3uxh
From Proteopedia
(Difference between revisions)
m (Protected "3uxh" [edit=sysop:move=sysop]) |
|||
Line 1: | Line 1: | ||
- | + | [[Image:3uxh.jpg|left|200px]] | |
- | The | + | <!-- |
+ | The line below this paragraph, containing "STRUCTURE_3uxh", creates the "Structure Box" on the page. | ||
+ | You may change the PDB parameter (which sets the PDB file loaded into the applet) | ||
+ | or the SCENE parameter (which sets the initial scene displayed when the page is loaded), | ||
+ | or leave the SCENE parameter empty for the default display. | ||
+ | --> | ||
+ | {{STRUCTURE_3uxh| PDB=3uxh | SCENE= }} | ||
- | + | ===Design, Synthesis and Biological Evaluation of Potetent Quinoline and Pyrroloquinoline Ammosamide Analogues as Inhibitors of Quinone Reductase 2=== | |
- | + | ||
+ | <!-- | ||
+ | The line below this paragraph, {{ABSTRACT_PUBMED_22206487}}, adds the Publication Abstract to the page | ||
+ | (as it appears on PubMed at http://www.pubmed.gov), where 22206487 is the PubMed ID number. | ||
+ | --> | ||
+ | {{ABSTRACT_PUBMED_22206487}} | ||
+ | |||
+ | ==About this Structure== | ||
+ | [[3uxh]] is a 2 chain structure 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=3UXH OCA]. | ||
+ | |||
+ | ==Reference== | ||
+ | <ref group="xtra">PMID:022206487</ref><references group="xtra"/> | ||
+ | [[Category: Homo sapiens]] | ||
+ | [[Category: Cushman, M.]] | ||
+ | [[Category: Fanwick, P E.]] | ||
+ | [[Category: Jensen, K C.]] | ||
+ | [[Category: Mesecar, A D.]] | ||
+ | [[Category: Narasimha, R.]] | ||
+ | [[Category: Cytosol]] | ||
+ | [[Category: Oxidoreductase-inhibitor complex]] | ||
+ | [[Category: Quinone reductase]] |
Revision as of 10:46, 18 January 2012
Design, Synthesis and Biological Evaluation of Potetent Quinoline and Pyrroloquinoline Ammosamide Analogues as Inhibitors of Quinone Reductase 2
Template:ABSTRACT PUBMED 22206487
About this Structure
3uxh is a 2 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
- Reddy PV, Jensen KC, Mesecar AD, Fanwick PE, Cushman M. Design, synthesis, and biological evaluation of potent quinoline and pyrroloquinoline ammosamide analogues as inhibitors of quinone reductase 2. J Med Chem. 2012 Jan 12;55(1):367-77. Epub 2011 Dec 29. PMID:22206487 doi:10.1021/jm201251c