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6qb7
From Proteopedia
(Difference between revisions)
(New page: '''Unreleased structure''' The entry 6qb7 is ON HOLD Authors: Pinkas, D.M., Bufton, J.C., Williams, E.P., Strain-Damerell, C., Kupinska, K., Burgess-Brown, N.A., von Delft, F., Arrowsmi...) |
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| - | '''Unreleased structure''' | ||
| - | + | ==Structure of the H1 domain of human KCTD16== | |
| - | + | <StructureSection load='6qb7' size='340' side='right'caption='[[6qb7]], [[Resolution|resolution]] 2.23Å' scene=''> | |
| - | + | == Structural highlights == | |
| - | + | <table><tr><td colspan='2'>[[6qb7]] is a 5 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6QB7 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6QB7 FirstGlance]. <br> | |
| - | + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.23Å</td></tr> | |
| - | [[Category: | + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=PO4:PHOSPHATE+ION'>PO4</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=6qb7 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6qb7 OCA], [https://pdbe.org/6qb7 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6qb7 RCSB], [https://www.ebi.ac.uk/pdbsum/6qb7 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6qb7 ProSAT]</span></td></tr> |
| - | [[Category: Arrowsmith | + | </table> |
| - | [[Category: | + | == Function == |
| - | [[Category: | + | [https://www.uniprot.org/uniprot/KCD16_HUMAN KCD16_HUMAN] Auxiliary subunit of GABA-B receptors that determine the pharmacology and kinetics of the receptor response. Increases agonist potency and markedly alter the G-protein signaling of the receptors by accelerating onset and promoting desensitization (By similarity). |
| - | [[Category: Bullock | + | __TOC__ |
| - | [[Category: | + | </StructureSection> |
| - | [[Category: | + | [[Category: Homo sapiens]] |
| - | [[Category: | + | [[Category: Large Structures]] |
| - | [[Category: | + | [[Category: Arrowsmith CH]] |
| - | [[Category: Strain-Damerell | + | [[Category: Bountra C]] |
| - | [[Category: | + | [[Category: Bufton JC]] |
| - | [[Category: | + | [[Category: Bullock AN]] |
| + | [[Category: Burgess-Brown NA]] | ||
| + | [[Category: Edwards AM]] | ||
| + | [[Category: Kupinska K]] | ||
| + | [[Category: Pinkas DM]] | ||
| + | [[Category: Strain-Damerell C]] | ||
| + | [[Category: Williams EP]] | ||
| + | [[Category: Von Delft F]] | ||
Current revision
Structure of the H1 domain of human KCTD16
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