• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
The drug-binding activity of the multidrug-responding transcriptional regulator BmrR resides in its C-terminal domain.多药响应转录调节因子BmrR的药物结合活性位于其C末端结构域。
J Bacteriol. 1996 Mar;178(5):1473-5. doi: 10.1128/jb.178.5.1473-1475.1996.
2
A protein that activates expression of a multidrug efflux transporter upon binding the transporter substrates.一种在结合转运体底物后激活多药外排转运体表达的蛋白质。
J Biol Chem. 1994 Nov 11;269(45):28506-13.
3
Preliminary structural studies on the multi-ligand-binding domain of the transcription activator, BmrR, from Bacillus subtilis.来自枯草芽孢杆菌的转录激活因子BmrR多配体结合结构域的初步结构研究。
Protein Sci. 1997 Nov;6(11):2465-8. doi: 10.1002/pro.5560061122.
4
Broad ligand specificity of the transcriptional regulator of the Bacillus subtilis multidrug transporter Bmr.
Biochem Biophys Res Commun. 1997 Oct 9;239(1):269-72. doi: 10.1006/bbrc.1997.7467.
5
Crystal structure of the transcription activator BmrR bound to DNA and a drug.与DNA和一种药物结合的转录激活因子BmrR的晶体结构。
Nature. 2001 Jan 18;409(6818):378-82. doi: 10.1038/35053138.
6
Structural basis of multidrug recognition by BmrR, a transcription activator of a multidrug transporter.多药转运蛋白转录激活因子BmrR对多种药物识别的结构基础
Cell. 1999 Feb 5;96(3):353-62. doi: 10.1016/s0092-8674(00)80548-6.
7
Structures of BmrR-drug complexes reveal a rigid multidrug binding pocket and transcription activation through tyrosine expulsion.BmrR-药物复合物的结构揭示了一个刚性的多药结合口袋以及通过酪氨酸排出实现的转录激活。
J Biol Chem. 2008 Sep 26;283(39):26795-804. doi: 10.1074/jbc.M804191200. Epub 2008 Jul 25.
8
The ostensible paradox of multidrug recognition.
J Mol Microbiol Biotechnol. 2001 Apr;3(2):151-4.
9
Two highly similar multidrug transporters of Bacillus subtilis whose expression is differentially regulated.枯草芽孢杆菌的两种高度相似的多药转运蛋白,其表达受到差异调节。
J Bacteriol. 1995 Jul;177(14):3904-10. doi: 10.1128/jb.177.14.3904-3910.1995.
10
Conformational plasticity of the coiled-coil domain of BmrR is required for bmr operator binding: the structure of unliganded BmrR.BmrR 卷曲螺旋结构域的构象可塑性是结合 bmr 操纵子所必需的:未配位 BmrR 的结构。
J Mol Biol. 2010 Apr 30;398(2):264-75. doi: 10.1016/j.jmb.2010.03.011. Epub 2010 Mar 15.

引用本文的文献

1
The bacterial multidrug resistance regulator BmrR distorts promoter DNA to activate transcription.细菌多药耐药调节蛋白 BmrR 扭曲启动子 DNA 以激活转录。
Nat Commun. 2020 Dec 8;11(1):6284. doi: 10.1038/s41467-020-20134-y.
2
Identification of the High-affinity Substrate-binding Site of the Multidrug and Toxic Compound Extrusion (MATE) Family Transporter from Pseudomonas stutzeri.嗜麦芽窄食单胞菌多药及有毒化合物外排(MATE)家族转运蛋白高亲和力底物结合位点的鉴定
J Biol Chem. 2016 Jul 22;291(30):15503-14. doi: 10.1074/jbc.M116.728618. Epub 2016 May 27.
3
Crystal structure of an integron gene cassette-associated protein from Vibrio cholerae identifies a cationic drug-binding module.霍乱弧菌整合子基因盒相关蛋白的晶体结构鉴定出一种阳离子药物结合模块。
PLoS One. 2011 Mar 3;6(3):e16934. doi: 10.1371/journal.pone.0016934.
4
Distribution and physiology of ABC-type transporters contributing to multidrug resistance in bacteria.细菌中导致多药耐药的ABC型转运蛋白的分布与生理学
Microbiol Mol Biol Rev. 2007 Sep;71(3):463-76. doi: 10.1128/MMBR.00001-07.
5
Crystal structures of multidrug binding protein TtgR in complex with antibiotics and plant antimicrobials.多药结合蛋白TtgR与抗生素及植物抗菌剂复合物的晶体结构。
J Mol Biol. 2007 Jun 8;369(3):829-40. doi: 10.1016/j.jmb.2007.03.062. Epub 2007 Mar 30.
6
Bile salts modulate expression of the CmeABC multidrug efflux pump in Campylobacter jejuni.胆汁盐可调节空肠弯曲杆菌中CmeABC多药外排泵的表达。
J Bacteriol. 2005 Nov;187(21):7417-24. doi: 10.1128/JB.187.21.7417-7424.2005.
7
Investigation of ligand binding to the multidrug resistance protein EmrE by isothermal titration calorimetry.通过等温滴定量热法研究配体与多药耐药蛋白EmrE的结合
Biophys J. 2005 Jan;88(1):475-82. doi: 10.1529/biophysj.104.049247. Epub 2004 Oct 22.
8
Regulation of bacterial drug export systems.细菌药物外排系统的调控
Microbiol Mol Biol Rev. 2002 Dec;66(4):671-701, table of contents. doi: 10.1128/MMBR.66.4.671-701.2002.
9
The staphylococcal QacR multidrug regulator binds a correctly spaced operator as a pair of dimers.葡萄球菌QacR多药调控因子以二聚体对的形式结合正确间隔的操纵基因。
J Bacteriol. 2001 Dec;183(24):7102-9. doi: 10.1128/JB.183.24.7102-7109.2001.
10
Molecular properties of bacterial multidrug transporters.细菌多药转运蛋白的分子特性
Microbiol Mol Biol Rev. 2000 Dec;64(4):672-93. doi: 10.1128/MMBR.64.4.672-693.2000.

本文引用的文献

1
Multidrug resistance pumps in bacteria: variations on a theme.细菌中的多药耐药泵:同一主题的变体
Trends Biochem Sci. 1994 Mar;19(3):119-23. doi: 10.1016/0968-0004(94)90204-6.
2
Prevention of drug access to bacterial targets: permeability barriers and active efflux.防止药物作用于细菌靶点:通透性屏障与主动外排
Science. 1994 Apr 15;264(5157):382-8. doi: 10.1126/science.8153625.
3
Biochemistry of multidrug resistance mediated by the multidrug transporter.多药转运蛋白介导的多药耐药的生物化学
Annu Rev Biochem. 1993;62:385-427. doi: 10.1146/annurev.bi.62.070193.002125.
4
A protein that activates expression of a multidrug efflux transporter upon binding the transporter substrates.一种在结合转运体底物后激活多药外排转运体表达的蛋白质。
J Biol Chem. 1994 Nov 11;269(45):28506-13.
5
A thioredoxin gene fusion expression system that circumvents inclusion body formation in the E. coli cytoplasm.一种可避免在大肠杆菌细胞质中形成包涵体的硫氧还蛋白基因融合表达系统。
Biotechnology (N Y). 1993 Feb;11(2):187-93. doi: 10.1038/nbt0293-187.
6
Autogenous transcriptional activation of a thiostrepton-induced gene in Streptomyces lividans.硫链丝菌素诱导的天蓝色链霉菌基因的自体转录激活
EMBO J. 1993 Aug;12(8):3183-91. doi: 10.1002/j.1460-2075.1993.tb05987.x.
7
Two highly similar multidrug transporters of Bacillus subtilis whose expression is differentially regulated.枯草芽孢杆菌的两种高度相似的多药转运蛋白,其表达受到差异调节。
J Bacteriol. 1995 Jul;177(14):3904-10. doi: 10.1128/jb.177.14.3904-3910.1995.
8
The MerR metalloregulatory protein binds mercuric ion as a tricoordinate, metal-bridged dimer.MerR金属调节蛋白作为一种三配位、金属桥连二聚体结合汞离子。
Science. 1990 Feb 23;247(4945):946-8. doi: 10.1126/science.2305262.
9
Efflux-mediated multidrug resistance in Bacillus subtilis: similarities and dissimilarities with the mammalian system.枯草芽孢杆菌中由外排介导的多药耐药性:与哺乳动物系统的异同
Proc Natl Acad Sci U S A. 1991 Jun 1;88(11):4781-5. doi: 10.1073/pnas.88.11.4781.
10
Untwist and shout: a heavy metal-responsive transcriptional regulator.解开缠绕并呼喊:一种重金属响应转录调节因子。
J Bacteriol. 1992 May;174(10):3097-101. doi: 10.1128/jb.174.10.3097-3101.1992.

多药响应转录调节因子BmrR的药物结合活性位于其C末端结构域。

The drug-binding activity of the multidrug-responding transcriptional regulator BmrR resides in its C-terminal domain.

作者信息

Markham P N, Ahmed M, Neyfakh A A

机构信息

Department of Medicinal Chemistry and Pharmacognosy, University of Illinois at Chicago 60612, USA.

出版信息

J Bacteriol. 1996 Mar;178(5):1473-5. doi: 10.1128/jb.178.5.1473-1475.1996.

DOI:10.1128/jb.178.5.1473-1475.1996
PMID:8631728
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC177825/
Abstract

Rhodamine and tetraphenylphosphonium, the substrates of the Bacillus subtilis multidrug efflux transporter Bmr, induce the expression of Bmr through direct interaction with its transcriptional activator BmrR. Here we show that the C-terminal domain of BmrR, expressed individually, binds both these compounds and therefore can be used as a model for molecular analysis of the phenomenon of multidrug recognition.

摘要

若丹明和四苯基鏻是枯草芽孢杆菌多药外排转运蛋白Bmr的底物,它们通过与转录激活因子BmrR直接相互作用来诱导Bmr的表达。我们在此表明,单独表达的BmrR的C末端结构域能结合这两种化合物,因此可作为多药识别现象分子分析的模型。