Cargando…
GASS-WEB: a web server for identifying enzyme active sites based on genetic algorithms
Enzyme active sites are important and conserved functional regions of proteins whose identification can be an invaluable step toward protein function prediction. Most of the existing methods for this task are based on active site similarity and present limitations including performing only exact mat...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5570142/ https://www.ncbi.nlm.nih.gov/pubmed/28459991 http://dx.doi.org/10.1093/nar/gkx337 |
_version_ | 1783259127661723648 |
---|---|
author | Moraes, João P. A. Pappa, Gisele L. Pires, Douglas E. V. Izidoro, Sandro C. |
author_facet | Moraes, João P. A. Pappa, Gisele L. Pires, Douglas E. V. Izidoro, Sandro C. |
author_sort | Moraes, João P. A. |
collection | PubMed |
description | Enzyme active sites are important and conserved functional regions of proteins whose identification can be an invaluable step toward protein function prediction. Most of the existing methods for this task are based on active site similarity and present limitations including performing only exact matches on template residues, template size restraints, despite not being capable of finding inter-domain active sites. To fill this gap, we proposed GASS-WEB, a user-friendly web server that uses GASS (Genetic Active Site Search), a method based on an evolutionary algorithm to search for similar active sites in proteins. GASS-WEB can be used under two different scenarios: (i) given a protein of interest, to match a set of specific active site templates; or (ii) given an active site template, looking for it in a database of protein structures. The method has shown to be very effective on a range of experiments and was able to correctly identify >90% of the catalogued active sites from the Catalytic Site Atlas. It also managed to achieve a Matthew correlation coefficient of 0.63 using the Critical Assessment of protein Structure Prediction (CASP 10) dataset. In our analysis, GASS was ranking fourth among 18 methods. GASS-WEB is freely available at http://gass.unifei.edu.br/. |
format | Online Article Text |
id | pubmed-5570142 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-55701422017-08-29 GASS-WEB: a web server for identifying enzyme active sites based on genetic algorithms Moraes, João P. A. Pappa, Gisele L. Pires, Douglas E. V. Izidoro, Sandro C. Nucleic Acids Res Web Server Issue Enzyme active sites are important and conserved functional regions of proteins whose identification can be an invaluable step toward protein function prediction. Most of the existing methods for this task are based on active site similarity and present limitations including performing only exact matches on template residues, template size restraints, despite not being capable of finding inter-domain active sites. To fill this gap, we proposed GASS-WEB, a user-friendly web server that uses GASS (Genetic Active Site Search), a method based on an evolutionary algorithm to search for similar active sites in proteins. GASS-WEB can be used under two different scenarios: (i) given a protein of interest, to match a set of specific active site templates; or (ii) given an active site template, looking for it in a database of protein structures. The method has shown to be very effective on a range of experiments and was able to correctly identify >90% of the catalogued active sites from the Catalytic Site Atlas. It also managed to achieve a Matthew correlation coefficient of 0.63 using the Critical Assessment of protein Structure Prediction (CASP 10) dataset. In our analysis, GASS was ranking fourth among 18 methods. GASS-WEB is freely available at http://gass.unifei.edu.br/. Oxford University Press 2017-07-03 2017-04-29 /pmc/articles/PMC5570142/ /pubmed/28459991 http://dx.doi.org/10.1093/nar/gkx337 Text en © The Author(s) 2017. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Web Server Issue Moraes, João P. A. Pappa, Gisele L. Pires, Douglas E. V. Izidoro, Sandro C. GASS-WEB: a web server for identifying enzyme active sites based on genetic algorithms |
title | GASS-WEB: a web server for identifying enzyme active sites based on genetic algorithms |
title_full | GASS-WEB: a web server for identifying enzyme active sites based on genetic algorithms |
title_fullStr | GASS-WEB: a web server for identifying enzyme active sites based on genetic algorithms |
title_full_unstemmed | GASS-WEB: a web server for identifying enzyme active sites based on genetic algorithms |
title_short | GASS-WEB: a web server for identifying enzyme active sites based on genetic algorithms |
title_sort | gass-web: a web server for identifying enzyme active sites based on genetic algorithms |
topic | Web Server Issue |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5570142/ https://www.ncbi.nlm.nih.gov/pubmed/28459991 http://dx.doi.org/10.1093/nar/gkx337 |
work_keys_str_mv | AT moraesjoaopa gasswebawebserverforidentifyingenzymeactivesitesbasedongeneticalgorithms AT pappagiselel gasswebawebserverforidentifyingenzymeactivesitesbasedongeneticalgorithms AT piresdouglasev gasswebawebserverforidentifyingenzymeactivesitesbasedongeneticalgorithms AT izidorosandroc gasswebawebserverforidentifyingenzymeactivesitesbasedongeneticalgorithms |