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3g5e
From Proteopedia
(Difference between revisions)
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| + | [[Image:3g5e.jpg|left|200px]] | ||
| - | The | + | <!-- |
| + | The line below this paragraph, containing "STRUCTURE_3g5e", creates the "Structure Box" on the page. | ||
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| + | {{STRUCTURE_3g5e| PDB=3g5e | SCENE= }} | ||
| - | + | ===Human aldose reductase complexed with IDD 740 inhibitor=== | |
| - | Description: Human aldose reductase complexed with IDD 740 inhibitor | ||
| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed | + | <!-- |
| + | The line below this paragraph, {{ABSTRACT_PUBMED_19250825}}, adds the Publication Abstract to the page | ||
| + | (as it appears on PubMed at http://www.pubmed.gov), where 19250825 is the PubMed ID number. | ||
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| + | {{ABSTRACT_PUBMED_19250825}} | ||
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| + | ==About this Structure== | ||
| + | 3G5E is a 1 chain structure of 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]. | ||
| + | |||
| + | ==Reference== | ||
| + | <ref group="xtra">PMID:19250825</ref><references group="xtra"/> | ||
| + | [[Category: Aldehyde reductase]] | ||
| + | [[Category: Homo sapiens]] | ||
| + | [[Category: Podjarny, A D.]] | ||
| + | [[Category: Zandt, M C.Van.]] | ||
| + | [[Category: Acetylation]] | ||
| + | [[Category: Aldose reductase]] | ||
| + | [[Category: Cataract]] | ||
| + | [[Category: Cytoplasm]] | ||
| + | [[Category: Diabetes]] | ||
| + | [[Category: Inhibition]] | ||
| + | [[Category: Nadp]] | ||
| + | [[Category: Oxidoreductase]] | ||
| + | [[Category: Phosphoprotein]] | ||
| + | [[Category: Polymorphism]] | ||
| + | |||
| + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Mar 25 12:40:03 2009'' | ||
Revision as of 10:40, 25 March 2009
Human aldose reductase complexed with IDD 740 inhibitor
Template:ABSTRACT PUBMED 19250825
About this Structure
3G5E is a 1 chain structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.
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
Page seeded by OCA on Wed Mar 25 12:40:03 2009
