|
89
|
305
|
5hvjA |
Crystal structure of limk1 d460n mutant in complex with amp-pnp |
|
70
|
268
|
5hi2A |
Braf kinase domain b3ac loop deletion mutant in complex with sorafenib |
|
79
|
283
|
5hkmA |
Discovery of novel 7-azaindoles as pdk1 inhibitors |
|
265
|
948
|
5g2nA |
X-ray structure of pi3kinase gamma in complex with copanlisib |
|
83
|
288
|
5ho8A |
Discovery of novel 7-azaindoles as pdk1 inhibitors |
|
89
|
292
|
4zy6A |
Crystal structure of p21-activated kinase 1 in complex with an inhibitor compound 29 |
|
99
|
347
|
5hlpA |
X-ray crystal structure of gsk3b in complex with brd3937 |
|
105
|
251
|
4zdrA |
Crystal structure of 14-3-3[zeta]-lkb1 fusion protein |
|
113
|
331
|
5h8bA |
Crystal structure of ck2 with compound 2 |
|
257
|
951
|
5g55A |
3-quinoline carboxamides inhibitors of pi3k |
|
105
|
326
|
5h8gA |
Crystal structure of ck2 with compound 7b |
|
86
|
297
|
5ikwA |
Crystal structure of bmp-2-inducible kinase in complex with an indazole inhibitor |
|
115
|
331
|
5h8eA |
Crystal structure of ck2 with compound 7h |
|
78
|
269
|
5hidA |
Braf kinase domain b3ac loop deletion mutant in complex with az628 |
|
86
|
302
|
5i3oA |
Crystal structure of bmp-2-inducible kinase in complex with an indazole inhibitor |
|
81
|
289
|
5hngA |
Discovery of novel 7-azaindoles as pdk1 inhibitors |
|
114
|
403
|
5hgiA |
Crystal structure of apo human ire1 alpha |
|
0
|
14
|
5hgvB |
Structure of an o-glcnac transferase point mutant, d554n in complex with peptide |
|
103
|
296
|
4yp8A |
Irak4-inhibitor co-structure |
|
172
|
598
|
5gqrB |
Crystal structure of pxy-cle41-serk2 |
|
86
|
296
|
5ax9A |
Crystal structure of the kinase domain of human traf2 and nck-interacting protein kinase in complex with compund 9 |
|
172
|
607
|
5gijB |
Crystal structure of tdr-tdif complex |
|
0
|
10
|
5g04S |
Structure of the human apc-cdc20-hsl1 complex |
|
35
|
93
|
5gpgB |
Co-crystal structure of the fk506 binding domain of human fkbp25, rapamycin and the frb domain of human mtor |
|
198
|
599
|
5gr9B |
Crystal structure of pxy-tdif/cle41 |
|
52
|
185
|
5gqrK |
Crystal structure of pxy-cle41-serk2 |
|
86
|
265
|
5g15A |
Structure aurora a (122-403) bound to activating monobody mb1 and amppcp |
|
112
|
329
|
5b0xA |
Crystal structure of the ck2a/benzoic acid derivative complex |
|
87
|
263
|
5g1xA |
Crystal structure of aurora-a kinase in complex with n-myc |
|
298
|
945
|
5dxtA |
P110alpha with gdc-0326 |
|
90
|
276
|
5av1A |
Crystal structure of dapk1 in the presence of bromide ions. |
|
98
|
348
|
5f95A |
Crystal structure of gsk3b in complex with compound 18: 2-[(cyclopropylcarbonyl)amino]-n-(4-phenylpyridin-3-yl)pyridine-4-carboxamide |
|
86
|
268
|
5eykA |
Crystal structure of aurora b in complex with bi 847325 |
|
79
|
273
|
5fd2A |
B-raf wild-type kinase domain in complex with a purinylpyridinylamino-based inhibitor |
|
90
|
276
|
5auxA |
Crystal structure of dapk1 in complex with kaempferol. |
|
75
|
262
|
4ztsA |
Human aurora a catalytic domain bound to fk1142 |
|
89
|
276
|
5auzA |
Crystal structure of dapk1 in complex with genistein. |
|
75
|
262
|
4ztqA |
Human aurora a catalytic domain bound to fk932 |
|
94
|
295
|
4ztlA |
Irak4-inhibitor co-structure |
|
89
|
276
|
5av2A |
Crystal structure of dapk1-kaempferol complex in the presence of bromide ions. |
|
91
|
276
|
5auwA |
Crystal structure of dapk1 in complex with quercetin. |
|
98
|
297
|
4ztnA |
Irak4-inhibitor co-structure |
|
97
|
346
|
5f94A |
Crystal structure of gsk3b in complex with compound 15: 2-[(cyclopropylcarbonyl)amino]-n-(4-methoxypyridin-3-yl)pyridine-4-carboxamide |
|
26
|
55
|
5f5pC |
Molecular basis for shroom2 recognition by rock1 |
|
87
|
276
|
5auyA |
Crystal structure of dapk1 in complex with morin. |
|
119
|
538
|
5ezvA |
X-ray crystal structure of amp-activated protein kinase alpha-2/alpha-1 rim chimaera (alpha-2(1-347)/alpha-1(349-401)/alpha-2(397-end) beta-1 gamma-1) co-crystallized with c2 (5-(5-hydroxyl-isoxazol-3-yl)-furan-2-phosphonic acid) |
|
93
|
294
|
5fqdC |
Structural basis of lenalidomide induced ck1a degradation by the crl4crbn ubiquitin ligase |
|
92
|
276
|
5auvA |
Crystal structure of dapk1 in complex with apigenin. |
|
70
|
262
|
4ztrA |
Human aurora a catalytic domain bound to fk1141 |
|
92
|
276
|
5av3A |
Crystal structure of dapk1-kaempferol complex in the presence of iodide ions. |
