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RNA Dependent RNA Polymerases: Insights from Structure, Function and Evolution
RNA dependent RNA polymerase (RdRp) is one of the most versatile enzymes of RNA viruses that is indispensable for replicating the genome as well as for carrying out transcription. The core structural features of RdRps are conserved, despite the divergence in their sequences. The structure of RdRp re...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5850383/ https://www.ncbi.nlm.nih.gov/pubmed/29439438 http://dx.doi.org/10.3390/v10020076 |
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author | Venkataraman, Sangita Prasad, Burra V L S Selvarajan, Ramasamy |
author_facet | Venkataraman, Sangita Prasad, Burra V L S Selvarajan, Ramasamy |
author_sort | Venkataraman, Sangita |
collection | PubMed |
description | RNA dependent RNA polymerase (RdRp) is one of the most versatile enzymes of RNA viruses that is indispensable for replicating the genome as well as for carrying out transcription. The core structural features of RdRps are conserved, despite the divergence in their sequences. The structure of RdRp resembles that of a cupped right hand and consists of fingers, palm and thumb subdomains. The catalysis involves the participation of conserved aspartates and divalent metal ions. Complexes of RdRps with substrates, inhibitors and metal ions provide a comprehensive view of their functional mechanism and offer valuable insights regarding the development of antivirals. In this article, we provide an overview of the structural aspects of RdRps and their complexes from the Group III, IV and V viruses and their structure-based phylogeny. |
format | Online Article Text |
id | pubmed-5850383 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-58503832018-03-16 RNA Dependent RNA Polymerases: Insights from Structure, Function and Evolution Venkataraman, Sangita Prasad, Burra V L S Selvarajan, Ramasamy Viruses Review RNA dependent RNA polymerase (RdRp) is one of the most versatile enzymes of RNA viruses that is indispensable for replicating the genome as well as for carrying out transcription. The core structural features of RdRps are conserved, despite the divergence in their sequences. The structure of RdRp resembles that of a cupped right hand and consists of fingers, palm and thumb subdomains. The catalysis involves the participation of conserved aspartates and divalent metal ions. Complexes of RdRps with substrates, inhibitors and metal ions provide a comprehensive view of their functional mechanism and offer valuable insights regarding the development of antivirals. In this article, we provide an overview of the structural aspects of RdRps and their complexes from the Group III, IV and V viruses and their structure-based phylogeny. MDPI 2018-02-10 /pmc/articles/PMC5850383/ /pubmed/29439438 http://dx.doi.org/10.3390/v10020076 Text en © 2018 by the authors. 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 Venkataraman, Sangita Prasad, Burra V L S Selvarajan, Ramasamy RNA Dependent RNA Polymerases: Insights from Structure, Function and Evolution |
title | RNA Dependent RNA Polymerases: Insights from Structure, Function and Evolution |
title_full | RNA Dependent RNA Polymerases: Insights from Structure, Function and Evolution |
title_fullStr | RNA Dependent RNA Polymerases: Insights from Structure, Function and Evolution |
title_full_unstemmed | RNA Dependent RNA Polymerases: Insights from Structure, Function and Evolution |
title_short | RNA Dependent RNA Polymerases: Insights from Structure, Function and Evolution |
title_sort | rna dependent rna polymerases: insights from structure, function and evolution |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5850383/ https://www.ncbi.nlm.nih.gov/pubmed/29439438 http://dx.doi.org/10.3390/v10020076 |
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