4.5 Article

A Unified Nomenclature and Amino Acid Numbering for Human PTEN

Journal

SCIENCE SIGNALING
Volume 7, Issue 332, Pages -

Publisher

AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/scisignal.2005560

Keywords

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Funding

  1. Medical Research Council [G0801865, G0802289] Funding Source: researchfish
  2. Division Of Chemistry
  3. Direct For Mathematical & Physical Scien [1216827] Funding Source: National Science Foundation
  4. Grants-in-Aid for Scientific Research [26640081, 26114005] Funding Source: KAKEN
  5. MRC [G0802289, G0801865] Funding Source: UKRI
  6. Medical Research Council [G0801865, G0802289] Funding Source: Medline
  7. NCI NIH HHS [R01 CA053840, R01 CA154986] Funding Source: Medline
  8. NIGMS NIH HHS [R01 GM055989, R01 GM034933] Funding Source: Medline

Ask authors/readers for more resources

The tumor suppressor PTEN is a major brake for cell transformation, mainly due to its phosphatidylinositol 3,4,5-trisphosphate [PI(3,4,5)P-3] phosphatase activity that directly counteracts the oncogenicity of phosphoinositide 3-kinase (PI3K). PTEN mutations are frequent in tumors and in the germ line of patients with tumor predisposition or with neurological or cognitive disorders, which makes the PTEN gene and protein a major focus of interest in current biomedical research. After almost two decades of intense investigation on the 403-residue-long PTEN protein, a previously uncharacterized form of PTEN has been discovered that contains 173 amino-terminal extra amino acids, as a result of an alternate translation initiation site. To facilitate research in the field and to avoid ambiguities in the naming and identification of PTEN amino acids from publications and databases, we propose here a unifying nomenclature and amino acid numbering for this longer form of PTEN.

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