1k0a: Difference between revisions

Revision as of 19:45, 28 July 2008

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:1k0a.png

Template:STRUCTURE 1k0a

Ure2p in Complex with S-hexylglutathioneUre2p in Complex with S-hexylglutathione

Template:ABSTRACT PUBMED 11695904

About this StructureAbout this Structure

1K0A is a Single protein structure of sequence from Saccharomyces cerevisiae. Full crystallographic information is available from OCA.

ReferenceReference

Crystal structures of the yeast prion Ure2p functional region in complex with glutathione and related compounds., Bousset L, Belrhali H, Melki R, Morera S, Biochemistry. 2001 Nov 13;40(45):13564-73. PMID:11695904

Page seeded by OCA on Mon Jul 28 19:45:35 2008

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

OCA

@@ Line 1: / Line 1: @@
-[[Image:1k0a.jpg|left|200px]]
+{{Seed}}
+[[Image:1k0a.png|left|200px]]
 <!--
@@ Line 9: / Line 10: @@
 {{STRUCTURE_1k0a|  PDB=1k0a  |  SCENE=  }}
-'''Ure2p in Complex with S-hexylglutathione'''
+===Ure2p in Complex with S-hexylglutathione===
-==Overview==
+<!--
-The [URE3] phenotype in yeast Saccharomyces cerevisiae is due to an altered prion form of Ure2p, a protein involved in nitrogen catabolism. To understand possible conformational changes at the origin of prion propagation, we previously solved the crystal structure of the Ure2p functional region [Bousset et al. (2001) Structure 9, 39-46]. We showed the protein to have a fold similar to that of the beta class of glutathione S-transferases (GSTs). Here we report crystal structures of the Ure2p functional region (extending from residues 95-354) in complex with glutathione (GSH), the substrate of all GSTs, and two widely used GST inhibitors, namely, S-hexylglutathione and S-p-nitrobenzylglutathione. In a manner similar to what is observed in many GSTs, ligand binding is not accompanied by a significant change in the conformation of the protein. We identify one GSH and one hydrophobic electrophile binding site per monomer as observed in all other GSTs. The sulfur group of GSH, that conjugates electrophiles, is located near the amide group of Asn124, allowing a hydrogen bond to be formed. Biochemical data indicate that GSH binds to Ure2p with high affinity. Its binding affects Ure2p oligomerization but has no effect on the assembly of the protein into amyloid fibrils. Despite results indicating that Ure2p lacks GST activity, we propose that Ure2p is a member of the GST superfamily that may describe a novel GST class. Our data bring new insights into the function of the Ure2p active region.
+The line below this paragraph, {{ABSTRACT_PUBMED_11695904}}, adds the Publication Abstract to the page
+(as it appears on PubMed at http://www.pubmed.gov), where 11695904 is the PubMed ID number.
+-->
+{{ABSTRACT_PUBMED_11695904}}
 ==About this Structure==
@@ Line 28: / Line 32: @@
 [[Category: Nitrate assimilation]]
 [[Category: Structural genomic]]
-''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Fri May  2 22:08:29 2008''
+''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Jul 28 19:45:35 2008''