Dissection of the ATPase active site of P1 ParA reveals multiple active forms essential for plasmid partition

Journal of Biological Chemistry

Volumn 288, Issue 24, 2013, Pages 17823-17831

  Vecchiarelli, Anthony G ^a,b   Havey, James C ^a,c   Ing, Lori L ^a   Wong, Erin O Y ^a   Waples, William G ^a   Funnell, Barbara E ^a  

^a UNIVERSITY OF TORONTO   (Canada)

^b NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES   (United States)

^c YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ATP-ASE ACTIVITY; ATP-BINDING SITE; BACTERIAL CHROMOSOMES; BACTERIAL PLASMID; DNA BINDING ACTIVITY; DNA-BINDING PROTEIN; REPRESSOR ACTIVITY; TRANSCRIPTIONAL REPRESSORS;

AMINO ACIDS; CHROMOSOMES; GENE EXPRESSION; PROTEINS;

DNA;

ADENOSINE TRIPHOSPHATASE; ARGININE; BACTERIAL PROTEIN; GLUTAMIC ACID; GLUTAMINE; LYSINE; P1 PARA PROTEIN; PROTEIN PARB; PROTEIN PARPD; UNCLASSIFIED DRUG;

AMINO ACID SUBSTITUTION; ARTICLE; BINDING SITE; COMPLEX FORMATION; CONTROLLED STUDY; ENZYME ACTIVE SITE; ENZYME ACTIVITY; ENZYME ANALYSIS; ENZYME LOCALIZATION; GENE MUTATION; HYDROLYSIS; IN VITRO STUDY; IN VIVO STUDY; NONHUMAN; PHENOTYPE; PLASMID; PRIORITY JOURNAL; PROTEIN BINDING; PROTEIN MOTIF; PROTEIN PROTEIN INTERACTION;

ATP BINDING; ATPASES; CHROMOSOME DYNAMICS; DNA BINDING PROTEIN; ENZYME MUTATION; ESCHERICHIA COLI; FLUORESCENCE; PLASMID; PROTEIN DNA-INTERACTION; SEGREGATION;

ADENOSINE TRIPHOSPHATASES; ADENOSINE TRIPHOSPHATE; AMINO ACID SUBSTITUTION; CATALYTIC DOMAIN; DNA PRIMASE; DNA, BACTERIAL; ESCHERICHIA COLI; ESCHERICHIA COLI PROTEINS; HYDROLYSIS; PHENOTYPE; PLASMIDS; PROMOTER REGIONS, GENETIC; PROTEIN BINDING;

BACTERIA (MICROORGANISMS);

EID: 84879045680     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M113.469981     Document Type: Article

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