Pregled bibliografske jedinice broj: 530327
Structural basis for the methylation of A1408 in 16S rRNA by a panaminoglycoside resistance methyltransferase NpmA from a clinical isolate and analysis of the NpmA interactions with the 30S ribosomal subunit
Structural basis for the methylation of A1408 in 16S rRNA by a panaminoglycoside resistance methyltransferase NpmA from a clinical isolate and analysis of the NpmA interactions with the 30S ribosomal subunit // Book of Abstracts
Beč, Austrija, 2011. str. 53-53 (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 530327 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Structural basis for the methylation of A1408 in 16S rRNA by a panaminoglycoside resistance methyltransferase NpmA from a clinical isolate and analysis of the NpmA interactions with the 30S ribosomal subunit
Autori
Husain, Nilofer ; Obranić (Čubrilo), Sonja ; Koscinski, Lukasz ; Seetharaman, J. ; Babić, Fedora ; Bujnicki, Janusz M. ; Maravić-Vlahoviček, Gordana ; Sivaraman, J.
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Book of Abstracts
/ - , 2011, 53-53
Skup
The 3rd EMBO Meeting - Advancing the Life Sciences
Mjesto i datum
Beč, Austrija, 10.09.2011. - 13.09.2011
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
Antibiotic resistance; Methyltransferase; NpmA; Aminoglycosides; Sisomicin; Kanamycin; Apramycin; Tobramycin; footprinting; NpmA-30S subunit model
Sažetak
Background: NpmA, a methyltransferase that confers high level-resistance to aminoglycoside antibiotics was identified in an Escherichia coli clinical isolate. It belongs to the kanamycin–apramycin methyltransferase (Kam) family and specifically methylates the 16S rRNA at the N1 position of A1408. NpmA is plasmid-encoded and can be transferred between pathogenic bacteria, therefore posing a threat to the successful use of aminoglycosides in clinical practice. Observations: We determined the structures of apo-NpmA and its complexes with cofacor S-adenosylmethionine and reaction by-product S-adenosylhomocysteine at 2.4, 2.7 and 1.68 Angstrom, respectively. We generated 12 NpmA variants with alanine substitutions of evolutionary conserved amino acids and studied their ability to bind the cofactor, to methylate A1408 in the 30S subunit, and to confer resistance to kanamycin in vivo. Residues D30, W107 and W197 were found to be essential. We have also analyzed the interactions between NpmA and the 30S subunit by footprinting experiments and computational docking. Helices 24, 42 and 44 were found to be the main NpmA-binding site. Both experimental and theoretical analyses suggest that NpmA flips out the target nucleotide A1408 to carry out the methylation. Conclusions: The results presented here will assist in the development of specific NpmA inhibitors that could restore the potential of aminoglycoside antibiotics.
Izvorni jezik
Engleski
Znanstvena područja
Biologija
POVEZANOST RADA
Projekti:
006-0982913-1219 - Molekularne osnove djelovanja antibiotika i mehanizmi bakterijske rezistencije (Maravić Vlahoviček, Gordana, MZOS ) ( CroRIS)
Ustanove:
Farmaceutsko-biokemijski fakultet, Zagreb
