Ubigo-X: Protein ubiquitination site prediction using ensemble learning with image-based feature representation and weighted voting.

IF 4.1 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Computational and structural biotechnology journal Pub Date : 2025-07-14 eCollection Date: 2025-01-01 DOI:10.1016/j.csbj.2025.07.025
Disline Manli Tantoh, Jen-Chieh Yu, Ching-Hsuan Chien, Wei-Yi Yeh, Yen-Wei Chu
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引用次数: 0

Abstract

Accurate ubiquitination identification is crucial in biological function analysis. We developed Ubigo-X, a novel protein ubiquitination prediction tool. Our training data, sourced from the Protein Lysine Modification Database (PLMD 3.0), comprised 53,338 ubiquitination and 71,399 non-ubiquitination sites, retained after CD-HIT and CD-HIT-2d sequence filtering. Three sub-models: Single-Type sequence-based features (Single-Type SBF), k-mer sequence-based features (Co-Type SBF), and structure-based and function-based features (S-FBF), were developed. Single-Type SBF used amino acid composition (AAC), amino acid index (AAindex), and one-hot encoding; Co-Type SBF used Single-Type SBF via k-mer encoding; and S-FBF used secondary structure, relative solvent accessibility (RSA)/absolute solvent-accessible area (ASA), and signal peptide cleavage sites. S-FBF was trained using XGBoost, while Single-Type SBF and Co-Type SBF were transformed into image-based features and trained using Resnet34. Ubigo-X was developed by combining the three models via a weighted voting strategy. Independent testing using PhosphoSitePlus data (65,421 ubiquitination and 61,222 non-ubiquitination sites) retained after filtering yielded 0.85, 0.79, and 0.58 for area under the curve (AUC), accuracy (ACC), and Matthews correlation coefficient (MCC), respectively. Further testing on imbalanced PhosphoSitePlus data (1:8 positive-to-negative sample ratio) yielded 0.94 AUC, 0.85 ACC, and 0.55 MCC. Using the GPS-Uber data, the AUC, ACC, and MCC were 0.81, 0.59, and 0.27, respectively. In conclusion, Ubigo-X outperformed existing tools in MCC (for both balanced and unbalanced data) and AUC and ACC (for balanced data), highlighting the efficacy of integrating image-based feature representation and weighted voting in ubiquitination prediction. Ubigo-X is a potential species-neutral ubiquitination site prediction tool, accessible at http://merlin.nchu.edu.tw/ubigox/.

Abstract Image

Abstract Image

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Ubigo-X:基于图像特征表示和加权投票的集成学习的蛋白质泛素化位点预测。
准确的泛素化鉴定在生物学功能分析中至关重要。我们开发了Ubigo-X,一个新的蛋白质泛素化预测工具。我们的训练数据来自蛋白质赖氨酸修饰数据库(PLMD 3.0),包括53338个泛素化位点和71399个非泛素化位点,经过CD-HIT和CD-HIT-2d序列过滤后保留。建立了基于单一序列的特征(Single-Type SBF)、基于k-mer序列的特征(Co-Type SBF)和基于结构和功能的特征(S-FBF)三个子模型。单一型SBF采用氨基酸组成(AAC)、氨基酸指数(AAindex)和单热编码;共型SBF采用k-mer编码的单型SBF;S-FBF采用二级结构、相对溶剂可及性(RSA)/绝对溶剂可及性面积(ASA)和信号肽裂解位点。使用XGBoost对S-FBF进行训练,将Single-Type SBF和Co-Type SBF转化为基于图像的特征,使用Resnet34进行训练。Ubigo-X是通过加权投票策略将三种模型结合起来开发的。使用过滤后保留的PhosphoSitePlus数据(65,421个泛素化位点和61,222个非泛素化位点)进行独立测试,曲线下面积(AUC)、准确度(ACC)和马修斯相关系数(MCC)分别为0.85、0.79和0.58。进一步测试不平衡的PhosphoSitePlus数据(1:8的阳性与阴性样本比例)得到0.94 AUC, 0.85 ACC和0.55 MCC。利用GPS-Uber数据,AUC、ACC和MCC分别为0.81、0.59和0.27。总之,Ubigo-X在MCC(用于平衡和不平衡数据)和AUC和ACC(用于平衡数据)方面优于现有工具,突出了在泛素化预测中集成基于图像的特征表示和加权投票的有效性。Ubigo-X是一种潜在的物种中性泛素化位点预测工具,可访问http://merlin.nchu.edu.tw/ubigox/。
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来源期刊
Computational and structural biotechnology journal
Computational and structural biotechnology journal Biochemistry, Genetics and Molecular Biology-Biophysics
CiteScore
9.30
自引率
3.30%
发文量
540
审稿时长
6 weeks
期刊介绍: Computational and Structural Biotechnology Journal (CSBJ) is an online gold open access journal publishing research articles and reviews after full peer review. All articles are published, without barriers to access, immediately upon acceptance. The journal places a strong emphasis on functional and mechanistic understanding of how molecular components in a biological process work together through the application of computational methods. Structural data may provide such insights, but they are not a pre-requisite for publication in the journal. Specific areas of interest include, but are not limited to: Structure and function of proteins, nucleic acids and other macromolecules Structure and function of multi-component complexes Protein folding, processing and degradation Enzymology Computational and structural studies of plant systems Microbial Informatics Genomics Proteomics Metabolomics Algorithms and Hypothesis in Bioinformatics Mathematical and Theoretical Biology Computational Chemistry and Drug Discovery Microscopy and Molecular Imaging Nanotechnology Systems and Synthetic Biology
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