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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,...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Molecular Diversity Preservation International (MDPI)
2014
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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. |
format | Online Article Text |
id | pubmed-3907873 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Molecular Diversity Preservation International (MDPI) |
record_format | MEDLINE/PubMed |
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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