8iu2: Difference between revisions
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New page: '''Unreleased structure''' The entry 8iu2 is ON HOLD Authors: Li, J., Zhang, J. Description: Cryo-EM structure of Long-wave-sensitive opsin 1 Category: Unreleased Structures [[Cate... |
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==Cryo-EM structure of Long-wave-sensitive opsin 1== | |||
<StructureSection load='8iu2' size='340' side='right'caption='[[8iu2]], [[Resolution|resolution]] 3.35Å' scene=''> | |||
== Structural highlights == | |||
<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> | |||
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 3.35Å</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> | ||
[[Category: Li | <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> | ||
[[Category: Zhang | </table> | ||
== Disease == | |||
[https://www.uniprot.org/uniprot/OPSR_HUMAN OPSR_HUMAN] X-linked cone dysfunction syndrome with myopia;Blue cone monochromatism;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. | |||
== Function == | |||
[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. | |||
__TOC__ | |||
</StructureSection> | |||
[[Category: Bos taurus]] | |||
[[Category: Homo sapiens]] | |||
[[Category: Large Structures]] | |||
[[Category: Cheng XY]] | |||
[[Category: Li J]] | |||
[[Category: Li YY]] | |||
[[Category: Lu QY]] | |||
[[Category: Peng Q]] | |||
[[Category: Zhang J]] | |||
Latest revision as of 15:04, 30 October 2024
Cryo-EM structure of Long-wave-sensitive opsin 1Cryo-EM structure of Long-wave-sensitive opsin 1
Structural highlights
DiseaseOPSR_HUMAN X-linked cone dysfunction syndrome with myopia;Blue cone monochromatism;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. FunctionOPSR_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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