4icc

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{{STRUCTURE_4icc| PDB=4icc | SCENE= }}
{{STRUCTURE_4icc| PDB=4icc | SCENE= }}
===Crystal structure of human AKR1B10 complexed with NADP+ and JF0064===
===Crystal structure of human AKR1B10 complexed with NADP+ and JF0064===
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{{ABSTRACT_PUBMED_24598757}}
==Function==
==Function==
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==Reference==
==Reference==
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<references group="xtra"/><references/>
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<ref group="xtra">PMID:024598757</ref><references group="xtra"/><references/>
[[Category: Cousido-Siah, A.]]
[[Category: Cousido-Siah, A.]]
[[Category: Farres, J.]]
[[Category: Farres, J.]]

Revision as of 09:03, 19 March 2014

Template:STRUCTURE 4icc

Contents

Crystal structure of human AKR1B10 complexed with NADP+ and JF0064

Template:ABSTRACT PUBMED 24598757

Function

[AK1BA_HUMAN] Acts as all-trans-retinaldehyde reductase. Can efficiently reduce aliphatic and aromatic aldehydes, and is less active on hexoses (in vitro). May be responsible for detoxification of reactive aldehydes in the digested food before the nutrients are passed on to other organs.[1]

About this Structure

4icc is a 1 chain structure. Full crystallographic information is available from OCA.

Reference

  • Cousido-Siah A, Ruiz FX, Mitschler A, Porte S, de Lera AR, Martin MJ, Manzanaro S, de la Fuente JA, Terwesten F, Betz M, Klebe G, Farres J, Pares X, Podjarny A. Identification of a novel polyfluorinated compound as a lead to inhibit the human enzymes aldose reductase and AKR1B10: structure determination of both ternary complexes and implications for drug design. Acta Crystallogr D Biol Crystallogr. 2014 Mar;70(Pt 3):889-903. doi:, 10.1107/S1399004713033452. Epub 2014 Feb 27. PMID:24598757 doi:http://dx.doi.org/10.1107/S1399004713033452
  1. ↑ Gallego O, Ruiz FX, Ardevol A, Dominguez M, Alvarez R, de Lera AR, Rovira C, Farres J, Fita I, Pares X. Structural basis for the high all-trans-retinaldehyde reductase activity of the tumor marker AKR1B10. Proc Natl Acad Sci U S A. 2007 Dec 26;104(52):20764-9. Epub 2007 Dec 17. PMID:18087047

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OCA

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