|
124
|
447
|
2c0oA |
Src family kinase hck with bound inhibitor a-770041 |
|
80
|
296
|
2c5nA |
Differential binding of inhibitors to active and inactive cdk2 provides insights for drug design |
|
78
|
264
|
2c6dA |
Aurora a kinase activated mutant (t287d) in complex with adpnp |
|
125
|
447
|
2c0tA |
Src family kinase hck with bound inhibitor a-641359 |
|
78
|
265
|
2c3jA |
Identification of a buried pocket for potent and selective inhibition of chk1: prediction and verification |
|
107
|
337
|
2c1aA |
Structure of camp-dependent protein kinase complexed with isoquinoline-5-sulfonic acid (2-(2-(4-chlorobenzyloxy)ethylamino) ethyl)amide |
|
61
|
288
|
2bvaA |
Crystal structure of the human p21-activated kinase 4 |
|
76
|
275
|
2broA |
Structure-based design of novel chk1 inhibitors: insights into hydrogen bonding and protein-ligand affinity |
|
80
|
275
|
2br1A |
Structure-based design of novel chk1 inhibitors: insights into hydrogen bonding and protein-ligand affinity |
|
71
|
298
|
2btsA |
Structure of cdk2 complexed with pnu-230032 |
|
74
|
263
|
2brgA |
Structure-based design of novel chk1 inhibitors: insights into hydrogen bonding and protein-ligand affinity |
|
82
|
273
|
2bzkB |
Crystal structure of the human pim1 in complex with amppnp and pimtide |
|
90
|
302
|
2bpmA |
Structure of cdk2-cyclin a with pha-630529 |
|
84
|
273
|
2bzjA |
Crystal structure of the human pim1 in complex with a ruthenium organometallic ligand ru3 |
|
78
|
275
|
2brbA |
Structure-based design of novel chk1 inhibitors: insights into hydrogen bonding and protein-ligand affinity |
|
87
|
271
|
2bfyA |
Complex of aurora-b with incenp and hesperadin. |
|
102
|
355
|
2bajA |
P38alpha bound to pyrazolourea |
|
80
|
298
|
2bheA |
Human cyclin dependent protein kinase 2 in complex with the inhibitor 5-bromo-indirubine |
|
87
|
295
|
2bujA |
Crystal structure of the human serine-threonine kinase 16 in complex with staurosporine |
|
73
|
268
|
2brmA |
Structure-based design of novel chk1 inhibitors: insights into hydrogen bonding and protein-ligand affinity |
|
81
|
274
|
2bilB |
The human protein kinase pim1 in complex with its consensus peptide pimtide |
|
101
|
353
|
2b9iA |
Crystal structure of fus3 with a docking motif from msg5 |
|
75
|
271
|
2brnA |
Structure-based design of novel chk1 inhibitors: insights into hydrogen bonding and protein-ligand affinity |
|
79
|
266
|
2brhA |
Structure-based design of novel chk1 inhibitors: insights into hydrogen bonding and protein-ligand affinity |
|
82
|
287
|
2biyA |
Structure of pdk1-s241a mutant kinase domain |
|
77
|
272
|
2bdfA |
Src kinase in complex with inhibitor ap23451 |
|
101
|
353
|
2b9jA |
Crystal structure of fus3 with a docking motif from far1 |
|
69
|
298
|
2btrA |
Structure of cdk2 complexed with pnu-198873 |
|
76
|
268
|
2bmcA |
Aurora-2 t287d t288d complexed with pha-680632 |
|
87
|
273
|
2bikB |
Human pim1 phosphorylated on ser261 |
|
113
|
309
|
2bdwA |
Crystal structure of the auto-inhibited kinase domain of calcium/calmodulin activated kinase ii |
|
105
|
353
|
2b9hA |
Crystal structure of fus3 with a docking motif from ste7 |
|
100
|
353
|
2b9fA |
Crystal structure of non-phosphorylated fus3 |
|
193
|
640
|
2bcjA |
Crystal structure of g protein-coupled receptor kinase 2 in complex with galpha-q and gbetagamma subunits |
|
104
|
349
|
2bakA |
P38alpha map kinase bound to mpaq |
|
78
|
298
|
2b52A |
Human cyclin dependent kinase 2 (cdk2) complexed with dph-042562 |
|
76
|
268
|
2aypA |
Crystal structure of chk1 with an indol inhibitor |
|
91
|
302
|
2bkzA |
Structure of cdk2-cyclin a with pha-404611 |
|
79
|
265
|
2bdjA |
Src kinase in complex with inhibitor ap23464 |
|
106
|
349
|
2balA |
P38alpha map kinase bound to pyrazoloamine |
|
91
|
290
|
2b7aA |
The structural basis of janus kinase 2 inhibition by a potent and specific pan-janus kinase inhibitor |
|
88
|
270
|
2bfxA |
Mechanism of aurora-b activation by incenp and inhibition by hesperadin. |
|
107
|
347
|
2baqA |
P38alpha bound to ro3201195 |
|
85
|
300
|
2auhA |
Crystal structure of the grb14 bps region in complex with the insulin receptor tyrosine kinase |
|
76
|
298
|
2bhhA |
Human cyclin dependent protein kinase 2 in complex with the inhibitor 4-hydroxypiperindinesulfonyl-indirubine |
|
91
|
297
|
2b4sB |
Crystal structure of a complex between ptp1b and the insulin receptor tyrosine kinase |
|
75
|
298
|
2b54A |
Human cyclin dependent kinase 2 (ckd2)complexed with din-232305 |
|
95
|
289
|
2aqxA |
Crystal structure of the catalytic and cam-binding domains of inositol 1,4,5-trisphosphate 3-kinase b |
|
79
|
298
|
2b55A |
Human cyclin dependent kinase 2 (cdk2) complexed with indenopyraxole din-101312 |
|
81
|
298
|
2b53A |
Human cyclin dependent kinase 2 (cdk2) complexed with din-234325 |
