8s9s: Difference between revisions
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The entry | ==Structure of the human ER membrane protein complex (EMC) in GDN== | ||
<StructureSection load='8s9s' size='340' side='right'caption='[[8s9s]], [[Resolution|resolution]] 3.60Å' scene=''> | |||
== Structural highlights == | |||
<table><tr><td colspan='2'>[[8s9s]] is a 9 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=8S9S OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8S9S FirstGlance]. <br> | |||
</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=NAG:N-ACETYL-D-GLUCOSAMINE'>NAG</scene>, <scene name='pdbligand=PCW:1,2-DIOLEOYL-SN-GLYCERO-3-PHOSPHOCHOLINE'>PCW</scene></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=8s9s FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8s9s OCA], [https://pdbe.org/8s9s PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8s9s RCSB], [https://www.ebi.ac.uk/pdbsum/8s9s PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8s9s ProSAT]</span></td></tr> | ||
</table> | |||
== Disease == | |||
[https://www.uniprot.org/uniprot/EMC1_HUMAN EMC1_HUMAN] Global developmental delay-visual anomalies-progressive cerebellar atrophy-truncal hypotonia syndrome. The disease is caused by mutations affecting the gene represented in this entry. | |||
== Function == | |||
[https://www.uniprot.org/uniprot/EMC1_HUMAN EMC1_HUMAN] | |||
__TOC__ | |||
</StructureSection> | |||
[[Category: Homo sapiens]] | |||
[[Category: Large Structures]] | |||
[[Category: Nguyen V]] | |||
[[Category: Tomaleri GP]] | |||
[[Category: Voorhees RM]] | |||
Latest revision as of 10:03, 18 May 2023
Structure of the human ER membrane protein complex (EMC) in GDNStructure of the human ER membrane protein complex (EMC) in GDN
Structural highlights
DiseaseEMC1_HUMAN Global developmental delay-visual anomalies-progressive cerebellar atrophy-truncal hypotonia syndrome. The disease is caused by mutations affecting the gene represented in this entry. Function |
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