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7SPY

Get3 bound to ATP from G. intestinalis in the closed form

7SPY の概要
エントリーDOI10.2210/pdb7spy/pdb
分子名称ATPase ASNA1 homolog, ADENOSINE-5'-TRIPHOSPHATE, MAGNESIUM ION, ... (6 entities in total)
機能のキーワードtail-anchored membrane protein targeting deviant walker a atpase targeting factor, chaperone
由来する生物種Giardia intestinalis (strain ATCC 50803 / WB clone C6) (Giardia lamblia)
タンパク質・核酸の鎖数1
化学式量合計40637.71
構造登録者
Fry, M.Y.,Maggiolo, A.O.,Clemons Jr., W.M. (登録日: 2021-11-04, 公開日: 2022-07-20, 最終更新日: 2023-10-18)
主引用文献Fry, M.Y.,Najdrova, V.,Maggiolo, A.O.,Saladi, S.M.,Dolezal, P.,Clemons Jr., W.M.
Structurally derived universal mechanism for the catalytic cycle of the tail-anchored targeting factor Get3.
Nat.Struct.Mol.Biol., 29:820-830, 2022
Cited by
PubMed Abstract: Tail-anchored (TA) membrane proteins, accounting for roughly 2% of proteomes, are primarily targeted posttranslationally to the endoplasmic reticulum membrane by the guided entry of TA proteins (GET) pathway. For this complicated process, it remains unknown how the central targeting factor Get3 uses nucleotide to facilitate large conformational changes to recognize then bind clients while also preventing exposure of hydrophobic surfaces. Here, we identify the GET pathway in Giardia intestinalis and present the structure of the Get3-client complex in the critical postnucleotide-hydrolysis state, demonstrating that Get3 reorganizes the client-binding domain (CBD) to accommodate and shield the client transmembrane helix. Four additional structures of GiGet3, spanning the nucleotide-free (apo) open to closed transition and the ATP-bound state, reveal the details of nucleotide stabilization and occluded CBD. This work resolves key conundrums and allows for a complete model of the dramatic conformational landscape of Get3.
PubMed: 35851188
DOI: 10.1038/s41594-022-00798-4
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.23 Å)
構造検証レポート
Validation report summary of 7spy
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2026-04-15に公開中

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