5ldz

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m (Protected "5ldz" [edit=sysop:move=sysop])
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'''Unreleased structure'''
 
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The entry 5ldz is ON HOLD
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==Quadruple space group ambiguity due to rotational and translational non-crystallographic symmetry in human liver fructose-1,6-bisphosphatase==
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<StructureSection load='5ldz' size='340' side='right'caption='[[5ldz]], [[Resolution|resolution]] 2.20&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[5ldz]] is a 6 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=5LDZ OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=5LDZ FirstGlance]. <br>
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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]] 2.2&#8491;</td></tr>
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<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=CL:CHLORIDE+ION'>CL</scene>, <scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene>, <scene name='pdbligand=ZN:ZINC+ION'>ZN</scene></td></tr>
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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=5ldz FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5ldz OCA], [https://pdbe.org/5ldz PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5ldz RCSB], [https://www.ebi.ac.uk/pdbsum/5ldz PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5ldz ProSAT]</span></td></tr>
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</table>
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== Disease ==
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[https://www.uniprot.org/uniprot/F16P1_HUMAN F16P1_HUMAN] Defects in FBP1 are the cause of fructose-1,6-bisphosphatase deficiency (FBPD) [MIM:[https://omim.org/entry/229700 229700]. FBPD is inherited as an autosomal recessive disorder mainly in the liver and causes life-threatening episodes of hypoglycemia and metabolic acidosis (lactacidemia) in newborn infants or young children.<ref>PMID:9382095</ref> <ref>PMID:12126934</ref>
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== Function ==
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[https://www.uniprot.org/uniprot/F16P1_HUMAN F16P1_HUMAN]
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Authors: Ruf, A., Tetaz, T., Schott, B., Joseph, C., Rudolph, M.G.
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==See Also==
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*[[Fructose-1%2C6-bisphosphatase 3D structures|Fructose-1%2C6-bisphosphatase 3D structures]]
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Description: Crystal structure of apo human liver FBPASE in the T state
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== References ==
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[[Category: Unreleased Structures]]
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<references/>
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[[Category: Ruf, A]]
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__TOC__
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[[Category: Tetaz, T]]
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</StructureSection>
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[[Category: Joseph, C]]
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[[Category: Homo sapiens]]
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[[Category: Rudolph, M.G]]
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[[Category: Large Structures]]
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[[Category: Schott, B]]
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[[Category: Joseph C]]
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[[Category: Rudolph MG]]
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[[Category: Ruf A]]
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[[Category: Schott B]]
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[[Category: Tetaz T]]

Current revision

Quadruple space group ambiguity due to rotational and translational non-crystallographic symmetry in human liver fructose-1,6-bisphosphatase

PDB ID 5ldz

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