4.6 Article

Functional characterization of Narc 1, a novel proteinase related to proteinase K

Journal

ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS
Volume 420, Issue 1, Pages 55-67

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.abb.2003.09.011

Keywords

Narc 1; proteinase K; subtilase; convertase; autoprocessing; mutational analysis; P-domain; RGD motif

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The NARC 1 gene encodes a novel proteinase K family proteinase. The domain structure of rat Narc 1 resembles that of the subtilisin-like proprotein convertases (SPCs), except that rNarc 1 lacks the canonical P-domain of SPCs, retaining only the RGD motif as part of what might be a cryptically functioning P-domain. Narc 1 undergoes autocatalytic intramolecular processing at the site LVFAQdown arrow, resulting in the cleavage of its prosegment and the generation of an active proteinase with a broad alkaline pH optimum and no apparent calcium requirement for activity. Both primary and secondary structural determinants influence Narc 1 substrate recognition. Our functional characterization of Narc 1 reinforces the inference drawn from the analysis of its predicted structure that this enzyme is most closely related to representatives of the proteinase K family, but that it is also sufficiently different to warrant its possible classification in a separate sub-family. (C) 2003 Elsevier Inc. All rights reserved.

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