Evidence map›Paper›PMID 33850482›Full record

ArticleInternational journal of peptide research and therapeutics2021

Identification of Potential Peptide Inhibitors of ACE-2 Target of SARS-CoV-2 from Buckwheat & Quinoa.

Ashok Nanjaiah Rangaswamy, Arpitha Ashok, Pradeep Hanumanthappa, Aparanji Sinduvalli Chandrashekaramurthy, Monika Kumbaiah, Pratibha Hiregouda, Vaishali Sharma, Aparna Huligerepura Sosalegowda

Open access · bronzeAbstract read
In one paragraph

Article in International journal of peptide research and therapeutics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

3 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
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

8 authors at 1 institution in 1 country.

Ashok Nanjaiah RangaswamyDepartment of Studies in Biotechnology, University of Mysore, Manasagangothri, Mysore, Karnataka 570 006 India.
Arpitha AshokDepartment of Studies in Biotechnology, University of Mysore, Manasagangothri, Mysore, Karnataka 570 006 India.
Pradeep HanumanthappaDepartment of Studies in Biotechnology, University of Mysore, Manasagangothri, Mysore, Karnataka 570 006 India.
Aparanji Sinduvalli ChandrashekaramurthyDepartment of Studies in Biotechnology, University of Mysore, Manasagangothri, Mysore, Karnataka 570 006 India.
Monika KumbaiahDepartment of Studies in Biotechnology, University of Mysore, Manasagangothri, Mysore, Karnataka 570 006 India.
Pratibha HiregoudaDepartment of Studies in Biotechnology, University of Mysore, Manasagangothri, Mysore, Karnataka 570 006 India.
Vaishali SharmaDepartment of Studies in Biotechnology, University of Mysore, Manasagangothri, Mysore, Karnataka 570 006 India.
Aparna Huligerepura SosalegowdaDepartment of Studies in Biotechnology, University of Mysore, Manasagangothri, Mysore, Karnataka 570 006 India.
University of Mysore · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It is well established fact that peptides from various foods offer human health benefits displaying diverse functionalities. Millets considered as super foods is a major alternative in recent days for traditional diet being rich in proteins and fibre along with trace minerals and vitamins. In this connection, proteins from Buckwheat and Quinoa were digested by in vitro simulation digestion for the generation of peptides, analyzed by nLC-MS/MS and the functional annotations of the identified proteins/peptides were carried out. The study led to the identification of 34 small peptides and their parent proteins clustered into 4 gene functional groups and their localization prediction indicated their involvement in energy metabolism, transport and storage. Interestingly, the identified peptides maximally displayed DPP-IV and ACE inhibitions. The present study was extended to unravel ACE-2 inhibition targeting COVID-19 by selecting ACE-2-Spike binding domain for molecular docking studies. The NWRTVKYG interacted with the ACE-2-Spike interface displaying the feasible binding energy (- 213.63) and docking score (- 12.43) and the MD simulation revealed the ability of the peptide in stabilizing the protein-peptide composite. The present investigation thus establishes newer vista for food derived peptides having ACE-2 inhibitory potential as tentative strategy for SARS-CoV-2 therapeutics.

Indexed as

ACE-2Functional annotationMolecular dynamicsnLC-MS/MSPeptides

Identifiers

PMID33850482
PMCPMC8030649
OpenAlexW3154675071

What OpenQuestion holds

Textmetadata
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.