Evidence map›Paper›PMID 26457432›Full record

ArticleActa crystallographica. Section D, Biological crystallography2015

Comparison of epsilon- and delta-class glutathione S-transferases: the crystal structures of the glutathione S-transferases DmGSTE6 and DmGSTE7 from Drosophila melanogaster.

Michele Scian, Isolde Le Trong, Aslam M A Mazari, Bengt Mannervik, William M Atkins, Ronald E Stenkamp

Open access · hybridAbstract readComparative Study
In one paragraph

Article in Acta crystallographica. Section D, Biological crystallography, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

10 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Article
  3. Structural Analysis of theBiomolecules · 2024
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  6. Review
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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 at 2 institutions in 2 countries.

Michele ScianDepartment of Medicinal Chemistry, University of Washington, Box 357610, Seattle, WA 98195-7610, USA.
Isolde Le TrongDepartment of Biological Structure, University of Washington, Box 357420, Seattle, WA 98195-7420, USA.
Aslam M A MazariDepartment of Neurochemistry, Arrhenius Laboratories, Stockholm University, SE-10 691 Stockholm, Sweden.
Bengt MannervikDepartment of Neurochemistry, Arrhenius Laboratories, Stockholm University, SE-10 691 Stockholm, Sweden.
William M AtkinsDepartment of Medicinal Chemistry, University of Washington, Box 357610, Seattle, WA 98195-7610, USA.
Ronald E StenkampDepartment of Biological Structure, University of Washington, Box 357420, Seattle, WA 98195-7420, USA.
University of Washington · USStockholm University · SE

Funding

X-ray Absorption Spectroscopy (XAS) pp.711-759P41GM103393 · NIGMS · STANFORD UNIVERSITY · PI HODGSON, KEITH O · 2012 to 2019
$30.6M
NIGMS NIH HHS P41 GM103393NIGMS NIH HHS P41GM103393
6 · The paper itself

Abstract

Cytosolic glutathione transferases (GSTs) comprise a large family of enzymes with canonical structures that diverge functionally and structurally among mammals, invertebrates and plants. Whereas mammalian GSTs have been characterized extensively with regard to their structure and function, invertebrate GSTs remain relatively unstudied. The invertebrate GSTs do, however, represent potentially important drug targets for infectious diseases and agricultural applications. In addition, it is essential to fully understand the structure and function of invertebrate GSTs, which play important roles in basic biological processes. Invertebrates harbor delta- and epsilon-class GSTs, which are not found in other organisms. Drosophila melanogaster GSTs (DmGSTs) are likely to contribute to detoxication or antioxidative stress during development, but they have not been fully characterized. Here, the structures of two epsilon-class GSTs from Drosophila, DmGSTE6 and DmGSTE7, are reported at 2.1 and 1.5 Å resolution, respectively, and are compared with other GSTs to identify structural features that might correlate with their biological functions. The structures of DmGSTE6 and DmGSTE7 are remarkably similar; the structures do not reveal obvious sources of the minor functional differences that have been observed. The main structural difference between the epsilon- and delta-class GSTs is the longer helix (A8) at the C-termini of the epsilon-class enzymes.

Indexed as

Amino Acid SequenceAnimalsBinding SitesDrosophila melanogasterDrosophila ProteinsGlutathioneGlutathione TransferaseModels, MolecularMolecular Sequence DataProtein ConformationProtein StabilitySequence AlignmentTemperatureDrosophila ProteinsGlutathioneGlutathione TransferaseGSTE6 protein, DrosophilaGSTE7 protein, Drosophiladetoxicationglutathione bindingglutathione S-transferase

Identifiers

PMID26457432
PMCPMC4601370
OpenAlexW2220337495

What OpenQuestion holds

Textmetadata
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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.