SARS_CoV_2 mutation literature information.


  mRNA-1273 Vaccine-elicited Neutralization of SARS-CoV-2 Omicron in Adolescents and Children.
 PMID: 35118475       2022       medRxiv
Method: The Omicron (B.1.1.529) variant contained spike mutations A67V, Delta69-70, T95I, G142D, Delta143-145, Delta211, L212I, +214EPE, G339D, S371L, S373P, S375F, K417N, N440K, G446S, S477N, T478K, E484A, Q493R, G496S, Q498R, N501Y, Y505H, T547K,


  Binding of Human ACE2 and RBD of Omicron Enhanced by Unique Interaction Patterns Among SARS-CoV-2 Variants of Concern.
 PMID: 35118473       2022       bioRxiv
Abstract: We report that the Omicron brings an enhanced Method: In each variant, the Alpha includes N501Y mutation, Delta has L452R and T478K mutations, and Omicron contains 15 mutated amino acids, i.e., G339D, S371L, S373P, S375F, K417N, N440K, G446S, S477N, T478K, E484A, Q483K/R, G496S, Q498R, N501Y, and Y505H (see also Figures 1B and 2D).


  Divergent SARS-CoV-2 Omicron-reactive T and B cell responses in COVID-19 vaccine recipients.
 PMID: 35113647       2022       Science immunology
Method: The delta variant contained the following spike changes: T19R, G142D, del156-157, R158G, A222V, L452R, T478K, D614G, P681R and D950N.
Method: The omicron variant contained the following spike mutations: A67VS, del69-70, T95I, G142-, del143-144, Y145D, del211, L212I, ins215EPE, G339D, S371L, S373P, S375F, K417N,


  Mutations in the receptor-binding domain of human SARS CoV-2 spike protein increases its affinity to bind human ACE-2 receptor.
 PMID: 35109768       2022       Journal of biomolecular structure & dynamics
Abstract: Here, we use the crystal structure of the RBD in complex with ACE-2 available in the public domain and analyse the 250 ns molecular dynamics (MD) simulations of wild-type and mutants; K417N, K417T, N440K, N501Y, L452R, T478K, E484K and S494P.


  Omicron and Delta variant of SARS-CoV-2: A comparative computational study of spike protein.
 PMID: 34914115       2022       Journal of medical virology
Abstract: Based on docking studies, the Q493R, N501Y, S371L, S373P, S375F, Q498R, and T478K mutations contribute significantly to high binding affinity with human ACE2.


  The antibody response to SARS-CoV-2 Beta underscores the antigenic distance to other variants.
 PMID: 34921776       2022       Cell host & microbe
Introduction: The RBD mutations found in Alpha (N501Y), Beta (K417N, E484K, and N501Y), Gamma (K417T, E484K, and N501Y), and Delta (L452R and T478K) are located in or closely adjacent to the ACE2-interacting surface where they have the potential to modulate ACE2 interaction or disrupt the binding of neutralizing mAbs.
Figure: (A-F) Neutralization assays performed against Victoria, Alpha (N501Y), Beta (K417N, E484K, and N501Y), Gamma (K417T,  PMID: 34915409       2022       International immunopharmacology
Introduction: Currently, there are four variants of concerns: Alpha variant (B.1.1.7; RBD mutations: N501Y, A570D), Beta (B.1.351; RBD mutations: K417N, E484K, and N501Y), Gamma (P.1, B.1.1.28.1; RBD mutations: K417N/T, E484K, and N501Y) and Delta (B.1.617.2; RBD mutations: L452R, T478K).


  Aggregation of high-frequency RBD mutations of SARS-CoV-2 with three VOCs did not cause significant antigenic drift.
 PMID: 35032057       2022       Journal of medical virology
Introduction: As of March 2021, the 15 most commonly observed mutations in the RBD were as follows: V3
Figure: The 15 most commonly observed mutations in the RBD were as follows: N501Y, S477N, N439K, L452R, E484K, K417N, Y453F, S494P, A520S, N501T, T478K, V367F, S477R, P384L, and A522S, which were located at 13 sites in the RBD.


  Genetic variations from successive whole genome sequencing during COVID-19 treatment in five individuals.
 PMID: 35035981       2022       New microbes and new infections
Table: T478K


  Efficacy of mRNA, adenoviral vector, and perfusion protein COVID-19 vaccines.
 PMID: 34906769       2022       Biomedicine & pharmacotherapy
Introduction: Consequently, ten mutations in the spike protein of B.1.617.2 strain, including T19R, (G142D*), 156/157del, R158G, L452R, T478K, D614G, P681R, and D950N were identified.
Table: T478K



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