In Silico Identification of Potent PPAR- Agonists from Traditional Chinese Medicine: A Bioactivity Prediction, Virtual Screening, and Molecular Dynamics Study
Figure 8
Secondary structure assignments and secondary structural feature ratio variations of PPAR- complexes over 40 ns MD simulation. Residues 1–65 in -axis correspond to residues 207–271, residues 66-250 in -axis correspond to residues 276–460, and residues 251–262 in -axis correspond to residues 465–476.
