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

  • Marian A G de Boer-van den Berg
  • , Magda M W Ulrich
  • , H. Coenraad Hemker
  • , Berry A M Soute
  • , Cees Vermeer*
  • *Corresponding author for this work
  • University of Limburg

Research output: Contribution to journalArticleAcademicpeer-review

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.

Original languageEnglish
Pages (from-to)94-98
Number of pages5
JournalBiochimica et Biophysica Acta (BBA)/Protein Structure and Molecular
Volume831
Issue number1
DOIs
Publication statusPublished - 20 Sept 1985

Keywords

  • (Bovine liver)
  • Carboxylase
  • Descarboxyfactor
  • Vitamin K
  • Warfarin

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