3g5e
From Proteopedia
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{{STRUCTURE_3g5e| PDB=3g5e | SCENE= }} | {{STRUCTURE_3g5e| PDB=3g5e | SCENE= }} | ||
===Human aldose reductase complexed with IDD 740 inhibitor=== | ===Human aldose reductase complexed with IDD 740 inhibitor=== | ||
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{{ABSTRACT_PUBMED_19250825}} | {{ABSTRACT_PUBMED_19250825}} | ||
==About this Structure== | ==About this Structure== | ||
| - | + | [[3g5e]] is a 1 chain structure of [[Aldose Reductase]] 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=3G5E OCA]. | |
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| + | ==See Also== | ||
| + | *[[Aldose Reductase|Aldose Reductase]] | ||
==Reference== | ==Reference== | ||
| - | <ref group="xtra">PMID: | + | <ref group="xtra">PMID:019250825</ref><references group="xtra"/> |
[[Category: Aldehyde reductase]] | [[Category: Aldehyde reductase]] | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Podjarny, A D.]] | [[Category: Podjarny, A D.]] | ||
[[Category: Zandt, M C.Van.]] | [[Category: Zandt, M C.Van.]] | ||
| - | [[Category: Acetylation]] | ||
[[Category: Aldose reductase]] | [[Category: Aldose reductase]] | ||
[[Category: Cataract]] | [[Category: Cataract]] | ||
| - | [[Category: Cytoplasm]] | ||
[[Category: Diabetes]] | [[Category: Diabetes]] | ||
[[Category: Inhibition]] | [[Category: Inhibition]] | ||
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[[Category: Oxidoreductase]] | [[Category: Oxidoreductase]] | ||
[[Category: Phosphoprotein]] | [[Category: Phosphoprotein]] | ||
| - | [[Category: Polymorphism]] | ||
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| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Mar 25 12:40:03 2009'' | ||
Revision as of 04:11, 26 July 2012
Contents |
Human aldose reductase complexed with IDD 740 inhibitor
Template:ABSTRACT PUBMED 19250825
About this Structure
3g5e is a 1 chain structure of Aldose Reductase with sequence from Homo sapiens. Full crystallographic information is available from OCA.
See Also
Reference
- Van Zandt MC, Doan B, Sawicki DR, Sredy J, Podjarny AD. Discovery of [3-(4,5,7-trifluoro-benzothiazol-2-ylmethyl)-pyrrolo[2,3-b]pyridin-1-yl]ac etic acids as highly potent and selective inhibitors of aldose reductase for treatment of chronic diabetic complications. Bioorg Med Chem Lett. 2009 Apr 1;19(7):2006-8. Epub 2009 Feb 12. PMID:19250825 doi:10.1016/j.bmcl.2009.02.037
