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Structure of pig heart citrate synthase at 1.78 A resolution.

Authors :
Larson, Steven B
Larson, Steven B
Day, John S
Nguyen, Chieugiang
Cudney, Robert
McPherson, Alexander
Larson, Steven B
Larson, Steven B
Day, John S
Nguyen, Chieugiang
Cudney, Robert
McPherson, Alexander
Source :
Acta crystallographica. Section F, Structural biology and crystallization communications; vol 65, iss Pt 5, 430-434; 1744-3091
Publication Year :
2009

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.

Details

Database :
OAIster
Journal :
Acta crystallographica. Section F, Structural biology and crystallization communications; vol 65, iss Pt 5, 430-434; 1744-3091
Notes :
application/pdf, Acta crystallographica. Section F, Structural biology and crystallization communications vol 65, iss Pt 5, 430-434 1744-3091
Publication Type :
Electronic Resource
Accession number :
edsoai.on1367446135
Document Type :
Electronic Resource