Publication:
The specification of observed covid-19 in england: A review of auto-mutation

dc.contributor.authorNajaflou N., Monajjemi M., Attarikhasraghi N., Kandemirli F., Mollaamin F.
dc.contributor.authorNajaflou, N, Monajjemi, M, Attarikhasraghi, N, Kandemirli, F, Mollaamin, F
dc.date.accessioned2023-05-09T20:15:40Z
dc.date.available2023-05-09T20:15:40Z
dc.date.issued2021-01-01
dc.date.issued2021.01.01
dc.description.abstractGenomic sequencing helps us understand COVID-19 and its spread. It can also help guide treatments in the future and see the impact of interventions. In epidemics, genome structure is important for recognizing any small change in the COVID-19 behavior at any population scale to understand the spreading mechanism and whether different strains are emerging. The viral spike (S) protein amino acid sequence viral genomic sequences and other mutated spike proteins are related to the advanced genome of mRNA We analyzed some major S protein mutation which was represented in a high percentage of all the analyzed sequences. Spike-D614G mutation is a terrible phenomenon that has been spread in Europe in early February and has been started rapidly to become the dominant form in new regions. In the United States, the genotypic distribution in California and Washington was similar to Asian countries, while other US states' distribution was comparable to Europe. To gain insight into the D614G mutation consequences, homology modeling using a multi-template threading mechanism with ab initio structural refinement was performed for the S protein region. The D614 model predicted a random coil structure in the Furin domain, and this mutation may confer a competitive advantage at the Furin binding domain that may contribute to the rise of the D614G virus mutant. Due to resistance to any pandemic interventions, mutations should be evaluated in viewpoints of time and geographical situation in the wide phylogenetic domains to announce an early warning system for new mutations.
dc.identifier.doi10.33263/BRIAC116.1479414808
dc.identifier.endpage14808
dc.identifier.issn2069-5837
dc.identifier.scopus2-s2.0-85104820195
dc.identifier.startpage14794
dc.identifier.urihttps://hdl.handle.net/20.500.12597/14902
dc.identifier.volume11
dc.identifier.wosWOS:000640664600079
dc.relation.ispartofBiointerface Research in Applied Chemistry
dc.relation.ispartofBIOINTERFACE RESEARCH IN APPLIED CHEMISTRY
dc.rightstrue
dc.subjectCOVID-19 | COVID-19 footprint in spike. mutation | England Coronavirus | Evolutionary | Spike protein
dc.titleThe specification of observed covid-19 in england: A review of auto-mutation
dc.titleThe Specification of Observed COVID-19 in England: A Review of Auto-Mutation
dc.typeArticle
dspace.entity.typePublication
oaire.citation.issue6
oaire.citation.volume11
relation.isScopusOfPublicatione17d14ef-bcdb-4d39-a44a-2c8b5129c46b
relation.isScopusOfPublication.latestForDiscoverye17d14ef-bcdb-4d39-a44a-2c8b5129c46b
relation.isWosOfPublication71704010-06b8-41d0-9545-56f1622bf050
relation.isWosOfPublication.latestForDiscovery71704010-06b8-41d0-9545-56f1622bf050

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