4DPG
Crystal Structure of Human LysRS: P38/AIMP2 Complex I
4DPG の概要
| エントリーDOI | 10.2210/pdb4dpg/pdb |
| 関連するPDBエントリー | 4DPJ |
| 分子名称 | Lysine--tRNA ligase, Aminoacyl tRNA synthase complex-interacting multifunctional protein 2, LYSINE, ... (7 entities in total) |
| 機能のキーワード | lysyl-trna synthetase, lysrs, p38, aimp2, multi trna synthetase complex sub-complex, ligase-apoptosis complex, ligase/apoptosis |
| 由来する生物種 | Homo sapiens (human) 詳細 |
| 細胞内の位置 | Isoform Cytoplasmic: Cytoplasm, cytosol . Isoform Mitochondrial: Mitochondrion : Q15046 Cytoplasm, cytosol : Q13155 |
| タンパク質・核酸の鎖数 | 12 |
| 化学式量合計 | 503812.56 |
| 構造登録者 | |
| 主引用文献 | Ofir-Birin, Y.,Fang, P.,Bennett, S.P.,Zhang, H.M.,Wang, J.,Rachmin, I.,Shapiro, R.,Song, J.,Dagan, A.,Pozo, J.,Kim, S.,Marshall, A.G.,Schimmel, P.,Yang, X.L.,Nechushtan, H.,Razin, E.,Guo, M. Structural Switch of Lysyl-tRNA Synthetase between Translation and Transcription. Mol.Cell, 49:30-42, 2013 Cited by PubMed Abstract: Lysyl-tRNA synthetase (LysRS), a component of the translation apparatus, is released from the cytoplasmic multi-tRNA synthetase complex (MSC) to activate the transcription factor MITF in stimulated mast cells through undefined mechanisms. Here we show that Ser207 phosphorylation provokes a new conformer of LysRS that inactivates its translational function but activates its transcriptional function. The crystal structure of an MSC subcomplex established that LysRS is held in the MSC by binding to the N terminus of the scaffold protein p38/AIMP2. Phosphorylation-created steric clashes at the LysRS domain interface disrupt its binding grooves for p38/AIMP2, releasing LysRS and provoking its nuclear translocation. This alteration also exposes the C-terminal domain of LysRS to bind to MITF and triggers LysRS-directed production of the second messenger Ap(4)A that activates MITF. Thus our results establish that a single conformational change triggered by phosphorylation leads to multiple effects driving an exclusive switch of LysRS function from translation to transcription. PubMed: 23159739DOI: 10.1016/j.molcel.2012.10.010 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (2.844 Å) |
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