2M2C
Solution structure of Duplex DNA
2M2C の概要
エントリーDOI | 10.2210/pdb2m2c/pdb |
NMR情報 | BMRB: 18907 |
分子名称 | DNA (5'-D(*GP*CP*GP*CP*AP*TP*GP*CP*TP*AP*CP*GP*CP*G)-3'), DNA (5'-D(*CP*GP*CP*GP*TP*AP*GP*CP*AP*TP*GP*CP*GP*C)-3') (2 entities in total) |
機能のキーワード | duplex dna, gg28, dna |
由来する生物種 | Synthetic DNA 詳細 |
タンパク質・核酸の鎖数 | 2 |
化学式量合計 | 8563.56 |
構造登録者 | |
主引用文献 | Ghosh, A.,Kar, R.K.,Jana, J.,Saha, A.,Jana, B.,Krishnamoorthy, J.,Kumar, D.,Ghosh, S.,Chatterjee, S.,Bhunia, A. Indolicidin targets duplex DNA: structural and mechanistic insight through a combination of spectroscopy and microscopy. Chemmedchem, 9:2052-2058, 2014 Cited by PubMed Abstract: Indolicidin (IR13), a 13-residue antimicrobial peptide from the cathelicidin family, is known to exhibit a broad spectrum of antimicrobial activity against various microorganisms. This peptide inhibits bacterial DNA synthesis resulting in cell filamentation. However, the precise mechanism remains unclear and requires further investigation. The central PWWP motif of IR13 provides a unique structural element that can wrap around, and thus stabilize, duplex B-type DNA structures. Replacements of the central Trp-Trp pair with Ala-Ala, His-His, or Phe-Phe residues in the PxxP motif significantly affects the ability of the peptide to stabilize duplex DNA. Results of microscopy studies in conjunction with spectroscopic data confirm that the DNA duplex is stabilized by IR13, thereby inhibiting DNA replication and transcription. In this study we provide high-resolution structural information on the interaction between indolicidin and DNA, which will be beneficial for the design of novel therapeutic antibiotics based on peptide scaffolds. PubMed: 25044630DOI: 10.1002/cmdc.201402215 主引用文献が同じPDBエントリー |
実験手法 | SOLUTION NMR |
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