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• W2034337686 abstract "Activity assays for tyrosine phosphatases are based on the hydrolysis of a arylphosphate moiety from a synthetic substrate yielding a spectroscopically active product. Many different substrates can be used for these assays with p-nitrophenyl phosphate (pNPP), fluorescein diphosphate (FDP), and 6,8-difluoro-4-methylumbellyferyl phosphate (DiFMUP) being the most efficient and versatile. Equally, larger molecules such as phosphotyrosyl peptides can also be used to mimic more natural substrates. Activity assays include the determinations of the rate of dephosphorylation and calculations of kinetic constants such as kcat and KM. These assays are useful to identify and characterize tyrosine phosphatases and are commonly used to evaluate the efficiency of inhibitors." @default.
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• W2034337686 date "2005-01-01" @default.
• W2034337686 modified "2023-10-18" @default.
• W2034337686 title "Protein tyrosine phosphatase: enzymatic assays" @default.
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• W2034337686 doi "https://doi.org/10.1016/j.ymeth.2004.07.002" @default.
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