AlphaPred
AlphaPred predicts alpha-turn residues in protein sequences using artificial neural networks trained on sequence-derived evolutionary and secondary structure features.
Key Features:
- Artificial Neural Network Prediction: Uses an artificial neural network (ANN) model trained with position-specific scoring matrices generated by PSI-BLAST and secondary structure predictions from PSIPRED.
- Two-Stage Neural Network Architecture: Implements a feed-forward back-propagation neural network with a single hidden layer consisting of a sequence-structure network followed by a structure-structure network for prediction refinement.
- Sequence-Derived Evolutionary Features: Utilizes PSI-BLAST-generated position-specific scoring matrices derived from multiple sequence alignments to capture evolutionary information.
- Secondary Structure Integration: Incorporates PSIPRED-predicted secondary structure information to improve alpha-turn prediction accuracy.
Scientific Applications:
- Protein Structure Prediction: Identifies alpha-turn residues to support analysis of protein folding, structural motifs, and conformational stability.
- Protein Function Analysis: Facilitates investigation of structural elements influencing protein interactions, enzymatic activity, and molecular recognition.
- Structural Bioinformatics Research: Supports studies of sequence–structure relationships in proteins using computational prediction of local structural motifs.
Methodology:
AlphaPred applies a two-stage feed-forward back-propagation artificial neural network trained on PSI-BLAST-derived position-specific scoring matrices and PSIPRED secondary structure predictions using a dataset of 193 non-homologous protein X-ray structures with five-fold cross-validation.
Topics
Collections
Details
- Tool Type:
- web application
- Operating Systems:
- Linux, Windows, Mac
- Added:
- 5/1/2017
- Last Updated:
- 11/24/2024
Operations
Publications
Kaur H, Raghava G. Prediction of α‐turns in proteins using PSI‐BLAST profiles and secondary structure information. Proteins: Structure, Function, and Bioinformatics. 2004;55(1):83-90. doi:10.1002/prot.10569. PMID:14997542.
DOI: 10.1002/prot.10569
PMID: 14997542