1pr9
From Proteopedia
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| - | {{Seed}} | ||
| - | [[Image:1pr9.png|left|200px]] | ||
| - | + | ==Human L-Xylulose Reductase Holoenzyme== | |
| - | + | <StructureSection load='1pr9' size='340' side='right'caption='[[1pr9]], [[Resolution|resolution]] 1.96Å' scene=''> | |
| - | + | == Structural highlights == | |
| - | + | <table><tr><td colspan='2'>[[1pr9]] 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=1PR9 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=1PR9 FirstGlance]. <br> | |
| - | + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.96Å</td></tr> | |
| - | + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=2HP:DIHYDROGENPHOSPHATE+ION'>2HP</scene>, <scene name='pdbligand=K:POTASSIUM+ION'>K</scene>, <scene name='pdbligand=NAP:NADP+NICOTINAMIDE-ADENINE-DINUCLEOTIDE+PHOSPHATE'>NAP</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=1pr9 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1pr9 OCA], [https://pdbe.org/1pr9 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=1pr9 RCSB], [https://www.ebi.ac.uk/pdbsum/1pr9 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=1pr9 ProSAT]</span></td></tr> | |
| - | + | </table> | |
| - | + | == Disease == | |
| - | + | [https://www.uniprot.org/uniprot/DCXR_HUMAN DCXR_HUMAN] Note=The enzyme defect in pentosuria has been shown to involve L-xylulose reductase. Essential pentosuria is an inborn error of metabolism characterized by the excessive urinary excretion of the pentose L-xylulose. | |
| - | + | == Function == | |
| - | < | + | [https://www.uniprot.org/uniprot/DCXR_HUMAN DCXR_HUMAN] Catalyzes the NADPH-dependent reduction of several pentoses, tetroses, trioses, alpha-dicarbonyl compounds and L-xylulose. Participates in the uronate cycle of glucose metabolism. May play a role in the water absorption and cellular osmoregulation in the proximal renal tubules by producing xylitol, an osmolyte, thereby preventing osmolytic stress from occurring in the renal tubules. |
| - | + | == Evolutionary Conservation == | |
| - | + | [[Image:Consurf_key_small.gif|200px|right]] | |
| - | + | Check<jmol> | |
| - | + | <jmolCheckbox> | |
| - | + | <scriptWhenChecked>; select protein; define ~consurf_to_do selected; consurf_initial_scene = true; script "/wiki/ConSurf/pr/1pr9_consurf.spt"</scriptWhenChecked> | |
| - | == | + | <scriptWhenUnchecked>script /wiki/extensions/Proteopedia/spt/initialview01.spt</scriptWhenUnchecked> |
| - | + | <text>to colour the structure by Evolutionary Conservation</text> | |
| - | + | </jmolCheckbox> | |
| - | == | + | </jmol>, as determined by [http://consurfdb.tau.ac.il/ ConSurfDB]. You may read the [[Conservation%2C_Evolutionary|explanation]] of the method and the full data available from [http://bental.tau.ac.il/new_ConSurfDB/main_output.php?pdb_ID=1pr9 ConSurf]. |
| - | < | + | <div style="clear:both"></div> |
| + | __TOC__ | ||
| + | </StructureSection> | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
| - | [[Category: | + | [[Category: Large Structures]] |
| - | [[Category: Carbone | + | [[Category: Carbone V]] |
| - | [[Category: Chung | + | [[Category: Chung RP-T]] |
| - | [[Category: Darmanin | + | [[Category: Darmanin C]] |
| - | [[Category: El-Kabbani | + | [[Category: El-Kabbani O]] |
| - | [[Category: Hara | + | [[Category: Hara A]] |
| - | [[Category: Ishikura | + | [[Category: Ishikura S]] |
| - | [[Category: Usami | + | [[Category: Usami N]] |
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Current revision
Human L-Xylulose Reductase Holoenzyme
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Categories: Homo sapiens | Large Structures | Carbone V | Chung RP-T | Darmanin C | El-Kabbani O | Hara A | Ishikura S | Usami N

