5WGQ
Estrogen Receptor Alpha Ligand Binding Domain in Complex with Estradiol and SRC2-BCP1
5WGQ の概要
エントリーDOI | 10.2210/pdb5wgq/pdb |
関連するBIRD辞書のPRD_ID | PRD_002318 |
分子名称 | Estrogen receptor, SRC2-BCP1, ESTRADIOL, ... (4 entities in total) |
機能のキーワード | breast cancer, stapled peptides, synthetic peptides, hormone., transcription, transcription-transcription inhibitor complex, transcription/transcription inhibitor |
由来する生物種 | Homo sapiens (Human) 詳細 |
タンパク質・核酸の鎖数 | 4 |
化学式量合計 | 62868.39 |
構造登録者 | Fanning, S.W.,Speltz, T.E.,Mayne, C.G.,Siddiqui, Z.,Greene, G.L.,Tajkhorshid, E.,Moore, T.W. (登録日: 2017-07-14, 公開日: 2018-06-13, 最終更新日: 2024-10-30) |
主引用文献 | Speltz, T.E.,Mayne, C.G.,Fanning, S.W.,Siddiqui, Z.,Tajkhorshid, E.,Greene, G.L.,Moore, T.W. A "cross-stitched" peptide with improved helicity and proteolytic stability. Org. Biomol. Chem., 16:3702-3706, 2018 Cited by PubMed Abstract: A new computational approach to obtain quantitative energy profiles for helix folding was used in the design of orthogonal hydrocarbon and lactam bicyclic peptides. The proteolytically stable, "cross-stitched" peptide SRC2-BCP1 shows nanomolar affinity for estrogen receptor α and X-ray crystallography confirms a helical binding pose. PubMed: 29725689DOI: 10.1039/c8ob00790j 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (2.3 Å) |
構造検証レポート
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