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4V92

Kluyveromyces lactis 80S ribosome in complex with CrPV-IRES

This is a non-PDB format compatible entry.
Summary for 4V92
Entry DOI10.2210/pdb4v92/pdb
Related4CUV 4CUW
EMDB information2604
Descriptor18S RRNA, ES7, ES8, ... (35 entities in total)
Functional Keywordseukaryotic, translation, initiation, ribosome, ires
Biological sourceKLUYVEROMYCES LACTIS
More
Total number of polymer chains35
Total formula weight1164743.46
Authors
Fernandez, I.S.,Bai, X.,Scheres, S.H.W.,Ramakrishnan, V. (deposition date: 2014-03-21, release date: 2014-07-09, Last modification date: 2024-10-09)
Primary citationFernandez, I.S.,Bai, X.,Murshudov, G.,Scheres, S.H.W.,Ramakrishnan, V.
Initiation of Translation by Cricket Paralysis Virus Ires Requires its Translocation in the Ribosome.
Cell(Cambridge,Mass.), 157:823-, 2014
Cited by
PubMed Abstract: The cricket paralysis virus internal ribosome entry site (CrPV-IRES) is a folded structure in a viral mRNA that allows initiation of translation in the absence of any host initiation factors. By using recent advances in single-particle electron cryomicroscopy, we have solved the structure of CrPV-IRES bound to the ribosome of the yeast Kluyveromyces lactis in both the canonical and rotated states at overall resolutions of 3.7 and 3.8 Å, respectively. In both states, the pseudoknot PKI of the CrPV-IRES mimics a tRNA/mRNA interaction in the decoding center of the A site of the 40S ribosomal subunit. The structure and accompanying factor-binding data show that CrPV-IRES binding mimics a pretranslocation rather than initiation state of the ribosome. Translocation of the IRES by elongation factor 2 (eEF2) is required to bring the first codon of the mRNA into the A site and to allow the start of translation.
PubMed: 24792965
DOI: 10.1016/J.CELL.2014.04.015
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (3.7 Å)
Structure validation

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