This old version of Proteopedia is provided for student assignments while the new version is undergoing repairs. Content and edits done in this old version of Proteopedia after March 1, 2026 will eventually be lost when it is retired in about June of 2026.
Apply for new accounts at the new Proteopedia. Your logins will work in both the old and new versions.
7ewh
From Proteopedia
(Difference between revisions)
m (Protected "7ewh" [edit=sysop:move=sysop]) |
|||
| (4 intermediate revisions not shown.) | |||
| Line 1: | Line 1: | ||
| - | '''Unreleased structure''' | ||
| - | + | ==Crystal structure of human PHGDH in complex with Homoharringtonine== | |
| + | <StructureSection load='7ewh' size='340' side='right'caption='[[7ewh]], [[Resolution|resolution]] 2.99Å' scene=''> | ||
| + | == Structural highlights == | ||
| + | <table><tr><td colspan='2'>[[7ewh]] 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=7EWH OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7EWH 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]] 2.99Å</td></tr> | ||
| + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=HMT:(3BETA)-O~3~-[(2R)-2,6-DIHYDROXY-2-(2-METHOXY-2-OXOETHYL)-6-METHYLHEPTANOYL]CEPHALOTAXINE'>HMT</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=7ewh FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7ewh OCA], [https://pdbe.org/7ewh PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7ewh RCSB], [https://www.ebi.ac.uk/pdbsum/7ewh PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7ewh 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: Cheng YS]] | ||
| + | [[Category: Hsieh CH]] | ||
| + | [[Category: Huang HC]] | ||
| + | [[Category: Juan HF]] | ||
| + | [[Category: Lee YS]] | ||
Current revision
Crystal structure of human PHGDH in complex with Homoharringtonine
| |||||||||||
Categories: Homo sapiens | Large Structures | Cheng YS | Hsieh CH | Huang HC | Juan HF | Lee YS
