|
83
|
298
|
1w98A |
The structural basis of cdk2 activation by cyclin e |
|
94
|
265
|
1w2dA |
Human inositol (1,4,5)-trisphosphate 3-kinase complexed with mn2+/adp/ins(1,3,4,5)p4 |
|
106
|
351
|
1wbwA |
Identification of novel p38 alpha map kinase inhibitors using fragment-based lead generation. |
|
109
|
351
|
1w83A |
P38 kinase crystal structure in complex with small molecule inhibitor |
|
103
|
351
|
1w84A |
P38 kinase crystal structure in complex with small molecule inhibitor |
|
91
|
322
|
1vzoA |
The structure of the n-terminal kinase domain of msk1 reveals a novel autoinhibitory conformation for a dual kinase protein |
|
105
|
351
|
1wboA |
Fragment based p38 inhibitors |
|
108
|
351
|
1wbsA |
Identification of novel p38 alpha map kinase inhibitors using fragment-based lead generation. |
|
108
|
351
|
1w7hA |
P38 kinase crystal structure in complex with small molecule inhibitor |
|
96
|
265
|
1w2cA |
Human inositol (1,4,5) trisphosphate 3-kinase complexed with mn2+/amppnp/ins(1,4,5)p3 |
|
88
|
299
|
1vr2A |
Human vascular endothelial growth factor receptor 2 (kdr) kinase domain |
|
99
|
303
|
1vjyA |
Crystal structure of a naphthyridine inhibitor of human tgf-beta type i receptor |
|
73
|
298
|
1v1kA |
Cdk2 in complex with a disubstituted 4, 6-bis anilino pyrimidine cdk4 inhibitor |
|
73
|
298
|
1vyzA |
Structure of cdk2 complexed with pnu-181227 |
|
100
|
340
|
1vebA |
Crystal structure of protein kinase a in complex with azepane derivative 5 |
|
73
|
284
|
1v0oA |
Structure of p. falciparum pfpk5-indirubin-5-sulphonate ligand complex |
|
98
|
348
|
1uv5A |
Glycogen synthase kinase 3 beta complexed with 6-bromoindirubin-3'-oxime |
|
86
|
287
|
1uu3A |
Structure of human pdk1 kinase domain in complex with ly333531 |
|
78
|
286
|
1unhA |
Structural mechanism for the inhibition of cdk5-p25 by roscovitine, aloisine and indirubin. |
|
80
|
286
|
1v0pA |
Structure of p. falciparum pfpk5-purvalanol b ligand complex |
|
82
|
289
|
1uvrA |
Structure of human pdk1 kinase domain in complex with bim-8 |
|
79
|
298
|
1urwA |
Cdk2 in complex with an imidazo[1,2-b]pyridazine |
|
88
|
355
|
1ukiA |
Structural basis for the selective inhibition of jnk1 by the scaffolding protein jip1 and sp600125 |
|
75
|
276
|
1uwhA |
The complex of wild type b-raf and bay439006. |
|
85
|
286
|
1uu8A |
Structure of human pdk1 kinase domain in complex with bim-1 |
|
83
|
292
|
1unlA |
Structural mechanism for the inhibition of cd5-p25 from the roscovitine, aloisine and indirubin. |
|
85
|
286
|
1uu9A |
Structure of human pdk1 kinase domain in complex with bim-3 |
|
81
|
296
|
1urcA |
Cyclin a binding groove inhibitor ace-arg-lys-leu-phe-gly |
|
93
|
355
|
1ukhA |
Structural basis for the selective inhibition of jnk1 by the scaffolding protein jip1 and sp600125 |
|
80
|
286
|
1v0bA |
Crystal structure of the t198a mutant of pfpk5 |
|
81
|
292
|
1ungA |
Structural mechanism for the inhibition of cdk5-p25 by roscovitine, aloisine and indirubin. |
|
66
|
276
|
1uwjA |
The complex of mutant v599e b-raf and bay439006. |
|
83
|
286
|
1uu7A |
Structure of human pdk1 kinase domain in complex with bim-2 |
|
100
|
309
|
1u5qA |
Crystal structure of the tao2 kinase domain: activation and specifity of a ste20p map3k |
|
71
|
276
|
1u54A |
Crystal structures of the phosphorylated and unphosphorylated kinase domains of the cdc42-associated tyrosine kinase ack1 bound to amp-pcp |
|
83
|
273
|
1u46A |
Crystal structure of the unphosphorylated kinase domain of the tyrosine kinase ack1 |
|
99
|
309
|
1u5rA |
Crystal structure of the tao2 kinase domain: activation and specifity of a ste20p map3k |
|
89
|
285
|
1u59A |
Crystal structure of the zap-70 kinase domain in complex with staurosporine |
|
77
|
272
|
1u54B |
Crystal structures of the phosphorylated and unphosphorylated kinase domains of the cdc42-associated tyrosine kinase ack1 bound to amp-pcp |
|
86
|
273
|
1u4dA |
Structure of the ack1 kinase domain bound to debromohymenialdisine |
|
66
|
299
|
1ua2A |
Crystal structure of human cdk7 |
|
95
|
282
|
1tqmA |
Crystal structure of a. fulgidus rio2 serine protein kinase bound to amppnp |
|
103
|
350
|
1tvoA |
The structure of erk2 in complex with a small molecule inhibitor |
|
60
|
256
|
1tzdA |
Crystal structure of the catalytic core of inositol 1,4,5-trisphosphate 3-kinase |
|
96
|
321
|
1tkiA |
Autoinhibited serine kinase domain of the giant muscle protein titin |
|
86
|
282
|
1tqpA |
Crystal structure of a. fulgidus rio2 serine protein kinase bound to atp |
|
91
|
282
|
1tqiA |
Crystal structure of a. fulgidus rio2 serine protein kinase |
|
87
|
336
|
1szmA |
Dual binding mode of bisindolylmaleimide 2 to protein kinase a (pka) |
|
99
|
311
|
1t46A |
Structural basis for the autoinhibition and sti-571 inhibition of c-kit tyrosine kinase |
|
109
|
340
|
1svgA |
Crystal structure of protein kinase a in complex with azepane derivative 4 |
