...
首页> 外文期刊>Acta crystallographica.Section D. Biological crystallography >A novel crystal form of pyrrolysyl-tRNA synthetase reveals the pre- and post-aminoacyl-tRNA synthesis conformational states of the adenylate and aminoacyl moieties and an asparagine residue in the catalytic site
【24h】

A novel crystal form of pyrrolysyl-tRNA synthetase reveals the pre- and post-aminoacyl-tRNA synthesis conformational states of the adenylate and aminoacyl moieties and an asparagine residue in the catalytic site

机译:小说pyrrolysyl-tRNA合成酶的晶体形式揭示了预处理和post-aminoacyl-tRNA腺苷酸的合成构象状态和氨酰基根和一个天冬酰胺残留在催化部位

获取原文
获取原文并翻译 | 示例
           

摘要

Structures of Methanosarcina mazei pyrrolysyl-tRNA synthetase (PylRS) have been determined in a novel crystal form. The triclinic form crystals contained two PylRS dimers (four monomer molecules) in the asymmetric unit, in which the two subunits in one dimer each bind N-(tert-butyloxycarbonyl)-l - lysyladenylate (BocLys-AMP) and the two subunits in the other dimer each bind AMP. The BocLys-AMP molecules adopt a curved conformation and the C position of BocLys-AMP protrudes from the active site. The Β7-Β8 hairpin structures in the four PylRS molecules represent distinct conformations of different states of the aminoacyl-tRNA synthesis reaction. Tyr384, at the tip of the Β7-Β8 hairpin, moves from the edge to the inside of the active-site pocket and adopts multiple conformations in each state. Furthermore, a new crystal structure of the BocLys-AMPPNP-bound form is also reported. The bound BocLys adopts an unusually bent conformation, which differs from the previously reported structure. It is suggested that the present BocLys-AMPPNP-bound, BocLys-AMP-bound and AMP-bound complexes represent the initial binding of an amino acid (or pre-aminoacyl-AMP synthesis), pre-aminoacyl-tRNA synthesis and post-aminoacyl-tRNA synthesis states, respectively. The conformational changes of Asn346 that accompany the aminoacyl-tRNA synthesis reaction have been captured by X-ray crystallographic analyses. The orientation of the Asn346 side chain, which hydrogen-bonds to the carbonyl group of the amino-acid substrate, shifts by a maximum of 85-90° around the CΒ atom.
机译:结构的甲烷八叠球菌属mazei pyrrolysyl-tRNA合成酶(PylRS)决定的新型晶体形式。包含两个PylRS二聚体(四个单体分子)的不对称单位,两个子单元每个绑定在一个二聚体N - (tert-butyloxycarbonyl) - l - lysyladenylate(BocLys-AMP)和两个子单元每个绑定AMP。BocLys-AMP分子二聚体采用弯曲的构象和C的位置BocLys-AMP突出于活动网站。Β7 - 8Β四PylRS发夹结构分子代表不同的构象不同的州的氨酰合成的反应。发夹,从边缘到内部活性部位口袋,采用多个每个州的构象。晶体结构的BocLys-AMPPNP-bound形式也报道。异常弯曲构象,这不同于之前报道的结构。建议目前BocLys-AMPPNP-bound,BocLys-AMP-bound和AMP-bound复合物代表一种氨基酸的最初的绑定(或pre-aminoacyl-AMP合成),pre-aminoacyl-tRNA合成和post-aminoacyl-tRNA合成,分别。氨酰Asn346伴随合成反应已经被x射线晶体分析。Asn346侧链,氢键羰基的氨基酸衬底,变化最大的85 - 90°CΒ原子。

著录项

获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号