Purification, crystallization and preliminary X-ray analysis of isocitrate dehydrogenase kinase/phosphatase from Escherichia coli

被引:9
|
作者
Zheng, Jimin [1 ]
Lee, Daniel C. [1 ]
Jia, Zongchao [1 ]
机构
[1] Queens Univ, Dept Biochem, Kingston, ON K7L 3N6, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
KINASE PHOSPHATASE; NUCLEOTIDE-SEQUENCE; PHOSPHORYLATION; ACEK;
D O I
10.1107/S1744309109014729
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The Escherichia coli aceK gene encodes isocitrate dehydrogenase kinase/phosphatase (EC 2.7.11.5), a bifunctional protein that phosphorylates and dephosphorylates isocitrate dehydrogenase (IDH), resulting in its inactivation and activation, respectively. This reversible (de) phosphorylation directs isocitrate, an intermediate of the citric acid cycle, to either go through the full cycle or to enter the glyoxylate bypass. In the present study, the AceK protein from E. coli has been purified and crystallized. Three crystal forms were obtained from very similar crystallization conditions. The crystals belong to space groups P4(1)2(1)2, P3(2)21 and P2(1)2(1)2(1) and diffracted X-rays to resolutions of 2.9, 3.0 and 2.7 angstrom, respectively.
引用
收藏
页码:536 / 539
页数:4
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