9uwv: Difference between revisions

From Proteopedia
Jump to navigationJump to search
OCA (talk | contribs)
m Protected "9uwv" [edit=sysop:move=sysop]
OCA (talk | contribs)
No edit summary
 
Line 1: Line 1:
'''Unreleased structure'''


The entry 9uwv is ON HOLD  until Paper Publication
==SalA bound Kappa Opioid Receptor in complex with Gi==
 
<StructureSection load='9uwv' size='340' side='right'caption='[[9uwv]], [[Resolution|resolution]] 3.30&Aring;' scene=''>
Authors: Wang, Y., Zhuang, Y., Xu, H.E.
== Structural highlights ==
 
<table><tr><td colspan='2'>[[9uwv]] is a 5 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=9UWV OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=9UWV FirstGlance]. <br>
Description: SalA bound Kappa Opioid Receptor in complex with Gi
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 3.3&#8491;</td></tr>
[[Category: Unreleased Structures]]
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=A1EQK:methyl+(2~{S},4~{a}~{R},6~{a}~{R},7~{R},9~{S},10~{a}~{S},10~{b}~{R})-9-acetyloxy-2-(furan-3-yl)-6~{a},10~{b}-dimethyl-4,10-bis(oxidanylidene)-2,4~{a},5,6,7,8,9,10~{a}-octahydro-1~{H}-benzo[f]isochromene-7-carboxylate'>A1EQK</scene></td></tr>
[[Category: Xu, H.E]]
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=9uwv FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=9uwv OCA], [https://pdbe.org/9uwv PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=9uwv RCSB], [https://www.ebi.ac.uk/pdbsum/9uwv PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=9uwv ProSAT]</span></td></tr>
[[Category: Zhuang, Y]]
</table>
[[Category: Wang, Y]]
== Function ==
[https://www.uniprot.org/uniprot/GNAI1_HUMAN GNAI1_HUMAN] Guanine nucleotide-binding proteins (G proteins) are involved as modulators or transducers in various transmembrane signaling systems. The G(i) proteins are involved in hormonal regulation of adenylate cyclase: they inhibit the cyclase in response to beta-adrenergic stimuli. The inactive GDP-bound form prevents the association of RGS14 with centrosomes and is required for the translocation of RGS14 from the cytoplasm to the plasma membrane. May play a role in cell division.<ref>PMID:17635935</ref> <ref>PMID:17264214</ref>
== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Bos taurus]]
[[Category: Homo sapiens]]
[[Category: Large Structures]]
[[Category: Rattus norvegicus]]
[[Category: Synthetic construct]]
[[Category: Wang Y]]
[[Category: Xu HE]]
[[Category: Zhuang Y]]

Latest revision as of 05:04, 27 May 2026

SalA bound Kappa Opioid Receptor in complex with Gi

9uwv, resolution 3.30Å

Drag the structure with the mouse to rotate

Proteopedia Page Contributors and Editors (what is this?)

OCA