|
82
|
274
|
3mssA |
Abl kinase in complex with imatinib and fragment (frag2) in the myristate site |
|
90
|
291
|
3lxnA |
Structural and thermodynamic characterization of the tyk2 and jak3 kinase domains in complex with cp-690550 and cmp-6 |
|
89
|
284
|
3lxkA |
Structural and thermodynamic characterization of the tyk2 and jak3 kinase domains in complex with cp-690550 and cmp-6 |
|
78
|
265
|
3miyA |
X-ray crystal structure of itk complexed with sunitinib |
|
88
|
285
|
3lxlA |
Structural and thermodynamic characterization of the tyk2 and jak3 kinase domains in complex with cp-690550 and cmp-6 |
|
73
|
261
|
3mj1A |
X-ray crystal structure of itk complexed with inhibitor ro5191614 |
|
81
|
259
|
3mj2A |
X-ray crystal structure of itk complexed with inhibitor bms-509744 |
|
97
|
291
|
3lxpA |
Structural and thermodynamic characterization of the tyk2 and jak3 kinase domains in complex with cp-690550 and cmp-6 |
|
68
|
277
|
3lokA |
Drug resistant csrc kinase domain in complex with covalent inhibitor pd168393 |
|
100
|
290
|
3lpbA |
Crystal structure of jak2 complexed with a potent 2,8-diaryl-quinoxaline inhibitor |
|
92
|
271
|
3lckA |
The kinase domain of human lymphocyte kinase (lck), activated form (auto-phosphorylated on tyr394) |
|
82
|
264
|
3kxzA |
The complex crystal structure of lck with a probe molecule w259 |
|
90
|
284
|
3kfaA |
Structural analysis of dfg-in and dfg-out dual src-abl inhibitors sharing a common vinyl purine template |
|
99
|
293
|
3krrA |
Crystal structure of jak2 complexed with a potent quinoxaline atp site inhibitor |
|
88
|
286
|
3kf4A |
Structural analysis of dfg-in and dfg-out dual src-abl inhibitors sharing a common vinyl purine template |
|
83
|
271
|
3kmmA |
Structure of human lck kinase with a small molecule inhibitor |
|
92
|
289
|
3kckA |
A novel chemotype of kinase inhibitors |
|
25
|
100
|
3k2mA |
Crystal structure of monobody ha4/abl1 sh2 domain complex |
|
88
|
287
|
3k5vA |
Structure of abl kinase in complex with imatinib and gnf-2 |
|
89
|
289
|
3jy9A |
Janus kinase 2 inhibitors |
|
81
|
267
|
3k54A |
Structures of human bruton's tyrosine kinase in active and inactive conformations suggests a mechanism of activation for tec family kinases. |
|
96
|
289
|
3io7A |
2-aminopyrazolo[1,5-a]pyrimidines as potent and selective inhibitors of jak2 |
|
97
|
289
|
3iokA |
2-aminopyrazolo[1,5-a]pyrimidines as potent and selective inhibitors of jak2 |
|
88
|
286
|
3ik3A |
Ap24534, a pan-bcr-abl inhibitor for chronic myeloid leukemia, potently inhibits the t315i mutant and overcomes mutation-based resistance |
|
81
|
277
|
3h3cA |
Crystal structure of pyk2 in complex with sulfoximine-substituted trifluoromethylpyrimidine analog |
|
15
|
107
|
3hckA |
Nmr ensemble of the uncomplexed human hck sh2 domain, 20 structures |
|
85
|
268
|
3hmiA |
The crystal structure of human abl2 in complex with 5-amino-3-{[4-(aminosulfonyl)phenyl]amino}-n-(2,6-difluorophenyl)-1h-1,2,4-triazole-1-carbothioamide |
|
55
|
133
|
3gm3A |
Crystal structure of the focal adhesion targeting (fat) domain of pyk2 |
|
11
|
59
|
3h0fA |
Crystal structure of the human fyn sh3 r96w mutant |
|
11
|
59
|
3h0iA |
Human fyn sh3 domain r96i mutant, crystal form ii |
|
51
|
127
|
3gm2A |
Crystal structure of the focal adhesion targeting (fat) domain of pyk2 |
|
91
|
267
|
3genA |
The 1.6 a crystal structure of human bruton's tyrosine kinase bound to a pyrrolopyrimidine-containing compound |
|
10
|
63
|
3h0hA |
Human fyn sh3 domain r96i mutant, crystal form i |
|
57
|
140
|
3gm1A |
Crystal structure of the focal adhesion targeting (fat) domain of pyk2 in complex with paxillin ld4 motif-derived peptides |
|
77
|
286
|
3geqA |
Structural basis for the chemical rescue of src kinase activity |
|
83
|
278
|
3gvuA |
The crystal structure of human abl2 in complex with gleevec |
|
81
|
278
|
3g6gA |
Equally potent inhibition of c-src and abl by compounds that recognize inactive kinase conformations |
|
92
|
277
|
3fqsA |
Crystal structure of spleen tyrosine kinase complexed with r406 |
|
92
|
290
|
3fupA |
Crystal structures of jak1 and jak2 inhibitor complexes |
|
74
|
273
|
3fzrA |
Crystal structure of pyk2 complexed with pf-431396 |
|
78
|
276
|
3g6hA |
Src thr338ile inhibited in the dfg-asp-out conformation |
|
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 |
