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8hyi
From Proteopedia
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| - | '''Unreleased structure''' | ||
| - | + | ==Crystal structure of human P-cadherin MEC12 (X dimer) in complex with 2-(2-methyl-5-phenyl-1H-indole-3-yl)ethan-1-amine== | |
| - | + | <StructureSection load='8hyi' size='340' side='right'caption='[[8hyi]], [[Resolution|resolution]] 2.85Å' scene=''> | |
| - | + | == Structural highlights == | |
| - | + | <table><tr><td colspan='2'>[[8hyi]] is a 2 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=8HYI OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8HYI 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]] 2.85Å</td></tr> | |
| - | [[Category: | + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=22R:2-(2-methyl-5-phenyl-1H-indole-3-yl)ethan-1-amine'>22R</scene>, <scene name='pdbligand=CA:CALCIUM+ION'>CA</scene>, <scene name='pdbligand=DMS:DIMETHYL+SULFOXIDE'>DMS</scene></td></tr> |
| - | [[Category: | + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=8hyi FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8hyi OCA], [https://pdbe.org/8hyi PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8hyi RCSB], [https://www.ebi.ac.uk/pdbsum/8hyi PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8hyi ProSAT]</span></td></tr> |
| - | [[Category: | + | </table> |
| - | [[Category: Senoo | + | == Disease == |
| - | [[Category: | + | [https://www.uniprot.org/uniprot/CADH3_HUMAN CADH3_HUMAN] Hypotrichosis with juvenile macular degeneration;EEM syndrome. 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. |
| - | [[Category: Ueno | + | == Function == |
| + | [https://www.uniprot.org/uniprot/CADH3_HUMAN CADH3_HUMAN] Cadherins are calcium-dependent cell adhesion proteins. They preferentially interact with themselves in a homophilic manner in connecting cells; cadherins may thus contribute to the sorting of heterogeneous cell types. | ||
| + | __TOC__ | ||
| + | </StructureSection> | ||
| + | [[Category: Homo sapiens]] | ||
| + | [[Category: Large Structures]] | ||
| + | [[Category: Ito S]] | ||
| + | [[Category: Nagatoishi S]] | ||
| + | [[Category: Senoo A]] | ||
| + | [[Category: Tsumoto K]] | ||
| + | [[Category: Ueno G]] | ||
Current revision
Crystal structure of human P-cadherin MEC12 (X dimer) in complex with 2-(2-methyl-5-phenyl-1H-indole-3-yl)ethan-1-amine
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Categories: Homo sapiens | Large Structures | Ito S | Nagatoishi S | Senoo A | Tsumoto K | Ueno G
