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6AZ1

Cryo-EM structure of the small subunit of Leishmania ribosome bound to paromomycin

Summary for 6AZ1
Entry DOI10.2210/pdb6az1/pdb
Related6AZ3
EMDB information7024 7025
DescriptorRibosomal protein s1e, ribosomal protein S8, ribosomal protein S8e, ... (41 entities in total)
Functional Keywordsleishmania donovani, ribosome, aminoglycoside, paromomycin, ribosome-antibiotic complex, ribosome/antibiotic
Biological sourceLeishmania donovani
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Total number of polymer chains38
Total formula weight1416658.06
Authors
Shalev-Benami, M.,Zhang, Y.,Rozenberg, H.,Matzov, D.,Zimmerman, E.,Bashan, A.,Jaffe, C.L.,Yonath, A.,Skiniotis, G. (deposition date: 2017-09-09, release date: 2017-12-06, Last modification date: 2025-05-28)
Primary citationShalev-Benami, M.,Zhang, Y.,Rozenberg, H.,Nobe, Y.,Taoka, M.,Matzov, D.,Zimmerman, E.,Bashan, A.,Isobe, T.,Jaffe, C.L.,Yonath, A.,Skiniotis, G.
Atomic resolution snapshot of Leishmania ribosome inhibition by the aminoglycoside paromomycin.
Nat Commun, 8:1589-1589, 2017
Cited by
PubMed Abstract: Leishmania is a single-celled eukaryotic parasite afflicting millions of humans worldwide, with current therapies limited to a poor selection of drugs that mostly target elements in the parasite's cell envelope. Here we determined the atomic resolution electron cryo-microscopy (cryo-EM) structure of the Leishmania ribosome in complex with paromomycin (PAR), a highly potent compound recently approved for treatment of the fatal visceral leishmaniasis (VL). The structure reveals the mechanism by which the drug induces its deleterious effects on the parasite. We further show that PAR interferes with several aspects of cytosolic translation, thus highlighting the cytosolic rather than the mitochondrial ribosome as the primary drug target. The results also highlight unique as well as conserved elements in the PAR-binding pocket that can serve as hotspots for the development of novel therapeutics.
PubMed: 29150609
DOI: 10.1038/s41467-017-01664-4
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (2.7 Å)
Structure validation

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