Protein structure prediction using diversity controlled self-adaptive differential evolution with local search

In this paper, Protein Structure Prediction problem is solved using Diversity Controlled Self-Adaptive Differential Evolution with Local search (DCSaDE-LS). DCSaDE-LS, an improved version of Self-Adaptive Differential Evolution (SaDE), use simple fuzzy system to control the diversity of individuals...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Soft computing (Berlin, Germany) Germany), 2015-06, Vol.19 (6), p.1635-1646
Hauptverfasser: Sudha, S., Baskar, S., Amali, S. Miruna Joe, Krishnaswamy, S.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:In this paper, Protein Structure Prediction problem is solved using Diversity Controlled Self-Adaptive Differential Evolution with Local search (DCSaDE-LS). DCSaDE-LS, an improved version of Self-Adaptive Differential Evolution (SaDE), use simple fuzzy system to control the diversity of individuals and local search to maintain a balance between exploration and exploitation. DCSaDE-LS with four different local search replacement strategies are used. SaDE is also implemented for comparison purposes. Algorithms are tested on a peptide Met-enkephalin for force fields ECEPP/2, ECEPP/3 and CHARMM22. Results show that both DCSaDE-LS and SaDE produce the best energy for both force fields. Among the four replacement strategies, DCSaDE-LS1 strategy reports better results than other strategies and SaDE in terms of number of function evaluations, mean energy and success rate. Best conformations obtained using DCSaDE-LS is compared with native structure 1PLW and GEM structure Scheraga. Nonparametric statistical tests for multiple comparisons ( 1 × N ) with control method are implemented for CHARMM22 observations. A set of unique 100 best conformations obtained from DCSaDE-LS are clustered into 3 independent clusters suggesting the robustness of this methodology and the ability to explore the conformational space available and to populate the near native conformations.
ISSN:1432-7643
1433-7479
DOI:10.1007/s00500-014-1353-2