7NMA

Crystal structure of 14-3-3 sigma in complex with 13mer Amot-p130 peptide

7NMA の概要

• エントリーDOI: 10.2210/pdb7nma/pdb
• 分子名称: 14-3-3 protein sigma, Amot-p130 phosphopeptide (pS175), CHLORIDE ION, ... (5 entities in total)
• 機能のキーワード: protein-peptide complex, signaling protein
• 由来する生物種: Homo sapiens (Human); 詳細
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 29913.09

構造登録者

Centorrino, F.,Ottmann, C. (登録日: 2021-02-23, 公開日: 2022-01-12, 最終更新日: 2024-01-31)

主引用文献

Centorrino, F.,Andlovic, B.,Cossar, P.,Brunsveld, L.,Ottmann, C.
Fragment-based exploration of the 14-3-3/Amot-p130 interface.
Curr Res Struct Biol, 4:21-28, 2022

PubMed Abstract: The modulation of protein-protein interactions (PPIs) has developed into a well-established field of drug discovery. Despite the advances achieved in the field, many PPIs are still deemed as ' targets and the design of PPIs stabilizers remains a significant challenge. The application of fragment-based methods for the identification of drug leads and to evaluate the ' of the desired protein target has seen a remarkable development in recent years. In this study, we explore the molecular characteristics of the 14-3-3/Amot-p130 PPI and the conceptual possibility of targeting this interface using X-ray crystallography fragment-based screening. We report the first structural elucidation of the 14-3-3 binding motif of Amot-p130 and the characterization of the binding mode and affinities involved. We made use of fragments to probe the ' of the 14-3-3/Amot-p130 composite binding pocket. Here we disclose initial hits with promising stabilizing activity and an early-stage selectivity toward the Amot-p130 motifs over other representatives 14-3-3 partners. Our findings highlight the potential of using fragments to characterize and explore proteins' surfaces and might provide a starting point toward the development of small molecules capable of acting as .

PubMed: 35036934
DOI: 10.1016/j.crstbi.2021.12.003

実験手法

X-RAY DIFFRACTION (1.75 Å)