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About:
Following the rule: formation of the 6-helix bundle of the fusion core from severe acute respiratory syndrome coronavirus spike protein and identification of potent peptide inhibitors
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An Entity of Type :
schema:ScholarlyArticle
, within Data Space :
covidontheweb.inria.fr
associated with source
document(s)
Type:
Academic Article
research paper
schema:ScholarlyArticle
New Facet based on Instances of this Class
Attributes
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type
Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
has title
Following the rule: formation of the 6-helix bundle of the fusion core from severe acute respiratory syndrome coronavirus spike protein and identification of potent peptide inhibitors
Creator
Rao, Zihe
Yan, Huimin
Xiao, Gengfu
Tien, Po
Gao, George
Zheng, Congyi
Zhu, Jieqing
Liu, Yueyong
Xu, Yanhui
Yuan, Fang
Bell, John
Cole, David
Source
Elsevier; Medline; PMC
abstract
Abstract Severe acute respiratory syndrome (SARS) coronavirus (SARS-CoV) is a newly identified member of Family Coronaviridae. Coronavirus envelope spike protein S is a class I viral fusion protein which is characterized by the existence of two heptad repeat regions (HR1 and HR2) (forming a complex called fusion core). Here we report that by using in vitro bio-engineering techniques, SARS-CoV HR1 and HR2 bind to each other and form a typical 6-helix bundle. The HR2, either as a synthetic peptide or as a GST-fusion polypeptide, is a potent inhibitor of virus entry. The results do show that SARS-CoV follows the general fusion mechanism of class I viruses and this lays the ground for identification of virus fusion/entry inhibitors for this devastating emerging virus.
has issue date
2004-06-18
(
xsd:dateTime
)
bibo:doi
10.1016/j.bbrc.2004.04.141
bibo:pmid
15158473
has license
els-covid
sha1sum (hex)
f9f0b6eb74685972364b796a69bc0889d195707a
schema:url
https://doi.org/10.1016/j.bbrc.2004.04.141
resource representing a document's title
Following the rule: formation of the 6-helix bundle of the fusion core from severe acute respiratory syndrome coronavirus spike protein and identification of potent peptide inhibitors
has PubMed Central identifier
PMC7111185
has PubMed identifier
15158473
schema:publication
Biochemical and Biophysical Research Communications
resource representing a document's body
covid:f9f0b6eb74685972364b796a69bc0889d195707a#body_text
is
schema:about
of
named entity 'class I'
named entity 'fusion'
named entity 'inhibitor'
named entity 'spike'
named entity 'SEVERE ACUTE RESPIRATORY SYNDROME'
named entity 'REGIONS'
named entity 'VIRAL'
named entity 'TYPICAL'
named entity 'GENERAL'
named entity 'IDENTIFIED'
named entity 'IS A'
named entity 'PROTEIN S'
named entity 'HERE'
named entity 'REPEAT'
named entity 'RESULTS'
named entity 'CORONAVIRUS'
named entity 'PROTEIN '
named entity 'EITHER'
named entity 'FUSION PROTEIN'
named entity 'FOLLOWS'
named entity 'MEMBER OF'
named entity 'A CLASS'
named entity 'CLASS I'
named entity 'SARS-COV'
named entity 'BIND'
named entity 'ENGINEERING'
named entity 'FAMILY CORONAVIRIDAE'
named entity 'IN VITRO'
named entity 'ENVELOPE'
named entity 'MECHANISM'
named entity 'FORM'
named entity 'SYNTHETIC PEPTIDE'
named entity 'VIRUSES'
named entity 'BUNDLE'
named entity 'GROUND'
named entity 'SPIKE PROTEIN'
named entity 'IDENTIFICATION'
named entity 'HR1'
named entity 'USING'
named entity 'HELIX'
named entity 'LAYS'
named entity 'FUSION'
named entity 'VIRUS ENTRY'
named entity 'NEWLY'
named entity 'TECHNIQUES'
named entity 'HR2'
named entity 'COMPLEX'
named entity 'REPORT'
named entity 'CHARACTERIZED'
named entity 'POLYPEPTIDE'
named entity 'VIRUS'
named entity 'INHIBITOR'
named entity 'CORE'
covid:arg/f9f0b6eb74685972364b796a69bc0889d195707a
named entity 'envelope'
named entity 'virus'
named entity 'fusion protein'
named entity 'signal sequence'
named entity 'GST'
named entity 'coiled coil'
named entity 'Novagen'
named entity 'GST'
named entity 'polypeptides'
named entity 'IPTG'
named entity 'viral'
named entity 'HR1'
named entity 'spike protein'
named entity 'SARS-CoV'
named entity 'peptide'
named entity 'entry inhibitors'
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