2dpi: Difference between revisions

From Proteopedia
Jump to navigationJump to search
OCA (talk | contribs)
No edit summary
OCA (talk | contribs)
No edit summary
Line 1: Line 1:
[[Image:2dpi.gif|left|200px]]
{{Seed}}
[[Image:2dpi.png|left|200px]]


<!--
<!--
Line 9: Line 10:
{{STRUCTURE_2dpi|  PDB=2dpi  |  SCENE=  }}  
{{STRUCTURE_2dpi|  PDB=2dpi  |  SCENE=  }}  


'''Ternary complex of hPoli with DNA and dCTP'''
===Ternary complex of hPoli with DNA and dCTP===




==Overview==
<!--
The 1,N6-ethenodeoxyadenosine (epsilon dA) lesion is promutagenic and has been implicated in carcinogenesis. We show here that human Pol iota, a Y-family DNA polymerase, can promote replication through this lesion by proficiently incorporating a nucleotide opposite it. The structural basis of this action is rotation of the epsilon dA adduct to the syn conformation in the Pol iota active site and presentation of its 'Hoogsteen edge' for hydrogen-bonding with incoming dTTP or dCTP. We also show that Pol zeta carries out the subsequent extension reaction and that efficiency of extension from epsilon dA x T is notably higher than from epsilon dA x C. Together, our studies reveal for the first time how the exocyclic epsilon dA adduct is accommodated in a DNA polymerase active site, and they show that the combined action of Pol iota and Pol zeta provides for efficient and error-free synthesis through this potentially carcinogenic DNA lesion.
The line below this paragraph, {{ABSTRACT_PUBMED_16819516}}, adds the Publication Abstract to the page
(as it appears on PubMed at http://www.pubmed.gov), where 16819516 is the PubMed ID number.
-->
{{ABSTRACT_PUBMED_16819516}}


==About this Structure==
==About this Structure==
Line 31: Line 35:
[[Category: Ethenoda adduct]]
[[Category: Ethenoda adduct]]
[[Category: Lesion bypass]]
[[Category: Lesion bypass]]
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun May  4 00:54:53 2008''
 
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Jul 28 08:30:52 2008''