Difference between revisions of "Pseudophosphatases (obsolete)"
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* Receptor PTPs. Most receptor PTPs have two tandem phosphatase domains. The 2nd phosphatase domain has no or negligible activity. The 2nd domain can interact with 1st domain in both intra- and intermolecular manners <cite>denHertog02</cite>. | * Receptor PTPs. Most receptor PTPs have two tandem phosphatase domains. The 2nd phosphatase domain has no or negligible activity. The 2nd domain can interact with 1st domain in both intra- and intermolecular manners <cite>denHertog02</cite>. | ||
| − | === Controversial === | + | === Controversial pseudophosphatases === |
===== PTPRN (IA-2) and PTPRN2 ===== | ===== PTPRN (IA-2) and PTPRN2 ===== | ||
Human PTPRN and PTPRN2 have been proposed to be enzymatically inactive due to mutations at catalytic Cx5R motif and WPD motif <cite>Kharitidi13</cite>. However, PTPRN2 has been reported to be phosphatidylinositol phosphatase <cite>Caromile10</cite>. | Human PTPRN and PTPRN2 have been proposed to be enzymatically inactive due to mutations at catalytic Cx5R motif and WPD motif <cite>Kharitidi13</cite>. However, PTPRN2 has been reported to be phosphatidylinositol phosphatase <cite>Caromile10</cite>. | ||
Revision as of 05:03, 11 March 2015
List of pseudophosphatases
To be added.
Functions
- Receptor PTPs. Most receptor PTPs have two tandem phosphatase domains. The 2nd phosphatase domain has no or negligible activity. The 2nd domain can interact with 1st domain in both intra- and intermolecular manners [1].
Controversial pseudophosphatases
PTPRN (IA-2) and PTPRN2
Human PTPRN and PTPRN2 have been proposed to be enzymatically inactive due to mutations at catalytic Cx5R motif and WPD motif [2]. However, PTPRN2 has been reported to be phosphatidylinositol phosphatase [3].
PTPN23 (HD-PTP)
PTPN23 was reported to be catalytically inactive, - no phosphatase activity toward tyrosine or lipid. It was proposed that serine at position 1452 within Cx5R catalytic motif caused the inactivity. Replacing serine with alanine, which is found in catalytically active PTPs, can restore the phosphatase activity [4].
However, another study found SRC, E-cadherin, and beta-catenin are direct substrates of PTPN23 [5].
References
- Blanchetot C, Tertoolen LG, Overvoorde J, and den Hertog J. Intra- and intermolecular interactions between intracellular domains of receptor protein-tyrosine phosphatases. J Biol Chem. 2002 Dec 6;277(49):47263-9. DOI:10.1074/jbc.M205810200 |
- Kharitidi D, Manteghi S, and Pause A. Pseudophosphatases: methods of analysis and physiological functions. Methods. 2014 Jan 15;65(2):207-18. DOI:10.1016/j.ymeth.2013.09.009 |
- Caromile LA, Oganesian A, Coats SA, Seifert RA, and Bowen-Pope DF. The neurosecretory vesicle protein phogrin functions as a phosphatidylinositol phosphatase to regulate insulin secretion. J Biol Chem. 2010 Apr 2;285(14):10487-96. DOI:10.1074/jbc.M109.066563 |
