LMPD Database

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LMP005062

UniProt Annotations

Entry Information
Gene Namepyruvate dehydrogenase (lipoamide) beta
Protein EntryODPB_HUMAN
UniProt IDP11177
SpeciesHuman
Comments
Comment typeDescription
Alternative ProductsEvent=Alternative splicing; Named isoforms=3; Name=1; IsoId=P11177-1; Sequence=Displayed; Name=2; IsoId=P11177-2; Sequence=VSP_012675; Note=No experimental confirmation available.; Name=3; IsoId=P11177-3; Sequence=VSP_043364; Note=No experimental confirmation available.;
Catalytic ActivityPyruvate + [dihydrolipoyllysine-residue acetyltransferase] lipoyllysine = [dihydrolipoyllysine-residue acetyltransferase] S-acetyldihydrolipoyllysine + CO(2).
CofactorName=thiamine diphosphate; Xref=ChEBI
DiseasePyruvate dehydrogenase E1-beta deficiency (PDHBD) [MIM
FunctionThe pyruvate dehydrogenase complex catalyzes the overall conversion of pyruvate to acetyl-CoA and CO(2), and thereby links the glycolytic pathway to the tricarboxylic cycle.
InteractionP10515:DLAT; NbExp=7; IntAct=EBI-1035872, EBI-2959723;
Subcellular LocationMitochondrion matrix.
SubunitHeterotetramer of two PDHA1 and two PDHB subunits. The heterotetramer interacts with DLAT, and is part of the multimeric pyruvate dehydrogenase complex that contains multiple copies of pyruvate dehydrogenase (E1), dihydrolipoamide acetyltransferase (DLAT, E2) and lipoamide dehydrogenase (DLD, E3). These subunits are bound to an inner core composed of about 48 DLAT and 12 PDHX molecules. {ECO