| Literature DB >> 3543932 |
J W Suttie, J A Hoskins, J Engelke, A Hopfgartner, H Ehrlich, N U Bang, R M Belagaje, B Schoner, G L Long.
Abstract
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.Entities:
Mesh:
Substances:
Year: 1987 PMID: 3543932 PMCID: PMC304269 DOI: 10.1073/pnas.84.3.634
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205