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Description for Protein HTRA2

HtrA serine peptidase 2
17 total interacting proteins; 7 platelet interacting proteins
Icon Book Platelet Evidence (proteome studies/others : 2/0)
(platelet: 4)
Summary:
This gene encodes a serine protease. The protein has been localized in the endoplasmic reticulum and interacts with an alternatively spliced form of mitogen-activated protein kinase 14. The protein has also been localized to the mitochondria with release to the cytosol following apoptotic stimulus. The protein is thought to induce apoptosis by binding the apoptosis inhibitory protein baculoviral IAP repeat-containing 4. Nuclear localization of this protein has also been observed. Alternate splicing of this gene results in two transcript variants encoding different isoforms. Additional transcript variants have been described, but their full-length sequences have not been determined. [provided by RefSeq] (PubMed Links)
Domains and Motifs:
  • TM: Transmembrane domain
  • TRYPSIN: Trypsin-like serine protease
  • PDZ: Domain present in PSD-95, Dlg, and ZO-1/2.

  • Gene Ontology:
    Gene Ontology Annotations

    KEGG - Enzyme ID(s):
    3.4.21.108
    KEGG - Orthology:
    K08669
    KEGG - Pathway(s):
    hsa05012
    (The yellow boxes represents platelet proteins)
    Nomenclature / Alternative Names:
    Serine protease HTRA2 mitochondrial; High temperature requirement protein A2; Omi stress regulated endoprotease; Serine proteinase OMI; OMI; PRSS25; HtrA like serine protease; Protease serine 25; HtrA serine peptidase 2 isoform 1 preproprotein; HtrA serine peptidase 2 isoform 2
    Approved Symbol:
    HTRA2
    (De-) Phosphorylations:
    Total (de-) phosphorylation sites: 7
    Human (de-) phosphorylation sites: 7; 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):

    None Available


    Associated Genetic Diseases:

  • Parkinson disease 13(Pd);
  • Parkinson disease, susceptibility to(Pd)
  • Predicted Transmembrane Domains:
  • Isoform 2 : 1
  • Isoform 1 : 1
  • Additional Identifiers:

    HPRD: 05919 Entrez Gene ID: 27429 OMIM ID: 606441 Swissprot Accession: O43464