|
104
|
331
|
1pjkA |
Crystal structure of a c-terminal deletion mutant of human protein kinase ck2 catalytic subunit |
|
111
|
344
|
1q8uA |
The catalytic subunit of camp-dependent protein kinase in complex with rho-kinase inhibitor h-1152p |
|
96
|
352
|
1q41A |
Gsk-3 beta complexed with indirubin-3'-monoxime |
|
88
|
301
|
1py5A |
Crystal structure of tgf-beta receptor i kinase with inhibitor |
|
84
|
303
|
1pkgA |
Structure of a c-kit kinase product complex |
|
106
|
363
|
1q8zA |
The apoenzyme structure of the yeast sr protein kinase, sky1p |
|
74
|
298
|
1pxjA |
Human cyclin dependent kinase 2 complexed with the inhibitor 4-(2,4-dimethyl-thiazol-5-yl)-pyrimidin-2-ylamine |
|
107
|
337
|
1q61A |
Pka triple mutant model of pkb |
|
78
|
298
|
1pxkA |
Human cyclin dependent kinase 2 complexed with the inhibitor n-[4-(2,4-dimethyl-thiazol-5-yl)pyrimidin-2-yl]-n'-hydroxyiminoformamide |
|
83
|
297
|
1pkdA |
The crystal structure of ucn-01 in complex with phospho-cdk2/cyclin a |
|
100
|
337
|
1q8wA |
The catalytic subunit of camp-dependent protein kinase in complex with rho-kinase inhibitor fasudil (ha-1077) |
|
104
|
337
|
1q24A |
Pka double mutant model of pkb in complex with mgatp |
|
76
|
298
|
1pxiA |
Human cyclin dependent kinase 2 complexed with the inhibitor 4-(2,5-dichloro-thiophen-3-yl)-pyrimidin-2-ylamine |
|
107
|
345
|
1pmeA |
Structure of penta mutant human erk2 map kinase complexed with a specific inhibitor of human p38 map kinase |
|
116
|
362
|
1q8yA |
The structure of the yeast sr protein kinase, sky1p, with bound adp |
|
89
|
306
|
1p14A |
Crystal structure of a catalytic-loop mutant of the insulin receptor tyrosine kinase |
|
87
|
292
|
1p4fA |
Death associated protein kinase catalytic domain with bound inhibitor fragment |
|
181
|
640
|
1omwA |
Crystal structure of the complex between g protein-coupled receptor kinase 2 and heterotrimeric g protein beta 1 and gamma 2 subunits |
|
88
|
287
|
1opjA |
Structural basis for the auto-inhibition of c-abl tyrosine kinase |
|
96
|
308
|
1p4oA |
Structure of apo unactivated igf-1r kinase domain at 1.5a resolution. |
|
112
|
348
|
1oz1A |
P38 mitogen-activated kinase in complex with 4-azaindole inhibitor |
|
74
|
298
|
1p2aA |
The structure of cyclin dependent kinase 2 (ckd2) with a trisubstituted naphthostyril inhibitor |
|
69
|
298
|
1pf8A |
Crystal structure of human cyclin-dependent kinase 2 complexed with a nucleoside inhibitor |
|
110
|
348
|
1oukA |
The structure of p38 alpha in complex with a pyridinylimidazole inhibitor |
|
135
|
451
|
1oplA |
Structural basis for the auto-inhibition of c-abl tyrosine kinase |
|
89
|
277
|
1phkA |
Two structures of the catalytic domain of phosphorylase, kinase: an active protein kinase complexed with nucleotide, substrate-analogue and product |
|
112
|
349
|
1oveA |
The structure of p38 alpha in complex with a dihydroquinolinone |
|
85
|
297
|
1p5eA |
The structure of phospho-cdk2/cyclin a in complex with the inhibitor 4,5,6,7-tetrabromobenzotriazole (tbs) |
|
107
|
350
|
1ouyA |
The structure of p38 alpha in complex with a dihydropyrido-pyrimidine inhibitor |
|
138
|
449
|
1opkA |
Structural basis for the auto-inhibition of c-abl tyrosine kinase |
|
84
|
288
|
1okyA |
Structure of human pdk1 kinase domain in complex with staurosporine |
|
80
|
263
|
1ol7A |
Structure of human aurora-a 122-403 phosphorylated on thr287, thr288 |
|
70
|
298
|
1oiqA |
Imidazopyridines: a potent and selective class of cyclin-dependent kinase inhibitors identified through structure-based hybridisation |
|
98
|
350
|
1o9uA |
Glycogen synthase kinase 3 beta complexed with axin peptide |
|
84
|
286
|
1okzA |
Structure of human pdk1 kinase domain in complex with ucn-01 |
|
79
|
295
|
1okvA |
Cyclin a binding groove inhibitor h-arg-arg-leu-ile-phe-nh2 |
|
78
|
298
|
1oecA |
Fgfr2 kinase domain |
|
86
|
296
|
1ol2A |
Cyclin a binding groove inhibitor h-arg-arg-leu-asn-(p-f-phe)-nh2 |
|
78
|
296
|
1oirA |
Imidazopyridines: a potent and selective class of cyclin-dependent kinase inhibitors identified through structure-based hybridisation |
|
79
|
296
|
1ol1A |
Cyclin a binding groove inhibitor h-cit-cit-leu-ile-(p-f-phe)-nh2 |
|
92
|
265
|
1ol5A |
Structure of aurora-a 122-403, phosphorylated on thr287, thr288 and bound to tpx2 1-43 |
|
89
|
300
|
1oiuA |
Structure of human thr160-phospho cdk2/cyclin a complexed with a 6-cyclohexylmethyloxy-2-anilino-purine inhibitor |
|
84
|
296
|
1okwA |
Cyclin a binding groove inhibitor ac-arg-arg-leu-asn-(m-cl-phe)-nh2 |
|
70
|
296
|
1oitA |
Imidazopyridines: a potent and selective class of cyclin-dependent kinase inhibitors identified through structure-based hybridisation |
|
85
|
300
|
1oguA |
Structure of human thr160-phospho cdk2/cyclin a complexed with a 2-arylamino-4-cyclohexylmethyl-5-nitroso-6-aminopyrimidine inhibitor |
|
92
|
334
|
1o6kA |
Structure of activated form of pkb kinase domain s474d with gsk3 peptide and amp-pnp |
|
65
|
260
|
1ol6A |
Structure of unphosphorylated d274n mutant of aurora-a |
|
86
|
297
|
1oiyA |
Structure of human thr160-phospho cdk2/cyclin a complexed with a 6-cyclohexylmethyloxy-2-anilino-purine inhibitor |
|
92
|
337
|
1o6lA |
Crystal structure of an activated akt/protein kinase b (pkb-pif chimera) ternary complex with amp-pnp and gsk3 peptide |
|
111
|
325
|
1om1A |
Crystal structure of maize ck2 alpha in complex with iqa |
