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7BEQ

MicroED structure of the MyD88 TIR domain higher-order assembly

7BEQ の概要
エントリーDOI10.2210/pdb7beq/pdb
分子名称Myeloid differentiation primary response protein MyD88 (1 entity in total)
機能のキーワードmicroed, myd88, tir domain, higher-order assembly, protein binding
由来する生物種Homo sapiens (Human)
タンパク質・核酸の鎖数1
化学式量合計17833.85
構造登録者
主引用文献Clabbers, M.T.B.,Holmes, S.,Muusse, T.W.,Vajjhala, P.R.,Thygesen, S.J.,Malde, A.K.,Hunter, D.J.B.,Croll, T.I.,Flueckiger, L.,Nanson, J.D.,Rahaman, M.H.,Aquila, A.,Hunter, M.S.,Liang, M.,Yoon, C.H.,Zhao, J.,Zatsepin, N.A.,Abbey, B.,Sierecki, E.,Gambin, Y.,Stacey, K.J.,Darmanin, C.,Kobe, B.,Xu, H.,Ve, T.
MyD88 TIR domain higher-order assembly interactions revealed by microcrystal electron diffraction and serial femtosecond crystallography.
Nat Commun, 12:2578-2578, 2021
Cited by
PubMed Abstract: MyD88 and MAL are Toll-like receptor (TLR) adaptors that signal to induce pro-inflammatory cytokine production. We previously observed that the TIR domain of MAL (MAL) forms filaments in vitro and induces formation of crystalline higher-order assemblies of the MyD88 TIR domain (MyD88). These crystals are too small for conventional X-ray crystallography, but are ideally suited to structure determination by microcrystal electron diffraction (MicroED) and serial femtosecond crystallography (SFX). Here, we present MicroED and SFX structures of the MyD88 assembly, which reveal a two-stranded higher-order assembly arrangement of TIR domains analogous to that seen previously for MAL. We demonstrate via mutagenesis that the MyD88 assembly interfaces are critical for TLR4 signaling in vivo, and we show that MAL promotes unidirectional assembly of MyD88. Collectively, our studies provide structural and mechanistic insight into TLR signal transduction and allow a direct comparison of the MicroED and SFX techniques.
PubMed: 33972532
DOI: 10.1038/s41467-021-22590-6
主引用文献が同じPDBエントリー
実験手法
ELECTRON CRYSTALLOGRAPHY (3 Å)
構造検証レポート
Validation report summary of 7beq
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2024-10-30に公開中

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