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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DOI10.2210/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: 29473952
DOI: 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)
構造検証レポート
Validation report summary of 6f09
検証レポート(詳細版)ダウンロードをダウンロード

246905

件を2025-12-31に公開中

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