6eqj
From Proteopedia
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| - | '''Unreleased structure''' | ||
| - | + | ==Crystal Structure of Human Glycogenin-1 (GYG1) Tyr195pIPhe mutant, apo form== | |
| - | + | <StructureSection load='6eqj' size='340' side='right' caption='[[6eqj]], [[Resolution|resolution]] 2.18Å' scene=''> | |
| - | + | == Structural highlights == | |
| - | + | <table><tr><td colspan='2'>[[6eqj]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6EQJ OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6EQJ FirstGlance]. <br> | |
| - | + | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=EDO:1,2-ETHANEDIOL'>EDO</scene></td></tr> | |
| - | [[Category: | + | <tr id='NonStdRes'><td class="sblockLbl"><b>[[Non-Standard_Residue|NonStd Res:]]</b></td><td class="sblockDat"><scene name='pdbligand=PHI:IODO-PHENYLALANINE'>PHI</scene></td></tr> |
| - | [[Category: | + | <tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[http://en.wikipedia.org/wiki/Glycogenin_glucosyltransferase Glycogenin glucosyltransferase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.4.1.186 2.4.1.186] </span></td></tr> |
| - | [[Category: Bailey, H | + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6eqj FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6eqj OCA], [http://pdbe.org/6eqj PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6eqj RCSB], [http://www.ebi.ac.uk/pdbsum/6eqj PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6eqj ProSAT]</span></td></tr> |
| - | [[Category: | + | </table> |
| - | [[Category: | + | == Disease == |
| - | [[Category: | + | [[http://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 == | ||
| + | [[http://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__ | ||
| + | </StructureSection> | ||
| + | [[Category: Glycogenin glucosyltransferase]] | ||
| + | [[Category: Arrowsmith, C H]] | ||
| + | [[Category: Bailey, H J]] | ||
| + | [[Category: Bezerra, G A]] | ||
| + | [[Category: Bilyard, M K]] | ||
| + | [[Category: Bountra, C]] | ||
| + | [[Category: Davis, B G]] | ||
| + | [[Category: Edwards, A M]] | ||
[[Category: Kopec, J]] | [[Category: Kopec, J]] | ||
| - | [[Category: | + | [[Category: Lee, S Seo]] |
| - | [[Category: | + | [[Category: Yue, W W]] |
| - | [[Category: | + | [[Category: Glycogenin-1]] |
| - | [[Category: | + | [[Category: Hydrolase]] |
Revision as of 06:26, 20 December 2017
Crystal Structure of Human Glycogenin-1 (GYG1) Tyr195pIPhe mutant, apo form
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