PDB ID: 3S4P
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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 | PoSSuM |
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Download interaction data: 3S4P
Structure summary
Code : | 3S4P PDBj RCSB PDB PDBe | ||||||||||||
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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 | ||||||||||||
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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.
PubMed: 21905229 |