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6J02

Crystal structure of the SRCR domain of mouse SCARA1

6J02 の概要
エントリーDOI10.2210/pdb6j02/pdb
分子名称Macrophage scavenger receptor types I and II, CALCIUM ION (3 entities in total)
機能のキーワードscara1, cd204, scavenger receptor, srcr, endocytosis
由来する生物種Mus musculus (Mouse)
タンパク質・核酸の鎖数2
化学式量合計25858.94
構造登録者
Cheng, C.,Hu, Z. (登録日: 2018-12-20, 公開日: 2019-11-13, 最終更新日: 2024-10-23)
主引用文献Cheng, C.,Hu, Z.,Cao, L.,Peng, C.,He, Y.
The scavenger receptor SCARA1 (CD204) recognizes dead cells through spectrin.
J.Biol.Chem., 294:18881-18897, 2019
Cited by
PubMed Abstract: Scavenger receptor class A member 1 (SCARA1 or CD204) is an immune receptor highly expressed on macrophages. It forms homotrimers on the cell surface and plays important roles in regulating immune responses via its involvement in multiple pathways. However, both the structure and the functional roles of SCARA1 are not fully understood. Here, we determined the crystal structure of the C-terminal SRCR domain of SCARA1 at 1.8 Å resolution, revealing its Ca-binding site. Results from cell-based assays revealed that SCARA1 can recognize dead cells, rather than live cells, specifically through its SRCR domain and in a Ca-dependent manner. Furthermore, by combining MS and biochemical assays, we found that cellular spectrin is the binding target of SCARA1 on dead cells and that the SRCR domain of SCARA1 recognizes the SPEC repeats of spectrin in the presence of Ca We also found that macrophages can internalize dead cells or debris from both erythrocytes and other cells through the interaction between SCARA1 and spectrin, suggesting that SCARA1 could function as a scavenging receptor that recognizes dead cells. These results suggest that spectrin, which is one of the major components of the cytoskeleton, acts as a cellular marker that enables the recognition of dead cells by the immune system.
PubMed: 31653705
DOI: 10.1074/jbc.RA119.010110
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.803 Å)
構造検証レポート
Validation report summary of 6j02
検証レポート(詳細版)ダウンロードをダウンロード

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件を2026-02-04に公開中

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