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6plf
From Proteopedia
(Difference between revisions)
(New page: '''Unreleased structure''' The entry 6plf is ON HOLD Authors: Description: Category: Unreleased Structures) |
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| - | '''Unreleased structure''' | ||
| - | + | ==Crystal structure of human PHGDH complexed with Compound 1== | |
| + | <StructureSection load='6plf' size='340' side='right'caption='[[6plf]], [[Resolution|resolution]] 1.70Å' scene=''> | ||
| + | == Structural highlights == | ||
| + | <table><tr><td colspan='2'>[[6plf]] is a 2 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=6PLF OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6PLF FirstGlance]. <br> | ||
| + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.7Å</td></tr> | ||
| + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=EDO:1,2-ETHANEDIOL'>EDO</scene>, <scene name='pdbligand=ONV:4-{(1S)-1-[(5-chloro-6-{[(5S)-2-oxo-1,3-oxazolidin-5-yl]methoxy}-1H-indole-2-carbonyl)amino]-2-hydroxyethyl}benzoic+acid'>ONV</scene></td></tr> | ||
| + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=6plf FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6plf OCA], [https://pdbe.org/6plf PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6plf RCSB], [https://www.ebi.ac.uk/pdbsum/6plf PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6plf ProSAT]</span></td></tr> | ||
| + | </table> | ||
| + | == Disease == | ||
| + | [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. | ||
| + | == Function == | ||
| + | [https://www.uniprot.org/uniprot/SERA_HUMAN SERA_HUMAN] | ||
| - | + | ==See Also== | |
| - | + | *[[Phosphoglycerate dehydrogenase|Phosphoglycerate dehydrogenase]] | |
| - | + | __TOC__ | |
| - | [[Category: | + | </StructureSection> |
| + | [[Category: Homo sapiens]] | ||
| + | [[Category: Large Structures]] | ||
| + | [[Category: Lakshminarasimhan D]] | ||
| + | [[Category: Olland A]] | ||
| + | [[Category: Suto RK]] | ||
| + | [[Category: White A]] | ||
Current revision
Crystal structure of human PHGDH complexed with Compound 1
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