Key residues influencing binding affinities of 2019-nCoV with ACE2 in different species. Issue 2 (8th December 2020)
- Record Type:
- Journal Article
- Title:
- Key residues influencing binding affinities of 2019-nCoV with ACE2 in different species. Issue 2 (8th December 2020)
- Main Title:
- Key residues influencing binding affinities of 2019-nCoV with ACE2 in different species
- Authors:
- Fang, Senbiao
Zheng, Ruoqian
Lei, Chuqi
Wang, Jianxin
Zheng, Ruiqing
Li, Min - Abstract:
- Abstract: The Novel Coronavirus Disease 2019 (COVID-19) has become an international public health emergency, which poses the most serious threat to the human health around the world. Accumulating evidences have shown that the new coronavirus could not only infect human beings, but also can infect other species which might result in the cross-species infections . In this research, 1056 ACE2 protein sequences are collected from the NCBI database, and 173 species with >60% sequence identity compared with that of human beings are selected for further analysis. We find 14 polar residues forming the binding interface of ACE2/2019-nCoV-Spike complex play an important role in maintaining protein–protein stability. Among them, 8 polar residues at the same positions with that of human ACE2 are highly conserved, which ensure its basic binding affinity with the novel coronavirus. 5 of other 6 unconserved polar residues (positions at human ACE2: Q24, D30, K31, H34 and E35) are proved to have an effect on the binding patterns among species. We select 21 species keeping close contacts with human beings, construct their ACE2 three-dimensional structures by Homology Modeling method and calculate the binding free energies of their ACE2/2019-nCoV-Spike complexes. We find the ACE2 from all the 21 species possess the capabilities to bind with the novel coronavirus. Compared with the human beings, 8 species (cow, deer, cynomys, chimpanzee, monkey, sheep, dolphin and whale) present almost the sameAbstract: The Novel Coronavirus Disease 2019 (COVID-19) has become an international public health emergency, which poses the most serious threat to the human health around the world. Accumulating evidences have shown that the new coronavirus could not only infect human beings, but also can infect other species which might result in the cross-species infections . In this research, 1056 ACE2 protein sequences are collected from the NCBI database, and 173 species with >60% sequence identity compared with that of human beings are selected for further analysis. We find 14 polar residues forming the binding interface of ACE2/2019-nCoV-Spike complex play an important role in maintaining protein–protein stability. Among them, 8 polar residues at the same positions with that of human ACE2 are highly conserved, which ensure its basic binding affinity with the novel coronavirus. 5 of other 6 unconserved polar residues (positions at human ACE2: Q24, D30, K31, H34 and E35) are proved to have an effect on the binding patterns among species. We select 21 species keeping close contacts with human beings, construct their ACE2 three-dimensional structures by Homology Modeling method and calculate the binding free energies of their ACE2/2019-nCoV-Spike complexes. We find the ACE2 from all the 21 species possess the capabilities to bind with the novel coronavirus. Compared with the human beings, 8 species (cow, deer, cynomys, chimpanzee, monkey, sheep, dolphin and whale) present almost the same binding abilities, and 3 species (bat, pig and dog) show significant improvements in binding affinities. We hope this research could provide significant help for the future epidemic detection, drug and vaccine development and even the global eco-system protections. … (more)
- Is Part Of:
- Briefings in bioinformatics. Volume 22:Issue 2(2021)
- Journal:
- Briefings in bioinformatics
- Issue:
- Volume 22:Issue 2(2021)
- Issue Display:
- Volume 22, Issue 2 (2021)
- Year:
- 2021
- Volume:
- 22
- Issue:
- 2
- Issue Sort Value:
- 2021-0022-0002-0000
- Page Start:
- 963
- Page End:
- 975
- Publication Date:
- 2020-12-08
- Subjects:
- Genetics -- Data processing -- Periodicals
Molecular biology -- Data processing -- Periodicals
Genomes -- Data processing -- Periodicals
572.80285 - Journal URLs:
- http://bib.oxfordjournals.org ↗
http://www.oxfordjournals.org/content?genre=journal&issn=1477-4054 ↗
http://ukcatalogue.oup.com/ ↗
http://firstsearch.oclc.org ↗ - DOI:
- 10.1093/bib/bbaa329 ↗
- Languages:
- English
- ISSNs:
- 1467-5463
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 2283.958363
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 16774.xml