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6q6j

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m (Protected "6q6j" [edit=sysop:move=sysop])
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'''Unreleased structure'''
 
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The entry 6q6j is ON HOLD
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==Human phosphoserine phosphatase with substrate analogue homo-cysteic acid==
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<StructureSection load='6q6j' size='340' side='right'caption='[[6q6j]], [[Resolution|resolution]] 1.98&Aring;' scene=''>
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Authors: Wouters, J., Haufroid, M., Mirgaux, M.
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== Structural highlights ==
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<table><tr><td colspan='2'>[[6q6j]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6Q6J OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6Q6J FirstGlance]. <br>
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Description: Human phosphoserine phosphatase with substrate analogue homo-cysteic acid
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</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=CL:CHLORIDE+ION'>CL</scene>, <scene name='pdbligand=HJT:(2~{S})-2-azanyl-4-sulfo-butanoic+acid'>HJT</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/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>
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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=6q6j FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6q6j OCA], [http://pdbe.org/6q6j PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6q6j RCSB], [http://www.ebi.ac.uk/pdbsum/6q6j PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6q6j ProSAT]</span></td></tr>
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</table>
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== Disease ==
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[[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>
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== Function ==
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[[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>
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== References ==
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<references/>
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__TOC__
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</StructureSection>
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[[Category: Large Structures]]
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[[Category: Phosphoserine phosphatase]]
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[[Category: Haufroid, M]]
[[Category: Mirgaux, M]]
[[Category: Mirgaux, M]]
[[Category: Wouters, J]]
[[Category: Wouters, J]]
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[[Category: Haufroid, M]]
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[[Category: Human phosphoserine phosphatase]]
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[[Category: Hydrolase]]

Revision as of 05:45, 12 June 2019

Human phosphoserine phosphatase with substrate analogue homo-cysteic acid

PDB ID 6q6j

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