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6PNY

X-ray Structure of Flpp3

6PNY の概要
エントリーDOI10.2210/pdb6pny/pdb
関連するPDBエントリー2MU4
分子名称Flpp3 (2 entities in total)
機能のキーワードvirulence determinant, lipoprotein, allergen
由来する生物種Francisella tularensis subsp. tularensis (strain SCHU S4 / Schu 4)
タンパク質・核酸の鎖数1
化学式量合計13329.56
構造登録者
主引用文献Zook, J.,Shekhar, M.,Hansen, D.,Conrad, C.,Grant, T.,Gupta, C.,White, T.,Barty, A.,Basu, S.,Zhao, Y.,Zatsepin, N.,Ishchenko, A.,Batyuk, A.,Gati, C.,Li, C.,Galli, L.,Coe, J.,Hunter, M.,Liang, M.,Weierstall, U.,Nelson, G.,James, D.,Stauch, B.,Craciunescu, F.,Thifault, D.,Liu, W.,Cherezov, V.,Singharoy, A.,Fromme, P.
XFEL and NMR Structures of Francisella Lipoprotein Reveal Conformational Space of Drug Target against Tularemia.
Structure, 28:540-, 2020
Cited by
PubMed Abstract: Francisella tularensis is the causative agent for the potentially fatal disease tularemia. The lipoprotein Flpp3 has been identified as a virulence determinant of tularemia with no sequence homology outside the Francisella genus. We report a room temperature structure of Flpp3 determined by serial femtosecond crystallography that exists in a significantly different conformation than previously described by the NMR-determined structure. Furthermore, we investigated the conformational space and energy barriers between these two structures by molecular dynamics umbrella sampling and identified three low-energy intermediate states, transitions between which readily occur at room temperature. We have also begun to investigate organic compounds in silico that may act as inhibitors to Flpp3. This work paves the road to developing targeted therapeutics against tularemia and aides in our understanding of the disease mechanisms of tularemia.
PubMed: 32142641
DOI: 10.1016/j.str.2020.02.005
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.65 Å)
構造検証レポート
Validation report summary of 6pny
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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