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Integrating protein structural dynamics and evolutionary analysis with Bio3D
BACKGROUND: Popular bioinformatics approaches for studying protein functional dynamics include comparisons of crystallographic structures, molecular dynamics simulations and normal mode analysis. However, determining how observed displacements and predicted motions from these traditionally separate...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4279791/ https://www.ncbi.nlm.nih.gov/pubmed/25491031 http://dx.doi.org/10.1186/s12859-014-0399-6 |
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author | Skjærven, Lars Yao, Xin-Qiu Scarabelli, Guido Grant, Barry J |
author_facet | Skjærven, Lars Yao, Xin-Qiu Scarabelli, Guido Grant, Barry J |
author_sort | Skjærven, Lars |
collection | PubMed |
description | BACKGROUND: Popular bioinformatics approaches for studying protein functional dynamics include comparisons of crystallographic structures, molecular dynamics simulations and normal mode analysis. However, determining how observed displacements and predicted motions from these traditionally separate analyses relate to each other, as well as to the evolution of sequence, structure and function within large protein families, remains a considerable challenge. This is in part due to the general lack of tools that integrate information of molecular structure, dynamics and evolution. RESULTS: Here, we describe the integration of new methodologies for evolutionary sequence, structure and simulation analysis into the Bio3D package. This major update includes unique high-throughput normal mode analysis for examining and contrasting the dynamics of related proteins with non-identical sequences and structures, as well as new methods for quantifying dynamical couplings and their residue-wise dissection from correlation network analysis. These new methodologies are integrated with major biomolecular databases as well as established methods for evolutionary sequence and comparative structural analysis. New functionality for directly comparing results derived from normal modes, molecular dynamics and principal component analysis of heterogeneous experimental structure distributions is also included. We demonstrate these integrated capabilities with example applications to dihydrofolate reductase and heterotrimeric G-protein families along with a discussion of the mechanistic insight provided in each case. CONCLUSIONS: The integration of structural dynamics and evolutionary analysis in Bio3D enables researchers to go beyond a prediction of single protein dynamics to investigate dynamical features across large protein families. The Bio3D package is distributed with full source code and extensive documentation as a platform independent R package under a GPL2 license from http://thegrantlab.org/bio3d/. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12859-014-0399-6) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4279791 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42797912015-01-22 Integrating protein structural dynamics and evolutionary analysis with Bio3D Skjærven, Lars Yao, Xin-Qiu Scarabelli, Guido Grant, Barry J BMC Bioinformatics Software BACKGROUND: Popular bioinformatics approaches for studying protein functional dynamics include comparisons of crystallographic structures, molecular dynamics simulations and normal mode analysis. However, determining how observed displacements and predicted motions from these traditionally separate analyses relate to each other, as well as to the evolution of sequence, structure and function within large protein families, remains a considerable challenge. This is in part due to the general lack of tools that integrate information of molecular structure, dynamics and evolution. RESULTS: Here, we describe the integration of new methodologies for evolutionary sequence, structure and simulation analysis into the Bio3D package. This major update includes unique high-throughput normal mode analysis for examining and contrasting the dynamics of related proteins with non-identical sequences and structures, as well as new methods for quantifying dynamical couplings and their residue-wise dissection from correlation network analysis. These new methodologies are integrated with major biomolecular databases as well as established methods for evolutionary sequence and comparative structural analysis. New functionality for directly comparing results derived from normal modes, molecular dynamics and principal component analysis of heterogeneous experimental structure distributions is also included. We demonstrate these integrated capabilities with example applications to dihydrofolate reductase and heterotrimeric G-protein families along with a discussion of the mechanistic insight provided in each case. CONCLUSIONS: The integration of structural dynamics and evolutionary analysis in Bio3D enables researchers to go beyond a prediction of single protein dynamics to investigate dynamical features across large protein families. The Bio3D package is distributed with full source code and extensive documentation as a platform independent R package under a GPL2 license from http://thegrantlab.org/bio3d/. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12859-014-0399-6) contains supplementary material, which is available to authorized users. BioMed Central 2014-12-10 /pmc/articles/PMC4279791/ /pubmed/25491031 http://dx.doi.org/10.1186/s12859-014-0399-6 Text en © Skjærven et al.; licensee BioMed Central. 2014 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Software Skjærven, Lars Yao, Xin-Qiu Scarabelli, Guido Grant, Barry J Integrating protein structural dynamics and evolutionary analysis with Bio3D |
title | Integrating protein structural dynamics and evolutionary analysis with Bio3D |
title_full | Integrating protein structural dynamics and evolutionary analysis with Bio3D |
title_fullStr | Integrating protein structural dynamics and evolutionary analysis with Bio3D |
title_full_unstemmed | Integrating protein structural dynamics and evolutionary analysis with Bio3D |
title_short | Integrating protein structural dynamics and evolutionary analysis with Bio3D |
title_sort | integrating protein structural dynamics and evolutionary analysis with bio3d |
topic | Software |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4279791/ https://www.ncbi.nlm.nih.gov/pubmed/25491031 http://dx.doi.org/10.1186/s12859-014-0399-6 |
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