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      Two-Component Signal Transduction Systems of Pathogenic Bacteria As Targets for Antimicrobial Therapy: An Overview

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          Abstract

          The bacterial communities in a wide range of environmental niches sense and respond to numerous external stimuli for their survival. Primarily, a source they require to follow up this communication is the two-component signal transduction system (TCS), which typically comprises a sensor Histidine kinase for receiving external input signals and a response regulator that conveys a proper change in the bacterial cell physiology. For numerous reasons, TCSs have ascended as convincing targets for antibacterial drug design. Several studies have shown that TCSs are essential for the coordinated expression of virulence factors and, in some cases, for bacterial viability and growth. It has also been reported that the expression of antibiotic resistance determinants may be regulated by some TCSs. In addition, as a mode of signal transduction, phosphorylation of histidine in bacteria differs from normal serine/threonine and tyrosine phosphorylation in higher eukaryotes. Several studies have shown the molecular mechanisms by which TCSs regulate virulence and antibiotic resistance in pathogenic bacteria. In this review, we list some of the characteristics of the bacterial TCSs and their involvement in virulence and antibiotic resistance. Furthermore, this review lists and discusses inhibitors that have been reported to target TCSs in pathogenic bacteria.

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          Most cited references51

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          Two-component signal transduction.

          Most prokaryotic signal-transduction systems and a few eukaryotic pathways use phosphotransfer schemes involving two conserved components, a histidine protein kinase and a response regulator protein. The histidine protein kinase, which is regulated by environmental stimuli, autophosphorylates at a histidine residue, creating a high-energy phosphoryl group that is subsequently transferred to an aspartate residue in the response regulator protein. Phosphorylation induces a conformational change in the regulatory domain that results in activation of an associated domain that effects the response. The basic scheme is highly adaptable, and numerous variations have provided optimization within specific signaling systems. The domains of two-component proteins are modular and can be integrated into proteins and pathways in a variety of ways, but the core structures and activities are maintained. Thus detailed analyses of a relatively small number of representative proteins provide a foundation for understanding this large family of signaling proteins.
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            Drugs for bad bugs: confronting the challenges of antibacterial discovery.

            The sequencing of the first complete bacterial genome in 1995 heralded a new era of hope for antibacterial drug discoverers, who now had the tools to search entire genomes for new antibacterial targets. Several companies, including GlaxoSmithKline, moved back into the antibacterials area and embraced a genomics-derived, target-based approach to screen for new classes of drugs with novel modes of action. Here, we share our experience of evaluating more than 300 genes and 70 high-throughput screening campaigns over a period of 7 years, and look at what we learned and how that has influenced GlaxoSmithKline's antibacterials strategy going forward.
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              Histidine kinases and response regulator proteins in two-component signaling systems.

              Phosphotransfer-mediated signaling pathways allow cells to sense and respond to environmental stimuli. Autophosphorylating histidine protein kinases provide phosphoryl groups for response regulator proteins which, in turn, function as molecular switches that control diverse effector activities. Structural studies of proteins involved in two-component signaling systems have revealed a modular architecture with versatile conserved domains that are readily adapted to the specific needs of individual systems.
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                Author and article information

                Contributors
                Journal
                Front Microbiol
                Front Microbiol
                Front. Microbiol.
                Frontiers in Microbiology
                Frontiers Media S.A.
                1664-302X
                10 October 2017
                2017
                : 8
                : 1878
                Affiliations
                [1] 1Laboratório de Genética Celular e Molecular, Departamento de Biologia Geral, Instituto de Ciências Biológicas (ICB), Universidade Federal de Minas Gerais , Belo Horizonte, Brazil
                [2] 2Biochemistry Group, Department of Chemistry, Islamia College University , Peshawar, Pakistan
                [3] 3Centre for Genomics and Applied Gene Technology, Institute of Integrative Omics and Applied Biotechnology , Purba Medinipur, India
                [4] 4Department of Computer Science, Virginia Commonwealth University , Richmond, VA, United States
                [5] 5Instituto de Ciências Biológicas, Universidade Federal do Pará , Belém, Brazil
                [6] 6Instituto de Ciências da Saúde, Universidade Federal da Bahia , Salvador, Brazil
                Author notes

                Edited by: Miklos Fuzi, Semmelweis University, Hungary

                Reviewed by: Yixin Shi, Arizona State University, United States; Rodolfo García-Contreras, National Autonomous University of Mexico, Mexico

                *Correspondence: Vasco Azevedo, vascoariston@ 123456gmail.com Thiago L. P. Castro, castrotlp@ 123456gmail.com

                This article was submitted to Antimicrobials, Resistance and Chemotherapy, a section of the journal Frontiers in Microbiology

                Article
                10.3389/fmicb.2017.01878
                5641358
                29067003
                a70b5b1e-253b-48ee-805d-6c708e709b53
                Copyright © 2017 Tiwari, Jamal, Hassan, Carvalho, Almeida, Barh, Ghosh, Silva, Castro and Azevedo.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 18 March 2017
                : 14 September 2017
                Page count
                Figures: 1, Tables: 1, Equations: 0, References: 54, Pages: 7, Words: 0
                Categories
                Microbiology
                Mini Review

                Microbiology & Virology
                bacterial two-component signal transduction system,virulence and antibiotic resistance,inhibitors for kinases and response regulators

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