GeoEPred: A multimodal structure-aware geometric deep learning framework for Gram-negative bacterial secreted effector prediction with sequence semantics

Accurate prediction of effector proteins secreted by Gram-negative bacteria is important for elucidating bacterial pathogenic mechanisms and developing precise anti-infective strategies. Although existing methods have benefited from the strong sequence feature extraction capacity of pretrained protein language models, reliance on linear sequence information alone often fails to fully capture the three-dimensional conformational signals required for virulence functions. Meanwhile, conventional structure-based methods are limited by the scarcity of experimentally resolved protein structures. To address these challenges, we propose GeoEPred, a multimodal deep learning framework designed for the synergistic modeling of protein sequence and structure to identify Gram-negative bacterial effector proteins. Specifically, the model integrates sequence-contextual embeddings from a pretrained protein language model with three-dimensional structural representations predicted by ESMFold. A feature projection network refines fine-grained sequence signals associated with effector functions, while geometric vector perceptrons characterize inter-residue orientations, distances, and local spatial topology to capture potential structural conformational motifs. To further enable effective cross-modal fusion, we design a cross-modal alignment and feature-tokenized self-attention module. This module enhances consistency between the sequence-semantic and structural-geometric spaces through contrastive learning and models associations between linear functional motifs and spatial conformational patterns at a fine-grained token level. Extensive evaluations on multiple benchmark datasets show that GeoEPred achieves better predictive performance than existing leading models in T3SE, T4SE, and T6SE prediction tasks, while maintaining stable performance in remote homolog recognition scenarios. Moreover, the modular and extensible architecture of GeoEPred demonstrates strong generalization ability and substantial application potential for genome-scale effector protein discovery.

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Publication Details

Journal
PLoS Computational Biology
Published
2026-09-30
DOI
https://doi.org/10.1371/journal.pcbi.1014344
Primary Topic
Machine Learning in Bioinformatics
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article
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article

GeoEPred: A multimodal structure-aware geometric deep learning framework for Gram-negative bacterial secreted effector prediction with sequence semantics

Quan Zou, Yihang Lin, Hua Wang Shi, Nor Ashidi Mat Isa et al.
PLoS Computational Biology
Machine Learning in Bioinformatics
article

GeoEPred: A multimodal structure-aware geometric deep learning framework for Gram-negative bacterial secreted effector prediction with sequence semantics

Quan Zou, Yihang Lin, Hua Wang Shi, Nor Ashidi Mat Isa, Shouzhen Song, Dachen Liu, Leyi Wei, Hongfeng Wu
article en

Abstract

Accurate prediction of effector proteins secreted by Gram-negative bacteria is important for elucidating bacterial pathogenic mechanisms and developing precise anti-infective strategies. Although existing methods have benefited from the strong sequence feature extraction capacity of pretrained protein language models, reliance on linear sequence information alone often fails to fully capture the three-dimensional conformational signals required for virulence functions. Meanwhile, conventional structure-based methods are limited by the scarcity of experimentally resolved protein structures. To address these challenges, we propose GeoEPred, a multimodal deep learning framework designed for the synergistic modeling of protein sequence and structure to identify Gram-negative bacterial effector proteins. Specifically, the model integrates sequence-contextual embeddings from a pretrained protein language model with three-dimensional structural representations predicted by ESMFold. A feature projection network refines fine-grained sequence signals associated with effector functions, while geometric vector perceptrons characterize inter-residue orientations, distances, and local spatial topology to capture potential structural conformational motifs. To further enable effective cross-modal fusion, we design a cross-modal alignment and feature-tokenized self-attention module. This module enhances consistency between the sequence-semantic and structural-geometric spaces through contrastive learning and models associations between linear functional motifs and spatial conformational patterns at a fine-grained token level. Extensive evaluations on multiple benchmark datasets show that GeoEPred achieves better predictive performance than existing leading models in T3SE, T4SE, and T6SE prediction tasks, while maintaining stable performance in remote homolog recognition scenarios. Moreover, the modular and extensible architecture of GeoEPred demonstrates strong generalization ability and substantial application potential for genome-scale effector protein discovery.

PLoS Computational BiologyVol. 22(9)
Universiti Sains Malaysia (MY), University of Electronic Science and Technology of China (CN), Macao Polytechnic University (MO), Xiamen University of Technology (CN)
Openalex Percentile: Top 20%
Machine Learning in Bioinformatics
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