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Literature summary for 1.1.1.B25 extracted from

  • Yabe, K.; Matsuyama, Y.; Ando, Y.; Nakajima, H.; Hamasaki, T.
    Stereochemistry during aflatoxin biosynthesis: Conversion of norsolorinic acid to averufin (1993), Appl. Environ. Microbiol., 59, 2486-2492.
    View publication on PubMedView publication on EuropePMC

Localization

Localization Comment Organism GeneOntology No. Textmining
cytosol
-
Aspergillus parasiticus 5829
-

Natural Substrates/ Products (Substrates)

Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
norsolorinate + NADPH + H+ Aspergillus parasiticus
-
(1'S)-averantin + NADP+
-
?

Organism

Organism UniProt Comment Textmining
Aspergillus parasiticus
-
-
-
Aspergillus parasiticus NIAH-26
-
-
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
norsolorinate + NADPH + H+
-
Aspergillus parasiticus (1'S)-averantin + NADP+
-
?
norsolorinate + NADPH + H+ (1'S)-averantin is exclusively produced from norsolorinate in the presence of NADPH. Also, only (1'S)-averantin, and not (1'R)-averantin serves as a substrate for the reverse reaction from averantin to norsolorinate Aspergillus parasiticus (1'S)-averantin + NADP+
-
r