9xv1: Difference between revisions

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'''Unreleased structure'''


The entry 9xv1 is ON HOLD  until Paper Publication
==Crystal Structure of Fructose-1,6-bisphosphatase Complexed with a Covalent Inhibitor==
 
<StructureSection load='9xv1' size='340' side='right'caption='[[9xv1]], [[Resolution|resolution]] 1.96&Aring;' scene=''>
Authors: Cao, H., Huang, Z., Hu, X., Li, W., Chang, M., Zhang, Y., Chu, Y.
== Structural highlights ==
 
<table><tr><td colspan='2'>[[9xv1]] is a 4 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=9XV1 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=9XV1 FirstGlance]. <br>
Description: Crystal Structure of Fructose-1,6-bisphosphatase Complexed with a Covalent Inhibitor
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.96&#8491;</td></tr>
[[Category: Unreleased Structures]]
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=A1E1G:2-bromanyl-~{N}-[2-[4-[(3-phenylphenyl)carbamoylsulfamoyl]phenyl]ethyl]ethanamide'>A1E1G</scene></td></tr>
[[Category: Cao, H]]
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=9xv1 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=9xv1 OCA], [https://pdbe.org/9xv1 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=9xv1 RCSB], [https://www.ebi.ac.uk/pdbsum/9xv1 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=9xv1 ProSAT]</span></td></tr>
[[Category: Huang, Z]]
</table>
[[Category: Li, W]]
== Disease ==
[[Category: Hu, X]]
[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>
[[Category: Chu, Y]]
== Function ==
[[Category: Chang, M]]
[https://www.uniprot.org/uniprot/F16P1_HUMAN F16P1_HUMAN]
[[Category: Zhang, Y]]
== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Homo sapiens]]
[[Category: Large Structures]]
[[Category: Cao H]]
[[Category: Chang M]]
[[Category: Chu Y]]
[[Category: Hu X]]
[[Category: Huang Z]]
[[Category: Li W]]
[[Category: Zhang Y]]

Latest revision as of 05:31, 24 December 2025

Crystal Structure of Fructose-1,6-bisphosphatase Complexed with a Covalent Inhibitor

9xv1, resolution 1.96Å

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