|
96
|
309
|
2gcdA |
Tao2 kinase domain-staurosporine structure |
|
108
|
340
|
2gngA |
Protein kinase a fivefold mutant model of rho-kinase |
|
96
|
348
|
2ghmA |
Mutated map kinase p38 (mus musculus) in complex with inhbitor pg-895449 |
|
85
|
299
|
2g9xA |
Structure of thr 160 phosphorylated cdk2/cyclin a in complex with the inhibitor nu6271 |
|
75
|
273
|
2gdoA |
4-(aminoalkylamino)-3-benzimidazole-quinolinones as potent chk1 inhibitors |
|
109
|
337
|
2gfcA |
Camp-dependent protein kinase pka catalytic subunit with pki-5-24 |
|
86
|
272
|
2g2hA |
A src-like inactive conformation in the abl tyrosine kinase domain |
|
111
|
348
|
2gfsA |
P38 kinase crystal structure in complex with ro3201195 |
|
71
|
274
|
2g2iA |
A src-like inactive conformation in the abl tyrosine kinase domain |
|
88
|
349
|
2fysA |
Crystal structure of erk2 complex with kim peptide derived from mkp3 |
|
85
|
275
|
2g2fA |
A src-like inactive conformation in the abl tyrosine kinase domain |
|
73
|
355
|
2g01A |
Pyrazoloquinolones as novel, selective jnk1 inhibitors |
|
96
|
301
|
2g15A |
Structural characterization of autoinhibited c-met kinase |
|
106
|
349
|
2fsmX |
Mitogen activated protein kinase p38alpha (d176a+f327s) activating mutant form-b |
|
86
|
271
|
2g1tA |
A src-like inactive conformation in the abl tyrosine kinase domain |
|
68
|
274
|
2fh9A |
Structure and dimerization of the kinase domain from yeast snf1 |
|
81
|
275
|
2fumA |
Catalytic domain of protein kinase pknb from mycobacterium tuberculosis in complex with mitoxantrone |
|
109
|
349
|
2fsoX |
Mitogen activated protein kinase p38alpha (d176a) activating mutant |
|
103
|
351
|
2fslX |
Mitogen activated protein kinase p38alpha (d176a+f327s) activating mutant form-a |
|
132
|
466
|
2fo0A |
Organization of the sh3-sh2 unit in active and inactive forms of the c-abl tyrosine kinase |
|
106
|
348
|
2fstX |
Mitogen activated protein kinase p38alpha (d176a+f327l) activating mutant |
|
77
|
272
|
2fb8A |
Structure of the b-raf kinase domain bound to sb-590885 |
|
82
|
298
|
2fvdA |
Cyclin dependent kinase 2 (cdk2) with diaminopyrimidine inhibitor |
|
103
|
350
|
2ewaA |
Dual binding mode of pyridinylimidazole to map kinase p38 |
|
115
|
400
|
2etkA |
Crystal structure of rock 1 bound to hydroxyfasudil |
|
96
|
349
|
2fa2A |
Crystal structure of fus3 without a peptide from ste5 |
|
81
|
298
|
2exmA |
Human cdk2 in complex with isopentenyladenine |
|
125
|
400
|
2esmA |
Crystal structure of rock 1 bound to fasudil |
|
91
|
299
|
2fgiA |
Crystal structure of the tyrosine kinase domain of fgf receptor 1 in complex with inhibitor pd173074 |
|
108
|
336
|
2f7xE |
Protein kinase a bound to (s)-2-(1h-indol-3-yl)-1-[5-((e)-2-pyridin-4-yl-vinyl)-pyridin-3-yloxymethyl]-ethylamine |
|
79
|
282
|
2exeA |
Crystal structure of the phosphorylated clk3 |
|
86
|
272
|
2etmA |
Crystal structure of focal adhesion kinase domain complexed with 7h-pyrrolo [2,3-d] pyrimidine derivative |
|
92
|
287
|
2f4jA |
Structure of the kinase domain of an imatinib-resistant abl mutant in complex with the aurora kinase inhibitor vx-680 |
|
103
|
356
|
2excX |
Inhibitor complex of jnk3 |
|
116
|
346
|
2eu9A |
Crystal structure of clk3 |
|
69
|
296
|
2eufB |
X-ray structure of human cdk6-vcyclin in complex with the inhibitor pd0332991 |
|
108
|
336
|
2f7eE |
Pka complexed with (s)-2-(1h-indol-3-yl)-1-(5-isoquinolin-6-yl-pyridin-3-yloxymethyl-etylamine |
|
64
|
297
|
2f2cB |
X-ray structure of human cdk6-vcyclinwith the inhibitor aminopurvalanol |
|
107
|
336
|
2erzE |
Crystal structure of c-amp dependent kinase (pka) bound to hydroxyfasudil |
|
100
|
336
|
2f7zE |
Protein kinase a bound to (r)-1-(1h-indol-3-ylmethyl)-2-(2-pyridin-4-yl-[1,7]naphtyridin-5-yloxy)-ehylamine |
|
122
|
391
|
2f2uA |
Crystal structure of the rho-kinase kinase domain |
|
93
|
298
|
2f57A |
Crystal structure of the human p21-activated kinase 5 |
|
121
|
400
|
2etrA |
Crystal structure of rock i bound to y-27632 |
|
102
|
351
|
2f49A |
Crystal structure of fus3 in complex with a ste5 peptide |
|
108
|
353
|
2f9gA |
Crystal structure of fus3 phosphorylated on tyr182 |
|
85
|
307
|
2evaA |
Structural basis for the interaction of tak1 kinase with its activating protein tab1 |
|
112
|
353
|
2erkA |
Phosphorylated map kinase erk2 |
|
78
|
269
|
2e9uA |
Structure of h-chk1 complexed with a780125 |
|
76
|
269
|
2e9nA |
Structure of h-chk1 complexed with a767085 |
|
75
|
269
|
2e9pA |
Structure of h-chk1 complexed with a771129 |
