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6E54

Crystal structure of LpxC from Pseudomonas aeruginosa in complex with ligand PT802

6E54 の概要
エントリーDOI10.2210/pdb6e54/pdb
関連するPDBエントリー5UPG 5VWM 6C9C 6CAX 6DUI
分子名称UDP-3-O-acyl-N-acetylglucosamine deacetylase, (2S)-4-{4-[4-(benzyloxy)-2-fluorophenyl]-2-oxopyridin-1(2H)-yl}-N-hydroxy-2-methyl-2-(methylsulfonyl)butanamide, (2R)-4-{4-[4-(benzyloxy)-2-fluorophenyl]-2-oxopyridin-1(2H)-yl}-N-hydroxy-2-methyl-2-(methylsulfonyl)butanamide, ... (7 entities in total)
機能のキーワードinhibitor, structural genomics, seattle structural genomics center for infectious disease, ssgcid, lpxc, hydrolase-hydrolase inhibitor complex, hydrolase/hydrolase inhibitor
由来する生物種Pseudomonas aeruginosa
タンパク質・核酸の鎖数1
化学式量合計34755.65
構造登録者
Seattle Structural Genomics Center for Infectious Disease (SSGCID) (登録日: 2018-07-19, 公開日: 2019-06-26, 最終更新日: 2025-10-22)
主引用文献Delker, S.L.,Mayclin, S.J.,Phan, J.N.,Abendroth, J.,Lorimer, D.,Edwards, T.E.
Crystal structure of LpxC from Pseudomonas aeruginosa in complex with ligand PT802
to be published,
実験手法
X-RAY DIFFRACTION (1.65 Å)
構造検証レポート
Validation report summary of 6e54
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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