Fig. 8From: Endocrine disruption: In silico perspectives of interactions of di-(2-ethylhexyl)phthalate and its five major metabolites with progesterone receptorRibbon form representation of docking complex of human progesterone receptor (PR) with native co-complex ligand norethindrone (NET) (left panel). Amino-acid residues in the binding pocket of PR involved in interactions with NET (right panel)Back to article page