Using reverse docking to identify potential targets for ginsenosides
- Authors
- Park, Kichul; Cho, Art E.
- Issue Date
- 10월-2017
- Publisher
- KOREAN SOC GINSENG
- Keywords
- drug target; ginsenoside; ligand screening; protein docking; reverse docking
- Citation
- JOURNAL OF GINSENG RESEARCH, v.41, no.4, pp.534 - 539
- Indexed
- SCIE
SCOPUS
KCI
- Journal Title
- JOURNAL OF GINSENG RESEARCH
- Volume
- 41
- Number
- 4
- Start Page
- 534
- End Page
- 539
- URI
- https://scholar.korea.ac.kr/handle/2021.sw.korea/82034
- DOI
- 10.1016/j.jgr.2016.10.005
- ISSN
- 1226-8453
- Abstract
- Background: Ginsenosides are the main ingredients of ginseng, which, in traditional Eastern medicine, has been claimed to have therapeutic values for many diseases. In order to verify the effects of ginseng that have been empirically observed, we utilized the reverse docking method to screen for target proteins that are linked to specific diseases. Methods: We constructed a target protein database including 1,078 proteins associated with various kinds of diseases, based on the Potential Drug Target Database, with an added list of kinase proteins. We screened 26 kinds of ginsenosides of this target protein database using docking. Results: We found four potential target proteins for ginsenosides, based on docking scores. Implications of these " hit" targets are discussed. From this screening, we also found four targets linked to possible side effects and toxicities, based on docking scores. Conclusion: Our method and results can be helpful for finding new targets and developing new drugs from natural products. (C) 2016 The Korean Society of Ginseng, Published by Elsevier Korea LLC.
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Collections - Graduate School > Department of Biotechnology and Bioinformatics > 1. Journal Articles
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