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Functional discrimination of membrane proteins using machine learning techniques

BACKGROUND: Discriminating membrane proteins based on their functions is an important task in genome annotation. In this work, we have analyzed the characteristic features of amino acid residues in membrane proteins that perform major functions, such as channels/pores, electrochemical potential-driv...

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Autores principales: Gromiha, M Michael, Yabuki, Yukimitsu
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2375119/
https://www.ncbi.nlm.nih.gov/pubmed/18312695
http://dx.doi.org/10.1186/1471-2105-9-135
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author Gromiha, M Michael
Yabuki, Yukimitsu
author_facet Gromiha, M Michael
Yabuki, Yukimitsu
author_sort Gromiha, M Michael
collection PubMed
description BACKGROUND: Discriminating membrane proteins based on their functions is an important task in genome annotation. In this work, we have analyzed the characteristic features of amino acid residues in membrane proteins that perform major functions, such as channels/pores, electrochemical potential-driven transporters and primary active transporters. RESULTS: We observed that the residues Asp, Asn and Tyr are dominant in channels/pores whereas the composition of hydrophobic residues, Phe, Gly, Ile, Leu and Val is high in electrochemical potential-driven transporters. The composition of all the amino acids in primary active transporters lies in between other two classes of proteins. We have utilized different machine learning algorithms, such as, Bayes rule, Logistic function, Neural network, Support vector machine, Decision tree etc. for discriminating these classes of proteins. We observed that most of the algorithms have discriminated them with similar accuracy. The neural network method discriminated the channels/pores, electrochemical potential-driven transporters and active transporters with the 5-fold cross validation accuracy of 64% in a data set of 1718 membrane proteins. The application of amino acid occurrence improved the overall accuracy to 68%. In addition, we have discriminated transporters from other α-helical and β-barrel membrane proteins with the accuracy of 85% using k-nearest neighbor method. The classification of transporters and all other proteins (globular and membrane) showed the accuracy of 82%. CONCLUSION: The performance of discrimination with amino acid occurrence is better than that with amino acid composition. We suggest that this method could be effectively used to discriminate transporters from all other globular and membrane proteins, and classify them into channels/pores, electrochemical and active transporters.
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spelling pubmed-23751192008-05-10 Functional discrimination of membrane proteins using machine learning techniques Gromiha, M Michael Yabuki, Yukimitsu BMC Bioinformatics Research Article BACKGROUND: Discriminating membrane proteins based on their functions is an important task in genome annotation. In this work, we have analyzed the characteristic features of amino acid residues in membrane proteins that perform major functions, such as channels/pores, electrochemical potential-driven transporters and primary active transporters. RESULTS: We observed that the residues Asp, Asn and Tyr are dominant in channels/pores whereas the composition of hydrophobic residues, Phe, Gly, Ile, Leu and Val is high in electrochemical potential-driven transporters. The composition of all the amino acids in primary active transporters lies in between other two classes of proteins. We have utilized different machine learning algorithms, such as, Bayes rule, Logistic function, Neural network, Support vector machine, Decision tree etc. for discriminating these classes of proteins. We observed that most of the algorithms have discriminated them with similar accuracy. The neural network method discriminated the channels/pores, electrochemical potential-driven transporters and active transporters with the 5-fold cross validation accuracy of 64% in a data set of 1718 membrane proteins. The application of amino acid occurrence improved the overall accuracy to 68%. In addition, we have discriminated transporters from other α-helical and β-barrel membrane proteins with the accuracy of 85% using k-nearest neighbor method. The classification of transporters and all other proteins (globular and membrane) showed the accuracy of 82%. CONCLUSION: The performance of discrimination with amino acid occurrence is better than that with amino acid composition. We suggest that this method could be effectively used to discriminate transporters from all other globular and membrane proteins, and classify them into channels/pores, electrochemical and active transporters. BioMed Central 2008-03-03 /pmc/articles/PMC2375119/ /pubmed/18312695 http://dx.doi.org/10.1186/1471-2105-9-135 Text en Copyright © 2008 Gromiha and Yabuki; 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
Gromiha, M Michael
Yabuki, Yukimitsu
Functional discrimination of membrane proteins using machine learning techniques
title Functional discrimination of membrane proteins using machine learning techniques
title_full Functional discrimination of membrane proteins using machine learning techniques
title_fullStr Functional discrimination of membrane proteins using machine learning techniques
title_full_unstemmed Functional discrimination of membrane proteins using machine learning techniques
title_short Functional discrimination of membrane proteins using machine learning techniques
title_sort functional discrimination of membrane proteins using machine learning techniques
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2375119/
https://www.ncbi.nlm.nih.gov/pubmed/18312695
http://dx.doi.org/10.1186/1471-2105-9-135
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