Evidence map›Paper›PMID 40372465›Full record

ArticleBioinformatics (Oxford, England)2025

DeepAllo: allosteric site prediction using protein language model (pLM) with multitask learning.

Moaaz Khokhar, Ozlem Keskin, Attila Gursoy

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2025. 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
–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

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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.

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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

3 authors.

Moaaz KhokharDepartment of Computer Engineering, Koç University, 34450 Istanbul, Turkey.ORCID 0009-0008-1977-2736
Ozlem KeskinDepartment of Chemical and Biological Engineering, Koç University, 34450 Istanbul, Turkey.ORCID 0000-0002-4202-4049
Attila GursoyDepartment of Computer Engineering, Koç University, 34450 Istanbul, Turkey.ORCID 0000-0002-2297-2113

Funding

Scientific and Technological Research Council of Türkiye 120C120
6 · The paper itself

Abstract

motivationAllostery, the process by which binding at one site perturbs a distant site, is being rendered as a key focus in the field of drug development with its substantial impact on protein function. The identification of allosteric pockets (sites) is a challenging task and several techniques have been developed, including Machine Learning to predict allosteric pockets that utilize both static and pocket features.

resultsOur work, DeepAllo, is the first study that combines fine-tuned protein language model (pLM) with FPocket features and shows an increase in prediction performance of allosteric sites over previous studies. The pLM model was fine-tuned on AlloSteric Database (ASD) in Multitask Learning setting and was further used as a feature extractor to train XGBoost and AutoML models. The best model predicts allosteric pockets with 89.66% F1 score and 90.5% of allosteric pockets in the top 3 positions, outperforming previous results. A case study has been performed on proteins with known allosteric pockets, which shows the proof of our approach. Moreover, an effort was made to explain the pLM by visualizing its attention mechanism among allosteric and non-allosteric residues. AVAILABILITY AND IMPLEMENTATION: The source code is available on GitHub (https://github.com/MoaazK/deepallo) and archived on Zenodo (DOI: 10.5281/zenodo.15255379). The trained model is hosted on Hugging Face (DOI: 10.57967/hf/5198). The dataset used for training and evaluation is archived on Zenodo (DOI: 10.5281/zenodo.15255437).

Indexed as

Allosteric SiteComputational BiologyMachine LearningProteinsSoftwareDatabases, ProteinModels, MolecularProteins

Identifiers

PMID40372465
PMCPMC12145174

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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 OpenQuestion graph.