|
81
|
268
|
3umwA |
Crystal structure of pim1 kinase in complex with inhibitor (z)-2-[(1h-indazol-3-yl)methylene]-6-methoxy-7-(piperazin-1-ylmethyl)benzofuran-3(2h)-one |
|
92
|
297
|
3tzmA |
Tgf-beta receptor type 1 in complex with sb431542 |
|
81
|
266
|
3up2A |
Aurora a in complex with rpm1686 |
|
84
|
298
|
3unjA |
Cdk2 in complex with inhibitor yl1-038-31 |
|
82
|
307
|
3uc4A |
The crystal structure of snf1-related kinase 2.6 |
|
116
|
347
|
3uvrA |
Human p38 map kinase in complex with km064 |
|
95
|
322
|
3ug2A |
Crystal structure of the mutated egfr kinase domain (g719s/t790m) in complex with gefitinib |
|
78
|
266
|
3uo4A |
Aurora a in complex with rpm1680 |
|
77
|
302
|
3ulzA |
Crystal structure of apo bak1 |
|
103
|
331
|
3u9cA |
Structure of a c-terminal deletion mutant of human protein kinase ck2 catalytic subunit with the atp-competitive inhibitor resorufin |
|
87
|
298
|
3ubdA |
Structure of n-terminal domain of rsk2 kinase in complex with flavonoid glycoside sl0101 |
|
79
|
299
|
3ujgA |
Crystal structure of snrk2.6 in complex with hab1 |
|
153
|
464
|
3upxA |
Calcium-dependent protein kinase 1 from toxoplasma gondii (tgcdpk1) in complex with inhibitor uw1300 |
|
71
|
263
|
3unzA |
Aurora a in complex with rpm1679 |
|
92
|
275
|
3u4wA |
Src in complex with dna-templated macrocyclic inhibitor mc4b |
|
112
|
355
|
3ttjA |
Crystal structure of jnk3 complexed with cc-359, a jnk inhibitor for the prevention of ischemia-reperfusion injury |
|
97
|
327
|
3txoA |
Pkc eta kinase in complex with a naphthyridine |
|
111
|
349
|
3u8wA |
Crystal structure of p38a mitogen-activated protein kinase in complex with a triazolopyridazinone inhibitor |
|
81
|
277
|
3tz7A |
Kinase domain of csrc in complex with rl103 |
|
79
|
265
|
3u9nA |
X-ray crystal structure of compound 1 bound to human chk1 kinase domain |
|
76
|
277
|
3tz9A |
Kinase domain of csrc in complex with rl130 |
|
81
|
277
|
3tz8A |
Kinase domain of csrc in complex with rl104 |
|
108
|
327
|
3u4uA |
Casein kinase 2 in complex with az-inhibitor |
|
107
|
355
|
3ttiA |
Crystal structure of jnk3 complexed with cc-930, an orally active anti-fibrotic jnk inhibitor |
|
76
|
273
|
3u51A |
Src in complex with dna-templated macrocyclic inhibitor mc1 |
|
114
|
396
|
3twjA |
Rho-associated protein kinase 1 (rock 1) in complex with rki1447 |
|
98
|
334
|
3tnqB |
Structure and allostery of the pka riib tetrameric holoenzyme |
|
79
|
279
|
3tkhA |
Crystal structure of chk1 in complex with inhibitor s01 |
|
114
|
394
|
3tv7A |
Human rho-associated protein kinase 1 (rock 1) in complex with rki1342 |
|
86
|
299
|
3tnwA |
Structure of cdk2/cyclin a in complex with can508 |
|
89
|
318
|
3tn8A |
Cdk9/cyclin t in complex with can508 |
|
87
|
305
|
3tt0A |
Co-structure of fibroblast growth factor receptor 1 kinase domain with 3-(2,6-dichloro-3,5-dimethoxy-phenyl)-1-{6-[4-(4-ethyl-piperazin-1-yl)-phenylamino]-pyrimidin-4-yl}-1-methyl-urea (bgj398) |
|
67
|
276
|
3tv6A |
Human b-raf kinase domain in complex with a methoxypyrazolopyridinyl benzamide inhibitor |
|
84
|
279
|
3tkiA |
Crystal structure of chk1 in complex with inhibitor s25 |
|
104
|
337
|
3tnpC |
Structure and allostery of the pka riib tetrameric holoenzyme |
|
82
|
319
|
3tniA |
Structure of cdk9/cyclin t f241l |
|
92
|
348
|
3tg1A |
Crystal structure of p38alpha in complex with a mapk docking partner |
|
73
|
276
|
3tv4A |
Human b-raf kinase domain in complex with an bromopyridine benzamide inhibitor |
|
101
|
349
|
3teiA |
Crystal structure of human erk2 complexed with a mapk docking peptide |
|
80
|
321
|
3tnhA |
Cdk9/cyclin t in complex with can508 |
|
119
|
414
|
3tkuA |
Mrck beta in complex with fasudil |
|
92
|
304
|
3tl8A |
The avrptob-bak1 complex reveals two structurally similar kinaseinteracting domains in a single type iii effector |
|
81
|
297
|
3tizA |
Cdk2 in complex with nsc 111848 |
|
92
|
290
|
3tjdA |
Co-crystal structure of jak2 with thienopyridine 19 |
|
81
|
297
|
3tiyA |
Cdk2 in complex with nsc 35676 |
|
161
|
503
|
3t8oA |
Rhodopsin kinase (grk1) l166k mutant at 2.5a resolution |
|
74
|
287
|
3tcpA |
Crystal structure of the catalytic domain of the proto-oncogene tyrosine-protein kinase mer in complex with inhibitor unc569 |
|
78
|
298
|
3ti1A |
Cdk2 in complex with sunitinib |
|
97
|
326
|
3tacA |
Crystal structure of the liprin-alpha/cask complex |
|
91
|
290
|
3tjcA |
Co-crystal structure of jak2 with thienopyridine 8 |
