Literature DB >> 27373148

2.8-Å Cryo-EM Structure of the Large Ribosomal Subunit from the Eukaryotic Parasite Leishmania.

Moran Shalev-Benami1, Yan Zhang2, Donna Matzov1, Yehuda Halfon1, Arie Zackay3, Haim Rozenberg1, Ella Zimmerman1, Anat Bashan1, Charles L Jaffe3, Ada Yonath4, Georgios Skiniotis5.   

Abstract

Leishmania is a single-cell eukaryotic parasite of the Trypanosomatidae family, whose members cause an array of tropical diseases. The often fatal outcome of infections, lack of effective vaccines, limited selection of therapeutic drugs, and emerging resistant strains, underline the need to develop strategies to combat these pathogens. The Trypanosomatid ribosome has recently been highlighted as a promising therapeutic target due to structural features that are distinct from other eukaryotes. Here, we present the 2.8-Å resolution structure of the Leishmania donovani large ribosomal subunit (LSU) derived from a cryo-EM map, further enabling the structural observation of eukaryotic rRNA modifications that play a significant role in ribosome assembly and function. The structure illustrates the unique fragmented nature of leishmanial LSU rRNA and highlights the irregular distribution of rRNA modifications in Leishmania, a characteristic with implications for anti-parasitic drug development.
Copyright © 2016. Published by Elsevier Inc.

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Year:  2016        PMID: 27373148      PMCID: PMC5835689          DOI: 10.1016/j.celrep.2016.06.014

Source DB:  PubMed          Journal:  Cell Rep            Impact factor:   9.423


  26 in total

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5.  Features and development of Coot.

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  33 in total

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Journal:  Proc Natl Acad Sci U S A       Date:  2016-10-10       Impact factor: 11.205

3.  On the interpretation of electron microscopic maps of biological macromolecules.

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7.  Ribosome Assembly in Trypanosomatids: A Novel Therapeutic Target.

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8.  Revising the Structural Diversity of Ribosomal Proteins Across the Three Domains of Life.

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10.  High-Resolution Cryo-EM Maps and Models: A Crystallographer's Perspective.

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