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- W2000765589 abstract "Docking results have enabled us to propose how resveratrol could act as a selective PGHS-1 peroxidase site inhibitor. The docking model has predicted a slightly less favorable ΔGbind (−17.9 kcal/mol) of the resveratrol to the PGHS-2 peroxidase site in comparison with its corresponding binding to the PGHS-1 (−20.4 kcal/mol). The formation of hydrogen bonds among the hydroxyl groups of the resveratrol phenyl rings, the backbone of Fe-heme and the carbonyl group of Leu294 inside the PGHS-1 peroxidase site, associated with the absence of His214 in the backbone of PGHS-1, are essential features that are required to maintain the aromatic rings of the natural product parallel to the Fe-heme group and transverse to the peroxidase access channel promoting a large steric hindrance at this site and its consequent selective inhibition." @default.
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- W2000765589 date "1998-09-01" @default.
- W2000765589 modified "2023-09-25" @default.
- W2000765589 title "Cloning and sequencing of members of the human placental protein 17 (PP17) family" @default.
- W2000765589 doi "https://doi.org/10.1016/s0143-4004(98)91208-5" @default.
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