9i3t: Difference between revisions
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New page: '''Unreleased structure''' The entry 9i3t is ON HOLD Authors: Description: Category: Unreleased Structures |
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The entry | ==Dark-state structure of human medium-wave-sensitive cone opsin (OPN1MW)== | ||
<StructureSection load='9i3t' size='340' side='right'caption='[[9i3t]], [[Resolution|resolution]] 3.70Å' scene=''> | |||
== Structural highlights == | |||
<table><tr><td colspan='2'>[[9i3t]] is a 3 chain structure with sequence from [https://en.wikipedia.org/wiki/Escherichia_coli Escherichia coli], [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] and [https://en.wikipedia.org/wiki/Synthetic_construct Synthetic construct]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=9I3T OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=9I3T FirstGlance]. <br> | |||
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 3.7Å</td></tr> | |||
[[Category: | <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> | ||
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=9i3t FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=9i3t OCA], [https://pdbe.org/9i3t PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=9i3t RCSB], [https://www.ebi.ac.uk/pdbsum/9i3t PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=9i3t ProSAT]</span></td></tr> | |||
</table> | |||
== Disease == | |||
[https://www.uniprot.org/uniprot/OPSG_HUMAN OPSG_HUMAN] Blue cone monochromatism;Cone rod dystrophy;X-linked cone dysfunction syndrome with myopia. 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. The disease is caused by variants affecting the gene represented in this entry. | |||
== Function == | |||
[https://www.uniprot.org/uniprot/OPSG_HUMAN OPSG_HUMAN] Visual pigments are the light-absorbing molecules that mediate vision. They consist of an apoprotein, opsin, covalently linked to cis-retinal.<ref>PMID:12051694</ref> <ref>PMID:1302020</ref> <ref>PMID:2937147</ref> [https://www.uniprot.org/uniprot/C562_ECOLX C562_ECOLX] Electron-transport protein of unknown function. | |||
== References == | |||
<references/> | |||
__TOC__ | |||
</StructureSection> | |||
[[Category: Escherichia coli]] | |||
[[Category: Homo sapiens]] | |||
[[Category: Large Structures]] | |||
[[Category: Synthetic construct]] | |||
[[Category: Isaikina P]] | |||
[[Category: Schmidt SL]] | |||
[[Category: Sen S]] | |||
Latest revision as of 04:34, 24 June 2026
Dark-state structure of human medium-wave-sensitive cone opsin (OPN1MW)
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