9GFC
HDM2 complexed with stapled peptide-like ligand
9GFC の概要
| エントリーDOI | 10.2210/pdb9gfc/pdb |
| 分子名称 | E3 ubiquitin-protein ligase Mdm2, Stapled peptide-like ligand (3 entities in total) |
| 機能のキーワード | stapled peptide, hdm2, peptide binding protein |
| 由来する生物種 | Homo sapiens (human) 詳細 |
| タンパク質・核酸の鎖数 | 7 |
| 化学式量合計 | 45225.46 |
| 構造登録者 | Perdriau, C.,Luton, A.,Zimmeter, K.,Neuville, M.,Saragaglia, C.,Peluso-lltis, C.,Osz, J.,Kauffmann, B.,Collie, G.,Rochel, N.,Guichard, G.,Pasco, M. (登録日: 2024-08-08, 公開日: 2025-02-12) |
| 主引用文献 | Perdriau, C.,Luton, A.,Zimmeter, K.,Neuville, M.,Saragaglia, C.,Peluso-Iltis, C.,Osz, J.,Kauffmann, B.,Collie, G.W.,Rochel, N.,Guichard, G.,Pasco, M. Guanidinium-Stapled Helical Peptides for Targeting Protein-Protein Interactions. Angew.Chem.Int.Ed.Engl., 64:e202416348-e202416348, 2025 Cited by PubMed Abstract: Peptide stapling has emerged as a versatile approach in drug discovery to reinforce secondary structure elements especially α-helices and improve properties of linear bioactive peptides. Inspired by the prevalence of arginine in protein-protein and protein-DNA interfaces, we investigated guanidinium-stapling as a means to constrain helical peptides. Guanidinium stapling was readily achieved on solid support, utilizing two orthogonally protected lysine or unatural α-amino acid residues with an amino function. This method allows for easy modulation of the nature and size of the staple as well as helix propensity. Evaluating a set of guanidinium-stapled peptides for their interaction with different protein targets identified several binders with increased target affinity. X-ray structure determination of four complexes revealed that all stapled peptides adopt a helical conformation upon protein binding. Notably, the disubstituted guanidinium generally exhibits a distinct cis/trans conformation and, in one instance, retains a conserved hydrogen bond with the protein surface. By identifying, for the first time, the guanidinium moiety as an effective helical peptide stapling group, this research significantly expands the repertoire of α-helix stapling techniques for the creation of useful protein mimics. PubMed: 39714600DOI: 10.1002/anie.202416348 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (2.501 Å) |
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