Crystallographic characterization of the N-terminal domain of PEX1

Acta Crystallogr D Biol Crystallogr. 2004 Nov;60(Pt 11):2098-9. doi: 10.1107/S090744490402428X. Epub 2004 Oct 20.

Abstract

Peroxisomal enzymes are responsible for several primary metabolism pathways, including beta-oxidation and lipid biosynthesis. PEX1 and PEX6 are hexameric AAA-type ATPases and both are necessary for the import of more than 50 peroxisomal resident proteins from the cytosol into peroxisomes. In this study, PEX1 N-terminal domain crystals have been prepared. The crystals belong to space group P3(1) or P3(2), with unit-cell parameters a = b = 63.5 A, c = 33.5 A, and contain one protein molecule per crystallographic asymmetric unit. An intensity data set was collected to a resolution of 2.05 A.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • ATPases Associated with Diverse Cellular Activities
  • Adenosine Triphosphatases / chemistry*
  • Adenosine Triphosphatases / genetics
  • Animals
  • Crystallization
  • Crystallography, X-Ray
  • Mice
  • Peptide Fragments / chemistry
  • Peptide Fragments / genetics
  • Protein Structure, Tertiary

Substances

  • Peptide Fragments
  • Adenosine Triphosphatases
  • ATPases Associated with Diverse Cellular Activities
  • Pex1 protein, mouse