6pe9
From Proteopedia
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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=6pe9 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6pe9 OCA], [https://pdbe.org/6pe9 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6pe9 RCSB], [https://www.ebi.ac.uk/pdbsum/6pe9 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6pe9 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=6pe9 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6pe9 OCA], [https://pdbe.org/6pe9 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6pe9 RCSB], [https://www.ebi.ac.uk/pdbsum/6pe9 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6pe9 ProSAT]</span></td></tr> | ||
</table> | </table> | ||
| - | == Disease == | ||
| - | [https://www.uniprot.org/uniprot/TNR5_HUMAN TNR5_HUMAN] Defects in CD40 are the cause of immunodeficiency with hyper-IgM type 3 (HIGM3) [MIM:[https://omim.org/entry/606843 606843]. A rare immunodeficiency syndrome characterized by normal or elevated serum IgM levels with absence of IgG, IgA, and IgE. It results in a profound susceptibility to bacterial infections.<ref>PMID:11675497</ref> | ||
| - | == Function == | ||
| - | [https://www.uniprot.org/uniprot/TNR5_HUMAN TNR5_HUMAN] Receptor for TNFSF5/CD40LG. | ||
<div style="background-color:#fffaf0;"> | <div style="background-color:#fffaf0;"> | ||
== Publication Abstract from PubMed == | == Publication Abstract from PubMed == | ||
Current revision
Crystal Structure of CD40 complexed to FAB516
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