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Vitamin K-dependent carboxylase: possible role of the substrate "propeptide" as an intracellular recognition site.
Author(s) -
John W. Suttie,
JoAnn Hoskins,
J. Engelke,
A Hopfgartner,
H. J. Ehrlich,
Nils U. Bang,
Rama M. Belagaje,
Brigitte Schoner,
George L. Long
Publication year - 1987
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.84.3.634
Subject(s) - protein precursor , biochemistry , peptide sequence , pyruvate carboxylase , biology , amino acid , enzyme , chemistry , gene
The liver microsomal vitamin K-dependent carboxylase catalyzes the posttranslational conversion of specific glutamate residues to gamma-carboxyglutamate residues in a limited number of proteins. A number of these proteins have been shown to contain a homologous basic amino acid-rich "propeptide" between the leader sequence and the amino terminus of the mature protein. Plasmids encoding protein C, a vitamin K-dependent protein, containing or lacking a propeptide region were constructed and the protein was expressed in Escherichia coli. The protein products were assayed as substrates in an in vitro vitamin K-dependent carboxylase system. Only proteins containing a propeptide region were substrates for the enzyme. These data support the hypothesis that this sequence of the primary gene product is an important recognition site for this processing enzyme.

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