5vg7: Difference between revisions
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==Crystal Structure of the R503Q missense variant of human PGM1== | |||
<StructureSection load='5vg7' size='340' side='right' caption='[[5vg7]], [[Resolution|resolution]] 1.95Å' scene=''> | |||
== Structural highlights == | |||
<table><tr><td colspan='2'>[[5vg7]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5VG7 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5VG7 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='NonStdRes'><td class="sblockLbl"><b>[[Non-Standard_Residue|NonStd Res:]]</b></td><td class="sblockDat"><scene name='pdbligand=SEP:PHOSPHOSERINE'>SEP</scene></td></tr> | ||
[[Category: Beamer, L | <tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[5epc|5epc]]</td></tr> | ||
[[Category: Stiers, K | <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> | ||
<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=5vg7 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5vg7 OCA], [http://pdbe.org/5vg7 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5vg7 RCSB], [http://www.ebi.ac.uk/pdbsum/5vg7 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5vg7 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 05:39, 20 June 2018
Crystal Structure of the R503Q missense variant of human PGM1
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