Combinatorial control of the specificity of protein tyrosine phosphatases

NK Tonks, BG Neel - Current opinion in cell biology, 2001 - Elsevier
NK Tonks, BG Neel
Current opinion in cell biology, 2001Elsevier
Protein tyrosine phosphatases (PTPs), the enzymes that dephosphorylate tyrosyl
phosphoproteins, were initially believed to be few in number and serve a 'housekeeping'role
in signal transduction. Recent work indicates that this is totally incorrect. Instead, PTPs
comprise a large superfamily whose members play critical roles in a wide variety of cellular
processes. Moreover, PTPs exhibit exquisite substrate specificity in vivo. Recent evidence
has led us to propose that members of the PTP family achieve selectivity through different …
Protein tyrosine phosphatases (PTPs), the enzymes that dephosphorylate tyrosyl phosphoproteins, were initially believed to be few in number and serve a ‘housekeeping’ role in signal transduction. Recent work indicates that this is totally incorrect. Instead, PTPs comprise a large superfamily whose members play critical roles in a wide variety of cellular processes. Moreover, PTPs exhibit exquisite substrate specificity in vivo. Recent evidence has led us to propose that members of the PTP family achieve selectivity through different combinations of specific targeting strategies and intrinsic catalytic domain specificity.
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