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PLoS Comput Biol. 2014 Apr 24;10(4):e1003539. doi: 10.1371/journal.pcbi.1003539. eCollection 2014 Apr.

Fast protein loop sampling and structure prediction using distance-guided sequential chain-growth Monte Carlo method.

Author information

1
Department of Bioengineering, University of Illinois at Chicago, Chicago, Illinois, United States of America.
2
Department of Statistics, Florida State University, Tallahassee, Florida, United States of America.

Abstract

Loops in proteins are flexible regions connecting regular secondary structures. They are often involved in protein functions through interacting with other molecules. The irregularity and flexibility of loops make their structures difficult to determine experimentally and challenging to model computationally. Conformation sampling and energy evaluation are the two key components in loop modeling. We have developed a new method for loop conformation sampling and prediction based on a chain growth sequential Monte Carlo sampling strategy, called Distance-guided Sequential chain-Growth Monte Carlo (DISGRO). With an energy function designed specifically for loops, our method can efficiently generate high quality loop conformations with low energy that are enriched with near-native loop structures. The average minimum global backbone RMSD for 1,000 conformations of 12-residue loops is 1:53 A° , with a lowest energy RMSD of 2:99 A° , and an average ensembleRMSD of 5:23 A° . A novel geometric criterion is applied to speed up calculations. The computational cost of generating 1,000 conformations for each of the x loops in a benchmark dataset is only about 10 cpu minutes for 12-residue loops, compared to ca 180 cpu minutes using the FALCm method. Test results on benchmark datasets show that DISGRO performs comparably or better than previous successful methods, while requiring far less computing time. DISGRO is especially effective in modeling longer loops (10-17 residues).

PMID:
24763317
PMCID:
PMC3998890
DOI:
10.1371/journal.pcbi.1003539
[Indexed for MEDLINE]
Free PMC Article

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