Detailed Information on Publication Record
2022
Improving ligand transport trajectory within flexible receptor in CaverDock
NĚMCOVÁ, Petra, Jana HOZZOVÁ and Jiří FILIPOVIČBasic information
Original name
Improving ligand transport trajectory within flexible receptor in CaverDock
Authors
NĚMCOVÁ, Petra (203 Czech Republic, belonging to the institution), Jana HOZZOVÁ (703 Slovakia, belonging to the institution) and Jiří FILIPOVIČ (203 Czech Republic, guarantor, belonging to the institution)
Edition
USA, SAC '22: Proceedings of the 37th ACM/SIGAPP Symposium on Applied Computing, p. 619-626, 8 pp. 2022
Publisher
Association for Computing Machinery
Other information
Language
English
Type of outcome
Stať ve sborníku
Field of Study
10201 Computer sciences, information science, bioinformatics
Country of publisher
United States of America
Confidentiality degree
není předmětem státního či obchodního tajemství
Publication form
electronic version available online
References:
RIV identification code
RIV/00216224:14610/22:00125815
Organization unit
Institute of Computer Science
ISBN
978-1-4503-8713-2
UT WoS
000946564100083
Keywords in English
CaverDock; ligand transport; flexible receptor; molecular docking; search heuristic; continuous space search
Tags
International impact, Reviewed
Změněno: 7/2/2024 16:11, Mgr. Marie Šípková, DiS.
Abstract
V originále
The receptor-ligand interactions are an important part of many biologically relevant processes. The small ligand molecule needs to pass via a tunnel into a receptor before the interaction of interest begins. Both receptor-ligand interaction and ligand pathway need to be studied. CaverDock is a computational tool that simulates the transport of the ligand in a tunnel. However, in its first version, CaverDock allowed only limited flexibility of the receptor, biasing the measured energy of ligand transportation. In this paper, we introduce two essential extensions to CaverDock. First, we combine its force field with AMBER, which allows to relax receptor’s geometry in tunnel bottlenecks. Second, we improve CaverDock heuristics for ligand trajectory search to obtain multiple variants of ligand trajectories, ideally with lower energy compared to the result of CaverDock 1.0. We experimentally demonstrate that the new heuristic is superior to the original one and that the receptor relaxation improves precision of CaverDock results.
Links
LM2018140, research and development project |
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MUNI/A/1145/2021, interní kód MU |
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