Common chaperone activity in the G-domain of trGTPase protects L11-L12 interaction on the ribosome

Nucleic Acids Research

Volumn 40, Issue 21, 2012, Pages 10851-10865

  Zhang, Dandan ^a   Liu, Guangqiao ^a   Xue, Jiaying ^a   Lou, Jizhong ^a   Nierhaus, Knud H ^b,c   Gong, Weimin ^a   Qin, Yan ^a  

^a INSTITUTE OF BIOPHYSICS   (China)

^b MAX PLANCK INSTITUTE FOR MOLECULAR GENETICS   (Germany)

^c CHARITÉ UNIVERSITÄTSMEDIZIN BERLIN   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

CHAPERONE; GUANOSINE TRIPHOSPHATASE; RIBOSOMAL PROTEIN L11; RIBOSOMAL PROTEIN L12; RIBOSOME PROTEIN; TRANSLATIONAL GUANOSINE TRIPHOSPHATASE; UNCLASSIFIED DRUG;

ARTICLE; BACTERIAL CELL; BACTERIAL STRAIN; BINDING AFFINITY; CELL GROWTH; CELL VIABILITY; CONTROLLED STUDY; ESCHERICHIA COLI; MUTAGENESIS; NONHUMAN; PRIORITY JOURNAL; PROTEIN BINDING; PROTEIN DOMAIN; PROTEIN FUNCTION; PROTEIN PROTEIN INTERACTION; PROTEIN STRUCTURE; PROTEIN SYNTHESIS; RIBOSOME; THERMUS THERMOPHILUS;

ESCHERICHIA COLI; ESCHERICHIA COLI PROTEINS; GTP PHOSPHOHYDROLASE-LINKED ELONGATION FACTORS; GTP-BINDING PROTEINS; HYDROPHOBIC AND HYDROPHILIC INTERACTIONS; MODELS, MOLECULAR; MOLECULAR CHAPERONES; PEPTIDE ELONGATION FACTOR G; PROTEIN INTERACTION DOMAINS AND MOTIFS; RIBOSOMAL PROTEINS; RIBOSOMES; STATIC ELECTRICITY; TRANSCRIPTIONAL ELONGATION FACTORS;

EID: 84870605357     PISSN: 03051048     EISSN: 13624962     Source Type: Journal    
DOI: 10.1093/nar/gks833     Document Type: Article

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