7ZJW の概要
| エントリーDOI | 10.2210/pdb7zjw/pdb |
| EMDBエントリー | 14751 |
| 分子名称 | eEFSec, 60S ribosomal protein L3, 60S ribosomal protein L4, ... (93 entities in total) |
| 機能のキーワード | selenocysteine, recoding, 80s, ribosome |
| 由来する生物種 | Homo sapiens (human) 詳細 |
| タンパク質・核酸の鎖数 | 86 |
| 化学式量合計 | 4626611.51 |
| 構造登録者 | |
| 主引用文献 | Hilal, T.,Killam, B.Y.,Grozdanovic, M.,Dobosz-Bartoszek, M.,Loerke, J.,Burger, J.,Mielke, T.,Copeland, P.R.,Simonovic, M.,Spahn, C.M.T. Structure of the mammalian ribosome as it decodes the selenocysteine UGA codon. Science, 376:1338-1343, 2022 Cited by PubMed Abstract: The elongation of eukaryotic selenoproteins relies on a poorly understood process of interpreting in-frame UGA stop codons as selenocysteine (Sec). We used cryo-electron microscopy to visualize Sec UGA recoding in mammals. A complex between the noncoding Sec-insertion sequence (SECIS), SECIS-binding protein 2 (SBP2), and 40 ribosomal subunit enables Sec-specific elongation factor eEFSec to deliver Sec. eEFSec and SBP2 do not interact directly but rather deploy their carboxyl-terminal domains to engage with the opposite ends of the SECIS. By using its Lys-rich and carboxyl-terminal segments, the ribosomal protein eS31 simultaneously interacts with Sec-specific transfer RNA (tRNA) and SBP2, which further stabilizes the assembly. eEFSec is indiscriminate toward l-serine and facilitates its misincorporation at Sec UGA codons. Our results support a fundamentally distinct mechanism of Sec UGA recoding in eukaryotes from that in bacteria. PubMed: 35709277DOI: 10.1126/science.abg3875 主引用文献が同じPDBエントリー |
| 実験手法 | ELECTRON MICROSCOPY (2.8 Å) |
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