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7NWI

Mammalian pre-termination 80S ribosome with Empty-A site bound by Blasticidin S

This is a non-PDB format compatible entry.
Summary for 7NWI
Entry DOI10.2210/pdb7nwi/pdb
EMDB information12633
DescriptorL8, Ribosomal protein L11, L13, ... (87 entities in total)
Functional Keywordsinhibitor 80s termination complex blasticidin s translation nmd, ribosome
Biological sourceOryctolagus cuniculus (Rabbit)
More
Total number of polymer chains84
Total formula weight3414474.92
Authors
Powers, K.T.,Yadav, S.K.N.,Bufton, J.C.,Schaffitzel, C. (deposition date: 2021-03-16, release date: 2021-07-07, Last modification date: 2024-11-20)
Primary citationPowers, K.T.,Stevenson-Jones, F.,Yadav, S.K.N.,Amthor, B.,Bufton, J.C.,Borucu, U.,Shen, D.,Becker, J.P.,Lavysh, D.,Hentze, M.W.,Kulozik, A.E.,Neu-Yilik, G.,Schaffitzel, C.
Blasticidin S inhibits mammalian translation and enhances production of protein encoded by nonsense mRNA.
Nucleic Acids Res., 49:7665-7679, 2021
Cited by
PubMed Abstract: Deciphering translation is of paramount importance for the understanding of many diseases, and antibiotics played a pivotal role in this endeavour. Blasticidin S (BlaS) targets translation by binding to the peptidyl transferase center of the large ribosomal subunit. Using biochemical, structural and cellular approaches, we show here that BlaS inhibits both translation elongation and termination in Mammalia. Bound to mammalian terminating ribosomes, BlaS distorts the 3'CCA tail of the P-site tRNA to a larger extent than previously reported for bacterial ribosomes, thus delaying both, peptide bond formation and peptidyl-tRNA hydrolysis. While BlaS does not inhibit stop codon recognition by the eukaryotic release factor 1 (eRF1), it interferes with eRF1's accommodation into the peptidyl transferase center and subsequent peptide release. In human cells, BlaS inhibits nonsense-mediated mRNA decay and, at subinhibitory concentrations, modulates translation dynamics at premature termination codons leading to enhanced protein production.
PubMed: 34157102
DOI: 10.1093/nar/gkab532
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (3.13 Å)
Structure validation

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