SARS_CoV_2 mutation literature information.


  Relative Consolidation of the Kappa Variant Pre-Dates the Massive Second Wave of COVID-19 in India.
 PMID: 34828410       2021       Genes
8Discussion: By virtue of sharing three critical mutations in the spike protein with the delta variant (L452R, E484Q and P681R), the kappa variant can be
Abstract: This relative consolidation of the kappa variant was significant, since it shared 3 of the 4 signature mutations (L452R, E484Q and P681R) observed in the spike protein of delta variant and thus was likely to be the precursor in its evolution.
Result: In addition, P681R mutation in the spike protein of the kappa variant was significant in view of its location being adjacent to the furin cleavage site and thereby having the potential to influence viral entry into the host cell.


  Curcumin Inhibits In Vitro SARS-CoV-2 Infection In Vero E6 Cells through Multiple Antiviral Mechanisms.
 PMID: 34833991       2021       Molecules (Basel, Switzerland)
Discussion: Taking into account that curcumin exhibited inhibition against D614G strain, through different treatment strategies, this compound was evaluated against infection by the Delta variant which contains mutations in the spike protein (L452R, T478K, P681R, and D614G) associated with an increase in viral infectivity, transmissibility and pathogenicity in individuals infected with SARS-CoV-2 and a decrease in antibody-mediated neutralization.


  Codon usage, phylogeny and binding energy estimation predict the evolution of SARS-CoV-2.
 PMID: 34841034       2021       One health (Amsterdam, Netherlands)
Introduction: P681R, which instead of operating on ACE2 receptor binding seems to primarily act on S1/S2 cleavage by furin.


  Phylogenomics and population genomics of SARS-CoV-2 in Mexico during the pre-vaccination stage reveals variants of interest B.1.1.28.4 and B.1.1.222 or B.1.1.519 and the nucleocapsid mutation S194L associated with symptoms.
 PMID: 34846283       2021       Microbial genomics
Figure: Right: positions of the important mutations S477N, T478K, E484K, D614G, P681H/R and T732A in two different regions.
Discussion: Like variant 20A/478K.V1, the latter VOC includes the mutations T478K and P681H/R.
Discussion: On the other hand, 20B/478K.V1, with mutations T478K, P681R/H and T732A in its spike protein, can undoubtedly be classified as a VOI, with the potential to become a VOC.

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