89
|
270
|
3dk7A |
Crystal structure of mutant abl kinase domain in complex with small molecule fragment |
78
|
275
|
3dqxA |
Chicken c-src kinase domain in complex with atpgs |
83
|
299
|
3dogA |
Structure of thr 160 phosphorylated cdk2/cyclin a in complex with the inhibitor n-&-n1 |
93
|
312
|
3dkfA |
Structure of met receptor tyrosine kinase in complex with inhibitor sgx-523 |
105
|
338
|
3dneA |
Camp-dependent protein kinase pka catalytic subunit with pki-5-24 |
85
|
296
|
3dkoA |
Complex between the kinase domain of human ephrin type-a receptor 7 (epha7) and inhibitor alw-ii-49-7 |
77
|
274
|
3dcvA |
Crystal structure of human pim1 kinase complexed with 4-(4-hydroxy-3-methyl-phenyl)-6-phenylpyrimidin-2(1h)-one |
86
|
312
|
3dpkA |
Cfms tyrosine kinase in complex with a pyridopyrimidinone inhibitor |
74
|
285
|
3dlsA |
Crystal structure of human pas kinase bound to adp |
101
|
312
|
3dkcA |
Structure of met receptor tyrosine kinase in complex with atp |
93
|
293
|
3dfcB |
Crystal structure of a glycine-rich loop mutant of the death associated protein kinase catalytic domain with amppnp |
85
|
299
|
3ddqA |
Structure of phosphorylated thr160 cdk2/cyclin a in complex with the inhibitor roscovitine |
105
|
336
|
3dndA |
Camp-dependent protein kinase pka catalytic subunit with pki-5-24 |
91
|
307
|
3dkgA |
Structure of mutant(y1248l) met receptor tyrosine kinase in complex with inhibitor sgx-523 |
79
|
263
|
3dj7A |
Crystal structure of the mouse aurora-a catalytic domain (asn186->gly, lys240->arg, met302->leu) in complex with compound 130. |
85
|
298
|
3ddpA |
Structure of phosphorylated thr160 cdk2/cyclin a in complex with the inhibitor cr8 |
84
|
270
|
3dk6A |
Crystal structure of mutant abl kinase domain in complex with small molecule fragment |
81
|
270
|
3dfaA |
Crystal structure of kinase domain of calcium-dependent protein kinase cgd3_920 from cryptosporidium parvum |
76
|
261
|
3dj5A |
Crystal structure of the mouse aurora-a catalytic domain (asn186->gly, lys240->arg, met302->leu) in complex with compound 290. |
76
|
261
|
3dj6A |
Crystal structure of the mouse aurora-a catalytic domain (asn186->gly, lys240->arg, met302->leu) in complex with compound 823. |
112
|
329
|
3dlzA |
Crystal structure of human haspin in complex with amp |
87
|
270
|
3dk3A |
Crystal structure of mutant abl kinase domain in complex with small molecule fragment |
85
|
292
|
3dgkA |
Crystal structure of a glycine-rich loop mutant of the death associated protein kinase catalytic domain |
111
|
349
|
3d7zA |
Crystal structure of p38 kinase in complex with a biphenyl amide inhibitor |
68
|
288
|
3d5vA |
Crystal structure of an activated (thr->asp) polo-like kinase 1 (plk1) catalytic domain. |
86
|
269
|
3d14A |
Crystal structure of mouse aurora a (asn186->gly, lys240->arg, met302->leu) in complex with 1-{5-[2-(thieno[3,2-d]pyrimidin-4-ylamino)-ethyl]- thiazol-2-yl}-3-(3-trifluoromethyl-phenyl)-urea |
74
|
287
|
3dbfA |
Crystal structure of an activated (thr->asp) polo-like kinase 1 (plk1) catalytic domain in complex with compound 562 |
77
|
287
|
3d5wA |
Crystal structure of a phosphorylated polo-like kinase 1 (plk1) catalytic domain in complex with adp. |
76
|
288
|
3d5uA |
Crystal structure of a wildtype polo-like kinase 1 (plk1) catalytic domain. |
72
|
287
|
3dbcA |
Crystal structure of an activated (thr->asp) polo-like kinase 1 (plk1) catalytic domain in complex with compound 257 |
73
|
287
|
3dbdA |
Crystal structure of an activated (thr->asp) polo-like kinase 1 (plk1) catalytic domain in complex with compound 094 |
108
|
400
|
3d9vA |
Crystal structure of rock i bound to h-1152p a di-methylated variant of fasudil |
72
|
276
|
3d7tB |
Structural basis for the recognition of c-src by its inactivator csk |
80
|
276
|
3d4qA |
Pyrazole-based inhibitors of b-raf kinase |
103
|
335
|
3d0eA |
Crystal structure of human akt2 in complex with gsk690693 |
108
|
349
|
3d83A |
Crystal structure of p38 kinase in complex with a biphenyl amide inhibitor |
95
|
300
|
3d94A |
Crystal structure of the insulin-like growth factor-1 receptor kinase in complex with pqip |
70
|
287
|
3db8A |
Crystal structure of an activated (thr->asp) polo-like kinase 1 (plk1) catalytic domain in complex with compound 041 |
67
|
268
|
3daeA |
Crystal structure of phosphorylated snf1 kinase domain |
82
|
274
|
3cxwA |
Crystal structure of human proto-oncogene serine threonine kinase (pim1) in complex with a consensus peptide and a beta carboline ligand i |
104
|
356
|
3da6A |
Crystal structure of human jnk3 complexed with n-(3-methyl-4-(3-(2-(methylamino)pyrimidin-4-yl)pyridin-2-yloxy)naphthalen-1-yl)-1h-benzo[d]imidazol-2-amine |
85
|
290
|
3dakA |
Crystal structure of domain-swapped osr1 kinase domain |
75
|
262
|
3d2iA |
Crystal structure of mouse aurora a (asn186->gly, lys240->arg, met302->leu) in complex with 1-{5-[2-(1-methyl-1h-pyrazolo[4,3-d]pyrimidin-7-ylamino)-ethyl]-thiazol-2-yl}-3-(3-trifluoromethyl-phenyl)-urea |
82
|
273
|
3cy3A |
Crystal structure of human proto-oncogene serine threonine kinase (pim1) in complex with a consensus peptide and the jnk inhibitor v |
73
|
262
|
3dajA |
Crystal structure of aurora a complexed with an inhibitor discovered through site-directed dynamic tethering |
71
|
286
|
3d5xA |
Crystal structure of an activated (thr->asp) polo-like kinase 1 (plk1) catalytic domain in complex with wortmannin. |
78
|
263
|
3d15A |
Crystal structure of mouse aurora a (asn186->gly, lys240->arg, met302->leu) in complex with 1-(3-chloro-phenyl)-3-{5-[2-(thieno[3,2-d]pyrimidin-4-ylamino)- ethyl]-thiazol-2-yl}-urea [sns-314] |
80
|
273
|
3cy2A |
Crystal structure of human proto-oncogene serine threonine kinase (pim1) in complex with a consensus peptide and a beta carboline ligand ii |
79
|
287
|
3db6A |
Crystal structure of an activated (thr->asp) polo-like kinase 1 (plk1) catalytic domain in complex with compound 902 |
61
|
263
|
3d7tA |
Structural basis for the recognition of c-src by its inactivator csk |