Protein Science · 2017 · 16 citations · 52 references
Life SciencesBioinformaticsChemistryProtein Structure PredictionStructural BioinformaticsStructural BiologyProtein StructureProtein Structure ModelingAll-atom ModelingDecoy SetsProtein Decoy SelectionProtein Structural AnalysisProtein Structure AssessmentProtein Structure DeterminationScoring FunctionsStatistical Potentials
We report a C-atom-based scoring function, named OPUS-CSF, for ranking protein structural models. Rather than using traditional Boltzmann formula, we built a scoring function (CSF score) based on the native distributions (derived from the entire PDB) of coordinate components of mainchain C (carbonyl) atoms on selected residues of peptide segments of 5, 7, 9, and 11 residues in length. In testing OPUS-CSF on decoy recognition, it maximally recognized 257 native structures out of 278 targets in 11 commonly used decoy sets, significantly outperforming other popular all-atom empirical potentials. The average correlation coefficient with TM-score was also comparable with those of other potentials. OPUS-CSF is a highly coarse-grained scoring function, which only requires input of partial mainchain information, and very fast. Thus, it is suitable for applications at early stage of structural building.
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The Amber biomolecular simulation programs
David A. Case, Thomas E. Cheatham, Tom Darden et al. · Journal of Computational Chemistry · 2005 · 9.6K citations · Full text