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3BM6

AmpC beta-lactamase in complex with a p.carboxyphenylboronic acid

3BM6 の概要
エントリーDOI10.2210/pdb3bm6/pdb
関連するPDBエントリー1C3B 1GA9 2I72
分子名称Beta-lactamase, 4-(dihydroxyboranyl)-2-({[4-(phenylsulfonyl)thiophen-2-yl]sulfonyl}amino)benzoic acid (3 entities in total)
機能のキーワードampc, beta-lactamases, cephalosporinase, serine hydrolase, covalent inhibition, antibiotic resistance, periplasm, hydrolase
由来する生物種Escherichia coli
細胞内の位置Periplasm: P00811
タンパク質・核酸の鎖数2
化学式量合計80110.45
構造登録者
Tondi, D. (登録日: 2007-12-12, 公開日: 2009-02-17, 最終更新日: 2024-10-09)
主引用文献Tondi, D.,Calo, S.,Shoichet, B.K.,Costi, M.P.
Structural study of phenyl boronic acid derivatives as AmpC beta-lactamase inhibitors.
Bioorg.Med.Chem.Lett., 20:3416-3419, 2010
Cited by
PubMed Abstract: A small set of boronic acids acting as low nanomolar inhibitors of AmpC beta-lactamase were designed and synthesized in the effort to improve affinity, pharmacokinetic properties, and to provide a valid lead compound. X-ray crystallography revealed the binary complex of the best inhibitor bound to the enzyme, highlighting possibilities for its further rational derivatization and chemical optimization.
PubMed: 20452208
DOI: 10.1016/j.bmcl.2010.04.007
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.1 Å)
構造検証レポート
Validation report summary of 3bm6
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2025-12-31に公開中

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