How PspGI, catalytic domain of EcoRII and Ecl18kI acquire specificities for different DNA targets

Nucleic Acids Research

Volumn 36, Issue 19, 2008, Pages 6101-6108

  Tamulaitis, Gintautas ^a   Zaremba, Mindaugas ^a   Szczepanowski, Roman H ^b,c   Bochtler, Matthias ^b,c,d   Siksnys, Virginijus ^a  

^a VILNIUS UNIVERSITY   (Lithuania)

^b INTERNATIONAL INSTITUTE OF MOLECULAR AND CELL BIOLOGY   (Poland)

^c MAX PLANCK INSTITUTE OF MOLECULAR CELL BIOLOGY AND GENETICS   (Germany)

^d CARDIFF UNIVERSITY   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

MUTANT PROTEIN; PROTEIN ECL18KL; PROTEIN ECORII; PROTEIN PSPGI; RESTRICTION ENDONUCLEASE; UNCLASSIFIED DRUG;

ARTICLE; BASE PAIRING; BINDING SITE; CONTROLLED STUDY; ENZYME SPECIFICITY; ENZYME SUBSTRATE; GENE MUTATION; GENE TARGETING; MOLECULAR INTERACTION; PRIORITY JOURNAL; PROTEIN DEGRADATION; PROTEIN DOMAIN; PROTEIN VARIANT; SEQUENCE ANALYSIS;

AMINO ACID SUBSTITUTION; BASE PAIRING; BINDING SITES; CATALYTIC DOMAIN; DEOXYRIBONUCLEASES, TYPE II SITE-SPECIFIC; DNA; ELECTROPHORETIC MOBILITY SHIFT ASSAY; MODELS, MOLECULAR; SUBSTRATE SPECIFICITY;

EID: 56049119613     PISSN: 03051048     EISSN: 13624962     Source Type: Journal    
DOI: 10.1093/nar/gkn621     Document Type: Article

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