|
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 |
|
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 |
|
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 |
|
76
|
261
|
3d2kA |
Crystal structure of mouse aurora a (asn186->gly, lys240->arg, met302->leu) in complex with [7-(2-{2-[3-(3-chloro-phenyl)-ureido]-thiazol-5-yl}-ethylamino)-pyrazolo[4,3-d]pyrimidin-1-yl]-acetic acid |
|
71
|
282
|
3dbqA |
Crystal structure of ttk kinase domain |
|
73
|
287
|
3dbeA |
Crystal structure of an activated (thr->asp) polo-like kinase 1 (plk1) catalytic domain in complex with compound 557 |
|
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 |
|
103
|
348
|
3ctqA |
Structure of map kinase p38 in complex with a 1-o-tolyl-1,2,3-triazole-4-carboxamide |
|
70
|
267
|
3cokA |
Crystal structure of plk4 kinase |
|
196
|
641
|
3cikA |
Human grk2 in complex with gbetagamma subunits |
|
97
|
310
|
3cpbA |
Crystal structure of the vegfr2 kinase domain in complex with a bisamide inhibitor |
|
96
|
312
|
3cp9A |
Crystal structure of the vegfr2 kinase domain in complex with a pyridone inhibitor |
|
94
|
335
|
3cquA |
Crystal structure of akt-1 complexed with substrate peptide and inhibitor |
|
102
|
352
|
3coiA |
Crystal structure of p38delta kinase |
|
89
|
305
|
3clyA |
Crystal structure of fgf receptor 2 (fgfr2) kinase domains trapped in trans-phosphorylation reaction |
|
89
|
298
|
3cjfA |
Crystal structure of vegfr2 in complex with a 3,4,5-trimethoxy aniline containing pyrimidine |
|
83
|
278
|
3cqeA |
Wee1 kinase complex with inhibitor pd074291 |
|
95
|
309
|
3cpcA |
Crystal structure of the vegfr2 kinase domain in complex with a pyridone inhibitor |
|
79
|
261
|
3cohA |
Crystal structure of aurora-a in complex with a pentacyclic inhibitor |
|
84
|
279
|
3ckxA |
Crystal structure of sterile 20-like kinase 3 (mst3, stk24) in complex with staurosporine |
|
98
|
335
|
3cqwA |
Crystal structure of akt-1 complexed with substrate peptide and inhibitor |
|
80
|
309
|
3cthA |
Crystal structure of the tyrosine kinase domain of the hepatocyte growth factor receptor c-met in complex with a aminopyridine based inhibitor |
|
85
|
270
|
3comA |
Crystal structure of mst1 kinase |
|
81
|
279
|
3ckwA |
Crystal structure of sterile 20-like kinase 3 (mst3, stk24) |
|
85
|
268
|
3cs9A |
Human abl kinase in complex with nilotinib |
|
83
|
281
|
3cr0A |
Wee1 kinase complex with inhibitor pd259_809 |
|
91
|
299
|
3cjgA |
Crystal structure of vegfr2 in complex with a 3,4,5-trimethoxy aniline containing pyrimidine |
|
84
|
310
|
3ctjA |
Crystal structure of the tyrosine kinase domain of the hepatocyte growth factor receptor c-met in complex with a aminopyridine based inhibitor |
|
132
|
503
|
3c51A |
Crystal structure of g protein coupled receptor kinase 1 bound to adp and magnesium chloride at 3.55a |
|
108
|
361
|
3byvA |
Crystal structure of toxoplasma gondii specific rhoptry antigen kinase domain |
|
162
|
503
|
3c4zA |
Crystal structure of g protein coupled receptor kinase 1 bound to adp and magnesium chloride at 1.84a |
|
74
|
280
|
3cekA |
Crystal structure of human dual specificity protein kinase (ttk) |
|
94
|
301
|
3c7qA |
Structure of vegfr2 kinase domain in complex with bibf1120 |
