5vec
From Proteopedia
(Difference between revisions)
| Line 1: | Line 1: | ||
| - | '''Unreleased structure''' | ||
| - | + | ==Crystal Structure of the R515L missense variant of human PGM1== | |
| - | + | <StructureSection load='5vec' size='340' side='right' caption='[[5vec]], [[Resolution|resolution]] 2.20Å' scene=''> | |
| - | + | == Structural highlights == | |
| - | + | <table><tr><td colspan='2'>[[5vec]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5VEC OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5VEC FirstGlance]. <br> | |
| - | + | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=GOL:GLYCEROL'>GOL</scene>, <scene name='pdbligand=MG:MAGNESIUM+ION'>MG</scene>, <scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene></td></tr> | |
| - | [[Category: | + | <tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[5epc|5epc]]</td></tr> |
| - | [[Category: Beamer, L | + | <tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[http://en.wikipedia.org/wiki/Phosphoglucomutase Phosphoglucomutase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=5.4.2.2 5.4.2.2] </span></td></tr> |
| - | [[Category: Stiers, K | + | <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=5vec FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5vec OCA], [http://pdbe.org/5vec PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5vec RCSB], [http://www.ebi.ac.uk/pdbsum/5vec PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5vec ProSAT]</span></td></tr> |
| + | </table> | ||
| + | == Disease == | ||
| + | [[http://www.uniprot.org/uniprot/PGM1_HUMAN PGM1_HUMAN]] PGM-CDG;Glycogen storage disease due to phosphoglucomutase deficiency. The disease is caused by mutations affecting the gene represented in this entry. | ||
| + | == Function == | ||
| + | [[http://www.uniprot.org/uniprot/PGM1_HUMAN PGM1_HUMAN]] This enzyme participates in both the breakdown and synthesis of glucose. | ||
| + | __TOC__ | ||
| + | </StructureSection> | ||
| + | [[Category: Phosphoglucomutase]] | ||
| + | [[Category: Beamer, L J]] | ||
| + | [[Category: Stiers, K M]] | ||
| + | [[Category: Isomerase]] | ||
| + | [[Category: Pgm1]] | ||
| + | [[Category: Phosphoglucomutase-1]] | ||
| + | [[Category: Phosphoryl transfer]] | ||
Revision as of 05:26, 27 June 2018
Crystal Structure of the R515L missense variant of human PGM1
| |||||||||||
