Evidence map›Paper›PMID 39977366›Full record

ArticleBioinformatics (Oxford, England)2025

Sul-BertGRU: an ensemble deep learning method integrating information entropy-enhanced BERT and directional multi-GRU for S-sulfhydration sites prediction.

Xirun Wei, Qiao Ning, Kuiyang Che, Zhaowei Liu, Hui Li, Shikai Guo

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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 3 papers.

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3citing papers in PubMed
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3 citing papers in PubMed.

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5 · Who and what money

Authors and funding

6 authors.

Xirun WeiDepartment of Information Science and Technology, Dalian Maritime University, Dalian 116026, P.R. China.
Qiao NingDepartment of Information Science and Technology, Dalian Maritime University, Dalian 116026, P.R. China.ORCID 0000-0002-4809-5104
Kuiyang CheDepartment of Information Science and Technology, Dalian Maritime University, Dalian 116026, P.R. China.
Zhaowei LiuDepartment of Information Science and Technology, Dalian Maritime University, Dalian 116026, P.R. China.
Hui LiDepartment of Information Science and Technology, Dalian Maritime University, Dalian 116026, P.R. China.
Shikai GuoDepartment of Information Science and Technology, Dalian Maritime University, Dalian 116026, P.R. China.

Funding

National Natural Science Foundation of China 62302075
6 · The paper itself

Abstract

motivationS-sulfhydration, a crucial post-translational protein modification, is pivotal in cellular recognition, signaling processes, and the development and progression of cardiovascular and neurological disorders, so identifying S-sulfhydration sites is crucial for studies in cell biology. Deep learning shows high efficiency and accuracy in identifying protein sites compared to traditional methods that often lack sensitivity and specificity in accurately locating nonsulfhydration sites. Therefore, we employ deep learning methods to tackle the challenge of pinpointing S-sulfhydration sites.

resultsIn this work, we introduce a deep learning approach called Sul-BertGRU, designed specifically for predicting S-sulfhydration sites in proteins, which integrates multi-directional gated recurrent unit (GRU) and BERT. First, Sul-BertGRU proposes an information entropy-enhanced BERT (IE-BERT) to preprocess protein sequences and extract initial features. Subsequently, confidence learning is employed to eliminate potential S-sulfhydration samples from the nonsulfhydration samples and select reliable negative samples. Then, considering the directional nature of the modification process, protein sequences are categorized into left, right, and full sequences centered on cysteines. We build a multi-directional GRU to enhance the extraction of directional sequence features and model the details of the enzymatic reaction involved in S-sulfhydration. Ultimately, we apply a parallel multi-head self-attention mechanism alongside a convolutional neural network to deeply analyze sequence features that might be missed at a local level. Sul-BertGRU achieves sensitivity, specificity, precision, accuracy, Matthews correlation coefficient, and area under the curve scores of 85.82%, 68.24%, 74.80%, 77.44%, 55.13%, and 77.03%, respectively. Sul-BertGRU demonstrates exceptional performance and proves to be a reliable method for predicting protein S-sulfhydration sites. AVAILABILITY AND IMPLEMENTATION: The source code and data are available at https://github.com/Severus0902/Sul-BertGRU/.

Indexed as

Computational BiologyDeep LearningProtein Processing, Post-TranslationalProteinsEntropyProteins

Identifiers

PMID39977366
PMCPMC11908646

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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.