SARS_CoV_2 mutation literature information.


  Ongoing global and regional adaptive evolution of SARS-CoV-2.
 PMID: 34292871       2021       Proc Natl Acad Sci U S A
Figure: Black nodes correspond to key amino acid substitutions S L18F, S A222V, S S477N, S N501Y, S D614G, S P681H, S T716I, N R203K, and N G204R.


  Mutational analysis in international isolates and drug repurposing against SARS-CoV-2 spike protein: molecular docking and simulation approach.
 PMID: 34307771       2021       Virusdisease
Table: L18F


  Long-Term Evolution of SARS-CoV-2 in an Immunocompromised Patient with Non-Hodgkin Lymphoma.
 PMID: 34319130       2021       mSphere
Discussion: Notably, a spike mutation (L18F) affecting this region has shown strong signs of convergent evolution, being harbored by the variant of concern (VOC) P.1 and being present in a high proportion of VOC B.1.351 viruses.


  SARS-CoV-2 in Transit: Characterization of SARS-CoV-2 Genomes From Venezuelan Migrants in Colombia.
 PMID: 34333122       2021       International journal of infectious diseases
Abstract: A mutation (L18F) in the N-terminal domain of the spike protein that has been associated with compromised binding of neutralizing antibodies was found in 2 of 30 (6.6%) genomes.


  Investigation of nonsynonymous mutations in the spike protein of SARS-CoV-2 and its interaction with the ACE2 receptor by molecular docking and MM/GBSA approach.
 PMID: 34346317       2021       Computers in biology and medicine
Abstract: Using the extensive bioinformatics pipeline, we screened the destabilizing (L8V, L8W, L18F, Y145H, M153T, F157S, G476S, L611F, A879S, C1247F, and C1254F) and stabilizing (H49Y, S50L, N501Y, D614G, A845V, and P1143L) nonsynonymous mutations in the S-protein.
Result: As a meta result, i-stable predicted, out of 62 nonsynonymous mutations, 40 nonsynonymous m


  Modelling conformational state dynamics and its role on infection for SARS-CoV-2 Spike protein variants.
 PMID: 34351895       2021       PLoS computational biology
Result: 501.V2 includes the mutations L18F, D80A, D215G, R246I, K417N, E484K, N501Y, D614G, A701V.
Result: P.1 variant includes the mutations L18F, T20N, P26S, D138Y, R190S, K417T, E484K, N501Y, D614G, H655Y, T1027I.


  Signatures in SARS-CoV-2 spike protein conferring escape to neutralizing antibodies.
 PMID: 34352039       2021       PLoS pathogens
Introduction: For example, in B.1.351 and P.1 lineages, mutations in amino acid residues at positions 18 (L18F) and at position 417 (S417N, or S417T in some P.1 cases) were observed.


  Correlates of SARS-CoV-2 Variants on Deaths, Case Incidence and Case Fatality Ratio among the Continents for the Period of 1 December 2020 to 15 March 2021.
 PMID: 34356077       2021       Genes
Abstract: Among the identified mutations, NSP2_T153M, NSP14_I42V and Spike_L18F mutations showed a positive correlation to CFR.
Conclusion: Among the identified mutations,
Result: Among the identified mutations, NSP2_T153M, NSP14_I42V and Spike_L18F mutations showed a positive correlation to CFR (Figure 2A-C).


  Mutation hotspots and spatiotemporal distribution of SARS-CoV-2 lineages in Brazil, February 2020-2021.
 PMID: 34363852       2021       Virus research
Table: L18F
Discussion: Of the 10 new amino acid mutations in the spike protein (L18F, T20N, P26S, D138Y, R190S, K417T, E484K, N501Y, H655Y, T1027I) compared to its immediate ancestor (B.1.1.28), molecular selection analyses found evidence that 8 of these 10 mutations are under diversifying positive selection.


  Molecular Evolution and Epidemiological Characteristics of SARS COV-2 in (Northwestern) Poland.
 PMID: 34372500       2021       Viruses
Result: The first one was DeltaH69V70 and N439 in lineage B.1.258 (20A), then D138Y with S477N observed for B.1.1.317 (20B), and finally A222V and L18F in the B.1.177 (20E EU1) strains.



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