Evidence map›Paper›PMID 26057936›Full record

ReviewFree radical biology & medicine2015

Structural basis of Keap1 interactions with Nrf2.

Peter Canning, Fiona J Sorrell, Alex N Bullock

Open access · hybridAbstract readReview
In one paragraph

Review in Free radical biology & medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 304 papers.

0numbers the graph read from it
0cells of the map it votes in
304citing papers in PubMed
12.5field-weighted citation impact, top 1% 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

304 citing papers in PubMed, 571 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Keap1-Inhibitory Peptides fromMolecules (Basel, Switzerland) · 2026
    Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Curcumin in High Doses Reverses the UV-B-InducedPharmaceuticals (Basel, Switzerland) · 2026
    Article
  15. Article
  16. Review
  17. Article
  18. Review
  19. Article
  20. Article

244 more citing papers are in PubMed but not listed here.

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

3 authors at 2 institutions in 1 country.

Peter CanningStructural Genomics Consortium, University of Oxford, Old Road Campus, Oxford OX3 7DQ, UK.
Fiona J SorrellStructural Genomics Consortium, University of Oxford, Old Road Campus, Oxford OX3 7DQ, UK.
Alex N BullockStructural Genomics Consortium, University of Oxford, Old Road Campus, Oxford OX3 7DQ, UK. Electronic address: alex.bullock@sgc.ox.ac.uk.
Genomics (United Kingdom) · GBUniversity of Oxford · GB

Funding

Wellcome Trust 092809/Z/10/ZWellcome Trust 106169
6 · The paper itself

Abstract

Keap1 is a highly redox-sensitive member of the BTB-Kelch family that assembles with the Cul3 protein to form a Cullin-RING E3 ligase complex for the degradation of Nrf2. Oxidative stress disables Keap1, allowing Nrf2 protein levels to accumulate for the transactivation of critical stress response genes. Consequently, the Keap1-Nrf2 system is extensively pursued for the development of protein-protein interaction inhibitors that will stabilize Nrf2 for therapeutic effect in conditions of neurodegeneration, inflammation, and cancer. Here we review current progress toward the structure determination of Keap1 and its protein complexes with Cul3, Nrf2 substrate, and small-molecule antagonists. Together the available structures establish a rational three-dimensional model to explain the two-site binding of Nrf2 as well as its efficient ubiquitination.

Indexed as

Models, MolecularAnimalsHumansIntracellular Signaling Peptides and ProteinsNF-E2-Related Factor 2Oxidative StressSignal TransductionIntracellular Signaling Peptides and ProteinsNF-E2-Related Factor 2BTBCullinFree radicalsKeap1KelchNrf2Ubiquitin

Identifiers

PMID26057936
PMCPMC4668279
OpenAlexW598738849

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.