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3-Hydroxybenzoyl-CoA is a molecule formed … 3-Hydroxybenzoyl-CoA is a molecule formed by condensing the thiol group of coenzyme A (CoA) with the carboxylic acid group of 3-hydroxybenzoic acid. Stable in acidic conditions, it is a tetraprotic acid due to the pyrophosphate and phosphate groups included. It derives from a benzoyl-CoA and a 3-hydroxybenzoic acid. In organisms such as plants, this can be formed using the 3-hydroxybenzoate—CoA ligase enzyme. This uses ATP, 3-hydroxybenzoate, and CoA as substrates. It can be reduced to 3-hydroxycyclohexa-1,5-diene-1-carbonyl-CoA by reduced ferredoxin and adenosine triphosphate using the benzoyl-CoA reductase enzyme. in this two hydrogen atoms are added to the benzene ring in a dearomatizing process.e benzene ring in a dearomatizing process.
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O1-{[(2R,3S,4R,5R)-5-(6-Amino-9H-purin-9-yl)-4-hydroxy-3-(phosphonooxy)oxolan-2-yl]methyl} O3-[(3R)-3-hydroxy-4-{[3-({2-[(3-hydroxybenzoyl)sulfanyl]ethyl}amino)-3-oxopropyl]amino}-2-methyl-4-oxobutyl] dihydrogen diphosphate
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Chemical structure of 3-Hydroxybenzoyl-CoA
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Chemical structure of 3-Hydroxybenzoyl-CoA
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3
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Chemical structure of 3-Hydroxybenzoyl-CoA
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300
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O1-{[-5--4-hydroxy-3-oxolan-2-yl]methyl} O3-[-3-hydroxy-4-{[3--3-oxopropyl]amino}-2-methyl-4-oxobutyl] dihydrogen diphosphate
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rdfs:comment |
3-Hydroxybenzoyl-CoA is a molecule formed … 3-Hydroxybenzoyl-CoA is a molecule formed by condensing the thiol group of coenzyme A (CoA) with the carboxylic acid group of 3-hydroxybenzoic acid. Stable in acidic conditions, it is a tetraprotic acid due to the pyrophosphate and phosphate groups included. It derives from a benzoyl-CoA and a 3-hydroxybenzoic acid. In organisms such as plants, this can be formed using the 3-hydroxybenzoate—CoA ligase enzyme. This uses ATP, 3-hydroxybenzoate, and CoA as substrates. 3-hydroxybenzoate, and CoA as substrates.
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rdfs:label |
3-Hydroxybenzoyl-CoA
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