4jq2
From Proteopedia
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- | {{STRUCTURE_4jq2| PDB=4jq2 | SCENE= }} | ||
- | ===AKR1C2 complex with sulindac=== | ||
- | == | + | ==AKR1C2 complex with sulindac== |
- | [[http://www.uniprot.org/uniprot/AK1C2_HUMAN AK1C2_HUMAN | + | <StructureSection load='4jq2' size='340' side='right'caption='[[4jq2]], [[Resolution|resolution]] 1.75Å' scene=''> |
+ | == Structural highlights == | ||
+ | <table><tr><td colspan='2'>[[4jq2]] 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=4JQ2 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4JQ2 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]] 1.75Å</td></tr> | ||
+ | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=EDO:1,2-ETHANEDIOL'>EDO</scene>, <scene name='pdbligand=NAP:NADP+NICOTINAMIDE-ADENINE-DINUCLEOTIDE+PHOSPHATE'>NAP</scene>, <scene name='pdbligand=PO4:PHOSPHATE+ION'>PO4</scene>, <scene name='pdbligand=SUZ:[(1Z)-5-FLUORO-2-METHYL-1-{4-[METHYLSULFINYL]BENZYLIDENE}-1H-INDEN-3-YL]ACETIC+ACID'>SUZ</scene>, <scene name='pdbligand=TLA:L(+)-TARTARIC+ACID'>TLA</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=4jq2 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4jq2 OCA], [https://pdbe.org/4jq2 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4jq2 RCSB], [https://www.ebi.ac.uk/pdbsum/4jq2 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4jq2 ProSAT]</span></td></tr> | ||
+ | </table> | ||
+ | == Disease == | ||
+ | [https://www.uniprot.org/uniprot/AK1C2_HUMAN AK1C2_HUMAN] Defects in AKR1C2 are a cause of 46,XY sex reversal type 8 (SRXY8) [MIM:[https://omim.org/entry/614279 614279]. A disorder of sex development. Affected individuals have a 46,XY karyotype but present as phenotypically normal females.<ref>PMID:21802064</ref> | ||
+ | == Function == | ||
+ | [https://www.uniprot.org/uniprot/AK1C2_HUMAN AK1C2_HUMAN] Works in concert with the 5-alpha/5-beta-steroid reductases to convert steroid hormones into the 3-alpha/5-alpha and 3-alpha/5-beta-tetrahydrosteroids. Catalyzes the inactivation of the most potent androgen 5-alpha-dihydrotestosterone (5-alpha-DHT) to 5-alpha-androstane-3-alpha,17-beta-diol (3-alpha-diol). Has a high bile-binding ability.<ref>PMID:8573067</ref> | ||
- | == | + | ==See Also== |
- | [[ | + | *[[Hydroxysteroid dehydrogenase 3D structures|Hydroxysteroid dehydrogenase 3D structures]] |
- | + | == References == | |
- | == | + | <references/> |
- | + | __TOC__ | |
- | + | </StructureSection> | |
- | + | [[Category: Homo sapiens]] | |
- | <references | + | [[Category: Large Structures]] |
- | [[Category: | + | [[Category: Flanagan JU]] |
- | [[Category: | + | [[Category: Squire CJ]] |
- | [[Category: | + | [[Category: Yosaatmadja Y]] |
- | [[Category: | + | |
- | [[Category: | + |
Current revision
AKR1C2 complex with sulindac
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