Evidence map›Paper›PMID 41497600›Full record

ArticlebioRxiv : the preprint server for biology2026

Predicting interaction-specific protein-protein interaction perturbations by missense variants with MutPred-PPI.

Ross Stewart, Florent Laval, Georges Coppin, Kerstin Spirohn-Fitzgerald, Maxime Tixhon, Tong Hao, Michael A Calderwood, Matthew Mort, David N Cooper, Marc Vidal and 1 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 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

11 authors.

Ross StewartKhoury College of Computer Sciences, Northeastern University, Boston, MA, USA.ORCID 0009-0006-4240-9308
Florent LavalCenter for Cancer Systems Biology (CCSB), Dana-Farber Cancer Institute, Boston, MA, USA.ORCID 0000-0001-7744-6199
Georges CoppinCenter for Cancer Systems Biology (CCSB), Dana-Farber Cancer Institute, Boston, MA, USA.ORCID 0000-0001-7647-3240
Kerstin Spirohn-FitzgeraldCenter for Cancer Systems Biology (CCSB), Dana-Farber Cancer Institute, Boston, MA, USA.ORCID 0000-0002-2071-1606
Maxime TixhonCenter for Cancer Systems Biology (CCSB), Dana-Farber Cancer Institute, Boston, MA, USA.ORCID 0009-0004-4289-6842
Tong HaoCenter for Cancer Systems Biology (CCSB), Dana-Farber Cancer Institute, Boston, MA, USA.ORCID 0000-0001-7908-3256
Michael A CalderwoodCenter for Cancer Systems Biology (CCSB), Dana-Farber Cancer Institute, Boston, MA, USA.ORCID 0000-0001-6475-1418
Matthew MortInstitute of Medical Genetics, School of Medicine, Cardiff University, Cardiff, UK.ORCID 0000-0002-3986-0935
David N CooperInstitute of Medical Genetics, School of Medicine, Cardiff University, Cardiff, UK.ORCID 0000-0002-8943-8484
Marc VidalCenter for Cancer Systems Biology (CCSB), Dana-Farber Cancer Institute, Boston, MA, USA.ORCID 0000-0003-3391-5410
Predrag RadivojacKhoury College of Computer Sciences, Northeastern University, Boston, MA, USA.ORCID 0000-0002-6769-0793

Funding

Molecular phenotyping of ~100,000 coding variants across Mendelian disease genesUM1HG011989 · NHGRI · DANA-FARBER CANCER INST · PI Marc Vidal · 2021 to 2026
$9.9M
Supporting IGVF by modeling genetics, function, and phenotype with machine learningU01HG012022 · NHGRI · NORTHEASTERN UNIVERSITY · PI Predrag Radivojac · 2021 to 2026
$3.4M
Fine-grained Annotation of the Protein Universe through a Community of PracticeR01GM145937 · NIGMS · IOWA STATE UNIVERSITY · PI Iddo Friedberg · 2024 to 2026
$1.3M
NHGRI NIH HHS U01 HG012022NHGRI NIH HHS UM1 HG011989NIGMS NIH HHS R01 GM145937Wellcome Trust
6 · The paper itself

Abstract

Disruption of protein-protein interactions (PPIs) is a major mechanism of a variant's deleterious effect. Computational tools are needed to assess such variants at scale, yet existing predictors rarely consider loss of specific interactions, particularly when variants perturb binding interfaces without significantly affecting protein stability. To address this problem, we present MutPred-PPI, a graph attention network that predicts interaction-specific (edgetic) effects of missense variants by operating on AlphaFold3-based protein complex contact graphs with protein language model embeddings imposed upon nodes. We systematically evaluated our model with stringent group cross-validation as well as benchmark data recently collected within the IGVF Consortium. MutPred-PPI outperformed all baseline methods across all evaluation criteria, achieving an AUC of 0.85 on seen proteins and 0.72 on previously unseen proteins in cross-validation, demonstrating strong generalizability despite scarce training data. To demonstrate biomedical relevance, we applied MutPred-PPI to variants from ClinVar, HGMD, COSMIC, gnomAD, and two

Identifiers

PMID41497600
PMCPMC12767517

What Socratic 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 Socratic graph.