8f7w
From Proteopedia
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- | '''Unreleased structure''' | ||
- | + | ==Gi bound kappa-opioid receptor in complex with dynorphin== | |
- | + | <StructureSection load='8f7w' size='340' side='right'caption='[[8f7w]], [[Resolution|resolution]] 3.19Å' scene=''> | |
- | + | == Structural highlights == | |
- | + | <table><tr><td colspan='2'>[[8f7w]] is a 6 chain structure with sequence from [https://en.wikipedia.org/wiki/Bos_taurus Bos taurus], [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens], [https://en.wikipedia.org/wiki/Rattus_norvegicus Rattus norvegicus] 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=8F7W OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8F7W FirstGlance]. <br> | |
- | + | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=CLR:CHOLESTEROL'>CLR</scene>, <scene name='pdbligand=PLM:PALMITIC+ACID'>PLM</scene></td></tr> | |
- | [[Category: | + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=8f7w FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8f7w OCA], [https://pdbe.org/8f7w PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8f7w RCSB], [https://www.ebi.ac.uk/pdbsum/8f7w PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8f7w ProSAT]</span></td></tr> |
- | [[Category: | + | </table> |
- | [[Category: | + | == Function == |
- | [[Category: Jain | + | [https://www.uniprot.org/uniprot/OPRK_HUMAN OPRK_HUMAN] G-protein coupled opioid receptor that functions as receptor for endogenous alpha-neoendorphins and dynorphins, but has low affinity for beta-endorphins. Also functions as receptor for various synthetic opioids and for the psychoactive diterpene salvinorin A. Ligand binding causes a conformation change that triggers signaling via guanine nucleotide-binding proteins (G proteins) and modulates the activity of down-stream effectors, such as adenylate cyclase. Signaling leads to the inhibition of adenylate cyclase activity. Inhibits neurotransmitter release by reducing calcium ion currents and increasing potassium ion conductance. Plays a role in the perception of pain. Plays a role in mediating reduced physical activity upon treatment with synthetic opioids. Plays a role in the regulation of salivation in response to synthetic opioids. May play a role in arousal and regulation of autonomic and neuroendocrine functions.<ref>PMID:12004055</ref> <ref>PMID:22437504</ref> <ref>PMID:7624359</ref> <ref>PMID:8060324</ref> |
- | [[Category: | + | == References == |
- | [[Category: Liu | + | <references/> |
- | [[Category: | + | __TOC__ |
- | [[Category: | + | </StructureSection> |
- | [[Category: | + | [[Category: Bos taurus]] |
- | [[Category: | + | [[Category: Homo sapiens]] |
- | [[Category: | + | [[Category: Large Structures]] |
- | [[Category: Yuan | + | [[Category: Rattus norvegicus]] |
- | [[Category: | + | [[Category: Synthetic construct]] |
+ | [[Category: DiBerto JF]] | ||
+ | [[Category: Jain MK]] | ||
+ | [[Category: Jiang Y]] | ||
+ | [[Category: Liu W]] | ||
+ | [[Category: Melcher K]] | ||
+ | [[Category: Roth BL]] | ||
+ | [[Category: Schmitz GP]] | ||
+ | [[Category: Wang Y]] | ||
+ | [[Category: Xu HE]] | ||
+ | [[Category: Yuan Q]] | ||
+ | [[Category: Zhou XE]] | ||
+ | [[Category: Zhuang Y]] |
Revision as of 10:11, 14 December 2022
Gi bound kappa-opioid receptor in complex with dynorphin
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Categories: Bos taurus | Homo sapiens | Large Structures | Rattus norvegicus | Synthetic construct | DiBerto JF | Jain MK | Jiang Y | Liu W | Melcher K | Roth BL | Schmitz GP | Wang Y | Xu HE | Yuan Q | Zhou XE | Zhuang Y