Isolation, crystallization and preliminary X-ray diffraction analysis of L-amino-acid oxidase from Vipera ammodytes ammodytes venom

Acta Crystallogr Sect F Struct Biol Cryst Commun. 2008 Oct 1;64(Pt 10):918-21. doi: 10.1107/S1744309108027036. Epub 2008 Sep 30.

Abstract

L-Amino-acid oxidase from the venom of Vipera ammodytes ammodytes, the most venomous snake in Europe, was isolated and crystallized using the sitting-drop vapour-diffusion method. The solution conditions under which the protein sample was monodisperse were optimized using dynamic light scattering prior to crystallization. The crystals belonged to space group C2, with unit-cell parameters a = 198.37, b = 96.38, c = 109.11 A, beta = 92.56 degrees . Initial diffraction data were collected to 2.6 A resolution. The calculated Matthews coefficient is approximately 2.6 A(3) Da(-1) assuming the presence of four molecules in the asymmetric unit.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Crystallization
  • Crystallography, X-Ray
  • L-Amino Acid Oxidase / chemistry*
  • L-Amino Acid Oxidase / isolation & purification
  • Solutions
  • Viper Venoms / chemistry*
  • Viper Venoms / isolation & purification
  • Viperidae
  • X-Ray Diffraction / methods

Substances

  • Solutions
  • Viper Venoms
  • L-Amino Acid Oxidase