Four categories of globular proteins, including all-α, all-β, α + β, and α /β types, are simplified as the off-lattice HNP model involving the secondary-structural information of each protein. The propensity of three types of residues,i.e., H, N, and P to form a secondary structure is investigated based on 146 protein samples. We find that P residues are easy to form α-helices, whereas H residues have a higher tendency to construct β-sheets. The statistical analysis also indicates that the occurrence of P residues is invariably higher than that of H residues, which is independent of protein category. Changes in bond- and non-bonded potential energies of all protein samples under a wide temperature range are presented by coarse-grained molecular dynamics(MD) simulation. The simulation results clearly show a linear relationship between the bond-stretching/bending potential energy and the reduced temperature. The bond-torsional and non-bonded potential energies show distinct transitions with temperature. The bond-torsional energy increases to the maximum and then decreases with the increase of temperature, which is opposite to the change in non-bonded potential energy. The transition temperature of non-bonded potential energy is independent of the protein category, while that of bond-torsional energy is closely related to the protein secondary structure, i.e., α-helix or β-sheet. The quantitatively bonded- and semiquantitatively non-bonded potential energy of 24 α + β and 23 α /β protein samples are successfully predicted according to the statistical results obtained from MD simulations.
