3BM6
AmpC beta-lactamase in complex with a p.carboxyphenylboronic acid
3BM6 の概要
| エントリーDOI | 10.2210/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 | |
| 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: 20452208DOI: 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) |
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