2LAI
Hyaloperonospora arabidopsidis Effector Protein ATR13
2LAI の概要
| エントリーDOI | 10.2210/pdb2lai/pdb |
| NMR情報 | BMRB: 17525 |
| 分子名称 | Avirulence protein ATR13 (1 entity in total) |
| 機能のキーワード | nucleolar localization, signaling protein |
| 由来する生物種 | Hyaloperonospora parasitica |
| タンパク質・核酸の鎖数 | 1 |
| 化学式量合計 | 11305.88 |
| 構造登録者 | Leonelli, L.,Pelton, J.G.,Wemmer, D.E.,Staskawicz, B.J. (登録日: 2011-03-15, 公開日: 2012-01-18, 最終更新日: 2024-05-01) |
| 主引用文献 | Leonelli, L.,Pelton, J.,Schoeffler, A.,Dahlbeck, D.,Berger, J.,Wemmer, D.E.,Staskawicz, B. Structural Elucidation and Functional Characterization of the Hyaloperonospora arabidopsidis Effector Protein ATR13. Plos Pathog., 7:e1002428-e1002428, 2011 Cited by PubMed Abstract: The oomycete Hyaloperonospora arabidopsidis (Hpa) is the causal agent of downy mildew on the model plant Arabidopsis thaliana and has been adapted as a model system to investigate pathogen virulence strategies and plant disease resistance mechanisms. Recognition of Hpa infection occurs when plant resistance proteins (R-genes) detect the presence or activity of pathogen-derived protein effectors delivered to the plant host. This study examines the Hpa effector ATR13 Emco5 and its recognition by RPP13-Nd, the cognate R-gene that triggers programmed cell death (HR) in the presence of recognized ATR13 variants. Herein, we use NMR to solve the backbone structure of ATR13 Emco5, revealing both a helical domain and a disordered internal loop. Additionally, we use site-directed and random mutagenesis to identify several amino acid residues involved in the recognition response conferred by RPP13-Nd. Using our structure as a scaffold, we map these residues to one of two surface-exposed patches of residues under diversifying selection. Exploring possible roles of the disordered region within the ATR13 structure, we perform domain swapping experiments and identify a peptide sequence involved in nucleolar localization. We conclude that ATR13 is a highly dynamic protein with no clear structural homologues that contains two surface-exposed patches of polymorphism, only one of which is involved in RPP13-Nd recognition specificity. PubMed: 22194684DOI: 10.1371/journal.ppat.1002428 主引用文献が同じPDBエントリー |
| 実験手法 | SOLUTION NMR |
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