-
1
-
-
58149305794
-
An empirical framework for binary interactome mapping
-
Venkatesan, K.; Rual, J. F.; Vazquez, A.; Stelzl, U.; Lemmens, I.; Hirozane-Kishikawa, T.; Hao, T.; Zenkner, M.; Xin, X.; Goh, K. I.; Yildirim, M. A.; Simonis, N.; Heinzmann, K.; Gebreab, F.; Sahalie, J. M.; Cevik, S.; Simon, C.; de Smet, Dann, E.; Smolyar, A.; Vinayagam, A.; Yu, H.; Szeto, D.; Borick, H.; Dricot, A.; Klitgord, N.; Murray, R. R.; Lin, C.; alowski, M.; Timm, J.; Rau, K.; Boone, C.; Braun, P.; Cusick, M. E.; Roth, F. P.; Hill, D. E.; Tavernier, J.; Wanker, E. E.; arabasi, A. L.; Vidal, M., An empirical framework for binary interactome mapping. Nat. Methods 2009, 6 (1), 83-90;
-
(2009)
Nat. Methods
, vol.6
, Issue.1
, pp. 83-90
-
-
Venkatesan, K.1
Rual, J.F.2
Vazquez, A.3
Stelzl, U.4
Lemmens, I.5
Hirozane-Kishikawa, T.6
Hao, T.7
Zenkner, M.8
Xin, X.9
Goh, K.I.10
Yildirim, M.A.11
Simonis, N.12
Heinzmann, K.13
Gebreab, F.14
Sahalie, J.M.15
Cevik, S.16
Simon, C.17
De Smet18
Dann, E.19
Smolyar, A.20
Vinayagam, A.21
Yu, H.22
Szeto, D.23
Borick, H.24
Dricot, A.25
Klitgord, N.26
Murray, R.R.27
Lin, C.28
Alowski, M.29
Timm, J.30
Rau, K.31
Boone, C.32
Braun, P.33
Cusick, M.E.34
Roth, F.P.35
Hill, D.E.36
Tavernier, J.37
Wanker, E.E.38
Arabasi, A.L.39
Vidal, M.40
more..
-
2
-
-
44349113144
-
Estimating the size of the human nteractome
-
tumpf, M. P.; Thorne, T.; de Silva, E.; Stewart, R.; An, H. J.; Lappe, M.; Wiuf, C., Estimating the size of the human nteractome. Proc. Natl. Acad. Sci. U.S.A. 2008, 105 (19), 6959-64.
-
(2008)
Proc. Natl. Acad. Sci. U.S.A
, vol.105
, Issue.19
, pp. 6959-6964
-
-
Tumpf, M.P.1
Thorne, T.2
De Silva, E.3
Stewart, R.4
An, H.J.5
Lappe, M.6
Wiuf, C.7
-
3
-
-
84866375308
-
Editorial: Toward the design of drugs on proteinprotein interactions
-
Sperandio, O., Editorial: Toward the design of drugs on proteinprotein interactions. Curr. Pharm. Des. 2012, 18 (30), 4585.
-
(2012)
Curr. Pharm. Des
, vol.18
, Issue.30
, pp. 4585
-
-
Sperandio, O.1
-
4
-
-
84863250545
-
Specific noncovalent interactions at protein-ligand interface: Implications for rational rug design
-
Zhou, P.; Huang, J.; Tian, F., Specific noncovalent interactions at protein-ligand interface: implications for rational rug design. Curr. Med. Chem. 2012, 19 (2), 226-38
-
(2012)
Curr. Med. Chem
, vol.19
, Issue.2
, pp. 226-238
-
-
Zhou, P.1
Huang, J.2
Tian, F.3
-
5
-
-
22144454687
-
Strategies for targeting protein-protein nteractions with synthetic agents
-
Yin, H.; Hamilton, A. D., Strategies for targeting protein-protein nteractions with synthetic agents. Angew. Chem. Int. Ed. Engl., 2005, 44 (27), 4130-63.
-
(2005)
Angew. Chem. Int. Ed. Engl
, vol.44
, Issue.27
, pp. 4130-4163
-
-
Yin, H.1
Hamilton, A.D.2
-
6
-
-
0000548829
-
Three-dimensional structure of peptide-protein complexes: Implications for recognition
-
Marshall, G., Three-dimensional structure of peptide-protein complexes: implications for recognition. Curr. Opin. truct. Biol. 1992, 2 (6), 904-919;
-
(1992)
Curr. Opin. Truct. Biol
, vol.2
, Issue.6
, pp. 904-919
-
-
Marshall, G.1
-
7
-
-
0003187567
-
The atomic structure of protein-protein ecognition sites
-
Lo Conte, L.; Chothia, C.; Janin, J., The atomic structure of protein-protein ecognition sites. J. Mol. Biol. 1999, 285 (5), 2177-98.
-
(1999)
J. Mol. Biol
, vol.285
, Issue.5
, pp. 2177-2198
-
-
Lo Conte, L.1
Chothia, C.2
Janin, J.3
-
8
-
-
37549040575
-
The challenge of drugging undruggable targets in cancer: Lessons learned from argeting BCL-2 family members
-
Verdine, G. L.; Walensky, L. D., The challenge of drugging undruggable targets in cancer: lessons learned from argeting BCL-2 family members. Clin. Cancer Res. 2007, 13 (24), 7264-70;
-
(2007)
Clin. Cancer Res
, vol.13
, Issue.24
, pp. 7264-7270
-
-
Verdine, G.L.1
Walensky, L.D.2
-
9
-
-
37249004920
-
Reaching or high-hanging fruit in drug discovery at protein-protein interfaces
-
Wells, J. A.; McClendon, C. L., Reaching or high-hanging fruit in drug discovery at protein-protein interfaces. Nature 2007, 450 (7172), 1001-9.
-
(2007)
Nature
, vol.450
, Issue.7172
, pp. 1001-1009
-
-
Wells, J.A.1
McClendon, C.L.2
-
10
-
-
50249154886
-
Small-molecule inhibitors of protein-protein interactions
-
Berg, T., mall-molecule inhibitors of protein-protein interactions. Curr. Opin. Drug Discovery Dev. 2008, 11 (5), 666-74;
-
(2008)
Curr. Opin. Drug Discovery Dev
, vol.11
, Issue.5
, pp. 666-674
-
-
Berg, T.1
-
11
-
-
79958143460
-
Modulators of protein-protein interactions: Novel approaches n targeting protein kinases and other pharmaceutically relevant biomolecules
-
Rechfeld, F.; Gruber, P.; Hofmann, J.; Kirchmair, J., Modulators of protein-protein interactions: novel approaches n targeting protein kinases and other pharmaceutically relevant biomolecules. Curr. Top. Med. Chem. 2011, 11 (11), 305-19;
-
(2011)
Curr. Top. Med. Chem
, vol.11
, Issue.11
, pp. 305-319
-
-
Rechfeld, F.1
Gruber, P.2
Hofmann, J.3
Kirchmair, J.4
-
12
-
-
84866368830
-
Discovery of Modulators of Protein Protein Interactions: Current Approaches nd Limitations
-
Meireles, L. M.; Mustata, G., Discovery of Modulators of Protein Protein Interactions: Current Approaches nd Limitations. Curr. Top. Med. Chem. 2010;
-
(2010)
Curr. Top. Med. Chem
-
-
Meireles, L.M.1
Mustata, G.2
-
13
-
-
3342908718
-
Emerging classes of protein-protein interaction inhibitors and new tools for their development
-
Pagliaro, L.; Felding, J.; Audouze, K.; Nielsen, S. J.; Terry, R. B.; rog-Jensen, C.; Butcher, S., Emerging classes of protein-protein interaction inhibitors and new tools for their development. Curr. Opin. Chem. Biol. 2004, 8 (4), 442-9;
-
(2004)
Curr. Opin. Chem. Biol
, vol.8
, Issue.4
, pp. 442-449
-
-
Pagliaro, L.1
Felding, J.2
Audouze, K.3
Nielsen, S.J.4
Terry, R.B.5
Rog-Jensen, C.6
Butcher, S.7
-
14
-
-
70450169243
-
Inhibition of protein-protein interactions using designed molecules
-
Wilson, A. J., Inhibition of protein-protein interactions using designed molecules. Chem Soc Rev 2009, 38 (12), 3289-300;
-
(2009)
Chem Soc Rev
, vol.38
, Issue.12
, pp. 3289-3300
-
-
Wilson, A.J.1
-
15
-
-
79960990847
-
Chemical and structural lessons from recent successes in protein-protein interaction inhibition (2P2I)
-
Morelli, X.; Bourgeas, R.; Roche, P., Chemical and structural lessons from recent successes in protein-protein interaction inhibition (2P2I). Curr. Opin. Chem. Biol. 2011, 15 (4), 475-81.
-
(2011)
Curr. Opin. Chem. Biol
, vol.15
, Issue.4
, pp. 475-481
-
-
Morelli, X.1
Bourgeas, R.2
Roche, P.3
-
16
-
-
34447290874
-
Protein-protein interaction inhibitors: Small molecules from screening techniques
-
Fletcher, S.; Hamilton, A. D., Protein-protein interaction inhibitors: small molecules from screening techniques. Curr. op. Med. Chem. 2007, 7 (10), 922-7;
-
(2007)
Curr. Op. Med. Chem
, vol.7
, Issue.10
, pp. 922-927
-
-
Fletcher, S.1
Hamilton, A.D.2
-
18
-
-
84870401411
-
Fragment based drug design: From experimental to omputational approaches
-
Kumar, A.; Voet, A.; Zhang, K. Y., Fragment based drug design: from experimental to omputational approaches. Curr. Med. Chem. 2012.
-
(2012)
Curr. Med. Chem
-
-
Kumar, A.1
Voet, A.2
Zhang, K.Y.3
-
19
-
-
79956188485
-
Computer-aided drug discovery and development
-
Zhang, S., Computer-aided drug discovery and development. Methods Mol Biol 2011, 716, 23-38.
-
(2011)
Methods Mol Biol
, vol.716
, pp. 23-38
-
-
Zhang, S.1
-
20
-
-
79959771257
-
Protein-ligand docking
-
Bottegoni, G., Protein-ligand docking. Front Biosci 17, 2289-306.
-
Front Biosci
, vol.17
, pp. 2289-2306
-
-
Bottegoni, G.1
-
21
-
-
0034081944
-
Evaluation of docking/scoring approaches: A comparative study based on MMP3 inhibitors
-
[10] Ha, S.; Andreani, R.; Robbins, A.; Muegge, I., Evaluation of docking/scoring approaches: a comparative study based on MMP3 inhibitors. J. Comput. Aided Mol. Des. 2000, 14 (5), 435-48.
-
(2000)
J. Comput. Aided Mol. Des
, vol.14
, Issue.5
, pp. 435-448
-
-
Ha, S.1
Andreani, R.2
Robbins, A.3
Muegge, I.4
-
22
-
-
45749117025
-
Ranking targets in structure-based virtual screening of three-dimensional rotein libraries: Methods and problems
-
Kellenberger, E.; Foata, N.; Rognan, D., Ranking targets in structure-based virtual screening of three-dimensional rotein libraries: methods and problems. J. Chem. Inf. Model. 2008, 48 (5), 1014-25.
-
(2008)
J. Chem. Inf. Model
, vol.48
, Issue.5
, pp. 1014-1025
-
-
Kellenberger, E.1
Foata, N.2
Rognan, D.3
-
23
-
-
77950839899
-
Designing focused chemical libraries enriched in protein-protein interaction inhibitors using achine-learning methods
-
Reynes, C.; Host, H.; Camproux, A. C.; Laconde, G.; Leroux, F.; Mazars, A.; Deprez, B.; Fahraeus, R.; Villoutreix, Sperandio, O., Designing focused chemical libraries enriched in protein-protein interaction inhibitors using achine-learning methods. PLoS Comput. Biol. 6 (3), e1000695;
-
PLoS Comput. Biol
, vol.6
, Issue.3
-
-
Reynes, C.1
Host, H.2
Camproux, A.C.3
Laconde, G.4
Leroux, F.5
Mazars, A.6
Deprez, B.7
Fahraeus, R.8
Villoutreix, S.9
-
24
-
-
77649233664
-
Rationalizing the chemical space of protein-protein interaction inhibitors
-
Sperandio, O.; Reynes, C. H.; Camproux, A. C.; illoutreix, B. O., Rationalizing the chemical space of protein-protein interaction inhibitors. Drug Discov. Today, 15 (5-6), 20-9;
-
Drug Discov. Today
, vol.15
, Issue.5-6
, pp. 20-29
-
-
Sperandio, O.1
Reynes, C.H.2
Camproux, A.C.3
Illoutreix, B.O.4
-
25
-
-
34648833340
-
Prediction of protein-protein interaction inhibitors by hemoinformatics and machine learning methods
-
Neugebauer, A.; Hartmann, R. W.; Klein, C. D., Prediction of protein-protein interaction inhibitors by hemoinformatics and machine learning methods. J. Med. Chem. 2007, 50 (19), 4665-8.
-
(2007)
J. Med. Chem
, vol.50
, Issue.19
, pp. 4665-4668
-
-
Neugebauer, A.1
Hartmann, R.W.2
Klein, C.D.3
-
27
-
-
77950522305
-
Pharmacophore based drug design approach as a practical process in drug discovery
-
Gao, Q.; Yang, L.; Zhu, Y., Pharmacophore based drug design approach as a practical process in drug discovery. Curr. omput. Aided Drug Des., 2010, 6 (1), 37-49.
-
(2010)
Curr. Omput. Aided Drug Des
, vol.6
, Issue.1
, pp. 37-49
-
-
Gao, Q.1
Yang, L.2
Zhu, Y.3
-
28
-
-
77955262882
-
Computational methodologies for compound database searching that utilize experimental roteinligand interaction information
-
Tan, L.; Batista, J.; Bajorath, J., Computational methodologies for compound database searching that utilize experimental roteinligand interaction information. Chem. Biol. Drug Des., 2010, 76 (3), 191-200.
-
(2010)
Chem. Biol. Drug Des
, vol.76
, Issue.3
, pp. 191-200
-
-
Tan, L.1
Batista, J.2
Bajorath, J.3
-
29
-
-
79952117000
-
Pharmacophore-based virtual screening
-
Horvath, D., Pharmacophore-based virtual screening. Methods Mol. Biol., 2011, 672, 261-98.
-
(2011)
Methods Mol. Biol
, vol.672
, pp. 261-298
-
-
Horvath, D.1
-
30
-
-
84866414275
-
Small-Molecule Inhibitors of Protein-Protein Interactions: How to Mimic a Protein Partner
-
Fry, D. C., Small-Molecule Inhibitors of Protein-Protein Interactions: How to Mimic a Protein Partner. Curr. Pharm. es. 2012.
-
(2012)
Curr. Pharm. Es
-
-
Fry, D.C.1
-
31
-
-
77955282104
-
Upregulation of Bcl2 inhibits apoptosisdriven BAX insertion but favors BAX relocalization in mitochondria
-
Teijido, O.; Dejean, L., Upregulation of Bcl2 inhibits apoptosisdriven BAX insertion but favors BAX relocalization in mitochondria. FEBS letters 2010, 584 (15), 3305-10.
-
(2010)
FEBS Letters
, vol.584
, Issue.15
, pp. 3305-3310
-
-
Teijido, O.1
Dejean, L.2
-
32
-
-
57049157033
-
BCL-2 family antagonists for cancer therapy
-
Lessene, G.; Czabotar, P. E.; Colman, P. M., BCL-2 family antagonists for cancer therapy. Nat. Rev. Drug Discov., 2008, 7 (12), 989-1000;
-
(2008)
Nat. Rev. Drug Discov
, vol.7
, Issue.12
, pp. 989-1000
-
-
Lessene, G.1
Czabotar, P.E.2
Colman, P.M.3
-
33
-
-
23444433257
-
Spontaneous immunity against BclxL in cancer patients
-
Andersen, M. H.; Reker, S.; Kvistborg, P.; Becker, J. C.; thor Straten, P., Spontaneous mmunity against BclxL in cancer patients. J. Immunol., 2005, 175 (4), 2709-14.
-
(2005)
J. Immunol
, vol.175
, Issue.4
, pp. 2709-2714
-
-
Andersen, M.H.1
Reker, S.2
Kvistborg, P.3
Becker, J.C.4
Thor, S.P.5
-
34
-
-
0033959744
-
MDM2-master regulator of the p53 tumor suppressor protein
-
Momand, J.; Wu, H. H.; asgupta, G., MDM2-master regulator of the p53 tumor suppressor protein. Gene 2000, 242 (1-2), 15-29;
-
(2000)
Gene
, vol.242
, Issue.1-2
, pp. 15-29
-
-
Momand, J.1
Wu, H.H.2
Asgupta, G.3
-
35
-
-
57049114832
-
The genetics of the p53 pathway, apoptosis and ancer therapy
-
Vazquez, A.; Bond, E. E.; Levine, A. J.; Bond, G. L., The genetics of the p53 pathway, apoptosis and ancer therapy. Nat. Rev. Drug Discov., 2008, 7 (12), 979-87;
-
(2008)
Nat. Rev. Drug Discov
, vol.7
, Issue.12
, pp. 979-987
-
-
Vazquez, A.1
Bond, E.E.2
Levine, A.J.3
Bond, G.L.4
-
36
-
-
0032417695
-
Overexpression of Mdm2 in mice reveals a p53-independent role for Mdm2 in tumorigenesis
-
Jones, S. N.; Hancock, A. R.; Vogel, H.; Donehower, L., Bradley, A., Overexpression of Mdm2 in mice reveals a p53-independent role for Mdm2 in tumorigenesis. Proc. Natl. cad. Sci. U.S.A. 1998, 95 (26), 15608-12;
-
(1998)
Proc. Natl. Cad. Sci. U.S.A
, vol.95
, Issue.26
, pp. 15608-15612
-
-
Jones, S.N.1
Hancock, A.R.2
Vogel, H.3
Donehower, L.4
Bradley, A.5
-
37
-
-
0030575937
-
Structure of the MDM2 oncoprotein bound to the p53 tumor suppressor transactivation domain
-
Kussie, P. H.; Gorina, S.; Marechal, V.; Elenbaas, B.; Moreau, J.; Levine, A.Pavletich, N. P., Structure of the MDM2 oncoprotein bound to the p53 tumor suppressor transactivation domain. Science 1996, 274 (5289), 948-53;
-
(1996)
Science
, vol.274
, Issue.5289
, pp. 948-953
-
-
Kussie, P.H.1
Gorina, S.2
Marechal, V.3
Elenbaas, B.4
Moreau, J.5
Levine, A.6
Pavletich, N.P.7
-
38
-
-
0030810926
-
Xlinked IAP is a direct inhibitor f cell-death proteases
-
Deveraux, Q. L.; Takahashi, R.; Salvesen, G. S.; Reed, J. C., Xlinked IAP is a direct inhibitor f cell-death proteases. Nature 1997, 388 (6639), 300-4;
-
(1997)
Nature
, vol.388
, Issue.6639
, pp. 300-304
-
-
Deveraux, Q.L.1
Takahashi, R.2
Salvesen, G.S.3
Reed, J.C.4
-
39
-
-
4143099131
-
Discovery of potent antagonists of the antiapoptotic protein XIAP for the treatment of cancer
-
Oost, T. K.; Sun, C.; Armstrong, R. C.; Al-Assaad, A. S.; Betz, F.; Deckwerth, T. L.; Ding, H.; Elmore, S. W.; Meadows, R. P.; Olejniczak, E. T.; Oleksijew, A.; Oltersdorf, T.; osenberg, S. H.; Shoemaker, A. R.; Tomaselli, K. J.; Zou, H.; Fesik, S. W., Discovery of potent antagonists of the antiapoptotic protein XIAP for the treatment of cancer. J. Med. Chem. 2004, 47 (18), 4417-26.
-
(2004)
J. Med. Chem
, vol.47
, Issue.18
, pp. 4417-4426
-
-
Oost, T.K.1
Sun, C.2
Armstrong, R.C.3
Al-Assaad, A.S.4
Betz, F.5
Deckwerth, T.L.6
Ding, H.7
Elmore, S.W.8
Meadows, R.P.9
Olejniczak, E.T.10
Oleksijew, A.11
Oltersdorf, T.12
Osenberg, S.H.13
Shoemaker, A.R.14
Tomaselli, K.J.15
Zou, H.16
Fesik, S.W.17
-
40
-
-
0035853803
-
Genetic analysis of the Escherichia coli tsZ.ZipA interaction in the yeast two-hybrid system
-
Characterization of FtsZ residues essential for the interactions with ipA and with FtsA
-
Haney, S. A.; Glasfeld, E.; Hale, C.; Keeney, D.; He, Z.; de Boer, P., Genetic analysis of the Escherichia coli tsZ.ZipA interaction in the yeast two-hybrid system. Characterization of FtsZ residues essential for the interactions with ipA and with FtsA. J. Biol. Chem 2001, 276 (15), 11980-7;
-
(2001)
J. Biol. Chem
, vol.276
, Issue.15
, pp. 11980-11987
-
-
Haney, S.A.1
Glasfeld, E.2
Hale, C.3
Keeney, D.4
He, Z.5
De Boer, P.6
-
41
-
-
47349109056
-
Drug-like inhibitors of protein-protein nteractions: A structural examination of effective protein mimicry
-
Fry, D. C., Drug-like inhibitors of protein-protein nteractions: a structural examination of effective protein mimicry. Curr. Protein Pept. Sci., 2008, 9 (3), 240-7;
-
(2008)
Curr. Protein Pept. Sci
, vol.9
, Issue.3
, pp. 240-247
-
-
Fry, D.C.1
-
42
-
-
4444340945
-
Combinatorial synthesis of substituted 3-(2-indolyl)piperidines and 2-phenyl indoles as nhibitors of ZipA-FtsZ interaction
-
Jennings, D.; Foreman, K. W.; Rush, T. S., III; Tsao, D. H.; Mosyak, L.; Kincaid, S. L.; Sukhdeo, M. N.; utherland, A. G.; Ding; Kenny, C. H.; Sabus, C. L.; Liu, H.; Dushin, E. G.; Moghazeh, S. L.; Labthavikul, P.; Petersen, P. J.; Tuckman, M.; Haney, S. A.; Ruzin, A. V., Combinatorial synthesis of substituted 3-(2-indolyl)piperidines and 2-phenyl indoles as nhibitors of ZipA-FtsZ interaction. Bioorg. Med. Chem. 2004, 12 (19), 5115-31;
-
(2004)
Bioorg. Med. Chem
, vol.12
, Issue.19
, pp. 5115-5131
-
-
Jennings, D.1
Foreman, K.W.2
Rush III, T.S.3
Tsao, D.H.4
Mosyak, L.5
Kincaid, S.L.6
Sukhdeo, M.N.7
Utherland, A.G.8
Ding9
Kenny, C.H.10
Sabus, C.L.11
Liu, H.12
Dushin, E.G.13
Moghazeh, S.L.14
Labthavikul, P.15
Petersen, P.J.16
Tuckman, M.17
Haney, S.A.18
Ruzin, A.V.19
-
43
-
-
10744230770
-
Design and synthesis of indolo[2,3-a]quinolizin-7-one nhibitors of the ZipA-FtsZ interaction
-
Jennings, L. D.; Foreman, K. W.; ush, T. S., III; Tsao, D. H.; Mosyak, L.; Li, Y.; Sukhdeo, M. N.; Ding, W.; Dushin, E. G.; Kenny, C. H.; Moghazeh, S. L.; etersen, P. J.; Ruzin, A. V.; Tuckman, M.; Sutherland, A. G., Design and synthesis of indolo[2,3-a]quinolizin-7-one nhibitors of the ZipA-FtsZ interaction. Bioorg. Med. Chem. Lett. 2004, 14 (6), 1427-31;
-
(2004)
Bioorg. Med. Chem. Lett
, vol.14
, Issue.6
, pp. 1427-1431
-
-
Jennings, L.D.1
Foreman, K.W.2
Ush III, T.S.3
Tsao, D.H.4
Mosyak, L.5
Li, Y.6
Sukhdeo, M.N.7
Ding, W.8
Dushin, E.G.9
Kenny, C.H.10
Moghazeh, S.L.11
Etersen, P.J.12
Ruzin, A.V.13
Tuckman, M.14
Sutherland, A.G.15
-
44
-
-
33750067690
-
Discovery of novel inhibitors of the ZipA/FtsZ complex by NMR fragment creening coupled with structure-based design
-
Tsao, D. H.; Sutherland, A.; Jennings, L. D.; Li, Y.; Rush, T. S., III; Alvarez, J. C.; Ding, W.; Dushin, E. G.; Dushin, R. G.; Haney, S. A.; Kenny, C. H.; alakian, A. K.; Nilakantan, R.; Mosyak, L., Discovery of novel inhibitors of the ZipA/FtsZ complex by NMR fragment creening coupled with structure-based design. Bioorg. Med. Chem. 2006, 14 (23), 7953-61.
-
(2006)
Bioorg. Med. Chem
, vol.14
, Issue.23
, pp. 7953-7961
-
-
Tsao, D.H.1
Sutherland, A.2
Jennings, L.D.3
Li, Y.4
Rush III, T.S.5
Alvarez, J.C.6
Ding, W.7
Dushin, E.G.8
Dushin, R.G.9
Haney, S.A.10
Kenny, C.H.11
Alakian, A.K.12
Nilakantan, R.13
Mosyak, L.14
-
45
-
-
0027096411
-
Non-peptide fibrinogen receptor antagonists
-
1. Discovery and design of exosite nhibitors
-
Hartman, G. D.; Egbertson, M. S.; Halczenko, W.; Laswell, W. L.; Duggan, M. E.; Smith, R. L.; Naylor, A. M.; anno, D.; Lynch, R. J.; Zhang, G.; et al., Non-peptide fibrinogen receptor antagonists. 1. Discovery and design of exosite nhibitors. J. Med. Chem. 1992, 35 (24), 4640-2;
-
(1992)
J. Med. Chem
, vol.35
, Issue.24
, pp. 4640-4642
-
-
Hartman, G.D.1
Egbertson, M.S.2
Halczenko, W.3
Laswell, W.L.4
Duggan, M.E.5
Smith, R.L.6
Naylor, A.M.7
Anno, D.8
Lynch, R.J.9
Zhang, G.10
-
46
-
-
50249106884
-
Structural basis for distinctive ecognition of fibrinogen gammaC peptide by the platelet integrin alphaIIbbeta3
-
Springer, T. A.; Zhu, J.; Xiao, T., Structural basis for distinctive ecognition of fibrinogen gammaC peptide by the platelet integrin alphaIIbbeta3. J. Cell. Biol. 2008, 182 (4), 791-800.
-
(2008)
J. Cell. Biol
, vol.182
, Issue.4
, pp. 791-800
-
-
Springer, T.A.1
Zhu, J.2
Xiao, T.3
-
47
-
-
84859173553
-
De novo design of small molecule inhibitors targeting the LEDGF/p75-HIV integrase interaction
-
Cavalluzzo, C.; Voet, A.; Christ, F.; Singh, B. K.; Sharma, A.; Debyser, Z.; Maeyer, M. D.; Eycken, E. V. d., De novo esign of small molecule inhibitors targeting the LEDGF/p75-HIV integrase interaction. RSC Advances 2012, 2 (3), 974
-
(2012)
RSC Advances
, vol.2
, Issue.3
, pp. 974
-
-
Cavalluzzo, C.1
Voet, A.2
Christ, F.3
Singh, B.K.4
Sharma, A.5
Debyser, Z.6
Maeyer, M.D.7
Eycken, E.V.D.8
-
48
-
-
77952553431
-
Rational design of small-molecule inhibitors of the EDGF/p75-integrase interaction and HIV replication
-
Christ, F.; Voet, A.; Marchand, A.; Nicolet, S.; Desimmie, B. A.; Marchand, D.; Bardiot, D.; Van der Veken, N. J.; Van emoortel, B.; Strelkov, S. V.; De Maeyer, M.; Chaltin, P.; Debyser, Z., Rational design of small-molecule inhibitors of the EDGF/p75-integrase interaction and HIV replication. Nat. Chem. Biol., 2010, 6 (6), 442-8;
-
(2010)
Nat. Chem. Biol
, vol.6
, Issue.6
, pp. 442-448
-
-
Christ, F.1
Voet, A.2
Marchand, A.3
Nicolet, S.4
Desimmie, B.A.5
Marchand, D.6
Bardiot, D.7
Van der Veken, N.J.8
Van Emoortel, B.9
Strelkov, S.V.10
De Maeyer, M.11
Chaltin, P.12
Debyser, Z.13
-
49
-
-
84878784225
-
Fragment hopping approach directed at design of HIV IN-LEDGF/p75 interaction inhibitors
-
De Luca, L.; Ferro, S.; orreale, F.; Christ, F.; Debyser, Z.; Chimirri, A.; Gitto, R., Fragment hopping approach directed at design of HIV IN-LEDGF/p75 interaction inhibitors. J. Enzyme Inhib. Med. Chem. 2012;
-
(2012)
J. Enzyme Inhib. Med. Chem
-
-
De Luca, L.1
Ferro, S.2
Orreale, F.3
Christ, F.4
Debyser, Z.5
Chimirri, A.6
Gitto, R.7
-
50
-
-
79960465042
-
Inhibition of the interaction between HIV-1 integrase and its cofactor LEDGF/p75: A promising approach in nti-retroviral therapy
-
De Luca, L.; Ferro, S.; Morreale, F.; himirri, A., Inhibition of the interaction between HIV-1 integrase and its cofactor LEDGF/p75: a promising approach in nti-retroviral therapy. Mini Rev. Med. Chem. 2011, 11 (8), 714-27;
-
(2011)
Mini Rev. Med. Chem
, vol.11
, Issue.8
, pp. 714-727
-
-
De Luca, L.1
Ferro, S.2
Morreale, F.3
Himirri, A.4
-
51
-
-
79959741307
-
Inhibitors of the interactions between HIV-1 IN and the cofactor LEDGF/p75
-
De Luca, L.; Ferro, S.; Morreale, F.; De Grazia, S.; himirri, A., Inhibitors of the interactions between HIV-1 IN and the cofactor LEDGF/p75. Chem. Med. Chem., 2011, 6 (7), 184-91;
-
(2011)
Chem. Med. Chem
, vol.6
, Issue.7
, pp. 184-191
-
-
De Luca, L.1
Ferro, S.2
Morreale, F.3
de Grazia, S.4
Himirri, A.5
-
52
-
-
77958015795
-
Small olecules targeting the interaction between HIV-1 integrase and LEDGF/p75 cofactor
-
De Luca, L.; Ferro, S.; Gitto, R.; Barreca, M. L.; Agnello, S.; Christ, F.; Debyser, Z.; Chimirri, A., Small olecules targeting the interaction between HIV-1 integrase and LEDGF/p75 cofactor. Bioorg. Med. Chem. 2010, 18 (21), 515-21.
-
(2010)
Bioorg. Med. Chem
, vol.18
, Issue.21
, pp. 515-521
-
-
De Luca, L.1
Ferro, S.2
Gitto, R.3
Barreca, M.L.4
Agnello, S.5
Christ, F.6
Debyser, Z.7
Chimirri, A.8
-
53
-
-
13744260574
-
Missing the target: Ubiquitin ligase drugs stall
-
Garber, K., Missing the target: ubiquitin ligase drugs stall. J. Natl. Cancer Inst. 2005, 97 (3), 166-7;
-
(2005)
J. Natl. Cancer Inst
, vol.97
, Issue.3
, pp. 166-167
-
-
Garber, K.1
-
54
-
-
84868522211
-
Emall-Molecule Inhibitors of the Interaction between the E3 Ligase VHL and HIF1alpha
-
Buckley, D.; Gustafson, J. L.; Van Molle, I.; Roth, A. G.; Tae, H. S.; Gareiss, P. C.; Jorgensen, W. L.; Ciulli, A.; Crews, C. M., Emall-Molecule Inhibitors of the Interaction between the E3 Ligase VHL and HIF1alpha. Angew Chem. Int. Ed. Engl., 2012;
-
(2012)
Angew Chem. Int. Ed. Engl
-
-
Buckley, D.1
Gustafson, J.L.2
van Molle, I.3
Roth, A.G.4
Tae, H.S.5
Gareiss, P.C.6
Jorgensen, W.L.7
Ciulli, A.8
Crews, C.M.9
-
55
-
-
84858201095
-
Targeting the von Hippel-Lindau E3 ubiquitin ligase using small molecules to disrupt the VHL/HIF-1alpha interaction
-
Buckley, D. L.; Van Molle, I.; Gareiss, P. C.; Tae, H. S.; Michel, J.; Noblin, D. J.; Jorgensen, W. L.; Ciulli, A.; rews, C. M., Targeting the von Hippel-Lindau E3 ubiquitin ligase using small molecules to disrupt the VHL/HIF-1alpha interaction. J. Am. Chem. Soc. 2012, 134 (10), 4465-8.
-
(2012)
J. Am. Chem. Soc
, vol.134
, Issue.10
, pp. 4465-4468
-
-
Buckley, D.L.1
van Molle, I.2
Gareiss, P.C.3
Tae, H.S.4
Michel, J.5
Noblin, D.J.6
Jorgensen, W.L.7
Ciulli, A.8
Rews, C.M.9
-
56
-
-
84860235383
-
Interleukin-2, Interleukin-7, T cell-mediated autoimmunity, and N-glycosylation
-
Grigorian, A.; Mkhikian, H.; Demetriou, M., Interleukin-2, Interleukin-7, T cell-mediated autoimmunity, and N-glycosylation. Ann. N. Y. Acad. Sci. 2012, 1253, 49-57
-
(2012)
Ann. N. Y. Acad. Sci
, vol.1253
, pp. 49-57
-
-
Grigorian, A.1
Mkhikian, H.2
Demetriou, M.3
-
57
-
-
84862868473
-
Small-molecule inhibitors of L-2/IL-2R: Lessons learned and applied
-
Wilson, C. G.; Arkin, M. R., Small-molecule inhibitors of L-2/IL-2R: lessons learned and applied. Curr. Top. Microbiol. Immunol. 2010, 348, 25-59;
-
(2010)
Curr. Top. Microbiol. Immunol
, vol.348
, pp. 25-59
-
-
Wilson, C.G.1
Arkin, M.R.2
-
58
-
-
0037414274
-
Discovery of a potent small olecule IL-2 inhibitor through fragment assembly
-
Braisted, A. C.; Oslob, J.; Delano, W. L.; Hyde, J.; McDowell, R. S.; Waal, N.; Yu, C.; Arkin, M. R.; Raimundo, B. C., Discovery of a potent small olecule IL-2 inhibitor through fragment assembly. J. Am. Chem. Soc. 2003, 125 (13), 3714-5.
-
(2003)
J. Am. Chem. Soc
, vol.125
, Issue.13
, pp. 3714-3715
-
-
Braisted, A.C.1
Oslob, J.2
Delano, W.L.3
Hyde, J.4
McDowell, R.S.5
Waal, N.6
Yu, C.7
Arkin, M.R.8
Raimundo, B.C.9
-
59
-
-
84866403586
-
Pharmacophore Modelling as a Virtual Screening Tool for the Discovery of Small Molecule roteinprotein Interaction Inhibitors
-
Voet, A.; Zhang, K. Y., Pharmacophore Modelling as a Virtual Screening Tool for the Discovery of Small Molecule roteinprotein Interaction Inhibitors. Curr. Pharm. Des. 2012, 18 (30), 4586-98.
-
(2012)
Curr. Pharm. Des
, vol.18
, Issue.30
, pp. 4586-4598
-
-
Voet, A.1
Zhang, K.Y.2
-
60
-
-
27744586067
-
Small-molecule inhibition of TNF-alpha
-
He, M. M.; Smith, A. S.; Oslob, J. D.; Flanagan, W. M.; Braisted, A. C.; Whitty, A.; Cancilla, M. T.; Wang, J.; ugovskoy, A. A.; Yoburn, J. C.; Fung, A. D.; Farrington, G.; Eldredge, J. K.; Day, E. S.; Cruz, L. A.; Cachero, T. G.; Miller, K.; Friedman, J. E.; Choong, I. C.; Cunningham, B. C., Small-molecule inhibition of TNF-alpha. Science 2005, 310 (5750), 1022-5;
-
(2005)
Science
, vol.310
, Issue.5750
, pp. 1022-1025
-
-
He, M.M.1
Smith, A.S.2
Oslob, J.D.3
Flanagan, W.M.4
Braisted, A.C.5
Whitty, A.6
Cancilla, M.T.7
Wang, J.8
Ugovskoy, A.A.9
Yoburn, J.C.10
Fung, A.D.11
Farrington, G.12
Eldredge, J.K.13
Day, E.S.14
Cruz, L.A.15
Cachero, T.G.16
Miller, K.17
Friedman, J.E.18
Choong, I.C.19
Cunningham, B.C.20
more..
-
61
-
-
33847619355
-
Optimization and determination of the absolute configuration of a series of otent nhibitors of human papillomavirus type-11 E1-E2 protein-protein interaction: A combined medicinal chemistry, NMR and omputational chemistry approach
-
Goudreau, N.; Cameron, D. R.; Deziel, R.; Hache, B.; Jakalian, A.; Malenfant, E.; Naud, J.; Ogilvie, W.O'Meara, J.; White, P. W.; Yoakim, C., Optimization and determination of the absolute configuration of a series of otent nhibitors of human papillomavirus type-11 E1-E2 protein-protein interaction: a combined medicinal chemistry, NMR and omputational chemistry approach. Bioorg. Med. Chem. 2007, 15 (7), 2690-700.
-
(2007)
Bioorg. Med. Chem
, vol.15
, Issue.7
, pp. 2690-2700
-
-
Goudreau, N.1
Cameron, D.R.2
Deziel, R.3
Hache, B.4
Jakalian, A.5
Malenfant, E.6
Naud, J.7
Ogilvie, W.8
O'Meara, J.9
White, P.W.10
Yoakim, C.11
-
62
-
-
1542466792
-
Annexin II regulates fibrin homeostasis and neoangiogenesis in vivo
-
Ling, Q.; Jacovina, A. T.; Deora, A.; Febbraio, M.; Simatov, R.; Silverstein, R. L.; Hempstead, B.; Mark, W. H.; Majjar, K. A., Annexin II regulates fibrin homeostasis and neoangiogenesis in vivo. J. Clin. Invest. 2004, 113 (1), 38-48;
-
(2004)
J. Clin. Invest
, vol.113
, Issue.1
, pp. 38-48
-
-
Ling, Q.1
Jacovina, A.T.2
Deora, A.3
Febbraio, M.4
Simatov, R.5
Silverstein, R.L.6
Hempstead, B.7
Mark, W.H.8
Ajjar, K.A.9
-
63
-
-
80052937405
-
Regulation of fibrinolysis y S100A10 in vivo
-
urette, A. P.; Madureira, P. A.; Phipps, K. D.; Miller, V. A.; Svenningsson, P.; Waisman, D. M., Regulation of fibrinolysis y S100A10 in vivo. Blood 2011, 118 (11), 3172-81.
-
(2011)
Blood
, vol.118
, Issue.11
, pp. 3172-3181
-
-
Urette, A.P.1
Madureira, P.A.2
Phipps, K.D.3
Miller, V.A.4
Svenningsson, P.5
Waisman, D.M.6
-
64
-
-
84864413157
-
Threedimensional pharmacophore design and biochemical screening identifies substituted 1,2,4-triazoles as inhibitors of the annexin A2-S100A10 protein interaction
-
eddy, T. R.; Li, C.; Fischer, P. M.; Dekker, L. V., Threedimensional pharmacophore design and biochemical screening identifies substituted 1,2,4-triazoles as inhibitors of the annexin A2-S100A10 protein interaction. Chem. Med. Chem., 2012, 7 (8), 1435-46.
-
(2012)
Chem. Med. Chem
, vol.7
, Issue.8
, pp. 1435-1446
-
-
Eddy, T.R.1
Li, C.2
Fischer, P.M.3
Dekker, L.V.4
-
65
-
-
13844320566
-
LigandScout: 3-D pharmacophores derived from protein-bound ligands and their use as virtual creening filters
-
Wolber, G.; Langer, T., LigandScout: 3-D pharmacophores derived from protein-bound ligands and their use as virtual creening filters. J. Chem Inf. Model. 2005, 45 (1), 160-9.
-
(2005)
J. Chem Inf. Model
, vol.45
, Issue.1
, pp. 160-169
-
-
Wolber, G.1
Langer, T.2
-
66
-
-
77953472798
-
In search of second-generation HIV integrase inhibitors: Targeting ntegration beyond strand transfer
-
Voet, A. R.; Maeyer, M. D.; Debyser, Z.; Christ, F., In search of second-generation HIV integrase inhibitors: targeting ntegration beyond strand transfer. Future Med. Chem., 2009, 1 (7), 1259-74.
-
(2009)
Future Med. Chem
, vol.1
, Issue.7
, pp. 1259-1274
-
-
Voet, A.R.1
Maeyer, M.D.2
Debyser, Z.3
Christ, F.4
-
67
-
-
0346036088
-
HIV-1 integrase forms stable tetramers and associates with LEDGF/p75 protein in human cells
-
Cherepanov, P.; Maertens, G.; Proost, P.; Devreese, B.; Van Beeumen, J.; Engelborghs, Y.; De Clercq, E.; Debyser, HIV-1 integrase forms stable tetramers and associates with LEDGF/p75 protein in human cells. J. Biol. Chem. 2003, 78 (1), 372-81;
-
(2003)
J. Biol. Chem
, vol.78
, Issue.1
, pp. 372-381
-
-
Cherepanov, P.1
Maertens, G.2
Proost, P.3
Devreese, B.4
van Beeumen, J.5
Engelborghs, Y.6
De Clercq, E.7
Debyser8
-
68
-
-
33751242046
-
Overexpression of the lens epithelium-derived growth factor/p75 integrase binding domain hibits human immunodeficiency virus replication
-
De Rijck, J.; Vandekerckhove, L.; Gijsbers, R.; Hombrouck, A.; Hendrix, J.; Vercammen, J.; Engelborghs; Christ, F.; Debyser, Z., Overexpression of the lens epithelium-derived growth factor/p75 integrase binding domain hibits human immunodeficiency virus replication. J. Virol. 2006, 80 (23), 11498-509.
-
(2006)
J. Virol
, vol.80
, Issue.23
, pp. 11498-11509
-
-
De Rijck, J.1
Vandekerckhove, L.2
Gijsbers, R.3
Hombrouck, A.4
Hendrix, J.5
Vercammen, J.6
Engelborghs Christ, F.7
Debyser, Z.8
-
69
-
-
28444445583
-
Structural basis for the recognition between HIV-1 integrase and transcriptional coactivator p75
-
Cherepanov, P.; Ambrosio, A. L.; Rahman, S.; Ellenberger, T.; Engelman, A., Structural basis for the recognition between HIV-1 integrase and transcriptional coactivator p75. Proc. Natl. Acad. Sci. U.S.A. 2005, 102 (48), 17308-13.
-
(2005)
Proc. Natl. Acad. Sci. U.S.A
, vol.102
, Issue.48
, pp. 17308-17313
-
-
Cherepanov, P.1
Ambrosio, A.L.2
Rahman, S.3
Ellenberger, T.4
Engelman, A.5
-
70
-
-
68149149956
-
Harmacophorebased discovery of small-molecule inhibitors of protein-protein interactions between HIV-1 integrase and ellular cofactor LEDGF/p75
-
De Luca, L.; Barreca, M. L.; Ferro, S.; Christ, F.; Iraci, N.; Gitto, R.; Monforte, A. M.; Debyser, Z.; Chimirri, A., harmacophorebased discovery of small-molecule inhibitors of protein-protein interactions between HIV-1 integrase and ellular cofactor LEDGF/p75. Chem. Med. Chem., 2009, 4 (8), 1311-6.
-
(2009)
Chem. Med. Chem
, vol.4
, Issue.8
, pp. 1311-1316
-
-
De Luca, L.1
Barreca, M.L.2
Ferro, S.3
Christ, F.4
Iraci, N.5
Gitto, R.6
Monforte, A.M.7
Debyser, Z.8
Chimirri, A.9
-
71
-
-
77956943427
-
Identification of the first non-peptidic small olecule inhibitor of the c-Abl/14-3-3 protein-protein interactions able to drive sensitive and Imatinib-resistant leukemia ells to apoptosis
-
Corradi, V.; Mancini, M.; Manetti, F.; Petta, S.; Santucci, M. A.; Botta, M., Identification of the first non-peptidic small olecule inhibitor of the c-Abl/14-3-3 protein-protein interactions able to drive sensitive and Imatinib-resistant leukemia ells to apoptosis. Bioorg. Med. Chem. Lett. 2010, 20 (20), 6133-7.
-
(2010)
Bioorg. Med. Chem. Lett
, vol.20
, Issue.20
, pp. 6133-6137
-
-
Corradi, V.1
Mancini, M.2
Manetti, F.3
Petta, S.4
Santucci, M.A.5
Botta, M.6
-
72
-
-
21444436802
-
A structural basis for 14-3-3sigma functional specificity
-
Wilker, E. W.; Grant, R. A.; Artim, S. C.; Yaffe, M. B., A structural basis for 14-3-3sigma functional specificity. J. Biol. Chem. 2005, 280 (19), 18891-8.
-
(2005)
J. Biol. Chem
, vol.280
, Issue.19
, pp. 18891-18898
-
-
Wilker, E.W.1
Grant, R.A.2
Artim, S.C.3
Yaffe, M.B.4
-
73
-
-
79954452616
-
Using molecular simulations to probe pharmaceutical materials
-
Cui, Y., Using molecular simulations to probe pharmaceutical materials. J. Pharma. Sci., 2011, 100 (6), 2000-19.
-
(2011)
J. Pharma. Sci
, vol.100
, Issue.6
, pp. 2000-2019
-
-
Cui, Y.1
-
74
-
-
0035289779
-
Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings
-
Lipinski, C. A.; Lombardo, F.; Dominy, B. W.; Feeney, P. J., Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings. Adv. Drug Deliv. Rev. 2001, 46 (1-3), 3-26.
-
(2001)
Adv. Drug Deliv. Rev
, vol.46
, Issue.1-3
, pp. 3-26
-
-
Lipinski, C.A.1
Lombardo, F.2
Dominy, B.W.3
Feeney, P.J.4
-
75
-
-
79951985419
-
A new nonpeptidic inhibitor of 14-3-3 induces apoptotic cell death in chronic myeloid leukemia sensitive or resistant to imatinib
-
Mancini, M.; Corradi, V.; Petta, S.; Barbieri, E.; Manetti, F.; Botta, M.; Santucci, M. A., A new nonpeptidic inhibitor of 14-3-3 induces apoptotic cell death in chronic myeloid leukemia sensitive or resistant to imatinib. J. Pharm. Exp. Ther. 2010, 336 (3), 596-604.
-
(2010)
J. Pharm. Exp. Ther
, vol.336
, Issue.3
, pp. 596-604
-
-
Mancini, M.1
Corradi, V.2
Petta, S.3
Barbieri, E.4
Manetti, F.5
Botta, M.6
Santucci, M.A.7
-
76
-
-
77952553431
-
Rational design of small-molecule inhibitors of the LEDGF/p75-integrase interaction and HIV replication
-
Christ, F.; Voet, A.; Marchand, A.; Nicolet, S.; Desimmie, B. A.; Marchand, D.; Bardiot, D.; Van der Veken, N. J.; Van Remoortel, B.; Strelkov, S. V.; De Maeyer, M.; Chaltin, P.; Debyser, Z., Rational design of small-molecule inhibitors of the LEDGF/p75-integrase interaction and HIV replication. Nat. Chem. Biol., 2010, 6 (6), 442-448.
-
(2010)
Nat. Chem. Biol
, vol.6
, Issue.6
, pp. 442-448
-
-
Christ, F.1
Voet, A.2
Marchand, A.3
Nicolet, S.4
Desimmie, B.A.5
Marchand, D.6
Bardiot, D.7
Van der Veken, N.J.8
Van Remoortel, B.9
Strelkov, S.V.10
De Maeyer, M.11
Chaltin, P.12
Debyser, Z.13
-
77
-
-
0032544311
-
Crystal structures of the catalytic domain of HIV-1 integrase free and complexed with its metal cofactor: High level of similarity of the active site with other viral integrases
-
Maignan, S.; Guilloteau, J. P.; Zhou-Liu, Q.; Clement-Mella, C.; Mikol, V., Crystal structures of the catalytic domain of HIV-1 integrase free and complexed with its metal cofactor: high level of similarity of the active site with other viral integrases. J. Mol. Biol. 1998, 282 (2), 359-68.
-
(1998)
J. Mol. Biol
, vol.282
, Issue.2
, pp. 359-368
-
-
Maignan, S.1
Guilloteau, J.P.2
Zhou-Liu, Q.3
Clement-Mella, C.4
Mikol, V.5
-
78
-
-
0035068122
-
Identification of a small-molecule binding site at the dimer interface of the HIV integrase catalytic domain
-
Molteni, V.; Greenwald, J.; Rhodes, D.; Hwang, Y.; Kwiatkowski, W.; Bushman, F. D.; Siegel, J. S.; Choe, S., Identification of a small-molecule binding site at the dimer interface of the HIV integrase catalytic domain. Acta crystallographica. Section D, Biological crystallography 2001, 57 (Pt 4), 536-44.
-
(2001)
Acta Crystallographica. Section D, Biological Crystallography
, vol.57
, Issue.Pt 4
, pp. 536-544
-
-
Molteni, V.1
Greenwald, J.2
Rhodes, D.3
Hwang, Y.4
Kwiatkowski, W.5
Bushman, F.D.6
Siegel, J.S.7
Choe, S.8
-
79
-
-
40749129190
-
Tetrazolium-based colorimetric assay for the detection of HIV replication inhibitors: Revisited 20 years later
-
Pannecouque, C.; Daelemans, D.; De Clercq, E., Tetrazolium-based colorimetric assay for the detection of HIV replication inhibitors: revisited 20 years later. Nat. Protoc., 2008, 3 (3), 427-34.
-
(2008)
Nat. Protoc
, vol.3
, Issue.3
, pp. 427-434
-
-
Pannecouque, C.1
Daelemans, D.2
De Clercq, E.3
-
80
-
-
84878796914
-
-
K.U.Leuven K.U.Leuven enters into license agreement with Pfizer
-
K.U.Leuven K.U.Leuven enters into license agreement with Pfizer http://lrd.kuleuven.be/en/news/kuleuven-enters-into-licenseagreement-with-pfizer.
-
-
-
-
81
-
-
84877923308
-
Development of Small Molecule PUMA Inhibitors for Mitigating Radiation-Induced Cell Death
-
Mustata, G.; Li, M.; Zevola, N.; Bakan, A.; Zhang, L.; Epperly, M.; Greenberger, J. S.; Yu, J.; Bahar, I., Development of Small Molecule PUMA Inhibitors for Mitigating Radiation-Induced Cell Death. Curr. Top. Med.Chem. 2010.
-
(2010)
Curr. Top. Med.Chem
-
-
Mustata, G.1
Li, M.2
Zevola, N.3
Bakan, A.4
Zhang, L.5
Epperly, M.6
Greenberger, J.S.7
Yu, J.8
Bahar, I.9
-
82
-
-
27744547091
-
Slug antagonizes p53-mediated apoptosis of hematopoietic progenitors by repressing puma
-
Wu, W. S.; Heinrichs, S.; Xu, D.; Garrison, S. P.; Zambetti, G. P.; Adams, J. M.; Look, A. T., Slug antagonizes p53-mediated apoptosis of hematopoietic progenitors by repressing puma. Cell 2005, 123 (4), 641-53;
-
(2005)
Cell
, vol.123
, Issue.4
, pp. 641-653
-
-
Wu, W.S.1
Heinrichs, S.2
Xu, D.3
Garrison, S.P.4
Zambetti, G.P.5
Adams, J.M.6
Look, A.T.7
-
83
-
-
44349122954
-
PUMA regulates intestinal progenitor cell radiosensitivity and gastrointestinal syndrome
-
Qiu, W.; Carson-Walter, E. B.; Liu, H.; Epperly, M.; Greenberger, J. S.; Zambetti, G. P.; Zhang, L.; Yu, J., PUMA regulates intestinal progenitor cell radiosensitivity and gastrointestinal syndrome. Cell stem cell 2008, 2 (6), 576-83;
-
(2008)
Cell Stem Cell
, vol.2
, Issue.6
, pp. 576-583
-
-
Qiu, W.1
Carson-Walter, E.B.2
Liu, H.3
Epperly, M.4
Greenberger, J.S.5
Zambetti, G.P.6
Zhang, L.7
Yu, J.8
-
84
-
-
1642580868
-
Radiation, the ideal cytotoxic agent for studying the cell biology of tissues such as the small intestine
-
Potten, C. S., Radiation, the ideal cytotoxic agent for studying the cell biology of tissues such as the small intestine. Radiat. Res. 2004, 161 (2), 123-36.
-
(2004)
Radiat. Res
, vol.161
, Issue.2
, pp. 123-136
-
-
Potten, C.S.1
-
85
-
-
42949110343
-
Structural plasticity underpins promiscuous binding of the prosurvival protein A1
-
Smits, C.; Czabotar, P. E.; Hinds, M. G.; Day, C. L., Structural plasticity underpins promiscuous binding of the prosurvival protein A1. Structure 2008, 16 (5), 818-29.
-
(2008)
Structure
, vol.16
, Issue.5
, pp. 818-829
-
-
Smits, C.1
Czabotar, P.E.2
Hinds, M.G.3
Day, C.L.4
-
86
-
-
45849104776
-
Structure of the BH3 domains from the p53-inducible BH3-only proteins Noxa and Puma in complex with Mcl-1
-
Day, C. L.; Smits, C.; Fan, F. C.; Lee, E. F.; Fairlie, W. D.; Hinds, M. G., Structure of the BH3 domains from the p53-inducible BH3-only proteins Noxa and Puma in complex with Mcl-1. J. Mol. Biol. 2008, 380 (5), 958-71.
-
(2008)
J. Mol. Biol
, vol.380
, Issue.5
, pp. 958-971
-
-
Day, C.L.1
Smits, C.2
Fan, F.C.3
Lee, E.F.4
Fairlie, W.D.5
Hinds, M.G.6
-
87
-
-
13844312649
-
ZINC--a free database of commercially available compounds for virtual screening
-
Irwin, J. J.; Shoichet, B. K., ZINC--a free database of commercially available compounds for virtual screening. J. Chem. Inf. Model. 2005, 45 (1), 177-82.
-
(2005)
J. Chem. Inf. Model
, vol.45
, Issue.1
, pp. 177-182
-
-
Irwin, J.J.1
Shoichet, B.K.2
-
88
-
-
0021871375
-
A computational procedure for determining energetically favorable binding sites on biologically important macromolecules
-
Goodford, P. J., A computational procedure for determining energetically favorable binding sites on biologically important macromolecules. J. Med. Chem. 1985, 28 (7), 849-57.
-
(1985)
J. Med. Chem
, vol.28
, Issue.7
, pp. 849-857
-
-
Goodford, P.J.1
-
89
-
-
0034645763
-
Knowledge-based scoring function to predict protein-ligand interactions
-
Gohlke, H.; Hendlich, M.; Klebe, G., Knowledge-based scoring function to predict protein-ligand interactions. J. Mol. Biol. 2000, 295 (2), 337-56;
-
(2000)
J. Mol. Biol
, vol.295
, Issue.2
, pp. 337-356
-
-
Gohlke, H.1
Hendlich, M.2
Klebe, G.3
-
90
-
-
80054943835
-
DSX: A knowledgebased scoring function for the assessment of protein-ligand complexes
-
Neudert, G.; Klebe, G., DSX: a knowledgebased scoring function for the assessment of protein-ligand complexes. J. Chem. Inf. Model. 2011, 51 (10), 2731-45.
-
(2011)
J. Chem. Inf. Model
, vol.51
, Issue.10
, pp. 2731-2745
-
-
Neudert, G.1
Klebe, G.2
-
91
-
-
44049097439
-
Small molecule inhibitors targeting HIV-1 reverse transcriptase dimerization
-
Grohmann, D.; Corradi, V.; Elbasyouny, M.; Baude, A.; Horenkamp, F.; Laufer, S. D.; Manetti, F.; Botta, M.; Restle, T., Small molecule inhibitors targeting HIV-1 reverse transcriptase dimerization. Chembiochem 2008, 9 (6), 916-22.
-
(2008)
Chembiochem
, vol.9
, Issue.6
, pp. 916-922
-
-
Grohmann, D.1
Corradi, V.2
Elbasyouny, M.3
Baude, A.4
Horenkamp, F.5
Laufer, S.D.6
Manetti, F.7
Botta, M.8
Restle, T.9
-
92
-
-
57549116404
-
Targets looking for drugs: A multistep computational protocol for the development of structure-based pharmacophores and their applications for hit discovery
-
Tintori, C.; Corradi, V.; Magnani, M.; Manetti, F.; Botta, M., Targets looking for drugs: a multistep computational protocol for the development of structure-based pharmacophores and their applications for hit discovery. J. Chem Inf. Model. 2008, 48 (11), 2166-79.
-
(2008)
J. Chem Inf. Model
, vol.48
, Issue.11
, pp. 2166-2179
-
-
Tintori, C.1
Corradi, V.2
Magnani, M.3
Manetti, F.4
Botta, M.5
-
93
-
-
0442297898
-
Mouse lysozyme M is important in pulmonary host defense against Klebsiella pneumoniae infection
-
Markart, P.; Korfhagen, T. R.; Weaver, T. E.; Akinbi, H. T., Mouse lysozyme M is important in pulmonary host defense against Klebsiella pneumoniae infection. Am. J. Respir. Crit. Care Med. 2004, 169 (4), 454-8;
-
(2004)
Am. J. Respir. Crit. Care Med
, vol.169
, Issue.4
, pp. 454-458
-
-
Markart, P.1
Korfhagen, T.R.2
Weaver, T.E.3
Akinbi, H.T.4
-
94
-
-
0034669924
-
Bacterial killing is enhanced by expression of lysozyme in the lungs of transgenic mice
-
Akinbi, H. T.; Epaud, R.; Bhatt, H.; Weaver, T. E., Bacterial killing is enhanced by expression of lysozyme in the lungs of transgenic mice. J. Immunol., 2000, 165 (10), 5760-6;
-
(2000)
J. Immunol
, vol.165
, Issue.10
, pp. 5760-5766
-
-
Akinbi, H.T.1
Epaud, R.2
Bhatt, H.3
Weaver, T.E.4
-
95
-
-
27644434474
-
Decreased clearance of Pseudomonas aeruginosa from airways of mice deficient in lysozyme M
-
Cole, A. M.; Thapa, D. R.; Gabayan, V.; Liao, H. I.; Liu, L.; Ganz, T., Decreased clearance of Pseudomonas aeruginosa from airways of mice deficient in lysozyme M. J. Leukocyte Biol. 2005, 78 (5), 1081-5.
-
(2005)
J. Leukocyte Biol
, vol.78
, Issue.5
, pp. 1081-1085
-
-
Cole, A.M.1
Thapa, D.R.2
Gabayan, V.3
Liao, H.I.4
Liu, L.5
Ganz, T.6
-
96
-
-
84866907888
-
Guards of the great wall: Bacterial lysozyme inhibitors
-
Callewaert, L.; Van Herreweghe, J. M.; Vanderkelen, L.; Leysen, S.; Voet, A.; Michiels, C. W., Guards of the great wall: bacterial lysozyme inhibitors. Trends Microbiol. 2012, 20 (10), 501-10.
-
(2012)
Trends Microbiol
, vol.20
, Issue.10
, pp. 501-510
-
-
Callewaert, L.1
Van Herreweghe, J.M.2
Vanderkelen, L.3
Leysen, S.4
Voet, A.5
Michiels, C.W.6
-
97
-
-
79951946086
-
Structure based discovery of small molecule suppressors targeting bacterial lysozyme inhibitors
-
Voet, A.; Callewaert, L.; Ulens, T.; Vanderkelen, L.; Vanherreweghe, J. M.; Michiels, C. W.; De Maeyer, M., Structure based discovery of small molecule suppressors targeting bacterial lysozyme inhibitors. Biochem. Biophys. Res. Commun. 2011, 405 (4), 527-32;
-
(2011)
Biochem. Biophys. Res. Commun
, vol.405
, Issue.4
, pp. 527-532
-
-
Voet, A.1
Callewaert, L.2
Ulens, T.3
Vanderkelen, L.4
Vanherreweghe, J.M.5
Michiels, C.W.6
De Maeyer, M.7
-
98
-
-
57049089908
-
Structural basis for the recognition of lysozyme by MliC, a periplasmic lysozyme inhibitor in Gram-negative bacteria
-
Yum, S.; Kim, M. J.; Xu, Y.; Jin, X. L.; Yoo, H. Y.; Park, J. W.; Gong, J. H.; Choe, K. M.; Lee, B. L.; Ha, N. C., Structural basis for the recognition of lysozyme by MliC, a periplasmic lysozyme inhibitor in Gram-negative bacteria. Biochem. Biophys. Res. Commun. 2009, 378 (2), 244-8.
-
(2009)
Biochem. Biophys. Res. Commun
, vol.378
, Issue.2
, pp. 244-248
-
-
Yum, S.1
Kim, M.J.2
Xu, Y.3
Jin, X.L.4
Yoo, H.Y.5
Park, J.W.6
Gong, J.H.7
Choe, K.M.8
Lee, B.L.9
Ha, N.C.10
-
99
-
-
0032466648
-
Continuum solvent studies of the stability of RNA hairpin loops and helices
-
Srinivasan, J.; Miller, J.; Kollman, P. A.; Case, D. A., Continuum solvent studies of the stability of RNA hairpin loops and helices. J. Biomol. Struct. Dyn. 1998, 16 (3), 671-82;
-
(1998)
J. Biomol. Struct. Dyn
, vol.16
, Issue.3
, pp. 671-682
-
-
Srinivasan, J.1
Miller, J.2
Kollman, P.A.3
Case, D.A.4
-
100
-
-
0034521981
-
Calculating structures and free energies of complex molecules: Combining molecular mechanics and continuum models
-
Kollman, P. A.; Massova, I.; Reyes, C.; Kuhn, B.; Huo, S.; Chong, L.; Lee, M.; Lee, T.; Duan, Y.; Wang, W.; Donini, O.; Cieplak, P.; Srinivasan, J.; Case, D. A.; Cheatham, T. E., III, Calculating structures and free energies of complex molecules: combining molecular mechanics and continuum models. Acc. Chem. Res. 2000, 33 (12), 889-97.
-
(2000)
Acc. Chem. Res
, vol.33
, Issue.12
, pp. 889-897
-
-
Kollman, P.A.1
Massova, I.2
Reyes, C.3
Kuhn, B.4
Huo, S.5
Chong, L.6
Lee, M.7
Lee, T.8
Duan, Y.9
Wang, W.10
Donini, O.11
Cieplak, P.12
Srinivasan, J.13
Case, D.A.14
Cheatham III, T.E.15
|