A single hydrophobic cleft in the Escherichia coli processivity clamp is sufficient to support cell viability and DNA damage-induced mutagenesis in vivo

BMC Molecular Biology

Volumn 11, Issue , 2010, Pages

  Sutton, Mark D ^a   Duzen, Jill M ^a,b   Scouten Ponticelli, Sarah K ^a  

^a UNIVERSITY AT BUFFALO   (United States)

^b ROSWELL PARK CANCER INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

HETERODIMER; BETA SUBUNIT, DNA POLYMERASE III; DINB PROTEIN, E COLI; DNA DIRECTED DNA POLYMERASE; DNA DIRECTED DNA POLYMERASE BETA; DNA DIRECTED DNA POLYMERASE GAMMA; DNA POLYMERASE V, E COLI; ESCHERICHIA COLI PROTEIN;

ALLELE; ARTICLE; CELL CYCLE PROGRESSION; CELL VIABILITY; DNA DAMAGE; DNA REPAIR; DNA REPLICATION; ESCHERICHIA COLI; HYDROPHOBICITY; IN VIVO STUDY; NONHUMAN; SITE DIRECTED MUTAGENESIS; TEMPERATURE SENSITIVITY; ULTRAVIOLET RADIATION; CHEMICAL PHENOMENA; DIMERIZATION; ENZYMOLOGY; GENETICS; METABOLISM; MICROBIAL VIABILITY; MUTAGENESIS; PHENOTYPE;

ESCHERICHIA COLI;

ALLELES; DIMERIZATION; DNA DAMAGE; DNA POLYMERASE BETA; DNA POLYMERASE III; DNA REPAIR; DNA REPLICATION; DNA-DIRECTED DNA POLYMERASE; ESCHERICHIA COLI; ESCHERICHIA COLI PROTEINS; HYDROPHOBIC AND HYDROPHILIC INTERACTIONS; MICROBIAL VIABILITY; MUTAGENESIS; PHENOTYPE; ULTRAVIOLET RAYS;

EID: 78650615835     PISSN: None     EISSN: 14712199     Source Type: Journal    
DOI: 10.1186/1471-2199-11-102     Document Type: Article

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