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. 2020 Jan 22;10(7):3626–3635. doi: 10.1039/c9ra09203j

Fig. 5. A stereo view of the crystal structure of thrombin and a stereodiagram of Z-GGRAMC acetate docked with licochalcone A. Inhibitor could bind to the active site (A), exosite I (C) of human thrombin. The detailed view represents the interactions between licochalcone A and the amino acids in the active site (B) and exosite I (D) of human thrombin.

Fig. 5