Literature DB >> 4041466

Vitamin K-dependent carboxylase: the carboxylation of exogenous substrates in different systems.

M A de Boer-van den Berg, M M Ulrich, H C Hemker, B A Soute, C Vermeer.   

Abstract

Two types of solid-phase carboxylase, SPC-II and SPC-X, have been prepared from the livers of warfarin-treated cows. Their enzymatic activities were compared with substrate-free carboxylase in microsomes from normal cows and substrate-bound carboxylase in microsomes from warfarin-treated cows. A number of exogenous substrates for carboxylase have been purified and tested. We found that large substrates, such as descarboxyprothrombin, are carboxylated only by substrate-free carboxylase and not by the substrate-bound enzyme. No differences in apparent Km values between solid-phase carboxylases II and X were observed.

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Year:  1985        PMID: 4041466     DOI: 10.1016/0167-4838(85)90154-2

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  2 in total

1.  Molecular cloning of matrix Gla protein: implications for substrate recognition by the vitamin K-dependent gamma-carboxylase.

Authors:  P A Price; J D Fraser; G Metz-Virca
Journal:  Proc Natl Acad Sci U S A       Date:  1987-12       Impact factor: 11.205

2.  A mutation in the propeptide of Factor IX leads to warfarin sensitivity by a novel mechanism.

Authors:  K Chu; S M Wu; T Stanley; D W Stafford; K A High
Journal:  J Clin Invest       Date:  1996-10-01       Impact factor: 14.808

  2 in total

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