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Ligands
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JS6 (1r,2r,3s,4r,6s)-4,6-diamino-2-{[3-O-(2,6-diamino-2,6-dideoxy-beta-L-idopyranosyl)-2-O-{2-[(2-phenylethyl)amino]ethyl}-beta-D-ribofuranosyl]oxy}-3-hydroxycyclohexyl 2-amino-2-deoxy-alpha-D-glucopyranoside
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Glycosylation
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Code : 3S4P   PDBj   RCSB PDB   PDBe
Header : RNA/ANTIBIOTIC
Title : Crystal structure of the bacterial ribosomal decoding site complexed with an amphiphilic paromomycin O2''-ether analogue
Release Data : 2011-09-21
Compound :
mol_id molecule chains
1 RNA (5'-R(P*GP*CP*GP*UP*CP*AP*CP*AP*CP*CP*GP*GP*UP*GP*AP*AP*GP*UP*CP*GP*C)-3') A,B
Source :
mol_id organism_scientific
1
synthetic: yes
other_details: Chemically synthesized
Authors : Szychowski, J., Kondo, J., Zahr, O., Auclair, K., Westhof, E., Hanessian, S., Keillor, J.W.
Keywords : aminoglycoside, antibiotics, ribosome, decoding site, RNA, RNA-ANTIBIOTIC complex
Exp. method : X-RAY DIFFRACTION ( 2.5600 Å )
Citation :

Inhibition of aminoglycoside-deactivating enzymes APH(3')-IIIa and AAC(6')-Ii by amphiphilic paromomycin O2''-ether analogues

Szychowski, J.,Kondo, J.,Zahr, O.  et al.
(2011)  Chemmedchem  6 : 1961 - 1966

PubMed: 21905229
DOI: 10.1002/cmdc.201100346