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Functional characterization of Narc 1, a novel proteinase related to proteinase K
Authors:Naureckiene Saule  Ma Linh  Sreekumar Kodangattil  Purandare Urmila  Lo C Frederick  Huang Ying  Chiang Lillian W  Grenier Jill M  Ozenberger Bradley A  Jacobsen J Steven  Kennedy Jeffrey D  DiStefano Peter S  Wood Andrew  Bingham Brendan
Institution:Neuroscience Discovery Research, Wyeth Research, CN 8000, Princeton, NJ 08543-8000, USA.
Abstract: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 LVFAQ/, 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.
Keywords:Narc 1  Proteinase K  Subtilase  Convertase  Autoprocessing  Mutational analysis  P-domain  RGD motif
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