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本文引用的文献

1
Regulation of enteric vapBC transcription: induction by VapC toxin dimer-breaking.肠内 vapBC 转录的调节:VapC 毒素二聚体断裂诱导。
Nucleic Acids Res. 2012 May;40(10):4347-57. doi: 10.1093/nar/gks029. Epub 2012 Jan 27.
2
Toxin-antitoxin systems of Mycobacterium smegmatis are essential for cell survival.分枝杆菌的毒素-抗毒素系统对细胞存活至关重要。
J Biol Chem. 2012 Feb 17;287(8):5340-56. doi: 10.1074/jbc.M111.286856. Epub 2011 Dec 23.
3
Crystal structure of the DNA-bound VapBC2 antitoxin/toxin pair from Rickettsia felis.菲氏立克次体 DNA 结合型 VapBC2 抗毒素/毒素对的晶体结构
Nucleic Acids Res. 2012 Apr;40(7):3245-58. doi: 10.1093/nar/gkr1167. Epub 2011 Dec 2.
4
Crystal structure of the VapBC toxin-antitoxin complex from Shigella flexneri reveals a hetero-octameric DNA-binding assembly.志贺氏菌 VapBC 毒素-抗毒素复合物的晶体结构揭示了一种异型八聚体 DNA 结合组装体。
J Mol Biol. 2011 Dec 16;414(5):713-22. doi: 10.1016/j.jmb.2011.10.024. Epub 2011 Oct 20.
5
Selective translation of leaderless mRNAs by specialized ribosomes generated by MazF in Escherichia coli.在大肠杆菌中,由 MazF 产生的无帽 mRNA 特异性核糖体进行无帽 mRNA 的选择性翻译。
Cell. 2011 Sep 30;147(1):147-57. doi: 10.1016/j.cell.2011.07.047. Epub 2011 Sep 22.
6
Toxins-antitoxins: diversity, evolution and function.毒素-抗毒素:多样性、进化和功能。
Crit Rev Biochem Mol Biol. 2011 Oct;46(5):386-408. doi: 10.3109/10409238.2011.600437. Epub 2011 Aug 5.
7
Bacterial persistence by RNA endonucleases.RNA 内切酶介导的细菌持续存在。
Proc Natl Acad Sci U S A. 2011 Aug 9;108(32):13206-11. doi: 10.1073/pnas.1100186108. Epub 2011 Jul 25.
8
Enteric virulence associated protein VapC inhibits translation by cleavage of initiator tRNA.肠致病性相关蛋白 VapC 通过切割起始 tRNA 抑制翻译。
Proc Natl Acad Sci U S A. 2011 May 3;108(18):7403-7. doi: 10.1073/pnas.1019587108. Epub 2011 Apr 18.
9
A novel mechanism of programmed cell death in bacteria by toxin-antitoxin systems corrupts peptidoglycan synthesis.毒素-抗毒素系统介导的细菌程序性细胞死亡的新机制会破坏肽聚糖的合成。
PLoS Biol. 2011 Mar;9(3):e1001033. doi: 10.1371/journal.pbio.1001033. Epub 2011 Mar 22.
10
Diversity of bacterial type II toxin-antitoxin systems: a comprehensive search and functional analysis of novel families.细菌 II 型毒素-抗毒素系统的多样性:新型家族的全面搜索和功能分析。
Nucleic Acids Res. 2011 Jul;39(13):5513-25. doi: 10.1093/nar/gkr131. Epub 2011 Mar 21.

来自大肠杆菌O157的ParE2-PaaA2毒素-抗毒素复合物在溶液和晶体中形成异十二聚体。

The ParE2-PaaA2 toxin-antitoxin complex from Escherichia coli O157 forms a heterodocecamer in solution and in the crystal.

作者信息

Sterckx Yann G J, Garcia-Pino Abel, Haesaerts Sarah, Jové Thomas, Geerts Lieselotte, Sakellaris Viktor, Van Melderen Laurence, Loris Remy

机构信息

Structural Biology Brussels, Department of Biotechnology, Vrije Universiteit Brussel, Pleinlaan 2, B-1050 Brussel, Belgium.

出版信息

Acta Crystallogr Sect F Struct Biol Cryst Commun. 2012 Jun 1;68(Pt 6):724-9. doi: 10.1107/S1744309112015230. Epub 2012 May 25.

DOI:10.1107/S1744309112015230
PMID:22684081
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3370921/
Abstract

Escherichia coli O157 paaR2-paaA2-parE2 constitutes a unique three-component toxin-antitoxin (TA) module encoding a toxin (ParE2) related to the classic parDE family but with an unrelated antitoxin called PaaA2. The complex between PaaA2 and ParE2 was purified and characterized by analytical gel filtration, dynamic light scattering and small-angle X-ray scattering. It consists of a particle with a radius of gyration of 3.95 nm and is likely to form a heterododecamer. Crystals of the ParE2-PaaA2 complex diffract to 3.8 Å resolution and belong to space group P3(1)21 or P3(2)21, with unit-cell parameters a = b = 142.9, c = 87.5 Å. The asymmetric unit is consistent with a particle of around 125 kDa, which is compatible with the solution data. Therefore, the ParE2-PaaA2 complex is the largest toxin-antitoxin complex identified to date and its quaternary arrangement is likely to be of biological significance.

摘要

大肠杆菌O157的paaR2 - paaA2 - parE2构成了一个独特的三组分毒素 - 抗毒素(TA)模块,该模块编码一种与经典parDE家族相关的毒素(ParE2),但其抗毒素名为PaaA2,与经典抗毒素无关。通过分析凝胶过滤、动态光散射和小角X射线散射对PaaA2和ParE2之间的复合物进行了纯化和表征。它由一个回转半径为3.95 nm的粒子组成,可能形成一个异十二聚体。ParE2 - PaaA2复合物的晶体衍射分辨率达到3.8 Å,属于空间群P3(1)21或P3(2)21,晶胞参数a = b = 142.9,c = 87.5 Å。不对称单元与一个约125 kDa的粒子一致,这与溶液数据相符。因此,ParE2 - PaaA2复合物是迄今为止鉴定出的最大的毒素 - 抗毒素复合物,其四级结构可能具有生物学意义。