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eVolver: an optimization engine for evolving protein sequences to stabilize the respective structures
BACKGROUND: Many structural bioinformatics approaches employ sequence profile-based threading techniques. To improve fold recognition rates, homology searching may include artificially evolved amino acid sequences, which were demonstrated to enhance the sensitivity of protein threading in targeting...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2013
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3735418/ https://www.ncbi.nlm.nih.gov/pubmed/23902875 http://dx.doi.org/10.1186/1756-0500-6-303 |
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author | Brylinski, Michal |
author_facet | Brylinski, Michal |
author_sort | Brylinski, Michal |
collection | PubMed |
description | BACKGROUND: Many structural bioinformatics approaches employ sequence profile-based threading techniques. To improve fold recognition rates, homology searching may include artificially evolved amino acid sequences, which were demonstrated to enhance the sensitivity of protein threading in targeting midnight zone templates. FINDINGS: We describe implementation details of eVolver, an optimization algorithm that evolves protein sequences to stabilize the respective structures by a variety of potentials, which are compatible with those commonly used in protein threading. In a case study focusing on LARG PDZ domain, we show that artificially evolved sequences have quite high capabilities to recognize the correct protein structures using standard sequence profile-based fold recognition. CONCLUSIONS: Computationally design protein sequences can be incorporated in existing sequence profile-based threading approaches to increase their sensitivity. They also provide a desired linkage between protein structure and function in in silico experiments that relate to e.g. the completeness of protein structure space, the origin of folds and protein universe. eVolver is freely available as a user-friendly webserver and a well-documented stand-alone software distribution at http://www.brylinski.org/evolver. |
format | Online Article Text |
id | pubmed-3735418 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-37354182013-08-07 eVolver: an optimization engine for evolving protein sequences to stabilize the respective structures Brylinski, Michal BMC Res Notes Technical Note BACKGROUND: Many structural bioinformatics approaches employ sequence profile-based threading techniques. To improve fold recognition rates, homology searching may include artificially evolved amino acid sequences, which were demonstrated to enhance the sensitivity of protein threading in targeting midnight zone templates. FINDINGS: We describe implementation details of eVolver, an optimization algorithm that evolves protein sequences to stabilize the respective structures by a variety of potentials, which are compatible with those commonly used in protein threading. In a case study focusing on LARG PDZ domain, we show that artificially evolved sequences have quite high capabilities to recognize the correct protein structures using standard sequence profile-based fold recognition. CONCLUSIONS: Computationally design protein sequences can be incorporated in existing sequence profile-based threading approaches to increase their sensitivity. They also provide a desired linkage between protein structure and function in in silico experiments that relate to e.g. the completeness of protein structure space, the origin of folds and protein universe. eVolver is freely available as a user-friendly webserver and a well-documented stand-alone software distribution at http://www.brylinski.org/evolver. BioMed Central 2013-07-31 /pmc/articles/PMC3735418/ /pubmed/23902875 http://dx.doi.org/10.1186/1756-0500-6-303 Text en Copyright © 2013 Brylinski; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Technical Note Brylinski, Michal eVolver: an optimization engine for evolving protein sequences to stabilize the respective structures |
title | eVolver: an optimization engine for evolving protein sequences to stabilize the respective structures |
title_full | eVolver: an optimization engine for evolving protein sequences to stabilize the respective structures |
title_fullStr | eVolver: an optimization engine for evolving protein sequences to stabilize the respective structures |
title_full_unstemmed | eVolver: an optimization engine for evolving protein sequences to stabilize the respective structures |
title_short | eVolver: an optimization engine for evolving protein sequences to stabilize the respective structures |
title_sort | evolver: an optimization engine for evolving protein sequences to stabilize the respective structures |
topic | Technical Note |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3735418/ https://www.ncbi.nlm.nih.gov/pubmed/23902875 http://dx.doi.org/10.1186/1756-0500-6-303 |
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