8w0r

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(New page: '''Unreleased structure''' The entry 8w0r is ON HOLD Authors: Sun, D., Masureel, M. Description: Human EBP complexed with compound 1 Category: Unreleased Structures [[Category: Mas...)
Current revision (05:55, 19 June 2024) (edit) (undo)
 
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'''Unreleased structure'''
 
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The entry 8w0r is ON HOLD
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==Human EBP complexed with compound 1==
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<StructureSection load='8w0r' size='340' side='right'caption='[[8w0r]], [[Resolution|resolution]] 2.80&Aring;' scene=''>
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Authors: Sun, D., Masureel, M.
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== Structural highlights ==
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<table><tr><td colspan='2'>[[8w0r]] 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=8W0R OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8W0R FirstGlance]. <br>
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Description: Human EBP complexed with compound 1
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 2.8&#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=A1AEU:1-methyl-1-[(oxan-4-yl)methyl]-5-(trifluoromethyl)spiro[indole-2,4-piperidin]-3(1H)-one'>A1AEU</scene></td></tr>
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[[Category: Masureel, M]]
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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=8w0r FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8w0r OCA], [https://pdbe.org/8w0r PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8w0r RCSB], [https://www.ebi.ac.uk/pdbsum/8w0r PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8w0r ProSAT]</span></td></tr>
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[[Category: Sun, D]]
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</table>
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== Disease ==
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[https://www.uniprot.org/uniprot/EBP_HUMAN EBP_HUMAN] MEND syndrome;X-linked dominant chondrodysplasia punctata. 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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== Function ==
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[https://www.uniprot.org/uniprot/EBP_HUMAN EBP_HUMAN] Catalyzes the conversion of Delta(8)-sterols to their corresponding Delta(7)-isomers.<ref>PMID:12760743</ref> <ref>PMID:8798407</ref> <ref>PMID:9894009</ref>
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== References ==
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<references/>
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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: Masureel M]]
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[[Category: Sun D]]

Current revision

Human EBP complexed with compound 1

PDB ID 8w0r

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