5ULI
Crystal Structure of mouse DXO in complex with (3'-NADP)+ and calcium ion
5ULI の概要
| エントリーDOI | 10.2210/pdb5uli/pdb |
| 分子名称 | Decapping and exoribonuclease protein, CALCIUM ION, [[(2R,3S,4R,5R)-5-(3-aminocarbonyl-4H-pyridin-1-yl)-3,4-bis(oxidanyl)oxolan-2-yl]methoxy-oxidanyl-phosphoryl] [(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-4-oxidanyl-3-phosphonooxy-oxolan-2-yl]methyl hydrogen phosphate, ... (4 entities in total) |
| 機能のキーワード | hydrolase, nadp |
| 由来する生物種 | Mus musculus (Mouse) |
| 細胞内の位置 | Nucleus : O70348 |
| タンパク質・核酸の鎖数 | 1 |
| 化学式量合計 | 43918.03 |
| 構造登録者 | |
| 主引用文献 | Jiao, X.,Doamekpor, S.K.,Bird, J.G.,Nickels, B.E.,Tong, L.,Hart, R.P.,Kiledjian, M. 5' End Nicotinamide Adenine Dinucleotide Cap in Human Cells Promotes RNA Decay through DXO-Mediated deNADding. Cell, 168:1015-1027.e10, 2017 Cited by PubMed Abstract: Eukaryotic mRNAs generally possess a 5' end N7 methyl guanosine (mG) cap that promotes their translation and stability. However, mammalian mRNAs can also carry a 5' end nicotinamide adenine dinucleotide (NAD) cap that, in contrast to the mG cap, does not support translation but instead promotes mRNA decay. The mammalian and fungal noncanonical DXO/Rai1 decapping enzymes efficiently remove NAD caps, and cocrystal structures of DXO/Rai1 with 3'-NADP illuminate the molecular mechanism for how the "deNADding" reaction produces NAD and 5' phosphate RNA. Removal of DXO from cells increases NAD-capped mRNA levels and enables detection of NAD-capped intronic small nucleolar RNAs (snoRNAs), suggesting NAD caps can be added to 5'-processed termini. Our findings establish NAD as an alternative mammalian RNA cap and DXO as a deNADding enzyme modulating cellular levels of NAD-capped RNAs. Collectively, these data reveal that mammalian RNAs can harbor a 5' end modification distinct from the classical mG cap that promotes rather than inhibits RNA decay. PubMed: 28283058DOI: 10.1016/j.cell.2017.02.019 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (2.1 Å) |
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