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1
SecA: a potential antimicrobial target.SecA:一种潜在的抗菌靶点。
Future Med Chem. 2015;7(8):989-1007. doi: 10.4155/fmc.15.42.
2
Alignment-independent QSAR analysis of SecA inhibitors.SecA抑制剂的非比对定量构效关系分析
Protein Pept Lett. 2013 Jul 1;20(7):802-7. doi: 10.2174/0929866511320070010.
3
Design, syntheses and evaluation of 4-oxo-5-cyano thiouracils as SecA inhibitors.4-氧代-5-氰基硫脲嘧啶作为SecA抑制剂的设计、合成与评价
Bioorg Med Chem. 2015 Jan 1;23(1):105-17. doi: 10.1016/j.bmc.2014.11.017. Epub 2014 Nov 20.
4
Design, synthesis and biological evaluation of rose bengal analogues as SecA inhibitors.设计、合成及新型孟加拉玫瑰红类似物作为 SecA 抑制剂的生物评价。
ChemMedChem. 2013 Aug;8(8):1384-93. doi: 10.1002/cmdc.201300216. Epub 2013 Jun 21.
5
Design, synthesis and antimicrobial activities of thiouracil derivatives containing triazolo-thiadiazole as SecA inhibitors.含三唑并噻二唑的硫脲嘧啶衍生物作为SecA抑制剂的设计、合成及抗菌活性
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Using Chemical Probes to Assess the Feasibility of Targeting SecA for Developing Antimicrobial Agents against Gram-Negative Bacteria.利用化学探针评估靶向SecA以开发抗革兰氏阴性菌抗菌剂的可行性。
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Evaluation of small molecule SecA inhibitors against methicillin-resistant Staphylococcus aureus.针对耐甲氧西林金黄色葡萄球菌的小分子SecA抑制剂的评估
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Traffic jam at the bacterial sec translocase: targeting the SecA nanomotor by small-molecule inhibitors.细菌Sec转位酶处的交通堵塞:小分子抑制剂靶向SecA纳米马达
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Exploration of Survival Traits, Probiotic Determinants, Host Interactions, and Functional Evolution of Bifidobacterial Genomes Using Comparative Genomics.利用比较基因组学探索双歧杆菌基因组的生存特征、益生菌决定因素、宿主相互作用及功能进化
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本文引用的文献

1
Design, syntheses and evaluation of 4-oxo-5-cyano thiouracils as SecA inhibitors.4-氧代-5-氰基硫脲嘧啶作为SecA抑制剂的设计、合成与评价
Bioorg Med Chem. 2015 Jan 1;23(1):105-17. doi: 10.1016/j.bmc.2014.11.017. Epub 2014 Nov 20.
2
Mechanisms of Rose Bengal inhibition on SecA ATPase and ion channel activities.孟加拉玫瑰红对SecA ATP酶和离子通道活性的抑制机制。
Biochem Biophys Res Commun. 2014 Nov 14;454(2):308-12. doi: 10.1016/j.bbrc.2014.10.070. Epub 2014 Oct 19.
3
ADP-dependent conformational changes distinguish Mycobacterium tuberculosis SecA2 from SecA1.ADP 依赖性构象变化区分结核分枝杆菌 SecA2 和 SecA1。
J Biol Chem. 2014 Jan 24;289(4):2307-17. doi: 10.1074/jbc.M113.533323. Epub 2013 Dec 2.
4
Selective transport by SecA2: an expanding family of customized motor proteins.SecA2介导的选择性转运:一类不断扩展的定制化驱动蛋白家族
Biochim Biophys Acta. 2014 Aug;1843(8):1674-86. doi: 10.1016/j.bbamcr.2013.10.019. Epub 2013 Oct 31.
5
Phospholipids induce conformational changes of SecA to form membrane-specific domains: AFM structures and implication on protein-conducting channels.磷脂诱导SecA构象变化以形成膜特异性结构域:原子力显微镜结构及其对蛋白质传导通道的影响
PLoS One. 2013 Aug 16;8(8):e72560. doi: 10.1371/journal.pone.0072560. eCollection 2013.
6
Design, synthesis and biological evaluation of rose bengal analogues as SecA inhibitors.设计、合成及新型孟加拉玫瑰红类似物作为 SecA 抑制剂的生物评价。
ChemMedChem. 2013 Aug;8(8):1384-93. doi: 10.1002/cmdc.201300216. Epub 2013 Jun 21.
7
Reconstitution of functionally efficient SecA-dependent protein-conducting channels: transformation of low-affinity SecA-liposome channels to high-affinity SecA-SecYEG-SecDF·YajC channels.重建具有功能效率的 SecA 依赖型蛋白传导通道:将低亲和力 SecA-脂质体通道转化为高亲和力 SecA-SecYEG-SecDF·YajC 通道。
Biochem Biophys Res Commun. 2013 Feb 15;431(3):388-92. doi: 10.1016/j.bbrc.2013.01.042. Epub 2013 Jan 18.
8
The bacterial Sec-translocase: structure and mechanism.细菌 Sec 转运酶:结构与机制。
Philos Trans R Soc Lond B Biol Sci. 2012 Apr 19;367(1592):1016-28. doi: 10.1098/rstb.2011.0201.
9
Fluorescein analogues inhibit SecA ATPase: the first sub-micromolar inhibitor of bacterial protein translocation.荧光素类似物抑制 SecA ATP 酶:首个亚毫摩尔级的细菌蛋白转位抑制剂。
ChemMedChem. 2012 Apr;7(4):571-7. doi: 10.1002/cmdc.201100594. Epub 2012 Feb 22.
10
A mechanism-based whole-cell screening assay to identify inhibitors of protein export in Escherichia coli by the Sec pathway.一种基于机制的全细胞筛选试验,用于鉴定大肠杆菌中通过Sec途径进行蛋白质输出的抑制剂。
J Biomol Screen. 2012 Apr;17(4):535-41. doi: 10.1177/1087057111431606. Epub 2012 Jan 10.

SecA:一种潜在的抗菌靶点。

SecA: a potential antimicrobial target.

作者信息

Chaudhary Arpana S, Chen Weixuan, Jin Jinshan, Tai Phang C, Wang Binghe

机构信息

Department of Chemistry, Center for Diagnostics & Therapeutics, & Center for Biotechnology & Drug Design, Georgia State University, Atlanta, GA 30303, USA.

Department of Biology, Center for Diagnostics & Therapeutics, & Center for Biotechnology & Drug Design, Georgia State University, Atlanta, GA 30303, USA.

出版信息

Future Med Chem. 2015;7(8):989-1007. doi: 10.4155/fmc.15.42.

DOI:10.4155/fmc.15.42
PMID:26062397
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4479503/
Abstract

There is a consensus in the medical profession of the pressing need for novel antimicrobial agents due to issues related to drug resistance. In practice, solutions to this problem to a large degree lie with the identification of new and vital targets in bacteria and subsequently designing their inhibitors. We consider SecA a very promising antimicrobial target. In this review, we compile and analyze information available on SecA to show that inhibition of SecA has a multitude of consequences. Furthermore, we discuss issues critical to the design and evaluation of SecA inhibitors.

摘要

由于耐药性问题,医学界已达成共识,迫切需要新型抗菌药物。实际上,解决这一问题的方法在很大程度上在于确定细菌中新的关键靶点,并随后设计其抑制剂。我们认为SecA是一个非常有前景的抗菌靶点。在本综述中,我们收集并分析了有关SecA的现有信息,以表明抑制SecA会产生多种后果。此外,我们还讨论了SecA抑制剂设计和评估的关键问题。