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

被引:136
作者
Naureckiene, S
Ma, L
Sreekumar, K
Purandare, U
Lo, CF
Huang, Y
Chiang, LW
Grenier, JM
Ozenberger, BA
Jacobsen, JS
Kennedy, JD
DiStefano, PS
Wood, A
Bingham, B
机构
[1] Wyeth Ayerst Res, Neurosci Discovery Res, Princeton, NJ 08543 USA
[2] Wyeth Ayerst Res, Prot Chem & Proteom, Cambridge, MA 02140 USA
[3] Millennium Pharmaceut Inc, Cambridge, MA 02139 USA
关键词
Narc; 1; proteinase K; subtilase; convertase; autoprocessing; mutational analysis; P-domain; RGD motif;
D O I
10.1016/j.abb.2003.09.011
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:55 / 67
页数:13
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