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8OVA

CRYO-EM STRUCTURE OF TRYPANOSOMA BRUCEI PROCYCLIC FORM 80S RIBOSOME : PARENTAL STRAIN

This is a non-PDB format compatible entry.
Summary for 8OVA
Entry DOI10.2210/pdb8ova/pdb
EMDB information17208 17249 17250
DescriptorLSUa rRNA, E-SITE TRNA, Ribosomal protein S10, ... (91 entities in total)
Functional Keywordscryo-em, trypanosoma brucei, 80s ribosome, ribosome
Biological sourceTrypanosoma brucei brucei
More
Total number of polymer chains86
Total formula weight3661530.75
Authors
Rajan, K.S.,Yonath, A. (deposition date: 2023-04-25, release date: 2023-11-29, Last modification date: 2025-10-01)
Primary citationRajan, K.S.,Madmoni, H.,Bashan, A.,Taoka, M.,Aryal, S.,Nobe, Y.,Doniger, T.,Galili Kostin, B.,Blumberg, A.,Cohen-Chalamish, S.,Schwartz, S.,Rivalta, A.,Zimmerman, E.,Unger, R.,Isobe, T.,Yonath, A.,Michaeli, S.
A single pseudouridine on rRNA regulates ribosome structure and function in the mammalian parasite Trypanosoma brucei.
Nat Commun, 14:7462-7462, 2023
Cited by
PubMed Abstract: Trypanosomes are protozoan parasites that cycle between insect and mammalian hosts and are the causative agent of sleeping sickness. Here, we describe the changes of pseudouridine (Ψ) modification on rRNA in the two life stages of the parasite using four different genome-wide approaches. CRISPR-Cas9 knock-outs of all four snoRNAs guiding Ψ on helix 69 (H69) of the large rRNA subunit were lethal. A single knock-out of a snoRNA guiding Ψ530 on H69 altered the composition of the 80S monosome. These changes specifically affected the translation of only a subset of proteins. This study correlates a single site Ψ modification with changes in ribosomal protein stoichiometry, supported by a high-resolution cryo-EM structure. We propose that alteration in rRNA modifications could generate ribosomes preferentially translating state-beneficial proteins.
PubMed: 37985661
DOI: 10.1038/s41467-023-43263-6
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (2.47 Å)
Structure validation

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