Mechanisms for defining supercoiling set point of DNA gyrase orthologs: II. The shape of the GyrA subunit C-terminal domain (CTD) is not a sole determinant for controlling supercoiling efficiency

Journal of Biological Chemistry

Volumn 287, Issue 22, 2012, Pages 18645-18654

  Tretter, Elsa M ^a   Berger, James M ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

C-TERMINAL DOMAINS; CATALYTIC PROPERTIES; CONTROL ELEMENTS; DNA GYRASES; DNA SEGMENTS; DNA STRANDS; DOUBLE-HELICAL; E. COLI; M. TUBERCULOSIS; MOLECULAR BASIS; MYCOBACTERIUM TUBERCULOSIS; ORTHOLOGS; PHYLOGENETIC INFERENCE; SETPOINTS; SPECIFIC ACTIVITY; SUPERCOILING; TOPOISOMERASES; TOPOLOGICAL STATE; TYPE II;

ENZYMES; ESCHERICHIA COLI; GENES; PLANTS (BOTANY); TUBES (COMPONENTS);

DNA;

ADENOSINE TRIPHOSPHATE; BACTERIAL ENZYME; DNA TOPOISOMERASE (ATP HYDROLYSING);

ARTICLE; CARBOXY TERMINAL SEQUENCE; CONTROLLED STUDY; DNA SUPERCOILING; ENZYME ACTIVITY; ENZYME CHEMISTRY; ENZYME MECHANISM; ENZYME METABOLISM; ENZYME STRUCTURE; ESCHERICHIA COLI; MYCOBACTERIUM TUBERCULOSIS; NONHUMAN; PHYLOGENY; PRIORITY JOURNAL; SPECIES DIFFERENCE; STRUCTURE ACTIVITY RELATION;

AMINO ACID SEQUENCE; CRYSTALLIZATION; DNA GYRASE; ESCHERICHIA COLI; MOLECULAR SEQUENCE DATA; SEQUENCE HOMOLOGY, AMINO ACID;

ESCHERICHIA COLI; MYCOBACTERIUM TUBERCULOSIS; PROTEOBACTERIA;

EID: 84861543031     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M112.345736     Document Type: Article

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