6GF2
The structure of the ubiquitin-like modifier FAT10 reveals a novel targeting mechanism for degradation by the 26S proteasome
6GF2 の概要
| エントリーDOI | 10.2210/pdb6gf2/pdb |
| NMR情報 | BMRB: 27466 |
| 分子名称 | Ubiquitin D (1 entity in total) |
| 機能のキーワード | fat10, ubiquitin-like modifier, proteasome, degradation, immune system |
| 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 | 9263.70 |
| 構造登録者 | Aichem, A.,Anders, S.,Catone, N.,Roessler, P.,Stotz, S.,Berg, A.,Schwab, R.,Scheuermann, S.,Bialas, J.,Schmidtke, G.,Peter, C.,Groettrup, M.,Wiesner, S. (登録日: 2018-04-29, 公開日: 2018-08-08, 最終更新日: 2024-06-19) |
| 主引用文献 | Aichem, A.,Anders, S.,Catone, N.,Stotz, S.,Berg, A.,Schwab, R.,Scheuermann, S.,Bialas, J.,Schutz-Stoffregen, M.C.,Schmidtke, G.,Peter, C.,Groettrup, M.,Wiesner, S. The structure of the ubiquitin-like modifier FAT10 reveals an alternative targeting mechanism for proteasomal degradation. Nat Commun, 9:3321-3321, 2018 Cited by PubMed Abstract: FAT10 is a ubiquitin-like modifier that directly targets proteins for proteasomal degradation. Here, we report the high-resolution structures of the two individual ubiquitin-like domains (UBD) of FAT10 that are joined by a flexible linker. While the UBDs of FAT10 show the typical ubiquitin-fold, their surfaces are entirely different from each other and from ubiquitin explaining their unique binding specificities. Deletion of the linker abrogates FAT10-conjugation while its mutation blocks auto-FAT10ylation of the FAT10-conjugating enzyme USE1 but not bulk conjugate formation. FAT10- but not ubiquitin-mediated degradation is independent of the segregase VCP/p97 in the presence but not the absence of FAT10's unstructured N-terminal heptapeptide. Stabilization of the FAT10 UBDs strongly decelerates degradation suggesting that the intrinsic instability of FAT10 together with its disordered N-terminus enables the rapid, joint degradation of FAT10 and its substrates without the need for FAT10 de-conjugation and partial substrate unfolding. PubMed: 30127417DOI: 10.1038/s41467-018-05776-3 主引用文献が同じPDBエントリー |
| 実験手法 | SOLUTION NMR |
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