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Automated 3D structure composition for large RNAs
Understanding the numerous functions that RNAs play in living cells depends critically on knowledge of their three-dimensional structure. Due to the difficulties in experimentally assessing structures of large RNAs, there is currently great demand for new high-resolution structure prediction methods...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3413140/ https://www.ncbi.nlm.nih.gov/pubmed/22539264 http://dx.doi.org/10.1093/nar/gks339 |
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author | Popenda, Mariusz Szachniuk, Marta Antczak, Maciej Purzycka, Katarzyna J. Lukasiak, Piotr Bartol, Natalia Blazewicz, Jacek Adamiak, Ryszard W. |
author_facet | Popenda, Mariusz Szachniuk, Marta Antczak, Maciej Purzycka, Katarzyna J. Lukasiak, Piotr Bartol, Natalia Blazewicz, Jacek Adamiak, Ryszard W. |
author_sort | Popenda, Mariusz |
collection | PubMed |
description | Understanding the numerous functions that RNAs play in living cells depends critically on knowledge of their three-dimensional structure. Due to the difficulties in experimentally assessing structures of large RNAs, there is currently great demand for new high-resolution structure prediction methods. We present the novel method for the fully automated prediction of RNA 3D structures from a user-defined secondary structure. The concept is founded on the machine translation system. The translation engine operates on the RNA FRABASE database tailored to the dictionary relating the RNA secondary structure and tertiary structure elements. The translation algorithm is very fast. Initial 3D structure is composed in a range of seconds on a single processor. The method assures the prediction of large RNA 3D structures of high quality. Our approach needs neither structural templates nor RNA sequence alignment, required for comparative methods. This enables the building of unresolved yet native and artificial RNA structures. The method is implemented in a publicly available, user-friendly server RNAComposer. It works in an interactive mode and a batch mode. The batch mode is designed for large-scale modelling and accepts atomic distance restraints. Presently, the server is set to build RNA structures of up to 500 residues. |
format | Online Article Text |
id | pubmed-3413140 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-34131402012-08-07 Automated 3D structure composition for large RNAs Popenda, Mariusz Szachniuk, Marta Antczak, Maciej Purzycka, Katarzyna J. Lukasiak, Piotr Bartol, Natalia Blazewicz, Jacek Adamiak, Ryszard W. Nucleic Acids Res Methods Online Understanding the numerous functions that RNAs play in living cells depends critically on knowledge of their three-dimensional structure. Due to the difficulties in experimentally assessing structures of large RNAs, there is currently great demand for new high-resolution structure prediction methods. We present the novel method for the fully automated prediction of RNA 3D structures from a user-defined secondary structure. The concept is founded on the machine translation system. The translation engine operates on the RNA FRABASE database tailored to the dictionary relating the RNA secondary structure and tertiary structure elements. The translation algorithm is very fast. Initial 3D structure is composed in a range of seconds on a single processor. The method assures the prediction of large RNA 3D structures of high quality. Our approach needs neither structural templates nor RNA sequence alignment, required for comparative methods. This enables the building of unresolved yet native and artificial RNA structures. The method is implemented in a publicly available, user-friendly server RNAComposer. It works in an interactive mode and a batch mode. The batch mode is designed for large-scale modelling and accepts atomic distance restraints. Presently, the server is set to build RNA structures of up to 500 residues. Oxford University Press 2012-08 2012-04-26 /pmc/articles/PMC3413140/ /pubmed/22539264 http://dx.doi.org/10.1093/nar/gks339 Text en © The Author(s) 2012. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Methods Online Popenda, Mariusz Szachniuk, Marta Antczak, Maciej Purzycka, Katarzyna J. Lukasiak, Piotr Bartol, Natalia Blazewicz, Jacek Adamiak, Ryszard W. Automated 3D structure composition for large RNAs |
title | Automated 3D structure composition for large RNAs |
title_full | Automated 3D structure composition for large RNAs |
title_fullStr | Automated 3D structure composition for large RNAs |
title_full_unstemmed | Automated 3D structure composition for large RNAs |
title_short | Automated 3D structure composition for large RNAs |
title_sort | automated 3d structure composition for large rnas |
topic | Methods Online |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3413140/ https://www.ncbi.nlm.nih.gov/pubmed/22539264 http://dx.doi.org/10.1093/nar/gks339 |
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