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Predicting gene ontology functions from protein's regional surface structures

BACKGROUND: Annotation of protein functions is an important task in the post-genomic era. Most early approaches for this task exploit only the sequence or global structure information. However, protein surfaces are believed to be crucial to protein functions because they are the main interfaces to f...

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Autores principales: Liu, Zhi-Ping, Wu, Ling-Yun, Wang, Yong, Chen, Luonan, Zhang, Xiang-Sun
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2233648/
https://www.ncbi.nlm.nih.gov/pubmed/18070366
http://dx.doi.org/10.1186/1471-2105-8-475
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author Liu, Zhi-Ping
Wu, Ling-Yun
Wang, Yong
Chen, Luonan
Zhang, Xiang-Sun
author_facet Liu, Zhi-Ping
Wu, Ling-Yun
Wang, Yong
Chen, Luonan
Zhang, Xiang-Sun
author_sort Liu, Zhi-Ping
collection PubMed
description BACKGROUND: Annotation of protein functions is an important task in the post-genomic era. Most early approaches for this task exploit only the sequence or global structure information. However, protein surfaces are believed to be crucial to protein functions because they are the main interfaces to facilitate biological interactions. Recently, several databases related to structural surfaces, such as pockets and cavities, have been constructed with a comprehensive library of identified surface structures. For example, CASTp provides identification and measurements of surface accessible pockets as well as interior inaccessible cavities. RESULTS: A novel method was proposed to predict the Gene Ontology (GO) functions of proteins from the pocket similarity network, which is constructed according to the structure similarities of pockets. The statistics of the networks were presented to explore the relationship between the similar pockets and GO functions of proteins. Cross-validation experiments were conducted to evaluate the performance of the proposed method. Results and codes are available at: . CONCLUSION: The computational results demonstrate that the proposed method based on the pocket similarity network is effective and efficient for predicting GO functions of proteins in terms of both computational complexity and prediction accuracy. The proposed method revealed strong relationship between small surface patterns (or pockets) and GO functions, which can be further used to identify active sites or functional motifs. The high quality performance of the prediction method together with the statistics also indicates that pockets play essential roles in biological interactions or the GO functions. Moreover, in addition to pockets, the proposed network framework can also be used for adopting other protein spatial surface patterns to predict the protein functions.
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spelling pubmed-22336482008-02-07 Predicting gene ontology functions from protein's regional surface structures Liu, Zhi-Ping Wu, Ling-Yun Wang, Yong Chen, Luonan Zhang, Xiang-Sun BMC Bioinformatics Research Article BACKGROUND: Annotation of protein functions is an important task in the post-genomic era. Most early approaches for this task exploit only the sequence or global structure information. However, protein surfaces are believed to be crucial to protein functions because they are the main interfaces to facilitate biological interactions. Recently, several databases related to structural surfaces, such as pockets and cavities, have been constructed with a comprehensive library of identified surface structures. For example, CASTp provides identification and measurements of surface accessible pockets as well as interior inaccessible cavities. RESULTS: A novel method was proposed to predict the Gene Ontology (GO) functions of proteins from the pocket similarity network, which is constructed according to the structure similarities of pockets. The statistics of the networks were presented to explore the relationship between the similar pockets and GO functions of proteins. Cross-validation experiments were conducted to evaluate the performance of the proposed method. Results and codes are available at: . CONCLUSION: The computational results demonstrate that the proposed method based on the pocket similarity network is effective and efficient for predicting GO functions of proteins in terms of both computational complexity and prediction accuracy. The proposed method revealed strong relationship between small surface patterns (or pockets) and GO functions, which can be further used to identify active sites or functional motifs. The high quality performance of the prediction method together with the statistics also indicates that pockets play essential roles in biological interactions or the GO functions. Moreover, in addition to pockets, the proposed network framework can also be used for adopting other protein spatial surface patterns to predict the protein functions. BioMed Central 2007-12-11 /pmc/articles/PMC2233648/ /pubmed/18070366 http://dx.doi.org/10.1186/1471-2105-8-475 Text en Copyright © 2007 Liu et al; 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 Research Article
Liu, Zhi-Ping
Wu, Ling-Yun
Wang, Yong
Chen, Luonan
Zhang, Xiang-Sun
Predicting gene ontology functions from protein's regional surface structures
title Predicting gene ontology functions from protein's regional surface structures
title_full Predicting gene ontology functions from protein's regional surface structures
title_fullStr Predicting gene ontology functions from protein's regional surface structures
title_full_unstemmed Predicting gene ontology functions from protein's regional surface structures
title_short Predicting gene ontology functions from protein's regional surface structures
title_sort predicting gene ontology functions from protein's regional surface structures
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2233648/
https://www.ncbi.nlm.nih.gov/pubmed/18070366
http://dx.doi.org/10.1186/1471-2105-8-475
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