9jk6: Difference between revisions
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The entry | ==Human VANGL1 hexamer== | ||
<StructureSection load='9jk6' size='340' side='right'caption='[[9jk6]], [[Resolution|resolution]] 3.00Å' scene=''> | |||
== Structural highlights == | |||
<table><tr><td colspan='2'>[[9jk6]] 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=9JK6 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=9JK6 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]] 3Å</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=9jk6 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=9jk6 OCA], [https://pdbe.org/9jk6 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=9jk6 RCSB], [https://www.ebi.ac.uk/pdbsum/9jk6 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=9jk6 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]] | |||
Latest revision as of 12:34, 25 December 2024
Human VANGL1 hexamerHuman VANGL1 hexamer
Structural highlights
DiseaseVANG1_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 |
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