AlloReverse: multiscale understanding among hierarchical allosteric regulations

Author:

Zha Jinyin123,Li Qian3,Liu Xinyi3,Lin Weidong34,Wang Tingting3,Wei Jiacheng3,Zhang Ziliang2,Lu Xun3,Wu Jing35,Ni Duan3ORCID,Song Kun24,Zhang Liang6,Lu Xuefeng5,Lu Shaoyong37ORCID,Zhang Jian1238ORCID

Affiliation:

1. State Key Laboratory of Functions and Applications of Medicinal Plants & School of Pharmacy, Guizhou Medical University , Guizhou 550025 , China

2. Wenzhou Medical University , Wenzhou 325035 , China

3. Medicinal Chemistry and Bioinformatics Center, Shanghai Jiao Tong University School of Medicine , Shanghai 200025 , China

4. Nutshell Therapeutics , Shanghai 201210 , China

5. Department of Assisted Reproduction, Shanghai Ninth People’s Hospital, Shanghai Jiao Tong University School of Medicine , Shanghai 200011 , China

6. Department of Biomedical Sciences, College of Veterinary Medicine and Life Sciences, City University of Hong Kong , Hong Kong 999077 , China

7. Institute of Energy Metabolism and Health, Shanghai Tenth People’s Hospital, Tongji University School of Medicine , Shanghai 200072 , China

8. School of Pharmaceutical Sciences, Zhengzhou University , Zhengzhou 450001 , China

Abstract

AbstractIncreasing 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/.

Funder

National Key R&D Program of China

National Natural Science Foundation of China

Shanghai Municipal Education Commission

Starry Night Science Fund of Zhejiang University Shanghai Institute for Advanced Study

High-Level Local Universities in Shanghai

Shanghai Jiao Tong University School of Medicine

Key Research and Development Program of Ningxia Hui Autonomous Region

Shanghai Health and Family Planning Commission

Shanghai Science and Technology Innovation Fund

Shanghai Sailing Program

Publisher

Oxford University Press (OUP)

Subject

Genetics

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