AlloSigMA 2: paving the way to designing allosteric effectors and to exploring allosteric effects of mutations

Page view(s)
34
Checked on Jul 11, 2024
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
Journal Title:
Nucleic Acids Research
Keywords:
Publication Date:
11 May 2020
Citation:
Zhen Wah Tan, Enrico Guarnera, Wei-Ven Tee, Igor N Berezovsky, AlloSigMA 2: paving the way to designing allosteric effectors and to exploring allosteric effects of mutations, Nucleic Acids Research, , gkaa338, https://doi.org/10.1093/nar/gkaa338
Abstract:
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 residueby-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.
License type:
http://creativecommons.org/licenses/by/4.0/
Funding Info:
There was no specific funding for the research done.
Description:
ISSN:
0305-1048
1362-4962
Files uploaded:

File Size Format Action
ib-nar-11-may-2020.pdf 3.94 MB PDF Open