Severe diffraction anisotropy, rotational pseudosymmetry and twinning complicate the refinement of a pentameric coiled-coil structure of NSP4 of rotavirus

Acta Crystallogr D Biol Crystallogr. 2012 Nov;68(Pt 11):1541-8. doi: 10.1107/S090744491203836X. Epub 2012 Oct 18.

Abstract

The crystal structure of the region spanning residues 95-146 of the rotavirus nonstructural protein NSP4 from the asymptomatic human strain ST3 was determined at a resolution of 2.5 Å. Severe diffraction anisotropy, rotational pseudosymmetry and twinning complicated the refinement of this structure. A systematic explanation confirming the crystal pathologies and describing how the structure was successfully refined is given in this report.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anisotropy
  • Crystallography, X-Ray
  • Glycoproteins / chemistry*
  • Humans
  • Models, Molecular
  • Rotavirus / chemistry*
  • Rotavirus Infections / virology*
  • Toxins, Biological / chemistry*
  • Viral Nonstructural Proteins / chemistry*

Substances

  • Glycoproteins
  • NS28 protein, rotavirus
  • Toxins, Biological
  • Viral Nonstructural Proteins