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Description for Protein PLOD3

procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3
8 total interacting proteins; 2 platelet interacting proteins
Icon Book Platelet Evidence (proteome studies/others : 2/0)
(alpha granules: 1; secretome: 1)
Summary:
The protein encoded by this gene is a membrane-bound homodimeric enzyme that is localized to the cisternae of the rough endoplasmic reticulum. The enzyme (cofactors iron and ascorbate) catalyzes the hydroxylation of lysyl residues in collagen-like peptides. The resultant hydroxylysyl groups are attachment sites for carbohydrates in collagen and thus are critical for the stability of intermolecular crosslinks. Some patients with Ehlers-Danlos syndrome type VIB have deficiencies in lysyl hydroxylase activity. [provided by RefSeq] (PubMed Links)
Domains and Motifs:
  • SP: Signal Peptide
  • P4HC: Prolyl 4-hydroxylase alpha subunit homologues.

  • Gene Ontology:
    Gene Ontology Annotations

    KEGG - Enzyme ID(s):
    1.14.11.4; 2.4.1.50; 2.4.1.66
    KEGG - Orthology:
    K13646
    KEGG - Pathway(s):
    hsa00310
    (The yellow boxes represents platelet proteins)
    Nomenclature / Alternative Names:
    Procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3v; LH3; Procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3
    Approved Symbol:
    PLOD3
    (De-) Phosphorylations:
    Total (de-) phosphorylation sites: 0
    No human (de-) phosphorylation sites; 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):

  • Succinic acid(db);
  • Vitamin C(db)


    Associated Genetic Diseases:

    None Available
  • Predicted Transmembrane Domains:
  • Isoform 1 : 0
  • Additional Identifiers:

    HPRD: 04347 Entrez Gene ID: 8985 OMIM ID: 603066 Swissprot Accession: Q9UG85O60568