4z3d: Difference between revisions
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New page: '''Unreleased structure''' The entry 4z3d is ON HOLD Authors: Ding, Y., Liang, Q. Description: Human carbonyl reductase 1 with glutathione in a protection configuration [[Category: Unr... |
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==Human carbonyl reductase 1 with glutathione in a protective configuration== | |||
<StructureSection load='4z3d' size='340' side='right'caption='[[4z3d]], [[Resolution|resolution]] 1.80Å' scene=''> | |||
== Structural highlights == | |||
<table><tr><td colspan='2'>[[4z3d]] is a 4 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=4Z3D OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4Z3D 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]] 1.8Å</td></tr> | |||
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=GSH:GLUTATHIONE'>GSH</scene>, <scene name='pdbligand=NDP:NADPH+DIHYDRO-NICOTINAMIDE-ADENINE-DINUCLEOTIDE+PHOSPHATE'>NDP</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=4z3d FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4z3d OCA], [https://pdbe.org/4z3d PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4z3d RCSB], [https://www.ebi.ac.uk/pdbsum/4z3d PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4z3d ProSAT]</span></td></tr> | |||
</table> | |||
== Function == | |||
[https://www.uniprot.org/uniprot/CBR1_HUMAN CBR1_HUMAN] NADPH-dependent reductase with broad substrate specificity. Catalyzes the reduction of a wide variety of carbonyl compounds including quinones, prostaglandins, menadione, plus various xenobiotics. Catalyzes the reduction of the antitumor anthracyclines doxorubicin and daunorubicin to the cardiotoxic compounds doxorubicinol and daunorubicinol. Can convert prostaglandin E2 to prostaglandin F2-alpha. Can bind glutathione, which explains its higher affinity for glutathione-conjugated substrates. Catalyzes the reduction of S-nitrosoglutathione.<ref>PMID:18449627</ref> <ref>PMID:15799708</ref> <ref>PMID:17912391</ref> <ref>PMID:18826943</ref> | |||
==See Also== | |||
*[[Carbonyl reductase 3D structures|Carbonyl reductase 3D structures]] | |||
== References == | |||
[[Category: | <references/> | ||
[[Category: Ding | __TOC__ | ||
[[Category: Liang | </StructureSection> | ||
[[Category: Homo sapiens]] | |||
[[Category: Large Structures]] | |||
[[Category: Ding Y]] | |||
[[Category: Liang Q]] | |||
Latest revision as of 09:04, 20 March 2024
Human carbonyl reductase 1 with glutathione in a protective configuration
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