• Title of article

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

  • Author/Authors

    Naureckiene، نويسنده , , Saule and Ma، نويسنده , , Linh and Sreekumar، نويسنده , , Kodangattil and Purandare، نويسنده , , Urmila and Frederick Lo، نويسنده , , C and Huang، نويسنده , , Ying and Chiang، نويسنده , , Lillian W and Grenier، نويسنده , , Jill M and Ozenberger، نويسنده , , Bradley A and Steven Jacobsen، نويسنده , , J and Kennedy، نويسنده , , Jeffrey D and DiStefano، نويسنده , , Peter E. and Wood، نويسنده , , Andrew and Bingham، نويسنده , , Brendan، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2003
  • Pages
    13
  • From page
    55
  • To page
    67
  • 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 , autoprocessing , Convertase , P-domain , RGD motif , mutational analysis
  • Journal title
    Archives of Biochemistry and Biophysics
  • Serial Year
    2003
  • Journal title
    Archives of Biochemistry and Biophysics
  • Record number

    1621427