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2VAZ

Model of the S15-mRNA complex fitted into the cryo-EM map of the 70S entrapment complex.

Summary for 2VAZ
Entry DOI10.2210/pdb2vaz/pdb
Related1P6G 1P87 2AVY 2AW7
EMDB information1391
DescriptorRPSO MRNA OPERATOR, 30S RIBOSOMAL PROTEIN S15 (2 entities in total)
Functional Keywordstranslation, platform-binding center, gene expression regulation, ribosomal protein, ribonucleoprotein, protein synthesis, translation initiation, ribosome, riboswitch, rna-binding, rrna-binding, rna pseudoknot, mrna structure, repressor protein
Biological sourceESCHERICHIA COLI
More
Total number of polymer chains2
Total formula weight69717.93
Authors
Marzi, S.,Myasnikov, A.G.,Serganov, A.,Ehresmann, C.,Romby, P.,Yusupov, M.,Klaholz, B.P. (deposition date: 2007-09-05, release date: 2007-10-02, Last modification date: 2024-05-08)
Primary citationMarzi, S.,Myasnikov, A.G.,Serganov, A.,Ehresmann, C.,Romby, P.,Yusupov, M.,Klaholz, B.P.
Structured Mrnas Regulate Translation Initiation by Binding to the Platform of the Ribosome.
Cell(Cambridge,Mass.), 130:1019-, 2007
Cited by
PubMed Abstract: Gene expression can be regulated at the level of initiation of protein biosynthesis via structural elements present at the 5' untranslated region of mRNAs. These folded mRNA segments may bind to the ribosome, thus blocking translation until the mRNA unfolds. Here, we report a series of cryo-electron microscopy snapshots of ribosomal complexes directly visualizing either the mRNA structure blocked by repressor protein S15 or the unfolded, active mRNA. In the stalled state, the folded mRNA prevents the start codon from reaching the peptidyl-tRNA (P) site inside the ribosome. Upon repressor release, the mRNA unfolds and moves into the mRNA channel allowing translation initiation. A comparative structure and sequence analysis suggests the existence of a universal stand-by site on the ribosome (the 30S platform) dedicated for binding regulatory 5' mRNA elements. Different types of mRNA structures may be accommodated during translation preinitiation and regulate gene expression by transiently stalling the ribosome.
PubMed: 17889647
DOI: 10.1016/J.CELL.2007.07.008
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (10 Å)
Structure validation

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