|
91
|
308
|
7khjA |
Crystal structure of kit kinase domain with a small molecule inhibitor, plx8512 in the dfg-in state |
|
88
|
308
|
7khkA |
Crystal structure of kit kinase domain with a small molecule inhibitor, plx9486 (bezuclastinib) in the dfg-in state |
|
104
|
327
|
7khgA |
Crystal structure of kit kinase domain with a small molecule inhibitor, plx3397 |
|
84
|
372
|
7n7mA |
Crystal structure of pi5p4kiialpha complex with bi-2536 |
|
85
|
372
|
7n7nA |
Crystal structure of pi5p4kiialpha complex with volasertib |
|
85
|
372
|
7n7kA |
Crystal structure of pi5p4kiialpha complex with amppnp |
|
87
|
372
|
7n7jA |
Crystal structure of pi5p4kiialpha complex with amppnp |
|
85
|
372
|
7n7lA |
Crystal structure of pi5p4kiialpha complex with bi-d1870 |
|
83
|
372
|
7n7oA |
Crystal structure of pi5p4kiialpha complex with palbociclib |
|
90
|
308
|
6xl4A |
Egfr(t790m/v948r) in complex with azd9291 and ddc4002 |
|
83
|
268
|
7mckA |
Structure of chk1 10-pt. mutant complex with lrrk2 inhibitor 18 |
|
115
|
400
|
6x10A |
Crystal structure of acetyltransferase eis from mycobacterium tuberculosis in complex with haloperidol |
|
114
|
400
|
6x6iAAA |
Crystal structure of acetyltransferase eis from mycobacterium tuberculosis in complex with inhibitor sgt543 |
|
116
|
400
|
6x6gAAA |
Crystal structure of acetyltransferase eis from mycobacterium tuberculosis in complex with droperidol |
|
106
|
400
|
6x6yAAA |
Crystal structure of acetyltransferase eis from mycobacterium tuberculosis in complex with inhibitor sgt1264 |
|
111
|
399
|
6x7aAAA |
Crystal structure of acetyltransferase eis from mycobacterium tuberculosis in complex with inhibitor sgt572 |
|
81
|
274
|
7k0vA |
Crystal structure of braf in complex with inhibitor gne-0749 |
|
86
|
272
|
6xloA |
Crystal structure of braf in complex with inhibitor |
|
92
|
316
|
6wxnA |
Egfr(t790m/v948r) in complex with ln3844 |
|
1
|
45
|
7ce4B |
Tankyrase2 catalytic domain in complex with k-476 |
|
47
|
162
|
7ce4A |
Tankyrase2 catalytic domain in complex with k-476 |
|
212
|
625
|
7kicA |
Prmt5:mep50 complexed with 5,5-bicyclic inhibitor compound 34 |
|
209
|
625
|
7kibA |
Prmt5:mep50 complexed with 5,5-bicyclic inhibitor compound 4 |
|
202
|
625
|
7kidA |
Prmt5:mep50 complexed with 5,5-bicyclic inhibitor compound 72 |
|
127
|
407
|
6xdfA |
Crystal structure of ire1a in complex with g-4100 |
|
74
|
311
|
7kidB |
Prmt5:mep50 complexed with 5,5-bicyclic inhibitor compound 72 |
|
132
|
404
|
6xdbA |
Crystal structure of ire1a in complex with g-6904 |
|
81
|
311
|
7kicB |
Prmt5:mep50 complexed with 5,5-bicyclic inhibitor compound 34 |
|
77
|
310
|
7kibB |
Prmt5:mep50 complexed with 5,5-bicyclic inhibitor compound 4 |
|
78
|
221
|
7k3dA |
The structure of ntmt1 in complex with compound dc1-13 |
|
47
|
152
|
6wc8A |
Hiv integrase core domain in complex with inhibitor 2-(5-(3-fluorophenyl)-2-(2-(thiophen-2-yl)ethynyl)-1- benzofuran-3-yl)ethanoic acid |
|
89
|
289
|
7m0kA |
Hpk1 in complex with compound 1 |
|
41
|
150
|
6we7A |
Hiv integrase core domain in complex with inhibitor 3-methyl-2-{5-methyl-2-[2-(thiophen-2-yl)ethynyl]-1- benzofuran-3-yl}butanoic acid |
|
96
|
293
|
7m0mA |
Hpk1 in complex with compound 1 |
|
52
|
189
|
6we3A |
Human parp14 (artd8), catalytic fragment in complex with compound 3 |
|
49
|
186
|
6we4A |
Human parp14 (artd8), catalytic fragment in complex with compound 2 |
|
90
|
288
|
7botA |
Human sirt2 in complex with myristoyl thiourea inhibitor, no.23 |
|
95
|
288
|
7bosA |
Human sirt2 in complex with myristoyl thiourea inhibitor, no.13 |
|
255
|
944
|
7jx0A |
Nvs-pi3-4 bound to the pi3kg catalytic subunit p110 gamma |
|
269
|
947
|
7jwzA |
Ipi-549 bound to the pi3kg catalytic subunit p110 gamma |
|
105
|
343
|
7ljeA |
Discovery of spirohydantoins as selective, orally bioavailable inhibitors of p300/cbp histone acetyltransferases |
|
41
|
150
|
6w42A |
Hiv integrase core domain in complex with inhibitor 2-(5-methyl-2-(2-(thiophen-2-yl)ethynyl)-1-benzofuran-3-yl)acetic acid |
|
91
|
288
|
7l25A |
Hpk1 in complex with compound 18 |
|
42
|
148
|
6w0uA |
Hiv integrase core domain in complex with inhibitor 2-(2-ethynyl-5-methyl-1-benzofuran-3-yl)acetic acid |
|
106
|
322
|
6vxuA |
Structure of human vaccinia-related kinase 1 (vrk1) bound to ach471 |
|
41
|
151
|
6vx2A |
Hiv integrase core domain in complex with inhibitor (5-methyl-1-benzofuran-3-yl)acetic acid |
|
89
|
326
|
6wadA |
Crystal structure of human protein arginine n-methyltransferase 6 (prmt6) in complex with mt2739 inhibitor |
|
92
|
296
|
6lxyA |
Irak4 in complex with inhibitor |
|
228
|
592
|
7k41A |
Bacterial o-glcnacase (oga) with compound |
|
462
|
1454
|
6w2jA |
Cps1 bound to allosteric inhibitor h3b-374 |
