|
Basic Characteristics of Mutations
|
|
Mutation Site
|
E484K |
|
Mutation Site Sentence
|
Novel Highly Divergent SARS-CoV-2 Lineage With the Spike Substitutions L249S and E484K. |
|
Mutation Level
|
Amino acid level |
|
Mutation Type
|
Nonsynonymous substitution |
|
Gene/Protein/Region
|
S |
|
Standardized Encoding Gene
|
S
|
|
Genotype/Subtype
|
- |
|
Viral Reference
|
-
|
|
Functional Impact and Mechanisms
|
|
Disease
|
COVID-19
|
|
Immune
|
- |
|
Target Gene
|
-
|
|
Clinical and Epidemiological Correlations
|
|
Clinical Information
|
- |
|
Treatment
|
- |
|
Location
|
Colombia |
|
Literature Information
|
|
PMID
|
34262921
|
|
Title
|
Novel Highly Divergent SARS-CoV-2 Lineage With the Spike Substitutions L249S and E484K
|
|
Author
|
Laiton-Donato K,Usme-Ciro JA,Franco-Munoz C,Alvarez-Diaz DA,Ruiz-Moreno HA,Reales-Gonzalez J,Prada DA,Corchuelo S,Herrera-Sepulveda MT,Naizaque J,Santamaria G,Wiesner M,Walteros DM,Ospina Martinez ML,Mercado-Reyes M
|
|
Journal
|
Frontiers in medicine
|
|
Journal Info
|
2021 Jun 28;8:697605
|
|
Abstract
|
COVID-19 pandemics has led to genetic diversification of SARS-CoV-2 and the appearance of variants with potential impact in transmissibility and viral escape from acquired immunity. We report a new and highly divergent lineage containing 21 distinctive mutations (10 non-synonymous, eight synonymous, and three substitutions in non-coding regions). The amino acid changes L249S and E484K located at the CTD and RBD of the Spike protein could be of special interest due to their potential biological role in the virus-host relationship. Further studies are required for monitoring the epidemiologic impact of this new lineage.
|
|
Sequence Data
|
EPI_ISL_1092008;EPI_ISL_1092007;EPI_ISL_1092006;EPI_ISL_1092005
|