Evidence map›Paper›PMID 19699750›Full record

ArticleJournal of molecular biology2009

Structural changes common to catalysis in the Tpx peroxiredoxin subfamily.

Andrea Hall, Banumathi Sankaran, Leslie B Poole, P Andrew Karplus

Open access · hybridAbstract read
In one paragraph

Article in Journal of molecular biology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

29 citing papers in PubMed, 50 citations in OpenAlex.

  1. Frustration in physiology and molecular medicine.Molecular aspects of medicine · 2025
    Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. The Human PathogenFrontiers in cellular and infection microbiology · 2020
    Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Crystal and solution structural studies of mouse phospholipid hydroperoxide glutathione peroxidase 4.Acta crystallographica. Section F, Structural biology communications · 2016
    Article
  13. Review
  14. Article
  15. A primer on peroxiredoxin biochemistry.Free radical biology & medicine · 2015
    Review
  16. Review
  17. Article
  18. Article
  19. Article
  20. 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

4 authors at 3 institutions in 1 country.

Andrea HallDepartment of Biochemistry and Biophysics, Oregon State University, Corvallis, OR 97331, USA.
Banumathi Sankaran
Leslie B Poole
P Andrew Karplus
Oregon State University · USLawrence Berkeley National Laboratory · USWake Forest University · US

Funding

Reducing Susceptibility to Environmental Stress Throughout the Life SpanP30ES000210 · NIEHS · OREGON STATE UNIVERSITY · PI BECKMAN, JOSEPH S · 1985 to 2015
$21.4M
Mechanistic Studies of Alkyl Hydroperoxide Reductase and Related Redox SystemsR01GM050389 · NIGMS · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI POOLE, LESLIE B · 1994 to 2013
$4.8M
NIEHS NIH HHS P30 ES000210NIEHS NIH HHS P30 ES00210NIGMS NIH HHS R01 GM050389NIGMS NIH HHS R01 GM50389
6 · The paper itself

Abstract

Thiol peroxidases (Tpxs) are dimeric 2-Cys peroxiredoxins from bacteria that preferentially reduce alkyl hydroperoxides. Catalysis requires two conserved residues, the peroxidatic cysteine and the resolving cysteine, which are located in helix alpha(2) and helix alpha(3), respectively. The partial unraveling of helices alpha(2) and alpha(3) during catalysis allows for the formation of an intramolecular disulfide between these two residues. Here, we present three structures of Escherichia coli Tpx representing the fully folded (peroxide binding site intact), locally unfolded (disulfide bond), and partially locally unfolded (transitional state) conformations. We also compare known Tpx crystal structures and analyze the sequence-conservation patterns among nearly 300 Tpx sequences. Twelve fully conserved Tpx-specific residues cluster at the active site and dimer interface, and an additional 37 highly conserved residues are mostly located in a cradle providing the environment for helix alpha(2). Using the structures determined here as representative fully folded, transitional, and locally unfolded Tpx conformations, we describe in detail the structural changes associated with catalysis in the Tpx subfamily. Key insights include the description of a conserved hydrophobic collar around the active site, a set of conserved packing interactions between helices alpha(2) and alpha(3) that allow the local unfolding of alpha(2) to trigger the partial unfolding of alpha(3), a conserved dimer interface that anchors the ends of helices alpha(2) and alpha(3) to stabilize the active site during structural transitions, and a conserved set of residues constituting a cradle that stabilizes the two discrete conformations of helix alpha(2) involved in catalysis. The involvement of the dimer interface in stabilizing active-site folding and in forming the hydrophobic collar implies that Tpx is an obligate homodimer and explains the high conservation of interface residues.

Indexed as

Protein ConformationAmino Acid SequenceCatalysisCatalytic DomainCrystallography, X-RayEscherichia coliEscherichia coli ProteinsIsoenzymesModels, MolecularMolecular Sequence DataPeriplasmic ProteinsPeroxidasesProtein MultimerizationSequence Homology, Amino AcidEscherichia coli ProteinsIsoenzymesPeriplasmic ProteinsPeroxidasesTpx protein, E coli

Identifiers

PMID19699750
PMCPMC3664093
OpenAlexW2154750161

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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.