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About:
Cell membrane proteins with high N-glycosylation, high expression and multiple interaction partners are preferred by mammalian viruses as receptors
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An Entity of Type :
schema:ScholarlyArticle
, within Data Space :
covidontheweb.inria.fr
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document(s)
Type:
Academic Article
research paper
schema:ScholarlyArticle
New Facet based on Instances of this Class
Attributes
Values
type
Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
has title
Cell membrane proteins with high N-glycosylation, high expression and multiple interaction partners are 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
Tan, Zhiying
Guo, Xinhong
Xu, Beibei
Source
Medline; PMC
abstract
MOTIVATION: Receptor mediated entry is the first step for viral infection. However, the question of how viruses select receptors remains unanswered. RESULTS: 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 are 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. This study could deepen our understanding of virus–receptor interaction. AVAILABILITY AND IMPLEMENTATION: The database of mammalian virus–host receptor interaction is available at http://www.computationalbiology.cn: 5000/viralReceptor. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
has issue date
2019-03-01
(
xsd:dateTime
)
bibo:doi
10.1093/bioinformatics/bty694
bibo:pmid
30102334
has license
no-cc
sha1sum (hex)
e9316292ca1d7b6faf5b2f1d2a5f450d238a601b
schema:url
https://doi.org/10.1093/bioinformatics/bty694
resource representing a document's title
Cell membrane proteins with high N-glycosylation, high expression and multiple interaction partners are preferred by mammalian viruses as receptors
has PubMed Central identifier
PMC7109886
has PubMed identifier
30102334
schema:publication
Bioinformatics
resource representing a document's body
covid:e9316292ca1d7b6faf5b2f1d2a5f450d238a601b#body_text
is
schema:about
of
named entity 'HIGH'
named entity 'N-GLYCOSYLATION'
named entity 'HIGH EXPRESSION'
named entity 'SUPPLEMENTARY INFORMATION'
named entity 'PARTNERS'
named entity 'PREFERRED'
named entity 'MULTIPLE'
named entity 'INTERACTION'
named entity 'VIRUSES'
named entity 'CELL MEMBRANE PROTEINS'
named entity 'RECEPTORS'
named entity 'MAMMALIAN'
named entity 'N-glycosylation'
named entity 'interaction partners'
named entity 'plasma membrane'
named entity 'cell membrane'
named entity 'virus receptor'
named entity 'amino acid'
named entity 'homolog'
named entity 'cytoplasmic'
named entity 'Cytoscape'
named entity 'gene'
named entity 'database'
named entity 'PPIs'
named entity 'virus'
named entity 'UniProt'
named entity 'interaction partners'
named entity 'mammal species'
named entity 'database'
named entity 'HMMER'
named entity 'NCBI'
named entity 'cell surface'
named entity 'p-value'
named entity 'Subcellular location'
named entity 'HTR2A'
named entity 'human tissues'
named entity 'Expression Atlas'
named entity 'mammal species'
named entity 'mammal species'
named entity 'UniProtKB'
named entity 'virus'
named entity 'cell membrane'
named entity 'RefSeq'
named entity 'amino acid'
named entity 'alpha helix'
named entity 'Viral myocarditis'
named entity 'virus'
named entity 'virus'
named entity 'virus receptor'
named entity 'protein'
named entity '10.5'
named entity 'viral species'
named entity 'virus'
named entity 'virus'
named entity 'mammal species'
named entity 'UniprotKB'
named entity 'NCBI'
named entity 'database'
named entity 'protein sequences'
named entity 'protein'
named entity '10.5'
named entity 'UniprotKB'
named entity 'PPIs'
named entity 'cytoplasm'
named entity '3D structure'
named entity 'cytoplasm'
named entity 'database'
named entity 'protein sequences'
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