Literature DB >> 21700205

Traffic jam at the bacterial sec translocase: targeting the SecA nanomotor by small-molecule inhibitors.

Kenneth Segers1, Jozef Anné.   

Abstract

The rapid rise of drug-resistant bacteria is one of the most serious unmet medical needs facing the world. Despite this increasing problem of antibiotic resistance, the number of different antibiotics available for the treatment of serious infections is dwindling. Therefore, there is an urgent need for new antibacterial drugs, preferably with novel modes of action to potentially avoid cross-resistance with existing antibacterial agents. In recent years, increasing attention has been paid to bacterial protein secretion as a potential antibacterial target. Among the different protein secretion pathways that are present in bacterial pathogens, the general protein secretory (Sec) pathway is widely considered as an attractive target for antibacterial therapy. One of the key components of the Sec pathway is the peripheral membrane ATPase SecA, which provides the energy for the translocation of preproteins across the bacterial cytoplasmic membrane. In this review, we will provide an overview of research efforts on the discovery and development of small-molecule SecA inhibitors. Furthermore, recent advances on the structure and function of SecA and their potential impact on antibacterial drug discovery will be discussed.
Copyright © 2011 Elsevier Ltd. All rights reserved.

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Year:  2011        PMID: 21700205     DOI: 10.1016/j.chembiol.2011.04.007

Source DB:  PubMed          Journal:  Chem Biol        ISSN: 1074-5521


  19 in total

1.  Gargantulide A, a complex 52-membered macrolactone showing antibacterial activity from Streptomyces sp.

Authors:  Jung-Rae Rho; Gurusamy Subramaniam; Hyukjae Choi; Eun-Hee Kim; Sok Peng Ng; K Yoganathan; Siewbee Ng; Antony D Buss; Mark S Butler; William H Gerwick
Journal:  Org Lett       Date:  2015-02-27       Impact factor: 6.005

Review 2.  The inhibition of type I bacterial signal peptidase: Biological consequences and therapeutic potential.

Authors:  Arryn Craney; Floyd E Romesberg
Journal:  Bioorg Med Chem Lett       Date:  2015-07-26       Impact factor: 2.823

3.  Mechanisms of Rose Bengal inhibition on SecA ATPase and ion channel activities.

Authors:  Ying-Hsin Hsieh; Ying-Ju Huang; Jin-Shan Jin; Liyan Yu; Hsiuchin Yang; Chun Jiang; Binghe Wang; Phang C Tai
Journal:  Biochem Biophys Res Commun       Date:  2014-10-19       Impact factor: 3.575

4.  Antibiotic adjuvants: diverse strategies for controlling drug-resistant pathogens.

Authors:  Erin E Gill; Octavio L Franco; Robert E W Hancock
Journal:  Chem Biol Drug Des       Date:  2015-01       Impact factor: 2.817

Review 5.  SecA inhibitors as potential antimicrobial agents: differential actions on SecA-only and SecA-SecYEG protein-conducting channels.

Authors:  Jinshan Jin; Ying-Hsin Hsieh; Arpana S Chaudhary; Jianmei Cui; John E Houghton; Sen-Fang Sui; Binghe Wang; Phang C Tai
Journal:  FEMS Microbiol Lett       Date:  2018-08-01       Impact factor: 2.742

Review 6.  SecA: a potential antimicrobial target.

Authors:  Arpana S Chaudhary; Weixuan Chen; Jinshan Jin; Phang C Tai; Binghe Wang
Journal:  Future Med Chem       Date:  2015       Impact factor: 3.808

7.  Identification of small-molecule inhibitors against SecA by structure-based virtual ligand screening.

Authors:  Evelien De Waelheyns; Kenneth Segers; Marios Frantzeskos Sardis; Jozef Anné; Gerry A F Nicolaes; Anastassios Economou
Journal:  J Antibiot (Tokyo)       Date:  2015-05-20       Impact factor: 2.649

8.  TetR-based gene regulation systems for Francisella tularensis.

Authors:  Eric D LoVullo; Cheryl N Miller; Martin S Pavelka; Thomas H Kawula
Journal:  Appl Environ Microbiol       Date:  2012-07-20       Impact factor: 4.792

Review 9.  The ins and outs of Mycobacterium tuberculosis protein export.

Authors:  Lauren S Ligon; Jennifer D Hayden; Miriam Braunstein
Journal:  Tuberculosis (Edinb)       Date:  2011-12-21       Impact factor: 3.131

10.  Acinetobacter baumannii Extracellular OXA-58 Is Primarily and Selectively Released via Outer Membrane Vesicles after Sec-Dependent Periplasmic Translocation.

Authors:  Yu-Ting Liao; Shu-Chen Kuo; Ming-Hsien Chiang; Yi-Tzu Lee; Wang-Chou Sung; You-Hsuan Chen; Te-Li Chen; Chang-Phone Fung
Journal:  Antimicrob Agents Chemother       Date:  2015-09-14       Impact factor: 5.191

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