9jk8: Difference between revisions
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The entry | ==Human VANGL1 in complex with PK1== | ||
<StructureSection load='9jk8' size='340' side='right'caption='[[9jk8]], [[Resolution|resolution]] 2.60Å' 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]] 2.6Å</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=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]] | |||
Latest revision as of 12:34, 25 December 2024
Human VANGL1 in complex with PK1Human VANGL1 in complex with PK1
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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