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8hyi

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'''Unreleased structure'''
 
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The entry 8hyi is ON HOLD
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==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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<StructureSection load='8hyi' size='340' side='right'caption='[[8hyi]], [[Resolution|resolution]] 2.85&Aring;' scene=''>
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Authors: Senoo, A., Ito, S., Ueno, G., Nagatoishi, S., Tsumoto, K.
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== Structural highlights ==
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<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>
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Description: 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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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.85&#8491;</td></tr>
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[[Category: Unreleased Structures]]
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<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>
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[[Category: Nagatoishi, S]]
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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=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>
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[[Category: Tsumoto, K]]
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</table>
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[[Category: Senoo, A]]
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== Disease ==
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[[Category: Ito, S]]
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[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.
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[[Category: Ueno, G]]
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== Function ==
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[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.
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__TOC__
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</StructureSection>
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[[Category: Homo sapiens]]
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[[Category: Large Structures]]
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[[Category: Ito S]]
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[[Category: Nagatoishi S]]
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[[Category: Senoo A]]
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[[Category: Tsumoto K]]
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[[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

PDB ID 8hyi

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