6PQA
GAVVGG segment 119-124 from human prion
6PQA の概要
エントリーDOI | 10.2210/pdb6pqa/pdb |
関連するPDBエントリー | 6PQ5 |
分子名称 | Major prion protein (2 entities in total) |
機能のキーワード | amyloid-like protofibril, protein fibril |
由来する生物種 | Homo sapiens (Human) |
タンパク質・核酸の鎖数 | 1 |
化学式量合計 | 458.51 |
構造登録者 | |
主引用文献 | Glynn, C.,Sawaya, M.R.,Ge, P.,Gallagher-Jones, M.,Short, C.W.,Bowman, R.,Apostol, M.,Zhou, Z.H.,Eisenberg, D.S.,Rodriguez, J.A. Cryo-EM structure of a human prion fibril with a hydrophobic, protease-resistant core. Nat.Struct.Mol.Biol., 27:417-423, 2020 Cited by PubMed Abstract: Self-templating assemblies of the human prion protein are clinically associated with transmissible spongiform encephalopathies. Here we present the cryo-EM structure of a denaturant- and protease-resistant fibril formed in vitro spontaneously by a 9.7-kDa unglycosylated fragment of the human prion protein. This human prion fibril contains two protofilaments intertwined with screw symmetry and linked by a tightly packed hydrophobic interface. Each protofilament consists of an extended beta arch formed by residues 106 to 145 of the prion protein, a hydrophobic and highly fibrillogenic disease-associated segment. Such structures of prion polymorphs serve as blueprints on which to evaluate the potential impact of sequence variants on prion disease. PubMed: 32284600DOI: 10.1038/s41594-020-0403-y 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (1.46 Å) |
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