| Literature DB >> 6100374 |
D M Gibson, J H Steinrauf, R A Parker.
Abstract
Steady-state and kinetic equations have been developed which characterize the rates of formation, interconversion, and degradation of an enzyme protein subject to reversible phosphorylation. The theoretical model system incorporates separate fractional degradative rate constants for the phosphorylated and dephosphorylated protein species. The classical models for interconvertible enzymes, and for protein turnover, are special limiting situations of the general model presented here.Mesh:
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Year: 1984 PMID: 6100374 DOI: 10.1007/bf00743237
Source DB: PubMed Journal: J Bioenerg Biomembr ISSN: 0145-479X Impact factor: 2.945