6M91

Monophosphorylated pSer33 b-Catenin peptide, b-TrCP/Skp1, NRX-103094 ternary complex

6M91 の概要

• エントリーDOI: 10.2210/pdb6m91/pdb
• 分子名称: F-box/WD repeat-containing protein 1A, S-phase kinase-associated protein 1, Catenin beta-1, ... (7 entities in total)
• 機能のキーワード: ubiquitin molecular glue enhancer, ligase
• 由来する生物種: Homo sapiens (Human); 詳細
• タンパク質・核酸の鎖数: 3
• 化学式量合計: 70040.58

構造登録者

Simonetta, K.R.,Clifton, M.C.,Walter, R.L.,Ranieri, G.M.,Carter, J.J. (登録日: 2018-08-22, 公開日: 2019-04-03, 最終更新日: 2024-10-23)

主引用文献

Simonetta, K.R.,Taygerly, J.,Boyle, K.,Basham, S.E.,Padovani, C.,Lou, Y.,Cummins, T.J.,Yung, S.L.,von Soly, S.K.,Kayser, F.,Kuriyan, J.,Rape, M.,Cardozo, M.,Gallop, M.A.,Bence, N.F.,Barsanti, P.A.,Saha, A.
Prospective discovery of small molecule enhancers of an E3 ligase-substrate interaction.
Nat Commun, 10:1402-1402, 2019

PubMed Abstract: Protein-protein interactions (PPIs) governing the recognition of substrates by E3 ubiquitin ligases are critical to cellular function. There is significant therapeutic potential in the development of small molecules that modulate these interactions; however, rational design of small molecule enhancers of PPIs remains elusive. Herein, we report the prospective identification and rational design of potent small molecules that enhance the interaction between an oncogenic transcription factor, β-Catenin, and its cognate E3 ligase, SCF. These enhancers potentiate the ubiquitylation of mutant β-Catenin by β-TrCP in vitro and induce the degradation of an engineered mutant β-Catenin in a cellular system. Distinct from PROTACs, these drug-like small molecules insert into a naturally occurring PPI interface, with contacts optimized for both the substrate and ligase within the same small molecule entity. The prospective discovery of 'molecular glue' presented here provides a paradigm for the development of small molecule degraders targeting hard-to-drug proteins.

PubMed: 30926793
DOI: 10.1038/s41467-019-09358-9

実験手法

X-RAY DIFFRACTION (2.4 Å)