3uzw: Difference between revisions

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New page: '''Unreleased structure''' The entry 3uzw is ON HOLD Authors: Chen, M., Christianson, D.W., Penning, T.M. Description: Crystal structure of 5beta-reductase (AKR1D1) E120H mutant in com...
 
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'''Unreleased structure'''


The entry 3uzw is ON HOLD
==Crystal structure of 5beta-reductase (AKR1D1) E120H mutant in complex with NADP+==
 
<StructureSection load='3uzw' size='340' side='right'caption='[[3uzw]], [[Resolution|resolution]] 1.89&Aring;' scene=''>
Authors: Chen, M., Christianson, D.W., Penning, T.M.
== Structural highlights ==
 
<table><tr><td colspan='2'>[[3uzw]] 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=3UZW OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=3UZW FirstGlance]. <br>
Description: Crystal structure of 5beta-reductase (AKR1D1) E120H mutant in complex with NADP+
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.892&#8491;</td></tr>
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=CL:CHLORIDE+ION'>CL</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=3uzw FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=3uzw OCA], [https://pdbe.org/3uzw PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=3uzw RCSB], [https://www.ebi.ac.uk/pdbsum/3uzw PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=3uzw ProSAT]</span></td></tr>
</table>
== Disease ==
[https://www.uniprot.org/uniprot/AK1D1_HUMAN AK1D1_HUMAN] Defects in AKR1D1 are the cause of congenital bile acid synthesis defect type 2 (CBAS2) [MIM:[https://omim.org/entry/235555 235555]; also known as cholestasis with delta(4)-3-oxosteroid 5-beta-reductase deficiency. Patients with this liver disease show absence or low levels of chenodeoxycholic acid and cholic acid in plasma and urine.<ref>PMID:12970144</ref> <ref>PMID:15030995</ref>
== Function ==
[https://www.uniprot.org/uniprot/AK1D1_HUMAN AK1D1_HUMAN] Efficiently catalyzes the reduction of progesterone, androstenedione, 17-alpha-hydroxyprogesterone and testosterone to 5-beta-reduced metabolites. The bile acid intermediates 7-alpha,12-alpha-dihydroxy-4-cholesten-3-one and 7-alpha-hydroxy-4-cholesten-3-one can also act as substrates.
== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Homo sapiens]]
[[Category: Large Structures]]
[[Category: Chen M]]
[[Category: Christianson DW]]
[[Category: Penning TM]]

Latest revision as of 14:12, 14 March 2024

Crystal structure of 5beta-reductase (AKR1D1) E120H mutant in complex with NADP+

3uzw, resolution 1.89Å

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