2LR3
Solution structure of the anti-fungal defensin DEF4 (MTR_8g070770) from Medicago truncatula (barrel clover)
2LR3 の概要
| エントリーDOI | 10.2210/pdb2lr3/pdb |
| NMR情報 | BMRB: 18345 |
| 分子名称 | Defensin (1 entity in total) |
| 機能のキーワード | fungal disease, antifungal agent, antifungal protein |
| 由来する生物種 | Medicago truncatula (Barrel medic) |
| タンパク質・核酸の鎖数 | 1 |
| 化学式量合計 | 5355.10 |
| 構造登録者 | |
| 主引用文献 | Sagaram, U.S.,El-Mounadi, K.,Buchko, G.W.,Berg, H.R.,Kaur, J.,Pandurangi, R.S.,Smith, T.J.,Shah, D.M. Structural and Functional Studies of a Phosphatidic Acid-Binding Antifungal Plant Defensin MtDef4: Identification of an RGFRRR Motif Governing Fungal Cell Entry. Plos One, 8:e82485-e82485, 2013 Cited by PubMed Abstract: MtDef4 is a 47-amino acid cysteine-rich evolutionary conserved defensin from a model legume Medicago truncatula. It is an apoplast-localized plant defense protein that inhibits the growth of the ascomycetous fungal pathogen Fusarium graminearum in vitro at micromolar concentrations. Little is known about the mechanisms by which MtDef4 mediates its antifungal activity. In this study, we show that MtDef4 rapidly permeabilizes fungal plasma membrane and is internalized by the fungal cells where it accumulates in the cytoplasm. Furthermore, analysis of the structure of MtDef4 reveals the presence of a positively charged γ-core motif composed of β2 and β3 strands connected by a positively charged RGFRRR loop. Replacement of the RGFRRR sequence with AAAARR or RGFRAA abolishes the ability of MtDef4 to enter fungal cells, suggesting that the RGFRRR loop is a translocation signal required for the internalization of the protein. MtDef4 binds to phosphatidic acid (PA), a precursor for the biosynthesis of membrane phospholipids and a signaling lipid known to recruit cytosolic proteins to membranes. Amino acid substitutions in the RGFRRR sequence which abolish the ability of MtDef4 to enter fungal cells also impair its ability to bind PA. These findings suggest that MtDef4 is a novel antifungal plant defensin capable of entering into fungal cells and affecting intracellular targets and that these processes are mediated by the highly conserved cationic RGFRRR loop via its interaction with PA. PubMed: 24324798DOI: 10.1371/journal.pone.0082485 主引用文献が同じPDBエントリー |
| 実験手法 | SOLUTION NMR |
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