Crystallization and preliminary X-ray diffraction analysis of Leishmania major dihydroorotate dehydrogenase

Acta Crystallogr Sect F Struct Biol Cryst Commun. 2006 Oct 1;62(Pt 10):1049-51. doi: 10.1107/S1744309106038966. Epub 2006 Sep 30.

Abstract

Dihydroorotate dehydrogenases (DHODHs) are flavin-containing enzymes that catalyze the oxidation of L-dihydroorotate to orotate, the fourth step in the de novo pyrimidine nucleotide synthesis pathway. In this study, DHODH from Leishmania major has been crystallized by the vapour-diffusion technique using lithium sulfate as the precipitating agent. The crystals belong to space group P6(1), with unit-cell parameters a = 143.7, c = 69.8 A. X-ray diffraction data were collected to 2.0 A resolution using an in-house rotating-anode generator. Analysis of the solvent content and the self-rotation function indicate the presence of two molecules in the asymmetric unit. The structure has been solved by the molecular-replacement technique.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Crystallization
  • Dihydroorotate Dehydrogenase
  • Leishmania major / enzymology*
  • Lithium Compounds / metabolism
  • Oxidoreductases Acting on CH-CH Group Donors / chemistry*
  • Oxidoreductases Acting on CH-CH Group Donors / isolation & purification
  • Sulfates / metabolism
  • X-Ray Diffraction

Substances

  • Dihydroorotate Dehydrogenase
  • Lithium Compounds
  • Sulfates
  • lithium sulfate
  • Oxidoreductases Acting on CH-CH Group Donors