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About:
Analysis of ACE2 Gene-Encoded Proteins Across Mammalian Species
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An Entity of Type :
schema:ScholarlyArticle
, within Data Space :
covidontheweb.inria.fr
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Type:
Academic Article
research paper
schema:ScholarlyArticle
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type
Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
has title
Analysis of ACE2 Gene-Encoded Proteins Across Mammalian Species
Creator
Li, Jing
Qi, Jianxun
Liu, Di
Cao, Ying
Ali, Ahmed
Liu, Wenjun
Kattoor, Jobin
Bai, Zhihua
Gong, Yue
Sun, Yeping
Tian, Xiaodong
Gong, Bai
Source
Medline; PMC
abstract
Human beings are currently experiencing a serious public health event. Novel coronavirus disease 2019 (COVID-19), caused by the novel severe acute respiratory syndrome coronavirus (SARS-CoV-2), has infected about 3 million people worldwide and killed more than 200,000, most being the elderly or people with potential chronic diseases or in immunosuppressive states. According to big data analysis, there are many proteins homologous to or interacting with the angiotensin-converting enzyme 2 (ACE2), which, therefore, may not be the only receptor for the novel coronavirus; other receptors may also exist in host cells of different species. These potential receptors may also play an important role in the infection process of the novel coronavirus. The current study aimed to discover such key proteins or receptors and analyze the susceptibility of different animals to the novel coronavirus, in order to reveal the transmission process of the virus in cross-species infection. We analyzed the proteins coded by the ACE2 gene in different mammalian species and predicted their correlation and homology with the human ACE2 receptor. The major finding of our predictive analysis suggested ACE2 gene-encoded proteins to be highly homologous across mammals. Based on their high homology, their possibility of binding the spike-protein of SARS-CoV-2 is quite high and species such as Felis catus, Bos taurus, Rattus norvegicus etc. may be potential susceptible hosts; special monitoring is particularly required for livestock that are in close contact with humans. Our results might provide ideas for the prevention and control of the novel coronavirus pneumonia.
has issue date
2020-07-03
(
xsd:dateTime
)
bibo:doi
10.3389/fvets.2020.00457
bibo:pmid
32719819
has license
cc-by
sha1sum (hex)
00a71a90b4fb896291913c6d290833ade77e2aa1
schema:url
https://doi.org/10.3389/fvets.2020.00457
resource representing a document's title
Analysis of ACE2 Gene-Encoded Proteins Across Mammalian Species
has PubMed Central identifier
PMC7349190
has PubMed identifier
32719819
schema:publication
Front Vet Sci
resource representing a document's body
covid:00a71a90b4fb896291913c6d290833ade77e2aa1#body_text
is
schema:about
of
named entity 'infection'
named entity 'receptors'
named entity 'severe acute respiratory syndrome coronavirus'
named entity 'pneumonia'
named entity 'correlation'
named entity 'key'
named entity 'STATES'
named entity 'REQUIRED'
named entity 'OUR'
named entity 'INFECTION'
named entity 'SARS-COV-2'
named entity 'interacting'
named entity 'control'
named entity 'exist'
named entity 'peptide'
named entity 'anti-fibrotic'
named entity 'SARS-CoV-2'
named entity 'amino acid'
named entity 'ACE2'
named entity 'ACE2'
named entity 'livestock'
named entity 'virus'
named entity 'SARS-CoV-2'
named entity 'C-terminal'
named entity 'MERS-CoV'
named entity 'RBD'
named entity 'SARS-CoV-2'
named entity 'livestock'
named entity 'protein sequence'
named entity 'Ang II'
named entity 'immunosuppressive'
named entity 'SARS-CoV'
named entity 'SARS-CoV-2'
named entity 'SARS-CoV-2'
named entity 'protein sequence'
named entity 'Angiotensin-converting enzyme'
named entity 'homology'
named entity 'immune response'
named entity 'decapeptide'
named entity 'data analysis'
named entity 'prevention and control'
named entity 'ACE2'
named entity 'severe acute respiratory syndrome coronavirus'
named entity 'severe acute respiratory syndrome coronavirus 2'
named entity 'N-terminal'
named entity 'protein sequences'
named entity 'mammalian species'
named entity 'protease'
named entity 'SARS-CoV-2'
named entity 'SARS-CoV-2'
named entity 'gene'
named entity 'immune recognition'
named entity 'protein sequences'
named entity 'Felis catus'
named entity 'ACE2'
named entity 'protein'
named entity 'infectious disease'
named entity 'vasodilator'
named entity 'protein'
named entity 'ACE2'
named entity 'protein sequences'
named entity 'mammals'
named entity 'infection'
named entity 'cross-species'
named entity 'virus'
named entity 'Needleman-Wunsch algorithm'
named entity 'Ang II'
named entity 'protein sequence'
named entity 'homologous proteins'
named entity 'ACE2'
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