PDBsum entry 4uke

Ribosome

PDB id: 4uke

Contents

Protein chains

213 a.a.

169 a.a.

150 a.a.

194 a.a.

137 a.a.

203 a.a.

197 a.a.

155 a.a.

185 a.a.

188 a.a.

172 a.a.

159 a.a.

98 a.a.

136 a.a.

135 a.a.

120 a.a.

126 a.a.

135 a.a.

148 a.a.

58 a.a.

100 a.a.

109 a.a.

127 a.a.

106 a.a.

112 a.a.

119 a.a.

99 a.a.

87 a.a.

77 a.a.

50 a.a.

52 a.a.

25 a.a.

105 a.a.

91 a.a.

143 a.a.

47 a.a.

Ligands

OHX ×15

Metals

_MG ×27

_ZN ×4

References listed in PDB file

Key reference

• Title: Structural basis for the inhibition of the eukaryotic ribosome.
• Authors: N.Garreau de loubresse, I.Prokhorova, W.Holtkamp, M.V.Rodnina, G.Yusupova, M.Yusupov.
• Ref.: Nature, 2014, 513, 517-522. [DOI no: 10.1038/nature13737]
• PubMed id: 25209664

Abstract

The ribosome is a molecular machine responsible for protein synthesis and a major target for small-molecule inhibitors. Compared to the wealth of structural information available on ribosome-targeting antibiotics in bacteria, our understanding of the binding mode of ribosome inhibitors in eukaryotes is currently limited. Here we used X-ray crystallography to determine 16 high-resolution structures of 80S ribosomes from Saccharomyces cerevisiae in complexes with 12 eukaryote-specific and 4 broad-spectrum inhibitors. All inhibitors were found associated with messenger RNA and transfer RNA binding sites. In combination with kinetic experiments, the structures suggest a model for the action of cycloheximide and lactimidomycin, which explains why lactimidomycin, the larger compound, specifically targets the first elongation cycle. The study defines common principles of targeting and resistance, provides insights into translation inhibitor mode of action and reveals the structural determinants responsible for species selectivity which could guide future drug development.