8COO
Solution structure of Zipcode binding protein 1 (ZBP1) KH3(DD)KH4 domains in complex with N6-Methyladenosine containing RNA
8COO の概要
| エントリーDOI | 10.2210/pdb8coo/pdb |
| 関連するPDBエントリー | 2N8M |
| NMR情報 | BMRB: 34660 |
| 分子名称 | Insulin-like growth factor 2 mRNA-binding protein 1, RNA_(5'-R(*(UP*CP*GP*GP*(6MZ)P*CP*U)-3') (2 entities in total) |
| 機能のキーワード | protein-rna interactions; nmr; binding mechanism; neuronal mrna granules; neuronal development; mrna local translation; zbp1; imp1; m6a-n6-methyladenosine rna;, rna binding protein |
| 由来する生物種 | Gallus gallus (chicken) 詳細 |
| タンパク質・核酸の鎖数 | 2 |
| 化学式量合計 | 22824.88 |
| 構造登録者 | |
| 主引用文献 | Nicastro, G.,Abis, G.,Klein, P.,Esteban-Serna, S.,Gallagher, C.,Chaves-Arquero, B.,Cai, Y.,Figueiredo, A.M.,Martin, S.R.,Patani, R.,Taylor, I.A.,Ramos, A. Direct m6A recognition by IMP1 underlays an alternative model of target selection for non-canonical methyl-readers. Nucleic Acids Res., 51:8774-8786, 2023 Cited by PubMed Abstract: m6A methylation provides an essential layer of regulation in organismal development, and is aberrant in a range of cancers and neuro-pathologies. The information encoded by m6A methylation is integrated into existing RNA regulatory networks by RNA binding proteins that recognise methylated sites, the m6A readers. m6A readers include a well-characterised class of dedicated proteins, the YTH proteins, as well as a broader group of multi-functional regulators where recognition of m6A is only partially understood. Molecular insight in this recognition is essential to build a mechanistic understanding of global m6A regulation. In this study, we show that the reader IMP1 recognises the m6A using a dedicated hydrophobic platform that assembles on the methyl moiety, creating a stable high-affinity interaction. This recognition is conserved across evolution and independent from the underlying sequence context but is layered upon the strong sequence specificity of IMP1 for GGAC RNA. This leads us to propose a concept for m6A regulation where methylation plays a context-dependent role in the recognition of selected IMP1 targets that is dependent on the cellular concentration of available IMP1, differing from that observed for the YTH proteins. PubMed: 37377445DOI: 10.1093/nar/gkad534 主引用文献が同じPDBエントリー |
| 実験手法 | SOLUTION NMR |
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