View source for 9jk8


==Human VANGL1 in complex with PK1==
<StructureSection load='9jk8' size='340' side='right'caption='[[9jk8]], [[Resolution|resolution]] 2.60&Aring;' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>[[9jk8]] is a 6 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=9JK8 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=9JK8 FirstGlance]. <br>
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 2.6&#8491;</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=9jk8 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=9jk8 OCA], [https://pdbe.org/9jk8 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=9jk8 RCSB], [https://www.ebi.ac.uk/pdbsum/9jk8 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=9jk8 ProSAT]</span></td></tr>
</table>
== Disease ==
[https://www.uniprot.org/uniprot/VANG1_HUMAN VANG1_HUMAN] Caudal regression syndrome. The disease is caused by variants affecting the gene represented in this entry.  The disease is caused by variants affecting the gene represented in this entry.
== Function ==
[https://www.uniprot.org/uniprot/VANG1_HUMAN VANG1_HUMAN] 
__TOC__
</StructureSection>
[[Category: Homo sapiens]]
[[Category: Large Structures]]
[[Category: Jian S]]
[[Category: Song Y]]
[[Category: Zhang Z]]
[[Category: Zheng P]]