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8cvz
From Proteopedia
(Difference between revisions)
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== Structural highlights == | == Structural highlights == | ||
<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> | <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='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 3.52Å</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 == | == 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 == | == 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. | |
| + | |||
| + | ==See Also== | ||
| + | *[[Glycogenin|Glycogenin]] | ||
__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
Current revision
Human glycogenin-1 and glycogen synthase-1 complex in the apo ordered state
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