4bss
From Proteopedia
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<StructureSection load='4bss' size='340' side='right'caption='[[4bss]], [[Resolution|resolution]] 3.20Å' scene=''> | <StructureSection load='4bss' size='340' side='right'caption='[[4bss]], [[Resolution|resolution]] 3.20Å' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
- | <table><tr><td colspan='2'>[[4bss]] is a 8 chain structure with sequence from [ | + | <table><tr><td colspan='2'>[[4bss]] is a 8 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=4BSS OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4BSS FirstGlance]. <br> |
- | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=NAG:N-ACETYL-D-GLUCOSAMINE'>NAG</scene> | + | </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=4bss FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4bss OCA], [https://pdbe.org/4bss PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4bss RCSB], [https://www.ebi.ac.uk/pdbsum/4bss PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4bss ProSAT]</span></td></tr> | |
- | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[ | + | |
</table> | </table> | ||
- | == Disease == | ||
- | [[http://www.uniprot.org/uniprot/RSPO1_HUMAN RSPO1_HUMAN]] Palmoplantar keratoderma - XX sex reversal - predisposition to squamous cell carcinoma. Keratoderma, palmoplantar, with squamous cell carcinoma of skin and sex reversal (PKKSCC) [MIM:[http://omim.org/entry/610644 610644]]: A recessive syndrome characterized by XX (female to male) SRY-independent sex reversal, palmoplantar hyperkeratosis and predisposition to squamous cell carcinoma of the skin. Note=The disease is caused by mutations affecting the gene represented in this entry. | ||
== Function == | == Function == | ||
- | [[ | + | [[https://www.uniprot.org/uniprot/LGR5_HUMAN LGR5_HUMAN]] Orphan receptor. Stem cell marker of the intestinal epithelium and the hair follicle. Target gene of Wnt signaling. |
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__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
- | [[Category: | + | [[Category: Homo sapiens]] |
[[Category: Large Structures]] | [[Category: Large Structures]] | ||
- | [[Category: Clevers | + | [[Category: Clevers H]] |
- | [[Category: Forneris | + | [[Category: Forneris F]] |
- | [[Category: Granneman | + | [[Category: Granneman JCM]] |
- | [[Category: Gros | + | [[Category: Gros P]] |
- | [[Category: Huch | + | [[Category: Huch M]] |
- | [[Category: | + | [[Category: Peng WC]] |
- | [[Category: | + | [[Category: De Lau W]] |
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Revision as of 17:05, 7 September 2022
Structure of the ectodomain of LGR5 in complex with R-spondin-1 (Fu1Fu2) in P21 crystal form
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Categories: Homo sapiens | Large Structures | Clevers H | Forneris F | Granneman JCM | Gros P | Huch M | Peng WC | De Lau W