Edge-count probabilities for the identification of local protein communities and their organization

We present a computational approach based on a local search strategy that discovers sets of proteins that preferentially interact with each other. Such sets are referred to as protein communities and are likely to represent functional modules. Preferential interaction between module members is quant...

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Veröffentlicht in:Proteins, structure, function, and bioinformatics structure, function, and bioinformatics, 2006-02, Vol.62 (3), p.800-818
Hauptverfasser: Farutin, Victor, Robison, Keith, Lightcap, Eric, Dancik, Vlado, Ruttenberg, Alan, Letovsky, Stanley, Pradines, Joel
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container_issue 3
container_start_page 800
container_title Proteins, structure, function, and bioinformatics
container_volume 62
creator Farutin, Victor
Robison, Keith
Lightcap, Eric
Dancik, Vlado
Ruttenberg, Alan
Letovsky, Stanley
Pradines, Joel
description We present a computational approach based on a local search strategy that discovers sets of proteins that preferentially interact with each other. Such sets are referred to as protein communities and are likely to represent functional modules. Preferential interaction between module members is quantified via an analytical framework based on a network null model known as the random graph with given expected degrees. Based on this framework, the concept of local protein community is generalized to that of community of communities. Protein communities and higher‐level structures are extracted from two yeast protein interaction data sets and a network of published interactions between human proteins. The high level structures obtained with the human network correspond to broad biological concepts such as signal transduction, regulation of gene expression, and intercellular communication. Many of the obtained human communities are enriched, in a statistically significant way, for proteins having no clear orthologs in lower organisms. This indicates that the extracted modules are quite coherent in terms of function. Proteins 2006. © 2005 Wiley‐Liss, Inc.
doi_str_mv 10.1002/prot.20799
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source MEDLINE; Wiley Online Library Journals Frontfile Complete
subjects Cell Adhesion
Cell Polarity
degree sequence
Humans
Models, Molecular
Nerve Net
Probability
protein interaction network
Protein Structure, Secondary
Proteins - chemistry
Proteins - physiology
random graph
random graph with given expected degrees
Receptors, Cell Surface - chemistry
Receptors, Cell Surface - physiology
Ribonucleoproteins, Small Nuclear - chemistry
Signal Transduction
title Edge-count probabilities for the identification of local protein communities and their organization
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