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8CD5

structure of HEX-1 from N. crassa crystallized in cellulo, diffracted at 100K and resolved using CrystFEL

8CD5 の概要
エントリーDOI10.2210/pdb8cd5/pdb
関連するPDBエントリー8CD4
分子名称Woronin body major protein (2 entities in total)
機能のキーワードnaturally crystallizing, woronin body, self-assembly, hex-1, in vivo, structural protein
由来する生物種Neurospora crassa
タンパク質・核酸の鎖数1
化学式量合計19150.66
構造登録者
主引用文献Schonherr, R.,Boger, J.,Lahey-Rudolph, J.M.,Harms, M.,Kaiser, J.,Nachtschatt, S.,Wobbe, M.,Duden, R.,Konig, P.,Bourenkov, G.,Schneider, T.R.,Redecke, L.
A streamlined approach to structure elucidation using in cellulo crystallized recombinant proteins, InCellCryst.
Nat Commun, 15:1709-1709, 2024
Cited by
PubMed Abstract: With the advent of serial X-ray crystallography on microfocus beamlines at free-electron laser and synchrotron facilities, the demand for protein microcrystals has significantly risen in recent years. However, by in vitro crystallization extensive efforts are usually required to purify proteins and produce sufficiently homogeneous microcrystals. Here, we present InCellCryst, an advanced pipeline for producing homogeneous microcrystals directly within living insect cells. Our baculovirus-based cloning system enables the production of crystals from completely native proteins as well as the screening of different cellular compartments to maximize chances for protein crystallization. By optimizing cloning procedures, recombinant virus production, crystallization and crystal detection, X-ray diffraction data can be collected 24 days after the start of target gene cloning. Furthermore, improved strategies for serial synchrotron diffraction data collection directly from crystals within living cells abolish the need to purify the recombinant protein or the associated microcrystals.
PubMed: 38402242
DOI: 10.1038/s41467-024-45985-7
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.56 Å)
構造検証レポート
Validation report summary of 8cd5
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2024-11-13に公開中

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