Evidence map›Paper›PMID 24756107›Full record

ArticlePLoS biology2014

Large-scale determination of sequence, structure, and function relationships in cytosolic glutathione transferases across the biosphere.

Susan T Mashiyama, M Merced Malabanan, Eyal Akiva, Rahul Bhosle, Megan C Branch, Brandan Hillerich, Kevin Jagessar, Jungwook Kim, Yury Patskovsky, Ronald D Seidel and 6 more

Open access · goldAbstract read
In one paragraph

Article in PLoS biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
6.7field-weighted citation impact, top 2% 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

42 citing papers in PubMed, 92 citations in OpenAlex.

  1. Predicting Functional Diversity Within Enzyme Families: A Practical Perspective.Chembiochem : a European journal of chemical biology · 2026
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  13. Redox and Thiols in Archaea.Antioxidants (Basel, Switzerland) · 2020
    Review
  14. Article
  15. Article
  16. A heterodimeric glutathioneThe Journal of biological chemistry · 2019
    Article
  17. Article
  18. Review
  19. Article
  20. The Journal of biological chemistry · 2018
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 5 institutions in 1 country.

Susan T MashiyamaDepartment of Bioengineering and Therapeutic Sciences, University of California, San Francisco, San Francisco, California, United States of America.
M Merced MalabananDepartment of Biochemistry, Vanderbilt University School of Medicine, Nashville, Tennessee, United States of America.
Eyal AkivaDepartment of Bioengineering and Therapeutic Sciences, University of California, San Francisco, San Francisco, California, United States of America.
Rahul BhosleDepartment of Biochemistry, Albert Einstein College of Medicine, Bronx, New York, United States of America.
Megan C BranchDepartment of Biochemistry, University of Wisconsin, Madison, Wisconsin, United States of America.
Brandan HillerichDepartment of Biochemistry, Albert Einstein College of Medicine, Bronx, New York, United States of America.
Kevin JagessarDepartment of Biochemistry, Vanderbilt University School of Medicine, Nashville, Tennessee, United States of America.
Jungwook KimDepartment of Biochemistry, Albert Einstein College of Medicine, Bronx, New York, United States of America.
Yury PatskovskyDepartment of Biochemistry, Albert Einstein College of Medicine, Bronx, New York, United States of America.
Ronald D SeidelDepartment of Biochemistry, Albert Einstein College of Medicine, Bronx, New York, United States of America.
Mark SteadDepartment of Biochemistry, Albert Einstein College of Medicine, Bronx, New York, United States of America.
Rafael ToroDepartment of Biochemistry, Albert Einstein College of Medicine, Bronx, New York, United States of America.
Matthew W VettingDepartment of Biochemistry, Albert Einstein College of Medicine, Bronx, New York, United States of America.
Steven C AlmoDepartment of Biochemistry, Albert Einstein College of Medicine, Bronx, New York, United States of America.
Richard N ArmstrongDepartments of Biochemistry and Chemistry, Vanderbilt University School of Medicine, Nashville, Tennessee, United States of America.
Patricia C BabbittDepartment of Bioengineering and Therapeutic Sciences, University of California, San Francisco, San Francisco, California, United States of America; Department of Pharmaceutical Chemistry, University of California, San Francisco, San Francisco, California, United States of America; California Institute for Quantitative Biosciences, University of California, San Francisco, San Francisco, California, United States of America.
Albert Einstein College of Medicine · USVanderbilt University · USUniversity of California, San Francisco · USQB3 · USUniversity of Wisconsin–Madison · US

Funding

Core H: MicrobiologyU54GM093342 · NIGMS · UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGN · PI CRONAN, JOHN E. · 2010 to 2015
$34.6M
Technical Assistance to Support the Development of a GM/CA CAT FacilityY1GM1104 · NIGMS · NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES · 2009 to 2011
$11.2M
Case Center for Synchrotron BiosciencesP30EB009998 · NIBIB · CASE WESTERN RESERVE UNIVERSITY · PI CHANCE, MARK R · 2009 to 2018
$8.4M
Resource for Biocomputing Visualization and InformaticsP41GM103311 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI FERRIN, THOMAS E · 2012 to 2017
$8.2M
MOLECULAR BIOPHYSICS TRAINING PROGRAM AT VANDERBILTT32GM008320 · NIGMS · VANDERBILT UNIVERSITY · PI CHAZIN, WALTER J. · 1989 to 2023
$7.9M
Laying the Foundation of Genomic EnzymologyR01GM060595 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BABBITT, PATRICIA CLEMENT · 2000 to 2018
$5.4M
NCI NIH HHS Y1 CO1020NIBIB NIH HHS P30 EB009998NIGMS NIH HHS P41 GM103311NIGMS NIH HHS R01 GM060595NIGMS NIH HHS R01 GM60595NIGMS NIH HHS T32 GM008320NIGMS NIH HHS U54 GM093342NIGMS NIH HHS Y1 GM1104
6 · The paper itself

Abstract

The cytosolic glutathione transferase (cytGST) superfamily comprises more than 13,000 nonredundant sequences found throughout the biosphere. Their key roles in metabolism and defense against oxidative damage have led to thousands of studies over several decades. Despite this attention, little is known about the physiological reactions they catalyze and most of the substrates used to assay cytGSTs are synthetic compounds. A deeper understanding of relationships across the superfamily could provide new clues about their functions. To establish a foundation for expanded classification of cytGSTs, we generated similarity-based subgroupings for the entire superfamily. Using the resulting sequence similarity networks, we chose targets that broadly covered unknown functions and report here experimental results confirming GST-like activity for 82 of them, along with 37 new 3D structures determined for 27 targets. These new data, along with experimentally known GST reactions and structures reported in the literature, were painted onto the networks to generate a global view of their sequence-structure-function relationships. The results show how proteins of both known and unknown function relate to each other across the entire superfamily and reveal that the great majority of cytGSTs have not been experimentally characterized or annotated by canonical class. A mapping of taxonomic classes across the superfamily indicates that many taxa are represented in each subgroup and highlights challenges for classification of superfamily sequences into functionally relevant classes. Experimental determination of disulfide bond reductase activity in many diverse subgroups illustrate a theme common for many reaction types. Finally, sequence comparison between an enzyme that catalyzes a reductive dechlorination reaction relevant to bioremediation efforts with some of its closest homologs reveals differences among them likely to be associated with evolution of this unusual reaction. Interactive versions of the networks, associated with functional and other types of information, can be downloaded from the Structure-Function Linkage Database (SFLD; http://sfld.rbvi.ucsf.edu).

Indexed as

Models, MolecularAmino Acid SequenceBase SequenceBinding SitesComputational BiologyDatabases, ProteinGlutathioneGlutathione TransferaseProtein Structure, TertiarySequence AlignmentStructure-Activity RelationshipGlutathioneGlutathione Transferase

Identifiers

PMID24756107
PMCPMC3995644
OpenAlexW1975738628

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.