|
178
|
600
|
3w1bA |
Crystal structure of human dna ligase iv-artemis complex (mercury derivative) |
|
165
|
447
|
3vw7A |
Crystal structure of human protease-activated receptor 1 (par1) bound with antagonist vorapaxar at 2.2 angstrom |
|
209
|
617
|
3w6wA |
Crystal structure of melb holo-protyrosinase from asperugillus oryzae |
|
83
|
269
|
3vw6A |
Crystal structure of human apoptosis signal-regulating kinase 1 (ask1) with imidazopyridine inhibitor |
|
90
|
322
|
3vvhA |
X-ray structure of the human mitogen-activated protein kinase kinase 1 (mek1) in complex with an inhibitor and mgatp |
|
91
|
251
|
3w68A |
Crystal structure of mouse alpha-tocopherol transfer protein in complex with alpha-tocopherol and phosphatidylinositol-(4,5)-bisphosphate |
|
92
|
320
|
3w2rA |
Egfr kinase domain t790m/l858r mutant with compound 4 |
|
71
|
263
|
3w16A |
Structure of aurora kinase a complexed to pyrazole-aminoquinoline inhibitor iii |
|
187
|
540
|
3vwaA |
Crystal structure of cex1p |
|
60
|
153
|
3w6dA |
Crystal structure of catalytic domain of chitinase from ralstonia sp. a-471 (e141q) in complex with tetrasaccharide |
|
86
|
347
|
3w55A |
The structure of erk2 in complex with fr148083 |
|
98
|
253
|
3w0aA |
Crystal structure analysis of vitamin d receptor |
|
52
|
261
|
3w2cA |
Structure of aurora kinase a complexed to benzoimidazole-indazole inhibitor xv |
|
116
|
284
|
3w7fA |
Crystal structure of the c(30) carotenoid dehydrosqualene synthase from staphylococcus aureus complexed with farnesyl thiopyrophosphate |
|
117
|
447
|
3vs6A |
Crystal structure of hck complexed with a pyrazolo-pyrimidine inhibitor tert-butyl {4-[4-amino-1-(propan-2-yl)-1h-pyrazolo[3,4-d]pyrimidin-3-yl]-2-methoxyphenyl}carbamate |
|
98
|
361
|
3vumA |
Crystal structure of a cysteine-deficient mutant m7 in map kinase jnk1 |
|
99
|
253
|
3w0jA |
Crystal structure of rat vdr ligand binding domain in complex with novel nonsecosteroidal ligands |
|
73
|
184
|
3vvyA |
Crystal strucuture of the ethidium-bound form of ramr (transcriptional regurator of tetr family) from salmonella typhimurium |
|
118
|
367
|
3vyuB |
Crystal structure of the hypc-hypd-hype complex (form ii) |
|
58
|
151
|
3w6cA |
Crystal structure of catalytic domain of chitinase from ralstonia sp. a-471 in complex with disaccharide |
|
174
|
596
|
3w5oA |
Crystal structure of human dna ligase iv |
|
67
|
263
|
3w18A |
Structure of aurora kinase a complexed to benzoimidazole-indazole inhibitor xiii |
|
53
|
141
|
3w4uA |
Human zeta-2 beta-2-s hemoglobin |
|
29
|
67
|
3w8iB |
Crystal structure of ccm3 in complex with the c-terminal regulatory domain of mst4 |
|
134
|
371
|
3vyrB |
Crystal structure of the hypc-hypd complex |
|
99
|
322
|
3w2pA |
Egfr kinase domain t790m/l858r mutant with compound 2 |
|
72
|
191
|
3vvxA |
Crystal strucuture of ramr (transcriptional regurator of tetr family) from salmonella typhimurium |
|
97
|
253
|
3w0yA |
Crystal structure analysis of vitamin d receptor |
|
72
|
227
|
3vmsA |
Crystal structure of staphylococcus aureus membrane-bound transglycosylase in complex with nbd-lipid ii |
|
100
|
253
|
3w5tA |
Crystal structure of complexes of vitamin d receptor ligand binding domain with lithocholic acid derivatives |
|
97
|
258
|
3w0hA |
Crystal structure of rat vdr ligand binding domain in complex with novel nonsecosteroidal ligands |
|
94
|
328
|
3vw8A |
Crystal structure of human c-met kinase domain with its inhibitor |
|
67
|
226
|
3vyhB |
Crystal structure of aw116r mutant of nitrile hydratase from pseudonocardia thermophilla |
|
105
|
296
|
3w6zA |
Crystal structure of nadp bound l-serine 3-dehydrogenase (k170m) from hyperthermophilic archaeon pyrobaculum calidifontis |
|
230
|
612
|
3vwsA |
Dengue serotype 3 rna-dependent rna polymerase bound to nitd-107 |
|
59
|
158
|
3w6eA |
Crystal structure of catalytic domain of chitinase from ralstonia sp. a-471 (e162q) |
|
95
|
321
|
3w2oA |
Egfr kinase domain t790m/l858r mutant with tak-285 |
|
95
|
251
|
3vt7A |
Crystal structures of rat vdr-lbd with w282r mutation |
|
72
|
184
|
3vw2A |
Crystal strucuture of the berberine-bound form of ramr (transcriptional regurator of tetr family) from salmonella typhimurium |
|
101
|
251
|
3vjtA |
Vitamin d receptor complex with a carborane compound |
|
84
|
267
|
3vqyA |
Crystal structure of the catalytic domain of pyrrolysyl-trna synthetase in complex with boclys and amppnp (form 2) |
|
104
|
359
|
3vugA |
Crystal structure of a cysteine-deficient mutant m2 in map kinase jnk1 |
|
143
|
407
|
3vm4A |
Cytochrome p450sp alpha (cyp152b1) in complex with (r)-ibuprophen |
|
125
|
286
|
3vpmA |
Crystal structure of human ribonucleotide reductase subunit m2 (hrrm2) mutant |
|
136
|
407
|
3vnoA |
Cytochrome p450sp alpha (cyp152b1) mutant r241e |
|
116
|
447
|
3vs2A |
Crystal structure of hck complexed with a pyrrolo-pyrimidine inhibitor 7-[cis-4-(4-methylpiperazin-1-yl)cyclohexyl]-5-(4-phenoxyphenyl)-7h-pyrrolo[2,3-d]pyrimidin-4-amine |
|
62
|
187
|
3voxA |
X-ray crystal structure of wild type hrtr in the apo form |
|
98
|
309
|
3vrnA |
Crystal structure of the tyrosine kinase binding domain of cbl-c |
|
98
|
251
|
3vt4A |
Crystal structures of rat vdr-lbd with r270l mutation |
|
103
|
271
|
3vn2A |
Crystal structure of ppargamma complexed with telmisartan |
