GeneSilico
GeneSilico predicts protein tertiary structures from amino acid sequences or multiple sequence alignments by integrating fold-recognition (FR) methods and converting FR results into full-atom 3D models to identify remote similarities between proteins.
Key Features:
- Input formats: Accepts amino acid sequences and user-supplied multiple sequence alignments (MSAs) for prediction.
- Fold-recognition integration: Integrates multiple fold-recognition (FR) methods to detect remote homologs.
- Consensus modeling: Combines results from different FR methods and infers a consensus to enhance prediction reliability.
- Full-atom model construction: Converts fold-recognition results into full-atom 3D protein models.
- Model quality assessment: Performs uniform quality assessment of generated 3D models.
- Multi-level prediction: Produces predictions at primary, secondary, and tertiary structure levels.
Scientific Applications:
- Remote similarity detection: Identifying remote similarities between proteins via fold-recognition methods.
- Structure generation: Producing full-atom 3D models for structural analysis.
- Consensus-based prediction: Improving the reliability of structural predictions through consensus of multiple FR methods.
- MSA-enhanced prediction: Enhancing prediction accuracy by using user-defined multiple sequence alignments instead of single-sequence methods.
Methodology:
Integrates multiple fold-recognition methods, accepts amino acid sequences or user-supplied MSAs, combines FR results into a consensus, converts FR results into full-atom 3D models, and performs uniform quality assessment while producing primary, secondary and tertiary structure predictions.
Topics
Details
- Tool Type:
- web application
- Operating Systems:
- Linux, Windows, Mac
- Added:
- 2/10/2017
- Last Updated:
- 11/25/2024
Operations
Data Inputs & Outputs
Protein quaternary structure prediction
Inputs
Outputs
Publications
Kurowski MA. GeneSilico protein structure prediction meta-server. Nucleic Acids Research. 2003;31(13):3305-3307. doi:10.1093/nar/gkg557. PMID:12824313. PMCID:PMC168964.