6F09
Binary complex of 14-3-3 zeta with ubiquitin specific protease 8 (USP8) pSer718 peptide
6F09 の概要
| エントリーDOI | 10.2210/pdb6f09/pdb |
| 分子名称 | 14-3-3 protein zeta/delta, Ubiquitin carboxyl-terminal hydrolase 8 (3 entities in total) |
| 機能のキーワード | 14-3-3, usp8, phosphosite, binary complex protein-peptide, signaling protein |
| 由来する生物種 | Homo sapiens (Human) 詳細 |
| 細胞内の位置 | Cytoplasm : P63104 P40818 |
| タンパク質・核酸の鎖数 | 8 |
| 化学式量合計 | 111689.88 |
| 構造登録者 | Centorrino, F.,Ballone, A.,Ottmann, C.,Guo, S.,Leysen, S. (登録日: 2017-11-17, 公開日: 2018-03-07, 最終更新日: 2024-10-16) |
| 主引用文献 | Centorrino, F.,Ballone, A.,Wolter, M.,Ottmann, C. Biophysical and structural insight into the USP8/14-3-3 interaction. FEBS Lett., 592:1211-1220, 2018 Cited by PubMed Abstract: The ubiquitin-specific protease 8 (USP8)/14-3-3 protein-protein interaction has recently been shown to exert a significant role in the pathogenesis of Cushing's disease (CD). USP8 is a deubiquitinase that prevents epidermal growth factor receptor (EGFR) degradation. Impairment of 14-3-3 binding leads to a higher deubiquitination of EGFR and results in a higher EGFR signaling and an increased production of adrenocorticotropic hormone. Here we report the high-resolution crystal structure of the 14-3-3 binding motif of USP8 surrounding Ser718 in complex with 14-3-3ζ and characterize the interaction with fluorescence polarization and isothermal titration calorimetry. Furthermore, we analyze the effect of USP8 mutations identified in CD on binding to 14-3-3. PubMed: 29473952DOI: 10.1002/1873-3468.13017 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (1.594 Å) |
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