Literature DB >> 1168073

Phosvitin phosphate content. Implications for protein kinase assay.

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.

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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


  3 in total

1.  Nuclear envelope of the seminal-vesicle epithelium.

Authors:  C M Veneziale; M E Utz; R C Steer; M J Wilson; K Ahmed
Journal:  Biochem J       Date:  1981-08-15       Impact factor: 3.857

2.  Effects of polyamines on prostatic chromatin- and non-histone-protein-associated protein kinase reactions.

Authors:  K Ahmed; M J Wilson; S A Goueli; H G Williams-Ashman
Journal:  Biochem J       Date:  1978-12-15       Impact factor: 3.857

3.  Polyamine-stimulated phosphorylation of prostatic spermine-binding protein is mediated only by cyclic AMP-independent protein kinases.

Authors:  S A Goueli; A T Davis; R A Hiipakka; S Liao; K Ahmed
Journal:  Biochem J       Date:  1985-09-01       Impact factor: 3.857

  3 in total

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