|
45
|
164
|
7km8A |
Crystal structure of dihydrofolate reductase (dhfr) from mycobacterium ulcerans agy99 in complex with nadp and inhibitor sddc-0001914, orthorhombic crystal from |
|
40
|
163
|
7km9A |
Crystal structure of dihydrofolate reductase (dhfr) from mycobacterium ulcerans agy99 in complex with nadp and inhibitor sddc-0001913, tetragonal crystal from |
|
42
|
163
|
7ki8A |
Crystal structure of dihydrofolate reductase (dhfr) from mycobacterium ulcerans agy99 in complex with nadp and inhibitor sddc-0001580 |
|
44
|
170
|
7ki9A |
Crystal structure of dihydrofolate reductase (dhfr) from mycobacterium ulcerans agy99 in complex with nadp and inhibitor sddc-0001912 |
|
40
|
163
|
7km7A |
Crystal structure of dihydrofolate reductase (dhfr) from mycobacterium ulcerans agy99 in complex with nadp and inhibitor sddc-0001914, tetragonal crystal from |
|
101
|
362
|
7mtuA |
Crystal structure of the catalytic domain of the inosine monophosphate dehydrogenase from bacillus anthracis in the complex with imp and the inhibitor p221 |
|
155
|
470
|
7ks8A |
Crystal structure of human cyp3a4 with the caged inhibitor |
|
137
|
469
|
7ksaA |
Crystal structure of human cyp3a4 with the caged inhibitor |
|
125
|
392
|
6x5yA |
Ido1 in complex with compound 4 |
|
132
|
374
|
7kyvA |
Crystal structure of plasmodium falciparum dihydroorotate dehydrogenase bound with inhibitor dsm634 (3-methyl-n-(1-(5-methylisoxazol-3-yl)ethyl)-4-(4-(trifluoromethyl)benzyl)-1h-pyrrole-2-carboxamide) |
|
152
|
381
|
7kykA |
Crystal structure of plasmodium falciparum dihydroorotate dehydrogenase bound with inhibitor dsm589 (ethyl 3-methyl-4-((4-(trifluoromethyl)benzo[d]oxazol-7-yl)methyl)-1h-pyrrole-2-carboxylate) |
|
147
|
378
|
7kz4A |
Crystal structure of plasmodium falciparum dihydroorotate dehydrogenase bound with inhibitor dsm705 (n-(1-(1h-1,2,4-triazol-3-yl)ethyl)-3-methyl-4-(1-(6-(trifluoromethyl)pyridin-3-yl)cyclopropyl)-1h-pyrrole-2-carboxamide) |
|
148
|
378
|
7l01A |
Crystal structure of plasmodium falciparum dihydroorotate dehydrogenase bound with inhibitor dsm782 (n-(1-(5-cyano-1h-pyrazol-3-yl)ethyl)-3-methyl-4-(1-(6-(trifluoromethyl)pyridin-3-yl)cyclopropyl)-1h-pyrrole-2-carboxamide) |
|
149
|
382
|
7kyyA |
Crystal structure of plasmodium falciparum dihydroorotate dehydrogenase bound with inhibitor dsm697 (3-methyl-n-(1-(5-methylisoxazol-3-yl)ethyl)-4-(6-(trifluoromethyl)-1h-indol-3-yl)-1h-pyrrole-2-carboxamide) |
|
153
|
393
|
7kzyA |
Crystal structure of plasmodium falciparum dihydroorotate dehydrogenase bound with inhibitor dsm778 (3-methyl-n-(1-(5-methyl-1h-pyrazol-3-yl)ethyl)-4-(1-(6-(trifluoromethyl)pyridin-3-yl)cyclopropyl)-1h-pyrrole-2-carboxamide) |
|
147
|
381
|
7l0kA |
Crystal structure of plasmodium falciparum dihydroorotate dehydrogenase bound with inhibitor dsm784 (3-(1-(3-methyl-4-((6-(trifluoromethyl)pyridin-3-yl)methyl)-1h-pyrrole-2-carboxamido)ethyl)-1h-pyrazole-5-carboxamide) |
|
40
|
159
|
7k6cA |
Crystal structure of dihydrofolate reductase (dhfr) from mycobacterium abscessus atcc 19977 / dsm 44196 with nadp and inhibitor p218 |
|
43
|
163
|
7k68A |
Crystal structure of dihydrofolate reductase (dhfr) from mycobacterium ulcerans agy99 in complex with nadp and inhibitor sddc-0001565 |
|
45
|
165
|
7k62A |
Crystal structure of dihydrofolate reductase from mycobacterium kansasii in complex with nadp and inhibitor p218 |
|
45
|
163
|
7k69A |
Crystal structure of dihydrofolate reductase (dhfr) from mycobacterium ulcerans agy99 in complex with nadp and inhibitor sddc-0001574 |
|
45
|
163
|
7k6aA |
Crystal structure of dihydrofolate reductase (dhfr) from mycobacterium ulcerans agy99 in complex with nadp and inhibitor sddc-0001575 |
|
143
|
365
|
6vndA |
Quaternary complex of human dihydroorotate dehydrogenase (dhodh) with flavin mononucleotide (fmn), orotic acid and ag-636 |
|
126
|
469
|
7kvjA |
Human cyp3a4 bound to an inhibitor |
|
149
|
469
|
7kvsA |
Human cyp3a4 bound to an inhibitor |
|
142
|
468
|
7kvoA |
Human cyp3a4 bound to an inhibitor |
|
159
|
465
|
7kmyA |
Structure of mtb lpd bound to 010705 |
|
145
|
470
|
7kvkA |
Human cyp3a4 bound to an inhibitor |
|
144
|
469
|
7kviA |
Human cyp3a4 bound to an inhibitor |
|
137
|
468
|
7kvqA |
Human cyp3a4 bound to an inhibitor |
|
130
|
468
|
7kvhA |
Human cyp3a4 bound to an inhibitor |
|
153
|
469
|
7kvpA |
Human cyp3a4 bound to an inhibitor |
|
140
|
468
|
7kvnA |
Human cyp3a4 bound to an inhibitor |
|
140
|
469
|
7kvmA |
Human cyp3a4 bound to an inhibitor |
|
116
|
331
|
6q0dA |
Crystal structure of ldha in complex with compound ncgc00384414-01 at 2.05 a resolution |
|
120
|
331
|
6q13A |
Crystal structure of ldha in complex with compound ncgc00420737-09 at 2.00 a resolution |
|
143
|
392
|
6wjyA |
Human ido1 in complex with compound 4-a |
|
64
|
187
|
6pc9A |
Crystal structure of ecdsba in a complex with purified methylpiperazinone 6 |
|
206
|
689
|
6ncfA |
The structure of stable-5-lipoxygenase bound to akba |
|
195
|
689
|
6n2wA |
The structure of stable-5-lipoxygenase bound to ndga |
|
133
|
421
|
6pobA |
Structure of human neuronal nitric oxide synthase r354a/g357d mutant heme domain in complex with 7-(3-(aminomethyl)-4-(thiazol-4-ylmethoxy)phenyl)-4-methylquinolin-2-amine |
|
129
|
418
|
6pmxA |
Structure of rat neuronal nitric oxide synthase heme domain in complex with 7-(3-(2-aminoethyl)phenyl)-4-methylquinolin-2-amine |
|
128
|
418
|
6pmvA |
Structure of rat neuronal nitric oxide synthase heme domain in complex with 7-(4-(2-aminoethyl)phenyl)-4-methylquinolin-2-amine |
|
127
|
418
|
6pn1A |
Structure of rat neuronal nitric oxide synthase heme domain in complex with 7-(3-(aminomethyl)-4-propoxyphenyl)-4-methylquinolin-2-amine |
|
134
|
421
|
6po9A |
Structure of human neuronal nitric oxide synthase r354a/g357d mutant heme domain in complex with 7-(3-(aminomethyl)-4-(pyridin-2-ylmethoxy)phenyl)-4-methylquinolin-2-amine |
|
132
|
421
|
6po5A |
Structure of human neuronal nitric oxide synthase r354a/g357d mutant heme domain in complex with 7-(3-(aminomethyl)-4-(cyclobutylmethoxy)phenyl)-4-methylquinolin-2-amine |
|
129
|
421
|
6po7A |
Structure of human neuronal nitric oxide synthase r354a/g357d mutant heme domain in complex with 7-(3-(aminomethyl)-4-(cyclopropylmethoxy)phenyl)-4-methylquinolin-2-amine |
|
131
|
421
|
6po8A |
Structure of human neuronal nitric oxide synthase r354a/g357d mutant heme domain in complex with 4-((4-(2-amino-4-methylquinolin-7-yl)-2-(aminomethyl)phenoxy)methyl)benzonitrile |
|
134
|
421
|
6pocA |
Structure of human neuronal nitric oxide synthase r354a/g357d mutant heme domain in complex with 7-(3-(aminomethyl)-4-(oxazol-4-ylmethoxy)phenyl)-4-methylquinolin-2-amine |
|
134
|
418
|
6pn0A |
Structure of rat neuronal nitric oxide synthase heme domain in complex with 7-(3-(aminomethyl)-4-ethoxyphenyl)-4-methylquinolin-2-amine |
|
131
|
418
|
6pmwA |
Structure of rat neuronal nitric oxide synthase heme domain in complex with 7-(4-(aminomethyl)phenyl)-4-methylquinolin-2-amine |
