7JFL
Crystal structure of human phosphorylated IRF-3 bound to CBP
7JFL の概要
エントリーDOI | 10.2210/pdb7jfl/pdb |
分子名称 | Interferon regulatory factor 3, CREB-binding protein (3 entities in total) |
機能のキーワード | transcription factor, phosphorylation, innate immunity, immune system |
由来する生物種 | Homo sapiens (Human) 詳細 |
タンパク質・核酸の鎖数 | 4 |
化学式量合計 | 58090.01 |
構造登録者 | |
主引用文献 | Jing, T.,Zhao, B.,Xu, P.,Gao, X.,Chi, L.,Han, H.,Sankaran, B.,Li, P. The Structural Basis of IRF-3 Activation upon Phosphorylation. J Immunol., 205:1886-1896, 2020 Cited by PubMed Abstract: The innate immune system is the first line of defense against bacterial and viral infections. The recognition of pathogen-associated molecular patterns by the RIG-I-like receptors, TLRs, and cGAS leads to the induction of IFN-I by activating the transcription factor IRF-3. Although the mechanism of IRF-3 activation has been extensively studied, the structural basis of IRF-3 activation upon phosphorylation is not fully understood. In this study, we determined the crystal structures of phosphorylated human and mouse IRF-3 bound to CREB-binding protein (CBP), which reveal that phosphorylated IRF-3 forms a dimer via pSer (pSer in mouse IRF-3) and a downstream LIS motif. Size-exclusion chromatography and cell-based studies show that mutations of key residues interacting with pSer severely impair IRF-3 activation and IFN-β induction. By contrast, phosphorylation of Ser within the LIS motif of human IRF-3 only plays a moderate role in IRF-3 activation. The mouse IRF-3/CBP complex structure reveals that the mechanism of mouse IRF-3 activation is similar but distinct from human IRF-3. These structural and functional studies reveal the detailed mechanism of IRF-3 activation upon phosphorylation. PubMed: 32826280DOI: 10.4049/jimmunol.2000026 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (1.68 Å) |
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