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Description for Protein CPT2

carnitine palmitoyltransferase 2
No Interacting Proteins
Icon Book Platelet Evidence (proteome studies/others : 1/0)
(platelet: 1)
Summary:
The protein encoded by this gene is a nuclear protein which is transported to the mitochondrial inner membrane. Together with carnitine palmitoyltransferase I, the encoded protein oxidizes long-chain fatty acids in the mitochondria. Defects in this gene are associated with mitochondrial long-chain fatty-acid (LCFA) oxidation disorders. [provided by RefSeq] (PubMed Links)
Domains and Motifs:
None Available
Gene Ontology:
Gene Ontology Annotations
KEGG - Enzyme ID(s):
2.3.1.21
KEGG - Orthology:
K08766
KEGG - Pathway(s):
hsa00071; hsa03320
(The yellow boxes represents platelet proteins)
Nomenclature / Alternative Names:
CPT 2
Approved Symbol:
CPT2
(De-) Phosphorylations:
Total (de-) phosphorylation sites: 11
Human (de-) phosphorylation sites: 11; 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):

  • B-Octylglucoside(db);
  • L-Carnitine(db);
  • Perhexiline(db)

    Associated Genetic Diseases:

  • Carnitine palmitoyltransferase II deficiency, infantile(Pd);
  • Carnitine palmitoyltransferase II deficiency, late-onset(Pd);
  • Carnitine palmitoyltransferase II deficiency, lethal neonatal(Pd);
  • Myopathy, variable(Pd)
    		• Predicted Transmembrane Domains:
  • Isoform 1 : 0
    • Additional Identifiers:

    HPRD: 02802 Entrez Gene ID: 1376 OMIM ID: 600650 Swissprot Accession: P23786;