Prediction of multi-type membrane proteins in human by an integrated approach.

Membrane proteins were found to be involved in various cellular processes performing various important functions, which are mainly associated to their types. However, it is very time-consuming and expensive for traditional biophysical methods to identify membrane protein types. Although some computa...

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Main Authors: Guohua Huang, Yuchao Zhang, Lei Chen, Ning Zhang, Tao Huang, Yu-Dong Cai
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24676214/?tool=EBI
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spelling doaj-9726ca5e02cb410e80378bad6da115e82021-03-04T09:36:42ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-0193e9355310.1371/journal.pone.0093553Prediction of multi-type membrane proteins in human by an integrated approach.Guohua HuangYuchao ZhangLei ChenNing ZhangTao HuangYu-Dong CaiMembrane proteins were found to be involved in various cellular processes performing various important functions, which are mainly associated to their types. However, it is very time-consuming and expensive for traditional biophysical methods to identify membrane protein types. Although some computational tools predicting membrane protein types have been developed, most of them can only recognize one kind of type. Therefore, they are not as effective as one membrane protein can have several types at the same time. To our knowledge, few methods handling multiple types of membrane proteins were reported. In this study, we proposed an integrated approach to predict multiple types of membrane proteins by employing sequence homology and protein-protein interaction network. As a result, the prediction accuracies reached 87.65%, 81.39% and 70.79%, respectively, by the leave-one-out test on three datasets. It outperformed the nearest neighbor algorithm adopting pseudo amino acid composition. The method is anticipated to be an alternative tool for identifying membrane protein types. New metrics for evaluating performances of methods dealing with multi-label problems were also presented. The program of the method is available upon request.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24676214/?tool=EBI
collection DOAJ
language English
format Article
sources DOAJ
author Guohua Huang
Yuchao Zhang
Lei Chen
Ning Zhang
Tao Huang
Yu-Dong Cai
spellingShingle Guohua Huang
Yuchao Zhang
Lei Chen
Ning Zhang
Tao Huang
Yu-Dong Cai
Prediction of multi-type membrane proteins in human by an integrated approach.
PLoS ONE
author_facet Guohua Huang
Yuchao Zhang
Lei Chen
Ning Zhang
Tao Huang
Yu-Dong Cai
author_sort Guohua Huang
title Prediction of multi-type membrane proteins in human by an integrated approach.
title_short Prediction of multi-type membrane proteins in human by an integrated approach.
title_full Prediction of multi-type membrane proteins in human by an integrated approach.
title_fullStr Prediction of multi-type membrane proteins in human by an integrated approach.
title_full_unstemmed Prediction of multi-type membrane proteins in human by an integrated approach.
title_sort prediction of multi-type membrane proteins in human by an integrated approach.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2014-01-01
description Membrane proteins were found to be involved in various cellular processes performing various important functions, which are mainly associated to their types. However, it is very time-consuming and expensive for traditional biophysical methods to identify membrane protein types. Although some computational tools predicting membrane protein types have been developed, most of them can only recognize one kind of type. Therefore, they are not as effective as one membrane protein can have several types at the same time. To our knowledge, few methods handling multiple types of membrane proteins were reported. In this study, we proposed an integrated approach to predict multiple types of membrane proteins by employing sequence homology and protein-protein interaction network. As a result, the prediction accuracies reached 87.65%, 81.39% and 70.79%, respectively, by the leave-one-out test on three datasets. It outperformed the nearest neighbor algorithm adopting pseudo amino acid composition. The method is anticipated to be an alternative tool for identifying membrane protein types. New metrics for evaluating performances of methods dealing with multi-label problems were also presented. The program of the method is available upon request.
url https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24676214/?tool=EBI
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