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The structures, together with mutagenesis studies, revealed distinct features of the CCK1R and CCK2R ligand-binding pockets that determine CCK1R selectivity for sulfated CCK-8 and SR146131, and CCK2R selectivity for gastrin-17, and thus highlighted the activation mechanism for both CCK1R and CCK2R

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Modelling of protective mechanism of iron (II)-polyphenol binding with OH-related molecular descriptors

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