Dual-specificity protein phosphatases are a subclass of protein tyrosine phosphatases that are uniquely able to hydrolyse the phosphate ester bond on both a tyrosine and a threonine or serine residue on the same protein. Dual-specificity phosphatases have a central role in the complex regulation of signalling pathways that are involved in cell stress responses, proliferation and death. Although this enzyme family is increasingly the target of drug discovery efforts in pharmaceutical companies, a summary of the salient developments in the biology and medicinal chemistry of dual-specificity phosphatases has been lacking. We hope that this comprehensive overview will stimulate further progress in the development of small-molecule inhibitors th...
The mammalian genome contains approximately 200 phosphatases that are responsible for catalytically ...
Dual-specificity protein phosphatases (DUSPs), which dephosphorylate both phosphoserine/threonine an...
With the recent clinical success of drugs targeting protein ki-nase activity, drug discovery efforts...
Dual specificity phosphatases (DUSPs) constitute a heterogeneous group of protein tyrosine phosphata...
Dual-specificity phosphatases (DSPs) are important, but poorly understood, cell signaling enzymes th...
Small molecules provide exceptionally useful tools for probing signaling targets relevant for cancer...
Several 'classical' protein tyrosine phosphatases are attractive therapeutic targets, including PTP1...
Dual-specificity phosphatases (DSPs) are important, but poorly understood, cell signaling enzymes th...
Dual specificity protein phosphatases (DSPases) are key regulators of signal transduction, oncogenes...
Phosphorylation of serine, threonine, and tyrosine controls fundamental mammalian cell events and is...
The gene family of protein phosphatases is a rich but under-exploited source of therapeutically vali...
Protein phosphorylation is the major mechanism for signaling and regulation of cellular activities. ...
Phosphatases constitute a wide class of enzymes which remove a phosphate group from the target subst...
Tyrosine phosphatases (PTPases) dephosphorylate phosphotyrosines while dual-specificity phosphatases...
Small molecules provide powerful tools to interrogate biological pathways but many important pathway...
The mammalian genome contains approximately 200 phosphatases that are responsible for catalytically ...
Dual-specificity protein phosphatases (DUSPs), which dephosphorylate both phosphoserine/threonine an...
With the recent clinical success of drugs targeting protein ki-nase activity, drug discovery efforts...
Dual specificity phosphatases (DUSPs) constitute a heterogeneous group of protein tyrosine phosphata...
Dual-specificity phosphatases (DSPs) are important, but poorly understood, cell signaling enzymes th...
Small molecules provide exceptionally useful tools for probing signaling targets relevant for cancer...
Several 'classical' protein tyrosine phosphatases are attractive therapeutic targets, including PTP1...
Dual-specificity phosphatases (DSPs) are important, but poorly understood, cell signaling enzymes th...
Dual specificity protein phosphatases (DSPases) are key regulators of signal transduction, oncogenes...
Phosphorylation of serine, threonine, and tyrosine controls fundamental mammalian cell events and is...
The gene family of protein phosphatases is a rich but under-exploited source of therapeutically vali...
Protein phosphorylation is the major mechanism for signaling and regulation of cellular activities. ...
Phosphatases constitute a wide class of enzymes which remove a phosphate group from the target subst...
Tyrosine phosphatases (PTPases) dephosphorylate phosphotyrosines while dual-specificity phosphatases...
Small molecules provide powerful tools to interrogate biological pathways but many important pathway...
The mammalian genome contains approximately 200 phosphatases that are responsible for catalytically ...
Dual-specificity protein phosphatases (DUSPs), which dephosphorylate both phosphoserine/threonine an...
With the recent clinical success of drugs targeting protein ki-nase activity, drug discovery efforts...