2GK7
Structural and Functional insights into the human Upf1 helicase core
2GK7 の概要
| エントリーDOI | 10.2210/pdb2gk7/pdb |
| 関連するPDBエントリー | 2GJK 2GK6 2GK8 |
| 分子名称 | Regulator of nonsense transcripts 1, PHOSPHATE ION (3 entities in total) |
| 機能のキーワード | upf1, helicase, nmd, hydrolase |
| 由来する生物種 | Homo sapiens (human) |
| 細胞内の位置 | Cytoplasm: Q92900 |
| タンパク質・核酸の鎖数 | 1 |
| 化学式量合計 | 70151.39 |
| 構造登録者 | |
| 主引用文献 | Cheng, Z.,Muhlrad, D.,Lim, M.K.,Parker, R.,Song, H. Structural and functional insights into the human Upf1 helicase core Embo J., 26:253-264, 2007 Cited by PubMed Abstract: Nonsense-mediated mRNA decay (NMD) is an mRNA surveillance pathway that recognizes and degrades aberrant mRNAs containing premature stop codons. A critical protein in NMD is Upf1p, which belongs to the helicase super family 1 (SF1), and is thought to utilize the energy of ATP hydrolysis to promote transitions in the structure of RNA or RNA-protein complexes. The crystal structure of the catalytic core of human Upf1p determined in three states (phosphate-, AMPPNP- and ADP-bound forms) reveals an overall structure containing two RecA-like domains with two additional domains protruding from the N-terminal RecA-like domain. Structural comparison combined with mutational analysis identifies a likely single-stranded RNA (ssRNA)-binding channel, and a cycle of conformational change coupled to ATP binding and hydrolysis. These conformational changes alter the likely ssRNA-binding channel in a manner that can explain how ATP binding destabilizes ssRNA binding to Upf1p. PubMed: 17159905DOI: 10.1038/sj.emboj.7601464 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (2.8 Å) |
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