7VQP
Vitamin D receptor complexed with a lithocholic acid derivative
7VQP の概要
| エントリーDOI | 10.2210/pdb7vqp/pdb |
| 分子名称 | Vitamin D3 receptor, Mediator of RNA polymerase II transcription subunit 1, 3-((R)-4-((3R,5R,8R,9S,10S,13R,14S,17R)-3-(2-hydroxy-2-methylpropyl)-10,13-dimethylhexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanamido)propanoic acid, ... (4 entities in total) |
| 機能のキーワード | vitamin d receptor, lithocholic acid, transcription |
| 由来する生物種 | Rattus norvegicus 詳細 |
| タンパク質・核酸の鎖数 | 2 |
| 化学式量合計 | 32669.69 |
| 構造登録者 | Kato, K.,Numoto, N.,Kagechika, H.,Tanatani, A.,Ito, N. (登録日: 2021-10-20, 公開日: 2022-03-09, 最終更新日: 2023-11-29) |
| 主引用文献 | Yoshihara, A.,Kawasaki, H.,Masuno, H.,Takada, K.,Numoto, N.,Ito, N.,Hirata, N.,Kanda, Y.,Ishizawa, M.,Makishima, M.,Kagechika, H.,Tanatani, A. Lithocholic Acid Amides as Potent Vitamin D Receptor Agonists. Biomolecules, 12:-, 2022 Cited by PubMed Abstract: 1α,25-Dihydroxyvitamin D [1α,25(OH)D, ] is an active form of vitamin D and regulates various biological phenomena, including calcium and phosphate homeostasis, bone metabolism, and immune response via binding to and activation of vitamin D receptor (VDR). Lithocholic acid (LCA, ) was identified as a second endogenous agonist of VDR, though its potency is very low. However, the lithocholic acid derivative () is a more potent agonist than 1α,25(OH)D, (), and its carboxyl group has similar interactions to the 1,3-dihydroxyl groups of with amino acid residues in the VDR ligand-binding pocket. Here, we designed and synthesized amide derivatives of in order to clarify the role of the carboxyl group. The synthesized amide derivatives showed HL-60 cell differentiation-inducing activity with potency that depended upon the substituent on the amide nitrogen atom. Among them, the -cyanoamide is more active than either or . PubMed: 35053278DOI: 10.3390/biom12010130 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (1.94 Å) |
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