Evidence map›Paper›PMID 41586464›Full record

ArticleActa crystallographica. Section D, Structural biology2026

Associating protein residues in the literature with structural data.

Melanie Vollmar, Simon Westrip, Sreenath Nair, Balakumaran Balasubramaniyan, Sameer Velankar, Louise Jones, Peter Strickland

Abstract read
In one paragraph

Article in Acta crystallographica. Section D, Structural biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

7 authors.

Melanie VollmarProtein Data Bank in Europe, European Molecular Biology Laboratory, European Bioinformatics Institute (EMBL-EBI), Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, United Kingdom.ORCID 0000-0002-9162-9159
Simon WestripInternational Union of Crystallography, 5 Abbey Square, Chester CH1 2HU, United Kingdom.ORCID 0000-0002-1287-9548
Sreenath NairProtein Data Bank in Europe, European Molecular Biology Laboratory, European Bioinformatics Institute (EMBL-EBI), Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, United Kingdom.
Balakumaran BalasubramaniyanProtein Data Bank in Europe, European Molecular Biology Laboratory, European Bioinformatics Institute (EMBL-EBI), Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, United Kingdom.
Sameer VelankarProtein Data Bank in Europe, European Molecular Biology Laboratory, European Bioinformatics Institute (EMBL-EBI), Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, United Kingdom.ORCID 0000-0002-8439-5964
Louise JonesInternational Union of Crystallography, 5 Abbey Square, Chester CH1 2HU, United Kingdom.
Peter StricklandInternational Union of Crystallography, 5 Abbey Square, Chester CH1 2HU, United Kingdom.ORCID 0000-0001-6555-0837

Funding

H2020 Marie Skłodowska-Curie Actions 945405
6 · The paper itself

Abstract

Protein structures are crucial in understanding the function, mechanism and disease-causing variants of proteins within any living cell. A number of experimental techniques are employed by researchers to determine such structures. Through structure inspection in molecular viewers, combined with supporting biochemical and biophysical experiments, scientists are able to identify the function of a protein, its reaction mechanism and effects caused by sequence variation. These detailed findings, supported by experimental results, are documented by being described in the scientific literature and by making the accompanying data open source. However, it has become increasingly difficult for a reader, in particular a non-expert, to access the correct additional information and assess the validity of the conclusions drawn based on experimental results. A reader is often required to resort to a number of different software packages to access the different data types. Here, we present a first-of-its-kind implementation of an artificial intelligence- and text-mining-supported software tool that allows the association of mentions in the text of one or more specific protein residues with their corresponding counterparts in the respective protein structure or structures. Our application allows a researcher to explore a residue of interest in the context of a publication and its respective protein structure, supported by its experimental evidence, in a single view. We describe model implementation, annotation extraction, downstream processing, dissemination and visualization at the IUCr and PDBe. The application presented is primarily aimed at readers of IUCr publications and users visiting the PDBe entry pages. However, we believe that in the future our application will be a valuable tool for reviewers of new submissions to IUCr journals and may even be useful as a curation tool involving the authors of a publication as annotation validators.

Indexed as

Data MiningProteinsSoftwareArtificial IntelligenceDatabases, ProteinModels, MolecularProtein ConformationProteinsknowledge linkinglarge language modelsprotein structuretext annotationstext mining

Identifiers

PMID41586464
PMCPMC12865887

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.