5n6c

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'''Unreleased structure'''
 
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The entry 5n6c is ON HOLD until Paper Publication
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==Crystal structure of human 3-phosphoglycerate dehydrogenase in complex with NAD and L-Tartrate==
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<StructureSection load='5n6c' size='340' side='right' caption='[[5n6c]], [[Resolution|resolution]] 2.30&Aring;' scene=''>
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Authors: Unterlass, J.E., Basle, A., Tucker, J., Cano, C., Noble, M.E.M., Curtin, N.J.
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== Structural highlights ==
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<table><tr><td colspan='2'>[[5n6c]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5N6C OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5N6C FirstGlance]. <br>
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Description: Crystal structure of human 3-phosphoglycerate dehydrogenase in complex with NAD and L-Tartrate
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</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=NAD:NICOTINAMIDE-ADENINE-DINUCLEOTIDE'>NAD</scene>, <scene name='pdbligand=TLA:L(+)-TARTARIC+ACID'>TLA</scene></td></tr>
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[[Category: Unreleased Structures]]
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<tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[http://en.wikipedia.org/wiki/Phosphoglycerate_dehydrogenase Phosphoglycerate dehydrogenase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.1.1.95 1.1.1.95] </span></td></tr>
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[[Category: Curtin, N.J]]
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<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=5n6c FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5n6c OCA], [http://pdbe.org/5n6c PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5n6c RCSB], [http://www.ebi.ac.uk/pdbsum/5n6c PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5n6c ProSAT]</span></td></tr>
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[[Category: Noble, M.E.M]]
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</table>
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[[Category: Unterlass, J.E]]
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== Disease ==
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[[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.
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__TOC__
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</StructureSection>
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[[Category: Phosphoglycerate dehydrogenase]]
[[Category: Basle, A]]
[[Category: Basle, A]]
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[[Category: Cano, C]]
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[[Category: Curtin, N J]]
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[[Category: Noble, M E.M]]
[[Category: Tucker, J]]
[[Category: Tucker, J]]
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[[Category: Cano, C]]
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[[Category: Unterlass, J E]]
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[[Category: Dehydrogenase]]
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[[Category: Enzymology]]
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[[Category: Oxidoreductase]]
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[[Category: Serine metabolism]]

Revision as of 07:37, 22 November 2017

Crystal structure of human 3-phosphoglycerate dehydrogenase in complex with NAD and L-Tartrate

5n6c, resolution 2.30Å

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