NLM DIR Seminar Schedule
UPCOMING SEMINARS
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July 15, 2025 Noam Rotenberg
Cell phenotypes in the biomedical literature: a systematic analysis and the NLM CellLink text mining corpus
RECENT SEMINARS
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July 3, 2025 Matthew Diller
Using Ontologies to Make Knowledge Computable -
July 1, 2025 Yoshitaka Inoue
Graph-Aware Interpretable Drug Response Prediction and LLM-Driven Multi-Agent Drug-Target Interaction Prediction -
June 10, 2025 Aleksandra Foerster
Interactions at pre-bonding distances and bond formation for open p-shell atoms: a step toward biomolecular interaction modeling using electrostatics -
June 3, 2025 MG Hirsch
Interactions among subclones and immunity controls melanoma progression -
May 29, 2025 Harutyun Sahakyan
In silico evolution of globular protein folds from random sequences
Scheduled Seminars on Nov. 16, 2021
Contact NLMDIRSeminarScheduling@mail.nih.gov with questions about this seminar.
Abstract:
Ribosomal RNA methylation is one of the main mechanisms of bacterial resistance to ribosome-targeting antibiotics. Methylation-dependent resistance has been described in drug-producing strains where resistance methyltransferases (MTs) are often encoded in the corresponding antibiotic biosynthetic gene clusters. It also has been found in pathogenic bacteria where this acquired resistance represents a significant medical problem. Several rRNA-specific MTs involved in antibiotic resistance have been identified and characterized. In this talk, I will present genomic and phylogenetic analyses of eight MT families involved in resistance to various classes of ribosome-targeting antibiotics. These include MTs conferring resistance to aminoglycosides, orthosomycins, RiPP thiopeptides, and macrolides. Within each family, subfamilies with antibiotic-resistance MTs were identified and their gene neighborhoods analyzed. I will discuss findings pointing to a great variability of genomic context for these MTs, as well as potential functional redundancy, overlapping of functions and possible dual housekeeping and antibiotic resistance function MTs.