Evidence-Based Complementary and Alternative Medicine / 2015 / Article / Fig 4

Research Article

1,2,3,4,6-Penta-O-galloylglucose within Galla Chinensis Inhibits Human LDH-A and Attenuates Cell Proliferation in MDA-MB-231 Breast Cancer Cells

Figure 4

Molecular docking studies (PGG inhibition of human LDH-A). (a) Structure of 1,2,3,4,6-O-galloy1-β-D-glucose, pentagalloylglucose. (b) Binding mode of compound CID65238, PGG, in the coenzyme active site of hLDH-A (PDB: 1∣10). (c) Simplified binding mode of compound CID65238, PGG, in the coenzyme binding site of hLDH-A (PDB: 1∣10).

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