Found 1200 chains in Genus chains table. Displaying 1 - 50. Applied filters: Proteins

Search results query: oxidoreductase/oxidoreductase inhibitor

Total Genus Sequence Length pdb Title
146 382 7s87A Crystal structure of dihydroorotate dehydrogenase from plasmodium falciparum in complex with orotate, fmn, and inhibitor ncgc00600348-01
186 523 7rybA S. cerevisiae cyp51 y140h/i471t - double mutant complexed with voriconazole
193 527 7ry8A S. cerevisiae cyp51 y140h mutant complexed with voriconazole
195 529 7ryaA S. cerevisiae cyp51 i471t mutant complexed with itraconazole
195 527 7ry9A S. cerevisiae cyp51 i471t mutant complexed with voriconazole
193 528 7ryxA S. cerevisiae cyp51 complexed with vt-1129
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
44 170 7ki9A Crystal structure of dihydrofolate reductase (dhfr) from mycobacterium ulcerans agy99 in complex with nadp and inhibitor sddc-0001912
42 163 7ki8A Crystal structure of dihydrofolate reductase (dhfr) from mycobacterium ulcerans agy99 in complex with nadp and inhibitor sddc-0001580
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
137 468 7kvqA Human cyp3a4 bound to an inhibitor
130 468 7kvhA Human cyp3a4 bound to an inhibitor
144 469 7kviA Human cyp3a4 bound to an inhibitor
140 468 7kvnA Human cyp3a4 bound to an inhibitor
153 469 7kvpA 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