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AlloSigMA 2: paving the way to designing allosteric effectors and to exploring allosteric effects of mutations
The AlloSigMA 2 server provides an interactive platform for exploring the allosteric signaling caused by ligand binding and/or mutations, for analyzing the allosteric effects of mutations and for detecting potential cancer drivers and pathogenic nsSNPs. It can also be used for searching latent allos...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7319554/ https://www.ncbi.nlm.nih.gov/pubmed/32392302 http://dx.doi.org/10.1093/nar/gkaa338 |
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author | Tan, Zhen Wah Guarnera, Enrico Tee, Wei-Ven Berezovsky, Igor N |
author_facet | Tan, Zhen Wah Guarnera, Enrico Tee, Wei-Ven Berezovsky, Igor N |
author_sort | Tan, Zhen Wah |
collection | PubMed |
description | The AlloSigMA 2 server provides an interactive platform for exploring the allosteric signaling caused by ligand binding and/or mutations, for analyzing the allosteric effects of mutations and for detecting potential cancer drivers and pathogenic nsSNPs. It can also be used for searching latent allosteric sites and for computationally designing allosteric effectors for these sites with required agonist/antagonist activity. The server is based on the implementation of the Structure-Based Statistical Mechanical Model of Allostery (SBSMMA), which allows one to evaluate the allosteric free energy as a result of the perturbation at per-residue resolution. The Allosteric Signaling Map (ASM) providing a comprehensive residue-by-residue allosteric control over the protein activity can be obtained for any structure of interest. The Allosteric Probing Map (APM), in turn, allows one to perform the fragment-based-like computational design experiment aimed at finding leads for potential allosteric effectors. The server can be instrumental in elucidating of allosteric mechanisms and actions of allosteric mutations, and in the efforts on design of new elements of allosteric control. The server is freely available at: http://allosigma.bii.a-star.edu.sg |
format | Online Article Text |
id | pubmed-7319554 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-73195542020-07-01 AlloSigMA 2: paving the way to designing allosteric effectors and to exploring allosteric effects of mutations Tan, Zhen Wah Guarnera, Enrico Tee, Wei-Ven Berezovsky, Igor N Nucleic Acids Res Web Server Issue The AlloSigMA 2 server provides an interactive platform for exploring the allosteric signaling caused by ligand binding and/or mutations, for analyzing the allosteric effects of mutations and for detecting potential cancer drivers and pathogenic nsSNPs. It can also be used for searching latent allosteric sites and for computationally designing allosteric effectors for these sites with required agonist/antagonist activity. The server is based on the implementation of the Structure-Based Statistical Mechanical Model of Allostery (SBSMMA), which allows one to evaluate the allosteric free energy as a result of the perturbation at per-residue resolution. The Allosteric Signaling Map (ASM) providing a comprehensive residue-by-residue allosteric control over the protein activity can be obtained for any structure of interest. The Allosteric Probing Map (APM), in turn, allows one to perform the fragment-based-like computational design experiment aimed at finding leads for potential allosteric effectors. The server can be instrumental in elucidating of allosteric mechanisms and actions of allosteric mutations, and in the efforts on design of new elements of allosteric control. The server is freely available at: http://allosigma.bii.a-star.edu.sg Oxford University Press 2020-07-02 2020-05-11 /pmc/articles/PMC7319554/ /pubmed/32392302 http://dx.doi.org/10.1093/nar/gkaa338 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by/4.0/ 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 reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Web Server Issue Tan, Zhen Wah Guarnera, Enrico Tee, Wei-Ven Berezovsky, Igor N AlloSigMA 2: paving the way to designing allosteric effectors and to exploring allosteric effects of mutations |
title | AlloSigMA 2: paving the way to designing allosteric effectors and to exploring allosteric effects of mutations |
title_full | AlloSigMA 2: paving the way to designing allosteric effectors and to exploring allosteric effects of mutations |
title_fullStr | AlloSigMA 2: paving the way to designing allosteric effectors and to exploring allosteric effects of mutations |
title_full_unstemmed | AlloSigMA 2: paving the way to designing allosteric effectors and to exploring allosteric effects of mutations |
title_short | AlloSigMA 2: paving the way to designing allosteric effectors and to exploring allosteric effects of mutations |
title_sort | allosigma 2: paving the way to designing allosteric effectors and to exploring allosteric effects of mutations |
topic | Web Server Issue |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7319554/ https://www.ncbi.nlm.nih.gov/pubmed/32392302 http://dx.doi.org/10.1093/nar/gkaa338 |
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