| Literature DB >> 1168073 |
K Ahmed, M J Wilson, A T Davis.
Abstract
The maximal rates of the protein kinase (ATP: protein phosphotransferase, EC 2.7.1.37) reaction studied with chicken egg yolk phosvitin as substrate are dependent on the level of dephosphorylation of phosvitin. 30 per cent dephospho-phosvitin gives the optimal initial rates. With varying levels of dephosphorylation, the apparent Km for the substrate also changes in a biphasic manner. If this factor is taken into account, and a suitable adjustment is made for the concentration of dephospho-phosvitin in the reaction it is possible to achieve maximal rates for the kinase reaction with phosvitin preparations of varying levels of dephosphorylation. Such a consideration is important for comparing the results of protein kinase studies using phosvitin as the substrate.Entities:
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Year: 1975 PMID: 1168073 DOI: 10.1016/0005-2744(75)90288-0
Source DB: PubMed Journal: Biochim Biophys Acta ISSN: 0006-3002