Protein function assignment through mining cross-species protein-protein interactions.

BACKGROUND: As we move into the post genome-sequencing era, an immediate challenge is how to make best use of the large amount of high-throughput experimental data to assign functions to currently uncharacterized proteins. We here describe CSIDOP, a new method for protein function assignment based o...

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Main Authors: Xue-Wen Chen, Mei Liu, Robert Ward
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2008-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC2216687?pdf=render
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spelling doaj-a9e118f3db014fa2b0c0fc7afeeebe702020-11-25T02:38:51ZengPublic Library of Science (PLoS)PLoS ONE1932-62032008-01-0132e156210.1371/journal.pone.0001562Protein function assignment through mining cross-species protein-protein interactions.Xue-Wen ChenMei LiuRobert WardBACKGROUND: As we move into the post genome-sequencing era, an immediate challenge is how to make best use of the large amount of high-throughput experimental data to assign functions to currently uncharacterized proteins. We here describe CSIDOP, a new method for protein function assignment based on shared interacting domain patterns extracted from cross-species protein-protein interaction data. METHODOLOGY/PRINCIPAL FINDINGS: The proposed method is assessed both biologically and statistically over the genome of H. sapiens. The CSIDOP method is capable of making protein function prediction with accuracy of 95.42% using 2,972 gene ontology (GO) functional categories. In addition, we are able to assign novel functional annotations for 181 previously uncharacterized proteins in H. sapiens. Furthermore, we demonstrate that for proteins that are characterized by GO, the CSIDOP may predict extra functions. This is attractive as a protein normally executes a variety of functions in different processes and its current GO annotation may be incomplete. CONCLUSIONS/SIGNIFICANCE: It can be shown through experimental results that the CSIDOP method is reliable and practical in use. The method will continue to improve as more high quality interaction data becomes available and is readily scalable to a genome-wide application.http://europepmc.org/articles/PMC2216687?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Xue-Wen Chen
Mei Liu
Robert Ward
spellingShingle Xue-Wen Chen
Mei Liu
Robert Ward
Protein function assignment through mining cross-species protein-protein interactions.
PLoS ONE
author_facet Xue-Wen Chen
Mei Liu
Robert Ward
author_sort Xue-Wen Chen
title Protein function assignment through mining cross-species protein-protein interactions.
title_short Protein function assignment through mining cross-species protein-protein interactions.
title_full Protein function assignment through mining cross-species protein-protein interactions.
title_fullStr Protein function assignment through mining cross-species protein-protein interactions.
title_full_unstemmed Protein function assignment through mining cross-species protein-protein interactions.
title_sort protein function assignment through mining cross-species protein-protein interactions.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2008-01-01
description BACKGROUND: As we move into the post genome-sequencing era, an immediate challenge is how to make best use of the large amount of high-throughput experimental data to assign functions to currently uncharacterized proteins. We here describe CSIDOP, a new method for protein function assignment based on shared interacting domain patterns extracted from cross-species protein-protein interaction data. METHODOLOGY/PRINCIPAL FINDINGS: The proposed method is assessed both biologically and statistically over the genome of H. sapiens. The CSIDOP method is capable of making protein function prediction with accuracy of 95.42% using 2,972 gene ontology (GO) functional categories. In addition, we are able to assign novel functional annotations for 181 previously uncharacterized proteins in H. sapiens. Furthermore, we demonstrate that for proteins that are characterized by GO, the CSIDOP may predict extra functions. This is attractive as a protein normally executes a variety of functions in different processes and its current GO annotation may be incomplete. CONCLUSIONS/SIGNIFICANCE: It can be shown through experimental results that the CSIDOP method is reliable and practical in use. The method will continue to improve as more high quality interaction data becomes available and is readily scalable to a genome-wide application.
url http://europepmc.org/articles/PMC2216687?pdf=render
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AT meiliu proteinfunctionassignmentthroughminingcrossspeciesproteinproteininteractions
AT robertward proteinfunctionassignmentthroughminingcrossspeciesproteinproteininteractions
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