2LR5
1H chemical shift assignments for micasin
2LR5 の概要
| エントリーDOI | 10.2210/pdb2lr5/pdb |
| NMR情報 | BMRB: 18347 |
| 分子名称 | micasin (1 entity in total) |
| 機能のキーワード | antimicrobial protein |
| 由来する生物種 | Arthroderma otae (Microsporum canis) |
| タンパク質・核酸の鎖数 | 1 |
| 化学式量合計 | 4067.70 |
| 構造登録者 | |
| 主引用文献 | Zhu, S.,Gao, B.,Harvey, P.J.,Craik, D.J. Dermatophytic defensin with antiinfective potential Proc.Natl.Acad.Sci.USA, 109:8495-8500, 2012 Cited by PubMed Abstract: Fungi are a newly emerging source of peptide antibiotics with therapeutic potential. Here, we report 17 new fungal defensin-like peptide (fDLP) genes and the detailed characterization of a corresponding synthetic fDLP (micasin) from a dermatophyte in terms of its structure, activity and therapeutic potential. NMR analysis showed that synthetic micasin adopts a "hallmark" cysteine-stabilized α-helical and β-sheet fold. It was active on both gram-positive and gram-negative bacteria, and importantly it killed two clinical isolates of methicillin-resistant Staphylococcus aureus and the opportunistic pathogen Pseudomonas aeruginosa at low micromolar concentrations. Micasin killed approximately 100% of treated bacteria within 3 h through a membrane nondisruptive mechanism of action, and showed extremely low hemolysis and high serum stability. Consistent with these functional properties, micasin increases survival in mice infected by the pathogenic bacteria in a peritonitis model. Our work represents a valuable approach to explore novel peptide antibiotics from a large resource of fungal genomes. PubMed: 22586077DOI: 10.1073/pnas.1201263109 主引用文献が同じPDBエントリー |
| 実験手法 | SOLUTION NMR |
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