3udd: Difference between revisions

Revision as of 07:21, 1 February 2012

3udd is a 2 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.

Shultz MD, Kirby CA, Stams T, Chin DN, Blank J, Charlat O, Cheng H, Cheung AK, Feng Y, Fortin PD, Hood T, Tyagi V, Xu M, Zhang B, Shao W. [1,2,4]Triazol-3-ylsulfanylmethyl)-3-phenyl-[1,2,4]oxadiazoles: Antagonists of the Wnt pathway that inhibit tankyrase 1&2 via novel adenosine pocket binding. J Med Chem. 2012 Jan 19. PMID:22260203 doi:10.1021/jm2011222

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-'''Unreleased structure'''
+[[Image:3udd.jpg|left|200px]]
-The entry 3udd is ON HOLD  until Paper Publication
+<!--
+The line below this paragraph, containing "STRUCTURE_3udd", 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_3udd|  PDB=3udd  |  SCENE=  }}
-Authors: Kirby, C.A., Stams, T.
+===Tankyrase-1 in complex with small molecule inhibitor===
-Description: Tankyrase-1 in complex with small molecule inhibitor
+<!--
+The line below this paragraph, {{ABSTRACT_PUBMED_22260203}}, adds the Publication Abstract to the page
+(as it appears on PubMed at http://www.pubmed.gov), where 22260203 is the PubMed ID number.
+-->
+{{ABSTRACT_PUBMED_22260203}}
+==About this Structure==
+[[3udd]] 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=3UDD OCA].
+==Reference==
+<ref group="xtra">PMID:022260203</ref><references group="xtra"/>
+[[Category: Homo sapiens]]
+[[Category: Kirby, C A.]]
+[[Category: Stams, T.]]
+[[Category: Transferase]]
+[[Category: Transferase-transferase inhibitor complex]]