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| | <StructureSection load='6j02' size='340' side='right'caption='[[6j02]], [[Resolution|resolution]] 1.80Å' scene=''> | | <StructureSection load='6j02' size='340' side='right'caption='[[6j02]], [[Resolution|resolution]] 1.80Å' scene=''> |
| | == Structural highlights == | | == Structural highlights == |
| - | <table><tr><td colspan='2'>[[6j02]] is a 2 chain structure with sequence from [http://en.wikipedia.org/wiki/Lk3_transgenic_mice Lk3 transgenic mice]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6J02 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6J02 FirstGlance]. <br> | + | <table><tr><td colspan='2'>[[6j02]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Mus_musculus Mus musculus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6J02 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6J02 FirstGlance]. <br> |
| - | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=CA:CALCIUM+ION'>CA</scene></td></tr> | + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.803Å</td></tr> |
| - | <tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">Msr1, Scvr ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=10090 LK3 transgenic mice])</td></tr> | + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=CA:CALCIUM+ION'>CA</scene></td></tr> |
| - | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6j02 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6j02 OCA], [http://pdbe.org/6j02 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6j02 RCSB], [http://www.ebi.ac.uk/pdbsum/6j02 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6j02 ProSAT]</span></td></tr> | + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=6j02 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6j02 OCA], [https://pdbe.org/6j02 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6j02 RCSB], [https://www.ebi.ac.uk/pdbsum/6j02 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6j02 ProSAT]</span></td></tr> |
| | </table> | | </table> |
| | == Function == | | == Function == |
| - | [[http://www.uniprot.org/uniprot/MSRE_MOUSE MSRE_MOUSE]] Membrane glycoproteins implicated in the pathologic deposition of cholesterol in arterial walls during atherogenesis. Two types of receptor subunits exist. These receptors mediate the endocytosis of a diverse group of macromolecules, including modified low density lipoproteins (LDL).[UniProtKB:P21757] | + | [https://www.uniprot.org/uniprot/MSRE_MOUSE MSRE_MOUSE] Membrane glycoproteins implicated in the pathologic deposition of cholesterol in arterial walls during atherogenesis. Two types of receptor subunits exist. These receptors mediate the endocytosis of a diverse group of macromolecules, including modified low density lipoproteins (LDL).[UniProtKB:P21757] |
| | <div style="background-color:#fffaf0;"> | | <div style="background-color:#fffaf0;"> |
| | == Publication Abstract from PubMed == | | == Publication Abstract from PubMed == |
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| | </StructureSection> | | </StructureSection> |
| | [[Category: Large Structures]] | | [[Category: Large Structures]] |
| - | [[Category: Lk3 transgenic mice]] | + | [[Category: Mus musculus]] |
| - | [[Category: Cheng, C]] | + | [[Category: Cheng C]] |
| - | [[Category: Hu, Z]] | + | [[Category: Hu Z]] |
| - | [[Category: Cd204]]
| + | |
| - | [[Category: Endocytosis]]
| + | |
| - | [[Category: Scara1]]
| + | |
| - | [[Category: Scavenger receptor]]
| + | |
| - | [[Category: Srcr]]
| + | |
| Structural highlights
Function
MSRE_MOUSE Membrane glycoproteins implicated in the pathologic deposition of cholesterol in arterial walls during atherogenesis. Two types of receptor subunits exist. These receptors mediate the endocytosis of a diverse group of macromolecules, including modified low density lipoproteins (LDL).[UniProtKB:P21757]
Publication Abstract from PubMed
Scavenger receptor class A member 1 (SCARA1 or CD204) is an immune receptor highly expressed on macrophages. It forms homotrimers on 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 A resolution, revealing its Ca2+-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 Ca2+-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 Ca2+. 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.
The scavenger receptor SCARA1(CD204) recognizes dead cells through spectrin.,Cheng C, Hu Z, Cao L, Peng C, He Y J Biol Chem. 2019 Oct 25. pii: RA119.010110. doi: 10.1074/jbc.RA119.010110. PMID:31653705[1]
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.
References
- ↑ Cheng C, Hu Z, Cao L, Peng C, He Y. The scavenger receptor SCARA1(CD204) recognizes dead cells through spectrin. J Biol Chem. 2019 Oct 25. pii: RA119.010110. doi: 10.1074/jbc.RA119.010110. PMID:31653705 doi:http://dx.doi.org/10.1074/jbc.RA119.010110
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