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8omk

From Proteopedia

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m (Protected "8omk" [edit=sysop:move=sysop])
Current revision (10:26, 10 January 2024) (edit) (undo)
 
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'''Unreleased structure'''
 
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The entry 8omk is ON HOLD
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==hKHK-C in complex with ADP & fructose 1-phosphate==
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<StructureSection load='8omk' size='340' side='right'caption='[[8omk]], [[Resolution|resolution]] 2.48&Aring;' scene=''>
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Authors: Ebenhoch, R., Pautsch, A.
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== Structural highlights ==
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<table><tr><td colspan='2'>[[8omk]] 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=8OMK OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8OMK FirstGlance]. <br>
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Description: hKHK-C in complex with ADP & fructose 1-phosphate
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.48&#8491;</td></tr>
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[[Category: Unreleased Structures]]
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<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=ADP:ADENOSINE-5-DIPHOSPHATE'>ADP</scene>, <scene name='pdbligand=F1X:1-O-PHOSPHONO-BETA-D-FRUCTOFURANOSE'>F1X</scene>, <scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene></td></tr>
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[[Category: Pautsch, A]]
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=8omk FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8omk OCA], [https://pdbe.org/8omk PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8omk RCSB], [https://www.ebi.ac.uk/pdbsum/8omk PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8omk ProSAT]</span></td></tr>
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[[Category: Ebenhoch, R]]
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</table>
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== Disease ==
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[https://www.uniprot.org/uniprot/KHK_HUMAN KHK_HUMAN] Defects in KHK are the cause of fructosuria (FRUCT) [MIM:[https://omim.org/entry/229800 229800]. Benign defect of intermediary metabolism.<ref>PMID:19237742</ref> <ref>PMID:7833921</ref>
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== Function ==
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[https://www.uniprot.org/uniprot/KHK_HUMAN KHK_HUMAN]
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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: Homo sapiens]]
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[[Category: Large Structures]]
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[[Category: Ebenhoch R]]
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[[Category: Pautsch A]]

Current revision

hKHK-C in complex with ADP & fructose 1-phosphate

PDB ID 8omk

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