Preferred Label : dihydrolipoyllysine-residue acetyltransferase;
MeSH definition : An enzyme that catalyzes the acetyltransferase reaction using ACETYL CoA as an acetyl
donor and dihydrolipoamide as acceptor to produce COENZYME A (CoA) and S-acetyldihydrolipoamide.
It forms the (E2) subunit of the PYRUVATE DEHYDROGENASE COMPLEX.;
MeSH synonym : dihydrolipoyl transacetylase; acetyl coa dihydrolipoamide s acetyltransferase; acetyltransferase, dihydrolipoyl; dihydrolipoamide acetyltransferase; pyruvate dehydrogenase complex e2; s-acetyltransferase, dihydrolipoamide; transacetylase, dihydrolipoyl; acetyl-coa-dihydrolipoamide s-acetyltransferase; s-acetyltransferase, acetyl-coa-dihydrolipoamide; dihydrolipoamide s-acetyltransferase; dihydrolipoamide s acetyltransferase; acetyltransferase, dihydrolipoyllysine-residue; acetyltransferase, dihydrolipoamide; dihydrolipoyl acetyltransferase; lipoate acetyltransferase; acetyltransferase, lipoate; dihydrolipoyllysine residue acetyltransferase;
MeSH Related Number : 9032-29-5 (CRN);
Registry Number MeSH : EC 2.3.1.12;
Wikipedia link : https://en.wikipedia.org/wiki/Dihydrolipoyllysine-residue acetyltransferase;
Is substance : O;
UNII : EC 2.3.1.12;
Origin ID : D051047;
UMLS CUI : C0058087;
Allowable qualifiers
Automatic exact mappings (from CISMeF team)
Currated CISMeF NLP mapping
Record concept(s)
Related MeSH Supplementary Concept(s)
Semantic type(s)
UMLS correspondences (same concept)
An enzyme that catalyzes the acetyltransferase reaction using ACETYL CoA as an acetyl
donor and dihydrolipoamide as acceptor to produce COENZYME A (CoA) and S-acetyldihydrolipoamide.
It forms the (E2) subunit of the PYRUVATE DEHYDROGENASE COMPLEX.
http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=FR&Expert=79244
2011
France
scientific and technical information
pyruvate dehydrogenase complex deficiency disease
dihydrolipoyllysine-residue acetyltransferase
pyruvate dehydrogenase complex deficiency
pyruvate dehydrogenase E2 deficiency
lactic acidosis, congenital infantile, due to LAD deficiency
dihydrolipoamide dehydrogenase
lactic acidosis, congenital infantile, due to LAD deficiency
pyruvate dehydrogenase E2 deficiency
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