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Description for Protein GCDH

glutaryl-CoA dehydrogenase
1 total interacting proteins; 1 platelet interacting proteins
Icon Book Platelet Evidence (proteome studies/others : 1/0)
(platelet: 4)
Summary:
The protein encoded by this gene belongs to the acyl-CoA dehydrogenase family. It catalyzes the oxidative decarboxylation of glutaryl-CoA to crotonyl-CoA and CO(2) in the degradative pathway of L-lysine, L-hydroxylysine, and L-tryptophan metabolism. It uses electron transfer flavoprotein as its electron acceptor. The enzyme exists in the mitochondrial matrix as a homotetramer of 45-kD subunits. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq] (PubMed Links)
Domains and Motifs:
None Available

Gene Ontology:
Gene Ontology Annotations

KEGG - Enzyme ID(s):
1.3.99.7
KEGG - Orthology:
K00252
KEGG - Pathway(s):
hsa00071; hsa00310; hsa00380; hsa01100
(The yellow boxes represents platelet proteins)
Nomenclature / Alternative Names:
GCD; ACAD5; Glutaryl-CoA dehydrogenase, mitochondrial; EC 1.3.99.7; Glutaryl-Coenzyme A dehydrogenase isoform a; Glutaryl-Coenzyme A dehydrogenase isoform b
Approved Symbol:
GCDH
(De-) Phosphorylations:
Total (de-) phosphorylation sites: 2
Human (de-) phosphorylation sites: 2; No platelet phosphorylation sites

Phosphorylation Targets:
Total phosphorylation targets: 0
Human phosphorylation targets: 0;Predicted platelet targets: 0
Protein Characteristics:
Isoform-specific Information
Icon DrugsAssociated Drugs (DrugBank Accession):

  • Flavin-Adenine Dinucleotide(db);
  • S-4-Nitrobutyryl-Coa(db)


    Associated Genetic Diseases:

  • Glutaric acidemia I(Pd)
  • Predicted Transmembrane Domains:
  • Isoform 2 : 0
  • Isoform 1 : 0
  • Additional Identifiers:

    HPRD: 01977 Entrez Gene ID: 2639 OMIM ID: 608801 Swissprot Accession: Q92947