Changing nucleotide specificity of the DEAD-box helicase Hera abrogates communication between the Q-motif and the P-loop

Biological Chemistry

Volumn 392, Issue 4, 2011, Pages 357-369

  Strohmeier, Julian ^a   Hertel, Ines ^b   Diederichsen, Ulf ^a   Rudolph, Markus G ^c   Klostermeier, Dagmar ^b,d  

^a UNIVERSITY OF GÖTTINGEN   (Germany)

^b UNIVERSITY OF BASEL   (Switzerland)

^c F HOFFMANN LA ROCHE LTD   (Switzerland)

^d UNIVERSITY OF MÜNSTER   (Germany)

Author keywords

8 oxo adenosine; Crystal structure; Hera; Hydrogen bond network; Nucleotide specificity; Ribosome biogenesis

Indexed keywords

8 OXO ADENOSINE; 8 OXO ADENOSINE TRIPHOSPHATE; ADENOSINE DERIVATIVE; ADENOSINE TRIPHOSPHATE; DEAD BOX PROTEIN; GLUTAMINE; UNCLASSIFIED DRUG;

AMINO TERMINAL SEQUENCE; ARTICLE; CRYSTAL STRUCTURE; ENZYME ACTIVITY; ENZYME SPECIFICITY; GLUTAMINE MOTIF; MUTATION; NONHUMAN; PRIORITY JOURNAL; PROTEIN BINDING; PROTEIN CONFORMATION; PROTEIN MOTIF; THERMUS THERMOPHILUS;

ADENINE; ADENOSINE DIPHOSPHATE; ADENOSINE MONOPHOSPHATE; AMINO ACID MOTIFS; CONSERVED SEQUENCE; CRYSTALLOGRAPHY, X-RAY; DEAD-BOX RNA HELICASES; HYDROGEN BONDING; MODELS, MOLECULAR; MUTATION; NUCLEOTIDES; PROTEIN STRUCTURE, TERTIARY; SUBSTRATE SPECIFICITY; THERMUS THERMOPHILUS;

THERMUS THERMOPHILUS;

EID: 79955415248     PISSN: 14316730     EISSN: 14374315     Source Type: Journal    
DOI: 10.1515/BC.2011.034     Document Type: Article

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