Single-molecule FRET reveals nucleotide-driven conformational changes in molecular machines and their link to RNA unwinding and DNA supercoiling

Biochemical Society Transactions

Volumn 39, Issue 2, 2011, Pages 611-616

  Klostermeier, Dagmar ^a,b  

^a UNIVERSITY OF BASEL   (Switzerland)

^b UNIVERSITY OF MÜNSTER   (Germany)

Author keywords

ATP hydrolysis; C terminal domain; DEAD box; Fluorescence resonance energy transfer (FRET); RNA binding domain; RNA recognition motif

Indexed keywords

ADENOSINE TRIPHOSPHATE; DEAD BOX PROTEIN; DNA; DNA TOPOISOMERASE (ATP HYDROLYSING); NUCLEOTIDE; RNA; RNA 23S;

AMINO TERMINAL SEQUENCE; CARBOXY TERMINAL SEQUENCE; CATALYSIS; CONFORMATIONAL TRANSITION; DNA CLEAVAGE; ENZYME REGULATION; FLUORESCENCE RESONANCE ENERGY TRANSFER; METHANOCALDOCOCCUS JANNASCHII; PRIORITY JOURNAL; PROTEIN BINDING; PROTEIN HYDROLYSIS; PROTEIN LOCALIZATION; PROTEIN STRUCTURE; REVIEW; RNA BINDING; SINGLE MOLECULE FLUORESCENCE RESONANCE ENERGY TRANSFER;

ADENOSINE TRIPHOSPHATE; ANIMALS; BACILLUS SUBTILIS; BACTERIAL PROTEINS; DEAD-BOX RNA HELICASES; DNA, SUPERHELICAL; FLUORESCENCE RESONANCE ENERGY TRANSFER; HUMANS; MACROMOLECULAR SUBSTANCES; MODELS, BIOLOGICAL; NUCLEIC ACID CONFORMATION; NUCLEOTIDES; RNA;

EID: 79953184339     PISSN: 03005127     EISSN: 14708752     Source Type: Journal    
DOI: 10.1042/BST0390611     Document Type: Review

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