Evidence map›Paper›PMID 35656479›Full record

ArticleRSC chemical biology2022

Understanding p300-transcription factor interactions using sequence variation and hybridization.

Fruzsina Hóbor, Zsófia Hegedüs, Amaurys Avila Ibarra, Vencel L Petrovicz, Gail J Bartlett, Richard B Sessions, Andrew J Wilson, Thomas A Edwards

Open access · goldAbstract read
In one paragraph

Article in RSC chemical biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

9 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Covalent Peptide-Based N-Myc/Aurora-A Inhibitors Bearing Sulfonyl Fluoride Warheads.Journal of peptide science : an official publication of the European Peptide Society · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Cited2 is a key regulator of placental development and plasticity.BioEssays : news and reviews in molecular, cellular and developmental biology · 2024
    Review
  8. Article
  9. Review
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

8 authors at 3 institutions in 2 countries.

Fruzsina HóborAstbury Centre for Structural Molecular Biology, University of Leeds, Woodhouse Lane Leeds LS2 9JT UK a.j.wilson@leeds.ac.uk t.a.edwards@leeds.ac.uk.
Zsófia HegedüsDepartment of Medical Chemistry, University of Szeged Dóm tér 8 H-6720 Szeged Hungary hegedus.zsofia@med.u-szeged.hu.ORCID https://orcid.org/0000-0002-5546-8167
Amaurys Avila IbarraSchool of Biochemistry, University of Bristol, Medical Sciences Building, University Walk Bristol BS8 1TD UK.
Vencel L PetroviczDepartment of Medical Chemistry, University of Szeged Dóm tér 8 H-6720 Szeged Hungary hegedus.zsofia@med.u-szeged.hu.
Gail J BartlettSchool of Biochemistry, University of Bristol, Medical Sciences Building, University Walk Bristol BS8 1TD UK.ORCID https://orcid.org/0000-0002-9932-2960
Richard B SessionsSchool of Biochemistry, University of Bristol, Medical Sciences Building, University Walk Bristol BS8 1TD UK.ORCID https://orcid.org/0000-0003-0320-0895
Andrew J WilsonAstbury Centre for Structural Molecular Biology, University of Leeds, Woodhouse Lane Leeds LS2 9JT UK a.j.wilson@leeds.ac.uk t.a.edwards@leeds.ac.uk.ORCID https://orcid.org/0000-0001-9852-6366
Thomas A EdwardsAstbury Centre for Structural Molecular Biology, University of Leeds, Woodhouse Lane Leeds LS2 9JT UK a.j.wilson@leeds.ac.uk t.a.edwards@leeds.ac.uk.ORCID https://orcid.org/0000-0002-1467-3674
University of Bristol · GBUniversity of Leeds · GBUniversity of Szeged · HU

Funding

Biotechnology and Biological Sciences Research Council BB/L01386X/1
6 · The paper itself

Abstract

The hypoxic response is central to cell function and plays a significant role in the growth and survival of solid tumours. HIF-1 regulates the hypoxic response by activating over 100 genes responsible for adaptation to hypoxia, making it a potential target for anticancer drug discovery. Although there is significant structural and mechanistic understanding of the interaction between HIF-1α and p300 alongside negative regulators of HIF-1α such as CITED2, there remains a need to further understand the sequence determinants of binding. In this work we use a combination of protein expression, chemical synthesis, fluorescence anisotropy and isothermal titration calorimetry for HIF-1α sequence variants and a HIF-1α-CITED hybrid sequence which we term CITIF. We show the HIF-1α sequence is highly tolerant to sequence variation through reduced enthalpic and less unfavourable entropic contributions, These data imply backbone as opposed to side chain interactions and ligand folding control the binding interaction and that sequence variations are tolerated as a result of adopting a more disordered bound interaction or "fuzzy" complex.

Identifiers

PMID35656479
PMCPMC9092470
OpenAlexW4226191416

What OpenQuestion holds

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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.