6zc3: Difference between revisions
From Proteopedia
Jump to navigationJump to search
New page: '''Unreleased structure''' The entry 6zc3 is ON HOLD Authors: Roske, Y., Heinemann, U., Oschkinat, H. Description: Small-molecule inhibitors of the PDZ domain of Dishevelled proteins i... |
No edit summary |
||
| (5 intermediate revisions by the same user not shown) | |||
| Line 1: | Line 1: | ||
==Small-molecule inhibitors of the PDZ domain of Dishevelled proteins interrupt Wnt signalling== | |||
<StructureSection load='6zc3' size='340' side='right'caption='[[6zc3]], [[Resolution|resolution]] 1.67Å' scene=''> | |||
== Structural highlights == | |||
<table><tr><td colspan='2'>[[6zc3]] is a 2 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=6ZC3 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6ZC3 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]] 1.67Å</td></tr> | |||
[[Category: | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=EDO:1,2-ETHANEDIOL'>EDO</scene>, <scene name='pdbligand=JOR:5-fluoranyl-2-(methylsulfonylamino)benzoic+acid'>JOR</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=6zc3 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6zc3 OCA], [https://pdbe.org/6zc3 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6zc3 RCSB], [https://www.ebi.ac.uk/pdbsum/6zc3 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6zc3 ProSAT]</span></td></tr> | ||
[[Category: Heinemann | </table> | ||
[[Category: Roske | == Disease == | ||
[https://www.uniprot.org/uniprot/DVL3_HUMAN DVL3_HUMAN] Autosomal dominant Robinow syndrome. The disease is caused by variants affecting the gene represented in this entry. | |||
== Function == | |||
[https://www.uniprot.org/uniprot/DVL3_HUMAN DVL3_HUMAN] Involved in the signal transduction pathway mediated by multiple Wnt genes.[UniProtKB:Q61062] | |||
__TOC__ | |||
</StructureSection> | |||
[[Category: Homo sapiens]] | |||
[[Category: Large Structures]] | |||
[[Category: Heinemann U]] | |||
[[Category: Oschkinat H]] | |||
[[Category: Roske Y]] | |||
Latest revision as of 13:46, 24 January 2024
Small-molecule inhibitors of the PDZ domain of Dishevelled proteins interrupt Wnt signalling
| ||||||||||||
