6eql: Difference between revisions
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==Crystal Structure of Human Glycogenin-1 (GYG1) Tyr195pIPhe mutant complexed with manganese and UDP== | |||
<StructureSection load='6eql' size='340' side='right' caption='[[6eql]], [[Resolution|resolution]] 2.38Å' scene=''> | |||
== Structural highlights == | |||
<table><tr><td colspan='2'>[[6eql]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6EQL OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6EQL FirstGlance]. <br> | |||
</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=2PE:NONAETHYLENE+GLYCOL'>2PE</scene>, <scene name='pdbligand=EDO:1,2-ETHANEDIOL'>EDO</scene>, <scene name='pdbligand=MN:MANGANESE+(II)+ION'>MN</scene>, <scene name='pdbligand=UDP:URIDINE-5-DIPHOSPHATE'>UDP</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=6eql FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6eql OCA], [http://pdbe.org/6eql PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6eql RCSB], [http://www.ebi.ac.uk/pdbsum/6eql PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6eql 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 complexed with manganese and UDP
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