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- W2046911811 abstract "Solvation is an important factor in the structure stabilization of proteins. The free energy of solvation has been commonly approximated by summing the products of the atomic solvation parameters (ASPs) and the solvent accessible surface areas, where the ASPs were obtained from thermodynamic experiments of small molecules. This summation was usually added to the force field without calibration. We propose deriving an optimized set of ASPs only by requiring that the minimized total energy of the experimentally known structure is the global minimum. This method is applied to a cyclic hexapeptide in DMSO and can also be extended to loops in proteins in water." @default.
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- W2046911811 date "1997-09-01" @default.
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- W2046911811 title "Novel Procedure for Developing Implicit Solvation Models for Peptides and Proteins" @default.
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- W2046911811 doi "https://doi.org/10.1021/jp972175+" @default.
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