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8G4Y

Structure of ZNRF3 ECD bound to peptide MK1-3.6.10

8G4Y の概要
エントリーDOI10.2210/pdb8g4y/pdb
分子名称E3 ubiquitin-protein ligase ZNRF3, MK1-3.6.10 (3 entities in total)
機能のキーワードubiquitin ligase, wnt signal, cell surface, ckp, ligase
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24162.19
構造登録者
Harris, S.F.,Wu, P. (登録日: 2023-02-10, 公開日: 2023-12-20, 最終更新日: 2024-10-23)
主引用文献Kschonsak, Y.T.,Gao, X.,Miller, S.E.,Hwang, S.,Marei, H.,Wu, P.,Li, Y.,Ruiz, K.,Dorighi, K.,Holokai, L.,Perampalam, P.,Tsai, W.K.,Kee, Y.S.,Agard, N.J.,Harris, S.F.,Hannoush, R.N.,de Sousa E Melo, F.
Potent and selective binders of the E3 ubiquitin ligase ZNRF3 stimulate Wnt signaling and intestinal organoid growth.
Cell Chem Biol, 31:1176-, 2024
Cited by
PubMed Abstract: Selective and precise activation of signaling transduction cascades is key for cellular reprogramming and tissue regeneration. However, the development of small- or large-molecule agonists for many signaling pathways has remained elusive and is rate limiting to realize the full clinical potential of regenerative medicine. Focusing on the Wnt pathway, here we describe a series of disulfide-constrained peptides (DCPs) that promote Wnt signaling activity by modulating the cell surface levels of ZNRF3, an E3 ubiquitin ligase that controls the abundance of the Wnt receptor complex FZD/LRP at the plasma membrane. Mechanistically, monomeric DCPs induce ZNRF3 ubiquitination, leading to its cell surface clearance, ultimately resulting in FZD stabilization. Furthermore, we engineered multimeric DCPs that induce expansive growth of human intestinal organoids, revealing a dependence between valency and ZNRF3 clearance. Our work highlights a strategy for the development of potent, biologically active Wnt signaling pathway agonists via targeting of ZNRF3.
PubMed: 38056465
DOI: 10.1016/j.chembiol.2023.11.006
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.41 Å)
構造検証レポート
Validation report summary of 8g4y
検証レポート(詳細版)ダウンロードをダウンロード

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件を2026-04-22に公開中

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