7rdv: Difference between revisions
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<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> | <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> | </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 == | == Function == | ||
[https://www.uniprot.org/uniprot/ | [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== | ==See Also== | ||
Latest revision as of 13:58, 6 November 2024
TFH TCR bound to MHC Class II IAd presenting aggrecan epitope
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