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Structural and Functional Roles of Coevolved Sites in Proteins

BACKGROUND: Understanding the residue covariations between multiple positions in protein families is very crucial and can be helpful for designing protein engineering experiments. These simultaneous changes or residue coevolution allow protein to maintain its overall structural-functional integrity...

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Autores principales: Chakrabarti, Saikat, Panchenko, Anna R.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2797611/
https://www.ncbi.nlm.nih.gov/pubmed/20066038
http://dx.doi.org/10.1371/journal.pone.0008591
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author Chakrabarti, Saikat
Panchenko, Anna R.
author_facet Chakrabarti, Saikat
Panchenko, Anna R.
author_sort Chakrabarti, Saikat
collection PubMed
description BACKGROUND: Understanding the residue covariations between multiple positions in protein families is very crucial and can be helpful for designing protein engineering experiments. These simultaneous changes or residue coevolution allow protein to maintain its overall structural-functional integrity while enabling it to acquire specific functional modifications. Despite the significant efforts in the field there is still controversy in terms of the preferable locations of coevolved residues on different regions of protein molecules, the strength of coevolutionary signal and role of coevolution in functional diversification. METHODOLOGY: In this paper we study the scale and nature of residue coevolution in maintaining the overall functionality and structural integrity of proteins. We employed a large scale study to investigate the structural and functional aspects of coevolved residues. We found that the networks representing the coevolutionary residue connections within our dataset are in general of ‘small-world’ type as they have clustering coefficient values higher than random networks and also show smaller mean shortest path lengths similar and/or lower than random and regular networks. We also found that altogether 11% of functionally important sites are coevolved with any other sites. Active sites are found more frequently to coevolve with any other sites (15%) compared to protein (11%) and ligand (9%) binding sites. Metal binding and active sites are also found to be more frequently coevolved with other metal binding and active sites, respectively. Analysis of the coupling between coevolutionary processes and the spatial distribution of coevolved sites reveals that a high fraction of coevolved sites are located close to each other. Moreover, ∼80% of charge compensatory substitutions within coevolved sites are found at very close spatial proximity (< = 5Å), pointing to the possible preservation of salt bridges in evolution. CONCLUSION: Our findings show that a noticeable fraction of functionally important sites undergo coevolution and also point towards compensatory substitutions as a probable coevolutionary mechanism within spatially proximal coevolved functional sites.
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spelling pubmed-27976112010-01-11 Structural and Functional Roles of Coevolved Sites in Proteins Chakrabarti, Saikat Panchenko, Anna R. PLoS One Research Article BACKGROUND: Understanding the residue covariations between multiple positions in protein families is very crucial and can be helpful for designing protein engineering experiments. These simultaneous changes or residue coevolution allow protein to maintain its overall structural-functional integrity while enabling it to acquire specific functional modifications. Despite the significant efforts in the field there is still controversy in terms of the preferable locations of coevolved residues on different regions of protein molecules, the strength of coevolutionary signal and role of coevolution in functional diversification. METHODOLOGY: In this paper we study the scale and nature of residue coevolution in maintaining the overall functionality and structural integrity of proteins. We employed a large scale study to investigate the structural and functional aspects of coevolved residues. We found that the networks representing the coevolutionary residue connections within our dataset are in general of ‘small-world’ type as they have clustering coefficient values higher than random networks and also show smaller mean shortest path lengths similar and/or lower than random and regular networks. We also found that altogether 11% of functionally important sites are coevolved with any other sites. Active sites are found more frequently to coevolve with any other sites (15%) compared to protein (11%) and ligand (9%) binding sites. Metal binding and active sites are also found to be more frequently coevolved with other metal binding and active sites, respectively. Analysis of the coupling between coevolutionary processes and the spatial distribution of coevolved sites reveals that a high fraction of coevolved sites are located close to each other. Moreover, ∼80% of charge compensatory substitutions within coevolved sites are found at very close spatial proximity (< = 5Å), pointing to the possible preservation of salt bridges in evolution. CONCLUSION: Our findings show that a noticeable fraction of functionally important sites undergo coevolution and also point towards compensatory substitutions as a probable coevolutionary mechanism within spatially proximal coevolved functional sites. Public Library of Science 2010-01-06 /pmc/articles/PMC2797611/ /pubmed/20066038 http://dx.doi.org/10.1371/journal.pone.0008591 Text en This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose.
spellingShingle Research Article
Chakrabarti, Saikat
Panchenko, Anna R.
Structural and Functional Roles of Coevolved Sites in Proteins
title Structural and Functional Roles of Coevolved Sites in Proteins
title_full Structural and Functional Roles of Coevolved Sites in Proteins
title_fullStr Structural and Functional Roles of Coevolved Sites in Proteins
title_full_unstemmed Structural and Functional Roles of Coevolved Sites in Proteins
title_short Structural and Functional Roles of Coevolved Sites in Proteins
title_sort structural and functional roles of coevolved sites in proteins
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2797611/
https://www.ncbi.nlm.nih.gov/pubmed/20066038
http://dx.doi.org/10.1371/journal.pone.0008591
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