7v0s: Difference between revisions
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The entry | ==Local refinement of RhAG/CE trimer, class 1 of erythrocyte ankyrin-1 complex== | ||
<StructureSection load='7v0s' size='340' side='right'caption='[[7v0s]], [[Resolution|resolution]] 2.50Å' scene=''> | |||
== Structural highlights == | |||
<table><tr><td colspan='2'>[[7v0s]] is a 4 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=7V0S OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7V0S 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]] 2.5Å</td></tr> | |||
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=AJP:Digitonin'>AJP</scene>, <scene name='pdbligand=CLR:CHOLESTEROL'>CLR</scene></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=7v0s FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7v0s OCA], [https://pdbe.org/7v0s PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7v0s RCSB], [https://www.ebi.ac.uk/pdbsum/7v0s PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7v0s ProSAT]</span></td></tr> | |||
</table> | |||
== Disease == | |||
[https://www.uniprot.org/uniprot/RHCE_HUMAN RHCE_HUMAN] Rh deficiency syndrome. The disease is caused by variants affecting the gene represented in this entry. | |||
== Function == | |||
[https://www.uniprot.org/uniprot/RHCE_HUMAN RHCE_HUMAN] May be part of an oligomeric complex which is likely to have a transport or channel function in the erythrocyte membrane. | |||
==See Also== | |||
*[[Ankyrin 3D structures|Ankyrin 3D structures]] | |||
__TOC__ | |||
[[Category: | </StructureSection> | ||
[[Category: Homo sapiens]] | |||
[[Category: Large Structures]] | |||
[[Category: Cali T]] | |||
[[Category: Clarke OB]] | |||
[[Category: Johnston JD]] | |||
[[Category: Kim K]] | |||
[[Category: Noble AJ]] | |||
[[Category: Vallese F]] | |||
[[Category: Yen LY]] | |||
Latest revision as of 12:39, 14 February 2024
Local refinement of RhAG/CE trimer, class 1 of erythrocyte ankyrin-1 complexLocal refinement of RhAG/CE trimer, class 1 of erythrocyte ankyrin-1 complex
Structural highlights
DiseaseRHCE_HUMAN Rh deficiency syndrome. The disease is caused by variants affecting the gene represented in this entry. FunctionRHCE_HUMAN May be part of an oligomeric complex which is likely to have a transport or channel function in the erythrocyte membrane. See Also |
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