84
|
299
|
4eoqA |
Thr 160 phosphorylated cdk2 wt - human cyclin a3 complex with atp |
86
|
298
|
4eokA |
Thr 160 phosphorylated cdk2 h84s, q85m, k89d - human cyclin a3 complex with the inhibitor nu6102 |
78
|
298
|
4ek6A |
Crystal structure of the cdk2 in complex with aminopyrazole inhibitor |
87
|
300
|
4eosA |
Thr 160 phosphorylated cdk2 wt - human cyclin a3 complex with the inhibitor ro3306 |
86
|
296
|
4ek4A |
Crystal structure of the cdk2 in complex with aminopyrazole inhibitor |
88
|
333
|
4ec8A |
Structure of full length cdk9 in complex with cyclint and drb |
82
|
298
|
4eorA |
Thr 160 phosphorylated cdk2 wt - human cyclin a3 complex with the inhibitor nu6102 |
88
|
298
|
4eolA |
Thr 160 phosphorylated cdk2 h84s, q85m, k89d - human cyclin a3 complex with the inhibitor ro3306 |
87
|
296
|
4ek3A |
Crystal structure of apo cdk2 |
91
|
300
|
4eopA |
Thr 160 phosphorylated cdk2 q131e - human cyclin a3 complex with the inhibitor ro3306 |
83
|
299
|
4eomA |
Thr 160 phosphorylated cdk2 h84s, q85m, q131e - human cyclin a3 complex with atp |
85
|
300
|
4eonA |
Thr 160 phosphorylated cdk2 h84s, q85m, q131e - human cyclin a3 complex with the inhibitor ro3306 |
85
|
299
|
4eoiA |
Thr 160 phosphorylated cdk2 k89d, q131e - human cyclin a3 complex with the inhibitor ro3306 |
82
|
296
|
4d1xA |
Cdk2 in complex with luciferin |
74
|
293
|
4d1zA |
Cdk2 in complex with a luciferin derivate |
80
|
333
|
4cxaA |
Crystal structure of the human cdk12-cyclin k complex bound to amppnp |
105
|
362
|
4crlA |
Crystal structure of human cdk8-cyclin c in complex with cortistatin a |
80
|
299
|
4cfxA |
Structure-based design of c8-substituted o6-cyclohexylmethoxyguanine cdk1 and 2 inhibitors. |
86
|
300
|
4cfwA |
Structure-based design of c8-substituted o6-cyclohexylmethoxyguanine cdk1 and 2 inhibitors. |
87
|
297
|
4cfmA |
Structure-based design of c8-substituted o6-cyclohexylmethoxyguanine cdk1 and 2 inhibitors. |
88
|
301
|
4cfvA |
Structure-based design of c8-substituted o6-cyclohexylmethoxyguanine cdk1 and 2 inhibitors. |
82
|
298
|
4bzdA |
Structure of cdk2 in complex with a benzimidazopyrimidine |
87
|
302
|
4cfuA |
Structure-based design of c8-substituted o6-cyclohexylmethoxyguanine cdk1 and 2 inhibitors. |
87
|
300
|
4cfnA |
Structure-based design of c8-substituted o6-cyclohexylmethoxyguanine cdk1 and 2 inhibitors. |
88
|
299
|
4bcoA |
Structure of cdk2 in complex with cyclin a and a 2-amino-4-heteroaryl- pyrimidine inhibitor |
87
|
299
|
4bcmA |
Structure of cdk2 in complex with cyclin a and a 2-amino-4-heteroaryl- pyrimidine inhibitor |
100
|
316
|
4bbmA |
Crystal structure of the human cdkl2 kinase domain with bound tcs 2312 |
83
|
299
|
4bcnA |
Structure of cdk2 in complex with cyclin a and a 2-amino-4-heteroaryl- pyrimidine inhibitor |
78
|
294
|
4bgqA |
Crystal structure of the human cdkl5 kinase domain |
80
|
299
|
4bckA |
Structure of cdk2 in complex with cyclin a and a 2-amino-4-heteroaryl- pyrimidine inhibitor |
76
|
298
|
4bcqA |
Structure of cdk2 in complex with cyclin a and a 2-amino-4-heteroaryl- pyrimidine inhibitor |
87
|
321
|
4bcgA |
Structure of cdk9 in complex with cyclin t and a 2-amino-4-heteroaryl- pyrimidine inhibitor |
81
|
298
|
4bghA |
Crystal structure of cdk2 in complex with pan-cdk inhibitor |
84
|
321
|
4bchA |
Structure of cdk9 in complex with cyclin t and a 2-amino-4-heteroaryl- pyrimidine inhibitor |
85
|
321
|
4bcfA |
Structure of cdk9 in complex with cyclin t and a 2-amino-4-heteroaryl- pyrimidine inhibitor |
78
|
291
|
4auaA |
Liganded x-ray crystal structure of cyclin dependent kinase 6 (cdk6) |
87
|
299
|
4bcpA |
Structure of cdk2 in complex with cyclin a and a 2-amino-4-heteroaryl- pyrimidine inhibitor |
83
|
321
|
4bcjA |
Structure of cdk9 in complex with cyclin t and a 2-amino-4-heteroaryl- pyrimidine inhibitor |
82
|
322
|
4bciA |
Structure of cdk9 in complex with cyclin t and a 2-amino-4-heteroaryl- pyrimidine inhibitor |
94
|
307
|
4aaaA |
Crystal structure of the human cdkl2 kinase domain |
80
|
298
|
4acmA |
Cdk2 in complex with 3-amino-6-(4-{[2-(dimethylamino)ethyl]sulfamoyl}-phenyl)-n-pyridin-3-ylpyrazine-2-carboxamide |
86
|
290
|
4aguA |
Crystal structure of the human cdkl1 kinase domain |
77
|
298
|
3wblA |
Crystal structure of cdk2 in complex with pyrazolopyrimidine inhibitor |
89
|
309
|
3zduA |
Crystal structure of the human cdkl3 kinase domain |
78
|
298
|
3uliA |
Human cyclin dependent kinase 2 (cdk2) bound to azabenzimidazole derivative |
84
|
298
|
3unjA |
Cdk2 in complex with inhibitor yl1-038-31 |
86
|
299
|
3tnwA |
Structure of cdk2/cyclin a in complex with can508 |
89
|
318
|
3tn8A |
Cdk9/cyclin t in complex with can508 |
80
|
321
|
3tnhA |
Cdk9/cyclin t in complex with can508 |
82
|
319
|
3tniA |
Structure of cdk9/cyclin t f241l |