3gam: Difference between revisions
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[[Image:3gam.png|left|200px]] | [[Image:3gam.png|left|200px]] | ||
{{STRUCTURE_3gam| PDB=3gam | SCENE= }} | {{STRUCTURE_3gam| PDB=3gam | SCENE= }} | ||
===Synthesis of Casimiroin and Optimization of Its Quinone Reductase 2 and Aromatase Inhibitory activity=== | ===Synthesis of Casimiroin and Optimization of Its Quinone Reductase 2 and Aromatase Inhibitory activity=== | ||
{{ABSTRACT_PUBMED_19265439}} | {{ABSTRACT_PUBMED_19265439}} | ||
==About this Structure== | ==About this Structure== | ||
[[3gam]] is a 2 chain structure of [[Quinone 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=3GAM OCA]. | |||
==See Also== | |||
*[[Quinone reductase|Quinone reductase]] | |||
==Reference== | ==Reference== | ||
<ref group="xtra">PMID: | <ref group="xtra">PMID:019265439</ref><references group="xtra"/> | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Cushman, M.]] | [[Category: Cushman, M.]] | ||
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[[Category: Sturdy, M.]] | [[Category: Sturdy, M.]] | ||
[[Category: Casimiroin]] | [[Category: Casimiroin]] | ||
[[Category: Fad]] | [[Category: Fad]] | ||
[[Category: Flavoprotein]] | [[Category: Flavoprotein]] | ||
| Line 40: | Line 30: | ||
[[Category: Oxidoreductase]] | [[Category: Oxidoreductase]] | ||
[[Category: Phosphoprotein]] | [[Category: Phosphoprotein]] | ||
[[Category: Qr2]] | [[Category: Qr2]] | ||
[[Category: Quinone reductase 2]] | [[Category: Quinone reductase 2]] | ||
Revision as of 01:36, 26 July 2012
Synthesis of Casimiroin and Optimization of Its Quinone Reductase 2 and Aromatase Inhibitory activity
Template:ABSTRACT PUBMED 19265439
About this Structure
3gam is a 2 chain structure of Quinone reductase with sequence from Homo sapiens. Full crystallographic information is available from OCA.
See Also
Reference
- Maiti A, Reddy PV, Sturdy M, Marler L, Pegan SD, Mesecar AD, Pezzuto JM, Cushman M. Synthesis of Casimiroin and Optimization of Its Quinone Reductase 2 and Aromatase Inhibitory Activities. J Med Chem. 2009 Mar 6. PMID:19265439 doi:10.1021/jm801335z