5cmn: Difference between revisions
From Proteopedia
Jump to navigationJump to search
No edit summary |
No edit summary |
||
| Line 1: | Line 1: | ||
==FLRT3 LRR domain in complex with LPHN3 Olfactomedin domain== | ==FLRT3 LRR domain in complex with LPHN3 Olfactomedin domain== | ||
<StructureSection load='5cmn' size='340' side='right' caption='[[5cmn]], [[Resolution|resolution]] 3.60Å' scene=''> | <StructureSection load='5cmn' size='340' side='right'caption='[[5cmn]], [[Resolution|resolution]] 3.60Å' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[5cmn]] is a 8 chain structure with sequence from [ | <table><tr><td colspan='2'>[[5cmn]] 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=5CMN OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=5CMN FirstGlance]. <br> | ||
</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=CA:CALCIUM+ION'>CA</scene>, <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=CA:CALCIUM+ION'>CA</scene>, <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=5cmn FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5cmn OCA], [https://pdbe.org/5cmn PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5cmn RCSB], [https://www.ebi.ac.uk/pdbsum/5cmn PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5cmn ProSAT]</span></td></tr> | |||
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[ | |||
</table> | </table> | ||
== Disease == | == Disease == | ||
[ | [https://www.uniprot.org/uniprot/FLRT3_HUMAN FLRT3_HUMAN] Kallmann syndrome. The disease is caused by mutations affecting distinct genetic loci, including the gene represented in this entry. Some patients carrying mutations in FLRT3 also have a mutation in another HH-associated gene including FGFR1, HS6ST1 and FGF17 (PubMed:23643382).<ref>PMID:23643382</ref> | ||
== Function == | == Function == | ||
[ | [https://www.uniprot.org/uniprot/FLRT3_HUMAN FLRT3_HUMAN] May have a function in cell adhesion and/or receptor signaling. | ||
<div style="background-color:#fffaf0;"> | <div style="background-color:#fffaf0;"> | ||
== Publication Abstract from PubMed == | == Publication Abstract from PubMed == | ||
| Line 22: | Line 20: | ||
</div> | </div> | ||
<div class="pdbe-citations 5cmn" style="background-color:#fffaf0;"></div> | <div class="pdbe-citations 5cmn" style="background-color:#fffaf0;"></div> | ||
==See Also== | |||
*[[Latrophilin|Latrophilin]] | |||
== References == | == References == | ||
<references/> | <references/> | ||
__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
[[Category: | [[Category: Homo sapiens]] | ||
[[Category: | [[Category: Large Structures]] | ||
[[Category: | [[Category: Arac D]] | ||
[[Category: | [[Category: Lu Y]] | ||
[[Category: | [[Category: Salzman G]] | ||