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Literature summary extracted from

  • Sedgwick, B.; Morris, C.
    Stereochemical course of hydrogen transfer catalysed be the enoyl reductase enzyme of the yeast fatty acid synthethase (1980), J. Chem. Soc. Chem. Commun., 1980, 96-97.
No PubMed abstract available

Natural Substrates/ Products (Substrates)

EC Number Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
1.3.1.10 additional information Saccharomyces cerevisiae part of fatty acid synthesis reducing double bonds of a great varity of acyl thioesters ?
-
 ?

Organism

EC Number Organism UniProt Comment Textmining
1.3.1.10 Saccharomyces cerevisiae
-
 scientific name not stated
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Reaction

EC Number Reaction Comment Organism Reaction ID
1.3.1.10 acyl-[acyl-carrier protein] + NADP+ = trans-2,3-dehydroacyl-[acyl-carrier protein] + NADPH + H+ anti addition via 2Si,3Si attack on double bond Saccharomyces cerevisiae
a

Substrates and Products (Substrate)

EC Number Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
1.3.1.10 crotonyl-N-acetyl-cysteamine + NADPH stereochemistry Saccharomyces cerevisiae butyryl-N-acetyl-cysteamine + NADP+
-
 ?
1.3.1.10 crotonyl-[acyl-carrier protein] + NADPH anti addition of hydrogen via a 2-Si,3-Si attack on the double bond Saccharomyces cerevisiae butyryl-[acyl-carrier protein] + NADP+
-
 ?
1.3.1.10 additional information part of fatty acid synthesis reducing double bonds of a great varity of acyl thioesters Saccharomyces cerevisiae ?
-
 ?