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The Macromolecular Machines that Duplicate the Escherichia coli Chromosome as Targets for Drug Discovery

DNA replication is an essential process. Although the fundamental strategies to duplicate chromosomes are similar in all free-living organisms, the enzymes of the three domains of life that perform similar functions in DNA replication differ in amino acid sequence and their three-dimensional structu...

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Autor principal: Kaguni, Jon M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5872134/
https://www.ncbi.nlm.nih.gov/pubmed/29538288
http://dx.doi.org/10.3390/antibiotics7010023
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author Kaguni, Jon M.
author_facet Kaguni, Jon M.
author_sort Kaguni, Jon M.
collection PubMed
description DNA replication is an essential process. Although the fundamental strategies to duplicate chromosomes are similar in all free-living organisms, the enzymes of the three domains of life that perform similar functions in DNA replication differ in amino acid sequence and their three-dimensional structures. Moreover, the respective proteins generally utilize different enzymatic mechanisms. Hence, the replication proteins that are highly conserved among bacterial species are attractive targets to develop novel antibiotics as the compounds are unlikely to demonstrate off-target effects. For those proteins that differ among bacteria, compounds that are species-specific may be found. Escherichia coli has been developed as a model system to study DNA replication, serving as a benchmark for comparison. This review summarizes the functions of individual E. coli proteins, and the compounds that inhibit them.
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spelling pubmed-58721342018-03-29 The Macromolecular Machines that Duplicate the Escherichia coli Chromosome as Targets for Drug Discovery Kaguni, Jon M. Antibiotics (Basel) Review DNA replication is an essential process. Although the fundamental strategies to duplicate chromosomes are similar in all free-living organisms, the enzymes of the three domains of life that perform similar functions in DNA replication differ in amino acid sequence and their three-dimensional structures. Moreover, the respective proteins generally utilize different enzymatic mechanisms. Hence, the replication proteins that are highly conserved among bacterial species are attractive targets to develop novel antibiotics as the compounds are unlikely to demonstrate off-target effects. For those proteins that differ among bacteria, compounds that are species-specific may be found. Escherichia coli has been developed as a model system to study DNA replication, serving as a benchmark for comparison. This review summarizes the functions of individual E. coli proteins, and the compounds that inhibit them. MDPI 2018-03-14 /pmc/articles/PMC5872134/ /pubmed/29538288 http://dx.doi.org/10.3390/antibiotics7010023 Text en © 2018 by the author. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Kaguni, Jon M.
The Macromolecular Machines that Duplicate the Escherichia coli Chromosome as Targets for Drug Discovery
title The Macromolecular Machines that Duplicate the Escherichia coli Chromosome as Targets for Drug Discovery
title_full The Macromolecular Machines that Duplicate the Escherichia coli Chromosome as Targets for Drug Discovery
title_fullStr The Macromolecular Machines that Duplicate the Escherichia coli Chromosome as Targets for Drug Discovery
title_full_unstemmed The Macromolecular Machines that Duplicate the Escherichia coli Chromosome as Targets for Drug Discovery
title_short The Macromolecular Machines that Duplicate the Escherichia coli Chromosome as Targets for Drug Discovery
title_sort macromolecular machines that duplicate the escherichia coli chromosome as targets for drug discovery
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5872134/
https://www.ncbi.nlm.nih.gov/pubmed/29538288
http://dx.doi.org/10.3390/antibiotics7010023
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