Crystallization and preliminary X-ray crystallographic studies of mavicyanin from Cucurbita pepo medullosa

被引:1
|
作者
Xie, Y
Inoue, T
Miyamoto, Y
Matsumura, H
Kataoka, K
Yamaguchi, K
Suzuki, S
Kai, Y [1 ]
机构
[1] Osaka Univ, Grad Sch Engn, Dept Chem Mat, Osaka 5650871, Japan
[2] Japan Sci & Technol Corp, PRESTO, Struct & Funct Biomol Grp, Kyoto 6040847, Japan
[3] Osaka Univ, Grad Sch Sci, Dept Chem, Osaka 5600043, Japan
关键词
D O I
10.1107/S0907444903011326
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Mavicyanin isolated from Cucurbita pepo medullosa is a glycosylated protein containing a single polypeptide chain of 109 amino-acid residues and is a member of the phytocyanin subclass of cupredoxins. Non-glycosylated recombinant mavicyanin, which was expressed in Escherichia coli, was crystallized by the hanging-drop vapour-diffusion method with ammonium sulfate as the precipitant at pH 5.5. The crystals belonged to the hexagonal space group P6(1) ( or P6(5)), with unit-cell parameters a = 64.0, c = 245.0 Angstrom, four molecules per asymmetric unit and a solvent content of 59%. X-ray diffraction data were collected to 1.6 Angstrom resolution. To solve the structure of mavicyanin, the MAD method as well as a Patterson search method using the structure of stellacyanin as a starting model are presently being utilized.
引用
收藏
页码:1474 / 1476
页数:3
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