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VFT modules constitute the binding pocket of various receptors activated by small molecules [ 13].
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These inhibitors can inhibit various CDKs by targeting the ATP binding pocket of CDKs, which is located in the deep cleft formed by N-lobe, C-lobe, and the hinge region in CDKs[1], [33].
Finally, docking results were analyzed by visualizing several interactions of compounds within binding pocket of proteins.
The binding pocket of this compound comprises of HIS44, TYR68, LEU46, GLY61, TYR36, LEU62 and LEU59.
c Comparison of the putative cation binding pocket of OsCAX1a and OsMHX1.
Molecular docking studies demonstrated that all compounds were well accommodated inside the binding pocket of BChE.
Figure 1 Compounds 1 and 2 fitted into the binding pocket of the CB2R receptor model.
The binding pocket of KQTSV on the PDZ domain is presented with grey surface.
Compound 4b forms three hydrogen bonds with the binding pocket of BuChE.
Forty-four bacidturic aciderivativeses (1 44) were docked into the binding pocket of urease.
By specifically comparing the substrate binding pocket of CALA to other binding pockets of α/β hydrolases, the binding pocket of Candida rugosa lipase was identified as being highly similar.
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