7YFK
The structure of human pregnane X receptor in complex with an SRC-1 coactivator peptide and a limonoid compound, nomilin
「7CHG」から置き換えられました7YFK の概要
エントリーDOI | 10.2210/pdb7yfk/pdb |
分子名称 | Nuclear receptor subfamily 1 group I member 2,Nuclear receptor coactivator 1, Nomilin (3 entities in total) |
機能のキーワード | complex, activator, transcription, drug binding, nuclear receptor |
由来する生物種 | Homo sapiens (human) 詳細 |
タンパク質・核酸の鎖数 | 2 |
化学式量合計 | 78143.82 |
構造登録者 | |
主引用文献 | Fan, S.,Yan, Y.,Xia, Y.,Zhou, Z.,Luo, L.,Zhu, M.,Han, Y.,Yao, D.,Zhang, L.,Fang, M.,Peng, L.,Yu, J.,Liu, Y.,Gao, X.,Guan, H.,Li, H.,Wang, C.,Wu, X.,Zhu, H.,Cao, Y.,Huang, C. Pregnane X receptor agonist nomilin extends lifespan and healthspan in preclinical models through detoxification functions. Nat Commun, 14:3368-3368, 2023 Cited by PubMed Abstract: Citrus fruit has long been considered a healthy food, but its role and detailed mechanism in lifespan extension are not clear. Here, by using the nematode C. elegans, we identified that nomilin, a bitter-taste limoloid that is enriched in citrus, significantly extended the animals' lifespan, healthspan, and toxin resistance. Further analyses indicate that this ageing inhibiting activity depended on the insulin-like pathway DAF-2/DAF-16 and nuclear hormone receptors NHR-8/DAF-12. Moreover, the human pregnane X receptor (hPXR) was identified as the mammalian counterpart of NHR-8/DAF-12 and X-ray crystallography showed that nomilin directly binds with hPXR. The hPXR mutations that prevented nomilin binding blocked the activity of nomilin both in mammalian cells and in C. elegans. Finally, dietary nomilin supplementation improved healthspan and lifespan in D-galactose- and doxorubicin-induced senescent mice as well as in male senescence accelerated mice prone 8 (SAMP8) mice, and induced a longevity gene signature similar to that of most longevity interventions in the liver of bile-duct-ligation male mice. Taken together, we identified that nomilin may extend lifespan and healthspan in animals via the activation of PXR mediated detoxification functions. PubMed: 37291126DOI: 10.1038/s41467-023-39118-9 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (2.1 Å) |
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