3D structure modeling of cytochrome P450 2C19 and its implication for personalized drug design |
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Authors: | Wang Jing-Fang Wei Dong-Qing Li Lin Zheng Si-Yuan Li Yi-Xue Chou Kuo-Chen |
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Affiliation: | College of Life Science and Biotechnology, Shanghai Jiaotong University, Shanghai 200240, China. |
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Abstract: | Cytochrome P450 2C19 (CYP2C19) is a member of the cytochrome P-450 enzyme superfamily and plays an important role in the metabolism of drugs. In order to gain insights for developing personalized drugs, the 3D (dimensional) structure of CYP2C19 has been developed based on the crystal structure of CYP2C9 (PDB code 1R90), and its structure-activity relationship with the ligands of CEC, Fluvoxamine, Lescol, and Ticlopidine investigated through the structure-activity relationship approach. By means of a series of docking studies, the binding pockets of CYP2C19 for the four compounds are explicitly defined that will be very useful for conducting mutagenesis studies, providing insights into personalization of drug treatments and stimulating novel strategies for finding desired personalized drugs. |
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Keywords: | CYP2C19 Cytochrome P-450 Structure-activity relationship CEC Fluvoxamine Lescol Ticlopidine Personalized drug design |
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