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7OI7

Cryo-EM structure of late human 39S mitoribosome assembly intermediates, state 2

Summary for 7OI7
Entry DOI10.2210/pdb7oi7/pdb
EMDB information12920
Descriptor39S ribosomal protein L2, mitochondrial, 39S ribosomal protein L16, mitochondrial, 39S ribosomal protein L17, mitochondrial, ... (57 entities in total)
Functional Keywords39s mitoribosome, ribosome biogenesis, ribosome
Biological sourceHomo sapiens (Human)
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Total number of polymer chains54
Total formula weight1782059.94
Authors
Cheng, J.,Berninghausen, O.,Beckmann, R. (deposition date: 2021-05-11, release date: 2021-09-15, Last modification date: 2024-07-10)
Primary citationCheng, J.,Berninghausen, O.,Beckmann, R.
A distinct assembly pathway of the human 39S late pre-mitoribosome.
Nat Commun, 12:4544-4544, 2021
Cited by
PubMed Abstract: Assembly of the mitoribosome is largely enigmatic and involves numerous assembly factors. Little is known about their function and the architectural transitions of the pre-ribosomal intermediates. Here, we solve cryo-EM structures of the human 39S large subunit pre-ribosomes, representing five distinct late states. Besides the MALSU1 complex used as bait for affinity purification, we identify several assembly factors, including the DDX28 helicase, MRM3, GTPBP10 and the NSUN4-mTERF4 complex, all of which keep the 16S rRNA in immature conformations. The late transitions mainly involve rRNA domains IV and V, which form the central protuberance, the intersubunit side and the peptidyltransferase center of the 39S subunit. Unexpectedly, we find deacylated tRNA in the ribosomal E-site, suggesting a role in 39S assembly. Taken together, our study provides an architectural inventory of the distinct late assembly phase of the human 39S mitoribosome.
PubMed: 34315873
DOI: 10.1038/s41467-021-24818-x
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (3.5 Å)
Structure validation

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