| Literature DB >> 24900542 |
Jiro Kondo1, Mai Koganei1, Tomoko Kasahara1.
Abstract
Sisomicin with an unsaturated sugar ring I displays better antibacterial activity than other structurally related aminoglycosides, such as gentamicin, tobramycin, and amikacin. In the present study, we have confirmed by X-ray analyses that the binding mode of sisomicin is basically similar but not identical to that of the related compounds having saturated ring I. A remarkable difference is found in the stacking interaction between ring I and G1491. While the typical saturated ring I with a chair conformation stacks on G1491 through CH/π interactions, the unsaturated ring I of sisomicin with a partially planar conformation can share its π-electron density with G1491 and fits well within the A-site helix.Entities:
Keywords: X-ray analysis; aminoglycoside; decoding; ribosome; stacking interaction
Year: 2012 PMID: 24900542 PMCID: PMC4025859 DOI: 10.1021/ml300145y
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345