|
128
|
401
|
4ellA |
Structure of the inactive retinoblastoma protein pocket domain |
|
96
|
257
|
4eolB |
Thr 160 phosphorylated cdk2 h84s, q85m, k89d - human cyclin a3 complex with the inhibitor ro3306 |
|
89
|
251
|
4ec9B |
Crystal structure of full-length cdk9 in complex with cyclin t |
|
94
|
257
|
4eopB |
Thr 160 phosphorylated cdk2 q131e - human cyclin a3 complex with the inhibitor ro3306 |
|
92
|
252
|
4ec8B |
Structure of full length cdk9 in complex with cyclint and drb |
|
96
|
258
|
4eooB |
Thr 160 phosphorylated cdk2 q131e - human cyclin a3 complex with atp |
|
91
|
257
|
4eonB |
Thr 160 phosphorylated cdk2 h84s, q85m, q131e - human cyclin a3 complex with the inhibitor ro3306 |
|
91
|
257
|
4eosB |
Thr 160 phosphorylated cdk2 wt - human cyclin a3 complex with the inhibitor ro3306 |
|
98
|
258
|
4eoiB |
Thr 160 phosphorylated cdk2 k89d, q131e - human cyclin a3 complex with the inhibitor ro3306 |
|
97
|
257
|
4eomB |
Thr 160 phosphorylated cdk2 h84s, q85m, q131e - human cyclin a3 complex with atp |
|
96
|
257
|
4eoqB |
Thr 160 phosphorylated cdk2 wt - human cyclin a3 complex with atp |
|
98
|
257
|
4eojB |
Thr 160 phosphorylated cdk2 h84s, q85m, k89d - human cyclin a3 complex with atp |
|
96
|
257
|
4eorB |
Thr 160 phosphorylated cdk2 wt - human cyclin a3 complex with the inhibitor nu6102 |
|
93
|
258
|
4eokB |
Thr 160 phosphorylated cdk2 h84s, q85m, k89d - human cyclin a3 complex with the inhibitor nu6102 |
|
86
|
246
|
4cxaB |
Crystal structure of the human cdk12-cyclin k complex bound to amppnp |
|
97
|
266
|
4crlB |
Crystal structure of human cdk8-cyclin c in complex with cortistatin a |
|
93
|
258
|
4cfmB |
Structure-based design of c8-substituted o6-cyclohexylmethoxyguanine cdk1 and 2 inhibitors. |
|
98
|
258
|
4cfwB |
Structure-based design of c8-substituted o6-cyclohexylmethoxyguanine cdk1 and 2 inhibitors. |
|
98
|
256
|
4cfnB |
Structure-based design of c8-substituted o6-cyclohexylmethoxyguanine cdk1 and 2 inhibitors. |
|
97
|
262
|
4cfvB |
Structure-based design of c8-substituted o6-cyclohexylmethoxyguanine cdk1 and 2 inhibitors. |
|
92
|
262
|
4cfuD |
Structure-based design of c8-substituted o6-cyclohexylmethoxyguanine cdk1 and 2 inhibitors. |
|
88
|
257
|
4bcqB |
Structure of cdk2 in complex with cyclin a and a 2-amino-4-heteroaryl- pyrimidine inhibitor |
|
99
|
255
|
4bcnD |
Structure of cdk2 in complex with cyclin a and a 2-amino-4-heteroaryl- pyrimidine inhibitor |
|
91
|
257
|
4bckB |
Structure of cdk2 in complex with cyclin a and a 2-amino-4-heteroaryl- pyrimidine inhibitor |
|
39
|
193
|
4bbrM |
Structure of rna polymerase ii-tfiib complex |
|
98
|
257
|
4bcmB |
Structure of cdk2 in complex with cyclin a and a 2-amino-4-heteroaryl- pyrimidine inhibitor |
|
89
|
252
|
4bchB |
Structure of cdk9 in complex with cyclin t and a 2-amino-4-heteroaryl- pyrimidine inhibitor |
|
87
|
253
|
4bcmD |
Structure of cdk2 in complex with cyclin a and a 2-amino-4-heteroaryl- pyrimidine inhibitor |
|
86
|
252
|
4bcjB |
Structure of cdk9 in complex with cyclin t and a 2-amino-4-heteroaryl- pyrimidine inhibitor |
|
81
|
256
|
4bcqD |
Structure of cdk2 in complex with cyclin a and a 2-amino-4-heteroaryl- pyrimidine inhibitor |
|
89
|
252
|
4bcfB |
Structure of cdk9 in complex with cyclin t and a 2-amino-4-heteroaryl- pyrimidine inhibitor |
|
98
|
257
|
4bcnB |
Structure of cdk2 in complex with cyclin a and a 2-amino-4-heteroaryl- pyrimidine inhibitor |
|
96
|
257
|
4bcpB |
Structure of cdk2 in complex with cyclin a and a 2-amino-4-heteroaryl- pyrimidine inhibitor |
|
91
|
252
|
4bciB |
Structure of cdk9 in complex with cyclin t and a 2-amino-4-heteroaryl- pyrimidine inhibitor |
|
89
|
252
|
4bcgB |
Structure of cdk9 in complex with cyclin t and a 2-amino-4-heteroaryl- pyrimidine inhibitor |
|
98
|
258
|
4bcoB |
Structure of cdk2 in complex with cyclin a and a 2-amino-4-heteroaryl- pyrimidine inhibitor |
|
102
|
348
|
4roeA |
Human tfiib-related factor 2 (brf2) and tbp bound to rpph1 promoter |
|
59
|
212
|
3x24B |
Crystal structure of nitrile hydratase mutant br56k complexed with trimethylacetonitrile, photo-activated for 120 min |
|
59
|
212
|
3x26B |
Crystal structure of nitrile hydratase mutant br56k complexed with trimethylacetonitrile, photo-activated for 5 min |
|
59
|
212
|
3x25B |
Crystal structure of nitrile hydratase mutant br56k complexed with trimethylacetonitrile, photo-activated for 700 min |
|
59
|
212
|
3wvdB |
Crystal structure of nitrile hydratase mutant br56k complexed with trimethylacetonitrile, photo-activated for 50 min |
|
59
|
212
|
3x28B |
Crystal structure of nitrile hydratase mutant br56k |
|
58
|
212
|
3wveB |
Crystal structure of nitrile hydratase mutant br56k complexed with trimethylacetonitrile, before photo-activation |
|
58
|
212
|
3x20B |
Crystal structure of nitrile hydratase mutant br56k complexed with trimethylacetonitrile, photo-activated for 25 min |
|
67
|
226
|
3vyhB |
Crystal structure of aw116r mutant of nitrile hydratase from pseudonocardia thermophilla |
|
42
|
152
|
3vygB |
Crystal structure of thiocyanate hydrolase mutant r136w |
|
283
|
1066
|
3tw7A |
Structure of rhizobium etli pyruvate carboxylase t882a crystallized without acetyl coenzyme-a |
|
331
|
1071
|
3tw6A |
Structure of rhizobium etli pyruvate carboxylase t882a with the allosteric activator, acetyl coenzyme-a |
|
84
|
252
|
3tn8B |
Cdk9/cyclin t in complex with can508 |
|
89
|
251
|
3tnhB |
Cdk9/cyclin t in complex with can508 |
