Literature DB >> 8338638

Prostaglandin H synthase as a limiting enzyme of prostaglandin synthesis: substrate-induced inactivation as a new kind of enzyme activity regulation.

S D Varfolomeyev1, A T Mevkh.   

Abstract

The properties of prostaglandin H synthase (PGHS) as a protein and as a rate-limiting enzyme of physiologically active prostanoid synthesis have been considered. Fast and dramatic changes in the protein structure were shown to accompany inactivation of PGHS in the course of the reaction. The conclusions derived from the study of the steady-state kinetics of the enzyme action are discussed, and a minimal kinetic scheme is proposed. The mechanism of substrate-induced inactivation of PGHS is suggested as a basis for the regulation at the prostanoid level. The mechanism is hypothesized to be a new regulatory mechanism of enzyme activity in biological systems.

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Year:  1993        PMID: 8338638

Source DB:  PubMed          Journal:  Biotechnol Appl Biochem        ISSN: 0885-4513            Impact factor:   2.431


  3 in total

1.  Ultralow concentrations of ibuprofen activate cell prostaglandin synthesis.

Authors:  M G Sergeeva; M V Gonchar; V V Chistyakov; A T Mevkh
Journal:  Appl Biochem Biotechnol       Date:  1996 Oct-Nov       Impact factor: 2.926

2.  Hydrogen peroxide-mediated alteration of the heme prosthetic group of metmyoglobin to an iron chlorin product: evidence for a novel oxidative pathway.

Authors:  K Sugiyama; R J Highet; A Woods; R J Cotter; Y Osawa
Journal:  Proc Natl Acad Sci U S A       Date:  1997-02-04       Impact factor: 11.205

3.  Inhibition of brain prostaglandin endoperoxide synthase-2 prevents the preparturient increase in fetal adrenocorticotropin secretion in the sheep fetus.

Authors:  Jason Gersting; Christine E Schaub; Maureen Keller-Wood; Charles E Wood
Journal:  Endocrinology       Date:  2008-05-01       Impact factor: 4.736

  3 in total

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