9uj1: Difference between revisions
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==Crystal Structure of AKR1C3 in Complex with an Osthole-Derived Inhibitor== | |||
<StructureSection load='9uj1' size='340' side='right'caption='[[9uj1]], [[Resolution|resolution]] 2.15Å' scene=''> | |||
== Structural highlights == | |||
<table><tr><td colspan='2'>[[9uj1]] 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=9UJ1 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=9UJ1 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]] 2.15Å</td></tr> | |||
[[Category: | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=A1EPD:(~{E})-4-(7-methoxy-2-oxidanylidene-chromen-8-yl)-2-methyl-~{N},~{N}-dipropyl-but-2-enamide'>A1EPD</scene>, <scene name='pdbligand=NAP:NADP+NICOTINAMIDE-ADENINE-DINUCLEOTIDE+PHOSPHATE'>NAP</scene></td></tr> | ||
[[Category: | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=9uj1 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=9uj1 OCA], [https://pdbe.org/9uj1 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=9uj1 RCSB], [https://www.ebi.ac.uk/pdbsum/9uj1 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=9uj1 ProSAT]</span></td></tr> | ||
[[Category: Liu | </table> | ||
[[Category: Zheng | == Function == | ||
[https://www.uniprot.org/uniprot/AK1C3_HUMAN AK1C3_HUMAN] Catalyzes the conversion of aldehydes and ketones to alcohols. Catalyzes the reduction of prostaglandin (PG) D2, PGH2 and phenanthrenequinone (PQ) and the oxidation of 9-alpha,11-beta-PGF2 to PGD2. Functions as a bi-directional 3-alpha-, 17-beta- and 20-alpha HSD. Can interconvert active androgens, estrogens and progestins with their cognate inactive metabolites. Preferentially transforms androstenedione (4-dione) to testosterone. | |||
__TOC__ | |||
</StructureSection> | |||
[[Category: Homo sapiens]] | |||
[[Category: Large Structures]] | |||
[[Category: Liu H]] | |||
[[Category: Sun M]] | |||
[[Category: Zheng X]] | |||
Latest revision as of 06:40, 22 April 2026
Crystal Structure of AKR1C3 in Complex with an Osthole-Derived Inhibitor
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