Evidence map›Paper›PMID 40463264›Full record

ArticlebioRxiv : the preprint server for biology2025

ProtFun: A Protein Function Prediction Model Using Graph Attention Networks with a Protein Large Language Model.

Muhammed Talo, Serdar Bozdag

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. 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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors.

Muhammed TaloDepartment of Computer Science and Engineering, University of North Texas, Denton, TX 76207, USA.ORCID 0000-0002-1595-5681
Serdar BozdagDepartment of Computer Science and Engineering, University of North Texas, Denton, TX 76207, USA.ORCID 0000-0002-4813-4310

Funding

lntegrating multi-omics datasets to infer phenotype-specific driver genes, regulatory interactions and drug responseR35GM133657 · NIGMS · UNIVERSITY OF NORTH TEXAS · PI Serdar Bozdag · 2019 to 2026
$3.1M
NIGMS NIH HHS R35 GM133657
6 · The paper itself

Abstract

Understanding protein functions facilitates the identification of the underlying causes of many diseases and guides the research for discovering new therapeutic targets and medications. With the advancement of high throughput technologies, obtaining novel protein sequences has been a routine process. However, determining protein functions experimentally is cost- and labor-prohibitive. Therefore, it is crucial to develop computational methods for automatic protein function prediction. In this study, we propose a multi-modal deep learning architecture called ProtFun to predict protein functions. ProtFun integrates protein large language model (LLM) embeddings as node features in a protein family network. Employing graph attention networks (GAT) on this protein family network, ProtFun learns protein embeddings, which are integrated with protein signature representations from InterPro to train a protein function prediction model. We evaluated our architecture using three benchmark datasets. Our results showed that our proposed approach outperformed current state-of-the-art methods for most cases. An ablation study also highlighted the importance of different components of ProtFun. The data and source code of ProtFun is available at https://github.com/bozdaglab/ProtFun under Creative Commons Attribution Non Commercial 4.0 International Public License.

Indexed as

Graph Attention NetworksGraph Neural NetworksLarge Language ModelsProtein Family NetworkProtein function prediction

Identifiers

PMID40463264
PMCPMC12132266

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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 OpenQuestion graph.