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DynOmics: dynamics of structural proteome and beyond

DynOmics (dynomics.pitt.edu) is a portal developed to leverage rapidly growing structural proteomics data by efficiently and accurately evaluating the dynamics of structurally resolved systems, from individual molecules to large complexes and assemblies, in the context of their physiological environ...

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Autores principales: Li, Hongchun, Chang, Yuan-Yu, Lee, Ji Young, Bahar, Ivet, Yang, Lee-Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5793847/
https://www.ncbi.nlm.nih.gov/pubmed/28472330
http://dx.doi.org/10.1093/nar/gkx385
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author Li, Hongchun
Chang, Yuan-Yu
Lee, Ji Young
Bahar, Ivet
Yang, Lee-Wei
author_facet Li, Hongchun
Chang, Yuan-Yu
Lee, Ji Young
Bahar, Ivet
Yang, Lee-Wei
author_sort Li, Hongchun
collection PubMed
description DynOmics (dynomics.pitt.edu) is a portal developed to leverage rapidly growing structural proteomics data by efficiently and accurately evaluating the dynamics of structurally resolved systems, from individual molecules to large complexes and assemblies, in the context of their physiological environment. At the core of the portal is a newly developed server, ENM 1.0, which permits users to efficiently generate information on the collective dynamics of any structure in PDB format, user-uploaded or database-retrieved. ENM 1.0 integrates two widely used elastic network models (ENMs)—the Gaussian Network Model (GNM) and the Anisotropic Network Model (ANM), extended to take account of molecular environment. It enables users to assess potentially functional sites, signal transduction or allosteric communication mechanisms, and protein–protein and protein–DNA interaction poses, in addition to delivering ensembles of accessible conformers reconstructed at atomic details based on the global modes of motions predicted by the ANM. The ‘environment’ is defined in a flexible manner, from lipid bilayer and crystal contacts, to substrate or ligands bound to a protein, or surrounding subunits in a multimeric structure or assembly. User-friendly interactive features permit users to easily visualize how the environment alter the intrinsic dynamics of the query systems. ENM 1.0 can be accessed at http://enm.pitt.edu/ or http://dyn.life.nthu.edu.tw/oENM/.
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spelling pubmed-57938472018-02-06 DynOmics: dynamics of structural proteome and beyond Li, Hongchun Chang, Yuan-Yu Lee, Ji Young Bahar, Ivet Yang, Lee-Wei Nucleic Acids Res Web Server Issue DynOmics (dynomics.pitt.edu) is a portal developed to leverage rapidly growing structural proteomics data by efficiently and accurately evaluating the dynamics of structurally resolved systems, from individual molecules to large complexes and assemblies, in the context of their physiological environment. At the core of the portal is a newly developed server, ENM 1.0, which permits users to efficiently generate information on the collective dynamics of any structure in PDB format, user-uploaded or database-retrieved. ENM 1.0 integrates two widely used elastic network models (ENMs)—the Gaussian Network Model (GNM) and the Anisotropic Network Model (ANM), extended to take account of molecular environment. It enables users to assess potentially functional sites, signal transduction or allosteric communication mechanisms, and protein–protein and protein–DNA interaction poses, in addition to delivering ensembles of accessible conformers reconstructed at atomic details based on the global modes of motions predicted by the ANM. The ‘environment’ is defined in a flexible manner, from lipid bilayer and crystal contacts, to substrate or ligands bound to a protein, or surrounding subunits in a multimeric structure or assembly. User-friendly interactive features permit users to easily visualize how the environment alter the intrinsic dynamics of the query systems. ENM 1.0 can be accessed at http://enm.pitt.edu/ or http://dyn.life.nthu.edu.tw/oENM/. Oxford University Press 2017-07-03 2017-05-03 /pmc/articles/PMC5793847/ /pubmed/28472330 http://dx.doi.org/10.1093/nar/gkx385 Text en © The Author(s) 2017. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Web Server Issue
Li, Hongchun
Chang, Yuan-Yu
Lee, Ji Young
Bahar, Ivet
Yang, Lee-Wei
DynOmics: dynamics of structural proteome and beyond
title DynOmics: dynamics of structural proteome and beyond
title_full DynOmics: dynamics of structural proteome and beyond
title_fullStr DynOmics: dynamics of structural proteome and beyond
title_full_unstemmed DynOmics: dynamics of structural proteome and beyond
title_short DynOmics: dynamics of structural proteome and beyond
title_sort dynomics: dynamics of structural proteome and beyond
topic Web Server Issue
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5793847/
https://www.ncbi.nlm.nih.gov/pubmed/28472330
http://dx.doi.org/10.1093/nar/gkx385
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