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Literature summary for 1.5.1.46 extracted from

  • Matuschek, M.; Wallwey, C.; Wollinsky, B.; Xie, X.; Li, S.
    In vitro conversion of chanoclavine-I aldehyde to the stereoisomers festuclavine and pyroclavine controlled by the second reduction step (2012), RSC Adv., 2, 3662-3669.
No PubMed abstract available

Organism

Organism UniProt Comment Textmining
Claviceps purpurea
-
-
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
chanoclavine-I aldehyde + GSH + NADPH + H+ the reaction occurs only in the presence of reduced glutathione Claviceps purpurea agroclavine + GSSG + NADP+
-
?
chanoclavine-I aldehyde + NADPH + H+
-
Claviceps purpurea festuclavine + pyroclavine + NADP+
-
?

Synonyms

Synonyms Comment Organism
agroclavine synthase
-
Claviceps purpurea
EasG
-
Claviceps purpurea

Cofactor

Cofactor Comment Organism Structure
FMN
-
Claviceps purpurea
NADPH NADPH is a better electron donor than NADH Claviceps purpurea