3oaw: Difference between revisions

Revision as of 14:40, 22 September 2010

This article has been automatically seeded. Changes to this page should pertain to the PDB entry only and not to the protein or biomolecule in general.

File:3oaw.jpg

Template:STRUCTURE 3oaw

4-Methylpteridineones as Orally Active and Selective PI3K/mTOR Dual Inhibitors4-Methylpteridineones as Orally Active and Selective PI3K/mTOR Dual Inhibitors

Template:ABSTRACT PUBMED 20817449

About this StructureAbout this Structure

3OAW is a 1 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.

ReferenceReference

^{[xtra 1]}

↑ Liu KK, Bagrodia S, Bailey S, Cheng H, Chen H, Gao L, Greasley S, Hoffman JE, Hu Q, Johnson TO, Knighton D, Liu Z, Marx MA, Nambu MD, Ninkovic S, Pascual B, Rafidi K, Rodgers CM, Smith GL, Sun S, Wang H, Yang A, Yuan J, Zou A. 4-Methylpteridinones as orally active and selective PI3K/mTOR dual inhibitors. Bioorg Med Chem Lett. 2010 Oct 15;20(20):6096-9. Epub 2010 Aug 14. PMID:20817449 doi:10.1016/j.bmcl.2010.08.045

Page seeded by OCA on Wed Sep 22 14:49:15 2010

Proteopedia Page Contributors and Editors (what is this?)Proteopedia Page Contributors and Editors (what is this?)

OCA

[1] Liu KK, Bagrodia S, Bailey S, Cheng H, Chen H, Gao L, Greasley S, Hoffman JE, Hu Q, Johnson TO, Knighton D, Liu Z, Marx MA, Nambu MD, Ninkovic S, Pascual B, Rafidi K, Rodgers CM, Smith GL, Sun S, Wang H, Yang A, Yuan J, Zou A. 4-Methylpteridinones as orally active and selective PI3K/mTOR dual inhibitors. Bioorg Med Chem Lett. 2010 Oct 15;20(20):6096-9. Epub 2010 Aug 14. PMID:20817449 doi:10.1016/j.bmcl.2010.08.045

[xtra 1]

@@ Line 1: / Line 1: @@
-'''Unreleased structure'''
+{{Seed}}
+[[Image:3oaw.jpg|left|200px]]
-The entry 3oaw is ON HOLD
+<!--
+The line below this paragraph, containing "STRUCTURE_3oaw", 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_3oaw|  PDB=3oaw  |  SCENE=  }}
-Authors: Knighton, D.R., Greasley, S.E., Rodgers, C.M.-L.
+===4-Methylpteridineones as Orally Active and Selective PI3K/mTOR Dual Inhibitors===
-Description: 4-Methylpteridineones as Orally Active and Selective PI3K/mTOR Dual Inhibitors
-''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Aug 18 11:25:59 2010''
+<!--
+The line below this paragraph, {{ABSTRACT_PUBMED_20817449}}, adds the Publication Abstract to the page
+(as it appears on PubMed at http://www.pubmed.gov), where 20817449 is the PubMed ID number.
+-->
+{{ABSTRACT_PUBMED_20817449}}
+==About this Structure==
+OAW is a 1 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=3OAW OCA].
+==Reference==
+<ref group="xtra">PMID:20817449</ref><references group="xtra"/>
+[[Category: Homo sapiens]]
+[[Category: Phosphatidylinositol-4,5-bisphosphate 3-kinase]]
+[[Category: Greasley, S E.]]
+[[Category: Knighton, D R.]]
+[[Category: Rodgers, C M.L.]]
+[[Category: Inhibition]]
+[[Category: Inhibitor complex.]]
+[[Category: Phosphoinositide kinase]]
+[[Category: Transferase-transferase]]
+[[Category: Transferase-transferase inhibitor complex]]
+''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Sep 22 14:49:15 2010''