3c3u
From Proteopedia
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[[Image:3c3u.png|left|200px]] | [[Image:3c3u.png|left|200px]] | ||
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{{STRUCTURE_3c3u| PDB=3c3u | SCENE= }} | {{STRUCTURE_3c3u| PDB=3c3u | SCENE= }} | ||
===Crystal structure of AKR1C1 in complex with NADP and 3,5-dichlorosalicylic acid=== | ===Crystal structure of AKR1C1 in complex with NADP and 3,5-dichlorosalicylic acid=== | ||
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{{ABSTRACT_PUBMED_18620380}} | {{ABSTRACT_PUBMED_18620380}} | ||
==About this Structure== | ==About this Structure== | ||
- | + | [[3c3u]] is a 1 chain structure of [[Hydroxysteroid dehydrogenase]] with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3C3U OCA]. | |
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+ | ==See Also== | ||
+ | *[[Hydroxysteroid dehydrogenase|Hydroxysteroid dehydrogenase]] | ||
==Reference== | ==Reference== | ||
- | <ref group="xtra">PMID: | + | <ref group="xtra">PMID:018620380</ref><references group="xtra"/> |
[[Category: 20-alpha-hydroxysteroid dehydrogenase]] | [[Category: 20-alpha-hydroxysteroid dehydrogenase]] | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
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[[Category: Akr1c1]] | [[Category: Akr1c1]] | ||
[[Category: Aldo-keto reductase]] | [[Category: Aldo-keto reductase]] | ||
- | [[Category: Cytoplasm]] | ||
[[Category: Nadp]] | [[Category: Nadp]] | ||
[[Category: Oxidoreductase]] | [[Category: Oxidoreductase]] | ||
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- | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Feb 18 05:36:19 2009'' |
Revision as of 12:00, 27 July 2012
Contents |
Crystal structure of AKR1C1 in complex with NADP and 3,5-dichlorosalicylic acid
Template:ABSTRACT PUBMED 18620380
About this Structure
3c3u is a 1 chain structure of Hydroxysteroid dehydrogenase with sequence from Homo sapiens. Full crystallographic information is available from OCA.
See Also
Reference
- Dhagat U, Endo S, Sumii R, Hara A, El-Kabbani O. Selectivity determinants of inhibitor binding to human 20alpha-hydroxysteroid dehydrogenase: crystal structure of the enzyme in ternary complex with coenzyme and the potent inhibitor 3,5-dichlorosalicylic acid. J Med Chem. 2008 Aug 14;51(15):4844-8. Epub 2008 Jul 12. PMID:18620380 doi:10.1021/jm8003575