1iry: Difference between revisions

From Proteopedia
Jump to navigationJump to search
← Older editNewer edit →
OCA (talk | contribs)
Bots, Bureaucrats, journal, Administrators
3,328,572 edits
No edit summary
OCA (talk | contribs)
Bots, Bureaucrats, journal, Administrators
3,328,572 edits
No edit summary
Line 1: Line 1:
[[Image:1iry.gif|left|200px]]
{{Seed}}
[[Image:1iry.png|left|200px]]


<!--
<!--
Line 9: Line 10:
{{STRUCTURE_1iry|  PDB=1iry  |  SCENE=  }}  
{{STRUCTURE_1iry|  PDB=1iry  |  SCENE=  }}  


'''Solution structure of the hMTH1, a nucleotide pool sanitization enzyme'''
===Solution structure of the hMTH1, a nucleotide pool sanitization enzyme===




==Overview==
<!--  
Oxygen radicals generated through normal cellular respiration processes can cause mutations in genomic and mitochondrial DNA. Human MTH1 hydrolyzes oxidized purine nucleoside triphosphates, such as 8-oxo-dGTP and 2-hydroxy-dATP, to monophosphates, thereby preventing the misincorporation of these oxidized nucleotides during replication. Here we present the solution structure of MTH1 solved by multidimensional heteronuclear NMR spectroscopy. The protein adopts a fold similar to that of Escherichia coli MutT, despite the low sequence similarity between these proteins outside the conserved Nudix motif. The substrate-binding pocket of MTH1, deduced from chemical shift perturbation experiments, is located at essentially the same position as in MutT; however, a pocket-forming helix is largely displaced in MTH1 (approximately 9 A) such that the shape of the pocket differs between the two proteins. Detailed analysis of the pocket-forming residues enabled us to identify Asn33 as one of the key residues in MTH1 for discriminating the oxidized form of purine, and mutation of this residue modifies the substrate specificity. We also show that MTH1 catalyzes hydrolysis of 8-oxo-dGTP through nucleophilic substitution of water at the beta-phosphate.
The line below this paragraph, {{ABSTRACT_PUBMED_15133035}}, adds the Publication Abstract to the page
(as it appears on PubMed at http://www.pubmed.gov), where 15133035 is the PubMed ID number.
-->
{{ABSTRACT_PUBMED_15133035}}


==About this Structure==
==About this Structure==
1IRY is a [[Single protein]] structure of 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=1IRY OCA].  
1IRY is a [[Single protein]] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1IRY OCA].  


==Reference==
==Reference==
Line 28: Line 32:
[[Category: Sakai, Y.]]
[[Category: Sakai, Y.]]
[[Category: Shirakawa, M.]]
[[Category: Shirakawa, M.]]
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Fri May 2 20:20:32 2008''
 
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Tue Jul 1 13:53:55 2008''

Revision as of 10:53, 1 July 2008

File:1iry.png

Template:STRUCTURE 1iry

Solution structure of the hMTH1, a nucleotide pool sanitization enzyme

Template:ABSTRACT PUBMED 15133035

About this Structure

1IRY is a Single protein structure of sequence from Homo sapiens. Full experimental information is available from OCA.

Reference

Structure of human MTH1, a Nudix family hydrolase that selectively degrades oxidized purine nucleoside triphosphates., Mishima M, Sakai Y, Itoh N, Kamiya H, Furuichi M, Takahashi M, Yamagata Y, Iwai S, Nakabeppu Y, Shirakawa M, J Biol Chem. 2004 Aug 6;279(32):33806-15. Epub 2004 May 7. PMID:15133035

Page seeded by OCA on Tue Jul 1 13:53:55 2008

Proteopedia Page Contributors and Editors (what is this?)

OCA

Retrieved from "https://proteopedia.org/index.php?title=1iry&oldid=613267"