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8cvy
From Proteopedia
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| - | '''Unreleased structure''' | ||
| - | + | ==Human glycogenin-1 and glycogen synthase-1 complex in the apo mobile state== | |
| - | + | <StructureSection load='8cvy' size='340' side='right'caption='[[8cvy]], [[Resolution|resolution]] 3.60Å' scene=''> | |
| - | + | == Structural highlights == | |
| - | + | <table><tr><td colspan='2'>[[8cvy]] is a 7 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=8CVY OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8CVY 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=8cvy FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8cvy OCA], [https://pdbe.org/8cvy PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8cvy RCSB], [https://www.ebi.ac.uk/pdbsum/8cvy PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8cvy ProSAT]</span></td></tr> | |
| - | [[Category: | + | </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__ | ||
| + | </StructureSection> | ||
| + | [[Category: Homo sapiens]] | ||
| + | [[Category: Large Structures]] | ||
| + | [[Category: Fastman NM]] | ||
| + | [[Category: Liu Y]] | ||
| + | [[Category: Tzitzilonis C]] | ||
Current revision
Human glycogenin-1 and glycogen synthase-1 complex in the apo mobile state
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