1M7W
HNF4a ligand binding domain with bound fatty acid
1M7W の概要
| エントリーDOI | 10.2210/pdb1m7w/pdb |
| 分子名称 | Hepatocyte nuclear factor 4-alpha, LAURIC ACID (3 entities in total) |
| 機能のキーワード | transcription factor |
| 由来する生物種 | Rattus rattus (black rat) |
| 細胞内の位置 | Nucleus: P22449 |
| タンパク質・核酸の鎖数 | 4 |
| 化学式量合計 | 113283.09 |
| 構造登録者 | Dhe-Paganon, S.,Duda, K.,Iwamoto, M.,Chi, Y.I.,Shoelson, S.E. (登録日: 2002-07-22, 公開日: 2003-07-01, 最終更新日: 2024-02-14) |
| 主引用文献 | Dhe-Paganon, S.,Duda, K.,Iwamoto, M.,Chi, Y.I.,Shoelson, S.E. Crystal structure of the HNF4 alpha ligand binding domain in complex with endogenous fatty acid ligand J.Biol.Chem., 277:37973-37976, 2002 Cited by PubMed Abstract: HNF4 alpha is an orphan member of the nuclear receptor family with prominent functions in liver, gut, kidney and pancreatic beta cells. We have solved the x-ray crystal structure of the HNF4 alpha ligand binding domain, which adopts a canonical fold. Two conformational states are present within each homodimer: an open form with alpha helix 12 (alpha 12) extended and collinear with alpha 10 and a closed form with alpha 12 folded against the body of the domain. Although the protein was crystallized without added ligands, the ligand binding pockets of both closed and open forms contain fatty acids. The carboxylic acid headgroup of the fatty acid ion pairs with the guanidinium group of Arg(226) at one end of the ligand binding pocket, while the aliphatic chain fills a long, narrow channel that is lined with hydrophobic residues. These findings suggest that fatty acids are endogenous ligands for HNF4 alpha and establish a framework for understanding how HNF4 alpha activity is enhanced by ligand binding and diminished by MODY1 mutations. PubMed: 12193589DOI: 10.1074/jbc.C200420200 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (2.8 Å) |
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