9IGO
PR3 S203A I221N W222N G223T mutant in complex with the extracellular domain of CD177
9IGO の概要
| エントリーDOI | 10.2210/pdb9igo/pdb |
| 分子名称 | Myeloblastin, CD177 antigen, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, ... (8 entities in total) |
| 機能のキーワード | serine protease, anca-antigen, cd177 receptor, surface proteins, glycoproteins, immune system |
| 由来する生物種 | Homo sapiens (human) 詳細 |
| タンパク質・核酸の鎖数 | 2 |
| 化学式量合計 | 49177.23 |
| 構造登録者 | |
| 主引用文献 | Zheng-Gerard, C.,Joha, J.,Carrasquero, M.,El Omari, K.,Lowe, E.,Dubey, S.,Draper, S.J.,Chang, Y.C.,Lin, H.H.,Salama, A.D.,McHugh, K.,Seiradake, E. Structures of proteinase 3 and the CD177 receptor complex reveal a major autoantibody epitope. Embo Rep., 27:1580-1606, 2026 Cited by PubMed Abstract: Granulomatosis with polyangiitis is a life-threatening systemic vasculitis, characterised by anti-neutrophil cytoplasmic autoantibodies (ANCA) most commonly against proteinase 3 (PR3), a protease expressed intracellularly and on the surface of neutrophils. Most cell surface PR3 is bound to the receptor CD177; however, the molecular mechanism of the interactions is not well understood. Here, we present crystal structures of CD177 in complex with PR3 and unliganded CD177. We describe a mainly hydrophobic binding interface between PR3 and CD177, involving the first two Ly6/uPAR (LU) domains of CD177. These form a globular structure which is connected to downstream domains via a flexible linker. Using a panel of PR3-ANCA-positive patient samples, we show that a significant proportion of ANCAs target the CD177-binding site of PR3 in these samples. Structure-guided mutation of the CD177-binding site on PR3 is effective in reducing PR3-ANCA binding. The results demonstrate that the CD177-binding surface of PR3 harbours a major PR3-ANCA epitope, and that the extent of binding to this surface varies between different patients. PubMed: 41703070DOI: 10.1038/s44319-026-00716-5 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (1.5 Å) |
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