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In Silico Discovery of Aminoacyl-tRNA Synthetase Inhibitors

Aminoacyl-tRNA synthetases (aaRSs) are enzymes that catalyze the transfer of amino acids to their cognate tRNA. They play a pivotal role in protein synthesis and are essential for cell growth and survival. The aaRSs are one of the leading targets for development of antibiotic agents. In this review,...

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Detalles Bibliográficos
Autores principales: Zhao, Yaxue, Meng, Qingqing, Bai, Linquan, Zhou, Huchen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International (MDPI) 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3907873/
https://www.ncbi.nlm.nih.gov/pubmed/24447926
http://dx.doi.org/10.3390/ijms15011358
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author Zhao, Yaxue
Meng, Qingqing
Bai, Linquan
Zhou, Huchen
author_facet Zhao, Yaxue
Meng, Qingqing
Bai, Linquan
Zhou, Huchen
author_sort Zhao, Yaxue
collection PubMed
description Aminoacyl-tRNA synthetases (aaRSs) are enzymes that catalyze the transfer of amino acids to their cognate tRNA. They play a pivotal role in protein synthesis and are essential for cell growth and survival. The aaRSs are one of the leading targets for development of antibiotic agents. In this review, we mainly focused on aaRS inhibitor discovery and development using in silico methods including virtual screening and structure-based drug design. These computational methods are relatively fast and cheap, and are proving to be of great benefit for the rational development of more potent aaRS inhibitors and other pharmaceutical agents that may usher in a much needed generation of new antibiotics.
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spelling pubmed-39078732014-01-31 In Silico Discovery of Aminoacyl-tRNA Synthetase Inhibitors Zhao, Yaxue Meng, Qingqing Bai, Linquan Zhou, Huchen Int J Mol Sci Review Aminoacyl-tRNA synthetases (aaRSs) are enzymes that catalyze the transfer of amino acids to their cognate tRNA. They play a pivotal role in protein synthesis and are essential for cell growth and survival. The aaRSs are one of the leading targets for development of antibiotic agents. In this review, we mainly focused on aaRS inhibitor discovery and development using in silico methods including virtual screening and structure-based drug design. These computational methods are relatively fast and cheap, and are proving to be of great benefit for the rational development of more potent aaRS inhibitors and other pharmaceutical agents that may usher in a much needed generation of new antibiotics. Molecular Diversity Preservation International (MDPI) 2014-01-20 /pmc/articles/PMC3907873/ /pubmed/24447926 http://dx.doi.org/10.3390/ijms15011358 Text en © 2014 by the authors; licensee MDPI, Basel, Switzerland http://creativecommons.org/licenses/by/3.0/ This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Zhao, Yaxue
Meng, Qingqing
Bai, Linquan
Zhou, Huchen
In Silico Discovery of Aminoacyl-tRNA Synthetase Inhibitors
title In Silico Discovery of Aminoacyl-tRNA Synthetase Inhibitors
title_full In Silico Discovery of Aminoacyl-tRNA Synthetase Inhibitors
title_fullStr In Silico Discovery of Aminoacyl-tRNA Synthetase Inhibitors
title_full_unstemmed In Silico Discovery of Aminoacyl-tRNA Synthetase Inhibitors
title_short In Silico Discovery of Aminoacyl-tRNA Synthetase Inhibitors
title_sort in silico discovery of aminoacyl-trna synthetase inhibitors
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3907873/
https://www.ncbi.nlm.nih.gov/pubmed/24447926
http://dx.doi.org/10.3390/ijms15011358
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