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2
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本文引用的文献

1
F(1)F(0) ATP synthase subunit c is targeted by the SRP to YidC in the E. coli inner membrane.F(1)F(0) ATP合酶亚基c在大肠杆菌内膜中被信号识别颗粒(SRP)靶向到YidC。
FEBS Lett. 2004 Oct 8;576(1-2):97-100. doi: 10.1016/j.febslet.2004.08.069.
2
The bacterial translocase: a dynamic protein channel complex.细菌转位酶:一种动态蛋白质通道复合体。
Cell Mol Life Sci. 2003 Oct;60(10):2034-52. doi: 10.1007/s00018-003-3006-y.
3
Depletion of SecDF-YajC causes a decrease in the level of SecG: implication for their functional interaction.SecDF-YajC 的缺失导致 SecG 水平下降:这暗示了它们之间的功能相互作用。
FEBS Lett. 2003 Aug 28;550(1-3):114-8. doi: 10.1016/s0014-5793(03)00847-0.
4
A conserved function of YidC in the biogenesis of respiratory chain complexes.YidC在呼吸链复合物生物合成中的保守功能。
Proc Natl Acad Sci U S A. 2003 May 13;100(10):5801-6. doi: 10.1073/pnas.0636761100. Epub 2003 Apr 30.
5
Crystal structure of bacterial multidrug efflux transporter AcrB.细菌多药外排转运蛋白AcrB的晶体结构
Nature. 2002 Oct 10;419(6907):587-93. doi: 10.1038/nature01050.
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Kinetic analysis of the translocation of fluorescent precursor proteins into Escherichia coli membrane vesicles.
J Biol Chem. 2002 Nov 29;277(48):46059-65. doi: 10.1074/jbc.M208449200. Epub 2002 Sep 10.
7
SecDFyajC forms a heterotetrameric complex with YidC.SecDFyajC与YidC形成异源四聚体复合物。
Mol Microbiol. 2002 Jun;44(5):1397-405. doi: 10.1046/j.1365-2958.2002.02972.x.
8
SecDFyajC is not required for the maintenance of the proton motive force.
FEBS Lett. 2001 Nov 9;508(1):103-6. doi: 10.1016/s0014-5793(01)03033-2.
9
The RND permease superfamily: an ancient, ubiquitous and diverse family that includes human disease and development proteins.耐药-结瘤-分裂(RND)转运蛋白超家族:一个古老、普遍且多样的家族,其中包括与人类疾病和发育相关的蛋白质。
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10
YidC, the Escherichia coli homologue of mitochondrial Oxa1p, is a component of the Sec translocase.YidC是线粒体Oxa1p在大肠杆菌中的同源物,是Sec转位酶的一个组成部分。
EMBO J. 2000 Feb 15;19(4):542-9. doi: 10.1093/emboj/19.4.542.

SecD和SecF的第一个大的周质环在SecDF发挥功能方面起着重要作用。

The large first periplasmic loop of SecD and SecF plays an important role in SecDF functioning.

作者信息

Nouwen Nico, Piwowarek Magdalena, Berrelkamp Greetje, Driessen Arnold J M

机构信息

Department of Microbiology, Groningen Biomolecular Sciences and Biotechnology Institute, University of Groningen, Kerklaan 30, 9751 NN Haren, The Netherlands.

出版信息

J Bacteriol. 2005 Aug;187(16):5857-60. doi: 10.1128/JB.187.16.5857-5860.2005.

DOI:10.1128/JB.187.16.5857-5860.2005
PMID:16077136
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1196081/
Abstract

A remarkable feature of proteins of the SecD and SecF family involved in protein translocation is that they possess a very large first periplasmic domain. Here we report that this large first periplasmic domain is not required for the SecD-SecF interaction but that it is important for catalyzing protein translocation.

摘要

参与蛋白质转运的SecD和SecF家族蛋白质的一个显著特征是它们拥有一个非常大的第一个周质结构域。我们在此报告,SecD与SecF相互作用并不需要这个大的第一个周质结构域,但它对催化蛋白质转运很重要。