6lkq

The Structural Basis for Inhibition of Ribosomal Translocation by Viomycin

spinqualitylabelsall models 6lkq, resolution 3.10Å Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image   Print3D Structural highlights 6lkq is a 10 chain structure with sequence from Escherichia coli. Full crystallographic information is available from OCA. For a guided tour on the structure components use FirstGlance. Method: X-ray diffraction, Resolution 3.1Å Ligands: 5OH, DPP, KBE, UAL Resources: FirstGlance, OCA, PDBe, RCSB, PDBsum, ProSAT Function C3TPN2_ECOLX Publication Abstract from PubMed Viomycin, an antibiotic that has been used to fight tuberculosis infections, is believed to block the translocation step of protein synthesis by inhibiting ribosomal subunit dissociation and trapping the ribosome in an intermediate state of intersubunit rotation. The mechanism by which viomycin stabilizes this state remains unexplained. To address this, we have determined cryo-EM and X-ray crystal structures of Escherichia coli 70S ribosome complexes trapped in a rotated state by viomycin. The 3.8-A resolution cryo-EM structure reveals a ribosome trapped in the hybrid state with 8.6 degrees intersubunit rotation and 5.3 degrees rotation of the 30S subunit head domain, bearing a single P/E state transfer RNA (tRNA). We identify five different binding sites for viomycin, four of which have not been previously described. To resolve the details of their binding interactions, we solved the 3.1-A crystal structure of a viomycin-bound ribosome complex, revealing that all five viomycins bind to ribosomal RNA. One of these (Vio1) corresponds to the single viomycin that was previously identified in a complex with a nonrotated classical-state ribosome. Three of the newly observed binding sites (Vio3, Vio4, and Vio5) are clustered at intersubunit bridges, consistent with the ability of viomycin to inhibit subunit dissociation. We propose that one or more of these same three viomycins induce intersubunit rotation by selectively binding the rotated state of the ribosome at dynamic elements of 16S and 23S rRNA, thus, blocking conformational changes associated with molecular movements that are required for translocation. The structural basis for inhibition of ribosomal translocation by viomycin.,Zhang L, Wang YH, Zhang X, Lancaster L, Zhou J, Noller HF Proc Natl Acad Sci U S A. 2020 Apr 27. pii: 2002888117. doi:, 10.1073/pnas.2002888117. PMID:32341159 From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

Proteopedia Page Contributors and Editors (what is this?)

OCA