6E54

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

6E54 の概要

• エントリーDOI: 10.2210/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,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: 2023-10-11)

• 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