Expression, purification, crystallization and preliminary X-ray diffraction studies of phosphoglycerate kinase from methicillin-resistant Staphylococcus aureus MRSA252

被引:7
作者
Roychowdhury, Amlan [1 ]
Mukherjee, Somnath [1 ]
Das, Amit Kumar [1 ]
机构
[1] Indian Inst Technol Kharagpur, Dept Biotechnol, Kharagpur 721302, W Bengal, India
来源
ACTA CRYSTALLOGRAPHICA SECTION F-STRUCTURAL BIOLOGY COMMUNICATIONS | 2011年 / 67卷
关键词
3-PHOSPHOGLYCERATE KINASE; GLYCERALDEHYDE-3-PHOSPHATE DEHYDROGENASE; CATALYTIC MECHANISM; CRYSTAL-STRUCTURE; OPEN CONFORMATION; DOMAIN CLOSURE; COMPLEX; ANGSTROM; BINDING; ENZYME;
D O I
10.1107/S1744309111007391
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Phosphoglycerate kinase (PGK) from methicillin-resistant Staphylococcus aureus MRSA252 has been cloned in pQE30 expression vector, overexpressed in Escherichia coli SG13009 (pREP4) cells and purified to homogeneity. The protein was crystallized from 0.15 M CaCl2, 0.1 M HEPES-NaOH pH 6.8, 20%(w/v) polyethylene glycol 2000 at 298 K by the hanging-drop vapour-diffusion method. The crystals belonged to space group P2(1), with unit-cell parameters a = 45.14, b = 74.75, c = 58.67 angstrom, beta = 95.72 degrees. X-ray diffraction data have been collected and processed to a maximum resolution of 2.3 angstrom. The presence of one molecule in the asymmetric unit gives a Matthews coefficient (V-M) of 2.26 angstrom(3) Da(-1) with a solvent content of 46%. The structure has been solved by molecular replacement and structure refinement is now in progress.
引用
收藏
页码:668 / 671
页数:4
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