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AlloReverse: multiscale understanding among hierarchical allosteric regulations

Increasing data in allostery are requiring analysis of coupling relationships among different allosteric sites on a single protein. Here, based on our previous efforts on reversed allosteric communication theory, we have developed AlloReverse, a web server for multiscale analysis of multiple alloste...

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Detalles Bibliográficos
Autores principales: Zha, Jinyin, Li, Qian, Liu, Xinyi, Lin, Weidong, Wang, Tingting, Wei, Jiacheng, Zhang, Ziliang, Lu, Xun, Wu, Jing, Ni, Duan, Song, Kun, Zhang, Liang, Lu, Xuefeng, Lu, Shaoyong, Zhang, Jian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10320067/
https://www.ncbi.nlm.nih.gov/pubmed/37070199
http://dx.doi.org/10.1093/nar/gkad279
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author Zha, Jinyin
Li, Qian
Liu, Xinyi
Lin, Weidong
Wang, Tingting
Wei, Jiacheng
Zhang, Ziliang
Lu, Xun
Wu, Jing
Ni, Duan
Song, Kun
Zhang, Liang
Lu, Xuefeng
Lu, Shaoyong
Zhang, Jian
author_facet Zha, Jinyin
Li, Qian
Liu, Xinyi
Lin, Weidong
Wang, Tingting
Wei, Jiacheng
Zhang, Ziliang
Lu, Xun
Wu, Jing
Ni, Duan
Song, Kun
Zhang, Liang
Lu, Xuefeng
Lu, Shaoyong
Zhang, Jian
author_sort Zha, Jinyin
collection PubMed
description Increasing data in allostery are requiring analysis of coupling relationships among different allosteric sites on a single protein. Here, based on our previous efforts on reversed allosteric communication theory, we have developed AlloReverse, a web server for multiscale analysis of multiple allosteric regulations. AlloReverse integrates protein dynamics and machine learning to discover allosteric residues, allosteric sites and regulation pathways. Especially, AlloReverse could reveal hierarchical relationships between different pathways and couplings among allosteric sites, offering a whole map of allostery. The web server shows a good performance in re-emerging known allostery. Moreover, we applied AlloReverse to explore global allostery on CDC42 and SIRT3. AlloReverse predicted novel allosteric sites and allosteric residues in both systems, and the functionality of sites was validated experimentally. It also suggests a possible scheme for combined therapy or bivalent drugs on SIRT3. Taken together, AlloReverse is a novel workflow providing a complete regulation map and is believed to aid target identification, drug design and understanding of biological mechanisms. AlloReverse is freely available to all users at https://mdl.shsmu.edu.cn/AlloReverse/ or http://www.allostery.net/AlloReverse/.
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spelling pubmed-103200672023-07-06 AlloReverse: multiscale understanding among hierarchical allosteric regulations Zha, Jinyin Li, Qian Liu, Xinyi Lin, Weidong Wang, Tingting Wei, Jiacheng Zhang, Ziliang Lu, Xun Wu, Jing Ni, Duan Song, Kun Zhang, Liang Lu, Xuefeng Lu, Shaoyong Zhang, Jian Nucleic Acids Res Web Server Issue Increasing data in allostery are requiring analysis of coupling relationships among different allosteric sites on a single protein. Here, based on our previous efforts on reversed allosteric communication theory, we have developed AlloReverse, a web server for multiscale analysis of multiple allosteric regulations. AlloReverse integrates protein dynamics and machine learning to discover allosteric residues, allosteric sites and regulation pathways. Especially, AlloReverse could reveal hierarchical relationships between different pathways and couplings among allosteric sites, offering a whole map of allostery. The web server shows a good performance in re-emerging known allostery. Moreover, we applied AlloReverse to explore global allostery on CDC42 and SIRT3. AlloReverse predicted novel allosteric sites and allosteric residues in both systems, and the functionality of sites was validated experimentally. It also suggests a possible scheme for combined therapy or bivalent drugs on SIRT3. Taken together, AlloReverse is a novel workflow providing a complete regulation map and is believed to aid target identification, drug design and understanding of biological mechanisms. AlloReverse is freely available to all users at https://mdl.shsmu.edu.cn/AlloReverse/ or http://www.allostery.net/AlloReverse/. Oxford University Press 2023-04-18 /pmc/articles/PMC10320067/ /pubmed/37070199 http://dx.doi.org/10.1093/nar/gkad279 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://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
Zha, Jinyin
Li, Qian
Liu, Xinyi
Lin, Weidong
Wang, Tingting
Wei, Jiacheng
Zhang, Ziliang
Lu, Xun
Wu, Jing
Ni, Duan
Song, Kun
Zhang, Liang
Lu, Xuefeng
Lu, Shaoyong
Zhang, Jian
AlloReverse: multiscale understanding among hierarchical allosteric regulations
title AlloReverse: multiscale understanding among hierarchical allosteric regulations
title_full AlloReverse: multiscale understanding among hierarchical allosteric regulations
title_fullStr AlloReverse: multiscale understanding among hierarchical allosteric regulations
title_full_unstemmed AlloReverse: multiscale understanding among hierarchical allosteric regulations
title_short AlloReverse: multiscale understanding among hierarchical allosteric regulations
title_sort alloreverse: multiscale understanding among hierarchical allosteric regulations
topic Web Server Issue
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10320067/
https://www.ncbi.nlm.nih.gov/pubmed/37070199
http://dx.doi.org/10.1093/nar/gkad279
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