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Crystallization and preliminary X-ray diffraction analysis of an Escherichia coli tRNAGly acceptor-stem microhelix

机译:大肠杆菌tRNAGly受体-茎微螺旋的结晶和初步X射线衍射分析

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摘要

The tRNAGly and glycyl-tRNA synthetase (GlyRS) system is an evolutionary special case within the class II aminoacyl-tRNA synthetases because two divergent types of GlyRS exist: an archaebacterial/human type and an eubacterial type. The tRNA identity elements which determine the correct aminoacylation process are located in the aminoacyl domain of tRNAGly. To obtain further insight concerning structural investigation of the identity elements, the Escherichia coli seven-base-pair tRNAGly acceptor-stem helix was crystallized. Data were collected to 2.0 Å resolution using synchrotron radiation. Crystals belong to space group P3121 or P3221, with unit-cell parameters a = b = 35.35, c = 130.82 Å, α = β = 90, γ = 120° and two molecules in the asymmetric unit.
机译:tRNA Gly 和甘氨酰-tRNA合成酶(GlyRS)系统是II类氨酰基-tRNA合成中的一个进化特例,因为存在两种不同类型的GlyRS:古细菌/人和真细菌。决定正确的氨酰化过程的tRNA同一性元件位于tRNA Gly 的氨酰基结构域中。为了进一步了解身份元素的结构,我们对大肠杆菌的七碱基对tRNA Gly 受体-茎螺旋进行了结晶。使用同步加速器辐射以2.0?Å的分辨率收集数据。晶体属于空间群P3121或P3221,其晶胞参数a = b = 35.35,c = 130.82,α=β= 90,γ= 120°,两个分子处于不对称单元中。

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