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4ZXB

Structure of the human insulin receptor ectodomain, IRDeltabeta construct, in complex with four Fab molecules

2DTG」から置き換えられました3LOH」から置き換えられました
4ZXB の概要
エントリーDOI10.2210/pdb4zxb/pdb
分子名称Fab 83-7 heavy chain, 2-acetamido-2-deoxy-beta-D-glucopyranose, Fab 83-7 light chain, ... (10 entities in total)
機能のキーワードreceptor tyrosine kinase extracellular domain antibody fragments, hormone receptor-immune system complex, hormone receptor/immune system
由来する生物種Mus musculus
詳細
タンパク質・核酸の鎖数5
化学式量合計202011.27
構造登録者
Croll, T.,Smith, B.J.,Margetts, M.B.,Whittaker, J.,Weiss, M.A.,Ward, C.W.,Lawrence, M.C. (登録日: 2015-05-20, 公開日: 2016-02-24, 最終更新日: 2024-11-20)
主引用文献Croll, T.I.,Smith, B.J.,Margetts, M.B.,Whittaker, J.,Weiss, M.A.,Ward, C.W.,Lawrence, M.C.
Higher-Resolution Structure of the Human Insulin Receptor Ectodomain: Multi-Modal Inclusion of the Insert Domain.
Structure, 24:469-476, 2016
Cited by
PubMed Abstract: Insulin receptor (IR) signaling is critical to controlling nutrient uptake and metabolism. However, only a low-resolution (3.8 Å) structure currently exists for the IR ectodomain, with some segments ill-defined or unmodeled due to disorder. Here, we revise this structure using new diffraction data to 3.3 Å resolution that allow improved modeling of the N-linked glycans, the first and third fibronectin type III domains, and the insert domain. A novel haptic interactive molecular dynamics strategy was used to aid fitting to low-resolution electron density maps. The resulting model provides a foundation for investigation of structural transitions in IR upon ligand binding.
PubMed: 26853939
DOI: 10.1016/j.str.2015.12.014
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (3.3 Å)
構造検証レポート
Validation report summary of 4zxb
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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