Biology – Quantitative Biology – Biomolecules
Scientific paper
2006-11-27
Biology
Quantitative Biology
Biomolecules
Structure, in press
Scientific paper
Natural proteins fold to a unique, thermodynamically dominant state. Modeling of the folding process and prediction of the native fold of proteins are two major unsolved problems in biophysics. Here, we show successful all-atom ab initio folding of a representative diverse set of proteins, using a minimalist transferable energy model that consists of two-body atom-atom interactions, hydrogen-bonding, and a local sequence energy term that models sequence-specific chain stiffness. Starting from a random coil, the native-like structure was observed during replica exchange Monte Carlo (REMC) simulation for most proteins regardless of their structural classes; the lowest energy structure was close to native- in the range of 2-6 A root-mean-square deviation (RMSD). Our results demonstrate that the successful all-atom folding of a protein chain to its native state is governed by only a few crucial energetic terms.
Chen William W.
Shakhnovich Eugene I.
Skolnick Jeffrey
Yang Jae Shick
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