872 CrossRef PubMed
-
(2009)
J. Med. Chem.
, vol.52
, pp. 1864-1872
-
-
Gujjar, R.1
Marwaha, A.2
El Mazouni, F.3
White, J.4
White, K.L.5
Creason, S.6
Shackleford, D.M.7
Baldwin, J.8
Charman, W.N.9
Buckner, F.S.10
-
129
-
-
45749119578
-
Triazolopyrimidine-based dihydroorotate dehydrogenase inhibitors with potent and selective activity against the malaria parasite Plasmodium falciparum
-
DOI 10.1021/jm8001026
-
Phillips, M. A., Gujjar, R., Malmquist, N. A., White, J., El Mazouni, F., Baldwin, J. and Rathod, P. K. (2008) Triazolopyrimidine-based dihydroorotate dehydrogenase inhibitors with potent and selective activity against the malaria parasite Plasmodium falciparum. J. Med. Chem. 51, 3649-3653 CrossRef PubMed (Pubitemid 351875021)
-
(2008)
Journal of Medicinal Chemistry
, vol.51
, Issue.12
, pp. 3649-3653
-
-
Phillips, M.A.1
Gujjar, R.2
Malmquist, N.A.3
White, J.4
El, M.F.5
Baldwin, J.6
Rathod, P.K.7
-
130
-
-
20444470318
-
High-throughput screening for potent and selective inhibitors of Plasmodium falciparum dihydroorotate dehydrogenase
-
DOI 10.1074/jbc.M501100200
-
Baldwin, J., Michnoff, C. H., Malmquist, N. A., White, J., Roth, M. G., Rathod, P. K. and Phillips, M. A. (2005) High-throughput screening for potent and selective inhibitors of Plasmodium falciparum dihydroorotate dehydrogenase. J. Biol. Chem. 280, 21847-21853 CrossRef PubMed (Pubitemid 40827835)
-
(2005)
Journal of Biological Chemistry
, vol.280
, Issue.23
, pp. 21847-21853
-
-
Baldwin, J.1
Michnoff, C.H.2
Malmquist, N.A.3
White, J.4
Roth, M.G.5
Rathod, P.K.6
Phillips, M.A.7
-
131
-
-
70350385202
-
Structural plasticity of malaria dihydroorotate dehydrogenase allows selective binding of diverse chemical scaffolds
-
CrossRef PubMed
-
Deng, X. Y., Gujjar, R., El Mazouni, F., Kaminsky, W., Malmquist, N. A., Goldsmith, E. J., Rathod, P. K. and Phillips, M. A. (2009) Structural plasticity of malaria dihydroorotate dehydrogenase allows selective binding of diverse chemical scaffolds. J. Biol. Chem. 284, 26999-27009 CrossRef PubMed
-
(2009)
J. Biol. Chem.
, vol.284
, pp. 26999-27009
-
-
Deng, X.Y.1
Gujjar, R.2
El Mazouni, F.3
Kaminsky, W.4
Malmquist, N.A.5
Goldsmith, E.J.6
Rathod, P.K.7
Phillips, M.A.8
-
132
-
-
77958511348
-
Novel inhibitors of Plasmodium falciparum dihydroorotate dehydrogenase with anti-malarial activity in the mouse model
-
CrossRef PubMed
-
Booker, M. L., Bastos, C. M., Kramer, M. L., Barker, R. H., Skerlj, R., Sidhu, A. B., Deng, X. Y., Celatka, C., Cortese, J. F., Bravo, J. E. G. et al. (2010) Novel inhibitors of Plasmodium falciparum dihydroorotate dehydrogenase with anti-malarial activity in the mouse model. J. Biol. Chem. 285, 33054-33064 CrossRef PubMed
-
(2010)
J. Biol. Chem.
, vol.285
, pp. 33054-33064
-
-
Booker, M.L.1
Bastos, C.M.2
Kramer, M.L.3
Barker, R.H.4
Skerlj, R.5
Sidhu, A.B.6
Deng, X.Y.7
Celatka, C.8
Cortese, J.F.9
Bravo, J.E.G.10
-
133
-
-
58049219752
-
Identification and characterization of small molecule inhibitors of Plasmodium falciparum dihydroorotate dehydrogenase
-
CrossRef PubMed
-
Patel, V., Booker, M., Kramer, M., Ross, L., Celatka, C. A., Kennedy, L. M., Dvorin, J. D., Duraisingh, M. T., Sliz, P., Wirth, D. F. and Clardy, J. (2008) Identification and characterization of small molecule inhibitors of Plasmodium falciparum dihydroorotate dehydrogenase. J. Biol. Chem. 283, 35078-35085 CrossRef PubMed
-
(2008)
J. Biol. Chem.
, vol.283
, pp. 35078-35085
-
-
Patel, V.1
Booker, M.2
Kramer, M.3
Ross, L.4
Celatka, C.A.5
Kennedy, L.M.6
Dvorin, J.D.7
Duraisingh, M.T.8
Sliz, P.9
Wirth, D.F.10
Clardy, J.11
-
134
-
-
84865808746
-
Factors influencing the specificity of inhibitor binding to the human and malaria parasite dihydroorotate dehydrogenases
-
CrossRef PubMed
-
Bedingfield, P. T. P., Cowen, D., Acklam, P., Cunningham, F., Parsons, M. R., McConkey, G. A., Fishwick, C. W. G. and Johnson, A. P. (2012) Factors influencing the specificity of inhibitor binding to the human and malaria parasite dihydroorotate dehydrogenases. J. Med. Chem. 55, 5841-5850 CrossRef PubMed
-
(2012)
J. Med. Chem.
, vol.55
, pp. 5841-5850
-
-
Bedingfield, P.T.P.1
Cowen, D.2
Acklam, P.3
Cunningham, F.4
Parsons, M.R.5
McConkey, G.A.6
Fishwick, C.W.G.7
Johnson, A.P.8
-
135
-
-
33646583490
-
Structure of Plasmodium falciparum dihydroorotate dehydrogenase with a bound inhibitor
-
DOI 10.1107/S0907444905042642
-
Hurt, D. E., Widom, J. and Clardy, J. (2006) Structure of Plasmodium falciparum dihydroorotate dehydrogenase with a bound inhibitor. Acta Crystallogr. D Biol. Crystallogr. 62, 312-323 CrossRef PubMed (Pubitemid 44185140)
-
(2006)
Acta Crystallographica Section D: Biological Crystallography
, vol.62
, Issue.3
, pp. 312-323
-
-
Hurt, D.E.1
Widom, J.2
Clardy, J.3
-
136
-
-
79958100876
-
Lead optimization of aryl and aralkyl amine-based triazolopyrimidine inhibitors of Plasmodium falciparum dihydroorotate dehydrogenase with antimalarial activity in mice
-
CrossRef PubMed
-
Gujjar, R., El Mazouni, F., White, K. L., White, J., Creason, S., Shackleford, D. M., Deng, X. Y., Charman, W. N., Bathurst, I., Burrows, J. et al. (2011) Lead optimization of aryl and aralkyl amine-based triazolopyrimidine inhibitors of Plasmodium falciparum dihydroorotate dehydrogenase with antimalarial activity in mice. J. Med. Chem. 54, 3935-3949 CrossRef PubMed
-
(2011)
J. Med. Chem.
, vol.54
, pp. 3935-3949
-
-
Gujjar, R.1
El Mazouni, F.2
White, K.L.3
White, J.4
Creason, S.5
Shackleford, D.M.6
Deng, X.Y.7
Charman, W.N.8
Bathurst, I.9
Burrows, J.10
-
137
-
-
48049096002
-
N-myristoyltransferase: A prospective drug target for protozoan parasites
-
CrossRef PubMed
-
Bowyer, P. W., Tate, E. W., Leatherbarrow, R. J., Holder, A. A., Smith, D. F. and Brown, K. A. (2008) N-myristoyltransferase: a prospective drug target for protozoan parasites. ChemMedChem 3, 402-408 CrossRef PubMed
-
(2008)
ChemMedChem
, vol.3
, pp. 402-408
-
-
Bowyer, P.W.1
Tate, E.W.2
Leatherbarrow, R.J.3
Holder, A.A.4
Smith, D.F.5
Brown, K.A.6
-
138
-
-
84861212906
-
Selective inhibitors of protozoan protein N-myristoyltransferases as starting points for tropical disease medicinal chemistry programs
-
CrossRef PubMed
-
Bell, A. S., Mills, J. E., Williams, G. P., Brannigan, J. A., Wilkinson, A. J., Parkinson, T., Leatherbarrow, R. J., Tate, E. W., Holder, A. A. and Smith, D. F. (2012) Selective inhibitors of protozoan protein N-myristoyltransferases as starting points for tropical disease medicinal chemistry programs. PLoS Negl. Trop. Dis. 6, e1625 CrossRef PubMed
-
(2012)
PLoS Negl. Trop. Dis.
, vol.6
-
-
Bell, A.S.1
Mills, J.E.2
Williams, G.P.3
Brannigan, J.A.4
Wilkinson, A.J.5
Parkinson, T.6
Leatherbarrow, R.J.7
Tate, E.W.8
Holder, A.A.9
Smith, D.F.10
-
139
-
-
84859790956
-
Discovery of Plasmodium vivax N-myristoyltransferase inhibitors: Screening, synthesis, and structural characterization of their binding mode
-
CrossRef PubMed
-
Goncalves, V., Brannigan, J. A., Whalley, D., Ansell, K. H., Saxty, B., Holder, A. A., Wilkinson, A. J., Tate, E. W. and Leatherbarrow, R. J. (2012) Discovery of Plasmodium vivax N-myristoyltransferase inhibitors: screening, synthesis, and structural characterization of their binding mode. J. Med. Chem. 55, 3578-3582 CrossRef PubMed
-
(2012)
J. Med. Chem.
, vol.55
, pp. 3578-3582
-
-
Goncalves, V.1
Brannigan, J.A.2
Whalley, D.3
Ansell, K.H.4
Saxty, B.5
Holder, A.A.6
Wilkinson, A.J.7
Tate, E.W.8
Leatherbarrow, R.J.9
-
140
-
-
84867757397
-
Design and synthesis of inhibitors of Plasmodium falciparum N-myristoyltransferase, a promising target for antimalarial drug discovery
-
CrossRef PubMed
-
Yu, Z. Y., Brannigan, J. A., Moss, D. K., Brzozowski, A. M., Wilkinson, A. J., Holder, A. A., Tate, E. W. and Leatherbarrow, R. J. (2012) Design and synthesis of inhibitors of Plasmodium falciparum N-myristoyltransferase, a promising target for antimalarial drug discovery. J. Med. Chem. 55, 8879-8890 CrossRef PubMed
-
(2012)
J. Med. Chem.
, vol.55
, pp. 8879-8890
-
-
Yu, Z.Y.1
Brannigan, J.A.2
Moss, D.K.3
Brzozowski, A.M.4
Wilkinson, A.J.5
Holder, A.A.6
Tate, E.W.7
Leatherbarrow, R.J.8
-
141
-
-
84872315887
-
Discovery of novel and ligand-efficient inhibitors of Plasmodium falciparum and Plasmodium vivax N-myristoyltransferase
-
CrossRef PubMed
-
Rackham, M. D., Brannigan, J. A., Moss, D. K., Yu, Z. Y., Wilkinson, A. J., Holder, A. A., Tate, E. W. and Leatherbarrow, R. J. (2013) Discovery of novel and ligand-efficient inhibitors of Plasmodium falciparum and Plasmodium vivax N-myristoyltransferase. J. Med. Chem. 56, 371-375 CrossRef PubMed
-
(2013)
J. Med. Chem.
, vol.56
, pp. 371-375
-
-
Rackham, M.D.1
Brannigan, J.A.2
Moss, D.K.3
Yu, Z.Y.4
Wilkinson, A.J.5
Holder, A.A.6
Tate, E.W.7
Leatherbarrow, R.J.8
-
142
-
-
84897471004
-
Design and synthesis of high affinity inhibitors of Plasmodium falciparum and Plasmodium vivax N-myristoyltransferases directed by ligand efficiency dependent lipophilicity (LELP)
-
CrossRef PubMed
-
Rackham, M. D., Brannigan, J. A., Rangachari, K., Meister, S., Wilkinson, A. J., Holder, A. A., Leatherbarrow, R. J. and Tate, E. W. (2014) Design and synthesis of high affinity inhibitors of Plasmodium falciparum and Plasmodium vivax N-myristoyltransferases directed by ligand efficiency dependent lipophilicity (LELP). J. Med. Chem. 57, 2773-2788 CrossRef PubMed
-
(2014)
J. Med. Chem.
, vol.57
, pp. 2773-2788
-
-
Rackham, M.D.1
Brannigan, J.A.2
Rangachari, K.3
Meister, S.4
Wilkinson, A.J.5
Holder, A.A.6
Leatherbarrow, R.J.7
Tate, E.W.8
-
143
-
-
84892956192
-
Validation of N-myristoyltransferase as an antimalarial drug target using an integrated chemical biology approach
-
CrossRef PubMed
-
Wright, M. H., Clough, B., Rackham, M. D., Rangachari, K., Brannigan, J. A., Grainger, M., Moss, D. K., Bottrill, A. R., Heal, W. P., Broncel, M. et al. (2014) Validation of N-myristoyltransferase as an antimalarial drug target using an integrated chemical biology approach. Nat. Chem. 6, 112-121 CrossRef PubMed
-
(2014)
Nat. Chem.
, vol.6
, pp. 112-121
-
-
Wright, M.H.1
Clough, B.2
Rackham, M.D.3
Rangachari, K.4
Brannigan, J.A.5
Grainger, M.6
Moss, D.K.7
Bottrill, A.R.8
Heal, W.P.9
Broncel, M.10
-
144
-
-
33645531531
-
Structure of the MTIP-MyoA complex, a key component of the malaria parasite invasion motor
-
CrossRef PubMed
-
Bosch, J., Turley, S., Daly, T. M., Bogh, S. M., Villasmil, M. L., Roach, C., Zhou, N., Morrisey, J. M., Vaidya, A. B., Bergman, L. W. and Hol, W. G. J. (2006) Structure of the MTIP-MyoA complex, a key component of the malaria parasite invasion motor. Proc. Natl. Acad. Sci. U.S.A. 103, 4852-4857 CrossRef PubMed
-
(2006)
Proc. Natl. Acad. Sci. U.S.A.
, vol.103
, pp. 4852-4857
-
-
Bosch, J.1
Turley, S.2
Daly, T.M.3
Bogh, S.M.4
Villasmil, M.L.5
Roach, C.6
Zhou, N.7
Morrisey, J.M.8
Vaidya, A.B.9
Bergman, L.W.10
Hol, W.G.J.11
-
145
-
-
34547682065
-
The Closed MTIP-Myosin A-Tail Complex from the Malaria Parasite Invasion Machinery
-
DOI 10.1016/j.jmb.2007.06.016, PII S0022283607007978
-
Bosch, J., Turley, S., Roach, C. M., Daly, T. M., Bergman, L. W. and Hol, W. G. J. (2007) The closed MTIP-myosin A-tail complex from the malaria parasite invasion machinery. J. Mol. Biol. 372, 77-88 CrossRef PubMed (Pubitemid 47223217)
-
(2007)
Journal of Molecular Biology
, vol.372
, Issue.1
, pp. 77-88
-
-
Bosch, J.1
Turley, S.2
Roach, C.M.3
Daly, T.M.4
Bergman, L.W.5
Hol, W.G.J.6
-
146
-
-
77952780117
-
Structure-based design of novel small-molecule inhibitors of Plasmodium falciparum
-
CrossRef PubMed
-
Kortagere, S., Welsh, W. J., Morrisey, J. M., Daly, T., Ejigiri, I., Sinnis, P., Vaidya, A. B. and Bergman, L. W. (2010) Structure-based design of novel small-molecule inhibitors of Plasmodium falciparum. J. Chem. Inf. Model. 50, 840-849 CrossRef PubMed
-
(2010)
J. Chem. Inf. Model.
, vol.50
, pp. 840-849
-
-
Kortagere, S.1
Welsh, W.J.2
Morrisey, J.M.3
Daly, T.4
Ejigiri, I.5
Sinnis, P.6
Vaidya, A.B.7
Bergman, L.W.8
-
147
-
-
13844312649
-
ZINC - A free database of commercially available compounds for virtual screening
-
DOI 10.1021/ci049714+
-
Irwin, J. J. and Shoichet, B. K. (2005) ZINC: a free database of commercially available compounds for virtual screening. J. Chem. Inf. Model. 45, 177-182 CrossRef PubMed (Pubitemid 40736970)
-
(2005)
Journal of Chemical Information and Modeling
, vol.45
, Issue.1
, pp. 177-182
-
-
Irwin, J.J.1
Shoichet, B.K.2
-
148
-
-
77952007992
-
Interaction between Plasmodium falciparum apical membrane antigen 1 and the rhoptry neck protein complex defines a key step in the erythrocyte invasion process of malaria parasites
-
CrossRef PubMed
-
Richard, D., MacRaild, C. A., Riglar, D. T., Chan, J. A., Foley, M., Baum, J., Ralph, S. A., Norton, R. S. and Cowman, A. F. (2010) Interaction between Plasmodium falciparum apical membrane antigen 1 and the rhoptry neck protein complex defines a key step in the erythrocyte invasion process of malaria parasites. J. Biol. Chem. 285, 14815-14822 CrossRef PubMed
-
(2010)
J. Biol. Chem.
, vol.285
, pp. 14815-14822
-
-
Richard, D.1
MacRaild, C.A.2
Riglar, D.T.3
Chan, J.A.4
Foley, M.5
Baum, J.6
Ralph, S.A.7
Norton, R.S.8
Cowman, A.F.9
-
149
-
-
80051699901
-
Apical membrane antigen 1 as an anti-malarial drug target
-
CrossRef PubMed
-
Macraild, C. A., Anders, R. F., Foley, M. and Norton, R. S. (2011) Apical membrane antigen 1 as an anti-malarial drug target. Curr. Top. Med. Chem. 11, 2039-2047 CrossRef PubMed
-
(2011)
Curr. Top. Med. Chem.
, vol.11
, pp. 2039-2047
-
-
Macraild, C.A.1
Anders, R.F.2
Foley, M.3
Norton, R.S.4
-
150
-
-
24644523245
-
Structure of AMA1 from Plasmodium falciparum reveals a clustering of polymorphisms that surround a conserved hydrophobic pocket
-
DOI 10.1073/pnas.0501808102
-
Bai, T., Becker, M., Gupta, A., Strike, P., Murphy, V. J., Anders, R. F. and Batchelor, A. H. (2005) Structure of AMA1 from Plasmodium falciparum reveals a clustering of polymorphisms that surround a conserved hydrophobic pocket. Proc. Natl. Acad. Sci. U.S.A. 102, 12736-12741 CrossRef PubMed (Pubitemid 41279435)
-
(2005)
Proceedings of the National Academy of Sciences of the United States of America
, vol.102
, Issue.36
, pp. 12736-12741
-
-
Bai, T.1
Becker, M.2
Gupta, A.3
Strike, P.4
Murphy, V.J.5
Anders, R.F.6
Batchelor, A.H.7
-
151
-
-
79952205663
-
Peptide inhibitors of the malaria surface protein, apical membrane antigen 1: Identification of key binding residues
-
CrossRef PubMed
-
Lee, E. F., Yao, S., Sabo, J. K., Fairlie, W. D., Stevenson, R. A., Harris, K. S., Anders, R. F., Foley, M. and Norton, R. S. (2011) Peptide inhibitors of the malaria surface protein, apical membrane antigen 1: identification of key binding residues. Biopolymers 95, 354-364 CrossRef PubMed
-
(2011)
Biopolymers
, vol.95
, pp. 354-364
-
-
Lee, E.F.1
Yao, S.2
Sabo, J.K.3
Fairlie, W.D.4
Stevenson, R.A.5
Harris, K.S.6
Anders, R.F.7
Foley, M.8
Norton, R.S.9
-
152
-
-
84864054673
-
Structural and functional insights into the malaria parasite moving junction complex
-
CrossRef PubMed
-
Vulliez-Le Normand, B., Tonkin, M. L., Lamarque, M. H., Langer, S., Hoos, S., Roques, M., Saul, F. A., Faber, B. W., Bentley, G. A., Boulanger, M. J. and Lebrun, M. (2012) Structural and functional insights into the malaria parasite moving junction complex. PLoS Pathog. 8, e1002755 CrossRef PubMed
-
(2012)
PLoS Pathog.
, vol.8
-
-
Vulliez-Le Normand, B.1
Tonkin, M.L.2
Lamarque, M.H.3
Langer, S.4
Hoos, S.5
Roques, M.6
Saul, F.A.7
Faber, B.W.8
Bentley, G.A.9
Boulanger, M.J.10
Lebrun, M.11
-
153
-
-
84881442475
-
Disrupting malaria parasite AMA1-RON2 interaction with a small molecule prevents erythrocyte invasion
-
CrossRef PubMed
-
Srinivasan, P., Yasgar, A., Luci, D. K., Beatty, W. L., Hu, X., Andersen, J., Narum, D. L., Moch, J. K., Sun, H., Haynes, J. D. et al. (2013) Disrupting malaria parasite AMA1-RON2 interaction with a small molecule prevents erythrocyte invasion. Nat. Commun. 4, 2261 CrossRef PubMed
-
(2013)
Nat. Commun.
, vol.4
, pp. 2261
-
-
Srinivasan, P.1
Yasgar, A.2
Luci, D.K.3
Beatty, W.L.4
Hu, X.5
Andersen, J.6
Narum, D.L.7
Moch, J.K.8
Sun, H.9
Haynes, J.D.10
-
154
-
-
51449114441
-
Malarial proteases and host cell egress: An 'emerging' cascade
-
CrossRef PubMed
-
Blackman, M. J. (2008) Malarial proteases and host cell egress: an 'emerging' cascade. Cell. Microbiol. 10, 1925-1934 CrossRef PubMed
-
(2008)
Cell. Microbiol.
, vol.10
, pp. 1925-1934
-
-
Blackman, M.J.1
-
155
-
-
46249106081
-
Roles of proteases during invasion and egress by Plasmodium and Toxoplasma
-
CrossRef PubMed
-
Dowse, T. J., Koussis, K., Blackman, M. J. and Soldati-Favre, D. (2008) Roles of proteases during invasion and egress by Plasmodium and Toxoplasma . Subcell. Biochem. 47, 121-139 CrossRef PubMed
-
(2008)
Subcell. Biochem.
, vol.47
, pp. 121-139
-
-
Dowse, T.J.1
Koussis, K.2
Blackman, M.J.3
Soldati-Favre, D.4
-
156
-
-
84880063851
-
In silico screening on the three-dimensional model of the Plasmodium vivax SUB1 protease leads to the validation of a novel anti-parasite compound
-
CrossRef PubMed
-
Bouillon, A., Giganti, D., Benedet, C., Gorgette, O., Petres, S., Crublet, E., Girard-Blanc, C., Witkowski, B., Menard, D., Nilges, M. et al. (2013) In silico screening on the three-dimensional model of the Plasmodium vivax SUB1 protease leads to the validation of a novel anti-parasite compound. J. Biol. Chem. 288, 18561-18573 CrossRef PubMed
-
(2013)
J. Biol. Chem.
, vol.288
, pp. 18561-18573
-
-
Bouillon, A.1
Giganti, D.2
Benedet, C.3
Gorgette, O.4
Petres, S.5
Crublet, E.6
Girard-Blanc, C.7
Witkowski, B.8
Menard, D.9
Nilges, M.10
-
157
-
-
84861678443
-
Plasmodium subtilisin-like protease 1 (SUB1): Insights into the active-site structure, specificity and function of a pan-malaria drug target
-
CrossRef PubMed
-
Withers-Martinez, C., Suarez, C., Fulle, S., Kher, S., Penzo, M., Ebejer, J. P., Koussis, K., Hackett, F., Jirgensons, A., Finn, P. and Blackman, M. J. (2012) Plasmodium subtilisin-like protease 1 (SUB1): insights into the active-site structure, specificity and function of a pan-malaria drug target. Int. J. Parasitol. 42, 597-612 CrossRef PubMed
-
(2012)
Int. J. Parasitol.
, vol.42
, pp. 597-612
-
-
Withers-Martinez, C.1
Suarez, C.2
Fulle, S.3
Kher, S.4
Penzo, M.5
Ebejer, J.P.6
Koussis, K.7
Hackett, F.8
Jirgensons, A.9
Finn, P.10
Blackman, M.J.11
-
158
-
-
0029157321
-
BTS1 encodes a geranylgeranyl diphosphate synthase in Saccharomyces cerevisiae
-
CrossRef PubMed
-
Jiang, Y., Proteau, P., Poulter, D. and Ferronovick, S. (1995) BTS1 encodes a geranylgeranyl diphosphate synthase in Saccharomyces cerevisiae. J. Biol. Chem. 270, 21793-21799 CrossRef PubMed
-
(1995)
J. Biol. Chem.
, vol.270
, pp. 21793-21799
-
-
Jiang, Y.1
Proteau, P.2
Poulter, D.3
Ferronovick, S.4
-
159
-
-
0032145868
-
Protein prenyl transferase activities of Plasmodium falciparum
-
DOI 10.1016/S0166-6851(98)00065-6, PII S0166685198000656
-
Chakrabarti, D., Azam, T., DelVecchio, C., Qiu, L. B., Park, Y. and Allen, C. M. (1998) Protein prenyl transferase activities of Plasmodium falciparum. Mol. Biochem. Parasitol. 94, 175-184 CrossRef PubMed (Pubitemid 28377284)
-
(1998)
Molecular and Biochemical Parasitology
, vol.94
, Issue.2
, pp. 175-184
-
-
Chakrabarti, D.1
Azam, T.2
Delvecchio, C.3
Qiu, L.4
Park, Y.-I.5
Allen, C.M.6
-
160
-
-
84863236969
-
Lipophilic analogs of zoledronate and risedronate inhibit Plasmodium geranylgeranyl diphosphate synthase (GGPPS) and exhibit potent antimalarial activity
-
CrossRef PubMed
-
No, J. H., Dossin, F. D., Zhang, Y. H., Liu, Y. L., Zhu, W., Feng, X. X., Yoo, J. A., Lee, E., Wang, K., Hui, R. et al. (2012) Lipophilic analogs of zoledronate and risedronate inhibit Plasmodium geranylgeranyl diphosphate synthase (GGPPS) and exhibit potent antimalarial activity. Proc. Natl. Acad. Sci. U.S.A. 109, 4058-4063 CrossRef PubMed
-
(2012)
Proc. Natl. Acad. Sci. U.S.A.
, vol.109
, pp. 4058-4063
-
-
No, J.H.1
Dossin, F.D.2
Zhang, Y.H.3
Liu, Y.L.4
Zhu, W.5
Feng, X.X.6
Yoo, J.A.7
Lee, E.8
Wang, K.9
Hui, R.10
-
161
-
-
79952799000
-
Molecular characterization of a novel geranylgeranyl pyrophosphate synthase from Plasmodium parasites
-
CrossRef PubMed
-
Artz, J. D., Wernimont, A. K., Dunford, J. E., Schapira, M., Dong, A. P., Zhao, Y., Lew, J., Russell, R. G. G., Ebetino, F. H., Oppermann, U. and Hui, R. (2011) Molecular characterization of a novel geranylgeranyl pyrophosphate synthase from Plasmodium parasites. J. Biol. Chem. 286, 3315-3322 CrossRef PubMed
-
(2011)
J. Biol. Chem.
, vol.286
, pp. 3315-3322
-
-
Artz, J.D.1
Wernimont, A.K.2
Dunford, J.E.3
Schapira, M.4
Dong, A.P.5
Zhao, Y.6
Lew, J.7
Russell, R.G.G.8
Ebetino, F.H.9
Oppermann, U.10
Hui, R.11
-
162
-
-
58149104159
-
Bisphosphonate inhibition of a Plasmodium farnesyl diphosphate synthase and a general method for predicting cell-based activity from enzyme data
-
CrossRef PubMed
-
Mukkamala, D., No, J. H., Cass, L. A., Chang, T. K. and Oldfield, E. (2008) Bisphosphonate inhibition of a Plasmodium farnesyl diphosphate synthase and a general method for predicting cell-based activity from enzyme data. J. Med. Chem. 51, 7827-7833 CrossRef PubMed
-
(2008)
J. Med. Chem.
, vol.51
, pp. 7827-7833
-
-
Mukkamala, D.1
No, J.H.2
Cass, L.A.3
Chang, T.K.4
Oldfield, E.5
-
163
-
-
0035866666
-
Bisphosphonates inhibit the growth of Trypanosoma brucei, Trypanosoma cruzi, Leishmania donovani, Toxoplasma gondii, and Plasmodium falciparum: A potential route to chemotherapy
-
DOI 10.1021/jm0002578
-
Martin, M. B., Grimley, J. S., Lewis, J. C., Heath, H. T., Bailey, B. N., Kendrick, H., Yardley, V., Caldera, A., Lira, R., Urbina, J. A. et al. (2001) Bisphosphonates inhibit the growth of Trypanosoma brucei, Trypanosoma cruzi, Leishmania donovani, Toxoplasma gondii, and Plasmodium falciparum: a potential route to chemotherapy. J. Med. Chem. 44, 909-916 CrossRef PubMed (Pubitemid 32861615)
-
(2001)
Journal of Medicinal Chemistry
, vol.44
, Issue.6
, pp. 909-916
-
-
Martin, M.B.1
Grimley, J.S.2
Lewis, J.C.3
Heath III, H.T.4
Bailey, B.N.5
Kendrick, H.6
Yardley, V.7
Caldera, A.8
Lira, R.9
Urbina, J.A.10
Moreno, S.N.J.11
Docampo, R.12
Croft, S.L.13
Oldfield, E.14
-
164
-
-
77956310878
-
Emerging principles in protease-based drug discovery
-
CrossRef PubMed
-
Drag, M. and Salvesen, G. S. (2010) Emerging principles in protease-based drug discovery. Nat. Rev. Drug Discov. 9, 690-701 CrossRef PubMed
-
(2010)
Nat. Rev. Drug Discov.
, vol.9
, pp. 690-701
-
-
Drag, M.1
Salvesen, G.S.2
-
165
-
-
0037154180
-
Four plasmepsins are active in the Plasmodium falciparum food vacuole, including a protease with an active-site histidine
-
DOI 10.1073/pnas.022630099
-
Banerjee, R., Liu, J., Beatty, W., Pelosof, L., Klemba, M. and Goldberg, D. E. (2002) Four plasmepsins are active in the Plasmodium falciparum food vacuole, including a protease with an active-site histidine. Proc. Natl. Acad. Sci. U.S.A. 99, 990-995 CrossRef PubMed (Pubitemid 34106623)
-
(2002)
Proceedings of the National Academy of Sciences of the United States of America
, vol.99
, Issue.2
, pp. 990-995
-
-
Banerjee, R.1
Liu, J.2
Beatty, W.3
Pelosof, L.4
Klemba, M.5
Goldberg, D.E.6
-
166
-
-
0035997361
-
Biological roles of proteases in parasitic protozoa
-
DOI 10.1146/annurev.biochem.71.090501.145453
-
Klemba, M. and Goldberg, D. E. (2002) Biological roles of proteases in parasitic protozoa. Annu. Rev. Biochem. 71, 275-305 CrossRef PubMed (Pubitemid 34800222)
-
(2002)
Annual Review of Biochemistry
, vol.71
, pp. 275-305
-
-
Klemba, M.1
Goldberg, D.E.2
-
167
-
-
0032971605
-
A distinct member of the aspartic proteinase gene family from the human malaria parasite Plasmodium falciparum
-
DOI 10.1016/S0014-5793(99)00276-8, PII S0014579399002768
-
Berry, C., Humphreys, M. J., Matharu, P., Granger, R., Horrocks, P., Moon, R. P., Certa, U., Ridley, R. G., Bur, D. and Kay, J. (1999) A distinct member of the aspartic proteinase gene family from the human malaria parasite Plasmodium falciparum. FEBS Lett. 447, 149-154 CrossRef PubMed (Pubitemid 29146076)
-
(1999)
FEBS Letters
, vol.447
, Issue.2-3
, pp. 149-154
-
-
Berry, C.1
Humphreys, M.J.2
Matharu, P.3
Granger, R.4
Horrocks, P.5
Moon, R.P.6
Certa, U.7
Ridley, R.G.8
Bur, D.9
Kay, J.10
-
168
-
-
0028211978
-
Order and specificity of the Plasmodium falciparum hemoglobin degradation pathway
-
Gluzman, I. Y., Francis, S. E., Oksman, A., Smith, C. E., Duffin, K. L. and Goldberg, D. E. (1994) Order and specificity of the Plasmodium falciparum hemoglobin degradation pathway. J. Clin. Invest. 93, 1602-1608 CrossRef PubMed (Pubitemid 24116398)
-
(1994)
Journal of Clinical Investigation
, vol.93
, Issue.4
, pp. 1602-1608
-
-
Gluzman, I.Y.1
Francis, S.E.2
Oksman, A.3
Smith, C.E.4
Duffin, K.L.5
Goldberg, D.E.6
-
169
-
-
57049113201
-
Development of protease inhibitors for protozoan infections
-
CrossRef PubMed
-
McKerrow, J. H., Rosenthal, P. J., Swenerton, R. and Doyle, P. (2008) Development of protease inhibitors for protozoan infections. Curr. Opin. Infect. Dis. 21, 668-672 CrossRef PubMed
-
(2008)
Curr. Opin. Infect. Dis.
, vol.21
, pp. 668-672
-
-
McKerrow, J.H.1
Rosenthal, P.J.2
Swenerton, R.3
Doyle, P.4
-
170
-
-
34250620398
-
Critical roles for the digestive vacuole plasmepsins of Plasmodium falciparum in vacuolar function
-
DOI 10.1111/j.1365-2958.2007.05768.x
-
Bonilla, J. A., Bonilla, T. D., Yowell, C. A., Fujioka, H. and Dame, J. B. (2007) Critical roles for the digestive vacuole plasmepsins of Plasmodium falciparum in vacuolar function. Mol. Microbiol. 65, 64-75 CrossRef PubMed (Pubitemid 46934483)
-
(2007)
Molecular Microbiology
, vol.65
, Issue.1
, pp. 64-75
-
-
Bonilla, J.A.1
Bonilla, T.D.2
Yowell, C.A.3
Fujioka, H.4
Dame, J.B.5
-
171
-
-
70350023620
-
Functional profiling, identification, and inhibition of plasmepsins in intraerythrocytic malaria parasites
-
CrossRef PubMed
-
Liu, K., Shi, H., Xiao, H., Chong, A. G., Bi, X., Chang, Y. T., Tan, K. S., Yada, R. Y. and Yao, S. Q. (2009) Functional profiling, identification, and inhibition of plasmepsins in intraerythrocytic malaria parasites. Angew. Chem. Int. Ed. Engl. 48, 8293-8297 CrossRef PubMed
-
(2009)
Angew. Chem. Int. Ed. Engl.
, vol.48
, pp. 8293-8297
-
-
Liu, K.1
Shi, H.2
Xiao, H.3
Chong, A.G.4
Bi, X.5
Chang, Y.T.6
Tan, K.S.7
Yada, R.Y.8
Yao, S.Q.9
-
172
-
-
66049110565
-
Recombinant plasmepsin 1 from the human malaria parasite Plasmodium falciparum: Enzymatic characterization, active site inhibitor design, and structural analysis
-
CrossRef PubMed
-
Liu, P., Marzahn, M. R., Robbins, A. H., Gutierrez-de-Teran, H., Rodriguez, D., McClung, S. H., Stevens, Jr, S. M., Yowell, C. A., Dame, J. B., McKenna, R. and Dunn, B. M. (2009) Recombinant plasmepsin 1 from the human malaria parasite Plasmodium falciparum: enzymatic characterization, active site inhibitor design, and structural analysis. Biochemistry 48, 4086-4099 CrossRef PubMed
-
(2009)
Biochemistry
, vol.48
, pp. 4086-4099
-
-
Liu, P.1
Marzahn, M.R.2
Robbins, A.H.3
Gutierrez-de-Teran, H.4
Rodriguez, D.5
McClung, S.H.6
Stevens Jr., S.M.7
Yowell, C.A.8
Dame, J.B.9
McKenna, R.10
Dunn, B.M.11
-
173
-
-
0029027901
-
Design and synthesis of HIV protease inhibitors containing allophenylnorstatine as a transition-state mimic
-
CrossRef PubMed
-
Kiso, Y. (1995) Design and synthesis of HIV protease inhibitors containing allophenylnorstatine as a transition-state mimic. Adv. Exp. Med. Biol. 362, 413-423 CrossRef PubMed
-
(1995)
Adv. Exp. Med. Biol.
, vol.362
, pp. 413-423
-
-
Kiso, Y.1
-
174
-
-
0029949211
-
The bioavailability of oral dosage forms of a new HIV-1 protease inhibitor, KNI-272, in beagle dogs
-
DOI 10.1002/(SICI)1099-081X(199603)17:2<125::AID-B
-
Kiriyama, A., Sugahara, M., Yoshikawa, Y., Kiso, Y. and Takada, K. (1996) The bioavailability of oral dosage forms of a new HIV-1 protease inhibitor, KNI-272, in beagle dogs. Biopharm. Drug Dispos. 17, 125-134 CrossRef PubMed (Pubitemid 26083020)
-
(1996)
Biopharmaceutics and Drug Disposition
, vol.17
, Issue.2
, pp. 125-134
-
-
Kiriyama, A.1
Sugahara, M.2
Yoshikawa, Y.3
Kiso, Y.4
Takada, K.5
-
175
-
-
82755161768
-
Structural studies of vacuolar plasmepsins
-
CrossRef PubMed
-
Bhaumik, P., Gustchina, A. and Wlodawer, A. (2012) Structural studies of vacuolar plasmepsins. Biochim. Biophys. Acta 1824, 207-223 CrossRef PubMed
-
(2012)
Biochim. Biophys. Acta
, vol.1824
, pp. 207-223
-
-
Bhaumik, P.1
Gustchina, A.2
Wlodawer, A.3
-
176
-
-
33646573016
-
Structure of the aspartic protease plasmepsin 4 from the malarial parasite Plasmodium malariae bound to an allophenylnorstatine-based inhibitor
-
DOI 10.1107/S0907444905041260
-
Clemente, J. C., Govindasamy, L., Madabushi, A., Fisher, S. Z., Moose, R. E., Yowell, C. A., Hidaka, K., Kimura, T., Hayashi, Y., Kiso, Y. et al. (2006) Structure of the aspartic protease plasmepsin 4 from the malarial parasite Plasmodium malariae bound to an allophenylnorstatine-based inhibitor. Acta Crystallogr. D Biol. Crystallogr. 62, 246-252 CrossRef PubMed (Pubitemid 44185133)
-
(2006)
Acta Crystallographica Section D: Biological Crystallography
, vol.62
, Issue.3
, pp. 246-252
-
-
Clemente, J.C.1
Govindasamy, L.2
Madabushi, A.3
Fisher, S.Z.4
Moose, R.E.5
Yowell, C.A.6
Hidaka, K.7
Kimura, T.8
Hayashi, Y.9
Kiso, Y.10
Agbandje-Mckenna, M.11
Dame, J.B.12
Dunn, B.M.13
McKenna, R.14
-
177
-
-
0037780064
-
High-affinity inhibition of a family of Plasmodium falciparum proteases by a designed adaptive inhibitor
-
DOI 10.1021/bi034131z
-
Nezami, A., Kimura, T., Hidaka, K., Kiso, A., Liu, J., Kiso, Y., Goldberg, D. E. and Freire, E. (2003) High-affinity inhibition of a family of Plasmodium falciparum proteases by a designed adaptive inhibitor. Biochemistry 42, 8459-8464 CrossRef PubMed (Pubitemid 36875411)
-
(2003)
Biochemistry
, vol.42
, Issue.28
, pp. 8459-8464
-
-
Nezami, A.1
Kimura, T.2
Hidaka, K.3
Kiso, A.4
Liu, J.5
Kiso, Y.6
Goldberg, D.E.7
Freire, E.8
-
178
-
-
79956214335
-
Crystal structures of the free and inhibited forms of plasmepsin I (PMI) from Plasmodium falciparum
-
CrossRef PubMed
-
Bhaumik, P., Horimoto, Y., Xiao, H., Miura, T., Hidaka, K., Kiso, Y., Wlodawer, A., Yada, R. Y. and Gustchina, A. (2011) Crystal structures of the free and inhibited forms of plasmepsin I (PMI) from Plasmodium falciparum. J. Struct. Biol. 175, 73-84 CrossRef PubMed
-
(2011)
J. Struct. Biol.
, vol.175
, pp. 73-84
-
-
Bhaumik, P.1
Horimoto, Y.2
Xiao, H.3
Miura, T.4
Hidaka, K.5
Kiso, Y.6
Wlodawer, A.7
Yada, R.Y.8
Gustchina, A.9
-
179
-
-
64649106677
-
Crystal structures of the histo-aspartic protease (HAP) from Plasmodium falciparum
-
CrossRef PubMed
-
Bhaumik, P., Xiao, H., Parr, C. L., Kiso, Y., Gustchina, A., Yada, R. Y. and Wlodawer, A. (2009) Crystal structures of the histo-aspartic protease (HAP) from Plasmodium falciparum. J. Mol. Biol. 388, 520-540 CrossRef PubMed
-
(2009)
J. Mol. Biol.
, vol.388
, pp. 520-540
-
-
Bhaumik, P.1
Xiao, H.2
Parr, C.L.3
Kiso, Y.4
Gustchina, A.5
Yada, R.Y.6
Wlodawer, A.7
-
180
-
-
80054768306
-
Structural insights into the activation and inhibition of histo-aspartic protease from Plasmodium falciparum
-
CrossRef PubMed
-
Bhaumik, P., Xiao, H., Hidaka, K., Gustchina, A., Kiso, Y., Yada, R. Y. and Wlodawer, A. (2011) Structural insights into the activation and inhibition of histo-aspartic protease from Plasmodium falciparum. Biochemistry 50, 8862-8879 CrossRef PubMed
-
(2011)
Biochemistry
, vol.50
, pp. 8862-8879
-
-
Bhaumik, P.1
Xiao, H.2
Hidaka, K.3
Gustchina, A.4
Kiso, Y.5
Yada, R.Y.6
Wlodawer, A.7
-
181
-
-
84871570163
-
Potent inhibitors of malarial aspartic proteases, the plasmepsins, by hydroformylation of substituted 7-azanorbornenes
-
CrossRef PubMed
-
Aureggi, V., Ehmke, V., Wieland, J., Schweizer, W. B., Bernet, B., Bur, D., Meyer, S., Rottmann, M., Freymond, C., Brun, R. et al. (2013) Potent inhibitors of malarial aspartic proteases, the plasmepsins, by hydroformylation of substituted 7-azanorbornenes. Chemistry 19, 155-164 CrossRef PubMed
-
(2013)
Chemistry
, vol.19
, pp. 155-164
-
-
Aureggi, V.1
Ehmke, V.2
Wieland, J.3
Schweizer, W.B.4
Bernet, B.5
Bur, D.6
Meyer, S.7
Rottmann, M.8
Freymond, C.9
Brun, R.10
-
182
-
-
79956153052
-
Identification of plasmepsin inhibitors as selective anti-malarial agents using ligand based drug design
-
CrossRef PubMed
-
McKay, P. B., Peters, M. B., Carta, G., Flood, C. T., Dempsey, E., Bell, A., Berry, C., Lloyd, D. G. and Fayne, D. (2011) Identification of plasmepsin inhibitors as selective anti-malarial agents using ligand based drug design. Bioorg. Med. Chem. Lett. 21, 3335-3341 CrossRef PubMed
-
(2011)
Bioorg. Med. Chem. Lett.
, vol.21
, pp. 3335-3341
-
-
McKay, P.B.1
Peters, M.B.2
Carta, G.3
Flood, C.T.4
Dempsey, E.5
Bell, A.6
Berry, C.7
Lloyd, D.G.8
Fayne, D.9
-
183
-
-
2942592064
-
Plasmodium falciparum cysteine protease falcipain-1 is not essential in erythrocytic stage malaria parasites
-
DOI 10.1073/pnas.0402738101
-
Sijwali, P. S., Kato, K., Seydel, K. B., Gut, J., Lehman, J., Klemba, M., Goldberg, D. E., Miller, L. H. and Rosenthal, P. J. (2004) Plasmodium falciparum cysteine protease falcipain-1 is not essential in erythrocytic stage malaria parasites. Proc. Natl. Acad. Sci. U.S.A. 101, 8721-8726 CrossRef PubMed (Pubitemid 38745838)
-
(2004)
Proceedings of the National Academy of Sciences of the United States of America
, vol.101
, Issue.23
, pp. 8721-8726
-
-
Sijwali, P.S.1
Kato, K.2
Seydel, K.B.3
Gut, J.4
Lehman, J.5
Klemba, M.6
Goldberg, D.E.7
Miller, L.H.8
Rosenthal, P.J.9
-
184
-
-
0037226491
-
Structure-activity relationships for inhibition of cysteine protease activity and development of Plasmodium falciparum by peptidyl vinyl sulfones
-
DOI 10.1128/AAC.47.1.154-160.2003
-
Shenai, B. R., Lee, B. J., Alvarez-Hernandez, A., Chong, P. Y., Emal, C. D., Neitz, R. J., Roush, W. R. and Rosenthal, P. J. (2003) Structure-activity relationships for inhibition of cysteine protease activity and development of Plasmodium falciparum by peptidyl vinyl sulfones. Antimicrob. Agents Chemother. 47, 154-160 CrossRef PubMed (Pubitemid 36070357)
-
(2003)
Antimicrobial Agents and Chemotherapy
, vol.47
, Issue.1
, pp. 154-160
-
-
Shenai, B.R.1
Lee, B.J.2
Alvarez-Hernandez, A.3
Chong, P.Y.4
Emal, C.D.5
Neitz, R.J.6
Roush, W.R.7
Rosenthal, P.J.8
-
185
-
-
33746791205
-
Structural basis for unique mechanisms of folding and hemoglobin binding by a malarial protease
-
DOI 10.1073/pnas.0600489103
-
Wang, S. X., Pandey, K. C., Somoza, J. R., Sijwali, P. S., Kortemme, T., Brinen, L. S., Fletterick, R. J., Rosenthal, P. J. and McKerrow, J. H. (2006) Structural basis for unique mechanisms of folding and hemoglobin binding by a malarial protease. Proc. Natl. Acad. Sci. U.S.A. 103, 11503-11508 CrossRef PubMed (Pubitemid 44182481)
-
(2006)
Proceedings of the National Academy of Sciences of the United States of America
, vol.103
, Issue.31
, pp. 11503-11508
-
-
Wang, S.X.1
Pandey, K.C.2
Somoza, J.R.3
Sijwali, P.S.4
Kortemme, T.5
Brinen, L.S.6
Fletterick, R.J.7
Rosenthal, P.J.8
McKerrow, J.H.9
-
186
-
-
61449267734
-
Structures of falcipain-2 and falcipain-3 bound to small molecule inhibitors: Implications for substrate specificity
-
CrossRef PubMed
-
Kerr, I. D., Lee, J. H., Pandey, K. C., Harrison, A., Sajid, M., Rosenthal, P. J. and Brinen, L. S. (2009) Structures of falcipain-2 and falcipain-3 bound to small molecule inhibitors: implications for substrate specificity. J. Med. Chem. 52, 852-857 CrossRef PubMed
-
(2009)
J. Med. Chem.
, vol.52
, pp. 852-857
-
-
Kerr, I.D.1
Lee, J.H.2
Pandey, K.C.3
Harrison, A.4
Sajid, M.5
Rosenthal, P.J.6
Brinen, L.S.7
-
187
-
-
84857769803
-
Falcipain inhibition as a promising antimalarial target
-
CrossRef PubMed
-
Marco, M. and Coteron, J. M. (2012) Falcipain inhibition as a promising antimalarial target. Curr. Top. Med. Chem. 12, 408-444 CrossRef PubMed
-
(2012)
Curr. Top. Med. Chem.
, vol.12
, pp. 408-444
-
-
Marco, M.1
Coteron, J.M.2
-
188
-
-
84880282478
-
Development of Plasmodium falciparum protease inhibitors in the past decade (2002-2012)
-
CrossRef PubMed
-
Perez, B., Teixeira, C., Gomes, J. R. and Gomes, P. (2013) Development of Plasmodium falciparum protease inhibitors in the past decade (2002-2012). Curr. Med. Chem. 20, 3049-3068 CrossRef PubMed
-
(2013)
Curr. Med. Chem.
, vol.20
, pp. 3049-3068
-
-
Perez, B.1
Teixeira, C.2
Gomes, J.R.3
Gomes, P.4
-
189
-
-
84894594903
-
Synthesis, biological evaluation, hydration site thermodynamics, and chemical reactivity analysis of α-keto substituted peptidomimetics for the inhibition of Plasmodium falciparum
-
CrossRef PubMed
-
Weldon, D. J., Shah, F., Chittiboyina, A. G., Sheri, A., Chada, R. R., Gut, J., Rosenthal, P. J., Shivakumar, D., Sherman, W., Desai, P. et al. (2014) Synthesis, biological evaluation, hydration site thermodynamics, and chemical reactivity analysis of α-keto substituted peptidomimetics for the inhibition of Plasmodium falciparum. Bioorg. Med. Chem. Lett. 24, 1274-1279 CrossRef PubMed
-
(2014)
Bioorg. Med. Chem. Lett.
, vol.24
, pp. 1274-1279
-
-
Weldon, D.J.1
Shah, F.2
Chittiboyina, A.G.3
Sheri, A.4
Chada, R.R.5
Gut, J.6
Rosenthal, P.J.7
Shivakumar, D.8
Sherman, W.9
Desai, P.10
-
190
-
-
78650319030
-
Total synthesis and antimalarial activity of symplostatin 4
-
CrossRef PubMed
-
Conroy, T., Guo, J. T., Hunt, N. H. and Payne, R. J. (2010) Total synthesis and antimalarial activity of symplostatin 4. Org. Lett. 12, 5576-5579 CrossRef PubMed
-
(2010)
Org. Lett.
, vol.12
, pp. 5576-5579
-
-
Conroy, T.1
Guo, J.T.2
Hunt, N.H.3
Payne, R.J.4
-
191
-
-
81755163141
-
Total synthesis, stereochemical assignment, and antimalarial activity of gallinamide A
-
CrossRef PubMed
-
Conroy, T., Guo, J. T., Linington, R. G., Hunt, N. H. and Payne, R. J. (2011) Total synthesis, stereochemical assignment, and antimalarial activity of gallinamide A. Chemistry 17, 13544-13552 CrossRef PubMed
-
(2011)
Chemistry
, vol.17
, pp. 13544-13552
-
-
Conroy, T.1
Guo, J.T.2
Linington, R.G.3
Hunt, N.H.4
Payne, R.J.5
-
192
-
-
39049108641
-
Symplocamide A, a potent cytotoxin and chymotrypsin inhibitor from the marine cyanobacterium Symploca sp.
-
DOI 10.1021/np070280x
-
Linington, R. G., Edwards, D. J., Shuman, C. F., McPhail, K. L., Matainaho, T. and Gerwick, W. H. (2008) Symplocamide A, a potent cytotoxin and chymotrypsin inhibitor from the marine cyanobacterium Symploca sp. J. Nat. Prod. 71, 22-27 CrossRef PubMed (Pubitemid 351236389)
-
(2008)
Journal of Natural Products
, vol.71
, Issue.1
, pp. 22-27
-
-
Linington, R.G.1
Edwards, D.J.2
Shuman, C.F.3
McPhail, K.L.4
Matainaho, T.5
Gerwick, W.H.6
-
193
-
-
84871579710
-
The antimalarial natural product symplostatin 4 is a nanomolar inhibitor of the food vacuole falcipains
-
CrossRef PubMed
-
Stolze, S. C., Deu, E., Kaschani, F., Li, N., Florea, B. I., Richau, K. H., Colby, T., van der Hoorn, R. A., Overkleeft, H. S., Bogyo, M. and Kaiser, M. (2012) The antimalarial natural product symplostatin 4 is a nanomolar inhibitor of the food vacuole falcipains. Chem. Biol. 19, 1546-1555 CrossRef PubMed
-
(2012)
Chem. Biol.
, vol.19
, pp. 1546-1555
-
-
Stolze, S.C.1
Deu, E.2
Kaschani, F.3
Li, N.4
Florea, B.I.5
Richau, K.H.6
Colby, T.7
Van Der Hoorn, R.A.8
Overkleeft, H.S.9
Bogyo, M.10
Kaiser, M.11
-
194
-
-
5644247394
-
A Plasmodium falciparum dipeptidyl aminopeptidase I participates in vacuolar hemoglobin degradation
-
DOI 10.1074/jbc.M408123200
-
Klemba, M., Gluzman, I. and Goldberg, D. E. (2004) A Plasmodium falciparum dipeptidyl aminopeptidase I participates in vacuolar hemoglobin degradation. J. Biol. Chem. 279, 43000-43007 CrossRef PubMed (Pubitemid 39372193)
-
(2004)
Journal of Biological Chemistry
, vol.279
, Issue.41
, pp. 43000-43007
-
-
Klemba, M.1
Gluzman, I.2
Goldberg, D.E.3
-
195
-
-
77956051319
-
Functional studies of Plasmodium falciparum dipeptidyl aminopeptidase I using small molecule inhibitors and active site probes
-
CrossRef PubMed
-
Deu, E., Leyva, M. J., Albrow, V. E., Rice, M. J., Ellman, J. A. and Bogyo, M. (2010) Functional studies of Plasmodium falciparum dipeptidyl aminopeptidase I using small molecule inhibitors and active site probes. Chem. Biol. 17, 808-819 CrossRef PubMed
-
(2010)
Chem. Biol.
, vol.17
, pp. 808-819
-
-
Deu, E.1
Leyva, M.J.2
Albrow, V.E.3
Rice, M.J.4
Ellman, J.A.5
Bogyo, M.6
-
196
-
-
84884251262
-
Plasmodium dipeptidyl aminopeptidases as malaria transmission-blocking drug targets
-
CrossRef PubMed
-
Tanaka, T. Q., Deu, E., Molina-Cruz, A., Ashburne, M. J., Ali, O., Suri, A., Kortagere, S., Bogyo, M. and Williamson, K. C. (2013) Plasmodium dipeptidyl aminopeptidases as malaria transmission-blocking drug targets. Antimicrob. Agents Chemother. 57, 4645-4652 CrossRef PubMed
-
(2013)
Antimicrob. Agents Chemother.
, vol.57
, pp. 4645-4652
-
-
Tanaka, T.Q.1
Deu, E.2
Molina-Cruz, A.3
Ashburne, M.J.4
Ali, O.5
Suri, A.6
Kortagere, S.7
Bogyo, M.8
Williamson, K.C.9
-
197
-
-
37249008065
-
Roles for two aminopeptidases in vacuolar hemoglobin catabolism in Plasmodium falciparum
-
DOI 10.1074/jbc.M703643200
-
Dalal, S. and Klemba, M. (2007) Roles for two aminopeptidases in vacuolar hemoglobin catabolism in Plasmodium falciparum. J. Biol. Chem. 282, 35978-35987 CrossRef PubMed (Pubitemid 350277126)
-
(2007)
Journal of Biological Chemistry
, vol.282
, Issue.49
, pp. 35978-35987
-
-
Dalal, S.1
Klemba, M.2
-
198
-
-
0025255254
-
Hemoglobin degradation in the malaria parasite Plasmodium falciparum: An ordered process in a unique organelle
-
CrossRef PubMed
-
Goldberg, D. E., Slater, A. F., Cerami, A. and Henderson, G. B. (1990) Hemoglobin degradation in the malaria parasite Plasmodium falciparum: an ordered process in a unique organelle. Proc. Natl. Acad. Sci. U.S.A. 87, 2931-2935 CrossRef PubMed
-
(1990)
Proc. Natl. Acad. Sci. U.S.A.
, vol.87
, pp. 2931-2935
-
-
Goldberg, D.E.1
Slater, A.F.2
Cerami, A.3
Henderson, G.B.4
-
199
-
-
0036183460
-
Hydrolysis of erythrocyte proteins by proteases of malaria parasites
-
CrossRef PubMed
-
Rosenthal, P. J. (2002) Hydrolysis of erythrocyte proteins by proteases of malaria parasites. Curr. Opin. Hematol. 9, 140-145 CrossRef PubMed
-
(2002)
Curr. Opin. Hematol.
, vol.9
, pp. 140-145
-
-
Rosenthal, P.J.1
-
200
-
-
80052154599
-
Bestatin-based chemical biology strategy reveals distinct roles for malaria M1- and M17-family aminopeptidases
-
CrossRef PubMed
-
Harbut, M. B., Velmourougane, G., Dalal, S., Reiss, G., Whisstock, J. C., Onder, O., Brisson, D., McGowan, S., Klemba, M. and Greenbaum, D. C. (2011) Bestatin-based chemical biology strategy reveals distinct roles for malaria M1- and M17-family aminopeptidases. Proc. Natl. Acad. Sci. U.S.A. 108, E526-534 CrossRef PubMed
-
(2011)
Proc. Natl. Acad. Sci. U.S.A.
, vol.108
-
-
Harbut, M.B.1
Velmourougane, G.2
Dalal, S.3
Reiss, G.4
Whisstock, J.C.5
Onder, O.6
Brisson, D.7
McGowan, S.8
Klemba, M.9
Greenbaum, D.C.10
-
201
-
-
77954761603
-
Downstream effects of haemoglobinase inhibition in Plasmodium falciparum-infected erythrocytes
-
CrossRef PubMed
-
Naughton, J. A., Nasizadeh, S. and Bell, A. (2010) Downstream effects of haemoglobinase inhibition in Plasmodium falciparum-infected erythrocytes. Mol. Biochem. Parasitol. 173, 81-87 CrossRef PubMed
-
(2010)
Mol. Biochem. Parasitol.
, vol.173
, pp. 81-87
-
-
Naughton, J.A.1
Nasizadeh, S.2
Bell, A.3
-
202
-
-
35748956443
-
The M18 aspartyl aminopeptidase of the human malaria parasite Plasmodium falciparum
-
DOI 10.1074/jbc.M704938200
-
Teuscher, F., Lowther, J., Skinner-Adams, T. S., Spielmann, T., Dixon, M. W., Stack, C. M., Donnelly, S., Mucha, A., Kafarski, P., Vassiliou, S. et al. (2007) The M18 aspartyl aminopeptidase of the human malaria parasite Plasmodium falciparum. J. Biol. Chem. 282, 30817-30826 CrossRef PubMed (Pubitemid 350041547)
-
(2007)
Journal of Biological Chemistry
, vol.282
, Issue.42
, pp. 30817-30826
-
-
Teuscher, F.1
Lowther, J.2
Skinner-Adams, T.S.3
Spielmann, T.4
Dixon, M.W.A.5
Stack, C.M.6
Donnelly, S.7
Mucha, A.8
Kafarski, P.9
Vassiliou, S.10
Gardiner, D.L.11
Dalton, J.P.12
Trenholme, K.R.13
-
203
-
-
77249144842
-
Structure of the Plasmodium falciparum M17 aminopeptidase and significance for the design of drugs targeting the neutral exopeptidases
-
CrossRef PubMed
-
McGowan, S., Oellig, C. A., Birru, W. A., Caradoc-Davies, T. T., Stack, C. M., Lowther, J., Skinner-Adams, T., Mucha, A., Kafarski, P., Grembecka, J. et al. (2010) Structure of the Plasmodium falciparum M17 aminopeptidase and significance for the design of drugs targeting the neutral exopeptidases. Proc. Natl. Acad. Sci. U.S.A. 107, 2449-2454 CrossRef PubMed
-
(2010)
Proc. Natl. Acad. Sci. U.S.A.
, vol.107
, pp. 2449-2454
-
-
McGowan, S.1
Oellig, C.A.2
Birru, W.A.3
Caradoc-Davies, T.T.4
Stack, C.M.5
Lowther, J.6
Skinner-Adams, T.7
Mucha, A.8
Kafarski, P.9
Grembecka, J.10
-
204
-
-
62449312343
-
Structural basis for the inhibition of the essential Plasmodium falciparum M1 neutral aminopeptidase
-
CrossRef PubMed
-
McGowan, S., Porter, C. J., Lowther, J., Stack, C. M., Golding, S. J., Skinner-Adams, T. S., Trenholme, K. R., Teuscher, F., Donnelly, S. M., Grembecka, J. et al. (2009) Structural basis for the inhibition of the essential Plasmodium falciparum M1 neutral aminopeptidase. Proc. Natl. Acad. Sci. U.S.A. 106, 2537-2542 CrossRef PubMed
-
(2009)
Proc. Natl. Acad. Sci. U.S.A.
, vol.106
, pp. 2537-2542
-
-
McGowan, S.1
Porter, C.J.2
Lowther, J.3
Stack, C.M.4
Golding, S.J.5
Skinner-Adams, T.S.6
Trenholme, K.R.7
Teuscher, F.8
Donnelly, S.M.9
Grembecka, J.10
-
205
-
-
37849041347
-
Identification of phosphinate dipeptide analog inhibitors directed against the Plasmodium falciparum M17 leucine aminopeptidase as lead antimalarial compounds
-
CrossRef PubMed
-
Skinner-Adams, T. S., Lowther, J., Teuscher, F., Stack, C. M., Grembecka, J., Mucha, A., Kafarski, P., Trenholme, K. R., Dalton, J. P. and Gardiner, D. L. (2007) Identification of phosphinate dipeptide analog inhibitors directed against the Plasmodium falciparum M17 leucine aminopeptidase as lead antimalarial compounds. J. Med. Chem. 50, 6024-6031 CrossRef PubMed
-
(2007)
J. Med. Chem.
, vol.50
, pp. 6024-6031
-
-
Skinner-Adams, T.S.1
Lowther, J.2
Teuscher, F.3
Stack, C.M.4
Grembecka, J.5
Mucha, A.6
Kafarski, P.7
Trenholme, K.R.8
Dalton, J.P.9
Gardiner, D.L.10
-
206
-
-
84879558016
-
Synthesis and structure-activity relationships of phosphonic arginine mimetics as inhibitors of the M1 and M17 aminopeptidases from Plasmodium falciparum
-
CrossRef PubMed
-
Kannan Sivaraman, K., Paiardini, A., Sienczyk, M., Ruggeri, C., Oellig, C. A., Dalton, J. P., Scammells, P. J., Drag, M. and McGowan, S. (2013) Synthesis and structure-activity relationships of phosphonic arginine mimetics as inhibitors of the M1 and M17 aminopeptidases from Plasmodium falciparum. J. Med. Chem. 56, 5213-5217 CrossRef PubMed
-
(2013)
J. Med. Chem.
, vol.56
, pp. 5213-5217
-
-
Kannan Sivaraman, K.1
Paiardini, A.2
Sienczyk, M.3
Ruggeri, C.4
Oellig, C.A.5
Dalton, J.P.6
Scammells, P.J.7
Drag, M.8
McGowan, S.9
-
207
-
-
84857153598
-
Fingerprinting the substrate specificity of M1 and M17 neutral aminopeptidases of human malaria, Plasmodium falciparum
-
CrossRef
-
Poreba, M., McGowan, S., Skinner-Adams, T., Trenholme, K. R., Gardiner, D. L., Whisstock, J. C., To, J., Salvesen, G. S., Drag, M. and Dalton, J. P. (2012) Fingerprinting the substrate specificity of M1 and M17 neutral aminopeptidases of human malaria, Plasmodium falciparum. PLoS ONE 2, e31938 CrossRef
-
(2012)
PLoS ONE
, vol.2
-
-
Poreba, M.1
McGowan, S.2
Skinner-Adams, T.3
Trenholme, K.R.4
Gardiner, D.L.5
Whisstock, J.C.6
To, J.7
Salvesen, G.S.8
Drag, M.9
Dalton, J.P.10
-
208
-
-
55549119591
-
Development of bestatin-based activity-based probes for metallo-aminopeptidases
-
CrossRef PubMed
-
Harbut, M. B., Velmourougane, G., Reiss, G., Chandramohanadas, R. and Greenbaum, D. C. (2008) Development of bestatin-based activity-based probes for metallo-aminopeptidases. Bioorg. Med. Chem. Lett. 18, 5932-5936 CrossRef PubMed
-
(2008)
Bioorg. Med. Chem. Lett.
, vol.18
, pp. 5932-5936
-
-
Harbut, M.B.1
Velmourougane, G.2
Reiss, G.3
Chandramohanadas, R.4
Greenbaum, D.C.5
-
209
-
-
79952788440
-
Synthesis of new (-)-bestatin-based inhibitor libraries reveals a novel binding mode in the S1 pocket of the essential malaria M1 metalloaminopeptidase
-
CrossRef PubMed
-
Velmourougane, G., Harbut, M. B., Dalal, S., McGowan, S., Oellig, C. A., Meinhardt, N., Whisstock, J. C., Klemba, M. and Greenbaum, D. C. (2011) Synthesis of new (-)-bestatin-based inhibitor libraries reveals a novel binding mode in the S1 pocket of the essential malaria M1 metalloaminopeptidase. J. Med. Chem. 54, 1655-1666 CrossRef PubMed
-
(2011)
J. Med. Chem.
, vol.54
, pp. 1655-1666
-
-
Velmourougane, G.1
Harbut, M.B.2
Dalal, S.3
McGowan, S.4
Oellig, C.A.5
Meinhardt, N.6
Whisstock, J.C.7
Klemba, M.8
Greenbaum, D.C.9
-
210
-
-
84871655128
-
Structure-activity relationships and blood distribution of antiplasmodial aminopeptidase-1 inhibitors
-
CrossRef PubMed
-
Deprez-Poulain, R., Flipo, M., Piveteau, C., Leroux, F., Dassonneville, S., Florent, I., Maes, L., Cos, P. and Deprez, B. (2012) Structure-activity relationships and blood distribution of antiplasmodial aminopeptidase-1 inhibitors. J. Med. Chem. 55, 10909-10917 CrossRef PubMed
-
(2012)
J. Med. Chem.
, vol.55
, pp. 10909-10917
-
-
Deprez-Poulain, R.1
Flipo, M.2
Piveteau, C.3
Leroux, F.4
Dassonneville, S.5
Florent, I.6
Maes, L.7
Cos, P.8
Deprez, B.9
-
211
-
-
33947632299
-
Novel selective inhibitors of the zinc plasmodial aminopeptidase PfA-M1 as potential antimalarial agents
-
DOI 10.1021/jm061169b
-
Flipo, M., Beghyn, T., Leroux, V., Florent, I., Deprez, B. P. and Deprez-Poulain, R. F. (2007) Novel selective inhibitors of the zinc plasmodial aminopeptidase PfA-M1 as potential antimalarial agents. J. Med. Chem. 50, 1322-1334 CrossRef PubMed (Pubitemid 46496331)
-
(2007)
Journal of Medicinal Chemistry
, vol.50
, Issue.6
, pp. 1322-1334
-
-
Flipo, M.1
Beghyn, T.2
Leroux, V.3
Florent, I.4
Deprez, B.P.5
Deprez-Poulain, R.F.6
-
212
-
-
84861161965
-
The aminopeptidase inhibitor CHR-2863 is an orally bioavailable inhibitor of murine malaria
-
CrossRef PubMed
-
Skinner-Adams, T. S., Peatey, C. L., Anderson, K., Trenholme, K. R., Krige, D., Brown, C. L., Stack, C., Nsangou, D. M., Mathews, R. T., Thivierge, K. et al. (2012) The aminopeptidase inhibitor CHR-2863 is an orally bioavailable inhibitor of murine malaria. Antimicrob. Agents Chemother. 56, 3244-3249 CrossRef PubMed
-
(2012)
Antimicrob. Agents Chemother.
, vol.56
, pp. 3244-3249
-
-
Skinner-Adams, T.S.1
Peatey, C.L.2
Anderson, K.3
Trenholme, K.R.4
Krige, D.5
Brown, C.L.6
Stack, C.7
Nsangou, D.M.8
Mathews, R.T.9
Thivierge, K.10
-
213
-
-
84865484501
-
X-ray crystal structure and specificity of the Plasmodium falciparum malaria aminopeptidase PfM18AAP
-
CrossRef PubMed
-
Sivaraman, K. K., Oellig, C. A., Huynh, K., Atkinson, S. C., Poreba, M., Perugini, M. A., Trenholme, K. R., Gardiner, D. L., Salvesen, G., Drag, M. et al. (2012) X-ray crystal structure and specificity of the Plasmodium falciparum malaria aminopeptidase PfM18AAP. J. Mol. Biol. 422, 495-507 CrossRef PubMed
-
(2012)
J. Mol. Biol.
, vol.422
, pp. 495-507
-
-
Sivaraman, K.K.1
Oellig, C.A.2
Huynh, K.3
Atkinson, S.C.4
Poreba, M.5
Perugini, M.A.6
Trenholme, K.R.7
Gardiner, D.L.8
Salvesen, G.9
Drag, M.10
-
214
-
-
84904096362
-
-
Probe Reports from the NIH Molecular Libraries Program
-
Schoenen, F. J., Weiner, W. S., Baillargeon, P., Brown, C. L., Chase, P., Ferguson, J., Fernandez-Vega, V., Ghosh, P., Hodder, P., Krise, J. P. et al. (2010) Inhibitors of the Plasmodium falciparum M18 aspartyl aminopeptidase. Probe Reports from the NIH Molecular Libraries Program
-
(2010)
Inhibitors of the Plasmodium Falciparum M18 Aspartyl Aminopeptidase
-
-
Schoenen, F.J.1
Weiner, W.S.2
Baillargeon, P.3
Brown, C.L.4
Chase, P.5
Ferguson, J.6
Fernandez-Vega, V.7
Ghosh, P.8
Hodder, P.9
Krise, J.P.10
-
215
-
-
77952696164
-
Drug discovery: Priming the antimalarial pipeline
-
CrossRef PubMed
-
Fidock, D. A. (2010) Drug discovery: priming the antimalarial pipeline. Nature 465, 297-298 CrossRef PubMed
-
(2010)
Nature
, vol.465
, pp. 297-298
-
-
Fidock, D.A.1
-
216
-
-
78349297187
-
Feeding the antimalarial pipeline
-
CrossRef PubMed
-
Schlitzer, M. and Ortmann, R. (2010) Feeding the antimalarial pipeline. ChemMedChem 5, 1837-1840 CrossRef PubMed
-
(2010)
ChemMedChem
, vol.5
, pp. 1837-1840
-
-
Schlitzer, M.1
Ortmann, R.2
-
217
-
-
12144287677
-
Plasmodium falciparum glycogen synthase kinase-3: Molecular model, expression, intracellular localisation and selective inhibitors
-
DOI 10.1016/j.bbapap.2003.11.023, PII S1570963903003753
-
Droucheau, E., Primot, A., Thomas, V., Mattei, D., Knockaert, M., Richardson, C., Sallicandro, P., Alano, P., Jafarshad, A., Baratte, B. et al. (2004) Plasmodium falciparum glycogen synthase kinase-3: molecular model, expression, intracellular localisation and selective inhibitors. Biochim. Biophys. Acta 1697, 181-196 CrossRef PubMed (Pubitemid 38326771)
-
(2004)
Biochimica et Biophysica Acta - Proteins and Proteomics
, vol.1697
, Issue.1-2
, pp. 181-196
-
-
Droucheau, E.1
Primot, A.2
Thomas, V.3
Mattei, D.4
Knockaert, M.5
Richardson, C.6
Sallicandro, P.7
Alano, P.8
Jafarshad, A.9
Baratte, B.10
Kunick, C.11
Parzy, D.12
Pearl, L.13
Doerig, C.14
Meijer, L.15
-
218
-
-
82555196646
-
Global kinomic and phospho-proteomic analyses of the human malaria parasite Plasmodium falciparum
-
CrossRef PubMed
-
Solyakov, L., Halbert, J., Alam, M. M., Semblat, J. P., Dorin-Semblat, D., Reininger, L., Bottrill, A. R., Mistry, S., Abdi, A., Fennell, C. et al. (2011) Global kinomic and phospho-proteomic analyses of the human malaria parasite Plasmodium falciparum. Nat. Commun. 2, 565 CrossRef PubMed
-
(2011)
Nat. Commun.
, vol.2
, pp. 565
-
-
Solyakov, L.1
Halbert, J.2
Alam, M.M.3
Semblat, J.P.4
Dorin-Semblat, D.5
Reininger, L.6
Bottrill, A.R.7
Mistry, S.8
Abdi, A.9
Fennell, C.10
-
219
-
-
78650798680
-
Suppression of Plasmodium berghei parasitemia by LiCl in an animal infection model
-
PubMed
-
Zakaria, N. A., Embi, N. and Sidek, H. M. (2010) Suppression of Plasmodium berghei parasitemia by LiCl in an animal infection model. Trop. Biomed. 27, 624-631 PubMed
-
(2010)
Trop. Biomed.
, vol.27
, pp. 624-631
-
-
Zakaria, N.A.1
Embi, N.2
Sidek, H.M.3
-
220
-
-
70350352301
-
Comparative investigation of the ATP-binding site of human and plasmodial glycogen synthase kinase-3
-
CrossRef
-
Kruggel, S. and Lemcke, T. (2009) Comparative investigation of the ATP-binding site of human and plasmodial glycogen synthase kinase-3. QSAR Comb. Sci. 28, 885-890 CrossRef
-
(2009)
QSAR Comb. Sci.
, vol.28
, pp. 885-890
-
-
Kruggel, S.1
Lemcke, T.2
-
221
-
-
79956047327
-
Bioinformatic analysis of glycogen synthase kinase 3: Human versus parasite kinases
-
CrossRef PubMed
-
Osolodkin, D. I., Zakharevich, N. V., Palyulin, V. A., Danilenko, V. N. and Zefirov, N. S. (2011) Bioinformatic analysis of glycogen synthase kinase 3: human versus parasite kinases. Parasitology 138, 725-735 CrossRef PubMed
-
(2011)
Parasitology
, vol.138
, pp. 725-735
-
-
Osolodkin, D.I.1
Zakharevich, N.V.2
Palyulin, V.A.3
Danilenko, V.N.4
Zefirov, N.S.5
-
222
-
-
84872298847
-
3,6-Diamino-4-(2-halophenyl)-2-benzoylthieno[2,3-b ]pyridine-5- carbonitriles are selective inhibitors of Plasmodium falciparum glycogen synthase kinase-3
-
CrossRef PubMed
-
Fugel, W., Oberholzer, A. E., Gschloessl, B., Dzikowski, R., Pressburger, N., Preu, L., Pearl, L. H., Baratte, B., Ratin, M., Okun, I. et al. (2013) 3,6-Diamino-4-(2-halophenyl)-2-benzoylthieno[2,3-b ]pyridine-5-carbonitriles are selective inhibitors of Plasmodium falciparum glycogen synthase kinase-3. J. Med. Chem. 56, 264-275 CrossRef PubMed
-
(2013)
J. Med. Chem.
, vol.56
, pp. 264-275
-
-
Fugel, W.1
Oberholzer, A.E.2
Gschloessl, B.3
Dzikowski, R.4
Pressburger, N.5
Preu, L.6
Pearl, L.H.7
Baratte, B.8
Ratin, M.9
Okun, I.10
-
223
-
-
0028060031
-
Roles of peptidyl-prolyl cis-trans isomerase and calcineurin in the mechanisms of antimalarial action of cyclosporin A, FK506, and rapamycin
-
DOI 10.1016/0006-2952(94)90279-8
-
Bell, A., Wernli, B. and Franklin, R. M. (1994) Roles of peptidyl-prolyl cis-trans isomerase and calcineurin in the mechanisms of antimalarial action of cyclosporine-A, FK506, and rapamycin. Biochem. Pharmacol. 48, 495-503 CrossRef PubMed (Pubitemid 24257012)
-
(1994)
Biochemical Pharmacology
, vol.48
, Issue.3
, pp. 495-503
-
-
Bell, A.1
Wernli, B.2
Franklin, R.M.3
-
224
-
-
0038546791
-
A bifunctional molecule that displays context-dependent cellular activity
-
DOI 10.1021/ja035176q
-
Braun, P. D., Barglow, K. T., Lin, Y. M., Akompong, T., Briesewitz, R., Ray, G. T., Haldar, K. and Wandless, T. J. (2003) A bifunctional molecule that displays context-dependent cellular activity. J. Am. Chem. Soc. 125, 7575-7580 CrossRef PubMed (Pubitemid 36750278)
-
(2003)
Journal of the American Chemical Society
, vol.125
, Issue.25
, pp. 7575-7580
-
-
Braun, P.D.1
Barglow, K.T.2
Lin, Y.-M.3
Akompong, T.4
Briesewitz, R.5
Ray, G.T.6
Haldar, K.7
Wandless, T.J.8
-
225
-
-
1242292029
-
Regulation of peptide bond cis/trans isomerization by enzyme catalysis and its implication in physiological processes
-
CrossRef
-
Fischer, G. and Aumuller, T. (2004) Regulation of peptide bond cis/trans isomerization by enzyme catalysis and its implication in physiological processes. Rev. Physiol. Biochem. Pharmacol. 148, 105-150 CrossRef
-
(2004)
Rev. Physiol. Biochem. Pharmacol.
, vol.148
, pp. 105-150
-
-
Fischer, G.1
Aumuller, T.2
-
226
-
-
84875481785
-
Structural insights into substrate binding by PvFKBP35, a peptidylprolyl cis-trans isomerase from the human malarial parasite Plasmodium vivax
-
CrossRef PubMed
-
Alag, R., Balakrishna, A. M., Rajan, S., Qureshi, I. A., Shin, J., Lescar, J., Gruber, G. and Yoon, H. S. (2013) Structural insights into substrate binding by PvFKBP35, a peptidylprolyl cis-trans isomerase from the human malarial parasite Plasmodium vivax . Eukaryot. Cell 12, 627-634 CrossRef PubMed
-
(2013)
Eukaryot. Cell
, vol.12
, pp. 627-634
-
-
Alag, R.1
Balakrishna, A.M.2
Rajan, S.3
Qureshi, I.A.4
Shin, J.5
Lescar, J.6
Gruber, G.7
Yoon, H.S.8
-
227
-
-
77955098310
-
NMR and crystallographic structures of the FK506 binding domain of human malarial parasite Plasmodium vivax FKBP35
-
CrossRef PubMed
-
Alag, R., Qureshi, I. A., Bharatham, N., Shin, J., Lescar, J. and Yoon, H. S. (2010) NMR and crystallographic structures of the FK506 binding domain of human malarial parasite Plasmodium vivax FKBP35. Protein Sci. 19, 1577-1586 CrossRef PubMed
-
(2010)
Protein Sci.
, vol.19
, pp. 1577-1586
-
-
Alag, R.1
Qureshi, I.A.2
Bharatham, N.3
Shin, J.4
Lescar, J.5
Yoon, H.S.6
-
228
-
-
44449107714
-
Crystal structure of the FK506 binding domain of Plasmodium falciparum FKBP35 in complex with FK506
-
DOI 10.1021/bi800004u
-
Kotaka, M., Ye, H., Alag, R., Hu, G. A., Bozdech, Z., Preiser, P. R., Yoon, H. S. and Lescar, J. (2008) Crystal structure of the FK506 binding domain of Plasmodium falciparum FKBP35 in complex with FK506. Biochemistry 47, 5951-5961 CrossRef PubMed (Pubitemid 351770025)
-
(2008)
Biochemistry
, vol.47
, Issue.22
, pp. 5951-5961
-
-
Kotaka, M.1
Ye, H.2
Alag, R.3
Hu, G.4
Bozdech, Z.5
Preiser, P.R.6
Ho, S.Y.7
Lescar, J.8
-
229
-
-
84883264897
-
Small molecule Plasmodium FKBP35 inhibitor as a potential antimalaria agent
-
CrossRef PubMed
-
Harikishore, A., Niang, M., Rajan, S., Preiser, P. R. and Yoon, H. S. (2013) Small molecule Plasmodium FKBP35 inhibitor as a potential antimalaria agent. Sci. Rep. 3, 2501 CrossRef PubMed
-
(2013)
Sci. Rep.
, vol.3
, pp. 2501
-
-
Harikishore, A.1
Niang, M.2
Rajan, S.3
Preiser, P.R.4
Yoon, H.S.5
-
230
-
-
84876002292
-
Quinolone-3-diarylethers: A new class of antimalarial drug
-
CrossRef PubMed
-
Nilsen, A., LaCrue, A. N., White, K. L., Forquer, I. P., Cross, R. M., Marfurt, J., Mather, M. W., Delves, M. J., Shackleford, D. M., Saenz, F. E. et al. (2013) Quinolone-3-diarylethers: a new class of antimalarial drug. Sci. Transl. Med. 5, 177ra37 CrossRef PubMed
-
(2013)
Sci. Transl. Med.
, vol.5
-
-
Nilsen, A.1
LaCrue, A.N.2
White, K.L.3
Forquer, I.P.4
Cross, R.M.5
Marfurt, J.6
Mather, M.W.7
Delves, M.J.8
Shackleford, D.M.9
Saenz, F.E.10
-
231
-
-
0346398368
-
Thioredoxin reductase and glutathione synthesis in Plasmodium falciparum
-
CrossRef PubMed
-
Muller, S. (2003) Thioredoxin reductase and glutathione synthesis in Plasmodium falciparum. Redox Rep. 8, 251-255 CrossRef PubMed
-
(2003)
Redox Rep.
, vol.8
, pp. 251-255
-
-
Muller, S.1
-
232
-
-
0025203611
-
Oxidative stress and the redox status of malaria-infected erythrocytes
-
PubMed
-
Hunt, N. H. and Stocker, R. (1990) Oxidative stress and the redox status of malaria-infected erythrocytes. Blood Cells 16, 499-526 PubMed
-
(1990)
Blood Cells
, vol.16
, pp. 499-526
-
-
Hunt, N.H.1
Stocker, R.2
-
233
-
-
84862231099
-
Discovery and biochemical characterization of Plasmodium thioredoxin reductase inhibitors from an antimalarial set
-
CrossRef PubMed
-
Theobald, A. J., Caballero, I., Coma, I., Colmenarejo, G., Cid, C., Gamo, F. J., Hibbs, M. J., Bass, A. L. and Thomas, D. A. (2012) Discovery and biochemical characterization of Plasmodium thioredoxin reductase inhibitors from an antimalarial set. Biochemistry 51, 4764-4771 CrossRef PubMed
-
(2012)
Biochemistry
, vol.51
, pp. 4764-4771
-
-
Theobald, A.J.1
Caballero, I.2
Coma, I.3
Colmenarejo, G.4
Cid, C.5
Gamo, F.J.6
Hibbs, M.J.7
Bass, A.L.8
Thomas, D.A.9
-
234
-
-
70350033518
-
Structural model of the Plasmodium falciparum thioredoxin reductase: A novel target for antimalarial drugs
-
PubMed
-
Banerjee, A. K., Arora, N. and Murty, U. S. N. (2009) Structural model of the Plasmodium falciparum thioredoxin reductase: a novel target for antimalarial drugs. J. Vector Borne Dis. 46, 171-183 PubMed
-
(2009)
J. Vector Borne Dis.
, vol.46
, pp. 171-183
-
-
Banerjee, A.K.1
Arora, N.2
Murty, U.S.N.3
-
235
-
-
84855819421
-
Investigation of a potential mechanism for the inhibition of SmTGR by auranofin and its implications for Plasmodium falciparum inhibition
-
CrossRef PubMed
-
Caroli, A., Simeoni, S., Lepore, R., Tramontano, A. and Via, A. (2012) Investigation of a potential mechanism for the inhibition of SmTGR by auranofin and its implications for Plasmodium falciparum inhibition. Biochem. Biophys. Res. Commun. 417, 576-581 CrossRef PubMed
-
(2012)
Biochem. Biophys. Res. Commun.
, vol.417
, pp. 576-581
-
-
Caroli, A.1
Simeoni, S.2
Lepore, R.3
Tramontano, A.4
Via, A.5
-
236
-
-
84865977017
-
Crystal structure of Plasmodium falciparum thioredoxin reductase, a validated drug target
-
CrossRef PubMed
-
Boumis, G., Giardina, G., Angelucci, F., Bellelli, A., Brunori, M., Dimastrogiovanni, D., Saccoccia, F. and Miele, A. E. (2012) Crystal structure of Plasmodium falciparum thioredoxin reductase, a validated drug target. Biochem. Biophys. Res. Commun. 425, 806-811 CrossRef PubMed
-
(2012)
Biochem. Biophys. Res. Commun.
, vol.425
, pp. 806-811
-
-
Boumis, G.1
Giardina, G.2
Angelucci, F.3
Bellelli, A.4
Brunori, M.5
Dimastrogiovanni, D.6
Saccoccia, F.7
Miele, A.E.8
-
237
-
-
79551573171
-
Autophagy in protists
-
CrossRef PubMed
-
Duszenko, M., Ginger, M. L., Brennand, A., Gualdron-Lopez, M., Colombo, M. I., Coombs, G. H., Coppens, I., Jayabalasingham, B., Langsley, G., de Castro, S. L. et al. (2011) Autophagy in protists. Autophagy 7, 127-158 CrossRef PubMed
-
(2011)
Autophagy
, vol.7
, pp. 127-158
-
-
Duszenko, M.1
Ginger, M.L.2
Brennand, A.3
Gualdron-Lopez, M.4
Colombo, M.I.5
Coombs, G.H.6
Coppens, I.7
Jayabalasingham, B.8
Langsley, G.9
De Castro, S.L.10
-
238
-
-
0141633042
-
Discovery of gene function by expression profiling of the malaria parasite life cycle
-
DOI 10.1126/science.1087025
-
Le Roch, K. G., Zhou, Y. Y., Blair, P. L., Grainger, M., Moch, J. K., Haynes, J. D., De la Vega, P., Holder, A. A., Batalov, S., Carucci, D. J. and Winzeler, E. A. (2003) Discovery of gene function by expression profiling of the malaria parasite life cycle. Science 301, 1503-1508 CrossRef PubMed (Pubitemid 37128535)
-
(2003)
Science
, vol.301
, Issue.5639
, pp. 1503-1508
-
-
Le, R.K.G.1
Zhou, Y.2
Blair, P.L.3
Grainger, M.4
Moch, J.K.5
Haynes, J.D.6
De La, V.P.7
Holder, A.A.8
Batalov, S.9
Carucci, D.J.10
Winzeler, E.A.11
-
239
-
-
84868506702
-
Structural characterization and inhibition of the Plasmodium Atg8-Atg3 interaction
-
CrossRef PubMed
-
Hain, A. U. P., Weltzer, R. R., Hammond, H., Jayabalasingham, B., Dinglasan, R. R., Graham, D. R. M., Colquhoun, D. R., Coppens, I. and Bosch, J. (2012) Structural characterization and inhibition of the Plasmodium Atg8-Atg3 interaction. J. Struct. Biol. 180, 551-562 CrossRef PubMed
-
(2012)
J. Struct. Biol.
, vol.180
, pp. 551-562
-
-
Hain, A.U.P.1
Weltzer, R.R.2
Hammond, H.3
Jayabalasingham, B.4
Dinglasan, R.R.5
Graham, D.R.M.6
Colquhoun, D.R.7
Coppens, I.8
Bosch, J.9
-
240
-
-
77954199478
-
Crystal structure of arginase from Plasmodium falciparum and implications for L-arginine depletion in malarial infection
-
CrossRef PubMed
-
Dowling, D. P., Ilies, M., Olszewski, K. L., Portugal, S., Mota, M. M., Llinas, M. and Christianson, D. W. (2010) Crystal structure of arginase from Plasmodium falciparum and implications for L-arginine depletion in malarial infection. Biochemistry 49, 5600-5608 CrossRef PubMed
-
(2010)
Biochemistry
, vol.49
, pp. 5600-5608
-
-
Dowling, D.P.1
Ilies, M.2
Olszewski, K.L.3
Portugal, S.4
Mota, M.M.5
Llinas, M.6
Christianson, D.W.7
-
241
-
-
0030768666
-
2-arginase by borate leads to the design of a transition state analogue inhibitor, 2(S)-amino-6-boronohexanoic acid
-
DOI 10.1021/ja971312d
-
Baggio, R., Elbaum, D., Kanyo, Z. F., Carroll, P. J., Cavalli, R. C., Ash, D. E. and Christianson, D. W. (1997) Inhibition of Mn2+ 2-arginase by borate leads to the design of a transition state analogue inhibitor, 2(S) -amino-6-boronohexanoic acid. J. Am. Chem. Soc. 119, 8107-8108 CrossRef (Pubitemid 27380279)
-
(1997)
Journal of the American Chemical Society
, vol.119
, Issue.34
, pp. 8107-8108
-
-
Baggio, R.1
Elbaum, D.2
Kanyo, Z.F.3
Carroll, P.J.4
Cavalli, R.C.5
Ash, D.E.6
Christianson, D.W.7
-
243
-
-
33749245660
-
Inhibitors of Plasmodium falciparum methionine aminopeptidase 1b possess antimalarial activity
-
DOI 10.1073/pnas.0604101103
-
Chen, X., Chong, C. R., Shi, L., Yoshimoto, T., Sullivan, Jr, D. J. and Liu, J. O. (2006) Inhibitors of Plasmodium falciparum methionine aminopeptidase 1b possess antimalarial activity. Proc. Natl. Acad. Sci. U.S.A. 103, 14548-14553 CrossRef PubMed (Pubitemid 44484787)
-
(2006)
Proceedings of the National Academy of Sciences of the United States of America
, vol.103
, Issue.39
, pp. 14548-14553
-
-
Chen, X.1
Chong, C.R.2
Shi, L.3
Yoshimoto, T.4
Sullivan Jr., D.J.5
Liu, J.O.6
-
244
-
-
84862286628
-
Selective and specific inhibition of the Plasmodium falciparum lysyl-tRNA synthetase by the fungal secondary metabolite cladosporin
-
CrossRef PubMed
-
Hoepfner, D., McNamara, C. W., Lim, C. S., Studer, C., Riedl, R., Aust, T., McCormack, S. L., Plouffe, D. M., Meister, S., Schuierer, S. et al. (2012) Selective and specific inhibition of the Plasmodium falciparum lysyl-tRNA synthetase by the fungal secondary metabolite cladosporin. Cell Host Microbe 11, 654-663 CrossRef PubMed
-
(2012)
Cell Host Microbe
, vol.11
, pp. 654-663
-
-
Hoepfner, D.1
McNamara, C.W.2
Lim, C.S.3
Studer, C.4
Riedl, R.5
Aust, T.6
McCormack, S.L.7
Plouffe, D.M.8
Meister, S.9
Schuierer, S.10
-
245
-
-
62549103382
-
Use of high-density tiling microarrays to identify mutations globally and elucidate mechanisms of drug resistance in Plasmodium falciparum
-
CrossRef PubMed
-
Dharia, N. V., Sidhu, A. B. S., Cassera, M. B., Westenberger, S. J., Bopp, S. E. R., Eastman, R. T., Plouffe, D., Batalov, S., Park, D. J., Volkman, S. K. et al. (2009) Use of high-density tiling microarrays to identify mutations globally and elucidate mechanisms of drug resistance in Plasmodium falciparum. Genome Biol. 10, R21 CrossRef PubMed
-
(2009)
Genome Biol.
, vol.10
-
-
Dharia, N.V.1
Sidhu, A.B.S.2
Cassera, M.B.3
Westenberger, S.J.4
Bopp, S.E.R.5
Eastman, R.T.6
Plouffe, D.7
Batalov, S.8
Park, D.J.9
Volkman, S.K.10
-
246
-
-
79959773283
-
Target identification and validation of novel antimalarials
-
CrossRef PubMed
-
McNamara, C. and Winzeler, E. A. (2011) Target identification and validation of novel antimalarials. Future Microbiol. 6, 693-704 CrossRef PubMed
-
(2011)
Future Microbiol.
, vol.6
, pp. 693-704
-
-
McNamara, C.1
Winzeler, E.A.2
-
247
-
-
83255176722
-
Imaging of Plasmodium liver stages to drive next-generation antimalarial drug discovery
-
CrossRef PubMed
-
Meister, S., Plouffe, D. M., Kuhen, K. L., Bonamy, G. M. C., Wu, T., Barnes, S. W., Bopp, S. E., Borboa, R., Bright, A. T., Che, J. W. et al. (2011) Imaging of Plasmodium liver stages to drive next-generation antimalarial drug discovery. Science 334, 1372-1377 CrossRef PubMed
-
(2011)
Science
, vol.334
, pp. 1372-1377
-
-
Meister, S.1
Plouffe, D.M.2
Kuhen, K.L.3
Bonamy, G.M.C.4
Wu, T.5
Barnes, S.W.6
Bopp, S.E.7
Borboa, R.8
Bright, A.T.9
Che, J.W.10
-
248
-
-
81555228431
-
A chemical genomic analysis of decoquinate, a Plasmodium falciparum cytochrome b inhibitor
-
CrossRef PubMed
-
Nam, T. G., McNamara, C. W., Bopp, S., Dharia, N. V., Meister, S., Bonamy, G. M. C., Plouffe, D. M., Kato, N., McCormack, S., Bursulaya, B. et al. (2011) A chemical genomic analysis of decoquinate, a Plasmodium falciparum cytochrome b inhibitor. ACS Chem. Biol. 6, 1214-1222 CrossRef PubMed
-
(2011)
ACS Chem. Biol.
, vol.6
, pp. 1214-1222
-
-
Nam, T.G.1
McNamara, C.W.2
Bopp, S.3
Dharia, N.V.4
Meister, S.5
Bonamy, G.M.C.6
Plouffe, D.M.7
Kato, N.8
McCormack, S.9
Bursulaya, B.10
-
249
-
-
0033782994
-
Aminoacyl-tRNA synthesis
-
CrossRef PubMed
-
Ibba, M. and Soll, D. (2000) Aminoacyl-tRNA synthesis. Annu. Rev. Biochem. 69, 617-650 CrossRef PubMed
-
(2000)
Annu. Rev. Biochem.
, vol.69
, pp. 617-650
-
-
Ibba, M.1
Soll, D.2
-
250
-
-
0027255483
-
Cognition, mechanism, and evolutionary relationships in aminoacyl-transfer RNA-synthetases
-
CrossRef PubMed
-
Carter, C. W. (1993) Cognition, mechanism, and evolutionary relationships in aminoacyl-transfer RNA-synthetases. Annu. Rev. Biochem. 62, 715-748 CrossRef PubMed
-
(1993)
Annu. Rev. Biochem.
, vol.62
, pp. 715-748
-
-
Carter, C.W.1
-
251
-
-
84877287995
-
Structural analysis of malaria-parasite lysyl-tRNA synthetase provides a platform for drug development
-
CrossRef PubMed
-
Khan, S., Garg, A., Camacho, N., Van Rooyen, J., Pole, A. K., Belrhali,
-
(2013)
Acta Crystallogr. D Biol. Crystallogr.
, vol.69
, pp. 785-795
-
-
Khan, S.1
Garg, A.2
Camacho, N.3
Van Rooyen, J.4
Pole, A.K.5
Belrhali, H.6
De Pouplana, L.R.7
Sharma, V.8
Sharma, A.9
-
252
-
-
60549102292
-
Fumagillin and fumarranol interact with P. Falciparum methionine aminopeptidase 2 and inhibit malaria parasite growth in vitro and in vivo
-
CrossRef PubMed
-
Chen, X., Xie, S., Bhat, S., Kumar, N., Shapiro, T. A. and Liu, J. O. (2009) Fumagillin and fumarranol interact with P. falciparum methionine aminopeptidase 2 and inhibit malaria parasite growth in vitro and in vivo. Chem. Biol. 16, 193-202 CrossRef PubMed
-
(2009)
Chem. Biol.
, vol.16
, pp. 193-202
-
-
Chen, X.1
Xie, S.2
Bhat, S.3
Kumar, N.4
Shapiro, T.A.5
Liu, J.O.6
-
253
-
-
80052023187
-
Crystal structure of Plasmodium falciparum phosphoglycerate kinase: Evidence for anion binding in the basic patch
-
CrossRef PubMed
-
Smith, C. D., Chattopadhyay, D. and Pal, B. (2011) Crystal structure of Plasmodium falciparum phosphoglycerate kinase: evidence for anion binding in the basic patch. Biochem. Biophys. Res. Commun. 412, 203-206 CrossRef PubMed
-
(2011)
Biochem. Biophys. Res. Commun.
, vol.412
, pp. 203-206
-
-
Smith, C.D.1
Chattopadhyay, D.2
Pal, B.3
-
254
-
-
79251597984
-
Specific inhibition of the aspartate aminotransferase of Plasmodium falciparum
-
CrossRef PubMed
-
Wrenger, C., Muller, I. B., Schifferdecker, A. J., Jain, R., Jordanova, R. and Groves, M. R. (2011) Specific inhibition of the aspartate aminotransferase of Plasmodium falciparum. J. Mol. Biol. 405, 956-971 CrossRef PubMed
-
(2011)
J. Mol. Biol.
, vol.405
, pp. 956-971
-
-
Wrenger, C.1
Muller, I.B.2
Schifferdecker, A.J.3
Jain, R.4
Jordanova, R.5
Groves, M.R.6
-
255
-
-
84892389030
-
Crystal structures of IspF from Plasmodium falciparum and Burkholderia cenocepacia: Comparisons inform antimicrobial drug target assessment
-
CrossRef PubMed
-
O'Rourke, P. E. F., Kalinowska-Tluscik, J., Fyfe, P. K., Dawson, A. and Hunter, W. N. (2014) Crystal structures of IspF from Plasmodium falciparum and Burkholderia cenocepacia : comparisons inform antimicrobial drug target assessment. BMC Struct. Biol. 14, 1 CrossRef PubMed
-
(2014)
BMC Struct. Biol.
, vol.14
, pp. 1
-
-
O'Rourke, P.E.F.1
Kalinowska-Tluscik, J.2
Fyfe, P.K.3
Dawson, A.4
Hunter, W.N.5
-
256
-
-
84888639629
-
Structure of the (E) -4-hydroxy-3-methyl-but-2-enyl-diphosphate reductase from Plasmodium falciparum
-
CrossRef PubMed
-
Rekittke, I., Olkhova, E., Wiesner, J., Demmer, U., Warkentin, E., Jomaa, H. and Ermler, U. (2013) Structure of the (E) -4-hydroxy-3-methyl-but-2-enyl- diphosphate reductase from Plasmodium falciparum. FEBS Lett. 587, 3968-3972 CrossRef PubMed
-
(2013)
FEBS Lett.
, vol.587
, pp. 3968-3972
-
-
Rekittke, I.1
Olkhova, E.2
Wiesner, J.3
Demmer, U.4
Warkentin, E.5
Jomaa, H.6
Ermler, U.7
-
257
-
-
84878950023
-
An appended domain results in an unusual architecture for malaria parasite tryptophanyl-tRNA synthetase
-
CrossRef PubMed
-
Khan, S., Garg, A., Sharma, A., Camacho, N., Picchioni, D., Saint-Leger, A., Ribas de Pouplana, L., Yogavel, M. and Sharma, A. (2013) An appended domain results in an unusual architecture for malaria parasite tryptophanyl-tRNA synthetase. PLoS ONE 8, e66224 CrossRef PubMed
-
(2013)
PLoS ONE
, vol.8
-
-
Khan, S.1
Garg, A.2
Sharma, A.3
Camacho, N.4
Picchioni, D.5
Saint-Leger, A.6
Ribas De Pouplana, L.7
Yogavel, M.8
Sharma, A.9
-
258
-
-
33845482665
-
Genome-scale protein expression and structural biology of Plasmodium falciparum and related Apicomplexan organisms
-
DOI 10.1016/j.molbiopara.2006.10.011, PII S0166685106003124
-
Vedadi, M., Lew, J., Artz, J., Amani, M., Zhao, Y., Dong, A. P., Wasney, G. A., Gao, M., Hills, T., Brokx, S. et al. (2007) Genome-scale protein expression and structural biology of Plasmodium falciparum and related apicomplexan organisms. Mol. Biochem. Parasitol. 151, 100-110 CrossRef PubMed (Pubitemid 44911074)
-
(2007)
Molecular and Biochemical Parasitology
, vol.151
, Issue.1
, pp. 100-110
-
-
Vedadi, M.1
Lew, J.2
Artz, J.3
Amani, M.4
Zhao, Y.5
Dong, A.6
Wasney, G.A.7
Gao, M.8
Hills, T.9
Brokx, S.10
Qiu, W.11
Sharma, S.12
Diassiti, A.13
Alam, Z.14
Melone, M.15
Mulichak, A.16
Wernimont, A.17
Bray, J.18
Loppnau, P.19
Plotnikova, O.20
Newberry, K.21
Sundararajan, E.22
Houston, S.23
Walker, J.24
Tempel, W.25
Bochkarev, A.26
Kozieradzki, I.27
Edwards, A.28
Arrowsmith, C.29
Roos, D.30
Kain, K.31
Hui, R.32
more..
-
259
-
-
70349463122
-
Crystallographic structure of the tetratricopeptide repeat domain of Plasmodium falciparum FKBP35 and its molecular interaction with Hsp90 C-terminal pentapeptide
-
CrossRef PubMed
-
Alag, R., Bharatham, N., Dong, A. P., Hills, T., Harikishore, A., Widjaja, A. A., Shochat, S. G., Hui, R. and Yoon, H. S. (2009) Crystallographic structure of the tetratricopeptide repeat domain of Plasmodium falciparum FKBP35 and its molecular interaction with Hsp90 C-terminal pentapeptide. Protein Sci. 18, 2115-2124 CrossRef PubMed
-
(2009)
Protein Sci.
, vol.18
, pp. 2115-2124
-
-
Alag, R.1
Bharatham, N.2
Dong, A.P.3
Hills, T.4
Harikishore, A.5
Widjaja, A.A.6
Shochat, S.G.7
Hui, R.8
Yoon, H.S.9
-
260
-
-
57649227299
-
Targeting a Uniquely Nonspecific Prenyl Synthase with Bisphosphonates to Combat Cryptosporidiosis
-
DOI 10.1016/j.chembiol.2008.10.017, PII S1074552108004481
-
Artz, J. D., Dunford, J. E., Arrowood, M. J., Dong, A. P., Chruszcz, M., Kavanagh, K. L., Minor, W., Russell, R. G. G., Ebetino, F. H., Oppermann, U. and Hui, R. (2008) Targeting a uniquely nonspecific prenyl synthase with bisphosphonates to combat cryptosporidiosis. Chem. Biol. 15, 1296-1306 CrossRef PubMed (Pubitemid 352841472)
-
(2008)
Chemistry and Biology
, vol.15
, Issue.12
, pp. 1296-1306
-
-
Artz, J.D.1
Dunford, J.E.2
Arrowood, M.J.3
Dong, A.4
Chruszcz, M.5
Kavanagh, K.L.6
Minor, W.7
Russell, R.G.G.8
Ebetino, F.H.9
Oppermann, U.10
Hui, R.11
-
261
-
-
34548587312
-
Crystal Structure of Plasmodium falciparum Spermidine Synthase in Complex with the Substrate Decarboxylated S-adenosylmethionine and the Potent Inhibitors 4MCHA and AdoDATO
-
DOI 10.1016/j.jmb.2007.07.053, PII S0022283607010066
-
Dufe, V. T., Qiu, W., Muller, I. B., Hui, R., Walter, R. D. and Al-Karadaghi, S. (2007) Crystal structure of Plasmodium falciparum spermidine synthase in complex with the substrate decarboxylated S -adenosylmethionine and the potent inhibitors 4MCHA and AdoDATO. J. Mol. Biol. 373, 167-177 CrossRef PubMed (Pubitemid 47390717)
-
(2007)
Journal of Molecular Biology
, vol.373
, Issue.1
, pp. 167-177
-
-
Dufe, V.T.1
Qiu, W.2
Muller, I.B.3
Hui, R.4
Walter, R.D.5
Al-Karadaghi, S.6
-
262
-
-
78349313044
-
The Clp chaperones and proteases of the human malaria parasite Plasmodium falciparum
-
CrossRef PubMed
-
El Bakkouri, M., Pow, A., Mulichak, A., Cheung, K. L. Y., Artz, J. D., Amani, M., Fell, S., de Koning-Ward, T. F., Goodman, C. D., McFaddens, G. I. et al. (2010) The Clp chaperones and proteases of the human malaria parasite Plasmodium falciparum. J. Mol. Biol. 404, 456-477 CrossRef PubMed
-
(2010)
J. Mol. Biol.
, vol.404
, pp. 456-477
-
-
El Bakkouri, M.1
Pow, A.2
Mulichak, A.3
Cheung, K.L.Y.4
Artz, J.D.5
Amani, M.6
Fell, S.7
De Koning-Ward, T.F.8
Goodman, C.D.9
McFaddens, G.I.10
-
263
-
-
84872296623
-
Structural insights into the inactive subunit of the apicoplast-localized caseinolytic protease complex of Plasmodium falciparum
-
CrossRef PubMed
-
El Bakkouri, M., Rathore, S., Calmettes, C., Wernimont, A. K., Liu, K. Y., Sinha, D., Asad, M., Jung, P., Hui, R., Mohmmed, A. and Houry, W. A. (2013) Structural insights into the inactive subunit of the apicoplast-localized caseinolytic protease complex of Plasmodium falciparum. J. Biol. Chem. 288, 1022-1031 CrossRef PubMed
-
(2013)
J. Biol. Chem.
, vol.288
, pp. 1022-1031
-
-
El Bakkouri, M.1
Rathore, S.2
Calmettes, C.3
Wernimont, A.K.4
Liu, K.Y.5
Sinha, D.6
Asad, M.7
Jung, P.8
Hui, R.9
Mohmmed, A.10
Houry, W.A.11
-
264
-
-
80051799844
-
Characterization of a new phosphatase from Plasmodium
-
CrossRef PubMed
-
Hills, T., Srivastava, A., Ayi, K., Wernimont, A. K., Kain, K., Waters, A. P., Hui, R. and Pizarro, J. C. (2011) Characterization of a new phosphatase from Plasmodium. Mol. Biochem. Parasitol. 179, 69-79 CrossRef PubMed
-
(2011)
Mol. Biochem. Parasitol.
, vol.179
, pp. 69-79
-
-
Hills, T.1
Srivastava, A.2
Ayi, K.3
Wernimont, A.K.4
Kain, K.5
Waters, A.P.6
Hui, R.7
Pizarro, J.C.8
-
265
-
-
79551482914
-
Structures of parasitic CDPK domains point to a common mechanism of activation
-
CrossRef PubMed
-
Wernimont, A. K., Amani, M., Qiu, W., Pizarro, J. C., Artz, J. D., Lin, Y. H., Lew, J., Hutchinson, A. and Hui, R. (2011) Structures of parasitic CDPK domains point to a common mechanism of activation. Proteins 79, 803-820 CrossRef PubMed
-
(2011)
Proteins
, vol.79
, pp. 803-820
-
-
Wernimont, A.K.1
Amani, M.2
Qiu, W.3
Pizarro, J.C.4
Artz, J.D.5
Lin, Y.H.6
Lew, J.7
Hutchinson, A.8
Hui, R.9
-
266
-
-
48449092811
-
Structures of substrate-and inhibitor-bound adenosine deaminase from a human malaria parasite show a dramatic conformational change and shed light on drug selectivity
-
CrossRef PubMed
-
Larson, E. T., Deng, W., Krumm, B. E., Napuli, A., Mueller, N., Van Voorhis, W. C., Buckner, F. S., Fan, E., Lauricella, A., DeTitta, G. et al. (2008) Structures of substrate-and inhibitor-bound adenosine deaminase from a human malaria parasite show a dramatic conformational change and shed light on drug selectivity. J. Mol. Biol. 381, 975-988 CrossRef PubMed
-
(2008)
J. Mol. Biol.
, vol.381
, pp. 975-988
-
-
Larson, E.T.1
Deng, W.2
Krumm, B.E.3
Napuli, A.4
Mueller, N.5
Van Voorhis, W.C.6
Buckner, F.S.7
Fan, E.8
Lauricella, A.9
DeTitta, G.10
-
267
-
-
84878506144
-
Designing the next generation of medicines for malaria control and eradication
-
CrossRef PubMed
-
Burrows, J. N., van Huijsduijnen, R. H., Moehrle, J. J., Oeuvray, C. and Wells, T. N. C. (2013) Designing the next generation of medicines for malaria control and eradication. Malar. J. 12, 187 CrossRef PubMed
-
(2013)
Malar. J.
, vol.12
, pp. 187
-
-
Burrows, J.N.1
Van Huijsduijnen, R.H.2
Moehrle, J.J.3
Oeuvray, C.4
Wells, T.N.C.5
-
268
-
-
84922687362
-
Structural biology for developing antimalarial compounds
-
CrossRef PubMed
-
Tanaka, N., Umeda, T., Kusakabe, Y., Nakanishi, M., Kitade, Y. and Nakamura, K. T. (2013) Structural biology for developing antimalarial compounds. Yakugaku Zasshi 133, 527-537 CrossRef PubMed
-
(2013)
Yakugaku Zasshi
, vol.133
, pp. 527-537
-
-
Tanaka, N.1
Umeda, T.2
Kusakabe, Y.3
Nakanishi, M.4
Kitade, Y.5
Nakamura, K.T.6
|