Literature DB >> 14696192

A new pairwise folding potential based on improved decoy generation and side-chain packing.

C Loose1, J L Klepeis, C A Floudas.   

Abstract

A new force field for pairwise residue interactions as a function of C(alpha) to C(alpha) distances is presented. The force field was developed through the solution of a linear programming formulation with large sets of constraints. The constraints are based on the construction of >80,000 low-energy decoys for a set of proteins and requiring the decoy energies for each protein system to be higher than the native conformation of that particular protein. The generation of a robust force field was facilitated by the use of a novel decoy generation process, which involved the rational selection of proteins to add to the training set and included a significant energy minimization of the decoys. The force field was tested on a large set of decoys for various proteins not included in the training set and shown to perform well compared with a leading force field in identifying the native conformation for these proteins. Copyright 2003 Wiley-Liss, Inc.

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Year:  2004        PMID: 14696192     DOI: 10.1002/prot.10521

Source DB:  PubMed          Journal:  Proteins        ISSN: 0887-3585


  10 in total

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5.  The impact of side-chain packing on protein docking refinement.

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8.  Simulating protein folding initiation sites using an alpha-carbon-only knowledge-based force field.

Authors:  Patrick M Buck; Christopher Bystroff
Journal:  Proteins       Date:  2009-08-01

9.  Incorporating Ab Initio energy into threading approaches for protein structure prediction.

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10.  Novel knowledge-based mean force potential at the profile level.

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Journal:  BMC Bioinformatics       Date:  2006-06-27       Impact factor: 3.169

  10 in total

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