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8cvz
From Proteopedia
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| - | ==== | + | ==Human glycogenin-1 and glycogen synthase-1 complex in the apo ordered state== |
| - | <StructureSection load='8cvz' size='340' side='right'caption='[[8cvz]]' scene=''> | + | <StructureSection load='8cvz' size='340' side='right'caption='[[8cvz]], [[Resolution|resolution]] 3.52Å' 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'>[[8cvz]] is a 10 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=8CVZ OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8CVZ 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=8cvz FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8cvz OCA], [https://pdbe.org/8cvz PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8cvz RCSB], [https://www.ebi.ac.uk/pdbsum/8cvz PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8cvz ProSAT]</span></td></tr> | </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=8cvz FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8cvz OCA], [https://pdbe.org/8cvz PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8cvz RCSB], [https://www.ebi.ac.uk/pdbsum/8cvz PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8cvz ProSAT]</span></td></tr> | ||
</table> | </table> | ||
| + | == Disease == | ||
| + | [[https://www.uniprot.org/uniprot/GLYG_HUMAN GLYG_HUMAN]] Glycogen storage disease due to glycogenin deficiency. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry. | ||
| + | == Function == | ||
| + | [[https://www.uniprot.org/uniprot/GLYG_HUMAN GLYG_HUMAN]] Self-glucosylates, via an inter-subunit mechanism, to form an oligosaccharide primer that serves as substrate for glycogen synthase. | ||
__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 apo ordered state
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