Crystallization and preliminary analysis of xenobiotic reductase B from Pseudomonas fluorescens I-C

被引:9
作者
Orville, AM [1 ]
Manning, L
Blehert, DS
Fox, BG
Chambliss, GH
机构
[1] Georgia Inst Technol, Sch Chem & Biochem, Atlanta, GA 30332 USA
[2] Univ Wisconsin, Dept Bacteriol, Madison, WI 53706 USA
[3] Univ Wisconsin, Coll Agr & Life Sci, Dept Biochem, Madison, WI 53706 USA
来源
ACTA CRYSTALLOGRAPHICA SECTION D-STRUCTURAL BIOLOGY | 2004年 / 60卷
关键词
D O I
10.1107/S0907444904010157
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Single crystals have been obtained of xenobiotic reductase B ( XenB), a flavoenzyme isolated and cloned from Pseudomonas fluorescens I-C. The enzyme catalyzes the NADPH-dependent elimination of nitrite from nitroglycerin with an approximately fivefold kinetic preference for the middle nitro group, primarily yielding 1,3-dinitroglycerol. X-ray diffraction data sets have been collected from native crystals to 2.3 Angstrom resolution. The space group is P4(1)2(1)2, with unit-cell parameters a = b = 140, c = 95.6 Angstrom. The asymmetric unit is likely to contain at least two XenB molecules ( V-M = 3.1 Angstrom(3) Da(-1), 60% solvent) and a molecular-replacement solution has been determined in order to solve the structure.
引用
收藏
页码:1289 / 1291
页数:3
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