6qb7: Difference between revisions

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'''Unreleased structure'''


The entry 6qb7 is ON HOLD
==Structure of the H1 domain of human KCTD16==
 
<StructureSection load='6qb7' size='340' side='right'caption='[[6qb7]], [[Resolution|resolution]] 2.23&Aring;' scene=''>
Authors: Pinkas, D.M., Bufton, J.C., Williams, E.P., Strain-Damerell, C., Kupinska, K., Burgess-Brown, N.A., von Delft, F., Arrowsmith, C.H., Edwards, A.M., Bountra, C., Bullock, A.N., Structural Genomics Consortium (SGC)
== 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>
Description: Structure of the H1 domain of human KCTD16
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.23&#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=PO4:PHOSPHATE+ION'>PO4</scene></td></tr>
[[Category: Williams, E.P]]
<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, C.H]]
</table>
[[Category: Burgess-Brown, N.A]]
== Function ==
[[Category: Von Delft, F]]
[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, A.N]]
__TOC__
[[Category: Bufton, J.C]]
</StructureSection>
[[Category: Pinkas, D.M]]
[[Category: Homo sapiens]]
[[Category: Edwards, A.M]]
[[Category: Large Structures]]
[[Category: Structural Genomics Consortium (Sgc)]]
[[Category: Arrowsmith CH]]
[[Category: Strain-Damerell, C]]
[[Category: Bountra C]]
[[Category: Bountra, C]]
[[Category: Bufton JC]]
[[Category: Kupinska, K]]
[[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]]

Latest revision as of 07:37, 1 May 2024

Structure of the H1 domain of human KCTD16

6qb7, resolution 2.23Å

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