|
58
|
211
|
3a8hB |
Crystal structure of nitrile hydratase mutant s113a complexed with trimethylacetamide |
|
58
|
212
|
3a8gB |
Crystal structure of nitrile hydratase mutant s113a complexed with trimethylacetonitrile |
|
46
|
153
|
2zzdB |
Recombinant thiocyanate hydrolase, air-oxidized form of holo-enzyme |
|
59
|
211
|
2zpfB |
Complex of fe-type nitrile hydratase with tert-butylisonitrile, photo-activated for 18min at 293k |
|
59
|
211
|
2zphB |
Complex of fe-type nitrile hydratase with tert-butylisonitrile, photo-activated for 340min at 293k |
|
59
|
211
|
2zpbB |
Nitrosylated fe-type nitrile hydratase |
|
59
|
211
|
2zpeB |
Nitrosylated fe-type nitrile hydratase with tert-butylisonitrile |
|
59
|
211
|
2zpiB |
Complex of fe-type nitrile hydratase with tert-butylisonitrile, photo-activated for 440min at 293k |
|
58
|
211
|
2zpgB |
Complex of fe-type nitrile hydratase with tert-butylisonitrile, photo-activated for 120min at 293k |
|
56
|
212
|
2zcfB |
Mutational study on alpha-gln90 of fe-type nitrile hydratase from rhodococcus sp. n771 |
|
89
|
258
|
2wpaB |
Optimisation of 6,6-dimethyl pyrrolo 3,4-c pyrazoles: identification of pha-793887, a potent cdk inhibitor suitable for intravenous dosing |
|
96
|
258
|
2x1nB |
Truncation and optimisation of peptide inhibitors of cdk2, cyclin a through structure guided design |
|
99
|
258
|
2wmbB |
Structural and thermodynamic consequences of cyclization of peptide ligands for the recruitment site of cyclin a |
|
96
|
257
|
2wihB |
Structure of cdk2-cyclin a with pha-848125 |
|
89
|
258
|
2whbB |
Truncation and optimisation of peptide inhibitors of cdk2, cyclin a through structure guided design |
|
95
|
257
|
2wxvB |
Structure of cdk2-cyclin a with a pyrazolo(4,3-h) quinazoline-3- carboxamide inhibitor |
|
93
|
258
|
2wipB |
Structure of cdk2-cyclin a complexed with 8-anilino-1-methyl-4,5-dihydro- 1h-pyrazolo[4,3-h] quinazoline-3-carboxylic acid |
|
100
|
258
|
2wmaB |
Structural and thermodynamic consequences of cyclization of peptide ligands for the recruitment site of cyclin a |
|
92
|
257
|
2wfyB |
Truncation and optimisation of peptide inhibitors of cdk2, cyclin a through structure guided design |
|
91
|
237
|
2w9fA |
Crystal structure of cdk4 in complex with a d-type cyclin |
|
47
|
149
|
2wj9A |
Ardb |
|
91
|
260
|
2w96A |
Crystal structure of cdk4 in complex with a d-type cyclin |
|
95
|
258
|
2wevB |
Truncation and optimisation of peptide inhibitors of cdk2, cyclin a through structure guided design |
|
91
|
246
|
2w99A |
Crystal structure of cdk4 in complex with a d-type cyclin |
|
91
|
246
|
2w9zA |
Crystal structure of cdk4 in complex with a d-type cyclin |
|
358
|
1152
|
2qf7A |
Crystal structure of a complete multifunctional pyruvate carboxylase from rhizobium etli |
|
97
|
257
|
2uzlB |
Crystal structure of human cdk2 complexed with a thiazolidinone inhibitor |
|
95
|
258
|
2uzdB |
Crystal structure of human cdk2 complexed with a thiazolidinone inhibitor |
|
94
|
258
|
2v22B |
Replace: a strategy for iterative design of cyclin binding groove inhibitors |
|
95
|
258
|
2uzbB |
Crystal structure of human cdk2 complexed with a thiazolidinone inhibitor |
|
98
|
258
|
2uzeB |
Crystal structure of human cdk2 complexed with a thiazolidinone inhibitor |
|
93
|
258
|
2uueB |
Replace: a strategy for iterative design of cyclin binding groove inhibitors |
|
130
|
345
|
2r7gA |
Structure of the retinoblastoma protein pocket domain in complex with adenovirus e1a cr1 domain |
|
72
|
216
|
2qgsA |
Crystal structure of se1688 protein from staphylococcus epidermidis. northeast structural genomics consortium target ser89 |
|
59
|
211
|
2qdyB |
Crystal structure of fe-type nhase from rhodococcus erythropolis aj270 |
|
103
|
312
|
2qq8A |
Crystal structure of the putative rabgap domain of human tbc1 domain family member 14 |
|
96
|
304
|
2qdjA |
Crystal structure of the retinoblastoma protein n-domain provides insight into tumor suppression, ligand interaction and holoprotein architecture |
|
121
|
313
|
2qfzA |
Crystal structure of human tbc1 domain family member 22a |
|
69
|
206
|
2phgA |
Model for vp16 binding to tfiib |
|
67
|
231
|
2pmiB |
Structure of the pho85-pho80 cdk-cyclin complex of the phosphate-responsive signal transduction pathway with bound atp-gamma-s |
|
64
|
232
|
2pk9B |
Structure of the pho85-pho80 cdk-cyclin complex of the phosphate-responsive signal transduction pathway |
|
63
|
256
|
2pk2A |
Cyclin box structure of the p-tefb subunit cyclin t1 derived from a fusion complex with eiav tat |
|
66
|
215
|
2pjqA |
Crystal structure of q88u62_lacpl from lactobacillus plantarum. northeast structural genomics target lpr71 |
|
28
|
176
|
2kr6A |
Solution structure of presenilin-1 ctf subunit |
|
31
|
142
|
2kmgA |
The structure of the klca and ardb proteins show a novel fold and antirestriction activity against type i dna restriction systems in vivo but not in vitro |
|
29
|
113
|
2lw4A |
Solution nmr structure of human transcription elongation factor a protein 2, central domain, northeast structural genomics consortium (nesg) target hr8682b |
|
97
|
260
|
2jgzB |
Crystal structure of phospho-cdk2 in complex with cyclin b |
|
95
|
257
|
2iw8B |
Structure of human thr160-phospho cdk2-cyclin a f82h-l83v-h84d mutant with an o6-cyclohexylmethylguanine inhibitor |
|
63
|
208
|
2in3A |
Crystal structure of a putative protein disulfide isomerase from nitrosomonas europaea |
|
94
|
257
|
2iw6B |
Structure of human thr160-phospho cdk2-cyclin a complexed with a bisanilinopyrimidine inhibitor |
