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Description for Protein WWP1

WW domain containing E3 ubiquitin protein ligase 1
29 total interacting proteins; 13 platelet interacting proteins
Icon Book Platelet Evidence (proteome studies/others : 0/0)
(Not detected in platelets)
Summary:
WW domain-containing proteins are found in all eukaryotes and play an important role in the regulation of a wide variety of cellular functions such as protein degradation, transcription, and RNA splicing. This gene encodes a protein which contains 4 tandem WW domains and a HECT (homologous to the E6-associated protein carboxyl terminus) domain. The encoded protein belongs to a family of NEDD4-like proteins, which are E3 ubiquitin-ligase molecules and regulate key trafficking decisions, including targeting of proteins to proteosomes or lysosomes. Alternative splicing of this gene generates at least 6 transcript variants; however, the full length nature of these transcripts has not been defined. [provided by RefSeq] (PubMed Links)
Domains and Motifs:
  • CC: Coiled Coil
  • C2: Protein kinase C conserved region 2 (CalB)
  • WW: Domain with 2 conserved Trp (W) residues

  • Gene Ontology:
    Gene Ontology Annotations

    KEGG - Enzyme ID(s):
    6.3.2.19
    KEGG - Orthology:
    K05633
    KEGG - Pathway(s):
    hsa04120; hsa04144
    (The yellow boxes represents platelet proteins)
    Nomenclature / Alternative Names:
    AIP5; Atropin 1 interacting protein 5; Nedd 4 like ubiquitin protein ligase; TGIF interacting ubiquitin ligase 1; Tiul1; hSDRP1; Nedd-4-like E3 ubiquitin-protein ligase WWP1; WW domain containing E3 ubiquitin protein ligase 1
    Approved Symbol:
    WWP1
    (De-) Phosphorylations:
    Total (de-) phosphorylation sites: 3
    Human (de-) phosphorylation sites: 3; 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:

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

    HPRD: 03811 Entrez Gene ID: 11059 OMIM ID: 602307 Swissprot Accession: Q9H0M0Q5YLC1