Evidence map›Paper›PMID 34194534›Full record

ReviewFuture virology2021

V483A: an emerging mutation hotspot of SARS-CoV-2.

Omar Ashwaq, Pratibha Manickavasagam, Sk Manirul Haque

Open access · greenAbstract readReview
In one paragraph

Review in Future virology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.1field-weighted citation impact, top 19% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. SARS-CoV-2 Mutations and their Viral Variants.Cytokine & growth factor reviews · 2022
    Review
  6. Article
  7. Review
  8. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 2 institutions in 2 countries.

Omar AshwaqDepartment of Chemical & Process Engineering Technology, Jubail Industrial College, Jubail Industrial City, 31961, Saudi Arabia.ORCID https://orcid.org/0000-0003-4477-7922
Pratibha ManickavasagamDepartment of Biotechnology, Indian Institute of Technology Hyderabad, Kandi, Telangana, India.ORCID https://orcid.org/0000-0002-7509-3593
Sk Manirul HaqueDepartment of Chemical & Process Engineering Technology, Jubail Industrial College, Jubail Industrial City, 31961, Saudi Arabia.ORCID https://orcid.org/0000-0003-2646-4164
Jubail Industrial College · SAIndian Institute of Technology Hyderabad · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

One of the many mutations that have occurred in the viral genome is the V483A mutation, which is a part of the receptor-binding motif present in the S1 domain of the spike protein. V483A mutant virus is popular in North America with 36 cases so far and frequently occurring in recent days. This review compares the wild-type and the V483A mutants to analyze certain factors like the interaction between the virus and host-cell interface, binding affinity, stability, partition energy, hydrophobicity, occurrence rate and transmissibility. This information can be of monumental importance in vaccine and drug development since the mutants can become resistant to the vaccines and monoclonal antibodies.

Indexed as

high transmissioninfectivityspike proteinsubstitution mutationV483Avirus–host cell interaction

Identifiers

PMID34194534
PMCPMC8223177
OpenAlexW3173360241

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.