|
80
|
269
|
4ftnA |
Crystal structure of the chk1 |
|
90
|
295
|
4g2fA |
Human epha3 kinase domain in complex with compound 7 |
|
83
|
278
|
4fttA |
Crystal structure of the chk1 |
|
85
|
281
|
4fzaB |
Crystal structure of mst4-mo25 complex |
|
80
|
278
|
4fsmA |
Crystal structure of the chk1 |
|
85
|
274
|
4fvqA |
Crystal structure of the jak2 pseudokinase domain (mg-atp-bound form) |
|
105
|
347
|
4fuxA |
Crystal structure of the erk2 complexed with e75 |
|
79
|
268
|
4ftqA |
Crystal structure of the chk1 |
|
67
|
271
|
4fk3A |
B-raf kinase v600e oncogenic mutant in complex with plx3203 |
|
66
|
264
|
3r22A |
Design, synthesis, and biological evaluation of pyrazolopyridine-sulfonamides as potent multiple-mitotic kinase (mmk) inhibitors (part i) |
|
94
|
292
|
4fijA |
Catalytic domain of human pak4 |
|
79
|
298
|
3qziA |
Cdk2 in complex with inhibitor kvr-1-126 |
|
85
|
377
|
4fieA |
Full-length human pak4 |
|
93
|
302
|
4fnyA |
Crystal structure of the r1275q anaplastic lymphoma kinase catalytic domain in complex with a benzoxazole inhibitor |
|
76
|
254
|
4fexA |
Crystal structure of the aminoglycoside phosphotransferase aph(3')-ia, with substrate kanamycin and small molecule inhibitor tyrphostin ag1478 |
|
83
|
298
|
4fkvA |
Crystal structure of the cdk2 in complex with oxindole inhibitor |
|
72
|
299
|
3r2bA |
Mk2 kinase bound to compound 5b |
|
78
|
298
|
4fkrA |
Crystal structure of the cdk2 in complex with oxindole inhibitor |
|
90
|
316
|
3r1nA |
Mk3 kinase bound to compound 5b |
|
81
|
298
|
3r1sA |
Cdk2 in complex with inhibitor kvr-1-127 |
|
72
|
279
|
4ficA |
Kinase domain of csrc in complex with a hinge region-binding fragment |
|
74
|
269
|
4fg7A |
Crystal structure of human calcium/calmodulin-dependent protein kinase i 1-293 in complex with atp |
|
100
|
310
|
4fobA |
Crystal structure of human anaplastic lymphoma kinase in complex with acyliminobenzimidazole inhibitor 1 |
|
79
|
298
|
4fkjA |
Crystal structure of the cdk2 in complex with aminopyrazole inhibitor |
|
83
|
298
|
3r6xA |
Cdk2 in complex with inhibitor kvr-1-158 |
|
77
|
296
|
4fksA |
Crystal structure of the cdk2 in complex with oxindole inhibitor |
|
80
|
298
|
3r28A |
Cdk2 in complex with inhibitor kvr-1-140 |
|
93
|
294
|
4fifA |
Catalytic domain of human pak4 with rpkplvdp peptide |
|
82
|
298
|
3qzgA |
Cdk2 in complex with inhibitor jws-6-76 |
|
111
|
350
|
4fmqA |
Crystal structure of human erk2 complexed with a mapk docking peptide |
|
77
|
266
|
4fewA |
Crystal structure of the aminoglycoside phosphotransferase aph(3')-ia, with substrate kanamycin and small molecule inhibitor pyrazolopyrimidine pp2 |
|
80
|
298
|
4fkwA |
Crystal structure of the cdk2 in complex with oxindole inhibitor |
|
81
|
275
|
4fc0A |
Crystal structure of human kinase domain of b-raf with a dfg-out inhibitor |
|
83
|
298
|
4fkpA |
Crystal structure of the cdk2 in complex with oxindole inhibitor |
|
84
|
298
|
3r1yA |
Cdk2 in complex with inhibitor kvr-1-134 |
|
82
|
298
|
4fkgA |
Crystal structure of the cdk2 in complex with aminopyrazole inhibitor |
|
80
|
271
|
3r02A |
The discovery of novel benzofuran-2-carboxylic acids as potent pim-1 inhibitors |
|
67
|
279
|
4feqA |
Inhibitor bound structure of the kinase domain of the murine receptor tyrosine kinase tyro3 (sky) |
|
102
|
322
|
4fnwA |
Crystal structure of the apo f1174l anaplastic lymphoma kinase catalytic domain |
|
117
|
333
|
4fbxA |
Complex structure of human protein kinase ck2 catalytic subunit crystallized in the presence of a bisubstrate inhibitor |
|
83
|
298
|
3r71A |
Cdk2 in complex with inhibitor kvr-1-162 |
|
109
|
327
|
3r0tA |
Crystal structure of human protein kinase ck2 alpha subunit in complex with the inhibitor cx-5279 |
|
74
|
263
|
3r21A |
Design, synthesis, and biological evaluation of pyrazolopyridine-sulfonamides as potent multiple-mitotic kinase (mmk) inhibitors (part i) |
|
85
|
231
|
4fjvA |
Crystal structure of human otubain2 and ubiquitin complex |
|
121
|
346
|
3qyzA |
Crystal structure of erk2 in complex with an inhibitor |
|
85
|
290
|
4fgbA |
Crystal structure of human calcium/calmodulin-dependent protein kinase i apo form |
|
98
|
310
|
4focA |
Crystal structure of human anaplastic lymphoma kinase in complex with acyliminobenzimidazole inhibitor 2 |
|
73
|
300
|
3r2yA |
Mk2 kinase bound to compound 1 |
|
79
|
274
|
3r01A |
The discovery of novel benzofuran-2-carboxylic acids as potent pim-1 inhibitors |
|
71
|
235
|
4fgrA |
X-ray structure of saicar synthetase (purc) from streptococcus pneumoniae complexed with adp and mg2+ |
