Found 1271 chains in Genus chains table. Displaying 51 - 100. Applied filters: Proteins

Search results query: oxidoreductase/oxidoreductase inhibitor

Total Genus Sequence Length pdb Title
154 486 5s9zA Pandda analysis group deposition -- crystal structure of trypanosoma brucei trypanothione reductase in complex with z2856434884
149 486 5sa1A Pandda analysis group deposition -- crystal structure of trypanosoma brucei trypanothione reductase in complex with z2856434944
78 237 7fbqA Human clic1 in complex with nsc602247
126 419 8fgdA Structure of rat neuronal nitric oxide synthase r349a mutant heme domain in complex with 6-(5-(2-(diethylamino)ethyl)-2,3-difluorophenethyl)-4-methylpyridin-2-amine
127 418 8fgbA Structure of rat neuronal nitric oxide synthase heme domain in complex with 4-(5-(2-(dimethylamino)ethyl)-2,3-difluorophenethyl)-6-methylpyrimidin-2-amine
132 418 8fgaA Structure of rat neuronal nitric oxide synthase heme domain in complex with 6-(5-(2-(dimethylamino)ethyl)-2,3-difluorophenethyl)-4-methylpyridin-2-amine
122 418 8fgvA Structure of rat neuronal nitric oxide synthase h692f mutant heme domain in complex with 6-(5-(2-(dimethylamino)ethyl)-2,3-difluorophenethyl)-4-methoxypyridin-2-amine
139 418 8fg9A Structure of rat neuronal nitric oxide synthase heme domain in complex with 6-(5-(2-(dimethylamino)ethyl)-2,3-difluorophenethyl)pyridin-2-amine
130 418 8fgcA Structure of rat neuronal nitric oxide synthase heme domain in complex with 6-(5-(2-aminoethyl)-2,3-difluorophenethyl)-4-methylpyridin-2-amine
185 494 7um9A Human aldh1a1 with bound compound cm38
62 188 7ttvA E.coli dsba in complex with 4-phenyl-2-(3-phenylpropyl)thiazole-5-carboxylic acid
122 406 7wyfA Plasmodium falciparum dihydroorotate dehydrogenase (dhodh) in complex with its inhibitor 50
49 157 7rgkA Dfra5 complexed with nadph and 5-(3-(7-(4-(aminomethyl)phenyl)benzo[d][1,3]dioxol-5-yl)but-1-yn-1-yl)-6-ethylpyrimidine-2,4-diamine (ucp1223)
48 157 7rgoA Dfra5 complexed with nadph and 4'-chloro-3'-(4-(2,4-diamino-6-ethylpyrimidin-5-yl)but-3-yn-2-yl)-[1,1'-biphenyl]-4-carboxamide (ucp1228)
47 156 7rgjA Dfra1 complexed with nadph and 5-(3-(7-(4-(aminomethyl)phenyl)benzo[d][1,3]dioxol-5-yl)but-1-yn-1-yl)-6-ethylpyrimidine-2,4-diamine (ucp1223)
64 188 7s1cA Crystal structure of e.coli dsba in complex with compound mips-0001897 (compound 1)
65 188 7s1lA Crystal structure of e.coli dsba in complex with compound mips-0001896 (compound 72)
66 188 7s1dA Crystal structure of e.coli dsba in complex with compound mips-0001877 (compound 39)
65 188 7s1fA Crystal structure of e.coli dsba in complex with compound mips-0001886 (compound 38)
48 164 7tj3A Crystal structure of a dihydrofolate reductase fola from stenotrophomonas maltophilia bound to nadp and p218
168 473 7sv2A Human cytochrome p450 (cyp) 3a5 ternary complex with azamulin
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
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)
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)
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)
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