Evidence map›Paper›PMID 42057657›Full record

ReviewBiochemical Society transactions2026

How intrinsically disordered regions shape the function of CREB-binding protein.

Grace Gilbert, Daniel A Bose

Abstract readReview
In one paragraph

Review in Biochemical Society transactions, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

2 authors.

Grace GilbertMolecular and Cellular Biology, School of Biosciences, The University of Sheffield, Sheffield S10 2TN, United Kingdom.ORCID 0009-0007-5656-9131
Daniel A BoseMolecular and Cellular Biology, School of Biosciences, The University of Sheffield, Sheffield S10 2TN, United Kingdom.ORCID 0000-0002-0276-6486

Funding

UKRI | Biotechnology and Biological Sciences Research Council (AFRC) BB/Y513453/1Wellcome Trust (WT) 213501/Z/18/Z
6 · The paper itself

Abstract

CREB-binding protein (CBP) is a histone acetyltransferase and transcriptional co-activator that operates across the genome at cis-regulatory elements (CREs) to regulate gene expression. Comprising the majority of the protein, CBP has intrinsically disordered regions (IDRs) that separate its folded domains. Whilst previously regarded as passive linkers, active roles for these IDRs within CBP are beginning to be uncovered. Firstly, the flexibility afforded by these regions and the presence of binding motifs within them establish CBP as an interaction specialist that is able to interact with many binding partners at diverse CREs. In addition, the IDRs of CBP allow it to undergo liquid-liquid phase separation, forming condensates with emerging roles in transcription. Finally, an IDR within CBP performs an autoregulatory function that makes histone acetyltransferase activity sensitive to changing conditions within the cell. To build a comprehensive understanding of CBP function going forwards, it will be necessary to consider the contributions of the IDRs in addition to the structured domains of CBP and how these are integrated for the regulation of this key transcriptional protein.

Indexed as

CREB-Binding ProteinIntrinsically Disordered ProteinsAnimalsHumansProtein BindingCREB-Binding ProteinIntrinsically Disordered Proteinsacetylationbiomolecular condensatesCBP/p300gene expression and regulationIDRsIntrinsically disordered proteins

Identifiers

PMID42057657
PMCPMC13142923

What Socratic holds

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LicenceCC BY
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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 Socratic graph.