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About:
Membrane proteins with high N-glycosylation, high expression, and multiple interaction partners were preferred by mammalian viruses as receptors
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schema:ScholarlyArticle
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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
Membrane proteins with high N-glycosylation, high expression, and multiple interaction partners were preferred by mammalian viruses as receptors
Creator
Zhang, Zheng
Ge, Xingyi
Jiang, Taijiao
Peng, Yousong
Zhu, Zhaozhong
Wu, Aiping
Tan, Zhongyang
Zhu, Haizhen
Cai, Zena
Chen, Wenjun
Xia, Zanxian
Guo, Xinhong
Xu, Beibei
Source
BioRxiv; MedRxiv
abstract
Receptor mediated entry is the first step for viral infection. However, the relationship between viruses and receptors is still obscure. Here, by manually curating a high-quality database of 268 pairs of mammalian virus-host receptor interaction, which included 128 unique viral species or sub-species and 119 virus receptors, we found the viral receptors were structurally and functionally diverse, yet they had several common features when compared to other cell membrane proteins: more protein domains, higher level of N-glycosylation, higher ratio of self-interaction and more interaction partners, and higher expression in most tissues of the host. Additionally, the receptors used by the same virus tended to co-evolve. Further correlation analysis between viral receptors and the tissue and host specificity of the virus shows that the virus receptor similarity was a significant predictor for mammalian virus cross-species. This work could deepen our understanding towards the viral receptor selection and help evaluate the risk of viral zoonotic diseases.
has issue date
2018-03-08
(
xsd:dateTime
)
bibo:doi
10.1101/271171
has license
biorxiv
sha1sum (hex)
fc6812d62536afc0018f27069e17aba0f4063d09
schema:url
https://doi.org/10.1101/271171
resource representing a document's title
Membrane proteins with high N-glycosylation, high expression, and multiple interaction partners were preferred by mammalian viruses as receptors
schema:publication
bioRxiv
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covid:fc6812d62536afc0018f27069e17aba0f4063d09#body_text
is
schema:about
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named entity 'features'
named entity 'virus'
named entity 'expression'
named entity 'cell membrane'
named entity 'similarity'
named entity 'receptor'
named entity 'host specificity'
named entity 'viruses'
named entity 'manually'
named entity 'viral'
named entity 'virus'
named entity 'N-glycosylation'
named entity 'This'
named entity 'high'
named entity 'virus'
named entity 'viruses'
named entity 'viral species'
named entity 'high-quality'
named entity 'N-glycosylation'
named entity 'cardiomyopathy'
named entity 'mammal species'
named entity 'protein'
named entity 'Arrhythmogenic'
named entity 'cytoplasm'
named entity 'sequence identity'
named entity 'Focal adhesion'
named entity 'KEGG'
named entity 'C3d'
named entity 'virus'
named entity 'viruses'
named entity 'virus'
named entity 'mammal species'
named entity 'Molecular Function'
named entity 'glycoprotein'
named entity 'protein sequences'
named entity 'membrane proteins'
named entity 'receptor protein'
named entity 'complement C3b'
named entity 'glycan'
named entity 'phylogenetic tree'
named entity 'mammal species'
named entity 'respiratory tract'
named entity 'statistical analysis'
named entity 'Receiver Operating Characteristic'
named entity 'host cell'
named entity 'virus receptor'
named entity 'homolog'
named entity 'vesicle'
named entity 'ligands'
named entity 'genetic distance'
named entity 'protein'
named entity 'interaction partners'
named entity 'Pfam'
named entity 'housekeeping gene'
named entity 'membrane protein'
named entity 'co-evolution'
named entity 'virus receptor'
named entity 'mammal species'
named entity 'low density lipoprotein receptor'
named entity 'protein domain'
named entity 'virus'
named entity 'mammal species'
named entity 'Biological Process'
named entity 'mammal species'
named entity 'cytokine'
named entity 'viral protein'
named entity 'interact'
named entity 'receptor protein'
named entity 'LDLR'
named entity 'Glycans'
named entity 'cytoplasmic'
named entity 'mammal species'
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