|
96
|
294
|
2x4fA |
The crystal structure of the human myosin light chain kinase loc340156. |
|
67
|
262
|
2x8eA |
Discovery of a novel class of triazolones as checkpoint kinase inhibitors - hit to lead exploration |
|
85
|
279
|
2x8dA |
Discovery of a novel class of triazolones as checkpoint kinase inhibitors - hit to lead exploration |
|
96
|
291
|
2x4zA |
Crystal structure of the human p21-activated kinase 4 in complex with pf-03758309 |
|
71
|
263
|
2x6eA |
Aurora-a bound to an inhibitor |
|
73
|
263
|
2x6dA |
Aurora-a bound to an inhibitor |
|
82
|
268
|
2x8iA |
Discovery of a novel class of triazolones as checkpoint kinase inhibitors - hit to lead exploration |
|
96
|
315
|
2wzjA |
Catalytic and uba domain of kinase mark2/(par-1) k82r, t208e double mutant |
|
0
|
10
|
2x39C |
Structure of 4-amino-n-(4-chlorobenzyl)-1-(7h-pyrrolo(2,3-d)pyrimidin- 4-yl)piperidine-4-carboxamide bound to pkb |
|
71
|
262
|
2wqeA |
Structure of s155r aurora-a somatic mutant |
|
18
|
99
|
2wwkT |
Crystal structure of the titin m10-obscurin like 1 ig f17r mutant complex |
|
77
|
263
|
2wmxA |
Crystal structure of checkpoint kinase 1 (chk1) in complex with inhibitors |
|
75
|
263
|
2wmqA |
Crystal structure of checkpoint kinase 1 (chk1) in complex with inhibitors |
|
79
|
296
|
2wtkC |
Structure of the heterotrimeric lkb1-stradalpha-mo25alpha complex |
|
76
|
263
|
2wmwA |
Crystal structure of checkpoint kinase 1 (chk1) in complex with inhibitors |
|
98
|
337
|
2x39A |
Structure of 4-amino-n-(4-chlorobenzyl)-1-(7h-pyrrolo(2,3-d)pyrimidin- 4-yl)piperidine-4-carboxamide bound to pkb |
|
18
|
100
|
2wwmD |
Crystal structure of the titin m10-obscurin like 1 ig complex in space group p1 |
|
72
|
262
|
2wtwA |
Aurora-a inhibitor structure (2nd crystal form) |
|
75
|
277
|
2wqoA |
Structure of nek2 bound to the aminopyridine cct241950 |
|
91
|
293
|
2wntA |
Crystal structure of the human ribosomal protein s6 kinase |
|
33
|
111
|
2x18A |
The crystal structure of the ph domain of human akt3 protein kinase |
|
94
|
303
|
2wtdA |
Crystal structure of chk2 in complex with an inhibitor |
|
71
|
262
|
2wmuA |
Crystal structure of checkpoint kinase 1 (chk1) in complex with inhibitors |
|
126
|
436
|
2wiuA |
Mercury-modified bacterial persistence regulator hipba |
|
65
|
164
|
2wviA |
Crystal structure of the n-terminal domain of bubr1 |
|
97
|
304
|
2wtjA |
Crystal structure of chk2 in complex with an inhibitor |
|
75
|
264
|
2wmsA |
Crystal structure of checkpoint kinase 1 (chk1) in complex with inhibitors |
|
77
|
264
|
2wmvA |
Crystal structure of checkpoint kinase 1 (chk1) in complex with inhibitors |
|
87
|
265
|
2wtvA |
Aurora-a inhibitor structure |
|
89
|
280
|
2wqnA |
Structure of adp-bound human nek7 |
|
89
|
302
|
2wtcA |
Crystal structure of chk2 in complex with an inhibitor |
|
88
|
281
|
2wqmA |
Structure of apo human nek7 |
|
78
|
264
|
2wmrA |
Crystal structure of checkpoint kinase 1 (chk1) in complex with inhibitors |
|
74
|
263
|
2wmtA |
Crystal structure of checkpoint kinase 1 (chk1) in complex with inhibitors |
|
95
|
303
|
2wtiA |
Crystal structure of chk2 in complex with an inhibitor |
|
21
|
99
|
2wp3T |
Crystal structure of the titin m10-obscurin like 1 ig complex |
|
120
|
352
|
2wb8A |
Crystal structure of haspin kinase |
|
92
|
301
|
2w7xA |
Cellular inhibition of checkpoint kinase 2 and potentiation of cytotoxic drugs by novel chk2 inhibitor pv1019 |
|
88
|
276
|
2w4jA |
X-ray structure of a dap-kinase 2-277 |
|
87
|
277
|
2w5bA |
Human nek2 kinase atpgammas-bound |
|
97
|
301
|
2w4kA |
X-ray structure of a dap-kinase 2-302 |
|
83
|
277
|
2w5hA |
Human nek2 kinase apo |
|
85
|
277
|
2w5aA |
Human nek2 kinase adp-bound |
|
78
|
263
|
2w1gA |
Structure determination of aurora kinase in complex with inhibitor |
|
73
|
263
|
2w1eA |
Structure determination of aurora kinase in complex with inhibitor |
|
88
|
301
|
2w0jA |
Crystal structure of chk2 in complex with nsc 109555, a specific inhibitor |
|
77
|
263
|
2w1cA |
Structure determination of aurora kinase in complex with inhibitor |
|
59
|
279
|
2vwiA |
Structure of the osr1 kinase, a hypertension drug target |
|
262
|
1077
|
2rd0A |
Structure of a human p110alpha/p85alpha complex |
|
72
|
263
|
2w1fA |
Structure determination of aurora kinase in complex with inhibitor |