7va1: Difference between revisions

From Proteopedia
Jump to navigationJump to search
OCA (talk | contribs)
No edit summary
OCA (talk | contribs)
No edit summary
Line 1: Line 1:
'''Unreleased structure'''


The entry 7va1 is ON HOLD  until 2024-02-27
==Crystal structure of human 3-phosphoglycerate dehydrogenase in complex with GDD-04-35==
 
<StructureSection load='7va1' size='340' side='right'caption='[[7va1]], [[Resolution|resolution]] 1.74&Aring;' scene=''>
Authors: Cen, Y., Gao, D., Zhou, J., Tian, P.
== Structural highlights ==
 
<table><tr><td colspan='2'>[[7va1]] is a 4 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=7VA1 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7VA1 FirstGlance]. <br>
Description: Crystal structure of human 3-phosphoglycerate dehydrogenase in complex with GDD-04-35
</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=5YP:4-[(3-ethanoylphenyl)sulfamoyl]-~{N}-[4-(3-fluorophenyl)-1,3-thiazol-2-yl]benzamide'>5YP</scene></td></tr>
[[Category: Unreleased Structures]]
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=7va1 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7va1 OCA], [https://pdbe.org/7va1 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7va1 RCSB], [https://www.ebi.ac.uk/pdbsum/7va1 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7va1 ProSAT]</span></td></tr>
[[Category: Cen, Y]]
</table>
[[Category: Gao, D]]
== Disease ==
[[Category: Zhou, J]]
[https://www.uniprot.org/uniprot/SERA_HUMAN SERA_HUMAN] Defects in PHGDH are the cause of phosphoglycerate dehydrogenase deficiency (PHGDH deficiency) [MIM:[https://omim.org/entry/601815 601815]. It is characterized by congenital microcephaly, psychomotor retardation, and seizures.
[[Category: Tian, P]]
== Function ==
[https://www.uniprot.org/uniprot/SERA_HUMAN SERA_HUMAN]
__TOC__
</StructureSection>
[[Category: Homo sapiens]]
[[Category: Large Structures]]
[[Category: Cen Y]]
[[Category: Gao D]]
[[Category: Tian P]]
[[Category: Zhou J]]