Evidence map›Paper›PMID 41318581›Full record

ArticleGenome biology2025

A scalable equivariant graph network framework for precise protein function prediction.

Zixu Ran, Xudong Guo, Tong Pan, Yue Bi, Yi Hao, Heyun Sun, Jiangning Song, Fuyi Li

Abstract read
In one paragraph

Article in Genome biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 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

8 authors.

Zixu Ran *College of Information Engineering, Northwest A&F University, Yangling, 712100, China.
Xudong Guo *College of Information Engineering, Northwest A&F University, Yangling, 712100, China.
Tong Pan *South Australian immunoGENomics Cancer Institute (SAiGENCI), The University of Adelaide, Adelaide, 5005, Australia.
Yue BiDepartment of Biochemistry and Molecular Biology, Monash University, Melbourne, 3168, Australia.
Yi HaoCollege of Information Engineering, Northwest A&F University, Yangling, 712100, China.
Heyun SunSouth Australian immunoGENomics Cancer Institute (SAiGENCI), The University of Adelaide, Adelaide, 5005, Australia.
Jiangning SongDepartment of Biochemistry and Molecular Biology, Monash University, Melbourne, 3168, Australia. Jiangning.Song@monash.edu.
Fuyi LiCollege of Information Engineering, Northwest A&F University, Yangling, 712100, China. fuyi.li@nwafu.edu.cn.

Funding

Australia National Health and Medical Research Council 2041439National Key Research and Development Program of China 2022YFF1000100National Natural Science Foundation of China 62202388Qin Chuangyuan Innovation and Entrepreneurship Talent Project QCYRCXM-2022-230
6 · The paper itself

Abstract

backgroundProtein function research helps in understanding the complex biological processes that occur within cells. However, the intricate nature of protein structures and functions, along with the rapid growth of protein sequence data, presents a pressing challenge to develop efficient computational methods for accurate protein annotation.

resultsIn this study, we propose ENGINE, a multi-channel deep learning framework designed for robust protein function prediction. ENGINE integrates an equivariant graph convolutional network model to capture geometric features from protein 3D structures, leverages the large language model ESM-C to encode evolutionary and sequence-derived information, and combines an innovative 3D sequence representation that unifies spatial and sequential signals. We demonstrate that ENGINE consistently surpasses current state-of-the-art methods across diverse protein function prediction benchmarks, demonstrating robust generalisation and high predictive accuracy. Beyond performance, ENGINE provides interpretable insights into key sequence features and structural motifs, enabling the identification of functionally critical residues and substructures within proteins. This facilitates a deeper mechanistic understanding of protein function annotation outcomes and supports hypothesis generation for downstream biological studies.

conclusionBy offering reliable predictions with biological interpretability, ENGINE contributes to advancing research into cellular processes and disease mechanisms. The model is available at GitHub ( https://github.com/ABILiLab/ENGINE ) and Zenodo ( https://doi.org/10.5281/zenodo.17221153 ), serving as a valuable tool for the broader scientific community.

Indexed as

Computational BiologyDeep LearningProteinsMolecular Sequence AnnotationProtein ConformationSoftwareProteins

Identifiers

PMID41318581
PMCPMC12665208

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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.