首页> 美国卫生研究院文献>Acta Crystallographica Section F: Structural Biology and Crystallization Communications >Cloning expression purification crystallization and preliminary structure determination of glucose-1-phosphate uridylyltransferase (UgpG) from Sphingomonas elodea ATCC 31461 bound to glucose-1-phosphate
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Cloning expression purification crystallization and preliminary structure determination of glucose-1-phosphate uridylyltransferase (UgpG) from Sphingomonas elodea ATCC 31461 bound to glucose-1-phosphate

机译:鞘氨醇单胞菌ATCC 31461与1-磷酸葡萄糖结合的葡萄糖-1-磷酸尿嘧啶转移酶(UgpG)的克隆表达纯化结晶和初步结构测定

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摘要

The cloning, expression, purification, crystallization and preliminary crystallographic analysis of glucose-1-phosphate uridylyltransferase (UgpG) from Sphingomonas elodea ATCC 31461 bound to glucose-1-phosphate are reported. Diffraction data sets were obtained from seven crystal forms in five different space groups, with highest resolutions ranging from 4.20 to 2.65 Å. The phase problem was solved for a P21 crystal form using multiple isomorphous replacement with anomalous scattering from an osmium derivative and a SeMet derivative. The best native crystal in space group P21 has unit-cell parameters a = 105.5, b = 85.7, c = 151.8 Å, β = 105.2°. Model building and refinement are currently under way.
机译:报道了与鞘氨醇-1-磷酸结合的鞘氨醇单胞菌ATCC 31461的葡萄糖-1-磷酸尿嘧啶转移酶(UgpG)的克隆,表达,纯化,结晶和初步晶体学分析。衍射数据集来自五个不同空间组中的七种晶体形式,最高分辨率范围为4.20至2.65 to。对于P21晶形,使用multiple同衍生物和SeMet衍生物的异常散射进行了多次同构置换,解决了相位问题。空间群P21中最好的天然晶体的晶胞参数a = 105.5,b = 85.7,c = 151.8Å,β= 105.2°。模型的建立和完善目前正在进行中。

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