8eq6: Difference between revisions

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'''Unreleased structure'''


The entry 8eq6 is ON HOLD  until 2024-10-07
==PD1 signaling receptor bound to FAB Complex==
 
<StructureSection load='8eq6' size='340' side='right'caption='[[8eq6]], [[Resolution|resolution]] 1.65&Aring;' scene=''>
Authors: Bjorkelid, C., Paluch, C., Robertson, N.J.
== Structural highlights ==
 
<table><tr><td colspan='2'>[[8eq6]] is a 3 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] and [https://en.wikipedia.org/wiki/Mus_musculus Mus musculus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=8EQ6 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8EQ6 FirstGlance]. <br>
Description: PD1 signaling receptor bound to FAB Complex
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.65&#8491;</td></tr>
[[Category: Unreleased Structures]]
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=8eq6 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8eq6 OCA], [https://pdbe.org/8eq6 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8eq6 RCSB], [https://www.ebi.ac.uk/pdbsum/8eq6 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8eq6 ProSAT]</span></td></tr>
[[Category: Bjorkelid, C]]
</table>
[[Category: Paluch, C]]
== Disease ==
[[Category: Robertson, N.J]]
[https://www.uniprot.org/uniprot/PDCD1_HUMAN PDCD1_HUMAN] Systemic lupus erythematosus;Multiple sclerosis. Systemic lupus erythematosus 2 (SLEB2) [MIM:[https://omim.org/entry/605218 605218]: A chronic, relapsing, inflammatory, and often febrile multisystemic disorder of connective tissue, characterized principally by involvement of the skin, joints, kidneys and serosal membranes. It is of unknown etiology, but is thought to represent a failure of the regulatory mechanisms of the autoimmune system. The disease is marked by a wide range of system dysfunctions, an elevated erythrocyte sedimentation rate, and the formation of LE cells in the blood or bone marrow. Note=Disease susceptibility is associated with variations affecting the gene represented in this entry.<ref>PMID:12402038</ref>
== Function ==
[https://www.uniprot.org/uniprot/PDCD1_HUMAN PDCD1_HUMAN] Inhibitory cell surface receptor involved in the regulation of T-cell function during immunity and tolerance. Upon ligand binding, inhibits T-cell effector functions in an antigen-specific manner. Possible cell death inducer, in association with other factors.<ref>PMID:21276005</ref>
== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Homo sapiens]]
[[Category: Large Structures]]
[[Category: Mus musculus]]
[[Category: Bjorkelid C]]
[[Category: Paluch C]]
[[Category: Robertson NJ]]

Revision as of 05:56, 11 October 2023

PD1 signaling receptor bound to FAB Complex

8eq6, resolution 1.65Å

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