4DKI
Structural Insights into the Anti- Methicillin-Resistant Staphylococcus aureus (MRSA) Activity of Ceftobiprole
4DKI の概要
| エントリーDOI | 10.2210/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 | |
| 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: 22815485DOI: 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) |
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