8cvx: Difference between revisions
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==== | ==Human glycogenin-1 and glycogen synthase-1 complex in the presence of glucose-6-phosphate== | ||
<StructureSection load='8cvx' size='340' side='right'caption='[[8cvx]]' scene=''> | <StructureSection load='8cvx' size='340' side='right'caption='[[8cvx]], [[Resolution|resolution]] 3.50Å' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id= OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol= FirstGlance]. <br> | <table><tr><td colspan='2'>[[8cvx]] is a 8 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=8CVX OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8CVX FirstGlance]. <br> | ||
</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=8cvx FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8cvx OCA], [https://pdbe.org/8cvx PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8cvx RCSB], [https://www.ebi.ac.uk/pdbsum/8cvx PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8cvx ProSAT]</span></td></tr> | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=G6P:ALPHA-D-GLUCOSE-6-PHOSPHATE'>G6P</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=8cvx FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8cvx OCA], [https://pdbe.org/8cvx PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8cvx RCSB], [https://www.ebi.ac.uk/pdbsum/8cvx PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8cvx ProSAT]</span></td></tr> | |||
</table> | </table> | ||
== Disease == | |||
[[https://www.uniprot.org/uniprot/GYS1_HUMAN GYS1_HUMAN]] Glycogen storage disease due to muscle and heart glycogen synthase deficiency. The disease is caused by variants affecting the gene represented in this entry. | |||
== Function == | |||
[[https://www.uniprot.org/uniprot/GYS1_HUMAN GYS1_HUMAN]] Transfers the glycosyl residue from UDP-Glc to the non-reducing end of alpha-1,4-glucan.[UniProtKB:P13834] | |||
__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
[[Category: Homo sapiens]] | |||
[[Category: Large Structures]] | [[Category: Large Structures]] | ||
[[Category: | [[Category: Fastman NM]] | ||
[[Category: Liu Y]] | |||
[[Category: Tzitzilonis C]] | |||
Revision as of 05:35, 8 September 2022
Human glycogenin-1 and glycogen synthase-1 complex in the presence of glucose-6-phosphate
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