Difference between revisions of "Phosphatase Subfamily PTEN"

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(References)
(Domain Structure)
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PTEN is found in almost all eukaryotes.
 
PTEN is found in almost all eukaryotes.
  
===Domain Structure===
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===Domain===
PTENs typically have a phosphatase domain followed by a C2 domain. Some homologs have PH (phospholipid-binding) or LIM domains. Yeast PTEN TEP1 lacks the C2 domain, but its functions as PTEN <cite>Heymont00</cite>.
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PTENs typically have a phosphatase domain followed by a C2 domain. C2 domain tethers PTEN to vesicles by specifically binding to phosphatidylinositol 3-phosphate (PI(3)P) (the signature lipid of endosomes) through the CBR3 loop (see [http://www.cell.com/molecular-cell/abstract/S1097-2765(15)00176-8?rss=yes here]).  
  
C2 domain tethers PTEN to vesicles by specifically binding to phosphatidylinositol 3-phosphate (PI(3)P) (the signature lipid of endosomes) through the CBR3 loop (see [http://www.cell.com/molecular-cell/abstract/S1097-2765(15)00176-8?rss=yes here]).
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The N-terminus of human PTEN contains a nuclear localization signal (NLS) (7-31), an overlapping PIP2-binding motif (PBM) (6-15) and  cytoplasmic localization signal (CLS) (19-25) (positions are numbered by human PTEN) <cite>Gil15</cite>.
  
The N-terminus contains a nuclear localization signal (NLS) (7-31), an overlapping PIP2-binding motif (PBM) (6-15) and  cytoplasmic localization signal (CLS) (19-25) (positions are numbered by human PTEN) <cite>Gil15</cite>.
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===== Fungi lost C2 domain =====
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Some homologs have PH (phospholipid-binding) or LIM domains. Yeast PTEN TEP1 lacks the C2 domain, but its functions as PTEN <cite>Heymont00</cite>. The C2 domain is actually absent from all fungi, but present in amoeba and basal eukaryotes (see technical notes).
  
 
===Functions===
 
===Functions===

Revision as of 15:59, 29 June 2015

Phosphatase Classification: Superfamily CC1: Family PTEN: Subfamily PTEN

PTEN subfamily is named after its single member in human, PTEN, which dephosphorylates phosphatidylinositol (3,4,5)-trisphosphate (PtdIns (3,4,5)P3 or PIP3). PTEN is one of the most commonly lost tumor suppressors in human cancer.

Evolution

PTEN is found in almost all eukaryotes.

Domain

PTENs typically have a phosphatase domain followed by a C2 domain. C2 domain tethers PTEN to vesicles by specifically binding to phosphatidylinositol 3-phosphate (PI(3)P) (the signature lipid of endosomes) through the CBR3 loop (see here).

The N-terminus of human PTEN contains a nuclear localization signal (NLS) (7-31), an overlapping PIP2-binding motif (PBM) (6-15) and cytoplasmic localization signal (CLS) (19-25) (positions are numbered by human PTEN) [1].

Fungi lost C2 domain

Some homologs have PH (phospholipid-binding) or LIM domains. Yeast PTEN TEP1 lacks the C2 domain, but its functions as PTEN [2]. The C2 domain is actually absent from all fungi, but present in amoeba and basal eukaryotes (see technical notes).

Functions

PTEN is a critical negative regulator of PI3K signaling. PI3K produce the lipid second messenger phosphatidylinositol 3,4,5-trisphosphate (PI (3,4,5)) trisphosphate (PI(3,4,5)P3/PIP3) in response to activation of receptor tyrosine kinases (RTKs), G-protein-coupled receptors, or membrane-bound oncogenes [3, 4]. It dephosphorylates the lipid second messenger, PI (3,4,5) [5]. It is tumor suppressor among the most frequently altered genes in cancer [6, 7].

References

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Error fetching PMID 25875300:
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  1. Error fetching PMID 25875300: [Gil15]
  2. Error fetching PMID 11070083: [Heymont00]
  3. Error fetching PMID 16847462: [Engelman06]
  4. Error fetching PMID 22358332: [Vanhaesebroeck12]
  5. Error fetching PMID 9593664: [Maehama98]
  6. Error fetching PMID 9072974: [Li97]
  7. Error fetching PMID 9090379: [Steck97]
All Medline abstracts: PubMed | HubMed