-
1
-
-
80051966197
-
Structural conservation of druggable hot spots in protein-protein interfaces
-
D. Kozakov Structural conservation of druggable hot spots in protein-protein interfaces Proc. Natl. Acad. Sci. U. S. A. 108 2011 13528 13533
-
(2011)
Proc. Natl. Acad. Sci. U. S. A.
, vol.108
, pp. 13528-13533
-
-
Kozakov, D.1
-
2
-
-
47349109056
-
Drug-like inhibitors of protein-protein interactions: A structural examination of effective protein mimicry
-
D.C. Fry Drug-like inhibitors of protein-protein interactions: a structural examination of effective protein mimicry Curr. Protein Pept. Sci. 9 2008 240 247
-
(2008)
Curr. Protein Pept. Sci.
, vol.9
, pp. 240-247
-
-
Fry, D.C.1
-
3
-
-
84862903158
-
Hydrogen-bonded synthetic mimics of protein secondary structure as disruptors of protein-protein interactions
-
M.J. Adler Hydrogen-bonded synthetic mimics of protein secondary structure as disruptors of protein-protein interactions Curr. Top. Microbiol. Immunol. 348 2011 1 23
-
(2011)
Curr. Top. Microbiol. Immunol.
, vol.348
, pp. 1-23
-
-
Adler, M.J.1
-
4
-
-
46449115901
-
The exploration of macrocycles for drug discovery - An underexploited structural class
-
E.M. Driggers The exploration of macrocycles for drug discovery - an underexploited structural class Nat. Rev. Drug Discov. 7 2008 608 624
-
(2008)
Nat. Rev. Drug Discov.
, vol.7
, pp. 608-624
-
-
Driggers, E.M.1
-
5
-
-
84860511479
-
Experiences in fragment-based drug discovery
-
C.W. Murray Experiences in fragment-based drug discovery Trends Pharmacol. Sci. 33 2012 224 232
-
(2012)
Trends Pharmacol. Sci.
, vol.33
, pp. 224-232
-
-
Murray, C.W.1
-
6
-
-
77955982439
-
Structural biology in fragment-based drug design
-
C.W. Murray, and T.L. Blundell Structural biology in fragment-based drug design Curr. Opin. Struct. Biol. 20 2010 497 507
-
(2010)
Curr. Opin. Struct. Biol.
, vol.20
, pp. 497-507
-
-
Murray, C.W.1
Blundell, T.L.2
-
7
-
-
33847381100
-
A decade of fragment-based drug design: Strategic advances and lessons learned
-
P.J. Hajduk, and J. Greer A decade of fragment-based drug design: strategic advances and lessons learned Nat. Rev. Drug Discov. 6 2007 211 219
-
(2007)
Nat. Rev. Drug Discov.
, vol.6
, pp. 211-219
-
-
Hajduk, P.J.1
Greer, J.2
-
8
-
-
33751204422
-
Fragment-based lead discovery: A chemical update
-
D.A. Erlanson Fragment-based lead discovery: a chemical update Curr. Opin. Biotechnol. 17 2006 643 652
-
(2006)
Curr. Opin. Biotechnol.
, vol.17
, pp. 643-652
-
-
Erlanson, D.A.1
-
9
-
-
35348922285
-
Fragment-based screening using X-ray crystallography and NMR spectroscopy
-
H. Jhoti Fragment-based screening using X-ray crystallography and NMR spectroscopy Curr. Opin. Chem. Biol. 11 2007 485 493
-
(2007)
Curr. Opin. Chem. Biol.
, vol.11
, pp. 485-493
-
-
Jhoti, H.1
-
10
-
-
0034618541
-
Privileged molecules for protein binding identified from NMR-based screening
-
P.J. Hajduk Privileged molecules for protein binding identified from NMR-based screening J. Med. Chem. 43 2000 3443 3447
-
(2000)
J. Med. Chem.
, vol.43
, pp. 3443-3447
-
-
Hajduk, P.J.1
-
11
-
-
79952429629
-
Experiences in fragment-based lead discovery
-
R.E. Hubbard, and J.B. Murray Experiences in fragment-based lead discovery Methods Enzymol. 493 2011 509 531
-
(2011)
Methods Enzymol.
, vol.493
, pp. 509-531
-
-
Hubbard, R.E.1
Murray, J.B.2
-
12
-
-
33750470057
-
Chemical screening methods to identify ligands that promote protein stability, protein crystallization, and structure determination
-
M. Vedadi Chemical screening methods to identify ligands that promote protein stability, protein crystallization, and structure determination Proc. Natl. Acad. Sci. U. S. A. 103 2006 15835 15840
-
(2006)
Proc. Natl. Acad. Sci. U. S. A.
, vol.103
, pp. 15835-15840
-
-
Vedadi, M.1
-
13
-
-
44949211332
-
Fragment-based activity space: Smaller is better
-
T. Hesterkamp, and M. Whittaker Fragment-based activity space: smaller is better Curr. Opin. Chem. Biol. 12 2008 260 268
-
(2008)
Curr. Opin. Chem. Biol.
, vol.12
, pp. 260-268
-
-
Hesterkamp, T.1
Whittaker, M.2
-
14
-
-
79952383501
-
From experimental design to validated hits a comprehensive walk-through of fragment lead identification using surface plasmon resonance
-
A.M. Giannetti From experimental design to validated hits a comprehensive walk-through of fragment lead identification using surface plasmon resonance Methods Enzymol. 493 2011 169 218
-
(2011)
Methods Enzymol.
, vol.493
, pp. 169-218
-
-
Giannetti, A.M.1
-
15
-
-
79952374737
-
Using computational techniques in fragment-based drug discovery
-
R.L. Desjarlais Using computational techniques in fragment-based drug discovery Methods Enzymol. 493 2011 137 155
-
(2011)
Methods Enzymol.
, vol.493
, pp. 137-155
-
-
Desjarlais, R.L.1
-
16
-
-
0038010557
-
Discovery and characterization of cooperative ligand binding in the adaptive region of interleukin-2
-
J. Hyde Discovery and characterization of cooperative ligand binding in the adaptive region of interleukin-2 Biochemistry 42 2003 6475 6483
-
(2003)
Biochemistry
, vol.42
, pp. 6475-6483
-
-
Hyde, J.1
-
17
-
-
79955556517
-
Discovery of a potent and highly selective PDK1 inhibitor via fragment-based drug discovery
-
D.A. Erlanson Discovery of a potent and highly selective PDK1 inhibitor via fragment-based drug discovery Bioorg. Med. Chem. Lett. 21 2011 3078 3083
-
(2011)
Bioorg. Med. Chem. Lett.
, vol.21
, pp. 3078-3083
-
-
Erlanson, D.A.1
-
18
-
-
4344654060
-
Discovery of an allosteric site in the caspases
-
J.A. Hardy Discovery of an allosteric site in the caspases Proc. Natl. Acad. Sci. U. S. A. 101 2004 12461 12466
-
(2004)
Proc. Natl. Acad. Sci. U. S. A.
, vol.101
, pp. 12461-12466
-
-
Hardy, J.A.1
-
19
-
-
0038274086
-
Discovery of a new phosphotyrosine mimetic for PTP1B using breakaway tethering
-
D.A. Erlanson Discovery of a new phosphotyrosine mimetic for PTP1B using breakaway tethering J. Am. Chem. Soc. 125 2003 5602 5603
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 5602-5603
-
-
Erlanson, D.A.1
-
20
-
-
0141726877
-
A 'rule of three' for fragment-based lead discovery?
-
M. Congreve A 'rule of three' for fragment-based lead discovery? Drug Discov. Today 8 2003 876 877
-
(2003)
Drug Discov. Today
, vol.8
, pp. 876-877
-
-
Congreve, M.1
-
21
-
-
79955843618
-
Simple one-pot synthesis of disulfide fragments for use in disulfide-exchange screening
-
M.A. Burlingame Simple one-pot synthesis of disulfide fragments for use in disulfide-exchange screening ACS Comb. Sci. 13 2011 205 208
-
(2011)
ACS Comb. Sci.
, vol.13
, pp. 205-208
-
-
Burlingame, M.A.1
-
22
-
-
2542643984
-
Integrating fragment assembly and biophysical methods in the chemical advancement of small-molecule antagonists of IL-2: An approach for inhibiting protein-protein interactions
-
B.C. Raimundo Integrating fragment assembly and biophysical methods in the chemical advancement of small-molecule antagonists of IL-2: an approach for inhibiting protein-protein interactions J. Med. Chem. 47 2004 3111 3130
-
(2004)
J. Med. Chem.
, vol.47
, pp. 3111-3130
-
-
Raimundo, B.C.1
-
23
-
-
0037414274
-
Discovery of a potent small molecule IL-2 inhibitor through fragment assembly
-
A.C. Braisted Discovery of a potent small molecule IL-2 inhibitor through fragment assembly J. Am. Chem. Soc. 125 2003 3714 3715
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 3714-3715
-
-
Braisted, A.C.1
-
24
-
-
79955038588
-
Turning a protein kinase on or off from a single allosteric site via disulfide trapping
-
J.D. Sadowsky Turning a protein kinase on or off from a single allosteric site via disulfide trapping Proc. Natl. Acad. Sci. U. S. A. 108 2011 6056 6061
-
(2011)
Proc. Natl. Acad. Sci. U. S. A.
, vol.108
, pp. 6056-6061
-
-
Sadowsky, J.D.1
-
25
-
-
0037452709
-
Binding of small molecules to an adaptive protein-protein interface
-
M.R. Arkin Binding of small molecules to an adaptive protein-protein interface Proc. Natl. Acad. Sci. U. S. A. 100 2003 1603 1608
-
(2003)
Proc. Natl. Acad. Sci. U. S. A.
, vol.100
, pp. 1603-1608
-
-
Arkin, M.R.1
-
26
-
-
84862868473
-
Small-molecule inhibitors of IL-2/IL-2R: Lessons learned and applied
-
C.G. Wilson, and M.R. Arkin Small-molecule inhibitors of IL-2/IL-2R: lessons learned and applied Curr. Top. Microbiol. Immunol. 348 2011 25 59
-
(2011)
Curr. Top. Microbiol. Immunol.
, vol.348
, pp. 25-59
-
-
Wilson, C.G.1
Arkin, M.R.2
-
27
-
-
37249004920
-
Reaching for high-hanging fruit in drug discovery at protein-protein interfaces
-
J.A. Wells, and C.L. McClendon Reaching for high-hanging fruit in drug discovery at protein-protein interfaces Nature 450 2007 1001 1009
-
(2007)
Nature
, vol.450
, pp. 1001-1009
-
-
Wells, J.A.1
McClendon, C.L.2
-
28
-
-
77953094954
-
Role of interleukin-2 in patients with HIV infection
-
S.L. Pett Role of interleukin-2 in patients with HIV infection Drugs 70 2010 1115 1130
-
(2010)
Drugs
, vol.70
, pp. 1115-1130
-
-
Pett, S.L.1
-
29
-
-
77955530237
-
Anti-interleukin-2 receptor antibodies-basiliximab and daclizumab-for the prevention of acute rejection in renal transplantation
-
J. Sageshima Anti-interleukin-2 receptor antibodies-basiliximab and daclizumab-for the prevention of acute rejection in renal transplantation Biologics 3 2009 319 336
-
(2009)
Biologics
, vol.3
, pp. 319-336
-
-
Sageshima, J.1
-
30
-
-
77954383661
-
T regulatory cells and transplantation tolerance
-
V.S. Gorantla T regulatory cells and transplantation tolerance Transpl. Rev. (Orlando) 24 2010 147 159
-
(2010)
Transpl. Rev. (Orlando)
, vol.24
, pp. 147-159
-
-
Gorantla, V.S.1
-
31
-
-
0030753124
-
Identification of a small molecule inhibitor of the IL-2/IL-2Ralpha receptor interaction which binds to IL-2
-
J.W. Tilley Identification of a small molecule inhibitor of the IL-2/IL-2Ralpha receptor interaction which binds to IL-2 J. Am. Chem. Soc. 119 1997 7589 7590
-
(1997)
J. Am. Chem. Soc.
, vol.119
, pp. 7589-7590
-
-
Tilley, J.W.1
-
32
-
-
16244416531
-
Identification of nonpeptidic small-molecule inhibitors of interleukin-2
-
N.D. Waal Identification of nonpeptidic small-molecule inhibitors of interleukin-2 Bioorg. Med. Chem. Lett. 15 2005 983 987
-
(2005)
Bioorg. Med. Chem. Lett.
, vol.15
, pp. 983-987
-
-
Waal, N.D.1
-
33
-
-
84866388293
-
Druggability of dynamic protein-protein interfaces
-
O. Ulucan Druggability of dynamic protein-protein interfaces Curr. Pharm. Des. 2012
-
(2012)
Curr. Pharm. Des.
-
-
Ulucan, O.1
-
34
-
-
34547583152
-
Transient pockets on protein surfaces involved in protein-protein interaction
-
S. Eyrisch, and V. Helms Transient pockets on protein surfaces involved in protein-protein interaction J. Med. Chem. 50 2007 3457 3464
-
(2007)
J. Med. Chem.
, vol.50
, pp. 3457-3464
-
-
Eyrisch, S.1
Helms, V.2
-
35
-
-
73349111643
-
Quantifying correlations between allosteric sites in thermodynamic ensembles
-
C.L. McClendon Quantifying correlations between allosteric sites in thermodynamic ensembles J. Chem. Theory Comput. 5 2009 2486 2502
-
(2009)
J. Chem. Theory Comput.
, vol.5
, pp. 2486-2502
-
-
McClendon, C.L.1
-
36
-
-
33750303565
-
Hot-spot mimicry of a cytokine receptor by a small molecule
-
C.D. Thanos Hot-spot mimicry of a cytokine receptor by a small molecule Proc. Natl. Acad. Sci. U. S. A. 103 2006 15422 15427
-
(2006)
Proc. Natl. Acad. Sci. U. S. A.
, vol.103
, pp. 15422-15427
-
-
Thanos, C.D.1
-
37
-
-
67649841614
-
The road less traveled: Modulating signal transduction enzymes by inhibiting their protein-protein interactions
-
M.R. Arkin, and A. Whitty The road less traveled: modulating signal transduction enzymes by inhibiting their protein-protein interactions Curr. Opin. Chem. Biol. 13 2009 284 290
-
(2009)
Curr. Opin. Chem. Biol.
, vol.13
, pp. 284-290
-
-
Arkin, M.R.1
Whitty, A.2
-
38
-
-
3042689209
-
Structural basis for the selective inhibition of JNK1 by the scaffolding protein JIP1 and SP600125
-
Y.S. Heo Structural basis for the selective inhibition of JNK1 by the scaffolding protein JIP1 and SP600125 EMBO J. 23 2004 2185 2195
-
(2004)
EMBO J.
, vol.23
, pp. 2185-2195
-
-
Heo, Y.S.1
-
39
-
-
1542286168
-
Phosphoinositide-dependent protein kinase 1, a sensor of protein conformation
-
R.M. Biondi Phosphoinositide-dependent protein kinase 1, a sensor of protein conformation Trends Biochem. Sci. 29 2004 136 142
-
(2004)
Trends Biochem. Sci.
, vol.29
, pp. 136-142
-
-
Biondi, R.M.1
-
40
-
-
34247368172
-
Lining the pockets of kinases and phosphatases
-
G. Gold Lining the pockets of kinases and phosphatases Curr. Opin. Struct. Biol. 16 2006 693 701
-
(2006)
Curr. Opin. Struct. Biol.
, vol.16
, pp. 693-701
-
-
Gold, G.1
-
41
-
-
58849093668
-
Identification of allosteric PIF-pocket ligands for PDK1 using NMR-based fragment screening and 1H-15N TROSY experiments
-
B.J. Stockman Identification of allosteric PIF-pocket ligands for PDK1 using NMR-based fragment screening and 1H-15N TROSY experiments Chem. Biol. Drug Des. 73 2009 179 188
-
(2009)
Chem. Biol. Drug Des.
, vol.73
, pp. 179-188
-
-
Stockman, B.J.1
-
42
-
-
33751583820
-
Allosteric activation of the protein kinase PDK1 with low molecular weight compounds
-
M. Engel Allosteric activation of the protein kinase PDK1 with low molecular weight compounds EMBO J 25 2006 5469 5480
-
(2006)
EMBO J
, vol.25
, pp. 5469-5480
-
-
Engel, M.1
|