|
103
|
350
|
2ewaA |
Dual binding mode of pyridinylimidazole to map kinase p38 |
|
96
|
349
|
2fa2A |
Crystal structure of fus3 without a peptide from ste5 |
|
103
|
356
|
2excX |
Inhibitor complex of jnk3 |
|
108
|
353
|
2f9gA |
Crystal structure of fus3 phosphorylated on tyr182 |
|
102
|
351
|
2f49A |
Crystal structure of fus3 in complex with a ste5 peptide |
|
112
|
353
|
2erkA |
Phosphorylated map kinase erk2 |
|
102
|
355
|
2bajA |
P38alpha bound to pyrazolourea |
|
101
|
353
|
2b9iA |
Crystal structure of fus3 with a docking motif from msg5 |
|
101
|
353
|
2b9jA |
Crystal structure of fus3 with a docking motif from far1 |
|
104
|
349
|
2bakA |
P38alpha map kinase bound to mpaq |
|
106
|
349
|
2balA |
P38alpha map kinase bound to pyrazoloamine |
|
107
|
347
|
2baqA |
P38alpha bound to ro3201195 |
|
105
|
353
|
2b9hA |
Crystal structure of fus3 with a docking motif from ste7 |
|
100
|
353
|
2b9fA |
Crystal structure of non-phosphorylated fus3 |
|
106
|
355
|
2b1pA |
Inhibitor complex of jnk3 |
|
104
|
348
|
1zyjA |
Human p38 map kinase in complex with inhibitor 1a |
|
107
|
351
|
1zzlA |
Crystal structure of p38 with triazolopyridine |
|
109
|
348
|
1zz2A |
Two classes of p38alpha map kinase inhibitors having a common diphenylether core but exhibiting divergent binding modes |
|
102
|
350
|
1yw2A |
Mutated mus musculus p38 kinase (mp38) |
|
100
|
348
|
1ywrA |
Crystal structure analysis of inactive p38 kinase domain in complex with a monocyclic pyrazolone inhibitor |
|
106
|
356
|
1yqjA |
Crystal structure of p38 alpha in complex with a selective pyridazine inhibitor |
|
101
|
350
|
1wzyA |
Crystal structure of human erk2 complexed with a pyrazolopyridazine derivative |
|
107
|
347
|
1wfcA |
Structure of apo, unphosphorylated, p38 mitogen activated protein kinase p38 (p38 map kinase) the mammalian homologue of the yeast hog1 protein |
|
108
|
351
|
1wbsA |
Identification of novel p38 alpha map kinase inhibitors using fragment-based lead generation. |
|
106
|
351
|
1wbwA |
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 |
|
111
|
351
|
1wbnA |
Fragment based p38 inhibitors |
|
109
|
351
|
1w83A |
P38 kinase crystal structure in complex with small molecule inhibitor |
|
112
|
351
|
1wbvA |
Identification of novel p38 alpha map kinase inhibitors using fragment-based lead generation. |
|
103
|
351
|
1w84A |
P38 kinase crystal structure in complex with small molecule inhibitor |
|
105
|
351
|
1wboA |
Fragment based p38 inhibitors |
|
110
|
351
|
1w82A |
P38 kinase crystal structure in complex with small molecule inhibitor |
|
113
|
351
|
1wbtA |
Identification of novel p38 alpha map kinase inhibitors using fragment-based lead generation. |
|
88
|
355
|
1ukiA |
Structural basis for the selective inhibition of jnk1 by the scaffolding protein jip1 and sp600125 |
|
93
|
355
|
1ukhA |
Structural basis for the selective inhibition of jnk1 by the scaffolding protein jip1 and sp600125 |
|
103
|
350
|
1tvoA |
The structure of erk2 in complex with a small molecule inhibitor |
|
105
|
348
|
1r39A |
The structure of p38alpha |
|
108
|
349
|
1r3cA |
The structure of p38alpha c162s mutant |
|
100
|
356
|
1pmuA |
The crystal structure of jnk3 in complex with a phenantroline inhibitor |
|
99
|
356
|
1pmvA |
The structure of jnk3 in complex with a dihydroanthrapyrazole inhibitor |
|
103
|
356
|
1pmnA |
Crystal structure of jnk3 in complex with an imidazole-pyrimidine inhibitor |
|
107
|
345
|
1pmeA |
Structure of penta mutant human erk2 map kinase complexed with a specific inhibitor of human p38 map kinase |
|
112
|
348
|
1oz1A |
P38 mitogen-activated kinase in complex with 4-azaindole inhibitor |
|
107
|
350
|
1ouyA |
The structure of p38 alpha in complex with a dihydropyrido-pyrimidine inhibitor |
|
112
|
349
|
1oveA |
The structure of p38 alpha in complex with a dihydroquinolinone |
|
110
|
348
|
1oukA |
The structure of p38 alpha in complex with a pyridinylimidazole inhibitor |
|
107
|
350
|
1lewA |
Crystal structure of map kinase p38 complexed to the docking site on its nuclear substrate mef2a |
|
107
|
348
|
1m7qA |
Crystal structure of p38 map kinase in complex with a dihydroquinazolinone inhibitor |
|
110
|
350
|
1lezA |
Crystal structure of map kinase p38 complexed to the docking site on its activator mkk3b |
|
99
|
348
|
1kv1A |
P38 map kinase in complex with inhibitor 1 |
