4JF4
OXA-23 meropenem complex
4JF4 の概要
| エントリーDOI | 10.2210/pdb4jf4/pdb |
| 関連するPDBエントリー | 4JF5 4JF6 |
| 分子名称 | Beta-lactamase, 1,2-ETHANEDIOL, (4R,5S)-3-{[(3S,5S)-5-(dimethylcarbamoyl)pyrrolidin-3-yl]sulfanyl}-5-[(2S,3R)-3-hydroxy-1-oxobutan-2-yl]-4-methyl-4,5-d ihydro-1H-pyrrole-2-carboxylic acid, ... (4 entities in total) |
| 機能のキーワード | beta-lactamase, hydrolase-hydrolase inhibitor complex, hydrolase/hydrolase inhibitor |
| 由来する生物種 | Acinetobacter baumannii |
| タンパク質・核酸の鎖数 | 2 |
| 化学式量合計 | 56126.89 |
| 構造登録者 | |
| 主引用文献 | Smith, C.A.,Antunes, N.T.,Stewart, N.K.,Toth, M.,Kumarasiri, M.,Chang, M.,Mobashery, S.,Vakulenko, S.B. Structural Basis for Carbapenemase Activity of the OXA-23 beta-Lactamase from Acinetobacter baumannii. Chem.Biol., 20:1107-1115, 2013 Cited by PubMed Abstract: Dissemination of Acinetobacter baumannii strains harboring class D β-lactamases producing resistance to carbapenem antibiotics severely limits our ability to treat deadly Acinetobacter infections. Susceptibility determination in the A. baumannii background and kinetic studies with a homogeneous preparation of OXA-23 β-lactamase, the major carbapenemase present in A. baumannii, document the ability of this enzyme to manifest resistance to last-resort carbapenem antibiotics. We also report three X-ray structures of OXA-23: apo OXA-23 at two different pH values, and wild-type OXA-23 in complex with meropenem, a carbapenem substrate. The structures and dynamics simulations reveal an important role for Leu166, whose motion regulates the access of a hydrolytic water molecule to the acyl-enzyme species in imparting carbapenemase activity. PubMed: 24012371DOI: 10.1016/j.chembiol.2013.07.015 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (2.14 Å) |
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