|
114
|
376
|
3cblA |
Crystal structure of human feline sarcoma viral oncogene homologue (v-fes) in complex with staurosporine and a consensus peptide |
|
79
|
273
|
3c4eA |
Pim-1 kinase domain in complex with 3-aminophenyl-7-azaindole |
|
95
|
300
|
3c0hA |
Cask cam-kinase domain- amppnp complex, p1 form |
|
112
|
328
|
3c13A |
Low ph-value crystal structure of emodin in complex with the catalytic subunit of protein kinase ck2 |
|
85
|
293
|
3cd8A |
X-ray structure of c-met with triazolopyridazine inhibitor. |
|
99
|
349
|
3c9wA |
Crystal structure of erk-2 with hypothemycin covalently bound |
|
61
|
275
|
3c4cA |
B-raf kinase in complex with plx4720 |
|
90
|
317
|
3c0gA |
Cask cam-kinase domain- 3'-amp complex, p1 form |
|
84
|
292
|
3ccnA |
X-ray structure of c-met with triazolopyridazine inhibitor. |
|
161
|
503
|
3c4wA |
Crystal structure of g protein coupled receptor kinase 1 bound to atp and magnesium chloride at 2.7a |
|
89
|
302
|
3c4fA |
Fgfr tyrosine kinase domain in complex with 3-(3-methoxybenzyl)-7-azaindole |
|
96
|
298
|
3c0iA |
Cask cam-kinase domain- 3'-amp complex, p212121 form |
|
91
|
276
|
3bz3A |
Crystal structure analysis of focal adhesion kinase with a methanesulfonamide diaminopyrimidine inhibitor |
|
99
|
356
|
3cgfA |
Irak-4 inhibitors (part ii)- a structure based assessment of imidazo[1,2 a]pyridine binding |
|
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 |
|
77
|
311
|
3c1xA |
Crystal structure of the tyrosine kinase domain of the hepatocyte growth factor receptor c-met in complex with a pyrrolotriazine based inhibitor |
|
90
|
272
|
3bymA |
X-ray co-crystal structure aminobenzimidazole triazine 1 bound to lck |
|
69
|
307
|
3ce3A |
Crystal structure of the tyrosine kinase domain of the hepatocyte growth factor receptor c-met in complex with a pyrrolopyridinepyridone based inhibitor |
|
162
|
504
|
3c50A |
Crystal structure of g protein coupled receptor kinase 1 bound to adp and magnesium chloride at 2.6a |
|
94
|
356
|
3cgoA |
Irak-4 inhibitors (part ii)- a structure based assessment of imidazo[1,2 a]pyridine binding |
|
104
|
376
|
3cd3A |
Crystal structure of phosphorylated human feline sarcoma viral oncogene homologue (v-fes) in complex with staurosporine and a consensus peptide |
|
155
|
504
|
3c4xA |
Crystal structure of g protein coupled receptor kinase 1 bound to atp and magnesium chloride at 2.9a |
|
91
|
297
|
3bu3A |
Crystal structure of the insulin receptor kinase in complex with irs2 krlb peptide |
|
83
|
287
|
3brbA |
Crystal structure of catalytic domain of the proto-oncogene tyrosine-protein kinase mer in complex with adp |
|
86
|
320
|
3blrA |
Crystal structure of human cdk9/cyclint1 in complex with flavopiridol |
|
88
|
278
|
3bqrA |
Crystal structure of human death associated protein kinase 3 (dapk3) in complex with an imidazo-pyridazine ligand |
|
81
|
319
|
3blqA |
Crystal structure of human cdk9/cyclint1 in complex with atp |
|
103
|
348
|
3bx5A |
P38 alpha map kinase complexed with bms-640994 |
|
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 |
|
88
|
278
|
3bi6A |
Wee1 kinase complex with inhibitor pd352396 |
|
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 |
|
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 |
|
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) |
|
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 |
|
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 |
|
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 |
