Found 320 chains in Genus chains table. Displaying 151 - 200. Applied filters: Proteins

Search results query: oxidoreductase/inhibitor

Total Genus Sequence Length pdb Title
134 421 6pncA Structure of human neuronal nitric oxide synthase r354a/g357d mutant heme domain in complex with 7-(3-(2-aminoethyl)phenyl)-4-methylquinolin-2-amine
127 420 6pnhA Structure of human neuronal nitric oxide synthase r354a/g357d mutant heme domain in complex with 7-(3-(aminomethyl)-4-isopropoxyphenyl)-4-methylquinolin-2-amine
120 413 6powA Structure of human endotheial nitric oxide synthase heme domain in complex with 7-(5-(aminomethyl)pyridin-3-yl)-4-methylquinolin-2-amine
128 418 6pn7A Structure of rat neuronal nitric oxide synthase heme domain in complex with 7-(3-(aminomethyl)-4-(thiazol-4-ylmethoxy)phenyl)-4-methylquinolin-2-amine
128 418 6pn9A Structure of rat neuronal nitric oxide synthase heme domain in complex with 7-(3-(aminomethyl)-4-(thiazol-5-ylmethoxy)phenyl)-4-methylquinolin-2-amine
132 418 6pn3A Structure of rat neuronal nitric oxide synthase heme domain in complex with 7-(3-(aminomethyl)-4-(cyclobutylmethoxy)phenyl)-4-methylquinolin-2-amine
118 413 6pozA Structure of human endothelial nitric oxide synthase heme domain in complex with 7-(3-(aminomethyl)-4-isopropoxyphenyl)-4-methylquinolin-2-amine
128 413 6pouA Structure of human endothelial nitric oxide synthase heme domain in complex with 7-(4-(2-aminoethyl)phenyl)-4-methylquinolin-2-amine
125 418 6pn8A Structure of rat neuronal nitric oxide synthase heme domain in complex with 7-(3-(aminomethyl)-4-(oxazol-4-ylmethoxy)phenyl)-4-methylquinolin-2-amine
125 421 6pndA Structure of human neuronal nitric oxide synthase r354a/g357d mutant heme domain in complex with 7-(3-(2-aminoethyl)phenyl)-4-methylquinolin-2-amine
128 418 6pmzA Structure of rat neuronal nitric oxide synthase heme domain in complex with 7-(5-(aminomethyl)pyridin-3-yl)-4-methylquinolin-2-amine
129 421 6potA Structure of human neuronal nitric oxide synthase r354a/g357d mutant heme domain in complex with 7-(3-(aminomethyl)-4-(thiazol-5-ylmethoxy)phenyl)-4-methylquinolin-2-amine
125 418 6pn6A Structure of rat neuronal nitric oxide synthase heme domain in complex with 7-(3-(aminomethyl)-4-(pyridin-3-ylmethoxy)phenyl)-4-methylquinolin-2-amine
136 389 6kpsA Crystal structure of indoleamine 2,3-dioxygenagse 1 (ido1) in complex with compound 36
134 390 6kofA Crystal structure of indoleamine 2,3-dioxygenagse 1 (ido1) in complex with compound 47
162 415 6u4jA Crystal structure of idh1 r132h mutant in complex with ft-2102
193 552 6v3rA Crystal structure of murine cycloxygenase in complex with a harmaline analog, 4,9-dihydro-3h-pyrido[3,4-b]indole
65 188 6pohA Crystal structure of ecdsba in complex alkyl ether 21
66 188 6poiA Crystal structure of ecdsba in complex phenyl ether 25
64 188 6poqA Crystal structure of ecdsba in complex with anisidine 16
64 188 6pmlA Crystal structure of ecdsba in complex benzyl ether 23
63 188 6pmfA Crystal structure of ecdsba in complex with aniline 15
135 393 6o3iA Crystal structure of human ido1 bound to navoximod (nlg-919)
40 154 6a9oA Rational discovery of a sod1 tryptophan oxidation inhibitor with therapeutic potential for amyotrophic lateral sclerosis
100 303 6plgA Crystal structure of human phgdh complexed with compound 15
107 305 6plfA Crystal structure of human phgdh complexed with compound 1
92 318 6dq4A Linked kdm5a jmj domain bound to the inhibitor gsk-j1
88 316 6dq5A Linked kdm5a jmj domain bound to the inhibitor n43 i.e. 3-((6-(4-acryloyl-1,4-diazepan-1-yl)-2-(pyridin-2-yl)pyrimidin-4-yl)amino)propanoic acid
94 317 6dq6A Linked kdm5a jmj domain bound to the inhibitor n44 i.e. 3-((2-(pyridin-2-yl)-6-(4-(vinylsulfonyl)-1,4-diazepan-1-yl)pyrimidin-4-yl)amino)propanoic acid
87 318 6dq8A Linked kdm5a jmj domain bound to the inhibitor n49 i.e. 2-((2-chlorophenyl)(2-(1-methylpyrrolidin-2-yl)ethoxy)methyl)thieno[3,2-b]pyridine-7-carboxylic acid
87 318 6dq9A Linked kdm5a jmj domain bound to the covalent inhibitor n69 i.e. [2-((3-acrylamidophenyl)(2-(piperidin-1-yl)ethoxy)methyl)thieno[3,2-b]pyridine-7-carboxylic acid]
87 318 6dqaA Linked kdm5a jmj domain bound to inhibitor n70 i.e.[2-((3-aminophenyl)(2-(piperidin-1-yl)ethoxy)methyl)thieno[3,2-b]pyridine-7-carboxylic acid]
86 318 6dqbA Linked kdm5a jmj domain forming covalent bond to inhibitor n71 i.e. 2-((3-(4-(dimethylamino)but-2-enamido)phenyl)(2-(piperidin-1-yl)ethoxy)methyl)thieno[3,2-b]pyridine-7-carboxylic acid
118 331 6badA Lactate dehydrogenase in complex with inhibitor (r)-3-((2-chlorophenyl)thio)-6-(3-((4-fluorophenyl)amino)phenyl)-4-hydroxy-6-(thiophen-3-yl)-5,6-dihydro-2h-pyran-2-one
118 331 6bb2A Lactate dehydrogenase in complex with inhibitor (s)-5-((2-chlorophenyl)thio)-6'-(4-fluorophenoxy)-4-hydroxy-2-(thiophen-3-yl)-2,3-dihydro-[2,2'-bipyridin]-6(1h)-one
194 552 6bl3A Crystal complex of cyclooxygenase-2 with indomethacin-butyldiamine-dansyl conjugate
203 552 6bl4A Crystal complex of cyclooxygenase-2 with indomethacin-ethylenediamine-dansyl conjugate
113 331 6bagA Lactate dehydrogenase in complex with inhibitor (r)-5-((2-chlorophenyl)thio)-6'-((4-fluorophenyl)amino)-4-hydroxy-2-(thiophen-3-yl)-2,3-dihydro-[2,2'-bipyridin]-6(1h)-one
121 321 6bulA Crystal structure of staphylococcus aureus ketol-acid reductoisomerase with hydroxyoxamate inhibitor 2
151 413 6o2yA Crystal structure of idh1 r132h mutant in complex with compound 24
154 413 6o2zA Crystal structure of idh1 r132h mutant in complex with compound 32
197 515 6d7kA Complex structure of methane monooxygenase hydroxylase in complex with inhibitory subunit
66 256 6ninB Rhodobacter sphaeroides bc1 with stigmatellin a
67 165 6d7kC Complex structure of methane monooxygenase hydroxylase in complex with inhibitory subunit
20 64 6d7kD Complex structure of methane monooxygenase hydroxylase in complex with inhibitory subunit
152 339 6d7kB Complex structure of methane monooxygenase hydroxylase in complex with inhibitory subunit
109 368 6j39A Crystal structure of cmis2 with inhibitor
156 428 6ninA Rhodobacter sphaeroides bc1 with stigmatellin a
52 179 6ninC Rhodobacter sphaeroides bc1 with stigmatellin a
86 318 6dq7A Linked kdm5a jmj domain bound to the potential hydrolysis product of inhibitor n45 i.e. 3-((6-(4-(2-cyano-3-methylbut-2-enoyl)-1,4-diazepan-1-yl)-2-(pyridin-2-yl)pyrimidin-4-yl)amino)propanoic acid