arXiv · physics/0310146
In-silico folding of a three helix protein and characterization of its free-energy landscape in an all-atom forcefield
Abstract
We report the reproducible first-principles folding of the 40 amino acid, three-helix headpiece of the HIV accessory protein in a recently developed all-atom free-energy forcefield. Six of twenty simulations using an adapted basin-hopping method converged to better than 3 Åbackbone RMS deviation to the experimental structure. Using over 60,000 low-energy conformations of this protein, we constructed a decoy tree that completely characterizes its folding funnel.
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T. Herges, W. Wenzel. 2003-10-29. In-silico folding of a three helix protein and characterization of its free-energy landscape in an all-atom forcefield. https://arxiv.org/abs/physics/0310146
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