7rdv
From Proteopedia
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(New page: '''Unreleased structure''' The entry 7rdv is ON HOLD Authors: Description: Category: Unreleased Structures) |
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- | '''Unreleased structure''' | ||
- | The entry | + | ==TFH TCR bound to MHC Class II IAd presenting aggrecan epitope== |
+ | <StructureSection load='7rdv' size='340' side='right'caption='[[7rdv]], [[Resolution|resolution]] 2.90Å' scene=''> | ||
+ | == Structural highlights == | ||
+ | <table><tr><td colspan='2'>[[7rdv]] is a 5 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=7RDV OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7RDV FirstGlance]. <br> | ||
+ | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.9000661Å</td></tr> | ||
+ | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=NAG:N-ACETYL-D-GLUCOSAMINE'>NAG</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=7rdv FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7rdv OCA], [https://pdbe.org/7rdv PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7rdv RCSB], [https://www.ebi.ac.uk/pdbsum/7rdv PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7rdv ProSAT]</span></td></tr> | ||
+ | </table> | ||
+ | == Disease == | ||
+ | [https://www.uniprot.org/uniprot/PGCA_HUMAN PGCA_HUMAN] Spondyloepimetaphyseal dysplasia, aggrecan type;Spondyloepiphyseal dysplasia, Kimberley type;Familial osteochondritis dissecans. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry. | ||
+ | == Function == | ||
+ | [https://www.uniprot.org/uniprot/PGCA_HUMAN PGCA_HUMAN] This proteoglycan is a major component of extracellular matrix of cartilagenous tissues. A major function of this protein is to resist compression in cartilage. It binds avidly to hyaluronic acid via an N-terminal globular region. | ||
- | + | ==See Also== | |
- | + | *[[MHC 3D structures|MHC 3D structures]] | |
- | + | *[[MHC II 3D structures|MHC II 3D structures]] | |
- | [[Category: | + | __TOC__ |
+ | </StructureSection> | ||
+ | [[Category: Homo sapiens]] | ||
+ | [[Category: Large Structures]] | ||
+ | [[Category: Mus musculus]] | ||
+ | [[Category: Lim JJ]] | ||
+ | [[Category: Reid H]] | ||
+ | [[Category: Rossjohn J]] |
Current revision
TFH TCR bound to MHC Class II IAd presenting aggrecan epitope
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