Structure of pig heart citrate synthase at 1.78 A resolution

Acta Crystallogr Sect F Struct Biol Cryst Commun. 2009 May 1;65(Pt 5):430-4. doi: 10.1107/S1744309109008343. Epub 2009 Apr 24.

Abstract

Pig heart citrate synthase was crystallized from a small-molecule cocktail containing cystamine dihydrochloride, aspartame and benzamidine hydrochloride. The structure was refined to an R factor of 0.179 (R(free) = 0.222) using synchrotron data to a resolution of 1.78 A. The model includes the full-length protein, a chloride ion, a sulfate ion, 305 water molecules and an unexpected moiety attached through a disulfide linkage to Cys184, which was modeled as a half-cystamine molecule generated by disulfide exchange with the cystamine in the small-molecule cocktail.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Citrate (si)-Synthase / chemistry*
  • Citrate (si)-Synthase / genetics
  • Crystallography, X-Ray
  • Models, Molecular
  • Myocardium / enzymology*
  • Protein Structure, Tertiary
  • Sus scrofa* / genetics

Substances

  • Citrate (si)-Synthase