-
1
-
-
67649141158
-
-
World Health Organization, World Health Organization, Geneva, Switzerland. Available at
-
World Health Organization. (2008) WHO World Malaria Report. World Health Organization, Geneva, Switzerland. Available at: http://malaria. who.int/wmr2008/.
-
(2008)
WHO World Malaria Report
-
-
-
2
-
-
17844404530
-
Amodiaquine alone, amodiaquine1sulfadoxine-pyrimethamine, amodiaquine1artesunate, and artemether-lumefantrine for outpatient treatment of malaria in Tanzanian children: A four-arm randomised effectiveness trial
-
Mutabingwa, T. K., Anthony, D., Heller, A., Hallett, R., Ahmed, J., Drakeley, C., Greenwood, B. M., and Whitty, C. J. (2005) Amodiaquine alone, amodiaquine1sulfadoxine-pyrimethamine, amodiaquine1artesunate, and artemether-lumefantrine for outpatient treatment of malaria in Tanzanian children: a four-arm randomised effectiveness trial. Lancet 365, 1474-1480.
-
(2005)
Lancet
, vol.365
, pp. 1474-1480
-
-
Mutabingwa, T.K.1
Anthony, D.2
Heller, A.3
Hallett, R.4
Ahmed, J.5
Drakeley, C.6
Greenwood, B.M.7
Whitty, C.J.8
-
3
-
-
0035126479
-
Triclosan offers protection against blood stages of malaria by inhibiting enoyl-ACP reductase of Plasmodium falciparum
-
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.
-
(2001)
Nat. Med.
, vol.7
, pp. 167-173
-
-
Surolia, N.1
Surolia, A.2
-
4
-
-
0030581109
-
Escherichia coli as a model for the regulation of dissociable (type II) fatty acid biosynthesis
-
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.
-
(1996)
Biochim. Biophys. Acta.
, vol.1302
, pp. 1-16
-
-
Rock, C.O.1
Cronan, J.E.2
-
5
-
-
0037411269
-
Structural and functional organization of the animal fatty acid synthase
-
DOI 10.1016/S0163-7827(02)00067-X
-
Smith, S., Witkowski, A., and Joshi, A. K. (2003) Structural and functional organization of the animal fatty acid synthase. Prog. Lipid Res. 42, 289-317. (Pubitemid 36411688)
-
(2003)
Progress in Lipid Research
, vol.42
, Issue.4
, pp. 289-317
-
-
Smith, S.1
Witkowski, A.2
Joshi, A.K.3
-
6
-
-
2342520626
-
Tropical infectious diseases: Metabolic maps and functions of the Plasmodium falciparum apicoplast
-
Ralph, S. A., van Dooren, G. G., Waller, R. F., Crawford, M. J., Fraunholz, M. J., Foth, B. J., Tonkin, C. J., Roos, D. S., and McFadden, G. I. (2004) Tropical infectious diseases: metabolic maps and functions of the Plasmodium falciparum apicoplast. Nat. Rev. Microbiol. 2, 203-216.
-
(2004)
Nat. Rev. Microbiol.
, vol.2
, pp. 203-216
-
-
Ralph, S.A.1
Van Dooren, G.G.2
Waller, R.F.3
Crawford, M.J.4
Fraunholz, M.J.5
Foth, B.J.6
Tonkin, C.J.7
Roos, D.S.8
McFadden, G.I.9
-
7
-
-
9144226932
-
FAS't inhibition of malaria
-
Surolia, A., Ramya, T. N., Ramya, V., and Surolia, N. (2004) 'FAS't inhibition of malaria. Biochem. J. 383, 401-412.
-
(2004)
Biochem. J.
, vol.383
, pp. 401-412
-
-
Surolia, A.1
Ramya, T.N.2
Ramya, V.3
Surolia, N.4
-
8
-
-
0037228888
-
A type II pathway for fatty acid biosynthesis presents drug targets in Plasmodium falciparum
-
Waller, R. F., Ralph, S. A., Reed, M. B., Su, V., Douglas, J. D., Minnikin, D. E., Cowman, A. F., Besra, G. S., and McFadden, G. I. (2003) A type II pathway for fatty acid biosynthesis presents drug targets in Plasmodium falciparum. Antimicrob. Agents. Chemother. 47, 297-301.
-
(2003)
Antimicrob. Agents. Chemother.
, vol.47
, pp. 297-301
-
-
Waller, R.F.1
Ralph, S.A.2
Reed, M.B.3
Su, V.4
Douglas, J.D.5
Minnikin, D.E.6
Cowman, A.F.7
Besra, G.S.8
McFadden, G.I.9
-
9
-
-
0030452311
-
A mechanism of drug action revealed by structural studies of enoyl reductase
-
Baldock, C., Rafferty, J. B., Sedelnikova, S. E., Baker, P. J., Stuitje, A. R., Slabas, A. R., Hawkes, T. R., and Rice, D. W. (1996) A mechanism of drug action revealed by structural studies of enoyl reductase. Science 274, 2107-2110.
-
(1996)
Science
, vol.274
, pp. 2107-2110
-
-
Baldock, C.1
Rafferty, J.B.2
Sedelnikova, S.E.3
Baker, P.J.4
Stuitje, A.R.5
Slabas, A.R.6
Hawkes, T.R.7
Rice, D.W.8
-
10
-
-
0033119057
-
Molecular basis of triclosan activity
-
Levy, C. W., Roujeinikova, A., Sedelnikova, S., Baker, P. J., Stuitje, A. R., Slabas, A. R., Rice, D. W., and Rafferty, J. B. (1999) Molecular basis of triclosan activity. Nature 398, 383-384.
-
(1999)
Nature
, vol.398
, pp. 383-384
-
-
Levy, C.W.1
Roujeinikova, A.2
Sedelnikova, S.3
Baker, P.J.4
Stuitje, A.R.5
Slabas, A.R.6
Rice, D.W.7
Rafferty, J.B.8
-
11
-
-
0032775211
-
Structural basis and mechanism of enoyl reductase inhibition by triclosan
-
Stewart, M. J., Parikh, S., Xiao, G., Tonge, P. J., and Kisker, C. (1999) Structural basis and mechanism of enoyl reductase inhibition by triclosan. J. Mol. Biol. 290, 859-865.
-
(1999)
J. Mol. Biol.
, vol.290
, pp. 859-865
-
-
Stewart, M.J.1
Parikh, S.2
Xiao, G.3
Tonge, P.J.4
Kisker, C.5
-
12
-
-
0032721424
-
Molecular basis for triclosan activity involves a flipping loop in the active site
-
Qiu, X., Janson, C. A., Court, R. I., Smyth, M. G., Payne, D. J., and Abdel-Meguid, S. S. (1999) Molecular basis for triclosan activity involves a flipping loop in the active site. Protein Sci. 8, 2529-2532.
-
(1999)
Protein Sci.
, vol.8
, pp. 2529-2532
-
-
Qiu, X.1
Janson, C.A.2
Court, R.I.3
Smyth, M.G.4
Payne, D.J.5
Abdel-Meguid, S.S.6
-
13
-
-
0032472224
-
Modification of the NADH of the isoniazid target (InhA) from Mycobacterium tuberculosis
-
Rozwarski, D. A., Grant, G. A., Barton, D. H., Jacobs, W. R., Jr., and Sacchettini, J. C. (1998) Modification of the NADH of the isoniazid target (InhA) from Mycobacterium tuberculosis. Science 279, 98-102.
-
(1998)
Science
, vol.279
, pp. 98-102
-
-
Rozwarski, D.A.1
Grant, G.A.2
Barton, D.H.3
Jacobs Jr., W.R.4
Sacchettini, J.C.5
-
14
-
-
0038757566
-
Targeting tuberculosis and malaria through inhibition of enoyl reductase: Compound activity and structural data
-
Kuo, M. R., Morbidoni, H. R., Alland, D., Sneddon, S. F., Gourlie, B. B., Staveski, M. M., Leonard, M., Gregory, J. S., Janjigian, A. D., Yee, C., Musser, J. M., Kreiswirth, B., Iwamoto, H., Perozzo, R., Jacobs, W. R., Jr., Sacchettini, J. C., and Fidock, D. A. (2003) Targeting tuberculosis and malaria through inhibition of enoyl reductase: compound activity and structural data. J. Biol. Chem. 278, 20851-20859.
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 20851-20859
-
-
Kuo, M.R.1
Morbidoni, H.R.2
Alland, D.3
Sneddon, S.F.4
Gourlie, B.B.5
Staveski, M.M.6
Leonard, M.7
Gregory, J.S.8
Janjigian, A.D.9
Yee, C.10
Musser, J.M.11
Kreiswirth, B.12
Iwamoto, H.13
Perozzo, R.14
Jacobs Jr., W.R.15
Sacchettini, J.C.16
Fidock, D.A.17
-
15
-
-
35448938486
-
Crystal structure of the Helicobacter pylori enoyl-acyl carrier protein reductase in complex with hydroxydiphenyl ether compounds, triclosan and diclosan
-
Lee, H. H., Moon, J., and Suh, S. W. (2007) Crystal structure of the Helicobacter pylori enoyl-acyl carrier protein reductase in complex with hydroxydiphenyl ether compounds, triclosan and diclosan. Proteins 69, 691-694.
-
(2007)
Proteins
, vol.69
, pp. 691-694
-
-
Lee, H.H.1
Moon, J.2
Suh, S.W.3
-
16
-
-
33947318051
-
Studies of Toxoplasma gondii and Plasmodium falciparum enoyl acyl carrier protein reductase and implications for the development of antiparasitic agents
-
Muench, S. P., Prigge, S. T., McLeod, R., Rafferty, J. B., Kirisits, M. J., Roberts, C. W., Mui, E. J., and Rice, D. W. (2007) Studies of Toxoplasma gondii and Plasmodium falciparum enoyl acyl carrier protein reductase and implications for the development of antiparasitic agents. Acta Crystallogr. D Biol. Crystallogr. 63, 328-338.
-
(2007)
Acta Crystallogr. D Biol. Crystallogr.
, vol.63
, pp. 328-338
-
-
Muench, S.P.1
Prigge, S.T.2
McLeod, R.3
Rafferty, J.B.4
Kirisits, M.J.5
Roberts, C.W.6
Mui, E.J.7
Rice, D.W.8
-
17
-
-
0037066782
-
Structural elucidation of the specificity of the antibacterial agent triclosan for malarial enoyl acyl carrier protein reductase
-
Perozzo, R., Kuo, M., Sidhu, A. S., Valiyaveettil, J. T., Bittman, R., Jacobs, W. R., Jr., 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.
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 13106-13114
-
-
Perozzo, R.1
Kuo, M.2
Sidhu, A.S.3
Valiyaveettil, J.T.4
Bittman, R.5
Jacobs Jr., W.R.6
Fidock, D.A.7
Sacchettini, J.C.8
-
18
-
-
0035861962
-
Kinetic determinants of the interaction of enoyl-ACP reductase from Plasmodium falciparum with its substrates and inhibitors
-
Kapoor, M., Dar, M. J., Surolia, A., and Surolia, N. (2001) Kinetic determinants of the interaction of enoyl-ACP reductase from Plasmodium falciparum with its substrates and inhibitors. Biochem. Biophys. Res. Commun. 289, 832-837.
-
(2001)
Biochem. Biophys. Res. Commun.
, vol.289
, pp. 832-837
-
-
Kapoor, M.1
Dar, M.J.2
Surolia, A.3
Surolia, N.4
-
19
-
-
4344702214
-
Slow-tight-binding inhibition of enoyl-acyl carrier protein reductase from Plasmodium falciparum by triclosan
-
Kapoor, M., Reddy, C. C., Krishnasastry, M. V., Surolia, N., and Surolia, A. (2004) Slow-tight-binding inhibition of enoyl-acyl carrier protein reductase from Plasmodium falciparum by triclosan. Biochem. J. 381, 719-724.
-
(2004)
Biochem. J.
, vol.381
, pp. 719-724
-
-
Kapoor, M.1
Reddy, C.C.2
Krishnasastry, M.V.3
Surolia, N.4
Surolia, A.5
-
20
-
-
4344567210
-
Kinetic and structural analysis of the increased affinity of enoyl- ACP (acyl-carrier protein) reductase for triclosan in the presence of NAD+
-
Kapoor, M., Mukhi, P. L., Surolia, N., Suguna, K., and Surolia, A. (2004) Kinetic and structural analysis of the increased affinity of enoyl- ACP (acyl-carrier protein) reductase for triclosan in the presence of NAD+. Biochem. J. 381, 725-733.
-
(2004)
Biochem. J.
, vol.381
, pp. 725-733
-
-
Kapoor, M.1
Mukhi, P.L.2
Surolia, N.3
Suguna, K.4
Surolia, A.5
-
21
-
-
4344584118
-
Mutational analysis of the triclosan-binding region of enoyl-ACP (acylcarrier protein) reductase from Plasmodium falciparum
-
Kapoor, M., Gopalakrishnapai, J., Surolia, N., and Surolia, A. (2004) Mutational analysis of the triclosan-binding region of enoyl-ACP (acylcarrier protein) reductase from Plasmodium falciparum. Biochem. J. 381, 735-741.
-
(2004)
Biochem. J.
, vol.381
, pp. 735-741
-
-
Kapoor, M.1
Gopalakrishnapai, J.2
Surolia, N.3
Surolia, A.4
-
22
-
-
4644355051
-
Structural basis for the variation in triclosan affinity to enoyl reductases
-
Pidugu, L. S., Kapoor, M., Surolia, N., Surolia, A., and Suguna, K. (2004) Structural basis for the variation in triclosan affinity to enoyl reductases. J. Mol. Biol. 343, 147-155.
-
(2004)
J. Mol. Biol.
, vol.343
, pp. 147-155
-
-
Pidugu, L.S.1
Kapoor, M.2
Surolia, N.3
Surolia, A.4
Suguna, K.5
-
23
-
-
33750036420
-
Novel diphenyl ethers: Design, docking studies, synthesis and inhibition of enoyl ACP reductase of Plasmodium falciparum and Escherichia coli
-
Chhibber, M., Kumar, G., Parasuraman, P., Ramya, T. N., 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.
-
(2006)
Bioorg. Med. Chem.
, vol.14
, pp. 8086-8098
-
-
Chhibber, M.1
Kumar, G.2
Parasuraman, P.3
Ramya, T.N.4
Surolia, N.5
Surolia, A.6
-
24
-
-
77449149677
-
Design, development, synthesis, and docking analysis of 20-substituted triclosan analogs as inhibitors for Plasmodium falciparum enoyl-ACP reductase
-
Kapoor, N., Banerjee, T., Babu, P., Maity, K., Surolia, N., and Surolia, A. (2009) Design, development, synthesis, and docking analysis of 20-substituted triclosan analogs as inhibitors for Plasmodium falciparum enoyl-ACP reductase. IUBMB Life 61, 1083-1091.
-
(2009)
IUBMB Life
, vol.61
, pp. 1083-1091
-
-
Kapoor, N.1
Banerjee, T.2
Babu, P.3
Maity, K.4
Surolia, N.5
Surolia, A.6
-
25
-
-
43749084141
-
Design, synthesis, and application of novel triclosan prodrugs as potential antimalarial and antibacterial agents
-
Mishra, S., Karmodiya, K., Parasuraman, P., Surolia, A., and Surolia, N. (2008) Design, synthesis, and application of novel triclosan prodrugs as potential antimalarial and antibacterial agents. Bioorg. Med. Chem. 16, 5536-5546.
-
(2008)
Bioorg. Med. Chem.
, vol.16
, pp. 5536-5546
-
-
Mishra, S.1
Karmodiya, K.2
Parasuraman, P.3
Surolia, A.4
Surolia, N.5
-
26
-
-
34250189143
-
Discovery of a rhodanine class of compounds as inhibitors of Plasmodium falciparum enoyl-acyl carrier protein reductase
-
Kumar, G., Parasuraman, P., Sharma, S. K., Banerjee, T., Karmodiya, K., Surolia, N., and Surolia, A. (2007) Discovery of a rhodanine class of compounds as inhibitors of Plasmodium falciparum enoyl-acyl carrier protein reductase. J. Med. Chem. 50, 2665-2675.
-
(2007)
J. Med. Chem.
, vol.50
, pp. 2665-2675
-
-
Kumar, G.1
Parasuraman, P.2
Sharma, S.K.3
Banerjee, T.4
Karmodiya, K.5
Surolia, N.6
Surolia, A.7
-
27
-
-
70350752494
-
Triclosan inhibit the growth of the late liver-stage of Plasmodium
-
Singh, A. P., Surolia, N., and Surolia, A. (2009) Triclosan inhibit the growth of the late liver-stage of Plasmodium. IUBMB Life 61, 923-928.
-
(2009)
IUBMB Life
, vol.61
, pp. 923-928
-
-
Singh, A.P.1
Surolia, N.2
Surolia, A.3
-
28
-
-
1642540581
-
Inhibition of the bacterial enoyl reductase FabI by triclosan: A structure-reactivity analysis of FabI inhibition by triclosan analogues
-
Sivaraman, S., Sullivan, T. J., Johnson, F., Novichenok, P., Cui, G., Simmerling, C., and Tonge, P. J. (2004) Inhibition of the bacterial enoyl reductase FabI by triclosan: a structure-reactivity analysis of FabI inhibition by triclosan analogues. J. Med. Chem. 47, 509-518.
-
(2004)
J. Med. Chem.
, vol.47
, pp. 509-518
-
-
Sivaraman, S.1
Sullivan, T.J.2
Johnson, F.3
Novichenok, P.4
Cui, G.5
Simmerling, C.6
Tonge, P.J.7
-
29
-
-
33750048012
-
High affinity InhA inhibitors with activity against drug-resistant strains of Mycobacterium tuberculosis
-
Sullivan, T. J., Truglio, J. J., Boyne, M. E., Novichenok, P., Zhang, X., Stratton, C. F., Li, H. J., Kaur, T., Amin, A., Johnson, F., Slayden, R. A., Kisker, C., and Tonge, P. J. (2006) High affinity InhA inhibitors with activity against drug-resistant strains of Mycobacterium tuberculosis. ACS Chem. Biol. 1, 43-53.
-
(2006)
ACS Chem. Biol.
, vol.1
, pp. 43-53
-
-
Sullivan, T.J.1
Truglio, J.J.2
Boyne, M.E.3
Novichenok, P.4
Zhang, X.5
Stratton, C.F.6
Li, H.J.7
Kaur, T.8
Amin, A.9
Johnson, F.10
Slayden, R.A.11
Kisker, C.12
Tonge, P.J.13
-
30
-
-
60849124512
-
Triclosan derivatives: Towards potent inhibitors of drug-sensitive and drug-resistant Mycobacterium tuberculosis
-
Freundlich, J. S., Wang, F., Vilcheze, C., Gulten, G., Langley, R., Schiehser, G. A., Jacobus, D. P., Jacobs, W. R., Jr., and Sacchettini, J. C. (2009) Triclosan derivatives: towards potent inhibitors of drug-sensitive and drug-resistant Mycobacterium tuberculosis. ChemMedChem 4, 241-248.
-
(2009)
ChemMedChem
, vol.4
, pp. 241-248
-
-
Freundlich, J.S.1
Wang, F.2
Vilcheze, C.3
Gulten, G.4
Langley, R.5
Schiehser, G.A.6
Jacobus, D.P.7
Jacobs Jr., W.R.8
Sacchettini, J.C.9
-
31
-
-
33644802299
-
Synthesis and biological activity of diaryl ether inhibitors of malarial enoyl acyl carrier protein reductase. II. 20-substituted triclosan derivatives
-
Freundlich, J. S., Yu, M., Lucumi, E., Kuo, M., Tsai, H. C., Valderramos, J. C., Karagyozov, L., Jacobs, W. R., Jr., Schiehser, G. A., Fidock, D. A., Jacobus, D. P., and Sacchettini, J. C. (2006) Synthesis and biological activity of diaryl ether inhibitors of malarial enoyl acyl carrier protein reductase. II. 20-substituted triclosan derivatives. Bioorg. Med. Chem. Lett. 16, 2163-2169.
-
(2006)
Bioorg. Med. Chem. Lett.
, vol.16
, 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
-
32
-
-
26844461350
-
Synthesis, biological activity, and X-ray crystal structural analysis of diaryl ether inhibitors of malarial enoyl acyl carrier protein reductase. I. 40-substituted triclosan derivatives
-
Freundlich, J. S., Anderson, J. W., Sarantakis, D., Shieh, H. M., Yu, M., Valderramos, J. C., Lucumi, E., Kuo, M., Jacobs, W. R., Jr., Fidock, D. A., Schiehser, G. A., Jacobus, D. P., and Sacchettini, J. C. (2005) Synthesis, biological activity, and X-ray crystal structural analysis of diaryl ether inhibitors of malarial enoyl acyl carrier protein reductase. I. 40-substituted triclosan derivatives. Bioorg. Med. Chem. Lett. 15, 5247-5252.
-
(2005)
Bioorg. Med. Chem. Lett.
, Issue.15
, 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
-
33
-
-
34548480189
-
X-ray structural analysis of Plasmodium falciparum enoyl acyl carrier protein reductase as a pathway toward the optimization of triclosan antimalarial efficacy
-
Freundlich, J. S., Wang, F., Tsai, H. C., Kuo, M., Shieh, H. M., Anderson, J. W., Nkrumah, L. J., Valderramos, J. C., Yu, M., Kumar, T. R., Valderramos, S. G., Jacobs, W. R., Jr., Schiehser, G. A., Jacobus, D. P., Fidock, D. A., and Sacchettini, J. C. (2007) X-ray structural analysis of Plasmodium falciparum enoyl acyl carrier protein reductase as a pathway toward the optimization of triclosan antimalarial efficacy. J. Biol. Chem. 282, 25436-25444.
-
(2007)
J. Biol. Chem.
, vol.282
, pp. 25436-25444
-
-
Freundlich, J.S.1
Wang, F.2
Tsai, H.C.3
Kuo, M.4
Shieh, H.M.5
Anderson, J.W.6
Nkrumah, L.J.7
Valderramos, J.C.8
Yu, M.9
Kumar, T.R.10
Valderramos, S.G.11
Jacobs Jr., W.R.12
Schiehser, G.A.13
Jacobus, D.P.14
Fidock, D.A.15
Sacchettini, J.C.16
-
35
-
-
0031059866
-
Processing of X-ray diffraction data collected in oscillation mode
-
Otwinowski, Z., and Minor, W. (1997) Processing of X-ray diffraction data collected in oscillation mode. Methods Enzymol. 276, 307-326.
-
(1997)
Methods Enzymol.
, vol.276
, pp. 307-326
-
-
Otwinowski, Z.1
Minor, W.2
-
36
-
-
0028103275
-
The CCP4 suite: Programs for protein crystallography
-
Collaborative Computational Project Number 4
-
Collaborative Computational Project Number 4. (1994) The CCP4 suite: programs for protein crystallography. Acta Crystallogr. D Biol. Crystallogr. 50, 760-763.
-
(1994)
Acta Crystallogr. D Biol. Crystallogr
, vol.50
, pp. 760-763
-
-
-
37
-
-
3042613550
-
Likelihoodenhanced fast rotation functions
-
Storoni, L. C., McCoy, A. J., and Read, R. J. (2004) Likelihoodenhanced fast rotation functions. Acta Crystallogr. D Biol. Crystallogr. 60, 432-438.
-
(2004)
Acta Crystallogr. D Biol. Crystallogr.
, vol.60
, pp. 432-438
-
-
Storoni, L.C.1
McCoy, A.J.2
Read, R.J.3
-
38
-
-
0030924992
-
Refinement of macromolecular structures by the maximum-likelihood method
-
Murshudov, G. N., Vagin, A. A., and Dodson, E. J. (1997) Refinement of macromolecular structures by the maximum-likelihood method. Acta Crystallogr. D Biol. Crystallogr. 53, 240-255.
-
(1997)
Acta Crystallogr. D Biol. Crystallogr.
, vol.53
, pp. 240-255
-
-
Murshudov, G.N.1
Vagin, A.A.2
Dodson, E.J.3
-
40
-
-
0000243829
-
PROCHECK: A program to check the stereochemical quality of protein structures
-
Laskowski, R. A., McArthur, M. W., Moss, D. S., and Thornton, J. M. (1993) PROCHECK: a program to check the stereochemical quality of protein structures. J Appl Crystallogr. 26, 283-291.
-
(1993)
J Appl Crystallogr.
, vol.26
, pp. 283-291
-
-
Laskowski, R.A.1
McArthur, M.W.2
Moss, D.S.3
Thornton, J.M.4
-
41
-
-
0001679473
-
ALIGN: A program to superimpose protein coordinates accounting for insertions and deletions
-
Cohen, G. H. (1997) ALIGN: a program to superimpose protein coordinates accounting for insertions and deletions. J Appl Crystallogr. 30, 1160-1161.
-
(1997)
J Appl Crystallogr.
, vol.30
, pp. 1160-1161
-
-
Cohen, G.H.1
-
42
-
-
3543012707
-
Crystallography & NMR system: A new software suite for macromolecular structure determination
-
Brünger, A. T., Adams, P. D., Clore, G. M., DeLano, W. L., Gros, P., Grosse-Kunstleve, R. W., Jiang, J. S., Kuszewski, J., Nilges, M., Pannu, N. S., Read, R. J., Rice, L. M., Simonson, T., and Warren, G. L. (1998) Crystallography & NMR system: a new software suite for macromolecular structure determination. Acta Crystallogr. D Biol. Crystallogr. 54, 905-921.
-
(1998)
Acta Crystallogr. D Biol. Crystallogr.
, vol.54
, pp. 905-921
-
-
Brünger, A.T.1
Adams, P.D.2
Clore, G.M.3
DeLano, W.L.4
Gros, P.5
Grosse-Kunstleve, R.W.6
Jiang, J.S.7
Kuszewski, J.8
Nilges, M.9
Pannu, N.S.10
Read, R.J.11
Rice, L.M.12
Simonson, T.13
Warren, G.L.14
-
43
-
-
7544226311
-
PRODRG: A tool for high-throughput crystallography of protein-ligand complexes
-
Schüttelkopf, A. W. and van Aalten, D. M. (2004) PRODRG: a tool for high-throughput crystallography of protein-ligand complexes. Acta Crystallogr. D Biol. Crystallogr. 60, 1355-1363.
-
(2004)
Acta Crystallogr. D Biol. Crystallogr.
, vol.60
, pp. 1355-1363
-
-
Schüttelkopf, A.W.1
Van Aalten, D.M.2
-
44
-
-
0032515066
-
Broad spectrum antimicrobial biocides target the FabI component of fatty acid synthesis
-
Heath, R. J., Yu, Y. T., Shapiro, M. A., Olson, E., and Rock, C. O. (1998) Broad spectrum antimicrobial biocides target the FabI component of fatty acid synthesis. J. Biol. Chem. 273, 30316-30320.
-
(1998)
J. Biol. Chem.
, vol.273
, pp. 30316-30320
-
-
Heath, R.J.1
Yu, Y.T.2
Shapiro, M.A.3
Olson, E.4
Rock, C.O.5
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