1q32: Difference between revisions

From Proteopedia
Jump to navigationJump to search
← Older editNewer edit →
OCA (talk | contribs)
Bots, Bureaucrats, journal, Administrators
3,331,613 edits
No edit summary
OCA (talk | contribs)
Bots, Bureaucrats, journal, Administrators
3,331,613 edits
No edit summary
Line 1: Line 1:
[[Image:1q32.gif|left|200px]]
{{Seed}}
[[Image:1q32.png|left|200px]]


<!--
<!--
Line 9: Line 10:
{{STRUCTURE_1q32|  PDB=1q32  |  SCENE=  }}  
{{STRUCTURE_1q32|  PDB=1q32  |  SCENE=  }}  


'''Crystal Structure Analysis of the Yeast Tyrosyl-DNA Phosphodiesterase'''
===Crystal Structure Analysis of the Yeast Tyrosyl-DNA Phosphodiesterase===




==Overview==
<!--  
Tyrosyl-DNA phosphodiesterase 1 (Tdp1) catalyzes the resolution of 3' and 5' phospho-DNA adducts. A defective mutant, associated with the recessive neurodegenerative disease SCAN1, accumulates Tdp1-DNA complexes in vitro. To assess the conservation of enzyme architecture, a 2.0 A crystal structure of yeast Tdp1 was determined that is very similar to human Tdp1. Poorly conserved regions of primary structure are peripheral to an essentially identical catalytic core. Enzyme mechanism was also conserved, because the yeast SCAN1 mutant (H(432)R) enhanced cell sensitivity to the DNA topoisomerase I (Top1) poison camptothecin. A more severe Top1-dependent lethality of Tdp1H(432)N was drug-independent, coinciding with increased covalent Top1-DNA and Tdp1-DNA complex formation in vivo. However, both H(432) mutants were recessive to wild-type Tdp1. Thus, yeast H(432) acts in the general acid/base catalytic mechanism of Tdp1 to resolve 3' phosphotyrosyl and 3' phosphoamide linkages. However, the distinct pattern of mutant Tdp1 activity evident in yeast cells, suggests a more severe defect in Tdp1H(432)N-catalyzed resolution of 3' phospho-adducts.
The line below this paragraph, {{ABSTRACT_PUBMED_17707402}}, adds the Publication Abstract to the page
(as it appears on PubMed at http://www.pubmed.gov), where 17707402 is the PubMed ID number.
-->
{{ABSTRACT_PUBMED_17707402}}


==About this Structure==
==About this Structure==
Line 34: Line 38:
[[Category: Transcription]]
[[Category: Transcription]]
[[Category: Tyrosyl-dna phosphodiesterase]]
[[Category: Tyrosyl-dna phosphodiesterase]]
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Jun 11 10:53:29 2008''
 
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Jul 28 16:17:29 2008''

Revision as of 13:17, 28 July 2008

File:1q32.png

Template:STRUCTURE 1q32

Crystal Structure Analysis of the Yeast Tyrosyl-DNA Phosphodiesterase

Template:ABSTRACT PUBMED 17707402

About this Structure

1Q32 is a Single protein structure of sequence from Saccharomyces cerevisiae. Full crystallographic information is available from OCA.

Reference

Mutation of a conserved active site residue converts tyrosyl-DNA phosphodiesterase I into a DNA topoisomerase I-dependent poison., He X, van Waardenburg RC, Babaoglu K, Price AC, Nitiss KC, Nitiss JL, Bjornsti MA, White SW, J Mol Biol. 2007 Sep 28;372(4):1070-81. Epub 2007 Aug 2. PMID:17707402

Page seeded by OCA on Mon Jul 28 16:17:29 2008

Proteopedia Page Contributors and Editors (what is this?)

OCA

Retrieved from "https://proteopedia.org/index.php?title=1q32&oldid=706615"