|
116
|
309
|
4h4cA |
Isph in complex with (e)-4-fluoro-3-methylbut-2-enyl diphosphate |
|
112
|
309
|
4h4eA |
Isph in complex with (e)-4-mercapto-3-methylbut-2-enyl diphosphate |
|
54
|
192
|
4hm4B |
Naphthalene 1,2-dioxygenase bound to indan |
|
54
|
192
|
4hm6B |
Naphthalene 1,2-dioxygenase bound to phenetole |
|
55
|
192
|
4hm1B |
Naphthalene 1,2-dioxygenase bound to 1-indanone |
|
54
|
192
|
4hm8B |
Naphthalene 1,2-dioxygenase bound to thioanisole |
|
151
|
446
|
4h80A |
Crystal structure of human aldh3a1 with its isozyme selective inhibitor - n-[4-(4-methylsulfonyl-2-nitroanilino)phenyl]acetamide |
|
165
|
448
|
4g3jA |
Sterol 14-alpha demethylase (cyp51) from trypanosoma brucei in complex with the vni derivative (r)-n-(1-(2,4-dichlorophenyl)-2-(1h-1,2,4-triazol-1-yl)ethyl)-4-(5-phenyl-1,3,4-oxadiazol-2-yl)benzamide [r-vni-triazole (vnt)] |
|
134
|
394
|
4g47A |
Structure of cytochrome p450 cyp121 in complex with 4-(1h-1,2,4-triazol-1-yl)phenol |
|
132
|
394
|
4g45A |
Structure of cytochrome cyp121 in complex with 2-methylquinolin-6-amine |
|
144
|
452
|
4gl7A |
Structure of human placental aromatase complexed with designed inhibitor hddg046 (compound 5) |
|
133
|
394
|
4g46A |
Structure of cytochrome p450 cyp121 in complex with 4-oxo-4,5,6,7-tetrahydrobenzofuran-3-carboxylate |
|
135
|
394
|
4g48A |
Structure of cyp121 in complex with 4-(4-phenoxy-1h-pyrazol-3-yl)benzene-1,3-diol |
|
132
|
394
|
4g44A |
Structure of p450 cyp121 in complex with lead compound mb286, 3-((1h-1,2,4-triazol-1-yl)methyl)aniline |
|
156
|
452
|
4gl5A |
Structure of human placental aromatase complexed with designed inhibitor hddg029 (compound 4) |
|
107
|
350
|
4gd4A |
Crystal structure of jmjd2a complexed with inhibitor |
|
166
|
448
|
4g7gA |
Sterol 14-alpha demethylase (cyp51) from trypanosoma brucei in complex with the vni derivative (r)-n-(1-(3,4'-difluorobiphenyl-4-yl)-2-(1h-imidazol-1-yl)ethyl)-4-(5-phenyl-1,3,4-oxadiazol-2-yl)benzamide [vni/vnf (vfv)] |
|
56
|
204
|
4g8zX |
Pcdhfr k37s/f69n double mutant tmp nadph ternary complex |
|
110
|
315
|
4gcaA |
Complex of aldose reductase with inhibitor idd 1219 |
|
131
|
394
|
4g2gA |
Crystal structure of mycobacterium tuberculosis cyp121 in complex with 4,4'-(1h-1,2,3-triazole-1,5-diyl)diphenol |
|
148
|
437
|
4g09A |
The crystal structure of the c366s mutant of hdh from brucella suis in complex with a substituted benzyl ketone |
|
130
|
394
|
4g1xA |
Crystal structure of mycobacterium tuberculosis cyp121 in complex with 4-(1h-1,2,4-triazol-1-yl)quinolin-6-amine |
|
203
|
552
|
4fm5A |
X-ray structure of des-methylflurbiprofen bound to murine cox-2 |
|
181
|
493
|
4fr8A |
Crystal structure of human aldehyde dehydrogenase-2 in complex with nitroglycerin |
|
79
|
230
|
4fglA |
Reduced quinone reductase 2 in complex with chloroquine |
|
137
|
455
|
4ff6A |
Mycobacterium tuberculosis dpre1 in complex with ct325 - monoclinic crystal form |
|
82
|
230
|
4fgkA |
Oxidized quinone reductase 2 in complex with chloroquine |
|
141
|
455
|
4fdoA |
Mycobacterium tuberculosis dpre1 in complex with ct319 |
|
108
|
261
|
4fj1A |
Crystal structure of the ternary complex between a fungal 17beta-hydroxysteroid dehydrogenase (holo form) and genistein |
|
106
|
260
|
4fj0A |
Crystal structure of the ternary complex between a fungal 17beta-hydroxysteroid dehydrogenase (holo form) and 3,7-dihydroxy flavone |
|
108
|
260
|
4fj2A |
Crystal structure of the ternary complex between a fungal 17beta-hydroxysteroid dehydrogenase (holo form) and biochanin a |
|
109
|
260
|
4fizA |
Crystal structure of the binary complex between a fungal 17beta-hydroxysteroid dehydrogenase (apo form) and coumestrol |
|
82
|
230
|
4fgjA |
Oxidized quinone reductase 2 in complex with primaquine |
|
162
|
469
|
4fdhA |
Structure of human aldosterone synthase, cyp11b2, in complex with fadrozole |
|
116
|
316
|
3r6iA |
Akr1c3 complex with meclofenamic acid |
|
139
|
455
|
4fdnA |
Mycobacterium tuberculosis dpre1 in complex with ct325 - hexagonal crystal form |
|
146
|
465
|
3r1bA |
Open crystal structure of cytochrome p450 2b4 covalently bound to the mechanism-based inactivator tert-butylphenylacetylene |
|
117
|
316
|
3r43A |
Akr1c3 complexed with mefenamic acid |
|
154
|
465
|
3r1aA |
Closed crystal structure of cytochrome p450 2b4 covalently bound to the mechanism-based inactivator tert-butylphenylacetylene |
|
115
|
317
|
3r58A |
Akr1c3 complex with naproxen |
|
61
|
225
|
3qlxA |
Candida glabrata dihydrofolate reductase complexed with nadph and 6-methyl-5-[(3r)-3-(3,4,5-trimethoxyphenyl)pent-1-yn-1-yl]pyrimidine-2,4-diamine (ucp112a) |
|
63
|
225
|
3qlzA |
Candida glabrata dihydrofolate reductase complexed with nadph and 5-[3-(2,5-dimethoxyphenyl)prop-1-yn-1-yl]-6-propylpyrimidine-2,4-diamine (ucp130b) |
|
56
|
192
|
3qlsA |
Candida albicans dihydrofolate reductase complexed with nadph and 6-methyl-5-[3-methyl-3-(3,4,5-trimethoxyphenyl)but-1-yn-1-yl]pyrimidine-2,4-diamine (ucp115a) |
|
59
|
192
|
3qlrA |
Candida albicans dihydrofolate reductase complexed with nadph and 6-methyl-5-[(3r)-3-(3,4,5-trimethoxyphenyl)pent-1-yn-1-yl]pyrimidine-2,4-diamine (ucp112a) |
|
99
|
270
|
3qqpA |
Crystal structure of 11beta-hydroxysteroid dehydrogenase 1 (11b-hsd1) in complex with urea inhibitor |
|
152
|
465
|
3qm4A |
Human cytochrome p450 (cyp) 2d6 - prinomastat complex |
|
58
|
219
|
3qfxA |
Trypanosoma brucei dihydrofolate reductase pyrimethamine complex |
|
188
|
552
|
3q7dA |
Structure of (r)-naproxen bound to mcox-2. |
|
161
|
465
|
3qu8A |
Crystal structure of a human cytochrome p450 2b6 (y226h/k262r) in complex with the inhibitor 4-(4-nitrobenzyl)pyridine. |
|
165
|
465
|
3qoaA |
Crystal structure of a human cytochrome p450 2b6 (y226h/k262r) in complex with the inhibitor 4-benzylpyridine. |
