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mBio. 2013 Dec 10;4(6):e00838-13. doi: 10.1128/mBio.00838-13.
2
Enteroaggregative Escherichia coli pathotype: a genetically heterogeneous emerging foodborne enteropathogen.聚集性大肠杆菌致病型:一种基因异质性的新发食源性肠道病原体。
FEMS Immunol Med Microbiol. 2012 Dec;66(3):281-98. doi: 10.1111/j.1574-695X.2012.01008.x. Epub 2012 Jul 31.
3
Improving the accuracy of macromolecular structure refinement at 7 Å resolution.提高 7Å 分辨率下大分子结构精修的准确性。
Structure. 2012 Jun 6;20(6):957-66. doi: 10.1016/j.str.2012.04.020.
4
Linking crystallographic model and data quality.链接晶体学模型和数据质量。
Science. 2012 May 25;336(6084):1030-3. doi: 10.1126/science.1218231.
5
Infection strategies of enteric pathogenic Escherichia coli.肠致病性大肠杆菌的感染策略。
Gut Microbes. 2012 Mar-Apr;3(2):71-87. doi: 10.4161/gmic.19182. Epub 2012 Mar 1.
6
Treatment of enterohemorrhagic Escherichia coli (EHEC) infection and hemolytic uremic syndrome (HUS).肠出血性大肠杆菌(EHEC)感染和溶血尿毒综合征(HUS)的治疗。
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Serine protease autotransporters of enterobacteriaceae (SPATEs): biogenesis and function.肠杆菌科丝氨酸蛋白酶自转运体(SPATEs):生物发生和功能。
Toxins (Basel). 2010 Jun;2(6):1179-206. doi: 10.3390/toxins2061179. Epub 2010 May 28.
8
Crystal structure of the passenger domain of the Escherichia coli autotransporter EspP.大肠杆菌自转运蛋白 EspP 的乘客结构域的晶体结构。
J Mol Biol. 2011 Nov 11;413(5):985-1000. doi: 10.1016/j.jmb.2011.09.028. Epub 2011 Sep 22.
9
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EMBO J. 2011 Aug 12;30(18):3864-74. doi: 10.1038/emboj.2011.279.
10
Overview of the CCP4 suite and current developments.CCP4软件包概述及当前进展
Acta Crystallogr D Biol Crystallogr. 2011 Apr;67(Pt 4):235-42. doi: 10.1107/S0907444910045749. Epub 2011 Mar 18.

肠聚集性大肠杆菌(EAEC)自转运肠毒素质粒编码毒素(Pet)乘客结构域的 X 射线晶体结构。

X-ray crystal structure of the passenger domain of plasmid encoded toxin(Pet), an autotransporter enterotoxin from enteroaggregative Escherichia coli (EAEC).

机构信息

Departamento de Salud Pública Facultad de Medicina UNAM, Ciudad Universitaria Coyoacán 04510, D.F., Mexico; Laboratorio de Patogenicidad Bacteriana, Unidad de Hemato Oncología e Investigación, Hospital Infantil de México Federico Gómez 06720, D.F., Mexico.

Department of Chemistry and Biochemistry, Arizona State University, Physical Sciences BLDG D-102, Tempe, AZ 85287, USA.

出版信息

Biochem Biophys Res Commun. 2014 Mar 7;445(2):439-44. doi: 10.1016/j.bbrc.2014.02.016. Epub 2014 Feb 12.

DOI:10.1016/j.bbrc.2014.02.016
PMID:24530907
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4005925/
Abstract

Autotransporters (ATs) represent a superfamily of proteins produced by a variety of pathogenic bacteria, which include the pathogenic groups of Escherichia coli (E. coli) associated with gastrointestinal and urinary tract infections. We present the first X-ray structure of the passenger domain from the Plasmid-encoded toxin (Pet) a 100 kDa protein at 2.3 Å resolution which is a cause of acute diarrhea in both developing and industrialized countries. Pet is a cytoskeleton-altering toxin that induces loss of actin stress fibers. While Pet (pdb code: 4OM9) shows only a sequence identity of 50% compared to the closest related protein sequence, extracellular serine protease plasmid (EspP) the structural features of both proteins are conserved. A closer structural look reveals that Pet contains a β-pleaded sheet at the sequence region of residues 181-190, the corresponding structural domain in EspP consists of a coiled loop. Secondary, the Pet passenger domain features a more pronounced beta sheet between residues 135 and 143 compared to the structure of EspP.

摘要

自动转运蛋白(ATs)是一类由多种致病菌产生的蛋白超家族,其中包括与胃肠道和尿路感染相关的致病性大肠杆菌(E. coli)群体。我们首次解析了质粒编码毒素(Pet)乘客结构域的 X 射线结构,该毒素分子量为 100kDa,分辨率为 2.3Å,是发展中国家和工业化国家急性腹泻的致病因素。Pet 是一种改变细胞骨架的毒素,可诱导肌动蛋白应力纤维的丧失。虽然 Pet(pdb 编号:4OM9)与最接近的相关蛋白序列,即细胞外丝氨酸蛋白酶质粒(EspP)相比,只有 50%的序列同一性,但这两种蛋白质的结构特征是保守的。更仔细的结构观察表明,Pet 在残基 181-190 处的序列区域包含一个β折叠片,而 EspP 中的相应结构域由一个卷曲环组成。其次,与 EspP 的结构相比,Pet 乘客结构域在残基 135 和 143 之间具有更明显的β片层。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eac1/4005925/2856b51aa077/nihms-567788-f0004.jpg
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