|
78
|
288
|
2z7rA |
Crystal structure of the n-terminal kinase domain of human rsk1 bound to staurosporine |
|
76
|
269
|
2ywpA |
Crystal structure of chk1 with a urea inhibitor |
|
85
|
306
|
2zm3A |
Complex structure of insulin-like growth factor receptor and isoquinolinedione inhibitor |
|
90
|
227
|
2zfyA |
Crystal structure of human otubain 1 |
|
73
|
285
|
2z7qA |
Crystal structure of the n-terminal kinase domain of human rsk-1 bound to amp-pcp |
|
77
|
239
|
2yzlA |
Crystal structure of phosphoribosylaminoimidazole-succinocarboxamide synthase with adp from methanocaldococcus jannaschii |
|
113
|
349
|
2zb1A |
Crystal structure of p38 in complex with biphenyl amide inhibitor |
|
71
|
280
|
2zmdA |
Crystal structure of human mps1 catalytic domain t686a mutant in complex with sp600125 inhibitor |
|
107
|
356
|
2zdtA |
Crystal structure of human jnk3 complexed with an isoquinolone inhibitor |
|
75
|
300
|
2z8cA |
Phosphorylated insulin receptor tyrosine kinase in complex with (4-{[5-carbamoyl-4-(3-methylanilino)pyrimidin-2-yl]amino}phenyl)acetic acid |
|
88
|
284
|
2z60A |
Crystal structure of the t315i mutant of abl kinase bound with ppy-a |
|
82
|
237
|
2ywvA |
Crystal structure of saicar synthetase from geobacillus kaustophilus |
|
80
|
271
|
2zm4A |
Crystal structure of imidazo quinoxaline 1 bound to the kinase domain of human lck, activated form (auto-phosphorylated on tyr394) |
|
111
|
349
|
2zb0A |
Crystal structure of p38 in complex with biphenyl amide inhibitor |
|
74
|
285
|
2z7sA |
Crystal structure of the n-terminal kinase domain of human rsk1 bound to purvalnol a |
|
69
|
279
|
2zmcA |
Crystal structure of human mitotic checkpoint kinase mps1 catalytic domain apo form |
|
103
|
355
|
2zduA |
Crystal structure of human jnk3 complexed with an isoquinolone inhibitor |
|
74
|
281
|
2z2wA |
Human wee1 kinase complexed with inhibitor pf0335770 |
|
107
|
349
|
2zazA |
Crystal structure of p38 in complex with 4-anilino quinoline inhibitor |
|
107
|
332
|
2zjwA |
Crystal structure of human ck2 alpha complexed with ellagic acid |
|
103
|
340
|
2z7lA |
Unphosphorylated mitogen activated protein kinase erk2 in complex with (4-{[5-carbamoyl-4-(3-methylanilino)pyrimidin 2-yl]amino}phenyl)acetic acid |
|
75
|
269
|
2yzaA |
Crystal structure of kinase domain of human 5'-amp-activated protein kinase alpha-2 subunit mutant (t172d) |
|
88
|
271
|
2zm1A |
Crystal structure of imidazo pyrazin 1 bound to the kinase domain of human lck, (auto-phosphorylated on tyr394) |
|
81
|
242
|
2z02A |
Crystal structure of phosphoribosylaminoimidazolesuccinocarboxamide synthase wit atp from methanocaldococcus jannaschii |
|
89
|
300
|
2ycrA |
Crystal structure of checkpoint kinase 2 in complex with inhibitor pv976 |
|
91
|
300
|
2ycqA |
Crystal structure of checkpoint kinase 2 in complex with inhibitor pv1115 |
|
78
|
267
|
2ym4A |
Crystal structure of checkpoint kinase 1 (chk1) in complex with inhibitors |
|
105
|
348
|
2yiwA |
Triazolopyridine inhibitors of p38 kinase |
|
80
|
262
|
2ydjA |
Discovery of checkpoint kinase inhibitor azd7762 by structure based design and optimization of thiophene carboxamide ureas |
|
80
|
264
|
2ym6A |
Crystal structure of checkpoint kinase 1 (chk1) in complex with inhibitors |
|
95
|
308
|
2yjsA |
Structure of c1156y mutant anaplastic lymphoma kinase |
|
86
|
268
|
2yerA |
Synthesis and evaluation of triazolones as checkpoint kinase 1 inhibitors |
|
82
|
263
|
2ym8A |
Crystal structure of checkpoint kinase 1 (chk1) in complex with inhibitors |
|
97
|
308
|
2yhvA |
Structure of l1196m mutant anaplastic lymphoma kinase |
|
83
|
268
|
2ydkA |
Discovery of checkpoint kinase inhibitor azd7762 by structure based design and optimization of thiophene carboxamide ureas |
|
113
|
351
|
2yixA |
Triazolopyridine inhibitors of p38 |
|
97
|
308
|
2yfxA |
Structure of l1196m mutant anaplastic lymphoma kinase in complex with crizotinib |
|
81
|
263
|
2ym3A |
Crystal structure of checkpoint kinase 1 (chk1) in complex with inhibitors |
|
94
|
300
|
2yirA |
Structural analysis of checkpoint kinase 2 in complex with inhibitor pv1352 |
|
89
|
300
|
2yiqA |
Structural analysis of checkpoint kinase 2 in complex with inhibitor pv1322 |
|
90
|
269
|
2yexA |
Synthesis and evaluation of triazolones as checkpoint kinase 1 inhibitors |
|
88
|
300
|
2yitA |
Structural analysis of checkpoint kinase 2 in complex with pv1162, a novel inhibitor |
|
92
|
301
|
2ycfA |
Crystal structure of checkpoint kinase 2 in complex with inhibitor pv1531 |
|
81
|
281
|
2yn8A |
Ephb4 kinase domain inhibitor complex |
|
94
|
301
|
2yjrA |
Structure of f1174l mutant anaplastic lymphoma kinase |
|
90
|
301
|
2ycsA |
Crystal structure of checkpoint kinase 2 in complex with pv788 |
|
75
|
263
|
2ym5A |
Crystal structure of checkpoint kinase 1 (chk1) in complex with inhibitors |
|
108
|
348
|
2yisA |
Triazolopyridine inhibitors of p38 kinase. |
|
83
|
279
|
2ydiA |
Discovery of checkpoint kinase inhibitor azd7762 by structure based design and optimization of thiophene carboxamide ureas |
|
79
|
265
|
2ym7A |
Crystal structure of checkpoint kinase 1 (chk1) in complex with inhibitors |
