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8OVJ

CRYO-EM STRUCTURE OF LEISHMANIA MAJOR 80S RIBOSOME : PARENTAL STRAIN

This is a non-PDB format compatible entry.
Summary for 8OVJ
Entry DOI10.2210/pdb8ovj/pdb
EMDB information17216
DescriptorLSUa_rRNA_chain_1, Putative ribosomal protein L1a, 60S ribosomal protein L11, ... (90 entities in total)
Functional Keywordscryo-em leishmania major 80s ribosome wild type, ribosome
Biological sourceLeishmania major strain Friedlin
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Total number of polymer chains85
Total formula weight3532343.38
Authors
Rajan, K.S.,Yonath, A. (deposition date: 2023-04-26, release date: 2024-05-08, Last modification date: 2024-10-16)
Primary citationRajan, K.S.,Aryal, S.,Hiregange, D.G.,Bashan, A.,Madmoni, H.,Olami, M.,Doniger, T.,Cohen-Chalamish, S.,Pescher, P.,Taoka, M.,Nobe, Y.,Fedorenko, A.,Bose, T.,Zimermann, E.,Prina, E.,Aharon-Hefetz, N.,Pilpel, Y.,Isobe, T.,Unger, R.,Spath, G.F.,Yonath, A.,Michaeli, S.
Structural and mechanistic insights into the function of Leishmania ribosome lacking a single pseudouridine modification.
Cell Rep, 43:114203-114203, 2024
Cited by
PubMed Abstract: Leishmania is the causative agent of cutaneous and visceral diseases affecting millions of individuals worldwide. Pseudouridine (Ψ), the most abundant modification on rRNA, changes during the parasite life cycle. Alterations in the level of a specific Ψ in helix 69 (H69) affected ribosome function. To decipher the molecular mechanism of this phenotype, we determine the structure of ribosomes lacking the single Ψ and its parental strain at ∼2.4-3 Å resolution using cryo-EM. Our findings demonstrate the significance of a single Ψ on H69 to its structure and the importance for its interactions with helix 44 and specific tRNAs. Our study suggests that rRNA modification affects translation of mRNAs carrying codon bias due to selective accommodation of tRNAs by the ribosome. Based on the high-resolution structures, we propose a mechanism explaining how the ribosome selects specific tRNAs.
PubMed: 38722744
DOI: 10.1016/j.celrep.2024.114203
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (2.4 Å)
Structure validation

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건을2024-11-06부터공개중

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