Target site cleavage by the monomeric restriction enzyme BcnI requires translocation to a random DNA sequence and a switch in enzyme orientation

Nucleic Acids Research

Volumn 39, Issue 20, 2011, Pages 8844-8856

  Sasnauskas, Giedrius ^a   Kostiuk, Georgij ^a   Tamulaitis, Gintautas ^a   Siksnys, Virginijus ^a  

^a VILNIUS UNIVERSITY   (Lithuania)

Author keywords

[No Author keywords available]

Indexed keywords

BACTERIAL ENZYME; DOUBLE STRANDED DNA; ENDONUCLEASE; ENZYME BCNI; UNCLASSIFIED DRUG;

AMINO ACID SEQUENCE; ARTICLE; BACTERIAL TRANSLOCATION; CATALYSIS; CONTROLLED STUDY; DIMERIZATION; DNA CLEAVAGE; DNA METHYLATION; DNA SEQUENCE; DNA STRAND; HYDROLYSIS; MOLECULAR DYNAMICS; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN METABOLISM; PROTEIN PURIFICATION; VDJ EXON;

BACTERIOPHAGE PHI X 174; BASE SEQUENCE; DEOXYRIBONUCLEASES, TYPE II SITE-SPECIFIC; DNA; DNA CLEAVAGE; DNA, SUPERHELICAL; DNA, VIRAL; KINETICS; PROTEIN TRANSPORT;

EID: 80455178757     PISSN: 03051048     EISSN: 13624962     Source Type: Journal    
DOI: 10.1093/nar/gkr588     Document Type: Article

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