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Literature summary for 1.3.8.1 extracted from

  • Battisti, C.; Forte, F.; Molinelli, M.; Funghini, S.; Pasquini, E.; Tassini, M.; Dotti, M.T.; Federico, A.
    A new case of short-chain acyl-CoA dehydrogenase deficiency: clinical, biochemical, genetic and (1)H-NMR spectroscopic studies (2007), Neurol. Sci., 28, 328-330.
    View publication on PubMed

Application

Application Comment Organism
medicine short-chain-acyl-CoA-dehydrogenase deficiency is an inborn error of mitochondrial fatty acid metabolism caused by rare mutations as well as common susceptibility variations in the SCAD gene Homo sapiens

Organism

Organism UniProt Comment Textmining
Homo sapiens
-
-
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
butyryl-CoA + electron acceptor
-
Homo sapiens 2-butenoyl-CoA + reduced acceptor
-
?

Synonyms

Synonyms Comment Organism
SCAD
-
Homo sapiens
short-chain acyl-CoA dehydrogenase
-
Homo sapiens