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6txp
From Proteopedia
(Difference between revisions)
(New page: '''Unreleased structure''' The entry 6txp is ON HOLD Authors: Hubert, L.-S., Ley, M., Heine, A., Klebe, G. Description: Human Aldose Reductase Mutant L300A in Complex with a Ligand wit...) |
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| - | '''Unreleased structure''' | ||
| - | + | ==Human Aldose Reductase Mutant L300A in Complex with a Ligand with an IDD Structure (3-({[2-(carboxymethoxy)-4-fluorobenzoyl]amino}methyl)benzoic acid)== | |
| + | <StructureSection load='6txp' size='340' side='right'caption='[[6txp]], [[Resolution|resolution]] 0.95Å' scene=''> | ||
| + | == Structural highlights == | ||
| + | <table><tr><td colspan='2'>[[6txp]] 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=6TXP OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6TXP 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]] 0.95Å</td></tr> | ||
| + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=4G7:3-({[2-(CARBOXYMETHOXY)-4-FLUOROBENZOYL]AMINO}METHYL)BENZOIC+ACID'>4G7</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=6txp FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6txp OCA], [https://pdbe.org/6txp PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6txp RCSB], [https://www.ebi.ac.uk/pdbsum/6txp PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6txp 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 L300A in Complex with a Ligand with an IDD Structure (3-({[2-(carboxymethoxy)-4-fluorobenzoyl]amino}methyl)benzoic acid)
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Categories: Homo sapiens | Large Structures | Heine A | Hubert L-S | Klebe G | Ley M
