3oeu

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-	'''Unreleased structure'''	+	[[Image:3oeu.jpg|left|200px]]
-	The entry 3oeu is ON HOLD	+	<!--
		+	The line below this paragraph, containing "STRUCTURE_3oeu", 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.
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		+	{{STRUCTURE_3oeu| PDB=3oeu | SCENE= }}
-	Authors: Sintchak, M.D.	+	===Structure of yeast 20S open-gate proteasome with Compound 24===
-	Description: Structure of yeast 20S open-gate proteasome with Compound 24	+
		+	<!--
		+	The line below this paragraph, {{ABSTRACT_PUBMED_20875739}}, adds the Publication Abstract to the page
		+	(as it appears on PubMed at http://www.pubmed.gov), where 20875739 is the PubMed ID number.
		+	-->
		+	{{ABSTRACT_PUBMED_20875739}}
		+
		+	==About this Structure==
		+	[[3oeu]] is a 28 chain structure with sequence from [http://en.wikipedia.org/wiki/Saccharomyces_cerevisiae Saccharomyces cerevisiae]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3OEU OCA].
		+
		+	==Reference==
		+	<ref group="xtra">PMID:020875739</ref><references group="xtra"/>
		+	[[Category: Proteasome endopeptidase complex]]
		+	[[Category: Saccharomyces cerevisiae]]
		+	[[Category: Sintchak, M D.]]
		+	[[Category: 20s proteasome]]
		+	[[Category: Hydrolase-hydrolase inhibitor complex]]

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Revision as of 06:42, 20 July 2011

Template:STRUCTURE 3oeu

Structure of yeast 20S open-gate proteasome with Compound 24

Template:ABSTRACT PUBMED 20875739

About this Structure

3oeu is a 28 chain structure with sequence from Saccharomyces cerevisiae. Full crystallographic information is available from OCA.

Reference

• Blackburn C, Barrett C, Blank JL, Bruzzese FJ, Bump N, Dick LR, Fleming P, Garcia K, Hales P, Hu Z, Jones M, Liu JX, Sappal DS, Sintchak MD, Tsu C, Gigstad KM. Optimization of a series of dipeptides with a P3 threonine residue as non-covalent inhibitors of the chymotrypsin-like activity of the human 20S proteasome. Bioorg Med Chem Lett. 2010 Nov 15;20(22):6581-6. Epub 2010 Sep 15. PMID:20875739 doi:10.1016/j.bmcl.2010.09.032