|
75
|
262
|
2xneA |
Structure of aurora-a bound to an imidazopyrazine inhibitor |
|
75
|
298
|
2xnbA |
Discovery and characterisation of 2-anilino-4-(thiazol-5-yl) pyrimidine transcriptional cdk inhibitors as anticancer agents |
|
100
|
303
|
2xirA |
Crystal structure of the vegfr2 kinase domain in complex with pf- 00337210 (n,2-dimethyl-6-(7-(2-morpholinoethoxy)quinolin-4-yloxy) benzofuran-3-carboxamide) |
|
68
|
267
|
2xf0A |
Crystal structure of checkpoint kinase 1 (chk1) in complex with inhibitors |
|
82
|
263
|
2xngA |
Structure of aurora-a bound to a selective imidazopyrazine inhibitor |
|
79
|
274
|
2xixA |
Protein kinase pim-1 in complex with fragment-1 from crystallographic fragment screen |
|
76
|
277
|
2xkeA |
Structure of nek2 bound to aminipyrazine compound 5 |
|
79
|
274
|
2xizA |
Protein kinase pim-1 in complex with fragment-3 from crystallographic fragment screen |
|
74
|
298
|
2xmyA |
Discovery and characterisation of 2-anilino-4-(thiazol-5-yl) pyrimidine transcriptional cdk inhibitors as anticancer agents |
|
83
|
284
|
2xckA |
Crystal structure of pdk1 in complex with a pyrazoloquinazoline inhibitor |
|
90
|
302
|
2xbjA |
Crystal structure of chk2 in complex with an inhibitor |
|
106
|
318
|
2x0gA |
X-ray structure of a dap-kinase calmodulin complex |
|
82
|
287
|
2xchA |
Crystal structure of pdk1 in complex with a pyrazoloquinazoline inhibitor |
|
73
|
262
|
2x81A |
Structure of aurora a in complex with mln8054 |
|
134
|
435
|
2xalA |
Lead derivative of inositol 1,3,4,5,6-pentakisphosphate 2-kinase from a. thaliana in complex with adp and ip6. |
|
92
|
288
|
2xa4A |
Inhibitors of jak2 kinase domain |
|
113
|
368
|
2x7gA |
Structure of human serine-arginine-rich protein-specific kinase 2 (srpk2) bound to purvalanol b |
|
134
|
435
|
2xamA |
Inositol 1,3,4,5,6-pentakisphosphate 2-kinase from a. thaliana in complex with adp and ip6. |
|
128
|
435
|
2xaoA |
Inositol 1,3,4,5,6-pentakisphosphate 2-kinase from a. thaliana in complex with ip5 |
|
89
|
311
|
2x2lA |
Crystal structure of phosphorylated ret tyrosine kinase domain with inhibitor |
|
67
|
262
|
2x8eA |
Discovery of a novel class of triazolones as checkpoint kinase inhibitors - hit to lead exploration |
|
71
|
263
|
2x6eA |
Aurora-a bound to an inhibitor |
|
96
|
294
|
2x4fA |
The crystal structure of the human myosin light chain kinase loc340156. |
|
99
|
307
|
2xb7A |
Structure of human anaplastic lymphoma kinase in complex with nvp- tae684 |
|
84
|
281
|
2x9fA |
Ephb4 kinase domain inhibitor complex |
|
85
|
279
|
2x8dA |
Discovery of a novel class of triazolones as checkpoint kinase inhibitors - hit to lead exploration |
|
86
|
330
|
2x7oA |
Crystal structure of tgfbri complexed with an indolinone inhibitor |
|
73
|
263
|
2x6dA |
Aurora-a bound to an inhibitor |
|
76
|
280
|
2x9eA |
Human mps1 in complex with nms-p715 |
|
96
|
291
|
2x4zA |
Crystal structure of the human p21-activated kinase 4 in complex with pf-03758309 |
|
80
|
299
|
2x7fA |
Crystal structure of the kinase domain of human traf2- and nck- interacting kinase with wee1chk1 inhibitor |
|
82
|
268
|
2x8iA |
Discovery of a novel class of triazolones as checkpoint kinase inhibitors - hit to lead exploration |
|
89
|
314
|
2x2kA |
Crystal structure of phosphorylated ret tyrosine kinase domain with inhibitor |
|
80
|
296
|
2x1nA |
Truncation and optimisation of peptide inhibitors of cdk2, cyclin a through structure guided design |
|
96
|
315
|
2wzjA |
Catalytic and uba domain of kinase mark2/(par-1) k82r, t208e double mutant |
|
115
|
348
|
2wu7A |
Crystal structure of the human clk3 in complex with v25 |
|
72
|
262
|
2wtwA |
Aurora-a inhibitor structure (2nd crystal form) |
|
75
|
277
|
2wqoA |
Structure of nek2 bound to the aminopyridine cct241950 |
|
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 |
|
84
|
302
|
2wxvA |
Structure of cdk2-cyclin a with a pyrazolo(4,3-h) quinazoline-3- carboxamide inhibitor |
|
94
|
303
|
2wtdA |
Crystal structure of chk2 in complex with an inhibitor |
|
87
|
305
|
2wqbA |
Structure of the tie2 kinase domain in complex with a thiazolopyrimidine inhibitor |
|
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 |
|
71
|
262
|
2wqeA |
Structure of s155r aurora-a somatic mutant |
|
101
|
303
|
2wotA |
Alk5 in complex with 4-((5,6-dimethyl-2-(2-pyridyl)-3-pyridyl)oxy)-n-(3,4,5-trimethoxyphenyl)pyridin-2-amine |
|
76
|
263
|
2wmwA |
Crystal structure of checkpoint kinase 1 (chk1) in complex with inhibitors |
|
89
|
314
|
2x2mA |
Crystal structure of phosphorylated ret tyrosine kinase domain with inhibitor |
|
91
|
293
|
2wntA |
Crystal structure of the human ribosomal protein s6 kinase |
