PMID:21421753: Difference between revisions
Fill PMID: Page! |
imported>Wikientrybot change PMID template to TableEdit version |
||
| (2 intermediate revisions by the same user not shown) | |||
| Line 1: | Line 1: | ||
{{RightTOC}} | {{RightTOC}} | ||
< | <!--box uid=d41d8cd98f00b204e9800998ecf8427e.179572.M5223919779e50--> | ||
< | <!-- | ||
****************************************************************************************** | |||
* | |||
* ** PLEASE DON'T EDIT THIS TABLE DIRECTLY. Use the edit table link under the table. ** | |||
* | |||
****************************************************************************************** --> | |||
{| id="M5223919779e50" class=" tableEdit PMID_info_table" | |||
|- | |- | ||
| | !align=left |Citation | ||
|| | |||
'''Foti, JJ and Walker, GC''' (2011) Efficient extension of slipped DNA intermediates by DinB is required to escape primer template realignment by DnaQ. ''J. Bacteriol.'' '''193''':2637-41 | |||
|- | |- | ||
| | !align=left |Abstract | ||
|| | |||
We show that Escherichia coli DinB polymerase, which creates single-base deletions, prefers to extend slipped DNA substrates with the skipped base at the -4 position. A DinB(Y79L) variant, which extends these substrates less efficiently in vitro, allows the proofreading function of polymerase III to reverse their formation in vivo. | |||
|- | |||
!align=left |Links | |||
|| | |||
[http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=21421753 PubMed] [http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3133156 PMC3133156] | |||
Online version:[http://dx.doi.org/10.1128/JB.00005-11 10.1128/JB.00005-11] | Online version:[http://dx.doi.org/10.1128/JB.00005-11 10.1128/JB.00005-11] | ||
|- | |||
!align=left |Keywords | |||
|| | |||
Amino Acid Substitution/genetics; DNA Polymerase III/metabolism; DNA Replication; DNA, Bacterial/biosynthesis; Escherichia coli/enzymology; Escherichia coli/physiology; Escherichia coli Proteins/genetics; Escherichia coli Proteins/metabolism; Models, Biological; Mutant Proteins/genetics; Mutant Proteins/metabolism; Mutation, Missense; Sequence Deletion | |||
|- class="tableEdit_footer" | |||
|<span class="tableEdit_editLink plainlinks">[{{SERVER}}{{SCRIPTPATH}}?title=Special:TableEdit&id=d41d8cd98f00b204e9800998ecf8427e.179572.M5223919779e50&page=179572&pagename={{FULLPAGENAMEE}}&type=1&template=PMID_info_table edit table]</span> || | |||
|} | |} | ||
< | <!--box uid=d41d8cd98f00b204e9800998ecf8427e.179572.M5223919779e50--> | ||
==Significance {{HelpIcon|Help:Literature}} == | ==Significance {{HelpIcon|Help:Literature}} == | ||
{{LitSignificance}} | {{LitSignificance}} | ||
| Line 19: | Line 38: | ||
==Annotations {{HelpIcon|Help:Literature}}== | ==Annotations {{HelpIcon|Help:Literature}}== | ||
<protect>< | <protect><annotationlinks/></protect> | ||
==EcoliWiki Links {{HelpIcon|Help:Literature}} == | ==EcoliWiki Links {{HelpIcon|Help:Literature}} == | ||
Latest revision as of 04:38, 15 September 2013
| Citation |
Foti, JJ and Walker, GC (2011) Efficient extension of slipped DNA intermediates by DinB is required to escape primer template realignment by DnaQ. J. Bacteriol. 193:2637-41 |
|---|---|
| Abstract |
We show that Escherichia coli DinB polymerase, which creates single-base deletions, prefers to extend slipped DNA substrates with the skipped base at the -4 position. A DinB(Y79L) variant, which extends these substrates less efficiently in vitro, allows the proofreading function of polymerase III to reverse their formation in vivo. |
| Links |
PubMed PMC3133156 Online version:10.1128/JB.00005-11 |
| Keywords |
Amino Acid Substitution/genetics; DNA Polymerase III/metabolism; DNA Replication; DNA, Bacterial/biosynthesis; Escherichia coli/enzymology; Escherichia coli/physiology; Escherichia coli Proteins/genetics; Escherichia coli Proteins/metabolism; Models, Biological; Mutant Proteins/genetics; Mutant Proteins/metabolism; Mutation, Missense; Sequence Deletion |
| edit table |
Significance
You can help EcoliWiki by summarizing why this paper is useful
Useful Materials and Methods
You can help Ecoliwiki by describing the useful materials (strains, plasmids, antibodies, etc) described in this paper.
Annotations
<annotationlinks/>
EcoliWiki Links
Add links to pages that link here (e.g. gene, product, method pages)
See also
References
See Help:References for how to manage references in EcoliWiki.