4KDT
Structure of an early native-like intermediate of beta2-microglobulin amyloidosis
4KDT の概要
| エントリーDOI | 10.2210/pdb4kdt/pdb |
| 分子名称 | Nanobody24, Beta-2-microglobulin, SULFATE ION, ... (5 entities in total) |
| 機能のキーワード | immunoglobulin fold, immune system |
| 由来する生物種 | Camelidae 詳細 |
| 細胞内の位置 | Secreted . Note=(Microbial infection) In the presence of M: P61769 |
| タンパク質・核酸の鎖数 | 4 |
| 化学式量合計 | 54422.11 |
| 構造登録者 | Vanderhaegen, S.,Fislage, M.,Pardon, E.,Versees, W.,Steyaert, J. (登録日: 2013-04-25, 公開日: 2013-08-28, 最終更新日: 2024-11-20) |
| 主引用文献 | Vanderhaegen, S.,Fislage, M.,Domanska, K.,Versees, W.,Pardon, E.,Bellotti, V.,Steyaert, J. Structure of an early native-like intermediate of beta 2-microglobulin amyloidogenesis. Protein Sci., 22:1349-1357, 2013 Cited by PubMed Abstract: To investigate early intermediates of β2-microglobulin (β2m) amyloidogenesis, we solved the structure of β2m containing the amyloidogenic Pro32Gly mutation by X-ray crystallography. One nanobody (Nb24) that efficiently blocks fibril elongation was used as a chaperone to co-crystallize the Pro32Gly β2m monomer under physiological conditions. The complex of P32G β2m with Nb24 reveals a trans peptide bond at position 32 of this amyloidogenic variant, whereas Pro32 adopts the cis conformation in the wild-type monomer, indicating that the cis to trans isomerization at Pro32 plays a critical role in the early onset of β2m amyloid formation. PubMed: 23904325DOI: 10.1002/pro.2321 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (2.6 Å) |
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