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4DKI

Structural Insights into the Anti- Methicillin-Resistant Staphylococcus aureus (MRSA) Activity of Ceftobiprole

4DKI の概要
エントリーDOI10.2210/pdb4dki/pdb
分子名称Penicillin-binding protein 2', (2R)-2-[(1R)-1-{[(2Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2-(hydroxyimino)acetyl]amino}-2-oxoethyl]-5-({2-oxo-1-[(3R)-pyr rolidin-3-yl]-2,5-dihydro-1H-pyrrol-3-yl}methyl)-3,6-dihydro-2H-1,3-thiazine-4-carboxylic acid, BICARBONATE ION, ... (6 entities in total)
機能のキーワードenzyme, hydrolase-antibiotic complex, hydrolase/antibiotic
由来する生物種Staphylococcus aureus
タンパク質・核酸の鎖数2
化学式量合計149800.43
構造登録者
Lovering, A.L.,Gretes, M.C.,Strynadka, N.C.J. (登録日: 2012-02-03, 公開日: 2012-08-01, 最終更新日: 2024-10-09)
主引用文献Lovering, A.L.,Gretes, M.C.,Safadi, S.S.,Danel, F.,de Castro, L.,Page, M.G.,Strynadka, N.C.
Structural Insights into the Anti-methicillin-resistant Staphylococcus aureus (MRSA) Activity of Ceftobiprole.
J.Biol.Chem., 287:32096-32102, 2012
Cited by
PubMed Abstract: Methicillin-resistant Staphylococcus aureus (MRSA) is an antibiotic-resistant strain of S. aureus afflicting hospitals and communities worldwide. Of greatest concern is its development of resistance to current last-line-of-defense antibiotics; new therapeutics are urgently needed to combat this pathogen. Ceftobiprole is a recently developed, latest generation cephalosporin and has been the first to show activity against MRSA by inhibiting essential peptidoglycan transpeptidases, including the β-lactam resistance determinant PBP2a, from MRSA. Here we present the structure of the complex of ceftobiprole bound to PBP2a. This structure provides the first look at the molecular details of an effective β-lactam-resistant PBP interaction, leading to new insights into the mechanism of ceftobiprole efficacy against MRSA.
PubMed: 22815485
DOI: 10.1074/jbc.M112.355644
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.9 Å)
構造検証レポート
Validation report summary of 4dki
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2026-02-11に公開中

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