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Optimized Null Model for Protein Structure Networks

Much attention has recently been given to the statistical significance of topological features observed in biological networks. Here, we consider residue interaction graphs (RIGs) as network representations of protein structures with residues as nodes and inter-residue interactions as edges. Degree-...

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Autores principales: Milenković, Tijana, Filippis, Ioannis, Lappe, Michael, Pržulj, Nataša
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2699654/
https://www.ncbi.nlm.nih.gov/pubmed/19557139
http://dx.doi.org/10.1371/journal.pone.0005967
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author Milenković, Tijana
Filippis, Ioannis
Lappe, Michael
Pržulj, Nataša
author_facet Milenković, Tijana
Filippis, Ioannis
Lappe, Michael
Pržulj, Nataša
author_sort Milenković, Tijana
collection PubMed
description Much attention has recently been given to the statistical significance of topological features observed in biological networks. Here, we consider residue interaction graphs (RIGs) as network representations of protein structures with residues as nodes and inter-residue interactions as edges. Degree-preserving randomized models have been widely used for this purpose in biomolecular networks. However, such a single summary statistic of a network may not be detailed enough to capture the complex topological characteristics of protein structures and their network counterparts. Here, we investigate a variety of topological properties of RIGs to find a well fitting network null model for them. The RIGs are derived from a structurally diverse protein data set at various distance cut-offs and for different groups of interacting atoms. We compare the network structure of RIGs to several random graph models. We show that 3-dimensional geometric random graphs, that model spatial relationships between objects, provide the best fit to RIGs. We investigate the relationship between the strength of the fit and various protein structural features. We show that the fit depends on protein size, structural class, and thermostability, but not on quaternary structure. We apply our model to the identification of significantly over-represented structural building blocks, i.e., network motifs, in protein structure networks. As expected, choosing geometric graphs as a null model results in the most specific identification of motifs. Our geometric random graph model may facilitate further graph-based studies of protein conformation space and have important implications for protein structure comparison and prediction. The choice of a well-fitting null model is crucial for finding structural motifs that play an important role in protein folding, stability and function. To our knowledge, this is the first study that addresses the challenge of finding an optimized null model for RIGs, by comparing various RIG definitions against a series of network models.
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spelling pubmed-26996542009-06-26 Optimized Null Model for Protein Structure Networks Milenković, Tijana Filippis, Ioannis Lappe, Michael Pržulj, Nataša PLoS One Research Article Much attention has recently been given to the statistical significance of topological features observed in biological networks. Here, we consider residue interaction graphs (RIGs) as network representations of protein structures with residues as nodes and inter-residue interactions as edges. Degree-preserving randomized models have been widely used for this purpose in biomolecular networks. However, such a single summary statistic of a network may not be detailed enough to capture the complex topological characteristics of protein structures and their network counterparts. Here, we investigate a variety of topological properties of RIGs to find a well fitting network null model for them. The RIGs are derived from a structurally diverse protein data set at various distance cut-offs and for different groups of interacting atoms. We compare the network structure of RIGs to several random graph models. We show that 3-dimensional geometric random graphs, that model spatial relationships between objects, provide the best fit to RIGs. We investigate the relationship between the strength of the fit and various protein structural features. We show that the fit depends on protein size, structural class, and thermostability, but not on quaternary structure. We apply our model to the identification of significantly over-represented structural building blocks, i.e., network motifs, in protein structure networks. As expected, choosing geometric graphs as a null model results in the most specific identification of motifs. Our geometric random graph model may facilitate further graph-based studies of protein conformation space and have important implications for protein structure comparison and prediction. The choice of a well-fitting null model is crucial for finding structural motifs that play an important role in protein folding, stability and function. To our knowledge, this is the first study that addresses the challenge of finding an optimized null model for RIGs, by comparing various RIG definitions against a series of network models. Public Library of Science 2009-06-26 /pmc/articles/PMC2699654/ /pubmed/19557139 http://dx.doi.org/10.1371/journal.pone.0005967 Text en Milenković et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Milenković, Tijana
Filippis, Ioannis
Lappe, Michael
Pržulj, Nataša
Optimized Null Model for Protein Structure Networks
title Optimized Null Model for Protein Structure Networks
title_full Optimized Null Model for Protein Structure Networks
title_fullStr Optimized Null Model for Protein Structure Networks
title_full_unstemmed Optimized Null Model for Protein Structure Networks
title_short Optimized Null Model for Protein Structure Networks
title_sort optimized null model for protein structure networks
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2699654/
https://www.ncbi.nlm.nih.gov/pubmed/19557139
http://dx.doi.org/10.1371/journal.pone.0005967
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