Aminoacyl-tRNA synthetases as drug targets
The Enzymes, ISSN: 1874-6047, Vol: 48, Page: 321-350
2020
- 10Citations
- 27Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations10
- Citation Indexes10
- 10
- CrossRef3
- Captures27
- Readers27
- 27
Article Description
Aminoacyl-tRNA synthetases (AARSs) have been considered very attractive drug-targets for decades. This interest probably emerged with the identification of differences in AARSs between prokaryotic and eukaryotic species, which provided a rationale for the development of antimicrobials targeting bacterial AARSs with minimal effect on the homologous human AARSs. Today we know that AARSs are not only attractive, but also valid drug targets as they are housekeeping proteins that: (i) play a fundamental role in protein translation by charging the corresponding amino acid to its cognate tRNA and preventing mistranslation mistakes [1], a critical process during fast growing conditions of microbes; and (ii) present significant differences between microbes and humans that can be used for drug development [2]. Together with the vast amount of available data on both pathogenic and mammalian AARSs, it is expected that, in the future, the numerous reported inhibitors of AARSs will provide the basis to develop new therapeutics for the treatment of human diseases. In this chapter, a detailed summary on the state-of-the-art in drug discovery and drug development for each aminoacyl-tRNA synthetase will be presented.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S1874604720300263; http://dx.doi.org/10.1016/bs.enz.2020.07.001; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85092721783&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/33837708; https://linkinghub.elsevier.com/retrieve/pii/S1874604720300263; https://dx.doi.org/10.1016/bs.enz.2020.07.001
Elsevier BV
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