Preferred Label : succinate-semialdehyde dehydrogenase;
MeSH definition : An enzyme that plays a role in the GLUTAMATE and butanoate metabolism pathways by
catalyzing the oxidation of succinate semialdehyde to SUCCINATE using NAD as a coenzyme.
Deficiency of this enzyme, causes 4-hydroxybutyricaciduria, a rare inborn error in
the metabolism of the neurotransmitter 4-aminobutyric acid (GABA).;
MeSH synonym : nad( )-dependent succinic semialdehyde dehydrogenase; dehydrogenase, succinate-semialdehyde; dehydrogenase, succinate semialdehyde; semialdehyde dehydrogenase, succinate; succinic semialdehyde dehydrogenase; dehydrogenase, succinic semialdehyde; semialdehyde dehydrogenase, succinic; succinate semialdehyde dehydrogenase;
MeSH Related Number : 9028-95-9 (CRN);
Registry Number MeSH : EC 1.2.1.24;
Wikipedia link : https://en.wikipedia.org/wiki/Succinate-semialdehyde dehydrogenase;
Is substance : O;
UNII : EC 1.2.1.24;
Origin ID : D050644;
UMLS CUI : C0075426;
Allowable qualifiers
Currated CISMeF NLP mapping
Record concept(s)
Related MeSH Supplementary Concept(s)
See also inter- (CISMeF)
Semantic type(s)
UMLS correspondences (same concept)
An enzyme that plays a role in the GLUTAMATE and butanoate metabolism pathways by
catalyzing the oxidation of succinate semialdehyde to SUCCINATE using NAD as a coenzyme.
Deficiency of this enzyme, causes 4-hydroxybutyricaciduria, a rare inborn error in
the metabolism of the neurotransmitter 4-aminobutyric acid (GABA).
http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=FR&Expert=22
2006
France
French
hydroxybutyrates
succinate-semialdehyde dehydrogenase
4-hydroxybutyric acid
rare diseases
succinic semialdehyde dehydrogenase deficiency
amino acid metabolism, inborn errors
hydroxybutyrates
scientific and technical information
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