7cvp

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
(New page: '''Unreleased structure''' The entry 7cvp is ON HOLD Authors: Wang, F., Lv, Z., Cheng, W., Lin, D., Miao, Q., Huang, Y. Description: The Crystal Structure of human PHGDH from Biortus. ...)
Current revision (16:17, 29 November 2023) (edit) (undo)
 
(2 intermediate revisions not shown.)
Line 1: Line 1:
-
'''Unreleased structure'''
 
-
The entry 7cvp is ON HOLD
+
==The Crystal Structure of human PHGDH from Biortus.==
 +
<StructureSection load='7cvp' size='340' side='right'caption='[[7cvp]], [[Resolution|resolution]] 2.50&Aring;' scene=''>
 +
== Structural highlights ==
 +
<table><tr><td colspan='2'>[[7cvp]] 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=7CVP OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7CVP 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]] 2.5&#8491;</td></tr>
 +
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=NAD:NICOTINAMIDE-ADENINE-DINUCLEOTIDE'>NAD</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=7cvp FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7cvp OCA], [https://pdbe.org/7cvp PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7cvp RCSB], [https://www.ebi.ac.uk/pdbsum/7cvp PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7cvp 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]
-
Authors: Wang, F., Lv, Z., Cheng, W., Lin, D., Miao, Q., Huang, Y.
+
==See Also==
-
 
+
*[[Phosphoglycerate dehydrogenase|Phosphoglycerate dehydrogenase]]
-
Description: The Crystal Structure of human PHGDH from Biortus.
+
__TOC__
-
[[Category: Unreleased Structures]]
+
</StructureSection>
-
[[Category: Huang, Y]]
+
[[Category: Homo sapiens]]
-
[[Category: Lin, D]]
+
[[Category: Large Structures]]
-
[[Category: Wang, F]]
+
[[Category: Cheng W]]
-
[[Category: Miao, Q]]
+
[[Category: Huang Y]]
-
[[Category: Lv, Z]]
+
[[Category: Lin D]]
-
[[Category: Cheng, W]]
+
[[Category: Lv Z]]
 +
[[Category: Miao Q]]
 +
[[Category: Wang F]]

Current revision

The Crystal Structure of human PHGDH from Biortus.

PDB ID 7cvp

Drag the structure with the mouse to rotate

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools