This old version of Proteopedia is provided for student assignments while the new version is undergoing repairs. Content and edits done in this old version of Proteopedia after March 1, 2026 will eventually be lost when it is retired in about June of 2026.
Apply for new accounts at the new Proteopedia. Your logins will work in both the old and new versions.
7xox
From Proteopedia
(Difference between revisions)
| Line 1: | Line 1: | ||
| - | ==== | + | ==Structural insights into human brain gut peptide cholecystokinin receptors== |
| - | <StructureSection load='7xox' size='340' side='right'caption='[[7xox]]' scene=''> | + | <StructureSection load='7xox' size='340' side='right'caption='[[7xox]], [[Resolution|resolution]] 3.10Å' scene=''> |
== Structural highlights == | == Structural highlights == | ||
| - | <table><tr><td colspan='2'>Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id= OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol= FirstGlance]. <br> | + | <table><tr><td colspan='2'>[[7xox]] is a 6 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] and [https://en.wikipedia.org/wiki/Mus_musculus Mus musculus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=7XOX OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7XOX FirstGlance]. <br> |
| - | </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=7xox FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7xox OCA], [https://pdbe.org/7xox PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7xox RCSB], [https://www.ebi.ac.uk/pdbsum/7xox PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7xox ProSAT]</span></td></tr> | + | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=TYS:O-SULFO-L-TYROSINE'>TYS</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=7xox FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7xox OCA], [https://pdbe.org/7xox PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7xox RCSB], [https://www.ebi.ac.uk/pdbsum/7xox PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7xox ProSAT]</span></td></tr> | ||
</table> | </table> | ||
| + | == Function == | ||
| + | [[https://www.uniprot.org/uniprot/GASR_HUMAN GASR_HUMAN]] Receptor for gastrin and cholecystokinin. The CKK-B receptors occur throughout the central nervous system where they modulate anxiety, analgesia, arousal, and neuroleptic activity. This receptor mediates its action by association with G proteins that activate a phosphatidylinositol-calcium second messenger system.<ref>PMID:8349705</ref> <ref>PMID:8185170</ref> <ref>PMID:7848914</ref> <ref>PMID:10913157</ref> <ref>PMID:11495676</ref> <ref>PMID:8221657</ref> Isoform 2 is constitutively activated and may regulate cancer cell proliferation via a gastrin-independent mechanism.<ref>PMID:8349705</ref> <ref>PMID:8185170</ref> <ref>PMID:7848914</ref> <ref>PMID:10913157</ref> <ref>PMID:11495676</ref> <ref>PMID:8221657</ref> | ||
| + | == References == | ||
| + | <references/> | ||
__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
| + | [[Category: Homo sapiens]] | ||
[[Category: Large Structures]] | [[Category: Large Structures]] | ||
| - | [[Category: | + | [[Category: Mus musculus]] |
| + | [[Category: Chen L]] | ||
| + | [[Category: Ding Y]] | ||
| + | [[Category: Ji S]] | ||
| + | [[Category: Liao Y]] | ||
| + | [[Category: Zhang H]] | ||
Revision as of 05:03, 8 September 2022
Structural insights into human brain gut peptide cholecystokinin receptors
| |||||||||||
Categories: Homo sapiens | Large Structures | Mus musculus | Chen L | Ding Y | Ji S | Liao Y | Zhang H
