6hyy: Difference between revisions

From Proteopedia
Jump to navigationJump to search
OCA (talk | contribs)
m Protected "6hyy" [edit=sysop:move=sysop]
OCA (talk | contribs)
No edit summary
Line 1: Line 1:
'''Unreleased structure'''


The entry 6hyy is ON HOLD
==Human phosphoserine phosphatase with serine and phosphate==
 
<StructureSection load='6hyy' size='340' side='right'caption='[[6hyy]], [[Resolution|resolution]] 1.57&Aring;' scene=''>
Authors: Wouters, J., Haufroid, M., Mirgaux, M.
== Structural highlights ==
 
<table><tr><td colspan='2'>[[6hyy]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6HYY OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6HYY FirstGlance]. <br>
Description: Human phosphoserine phosphatase with serine and phosphate
</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=CA:CALCIUM+ION'>CA</scene>, <scene name='pdbligand=MG:MAGNESIUM+ION'>MG</scene>, <scene name='pdbligand=PO4:PHOSPHATE+ION'>PO4</scene>, <scene name='pdbligand=SER:SERINE'>SER</scene></td></tr>
[[Category: Unreleased Structures]]
<tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[http://en.wikipedia.org/wiki/Phosphoserine_phosphatase Phosphoserine phosphatase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.1.3.3 3.1.3.3] </span></td></tr>
<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=6hyy FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6hyy OCA], [http://pdbe.org/6hyy PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6hyy RCSB], [http://www.ebi.ac.uk/pdbsum/6hyy PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6hyy ProSAT]</span></td></tr>
</table>
== Disease ==
[[http://www.uniprot.org/uniprot/SERB_HUMAN SERB_HUMAN]] Defects in PSPH are the cause of phosphoserine phosphatase deficiency (PSPHD)[MIM:[http://omim.org/entry/614023 614023]]. A disorder that results in pre- and postnatal growth retardation, moderate psychomotor retardation and facial features suggestive of Williams syndrome.<ref>PMID:14673469</ref> 
== Function ==
[[http://www.uniprot.org/uniprot/SERB_HUMAN SERB_HUMAN]] Catalyzes the last step in the biosynthesis of serine from carbohydrates. The reaction mechanism proceeds via the formation of a phosphoryl-enzyme intermediates.<ref>PMID:12777757</ref> 
== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Large Structures]]
[[Category: Phosphoserine phosphatase]]
[[Category: Haufroid, M]]
[[Category: Mirgaux, M]]
[[Category: Mirgaux, M]]
[[Category: Wouters, J]]
[[Category: Wouters, J]]
[[Category: Haufroid, M]]
[[Category: Human phosphoserine phosphatase]]
[[Category: Hydrolase]]

Revision as of 05:35, 12 June 2019

Human phosphoserine phosphatase with serine and phosphate

6hyy, resolution 1.57Å

Drag the structure with the mouse to rotate

Proteopedia Page Contributors and Editors (what is this?)

OCA