Our docking model shows that haloperidol in its highest ranked binding pose interacts with all residues in the binding pocket of Sigmar1, including Phe133, Glu172, Leu105, Met93, Leu95, Ile178, Val84, His154, and Val152, in line with previous studies pointing to Glu172 as an essential residue for Sigmar1 haloperidol binding 69, 70
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