Fig. 7From: 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 mono-[2-(carboxymethyl)hexyl]phthalate (2-cx-MMHP)(left panel). Amino-acid residues in the binding pocket of PR involved in interactions with 2-cx-MMHP (right panel)Back to article page