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All torsional modes of the sidechain (chi(1): rotation about the C-alpha-C-beta and chi(2): rotation about the C-beta-Se bonds) were investigated in the relaxed beta(L) backbone [(psi,phi), (a,a)] conformation. The relaxed potential energy surface (PES) obtained at the RHF/3-21G level of theory contained seven out of nine possible minima of the sidechain. All minima were re-optimized at the RHF/6-31G(d) and the B3LYP/6-31G(d) levels of theory. Two of the minima (g(+)a) and (g(-)g(+)) located at RHF/3-21G level of theory were annihilated when optimized at higher levels of theory. The frequency calculations for the found minima were used to construct the thermodynamic functions. The relative energies of the -CH2-SeH sidechain conformations have been compared with the relative energies of the analogous -CH2-SH and -CH2-OH sidechain conformers. 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