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8I45

Interaction between a fluoroquinolone derivative KG022 and RNAs: effect of base pairs 3' adjacent to the bulge out residues

Summary for 8I45
Entry DOI10.2210/pdb8i45/pdb
Related8I43 8I44
DescriptorRNA-G-3GC-uucg, 1-cyclopropyl-N-[3-(dimethylamino)propyl]-7-(4-ethylpiperazin-1-yl)-6-fluoranyl-4-oxidanylidene-quinoline-3-carboxamide (2 entities in total)
Functional Keywordsfluoroquinolone, rna, interaction, specificity
Biological sourceMus musculus
Total number of polymer chains1
Total formula weight6529.20
Authors
Ichijo, R.,Kamimura, T.,Kawai, G. (deposition date: 2023-01-18, release date: 2023-03-29, Last modification date: 2024-05-15)
Primary citationIchijo, R.,Kamimura, T.,Kawai, G.
Interaction between a fluoroquinolone derivative KG022 and RNAs: Effect of base pairs 3' adjacent to the bulged residues.
Front Mol Biosci, 10:1145528-1145528, 2023
Cited by
PubMed Abstract: RNA-targeted small molecules are a promising modality in drug discovery. Recently, we found that a fluoroquinolone derivative, KG022, can bind to RNAs with bulged C or G. To clarify the RNA specificity of KG022, we analyzed the effect of the base pair located at the 3'side of the bulged residue. It was found that KG022 prefers G-C and A-U base pairs at the 3'side. Solution structures of the complexes of KG022 with the four RNA molecules with bulged C or G and G-C or A-U base pairs at the 3'side of the bulged residue were determined to find that the fluoroquinolone moiety is located between two purine bases, and this may be the mechanism of the specificity. This work provides an important example of the specificity of RNA-targeted small molecules.
PubMed: 36999159
DOI: 10.3389/fmolb.2023.1145528
PDB entries with the same primary citation
Experimental method
SOLUTION NMR
Structure validation

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数据于2024-10-30公开中

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