2020
DOI: 10.1101/2020.01.20.913368
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Genomic and protein structure modelling analysis depicts the origin and infectivity of 2019-nCoV, a new coronavirus which caused a pneumonia outbreak in Wuhan, China

Abstract: 3Detailed genomic and structure-based analysis of a new coronavirus, namely 2019-nCoV, 2 4 1 9 2 1 9 3 author/funder. All rights reserved. No reuse allowed without permission.

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Cited by 114 publications
(128 citation statements)
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“…Till now most of the deaths have occurred in the elderly population due to novel coronavirus infection whereas, children and Table 2. Key interacting residues between RBD of spike protein of different corona viruses and host receptor ACE2 of human, bat, mouse civet and different avian species (modified from Dong et al 2020). 41 42 45 79 82 83 90 325 329 353 Amino Acid (aa) position relative to human ACE2…”
Section: Resultsmentioning
confidence: 99%
“…Till now most of the deaths have occurred in the elderly population due to novel coronavirus infection whereas, children and Table 2. Key interacting residues between RBD of spike protein of different corona viruses and host receptor ACE2 of human, bat, mouse civet and different avian species (modified from Dong et al 2020). 41 42 45 79 82 83 90 325 329 353 Amino Acid (aa) position relative to human ACE2…”
Section: Resultsmentioning
confidence: 99%
“…From previous reports, the interaction with ACE2 was responsible for SARS-CoV entering human cells [31 , 32] . Dong et al compared the structural similarity of the S protein in various viruses and speculated that SARS-CoV-2 could most likely use the same receptor as SARS-CoV [33] . Zhou et al conducted virus infectivity studies using HeLa cells with or without ACE2 proteins obtained from humans or animals and found that SARS-CoV-2 could invade all ACE2 proteinexpressing cells except for mouse cells [34] .…”
Section: Pathogenic Mechanismsmentioning
confidence: 99%
“…Analyzing of the genome of 2019-nCoV showed that this new virus shared around 80~90% sequence identity to SARS-CoV (2). Both bioinformatics modeling and in vitro experiments indicated that 2019-nCoV was more likely to use the angiotensin-converting enzyme 2 (ACE2) as the entry receptor (3,4). ACE2 is previously known as the receptor for SARS-CoV and HCoV-NL63 (5,6).…”
Section: Introductionmentioning
confidence: 99%