2RK4
Structure of M26I DJ-1
2RK4 の概要
エントリーDOI | 10.2210/pdb2rk4/pdb |
関連するPDBエントリー | 2RK3 |
分子名称 | Protein DJ-1 (2 entities in total) |
機能のキーワード | parkinson's disease, thij, pfpi, chaperone, cytoplasm, disease mutation, nucleus, oncogene, oxidation, parkinson disease, phosphorylation, polymorphism, ubl conjugation |
由来する生物種 | Homo sapiens (human) |
細胞内の位置 | Cytoplasm: Q99497 |
タンパク質・核酸の鎖数 | 1 |
化学式量合計 | 20970.17 |
構造登録者 | Lakshminarasimhan, M.,Maldonado, M.T.,Zhou, W.,Fink, A.L.,Wilson, M.A. (登録日: 2007-10-16, 公開日: 2008-01-15, 最終更新日: 2023-08-30) |
主引用文献 | Lakshminarasimhan, M.,Maldonado, M.T.,Zhou, W.,Fink, A.L.,Wilson, M.A. Structural Impact of Three Parkinsonism-Associated Missense Mutations on Human DJ-1. Biochemistry, 47:1381-1392, 2008 Cited by PubMed Abstract: A number of missense mutations in the oxidative stress response protein DJ-1 are implicated in rare forms of familial Parkinsonism. The best-characterized Parkinsonian DJ-1 missense mutation, L166P, disrupts homodimerization and results in a poorly folded protein. The molecular basis by which the other Parkinsonism-associated mutations disrupt the function of DJ-1, however, is incompletely understood. In this study we show that three different Parkinsonism-associated DJ-1 missense mutations (A104T, E163K, and M26I) reduce the thermal stability of DJ-1 in solution by subtly perturbing the structure of DJ-1 without causing major folding defects or loss of dimerization. Atomic resolution X-ray crystallography shows that the A104T substitution introduces water and a discretely disordered residue into the core of the protein, E163K disrupts a key salt bridge with R145, and M26I causes packing defects in the core of the dimer. The deleterious effect of each Parkinsonism-associated mutation on DJ-1 is dissected by analysis of engineered substitutions (M26L, A104V, and E163K/R145E) that partially alleviate each of the defects introduced by the A104T, E163K and M26I mutations. In total, our results suggest that the protective function of DJ-1 can be compromised by diverse perturbations in its structural integrity, particularly near the junctions of secondary structural elements. PubMed: 18181649DOI: 10.1021/bi701189c 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (1.15 Å) |
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