4ll9
From Proteopedia
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==Crystal structure of D3D4 domain of the LILRB1 molecule== | ==Crystal structure of D3D4 domain of the LILRB1 molecule== | ||
- | <StructureSection load='4ll9' size='340' side='right' caption='[[4ll9]], [[Resolution|resolution]] 2.69Å' scene=''> | + | <StructureSection load='4ll9' size='340' side='right'caption='[[4ll9]], [[Resolution|resolution]] 2.69Å' scene=''> |
== Structural highlights == | == Structural highlights == | ||
- | <table><tr><td colspan='2'>[[4ll9]] is a 3 chain structure with sequence from [ | + | <table><tr><td colspan='2'>[[4ll9]] is a 3 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4LL9 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4LL9 FirstGlance]. <br> |
- | </td></tr><tr id=' | + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.686Å</td></tr> |
- | <tr id=' | + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=IOD:IODIDE+ION'>IOD</scene></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=4ll9 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4ll9 OCA], [https://pdbe.org/4ll9 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4ll9 RCSB], [https://www.ebi.ac.uk/pdbsum/4ll9 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4ll9 ProSAT]</span></td></tr> | |
- | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[ | + | |
</table> | </table> | ||
+ | == Function == | ||
+ | [https://www.uniprot.org/uniprot/LIRB1_HUMAN LIRB1_HUMAN] Receptor for class I MHC antigens. Recognizes a broad spectrum of HLA-A, HLA-B, HLA-C and HLA-G alleles. Receptor for H301/UL18, a human cytomegalovirus class I MHC homolog. Ligand binding results in inhibitory signals and down-regulation of the immune response. Engagement of LILRB1 present on natural killer cells or T-cells by class I MHC molecules protects the target cells from lysis. Interaction with HLA-B or HLA-E leads to inhibition of the signal triggered by FCER1A and inhibits serotonin release. Inhibits FCGR1A-mediated phosphorylation of cellular proteins and mobilization of intracellular calcium ions.<ref>PMID:9285411</ref> <ref>PMID:9842885</ref> <ref>PMID:11907092</ref> | ||
<div style="background-color:#fffaf0;"> | <div style="background-color:#fffaf0;"> | ||
== Publication Abstract from PubMed == | == Publication Abstract from PubMed == | ||
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From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | ||
</div> | </div> | ||
+ | <div class="pdbe-citations 4ll9" style="background-color:#fffaf0;"></div> | ||
+ | |||
+ | ==See Also== | ||
+ | *[[Leukocyte immunoglobulin-like receptor|Leukocyte immunoglobulin-like receptor]] | ||
== References == | == References == | ||
<references/> | <references/> | ||
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</StructureSection> | </StructureSection> | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
- | [[Category: Gao | + | [[Category: Large Structures]] |
- | [[Category: Liu | + | [[Category: Gao GF]] |
- | [[Category: Nam | + | [[Category: Liu J]] |
- | [[Category: Qi | + | [[Category: Nam G]] |
- | [[Category: Ryu | + | [[Category: Qi J]] |
- | [[Category: Shi | + | [[Category: Ryu M]] |
- | [[Category: Song | + | [[Category: Shi Y]] |
- | [[Category: Wang | + | [[Category: Song H]] |
- | [[Category: Yan | + | [[Category: Wang Q]] |
- | + | [[Category: Yan J]] | |
- | + | ||
- | + |
Current revision
Crystal structure of D3D4 domain of the LILRB1 molecule
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Categories: Homo sapiens | Large Structures | Gao GF | Liu J | Nam G | Qi J | Ryu M | Shi Y | Song H | Wang Q | Yan J