How the BfiI restriction enzyme uses one active site to cut two DNA strands

Proceedings of the National Academy of Sciences of the United States of America

Volumn 100, Issue 11, 2003, Pages 6410-6415

  Sasnauskas, Giedrius ^a   Halford, Stephen E ^b   Siksnys, Virginijus ^a  

^a VILNIUS UNIVERSITY   (Lithuania)

^b UNIVERSITY OF BRISTOL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

DIMER; METAL ION; OLIGONUCLEOTIDE; PROTEIN BFI1; PROTEIN FOK1; PROTEIN SUBUNIT; RESTRICTION ENDONUCLEASE; UNCLASSIFIED DRUG;

ACIDITY; ARTICLE; DNA PROTEIN COMPLEX; DNA SEQUENCE; DNA STRAND; DOWNSTREAM PROCESSING; ENZYME ACTIVE SITE; IONIZATION; PH; PRIORITY JOURNAL; PROTEIN DEGRADATION;

BASE SEQUENCE; BINDING SITES; CATALYSIS; DEOXYRIBONUCLEASES, TYPE II SITE-SPECIFIC; DIMERIZATION; DNA; DNA PRIMERS; HYDROGEN-ION CONCENTRATION;

EID: 0038652096     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.1131003100     Document Type: Article

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