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2y5l
From Proteopedia
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<StructureSection load='2y5l' size='340' side='right'caption='[[2y5l]], [[Resolution|resolution]] 2.20Å' scene=''> | <StructureSection load='2y5l' size='340' side='right'caption='[[2y5l]], [[Resolution|resolution]] 2.20Å' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
| - | <table><tr><td colspan='2'>[[2y5l]] is a 8 chain structure with sequence from [ | + | <table><tr><td colspan='2'>[[2y5l]] 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=2Y5L OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2Y5L 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]] 2.2Å</td></tr> |
| - | <tr id=' | + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=RO8:N-{[(2Z)-5-BROMO-1,3-THIAZOL-2(3H)-YLIDENE]CARBAMOYL}-3-CHLOROBENZENESULFONAMIDE'>RO8</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=2y5l FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2y5l OCA], [https://pdbe.org/2y5l PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2y5l RCSB], [https://www.ebi.ac.uk/pdbsum/2y5l PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2y5l ProSAT]</span></td></tr> | |
| - | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[ | + | |
</table> | </table> | ||
== Disease == | == 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] | ||
<div style="background-color:#fffaf0;"> | <div style="background-color:#fffaf0;"> | ||
== Publication Abstract from PubMed == | == Publication Abstract from PubMed == | ||
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__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
| - | [[Category: | + | [[Category: Homo sapiens]] |
| - | + | ||
[[Category: Large Structures]] | [[Category: Large Structures]] | ||
| - | [[Category: Alvarez-sanchez | + | [[Category: Alvarez-sanchez r]] |
| - | [[Category: Benardeau | + | [[Category: Benardeau a]] |
| - | [[Category: Benz | + | [[Category: Benz j]] |
| - | [[Category: Gubler | + | [[Category: Gubler m]] |
| - | [[Category: Haap | + | [[Category: Haap w]] |
| - | [[Category: Hebeisen | + | [[Category: Hebeisen p]] |
| - | [[Category: Joseph | + | [[Category: Joseph c]] |
| - | [[Category: Kirchner | + | [[Category: Kirchner s]] |
| - | [[Category: Kitas | + | [[Category: Kitas e]] |
| - | [[Category: Kuhn | + | [[Category: Kuhn b]] |
| - | [[Category: Mohr | + | [[Category: Mohr p]] |
| - | [[Category: Ruf | + | [[Category: Ruf a]] |
| - | [[Category: Schott | + | [[Category: Schott b]] |
| - | [[Category: Tozzo | + | [[Category: Tozzo e]] |
| - | [[Category: Wessel | + | [[Category: Wessel hp]] |
| - | [[Category: Zutter | + | [[Category: Zutter u]] |
| - | + | ||
Current revision
orally active aminopyridines as inhibitors of tetrameric fructose 1,6- bisphosphatase
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Categories: Homo sapiens | Large Structures | Alvarez-sanchez r | Benardeau a | Benz j | Gubler m | Haap w | Hebeisen p | Joseph c | Kirchner s | Kitas e | Kuhn b | Mohr p | Ruf a | Schott b | Tozzo e | Wessel hp | Zutter u
