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Computer modeling of opioid interaction with the dimerized TLR4-MD2 complex. In silico docking of (−)-morphine (black stick and ball) to the 3D crystalline structure of the human MD2 (dark gray) and TLR4 (light) complex (Protein Data Bank ID 3FXI) demonstrates that the preferred docking location of (−)-morphine is to the LPS binding domain of MD2.
