2B50
Human Nuclear Receptor-Ligand Complex 2
2B50 の概要
| エントリーDOI | 10.2210/pdb2b50/pdb |
| 関連するPDBエントリー | 2AWH |
| 分子名称 | Peroxisome proliferator activated receptor delta, CALCIUM ION, heptyl beta-D-glucopyranoside, ... (5 entities in total) |
| 機能のキーワード | nuclear receptor, protein-ligand complex, ppar, gene regulation |
| 由来する生物種 | Homo sapiens (human) |
| タンパク質・核酸の鎖数 | 2 |
| 化学式量合計 | 63261.88 |
| 構造登録者 | Fyffe, S.A.,Alphey, M.S.,Buetow, L.,Smith, T.K.,Ferguson, M.A.J.,Sorensen, M.D.,Bjorkling, F.,Hunter, W.N. (登録日: 2005-09-27, 公開日: 2006-02-14, 最終更新日: 2024-03-13) |
| 主引用文献 | Fyffe, S.A.,Alphey, M.S.,Buetow, L.,Smith, T.K.,Ferguson, M.A.J.,Sorensen, M.D.,Bjorkling, F.,Hunter, W.N. Recombinant Human PPAR-beta/delta Ligand-binding Domain is Locked in an Activated Conformation by Endogenous Fatty Acids J.Mol.Biol., 356:1005-1013, 2006 Cited by PubMed Abstract: High-resolution crystallographic structures of recombinant human peroxisome proliferator-activated receptor ligand-binding domain (isotype beta/delta) reveal a fatty acid in the binding site. Mass spectrometry confirmed the presence of C16:0, C16:1, C18:0 and C18:1 in a ratio of approximately 3:2:1:4 with 11, Z-octadecenoic acid (cis-vaccenic acid) identified as the predominant species. These are endogenous fatty acids acquired from the bacterial expression system, and serve to lock the ligand-binding domain into the activated conformation. A requirement for crystal growth, the additive n-heptyl-beta-d-glucopyranoside, binds near the activation function helix where recognition of co-activator proteins occurs. Our observations suggest potential physiological ligands for human PPAR-beta/delta and highlight that reported binding studies must be treated with caution unless endogenous fatty acids have been removed from the sample prior to analysis. PubMed: 16405912DOI: 10.1016/j.jmb.2005.12.047 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (2 Å) |
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