7E4C
Crystal structure of MIF bound to compound11
7E4C の概要
エントリーDOI | 10.2210/pdb7e4c/pdb |
分子名称 | Macrophage migration inhibitory factor, CHLORIDE ION, SULFATE ION, ... (6 entities in total) |
機能のキーワード | tautomerase and cytokine, isomerase |
由来する生物種 | Homo sapiens (Human) |
タンパク質・核酸の鎖数 | 3 |
化学式量合計 | 38257.67 |
構造登録者 | |
主引用文献 | Yang, L.,Guo, D.,Fan, C. Identification and Structure-Activity Relationships of Dietary Flavonoids as Human Macrophage Migration Inhibitory Factor (MIF) Inhibitors. J.Agric.Food Chem., 69:10138-10150, 2021 Cited by PubMed Abstract: Dietary flavonoids are known to have anti-inflammatory and anticancer effects, but their influences on human macrophage migration inhibitory factor (MIF), a vital proinflammatory cytokine recognized as a therapeutic target for infectious diseases and cancers, have been rarely reported. Here, we identified 24 dietary flavonoids that could inhibit the tautomerase activity of MIF, five of which exerted IC values lower than the positive control ISO-1 in the micromolar range: morin (IC = 11.01 ± 0.45 μM) and amentoflavone (IC = 13.32 ± 0.64 μM) exhibited the most potent efficacy followed by apigenin (IC = 42.74 ± 4.20 μM), naringin (IC = 51.38 ± 2.12 μM), and fisetin (IC = 51.99 ± 0.63 μM). X-ray crystallography, molecular docking, and cellular experiments were utilized to illustrate the molecular binding details and structure-activity relationships. Scaffold modifications of flavonoids significantly influenced the potency. What stands out for morin is the unique 2'-OH substitution. In addition, amentoflavone situated at the MIF trimer pore may impact MIF-CD74 signaling. The results also showed that flavonoids could suppress cell chemotaxis and nitric oxide production in RAW264.7 cells. Our results elucidate the molecular mechanism of flavonoids acting on MIF and shed light on developing lead compounds against MIF-involved diseases. PubMed: 34459191DOI: 10.1021/acs.jafc.1c03367 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (1.644 Å) |
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