9EJC
Cryo-EM Structure of CXCL1-KSHV ORF74-Gi-scFv16 Complex
9EJC の概要
| エントリーDOI | 10.2210/pdb9ejc/pdb |
| 関連するPDBエントリー | 8W1A |
| EMDBエントリー | 48095 48100 |
| 分子名称 | Guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1, Guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-2, viral G-protein coupled receptor, ... (6 entities in total) |
| 機能のキーワード | kshv vgpcr, viral gpcr, kshv orf74, orf74-cxcl1, orf74 active, cxcl1 bound orf74, kshv orf74-cxcl1-gi-scfv16, viral protein, viral protein-signaling protein complex, viral protein/signaling protein |
| 由来する生物種 | Homo sapiens (human) 詳細 |
| タンパク質・核酸の鎖数 | 6 |
| 化学式量合計 | 168565.27 |
| 構造登録者 | |
| 主引用文献 | Park, J.B.,Sahoo, B.,Sahoo, A.R.,Kim, D.,Seo, H.D.,Bowman, J.,Kwak, M.J.,Suh, S.,Buck, M.,Dai, X.,Jung, J.U. Structural basis for ligand promiscuity and high signaling activity of Kaposi's Sarcoma-associated Herpesvirus-encoded GPCR. Nat Commun, 16:8403-8403, 2025 Cited by PubMed Abstract: Kaposi's Sarcoma-associated Herpesvirus encodes ORF74, a viral G protein-coupled receptor homologous to CXCR2, which plays a crucial role in Kaposi's Sarcoma development through its high basal signaling activity. Our cryoEM analysis of ORF74 in ligand-free, BRIL-fused ligand-free, and CXCL1/Gi-bound forms elucidates its ligand-independent signaling activity. A widely open, static extracellular cavity facilitates ligand promiscuity by enabling dynamic access and diverse binding modes. Structural alterations in CWxP, E/DRY, and NPxxY micro-switches stabilize the active conformation, leading to constitutive signaling. Metadynamics simulations reveal a dynamic ensemble between local switch structures corresponding to the inactive and active states, supporting spontaneous activation. CXCR2-ORF74 chimeras highlight intracellular loops 2 and 3 as key modulators of basal and agonist-induced activity. This study defines the structural basis of ORF74's ligand promiscuity, spontaneous activation, and high basal signaling, providing insights into its role in viral oncogenesis. PubMed: 40998787DOI: 10.1038/s41467-025-63457-4 主引用文献が同じPDBエントリー |
| 実験手法 | ELECTRON MICROSCOPY (2.98 Å) |
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