6rj2: Difference between revisions

Line 1:

~~'''Unreleased structure'''~~

~~The entry~~ 6rj2 is ~~ON HOLD until Paper Publication~~

==Crystal structure of PHGDH in complex with compound 40==

~~Authors~~:

== Structural highlights ==

<table><tr><td colspan='2'>[[6rj2]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6RJ2 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6RJ2 FirstGlance]. <br>

~~Description~~:

</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=K52:~{N}-[(1~{R})-1-[4-(ethanoylsulfamoyl)phenyl]ethyl]-2-methyl-5-phenyl-pyrazole-3-carboxamide'>K52</scene>, <scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene></td></tr>

[[Category: ~~Unreleased~~ Structures]]

<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=6rj2 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6rj2 OCA], [http://pdbe.org/6rj2 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6rj2 RCSB], [http://www.ebi.ac.uk/pdbsum/6rj2 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6rj2 ProSAT]</span></td></tr>

</table>

== Disease ==

[[http://www.uniprot.org/uniprot/SERA_HUMAN SERA_HUMAN]] Defects in PHGDH are the cause of phosphoglycerate dehydrogenase deficiency (PHGDH deficiency) [MIM:[http://omim.org/entry/601815 601815]]. It is characterized by congenital microcephaly, psychomotor retardation, and seizures.

__TOC__

</StructureSection>

[[Category: Large Structures]]

[[Category: Bader, G]]

[[Category: Wolkerstorfer, B]]

[[Category: Zoephel, A]]

[[Category: Dehydrogenase]]

[[Category: Oxidoreductase]]

[[Category: Protein-ligand complex]]

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@@ Line 1: / Line 1: @@
-'''Unreleased structure'''
-The entry 6rj2 is ON HOLD  until Paper Publication
+==Crystal structure of PHGDH in complex with compound 40==
+<StructureSection load='6rj2' size='340' side='right'caption='[[6rj2]], [[Resolution|resolution]] 2.00&Aring;' scene=''>
-Authors:
+== Structural highlights ==
+<table><tr><td colspan='2'>[[6rj2]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6RJ2 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6RJ2 FirstGlance]. <br>
-Description:
+</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=K52:~{N}-[(1~{R})-1-[4-(ethanoylsulfamoyl)phenyl]ethyl]-2-methyl-5-phenyl-pyrazole-3-carboxamide'>K52</scene>, <scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene></td></tr>
-[[Category: Unreleased Structures]]
+<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=6rj2 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6rj2 OCA], [http://pdbe.org/6rj2 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6rj2 RCSB], [http://www.ebi.ac.uk/pdbsum/6rj2 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6rj2 ProSAT]</span></td></tr>
+</table>
+== Disease ==
+[[http://www.uniprot.org/uniprot/SERA_HUMAN SERA_HUMAN]] Defects in PHGDH are the cause of phosphoglycerate dehydrogenase deficiency (PHGDH deficiency) [MIM:[http://omim.org/entry/601815 601815]]. It is characterized by congenital microcephaly, psychomotor retardation, and seizures.
+__TOC__
+</StructureSection>
+[[Category: Large Structures]]
+[[Category: Bader, G]]
+[[Category: Wolkerstorfer, B]]
+[[Category: Zoephel, A]]
+[[Category: Dehydrogenase]]
+[[Category: Oxidoreductase]]
+[[Category: Protein-ligand complex]]