Evidence map›Paper›PMID 31690005›Full record

ArticleBiology2019

Understanding the Effect of Structural Diversity in WRKY Transcription Factors on DNA Binding Efficiency through Molecular Dynamics Simulation.

Akshay Singh, Ajay Kumar Sharma, Nagendra Kumar Singh, Humira Sonah, Rupesh Deshmukh, Tilak Raj Sharma

Open access · goldAbstract read
In one paragraph

Article in Biology, 2019. 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
0.2field-weighted citation impact, top 46% 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, 14 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  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

6 authors at 3 institutions in 1 country.

Akshay SinghNational Agri-Food Biotechnology Institute (NABI), Mohali 140306, Punjab, India. akshaybioinfo@gmail.com.ORCID 0000-0001-7599-6699
Ajay Kumar SharmaMeerut Institute of Engineering and Technology, Meerut, Uttar Pradesh 250005, India. aks.ajayksharma@gmail.com.
Nagendra Kumar SinghNational Institute for Plant Biotechnology (NIPB), New Delhi 110012, India. nksingh@nrcpb.org.
Humira SonahNational Agri-Food Biotechnology Institute (NABI), Mohali 140306, Punjab, India. biohuma@gmail.com.ORCID 0000-0003-4796-6120
Rupesh DeshmukhNational Agri-Food Biotechnology Institute (NABI), Mohali 140306, Punjab, India. rupesh0deshmukh@gmail.com.ORCID 0000-0003-4167-6552
Tilak Raj SharmaNational Agri-Food Biotechnology Institute (NABI), Mohali 140306, Punjab, India. trsharma@nabi.res.in.
National Agri-Food Biotechnology Institute · INDr. A.P.J. Abdul Kalam Technical University · INNational Research Centre on Plant Biotechnology · IN

Funding

Science and Engineering Research Board JC Bose National Fellowship
6 · The paper itself

Abstract

A precise understanding of the molecular mechanism involved in stress conditions has great importance for crop improvement. Biomolecules, such as WRKY proteins, which are the largest transcription factor family that is widely distributed in higher plants, plays a significant role in plant defense response against various biotic and abiotic stressors. In the present study, an extensive homology-based three-dimensional model construction and subsequent interaction study of WRKY DNA-binding domain (DBD) in CcWRKY1 (Type I), CcWRKY51 (Type II), and CcWRKY70 (Type III) belonging to pigeonpea, a highly tolerant crop species, was performed. Evaluation of the generated protein models was done to check their reliability and accuracy based on the quantitative and qualitative parameters. The final model was subjected to investigate the comparative binding analysis of different types of WRKY-DBD with DNA-W-box (a cis-acting element) by protein-DNA docking and molecular dynamics (MD) simulation. The DNA binding specificity with WRKY variants was scrutinized through protein-DNA interaction using the HADDOCK server. The stability, as well as conformational changes of protein-DNA complex, was investigated through molecular dynamics (MD) simulations for 100 ns using GROMACS. Additionally, the comparative stability and dynamic behavior of each residue of the WRKY-DBD type were analyzed in terms of root mean square deviation (RMSD), root mean square fluctuation (RMSF)values of the backbone atoms for each frame taking the minimized structure as a reference. The details of DNA binding activity of three different types of WRKY-DBD provided here will be helpful to better understand the regulation of WRKY gene family members in plants.

Indexed as

DBDDNA bindingmolecular dynamics simulationmolecular modelingpigeonpeaprotein–DNA interactionWRKY transcription factor

Identifiers

PMID31690005
PMCPMC6956055
OpenAlexW2985426496

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.