SARS_CoV_2 mutation literature information.


  Geographic and Genomic Distribution of SARS-CoV-2 Mutations.
 PMID: 32793182       2020       Frontiers in microbiology
Table: P504L


  Characterizing SARS-CoV-2 mutations in the United States.
 PMID: 32818213       2020       Research square
Result: Similar to 27964C>T-(S24L), although 17858A>G-(Y541C), 17747C>T-(P504L) are in the final list in Table 2, more than 87% of t
Result: Table 4 shows that both high-frequency mutations Y541C and P504L have negative folding stability changes, which will destabilize the structure of NSP13.
Result: The other three mutations, 17747C>T-(P504L), 17858A>G-(Y541C), and 28144T>C-(L84S), occur mostly together and have similar numbers of frequencies.


  BioAider: An efficient tool for viral genome analysis and its application in tracing SARS-CoV-2 transmission.
 PMID: 32904401       2020       Sustainable cities and society
Figure: SARS-CoV (AY291315.1), SARS-CoV-2_referential (EPI_ISL_402119), SARS-CoV-2_NSP13-P504L_Y541C (EPI_ISL_413456), Bat-CoV RaTG13 (MN996532.1), Bat-CoV_RmYN02 (EPI_ISL_412977), Pangolin-CoV (EPI_ISL_410721), MERS-CoV (KC875821.1).


  Evaluation of the potency of FDA-approved drugs on wild type and mutant SARS-CoV-2 helicase (Nsp13).
 PMID: 32980406       2020       International journal of biological macromolecules
Conclusion: These mutations (P504L and Y541C) caused important exchanges in functional domain 2A of Nsp13 (helicase), a critical enzyme in the life cycle of the virus.
Result: Both P504L and Y541C mutations were in the 2A domain and caused a more hydrophobic 2A domain.
Result: In this way, the difference in sites P504L and Y541C, where there are amino acid changes, can be analyzed with reference to the wild type.

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