6a7b: Difference between revisions

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'''Unreleased structure'''


The entry 6a7b is ON HOLD  until Paper Publication
==AKR1C3 complexed with new inhibitor with novel scaffold==
 
<StructureSection load='6a7b' size='340' side='right'caption='[[6a7b]], [[Resolution|resolution]] 2.37&Aring;' scene=''>
Authors: Zheng, X., Zhao, Y., Zhang, H., Chen, Y.
== Structural highlights ==
 
<table><tr><td colspan='2'>[[6a7b]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6A7B OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6A7B FirstGlance]. <br>
Description: AKR1C3 complexed with new inhibitor with novel scaffold
</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=9S0:(4R)-6-amino-4-(4-hydroxy-3-methoxy-5-nitrophenyl)-3-propyl-1,4-dihydropyrano[2,3-c]pyrazole-5-carbonitrile'>9S0</scene>, <scene name='pdbligand=DMF:DIMETHYLFORMAMIDE'>DMF</scene>, <scene name='pdbligand=NAP:NADP+NICOTINAMIDE-ADENINE-DINUCLEOTIDE+PHOSPHATE'>NAP</scene></td></tr>
[[Category: Unreleased Structures]]
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6a7b FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6a7b OCA], [http://pdbe.org/6a7b PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6a7b RCSB], [http://www.ebi.ac.uk/pdbsum/6a7b PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6a7b ProSAT]</span></td></tr>
</table>
== Function ==
[[http://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: Large Structures]]
[[Category: Chen, Y]]
[[Category: Zhang, H]]
[[Category: Zhang, H]]
[[Category: Zhao, Y]]
[[Category: Zhao, Y]]
[[Category: Chen, Y]]
[[Category: Zheng, X]]
[[Category: Zheng, X]]
[[Category: Aldo-keto reductase family 1 member c3]]
[[Category: Oxidoreductase]]
[[Category: Prostaglandin f synthase]]
[[Category: Type 5 17-beta-hydroxysteroid dehydrogenase]]

Revision as of 05:44, 3 July 2019

AKR1C3 complexed with new inhibitor with novel scaffold

6a7b, resolution 2.37Å

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