89
|
277
|
3fqeA |
Crystal structure of spleen tyrosine kinase complexed with ym193306 |
92
|
272
|
3fqhA |
Crystal structure of spleen tyrosine kinase complexed with a 2-substituted 7-azaindole |
80
|
277
|
3g5dA |
Kinase domain of csrc in complex with dasatinib |
78
|
274
|
3fzpA |
Crystal structure of pyk2 complexed with atpgs |
81
|
272
|
3fzoA |
Crystal structure of pyk2-apo, proline-rich tyrosine kinase |
80
|
271
|
3fzsA |
Crystal structure of pyk2 complexed with birb796 |
85
|
271
|
3fztA |
Crystal structure of pyk2 complexed with pf-4618433 |
82
|
277
|
3f3uA |
Kinase domain of csrc in complex with inhibitor rl37 (type iii) |
81
|
279
|
3f6xA |
C-src kinase domain in complex with small molecule inhibitor |
6
|
57
|
3fj5A |
Crystal structure of the c-src-sh3 domain |
80
|
277
|
3f3tA |
Kinase domain of csrc in complex with inhibitor rl38 (type iii) |
84
|
277
|
3f3wA |
Drug resistant csrc kinase domain in complex with inhibitor rl45 (type ii) |
81
|
277
|
3f3vA |
Kinase domain of csrc in complex with inhibitor rl45 (type ii) |
85
|
276
|
3eqrA |
Crystal structure of ack1 with compound t74 |
96
|
290
|
3eyhA |
Crystal structures of jak1 and jak2 inhibitor complexes |
73
|
273
|
3et7A |
Crystal structure of pyk2 complexed with pf-2318841 |
83
|
274
|
3eqpA |
Crystal structure of ack1 with compound t95 |
70
|
278
|
3en7A |
Targeted polypharmacology: crystal structure of the c-src kinase domain in complex with s1, a multitargeted kinase inhibitor |
91
|
290
|
3eygA |
Crystal structures of jak1 and jak2 inhibitor complexes |
77
|
276
|
3en4A |
Targeted polypharmacology: crystal structure of the c-src kinase domain in complex with pp121, a multitargeted kinase inhibitor |
71
|
274
|
3en6A |
Targeted polypharmacology: crystal structure of the c-src kinase domain in complex with pp102, a multitargeted kinase inhibitor |
12
|
63
|
3eg3A |
Crystal structure of the n114a mutant of abl-sh3 domain |
78
|
276
|
3el8A |
Crystal structure of c-src in complex with pyrazolopyrimidine 5 |
14
|
63
|
3eg2A |
Crystal structure of the n114q mutant of abl-sh3 domain |
72
|
274
|
3en5A |
Targeted polypharmacology: crystal structure of the c-src kinase domain in complex with pp494, a multitargeted kinase inhibitor |
22
|
101
|
3eacA |
Crystal structure of sh2 domain of human csk (carboxyl-terminal src kinase), oxidized form. |
81
|
267
|
3emgA |
Discovery and sar of novel 4-thiazolyl-2-phenylaminopyrimidines as potent inhibitors of spleen tyrosine kinase (syk) |
10
|
57
|
3eguA |
Crystal structure of the n114a mutant of abl-sh3 domain |
25
|
102
|
3eazA |
Crystal structure of sh2 domain of human csk (carboxyl-terminal src kinase), c122s mutant. |
11
|
58
|
3eg1A |
Crystal structure of the n114q mutant of abl-sh3 domain complexed with a designed high-affinity peptide ligand: implications for sh3-ligand interactions |
68
|
277
|
3el7A |
Crystal structure of c-src in complex with pyrazolopyrimidine 3 |
12
|
56
|
3eg0A |
Crystal structure of the n114t mutant of abl-sh3 domain |
101
|
293
|
3e64A |
Fragment based discovery of jak-2 inhibitors |
99
|
293
|
3e62A |
Fragment based discovery of jak-2 inhibitors |
99
|
292
|
3e63A |
Fragment based discovery of jak-2 inhibitors |
89
|
270
|
3dk7A |
Crystal structure of mutant abl kinase domain in complex with small molecule fragment |
78
|
275
|
3dqxA |
Chicken c-src kinase domain in complex with atpgs |
85
|
279
|
3dqwA |
C-src kinase domain thr338ile mutant in complex with atpgs |
84
|
270
|
3dk6A |
Crystal structure of mutant abl kinase domain in complex with small molecule fragment |
87
|
270
|
3dk3A |
Crystal structure of mutant abl kinase domain in complex with small molecule fragment |
72
|
276
|
3d7tB |
Structural basis for the recognition of c-src by its inactivator csk |
73
|
263
|
3d7uA |
Structural basis for the recognition of c-src by its inactivator csk |
63
|
277
|
3d7uB |
Structural basis for the recognition of c-src by its inactivator csk |
61
|
263
|
3d7tA |
Structural basis for the recognition of c-src by its inactivator csk |
85
|
268
|
3cs9A |
Human abl kinase in complex with nilotinib |
83
|
281
|
3cr0A |
Wee1 kinase complex with inhibitor pd259_809 |
83
|
278
|
3cqeA |
Wee1 kinase complex with inhibitor pd074291 |
71
|
266
|
3cioA |
The kinase domain of escherichia coli tyrosine kinase etk |
12
|
58
|
3cqtA |
N53i v55l mutant of fyn sh3 domain |
114
|
376
|
3cblA |
Crystal structure of human feline sarcoma viral oncogene homologue (v-fes) in complex with staurosporine and a consensus peptide |