Crystallization and preliminary X-ray diffraction studies of D-glyceraldehyde-3-phosphate dehydrogenase from the hyperthermophilic archaeon Methanothermus fervidus

Acta Crystallogr D Biol Crystallogr. 1999 Jul;55(Pt 7):1353-5. doi: 10.1107/s0907444999005363.

Abstract

The homotetrameric holo-D-glyceraldehyde-3-phosphate dehydrogenase from the hyperthermophilic archaeon Methanothermus fervidus has been crystallized in the presence of NADP+ using the hanging-drop vapour-diffusion method. Crystals grew from a solution containing 2-methyl-2,4-pentanediol and magnesium acetate. A native data set has been collected to 2.1 A using synchrotron radiation and cryocooling. Diffraction data have been processed in the orthorhombic system (space group P21212) with unit-cell dimensions a = 136.7, b = 153.3, c = 74.9 A and one tetramer per asymmetric unit.

MeSH terms

  • Archaea / enzymology*
  • Crystallization
  • Crystallography, X-Ray
  • Enzyme Stability
  • Glyceraldehyde-3-Phosphate Dehydrogenases / chemistry*
  • Protein Conformation
  • Recombinant Proteins / chemistry

Substances

  • Recombinant Proteins
  • Glyceraldehyde-3-Phosphate Dehydrogenases

Associated data

  • PDB/1CF2