|
95
|
278
|
3cc6A |
Crystal structure of kinase domain of protein tyrosine kinase 2 beta (ptk2b) |
|
97
|
349
|
3c5uA |
P38 alpha map kinase complexed with a benzothiazole based inhibitor |
|
61
|
275
|
3c4cA |
B-raf kinase in complex with plx4720 |
|
90
|
317
|
3c0gA |
Cask cam-kinase domain- 3'-amp complex, p1 form |
|
83
|
287
|
3brbA |
Crystal structure of catalytic domain of the proto-oncogene tyrosine-protein kinase mer in complex with adp |
|
73
|
293
|
3blaA |
Synthetic gene encoded dcps bound to inhibitor dg153249 |
|
88
|
278
|
3bqrA |
Crystal structure of human death associated protein kinase 3 (dapk3) in complex with an imidazo-pyridazine ligand |
|
86
|
320
|
3blrA |
Crystal structure of human cdk9/cyclint1 in complex with flavopiridol |
|
103
|
348
|
3bx5A |
P38 alpha map kinase complexed with bms-640994 |
|
91
|
297
|
3bu3A |
Crystal structure of the insulin receptor kinase in complex with irs2 krlb peptide |
|
81
|
319
|
3blqA |
Crystal structure of human cdk9/cyclint1 in complex with atp |
|
77
|
271
|
3byuA |
Co-crystal structure of lck and aminopyrimidine reverse amide 23 |
|
102
|
347
|
3bv2A |
Morpholino pyrrolotriazine p38 alpha map kinase inhibitor compound 30 |
|
88
|
278
|
3bi6A |
Wee1 kinase complex with inhibitor pd352396 |
|
84
|
271
|
3byoA |
X-ray co-crystal structure of 2-amino-6-phenylpyrimido[5',4':5,6]pyrimido[1,2-a]benzimidazol-5(6h)-one 25 bound to lck |
|
89
|
297
|
3bu5A |
Crystal structure of the insulin receptor kinase in complex with irs2 krlb peptide and atp |
|
78
|
318
|
3blhA |
Crystal structure of human cdk9/cyclint1 |
|
81
|
293
|
3bl9A |
Synthetic gene encoded dcps bound to inhibitor dg157493 |
|
104
|
341
|
3bwjA |
Complex of pka with the bisubstrate protein kinase inhibitor lead compound arc-1034 |
|
89
|
297
|
3bu6A |
Crystal structure of the insulin receptor kinase in complex with irs2 krlb phosphopeptide |
|
101
|
348
|
3bv3A |
Morpholino pyrrolotriazine p38 alpha map kinase inhibitor compound 2 |
|
112
|
328
|
3bqcA |
High ph-value crystal structure of emodin in complex with the catalytic subunit of protein kinase ck2 |
|
114
|
373
|
3bkbA |
Crystal structure of human feline sarcoma viral oncogene homologue (v-fes) |
|
75
|
293
|
3bl7A |
Synthetic gene encoded dcps bound to inhibitor dg156844 |
|
82
|
272
|
3bysA |
Co-crystal structure of lck and aminopyrimidine amide 10b |
|
76
|
289
|
3bprA |
Crystal structure of catalytic domain of the proto-oncogene tyrosine-protein kinase mer in complex with inhibitor c52 |
|
81
|
289
|
3bceA |
Crystal structure of the erbb4 kinase |
|
87
|
276
|
3bhyA |
Crystal structure of human death associated protein kinase 3 (dapk3) in complex with a beta-carboline ligand |
|
83
|
277
|
3bizA |
Wee1 kinase complex with inhibitor pd331618 |
|
78
|
273
|
3bgzA |
Human pim-1 kinase in complex with diphenyl indole inhibitor vx3 |
|
78
|
314
|
3belA |
X-ray structure of egfr in complex with oxime inhibitor |
|
82
|
300
|
3bhuA |
Structure of phosphorylated thr160 cdk2/cyclin a in complex with the inhibitor meriolin 5 |
|
79
|
273
|
3bgqA |
Human pim-1 kinase in complex with an triazolo pyridazine inhibitor vx2 |
|
110
|
328
|
3be9A |
Structure-based design and synthesis of novel macrocyclic pyrazolo[1,5-a] [1,3,5]triazine compounds as potent inhibitors of protein kinase ck2 and their anticancer activities |
|
65
|
291
|
3bbtB |
Crystal structure of the erbb4 kinase in complex with lapatinib |
|
81
|
370
|
3begA |
Crystal structure of sr protein kinase 1 complexed to its substrate asf/sf2 |
|
90
|
293
|
3bhhA |
Crystal structure of human calcium/calmodulin-dependent protein kinase iib isoform 1 (camk2b) |
|
82
|
273
|
3bgpA |
Human pim-1 complexed with a benzoisoxazole inhibitor vx1 |
|
101
|
312
|
3be2A |
Crystal structure of the vegfr2 kinase domain in complex with a benzamide inhibitor |
|
85
|
300
|
3bhtA |
Structure of phosphorylated thr160 cdk2/cyclin a in complex with the inhibitor meriolin 3 |
|
96
|
320
|
3beaA |
Cfms tyrosine kinase (tie2 kid) in complex with a pyrimidinopyridone inhibitor |
|
82
|
300
|
3bhvA |
Structure of phosphorylated thr160 cdk2/cyclin a in complex with the inhibitor variolin b |
|
69
|
284
|
3bbwA |
Crystal structure of the erbb4 kinase in its inactive conformation |
|
73
|
263
|
3b2wA |
Crystal structure of pyrimidine amide 11 bound to lck |
|
96
|
311
|
3b8qA |
Crystal structure of the vegfr2 kinase domain in complex with a naphthamide inhibitor |
|
93
|
305
|
3b2tA |
Structure of phosphotransferase |
|
106
|
329
|
3axwA |
Crystal structure of human ck2alpha complexed with a potent inhibitor |
|
98
|
311
|
3b8rA |
Crystal structure of the vegfr2 kinase domain in complex with a naphthamide inhibitor |
|
116
|
334
|
3at2A |
Crystal structure of ck2alpha |
|
113
|
332
|
3at3A |
Crystal structure of ck2alpha with pyradine derivative |
