Evidence map›Paper›PMID 28192428›Full record

ArticlePloS one2017

A comparative study of cold- and warm-adapted Endonucleases A using sequence analyses and molecular dynamics simulations.

Davide Michetti, Bjørn Olav Brandsdal, Davide Bon, Geir Villy Isaksen, Matteo Tiberti, Elena Papaleo

Abstract readComparative Study
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–field-weighted citation impact
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

14 citing papers in PubMed.

  1. Article
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  5. Review
  6. Review
  7. Characterization of SdGA, a cold-adapted glucoamylase fromBiotechnology reports (Amsterdam, Netherlands) · 2021
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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.

Davide MichettiThe Centre for Theoretical and Computational Chemistry, Department of Chemistry, Faculty of Science and Technology, The Arctic University of Norway, Tromsø, Norway.
Bjørn Olav BrandsdalThe Centre for Theoretical and Computational Chemistry, Department of Chemistry, Faculty of Science and Technology, The Arctic University of Norway, Tromsø, Norway.
Davide BonThe Centre for Theoretical and Computational Chemistry, Department of Chemistry, Faculty of Science and Technology, The Arctic University of Norway, Tromsø, Norway.
Geir Villy IsaksenThe Centre for Theoretical and Computational Chemistry, Department of Chemistry, Faculty of Science and Technology, The Arctic University of Norway, Tromsø, Norway.
Matteo TibertiSchool of Biological and Chemical Sciences, Queen Mary University of London, Mile End Road, London E1 4NS, United Kingdom.
Elena PapaleoComputational Biology Laboratory, Danish Cancer Society Research Centre, Strandboulevarden 49, Copenhagen, Denmark.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The psychrophilic and mesophilic endonucleases A (EndA) from Aliivibrio salmonicida (VsEndA) and Vibrio cholera (VcEndA) have been studied experimentally in terms of the biophysical properties related to thermal adaptation. The analyses of their static X-ray structures was no sufficient to rationalize the determinants of their adaptive traits at the molecular level. Thus, we used Molecular Dynamics (MD) simulations to compare the two proteins and unveil their structural and dynamical differences. Our simulations did not show a substantial increase in flexibility in the cold-adapted variant on the nanosecond time scale. The only exception is a more rigid C-terminal region in VcEndA, which is ascribable to a cluster of electrostatic interactions and hydrogen bonds, as also supported by MD simulations of the VsEndA mutant variant where the cluster of interactions was introduced. Moreover, we identified three additional amino acidic substitutions through multiple sequence alignment and the analyses of MD-based protein structure networks. In particular, T120V occurs in the proximity of the catalytic residue H80 and alters the interaction with the residue Y43, which belongs to the second coordination sphere of the Mg2+ ion. This makes T120V an amenable candidate for future experimental mutagenesis.

Indexed as

Cold TemperatureMolecular Dynamics SimulationAliivibrio salmonicidaAmino Acid SequenceBacterial ProteinsBinding SitesEndodeoxyribonucleasesEnzyme StabilityHydrogen BondingHydrophobic and Hydrophilic InteractionsKineticsMembrane ProteinsMutationProtein Structure, TertiarySequence Homology, Amino AcidStatic ElectricityBacterial ProteinsendA protein, bacteriaEndodeoxyribonucleasesMembrane Proteins

Identifiers

PMID28192428
PMCPMC5305256

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Registered trials

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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.