Crystallization and preliminary X-ray crystallographic studies of the axin DIX domain

Acta Crystallogr Sect F Struct Biol Cryst Commun. 2007 Jun 1;63(Pt 6):529-31. doi: 10.1107/S1744309107022579. Epub 2007 May 18.

Abstract

Axin is a negative regulator of the canonical Wnt signalling pathway that mediates the phosphorylation of beta-catenin by glycogen synthase kinase 3beta. The DIX domain of rat axin, which is important for its homooligomerization and interactions with other regulators in the Wnt pathway, was purified and crystallized by the sitting-drop vapour-diffusion technique using polyethylene glycol 6000 and lithium sulfate as crystallization agents. Crystals belong to space group P6(1) or P6(5), with unit-cell parameters a = b = 91.49, c = 84.92 A. An X-ray diffraction data set has been collected to a nominal resolution of 2.9 A.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Axin Protein
  • Crystallization
  • Crystallography, X-Ray
  • Intracellular Signaling Peptides and Proteins / chemistry*
  • Intracellular Signaling Peptides and Proteins / metabolism
  • Microfilament Proteins / chemistry*
  • Microfilament Proteins / metabolism
  • Protein Structure, Tertiary
  • Rats
  • Repressor Proteins / chemistry*
  • Repressor Proteins / physiology
  • Signal Transduction / physiology
  • Wnt Proteins / chemistry
  • Wnt Proteins / physiology

Substances

  • Axin Protein
  • DIXDC1 protein, human
  • Intracellular Signaling Peptides and Proteins
  • Microfilament Proteins
  • Repressor Proteins
  • Wnt Proteins