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  • Title: Template-free protein structure prediction and quality assessment with an all-atom free-energy model.
    Author: Gopal SM, Klenin K, Wenzel W.
    Journal: Proteins; 2009 Nov 01; 77(2):330-41. PubMed ID: 19422063.
    Abstract:
    Biophysical forcefields have contributed less than originally anticipated to recent progress in protein structure prediction. Here, we have investigated the selectivity of a recently developed all-atom free-energy forcefield for protein structure prediction and quality assessment (QA). Using a heuristic method, but excluding homology, we generated decoy-sets for all targets of the CASP7 protein structure prediction assessment with <150 amino acids. The decoys in each set were then ranked by energy in short relaxation simulations and the best low-energy cluster was submitted as a prediction. For four of nine template-free targets, this approach generated high-ranking predictions within the top 10 models submitted in CASP7 for the respective targets. For these targets, our de-novo predictions had an average GDT_S score of 42.81, significantly above the average of all groups. The refinement protocol has difficulty for oligomeric targets and when no near-native decoys are generated in the decoy library. For targets with high-quality decoy sets the refinement approach was highly selective. Motivated by this observation, we rescored all server submissions up to 200 amino acids using a similar refinement protocol, but using no clustering, in a QA exercise. We found an excellent correlation between the best server models and those with the lowest energy in the forcefield. The free-energy refinement protocol may thus be an efficient tool for relative QA and protein structure prediction.
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