ResNetKhib
ResNetKhib: Deep learning-based prediction of cell type-specific lysine 2-hydroxyisobutylation sites
ResNetKhib predicts cell type-specific lysine 2-hydroxyisobutylation (Khib) sites in protein sequences using a residual network-based deep learning framework. It models Khib modifications associated with gene transcription, chromatin function regulation, purine metabolism, the pentose phosphate pathway, and glycolysis/gluconeogenesis across multiple species and cell types.
Key Features:
- Cell Type-Specific Prediction: Predicts Khib sites in four human cell types, mouse liver cells, and three rice cell types.
- Residual Network Architecture: Implements one-dimensional convolutional neural networks with ResNet-inspired residual connections.
- Transfer Learning Integration: Applies transfer learning to improve predictive performance across species and biological contexts.
- Performance Benchmarking: Evaluated using 10-fold cross-validation and independent testing; achieves AUC-ROC values ranging from 0.807 to 0.901 and outperforms random forest predictors.
Scientific Applications:
- Post-Translational Modification Analysis: Identifies Khib modification sites to support mechanistic studies of protein regulation and metabolic pathway involvement.
Methodology:
ResNetKhib employs one-dimensional convolutional neural networks with residual connections inspired by ResNet architecture and incorporates transfer learning. Model performance is assessed using 10-fold cross-validation and independent test datasets across human, mouse, and rice cell types.
Topics
Details
- Cost:
- Free of charge
- Tool Type:
- web application
- Operating Systems:
- Mac, Linux, Windows
- Added:
- 8/10/2023
- Last Updated:
- 11/24/2024
Operations
Data Inputs & Outputs
PTM site prediction
Inputs
Outputs
Publications
Jia X, Zhao P, Li F, Qin Z, Ren H, Li J, Miao C, Zhao Q, Akutsu T, Dou G, Chen Z, Song J. ResNetKhib: a novel cell type-specific tool for predicting lysine 2-hydroxyisobutylation sites via transfer learning. Briefings in Bioinformatics. 2023;24(2). doi:10.1093/bib/bbad063. PMID:36880172. PMCID:PMC10185920.