Emerging issues in receptor protein tyrosine phosphatase function: lifting fog or simply shifting?
Author(s) -
A. Petrone,
Jan Sap
Publication year - 2000
Publication title -
journal of cell science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.384
H-Index - 278
eISSN - 1477-9137
pISSN - 0021-9533
DOI - 10.1242/jcs.113.13.2345
Subject(s) - protein tyrosine phosphatase , biology , receptor tyrosine kinase , phosphorylation , tyrosine phosphorylation , proto oncogene tyrosine protein kinase src , microbiology and biotechnology , phosphatase , ror1 , tyrosine , protein phosphorylation , jak stat signaling pathway , signal transduction , sh2 domain , biochemistry , receptor , protein kinase a , platelet derived growth factor receptor , growth factor
Transmembrane (receptor) tyrosine phosphatases are intimately involved in responses to cell-cell and cell-matrix contact. Several important issues regarding the targets and regulation of this protein family are now emerging. For example, these phosphatases exhibit complex interactions with signaling pathways involving SRC family kinases, which result from their ability to control phosphorylation of both activating and inhibitory sites in these kinases and possibly also their substrates. Similarly, integrin signaling illustrates how phosphorylation of a single protein, or the activity of a pathway, can be controlled by multiple tyrosine phosphatases, attesting to the intricate integration of these enzymes in cellular regulation. Lastly, we are starting to appreciate the roles of intracellular topology, tyrosine phosphorylation and oligomerization among the many mechanisms regulating tyrosine phosphatase activity.
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