|
98
|
293
|
4d0xA |
Pyrrole-3-carboxamides as potent and selective jak2 inhibitors |
|
75
|
262
|
4dhfA |
Structure of aurora a mutant bound to biogenidec cpd 15 |
|
89
|
299
|
4d9tA |
Rsk2 c-terminal kinase domain with inhibitor (e)-methyl 3-(4-amino-7-(3-hydroxypropyl)-5-p-tolyl-7h-pyrrolo[2,3-d]pyrimidin-6-yl)-2-cyanoacrylate |
|
92
|
308
|
4ctcA |
Structure of the human anaplastic lymphoma kinase in complex with the inhibitor 7-amino-3-cyclopropyl-12-fluoro-1,10,16-trimethyl-16,17- dihydro-1h-8,4-(metheno)pyrazolo(4,3-h)(2,5,11) benzoxadiazacyclotetradecin-15(10h)-one |
|
110
|
350
|
4dliA |
Human p38 map kinase in complex with rl87 |
|
81
|
272
|
4d4yA |
Focal adhesion kinase catalytic domain |
|
101
|
334
|
4dglC |
Crystal structure of the ck2 tetrameric holoenzyme |
|
103
|
292
|
4d0wA |
Pyrrole-3-carboxamides as potent and selective jak2 inhibitors |
|
82
|
278
|
4dggA |
C-src kinase domain in complex with rm-1-176 |
|
87
|
294
|
4dehA |
Crystal structure of c-met in complex with triazolopyridinone inhibitor 3 |
|
74
|
293
|
4d1zA |
Cdk2 in complex with a luciferin derivate |
|
93
|
341
|
4crsA |
Human protein kinase n2 (pkn2, prkcl2) in complex with atpgammas |
|
82
|
273
|
4d55A |
Focal adhesion kinase catalytic domain |
|
110
|
336
|
4dh1A |
Low temperature x-ray structure of camp dependent protein kinase a catalytic subunit with low mg2+, atp and ip20 |
|
79
|
272
|
4d5hA |
Focal adhesion kinase catalytic domain |
|
109
|
336
|
4dh7A |
Low temperature x-ray structure of camp dependent protein kinase a catalytic subunit with high mg2+, amp-pnp and ip20' |
|
94
|
289
|
4d1sA |
Pyrrole-3-carboxamides as potent and selective jak2 inhibitors |
|
76
|
264
|
4debA |
Aurora a in complex with rk2-17-01 |
|
98
|
309
|
4ctbA |
Structure of the human anaplastic lymphoma kinase in complex with the inhibitor (5r)-8-amino-3-fluoro-5,19-dimethyl-20-oxo-5,18,19,20- tetrahydro-7,11-(azeno)pyrido(2',1':2,3)imidazo(4,5-h)(2,5,11) benzoxadiazacyclotetradecine-14-carbonitrile |
|
96
|
339
|
4dc2A |
Structure of pkc in complex with a substrate peptide from par-3 |
|
103
|
330
|
4cqgA |
The crystal structure of mpk38 in complex with otssp167, an orally- administrative melk selective inhibitor |
|
83
|
272
|
4d4rA |
Focal adhesion kinase catalytic domain |
|
112
|
350
|
4dfzE |
Crystal structure of myristoylated k7c catalytic subunit of camp-dependent protein kinase in complex with sp20 |
|
87
|
295
|
4degA |
Crystal structure of c-met in complex with triazolopyridazine inhibitor 2 |
|
63
|
282
|
4d28A |
Crystal structure of the kinase domain of cipk24/sos2 |
|
119
|
424
|
4cyjA |
Chaetomium thermophilum pan2:pan3 complex |
|
91
|
310
|
4dceA |
Crystal structure of human anaplastic lymphoma kinase in complex with a piperidine-carboxamide inhibitor |
|
86
|
271
|
4deeA |
Aurora a in complex with adp |
|
95
|
302
|
4d2rA |
Human igf in complex with a dyrk1b inhibitor |
|
110
|
326
|
4dgmA |
Crystal structure of maize ck2 in complex with the inhibitor apigenin |
|
87
|
274
|
4dflA |
Crystal structure of spleen tyrosine kinase complexed with a sulfonamidopyrazine piperidine inhibitor |
|
105
|
362
|
4crlA |
Crystal structure of human cdk8-cyclin c in complex with cortistatin a |
|
92
|
307
|
4d9uA |
Rsk2 c-terminal kinase domain, (e)-tert-butyl 3-(4-amino-7-(3-hydroxypropyl)-5-p-tolyl-7h-pyrrolo[2,3-d]pyrimidin-6-yl)-2-cyanoacrylate |
|
89
|
342
|
4dinA |
Novel localization and quaternary structure of the pka ri beta holoenzyme |
|
79
|
272
|
4d4sA |
Focal adhesion kinase catalytic domain |
|
105
|
336
|
4dh8A |
Room temperature x-ray structure of camp dependent protein kinase a catalytic subunit with high mg2+, amp-pnp and ip20 |
|
80
|
333
|
4cxaA |
Crystal structure of the human cdk12-cyclin k complex bound to amppnp |
|
96
|
294
|
4dawA |
Crystal structure of pak1 kinase domain with the ruthenium phthalimide complex |
|
75
|
272
|
4cqeA |
B-raf kinase v600e mutant in complex with a diarylthiazole b-raf inhibitor |
|
95
|
333
|
4d2pA |
Structure of melk in complex with inhibitors |
|
82
|
266
|
4deaA |
Aurora a in complex with yl1-038-18 |
|
89
|
296
|
4cztA |
Crystal structure of the kinase domain of cipk23 |
|
76
|
265
|
4dedA |
Aurora a in complex with yl1-038-21 |
|
76
|
280
|
4cv9A |
Mps1 kinase with 3-aminopyridin-2-one inhibitors |
|
74
|
274
|
4dbnA |
Crystal structure of the kinase domain of human b-raf with a [1,3]thiazolo[5,4-b]pyridine derivative |
|
108
|
336
|
4dh3A |
Low temperature x-ray structure of camp dependent protein kinase a catalytic subunit with high mg2+, atp and ip20 |
|
82
|
272
|
4d4vA |
Focal adhesion kinase catalytic domain |
|
105
|
336
|
4dh5A |
Room temperature x-ray structure of camp dependent protein kinase a catalytic subunit with high mg2+, adp, phosphate, and ip20 |
|
105
|
337
|
4dg3E |
Crystal structure of r336a mutant of camp-dependent protein kinase with unphosphorylated turn motif. |
|
110
|
417
|
4cyiA |
Chaetomium thermophilum pan3 |
