6td8
From Proteopedia
(Difference between revisions)
												
			
			 (New page: '''Unreleased structure'''  The entry 6td8 is ON HOLD  until Paper Publication  Authors: Hubert, L.-S., Ley, M., Heine, A., Klebe, G.  Description: Human Aldose Reductase Mutant L301A in C...)  | 
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| - | '''Unreleased structure'''  | ||
| - | + | ==Human Aldose Reductase Mutant L301A in Complex with a Ligand with an IDD Structure ({5-fluoro-2-[(3-nitrobenzyl)carbamoyl]phenoxy}acetic acid)==  | |
| + | <StructureSection load='6td8' size='340' side='right'caption='[[6td8]], [[Resolution|resolution]] 0.97Å' scene=''>  | ||
| + | == Structural highlights ==  | ||
| + | <table><tr><td colspan='2'>[[6td8]] is a 1 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=6TD8 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6TD8 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]] 0.97Å</td></tr>  | ||
| + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=30L:{5-FLUORO-2-[(3-NITROBENZYL)CARBAMOYL]PHENOXY}ACETIC+ACID'>30L</scene>, <scene name='pdbligand=CIT:CITRIC+ACID'>CIT</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=6td8 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6td8 OCA], [https://pdbe.org/6td8 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6td8 RCSB], [https://www.ebi.ac.uk/pdbsum/6td8 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6td8 ProSAT]</span></td></tr>  | ||
| + | </table>  | ||
| + | == Function ==  | ||
| + | [https://www.uniprot.org/uniprot/ALDR_HUMAN ALDR_HUMAN] Catalyzes the NADPH-dependent reduction of a wide variety of carbonyl-containing compounds to their corresponding alcohols with a broad range of catalytic efficiencies.  | ||
| - | + | ==See Also==  | |
| - | + | *[[Aldose reductase 3D structures|Aldose reductase 3D structures]]  | |
| - | + | __TOC__  | |
| - | [[Category:   | + | </StructureSection>  | 
| - | [[Category:   | + | [[Category: Homo sapiens]]  | 
| - | [[Category: Heine  | + | [[Category: Large Structures]]  | 
| - | [[Category: Hubert  | + | [[Category: Heine A]]  | 
| - | [[Category: Klebe  | + | [[Category: Hubert L-S]]  | 
| + | [[Category: Klebe G]]  | ||
| + | [[Category: Ley M]]  | ||
Current revision
Human Aldose Reductase Mutant L301A in Complex with a Ligand with an IDD Structure ({5-fluoro-2-[(3-nitrobenzyl)carbamoyl]phenoxy}acetic acid)
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Categories: Homo sapiens | Large Structures | Heine A | Hubert L-S | Klebe G | Ley M
