• Title of article

    Solution Structure of ASPP2 N-terminal Domain (N-ASPP2) Reveals a Ubiquitin-like Fold

  • Author/Authors

    Henning Tidow، نويسنده , , Antonina Andreeva، نويسنده , , Trevor J. Rutherford، نويسنده , , Alan R. Fersht، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2007
  • Pages
    11
  • From page
    948
  • To page
    958
  • Abstract
    Proteins of the ASPP family bind to p53 and regulate p53-mediated apoptosis. Two family members, ASPP1 and ASPP2, have pro-apoptotic functions while iASPP shows anti-apoptotic responses. However, both the mechanism of enhancement/repression of apoptosis and the molecular basis for their different responses remain unknown. To address the role of the N-termini of pro-apoptotic ASPP proteins, we solved the solution structure of N-ASPP2 (1–83) by NMR spectroscopy. The structure of this domain reveals a β-Grasp ubiquitin-like fold. Our findings suggest a possible role for the N-termini of ASPP proteins in binding to other proteins in the apoptotic response network and thus mediating their selective pro-apoptotic function.
  • Keywords
    ASPP2 , NMR , ubiquitin-like , ?-Grasp , solution structure
  • Journal title
    Journal of Molecular Biology
  • Serial Year
    2007
  • Journal title
    Journal of Molecular Biology
  • Record number

    1249636