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8iu2

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Current revision (10:08, 27 March 2024) (edit) (undo)
 
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'''Unreleased structure'''
 
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The entry 8iu2 is ON HOLD until 2025-03-23
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==Cryo-EM structure of Long-wave-sensitive opsin 1==
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<StructureSection load='8iu2' size='340' side='right'caption='[[8iu2]], [[Resolution|resolution]] 3.35&Aring;' scene=''>
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Authors: Peng, Q., Cheng, X.Y., Li, J., Lu, Q.Y., Li, Y.Y., Zhang, J.
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== Structural highlights ==
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<table><tr><td colspan='2'>[[8iu2]] is a 5 chain structure with sequence from [https://en.wikipedia.org/wiki/Bos_taurus Bos taurus] and [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=8IU2 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8IU2 FirstGlance]. <br>
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Description: Cryo-EM structure of Long-wave-sensitive opsin 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]] 3.35&#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=RET:RETINAL'>RET</scene></td></tr>
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[[Category: Lu, Q.Y]]
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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=8iu2 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8iu2 OCA], [https://pdbe.org/8iu2 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8iu2 RCSB], [https://www.ebi.ac.uk/pdbsum/8iu2 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8iu2 ProSAT]</span></td></tr>
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[[Category: Li, J]]
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</table>
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[[Category: Zhang, J]]
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== Disease ==
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[[Category: Peng, Q]]
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[https://www.uniprot.org/uniprot/OPSR_HUMAN OPSR_HUMAN] Blue cone monochromatism;X-linked cone dysfunction syndrome with myopia;NON RARE IN EUROPE: Partial color blindness, protan type;Cone rod dystrophy. The disease is caused by variants affecting the gene represented in this entry. The disease is caused by variants affecting the gene represented in this entry.
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[[Category: Cheng, X.Y]]
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== Function ==
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[[Category: Li, Y.Y]]
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[https://www.uniprot.org/uniprot/OPSR_HUMAN OPSR_HUMAN] Visual pigments are the light-absorbing molecules that mediate vision. They consist of an apoprotein, opsin, covalently linked to cis-retinal.
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__TOC__
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</StructureSection>
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[[Category: Bos taurus]]
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[[Category: Homo sapiens]]
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[[Category: Large Structures]]
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[[Category: Cheng XY]]
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[[Category: Li J]]
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[[Category: Li YY]]
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[[Category: Lu QY]]
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[[Category: Peng Q]]
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[[Category: Zhang J]]

Current revision

Cryo-EM structure of Long-wave-sensitive opsin 1

PDB ID 8iu2

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