5q04: Difference between revisions
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==Human liver fructose-1,6-bisphosphatase 1 (fructose 1,6-bisphosphate 1-phosphatase, E.C.3.1.3.11) complexed with the allosteric inhibitor 1-(4-bromo-5-chlorothiophen-2-yl)sulfonyl-3-(5-bromo-1,3-thiazol-2-yl)urea== | ==Human liver fructose-1,6-bisphosphatase 1 (fructose 1,6-bisphosphate 1-phosphatase, E.C.3.1.3.11) complexed with the allosteric inhibitor 1-(4-bromo-5-chlorothiophen-2-yl)sulfonyl-3-(5-bromo-1,3-thiazol-2-yl)urea== | ||
<StructureSection load='5q04' size='340' side='right' caption='[[5q04]], [[Resolution|resolution]] 2.50Å' scene=''> | <StructureSection load='5q04' size='340' side='right'caption='[[5q04]], [[Resolution|resolution]] 2.50Å' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[5q04]] is a 8 chain structure with sequence from [ | <table><tr><td colspan='2'>[[5q04]] is a 8 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=5Q04 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=5Q04 FirstGlance]. <br> | ||
</td></tr><tr id=' | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.502Å</td></tr> | ||
<tr id=' | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=95P:4-bromo-N-[(5-bromo-1,3-thiazol-2-yl)carbamoyl]-5-chlorothiophene-2-sulfonamide'>95P</scene></td></tr> | ||
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=5q04 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5q04 OCA], [https://pdbe.org/5q04 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5q04 RCSB], [https://www.ebi.ac.uk/pdbsum/5q04 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5q04 ProSAT]</span></td></tr> | |||
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[ | |||
</table> | </table> | ||
== Disease == | |||
[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> | |||
== Function == | |||
[https://www.uniprot.org/uniprot/F16P1_HUMAN F16P1_HUMAN] | |||
==See Also== | |||
*[[Fructose-1%2C6-bisphosphatase 3D structures|Fructose-1%2C6-bisphosphatase 3D structures]] | |||
== References == | |||
<references/> | |||
__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
[[Category: | [[Category: Homo sapiens]] | ||
[[Category: | [[Category: Large Structures]] | ||
[[Category: Alker | [[Category: Alker A]] | ||
[[Category: Banner | [[Category: Banner D]] | ||
[[Category: Benz | [[Category: Benz J]] | ||
[[Category: Burley | [[Category: Burley SK]] | ||
[[Category: Joseph | [[Category: Joseph C]] | ||
[[Category: Kuhn | [[Category: Kuhn B]] | ||
[[Category: Rudolph | [[Category: Rudolph MG]] | ||
[[Category: Ruf | [[Category: Ruf A]] | ||
[[Category: Shao | [[Category: Shao C]] | ||
[[Category: Tetaz | [[Category: Tetaz T]] | ||
[[Category: Yang | [[Category: Yang H]] | ||