SPOT-Disorder-Single
SPOT-Disorder-Single predicts intrinsically disordered regions (IDRs) in proteins using single-sequence information to enable disorder annotation without relying on evolutionary sequence profiles.
Key Features:
- Single-Sequence Approach: Operates using single-sequence data rather than evolutionary sequence profiles derived from multiple-sequence alignments.
- Deep Learning Ensemble: Employs an ensemble of deep recurrent and convolutional neural networks to model sequence-dependent disorder.
- Whole-Sequence Learning: Facilitates whole-sequence learning across entire protein sequences.
- Accuracy and Robustness: Outperforms SPOT-Disorder (a profile-based method) for proteins with few homologous sequences and performs comparably for long-disordered regions.
- Validation Across Test Sets: Validated across four independent test sets containing varying proportions of short- and long-disordered regions.
Scientific Applications:
- IDR Identification: Identification and annotation of intrinsically disordered regions (IDRs) in proteins.
- Protein Function and Interactions: Investigation of protein function and interaction networks influenced by disordered regions.
- Disease Mechanism Analysis: Study of disease mechanisms associated with misfolded or dysfunctional proteins linked to disordered regions.
Methodology:
Uses single-sequence input and an ensemble of deep recurrent and convolutional neural networks to perform whole-sequence learning.
Topics
Details
- Cost:
- Free of charge
- Tool Type:
- command-line tool, web application
- Operating Systems:
- Linux, Windows
- Added:
- 8/31/2022
- Last Updated:
- 11/24/2024
Operations
Publications
Hanson J, Paliwal K, Zhou Y. Accurate Single-Sequence Prediction of Protein Intrinsic Disorder by an Ensemble of Deep Recurrent and Convolutional Architectures. Journal of Chemical Information and Modeling. 2018;58(11):2369-2376. doi:10.1021/acs.jcim.8b00636. PMID:30395465.
PMID: 30395465
Funding: - National Health and Medical Research Council: 1121629
- Australian Research Council: DP180102060
Downloads
- Downloads pagehttp://zhouyq-lab.szbl.ac.cn/download/