|
189
|
494
|
8t0tA |
Structure of compound 4 bound to human aldh1a1 |
|
62
|
218
|
8j1kA |
Co-crystal structure of non-carboxylic acid inhibitor with phd2 |
|
231
|
662
|
8inlA |
Lsd1 in complex with s2172 |
|
146
|
393
|
7n14A |
Crystal structure of 4-(1h-1,2,4-triazol-1-yl)benzoic acid-bound cyp199a4 |
|
42
|
163
|
8f80A |
Crystal structure of dihydrofolate reductase (dhfr) from mycobacterium ulcerans agy99 in complex with nadp and inhibitor mam738 |
|
42
|
163
|
8f81A |
Crystal structure of dihydrofolate reductase (dhfr) from mycobacterium ulcerans agy99 in complex with nadp and inhibitor mam777 |
|
45
|
163
|
8f84A |
Crystal structure of dihydrofolate reductase (dhfr) from mycobacterium ulcerans agy99 in complex with nadp and inhibitor mam787 |
|
44
|
164
|
8f83A |
Crystal structure of dihydrofolate reductase (dhfr) from mycobacterium ulcerans agy99 in complex with nadp and inhibitor mam846 |
|
45
|
163
|
8f82A |
Crystal structure of dihydrofolate reductase (dhfr) from mycobacterium ulcerans agy99 in complex with nadp and inhibitor mam845 |
|
45
|
163
|
8f85A |
Crystal structure of dihydrofolate reductase (dhfr) from mycobacterium ulcerans agy99 in complex with nadp and inhibitor mam851 |
|
108
|
338
|
7u9sA |
Crystal structure of human d-amino acid oxidase in complex with inhibitor |
|
110
|
340
|
7u9uA |
Crystal structure of human d-amino acid oxidase in complex with inhibitor |
|
125
|
374
|
7rm6A |
Horse liver alcohol dehydrogenase in complex with nadh and n-cylcohexyl formamide |
|
75
|
287
|
8evoA |
Sulfatase from mycobacterium tuberculosis (rv3406) in complex with inhibitor fg2216 |
|
68
|
283
|
8evnA |
Sulfatase from mycobacterium tuberculosis (rv3406) in complex with n-oxalylglycine (nog) |
|
107
|
285
|
8g89A |
Hsd17b13 in complex with cofactor and inhibitor |
|
105
|
291
|
8g9vA |
Crystal structures of 17-beta-hydroxysteroid dehydrogenase 13 |
|
229
|
662
|
8ghdA |
The structure of h12-lox in hexameric form bound to inhibitor ml355 and arachidonic acid |
|
231
|
662
|
8gheA |
The structure of h12-lox in tetrameric form bound to endogenous inhibitor oleoyl-coa |
|
97
|
265
|
8g93A |
Crystal structures of 17-beta-hydroxysteroid dehydrogenase 13 |
|
148
|
413
|
8ektA |
Cyp51 from acanthamoeba castellanii in complex with the tetrazole-based ind inhibitor vt-1161(vt1) |
|
112
|
287
|
7y8lA |
Structure of scired-r2-v3 from streptomyces clavuligerus in complex with 5-(2,5-difluorophenyl)-3,4-dihydro-2h-pyrrole |
|
65
|
188
|
8dn0A |
E.coli dsba in complex with n-(2-fluorophenyl)-5-methylisoxazole-3-carboxamide |
|
108
|
287
|
7y8nA |
Structure of scired-r3-v4 from streptomyces clavuligerus in complex with 5-(2,5-difluorophenyl)-3,4-dihydro-2h-pyrrole |
|
117
|
371
|
8er0A |
X-ray crystal structure of tet(x6) bound to anhydrotetracycline |
|
134
|
388
|
8furA |
Crystal structure of human ido1 with compound 11 |
|
145
|
471
|
8ewmA |
Crystal structure of cyp3a4 bound to an inhibitor |
|
150
|
468
|
8ewrA |
Crystal structure of cyp3a4 bound to an inhibitor |
|
148
|
471
|
8ewqA |
Crystal structure of cyp3a4 bound to an inhibitor |
|
144
|
468
|
8exbA |
Crystal structure of cyp3a4 bound to an inhibitor |
|
151
|
471
|
8eweA |
Crystal structure of cyp3a4 bound to an inhibitor |
|
148
|
470
|
8ewpA |
Crystal structure of cyp3a4 bound to an inhibitor |
|
144
|
471
|
8ewsA |
Crystal structure of cyp3a4 bound to an inhibitor |
|
148
|
468
|
8ewdA |
Crystal structure of cyp3a4 bound to an inhibitor |
|
150
|
469
|
8ewnA |
Crystal structure of cyp3a4 bound to an inhibitor |
|
157
|
470
|
8ewlA |
Crystal structure of cyp3a4 bound to an inhibitor |
|
115
|
334
|
7ut5A |
Acinetobacter baumannii dihydroorotate dehydrogenase bound with inhibitor dsm186 |
|
144
|
464
|
8ct4A |
Cryo-em structure of mtb lpd bound to inhibitor complex with 2-((2-cyano-n,5-dimethyl-1h-indole)-7-sulfonamido)-n-(4-(oxetan-3-yl)-3,4-dihydro-2h-benzo[b] [1,4]oxazin-7-yl)acetamide |
|
44
|
170
|
7snwA |
1.80a resolution structure of nanoluc luciferase with bound inhibitor pc 16026576 |
|
127
|
404
|
7vo8A |
Structure of athppd complexed with lsy-1 |
|
131
|
418
|
7s3zA |
Structure of rat neuronal nitric oxide synthase heme domain in complex with n2-((3-((2-aminoquinolin-7-yl)methoxy)phenoxy)methyl)pyridine-2,6-diamine |
|
103
|
369
|
8ecgA |
Complex of hmg1 with pitavastatin |
|
127
|
418
|
7s40A |
Structure of rat neuronal nitric oxide synthase heme domain in complex with 7-((3-((((6-aminopyridin-2-yl)methyl)amino)methyl)phenoxy)methyl)quinolin-2-amine |
|
127
|
418
|
7s3xA |
Structure of rat neuronal nitric oxide synthase heme domain in complex with 7-((3-(((pyridin-2-ylmethyl)amino)methyl)phenoxy)methyl)quinolin-2-amine |
|
129
|
418
|
7s3yA |
Structure ofrat neuronal nitric oxide synthase heme domain in complex with 7-((3-(2-(6-aminopyridin-2-yl)ethyl)phenoxy)methyl)quinolin-2-amine |
|
140
|
469
|
7uazA |
Crystal structure of human cyp3a4 with the caged inhibitor |
|
131
|
468
|
7uayA |
Crystal structure of human cyp3a4 with the caged inhibitor |
|
136
|
367
|
8dhgA |
Dhodh in complex with ligand 19 |
|
138
|
366
|
8dhfA |
Dhodh in complex with ligand 11 |
|
133
|
367
|
8dhhA |
Dhodh in complex with ligand 29 |
