8s6a: Difference between revisions
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The entry | ==X-ray structure of Dishevelled 3 PDZ domain in a complex with a class III peptide ligand== | ||
<StructureSection load='8s6a' size='340' side='right'caption='[[8s6a]], [[Resolution|resolution]] 1.36Å' scene=''> | |||
== Structural highlights == | |||
<table><tr><td colspan='2'>[[8s6a]] is a 3 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=8S6A OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8S6A 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]] 1.36Å</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=8s6a FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8s6a OCA], [https://pdbe.org/8s6a PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8s6a RCSB], [https://www.ebi.ac.uk/pdbsum/8s6a PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8s6a ProSAT]</span></td></tr> | ||
</table> | |||
== 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: Barinka C]] | |||
[[Category: Komarek J]] | |||
Latest revision as of 10:17, 12 March 2025
X-ray structure of Dishevelled 3 PDZ domain in a complex with a class III peptide ligand
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