Evidence map›Paper›PMID 42450019›Full record

ReviewInternational journal of molecular sciences2026

A Global Analysis of the Complex Structural Organization of KCTD Proteins and Their Functional Implications.

Nicole Balasco, Luciana Esposito, Simone Di Micco, Luigi Vitagliano

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 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

4 authors.

Nicole BalascoInstitute of Molecular Biology and Pathology (IBPM), CNR c/o Department of Chemistry, Sapienza University of Rome, Piazzale A. Moro 5, 00185 Rome, Italy.ORCID 0000-0001-7862-9448
Luciana EspositoInstitute of Biostructures and Bioimaging (IBB), CNR, Via P. Castellino 111, 80131 Naples, Italy.ORCID 0000-0001-6431-2677
Simone Di MiccoEuropean Biomedical Research Institute of Salerno (EBRIS), Via S. De Renzi 50, 84125 Salerno, Italy.ORCID 0000-0002-4688-1080
Luigi VitaglianoInstitute of Biostructures and Bioimaging (IBB), CNR, Via P. Castellino 111, 80131 Naples, Italy.ORCID 0000-0002-3032-3375

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

KCTD proteins exhibit significant structural complexity, arising from their modular organization, oligomerization, and intricate biological partnerships. Although their biological importance has been assessed for two decades, the biochemical basis of their activities is only partially understood. This is certainly due to the limited structural information that was available until a few years ago. Fortunately, some recent insightful structural studies and the advent of machine-learning-based approaches are rapidly changing the scenario. By surveying the literature and structural databases and integrating this information with ad hoc 3D-structure predictions, we provide a detailed view of the structural biology of these proteins at different levels: individual domains, full-length oligomers, functional hetero-oligomers formed by different family members, and complexes with functional partners. Collectively, these surveys and analyses provide insights into the family's evolutionary history and its structure-function relationships. The family-wide coverage of structural information also indicates the extent to which structural similarities are reflected in functional analogies. Finally, the potential functional implications of the intricate architecture of these multimeric proteins and the tendency of their members to hetero-oligomerize are discussed from a functional perspective.

Indexed as

Intracellular Signaling Peptides and ProteinsAnimalsHumansModels, MolecularProtein BindingProtein ConformationProtein MultimerizationStructure-Activity RelationshipIntracellular Signaling Peptides and ProteinsAlphaFolddisease-associated mutationshetero-oligomersprotein–protein interactionsstructural biology

Identifiers

PMID42450019
PMCPMC13361646

What Socratic holds

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Registered trials

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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.