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Molecular basis of hemophilia B: a defective enzyme due to an unprocessed propeptide is caused by a point mutation in the factor IX precursor.
Author(s) -
David Diuguid,
MarieJosèphe Rabiet,
Bruce Furie,
Howard A. Liebman,
Bruce Furie
Publication year - 1986
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.83.16.5803
Subject(s) - protein precursor , point mutation , factor ix , mutant , biochemistry , cleavage (geology) , mutation , arginine , serine protease , serine , mutant protein , enzyme , microbiology and biotechnology , chemistry , protease , biology , amino acid , gene , fracture (geology) , paleontology
A mutant factor IX, designated factor IXCambridge, was isolated from a patient with hemophilia B. This protein includes an 18-residue propeptide attached to the NH2 terminus of factor IX. A point mutation at residue -1, from an arginine to a serine, precludes cleavage of the propeptide by a processing protease and interferes with gamma-carboxylation of the factor IX, indicating the importance of the leader sequence in substrate recognition by the vitamin K-dependent carboxylase. This represents an example of an enzyme defect due to the presence of a point mutation in a precursor protein (preproenzyme) that is the cause of a human hereditary disease. This defect will serve as a prototype for understanding the molecular basis of some forms of hemophilia and other hereditary enzyme deficiencies.

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