Drug pipeline
Full profile accessExplore the programs pursuing this target and their development progress.
- Drug candidates
- Developers
- Development stage
Target intelligence / Profile preview
The Helicobacter pylori ribosome is the essential macromolecular machinery responsible for translating genetic information into functional proteins within the bacterium (UniProt). It is composed of two major subunits: the small 30S subunit, which contains 16S ribosomal RNA (rRNA), and the large 50S subunit, which contains 5S and 23S rRNA (PubMed, PMID: 28254955). As a primary therapeutic target, the ribosome is the site of action for several key antibiotics used in H. pylori eradication regimens, such as macrolides and tetracyclines (StatPearls, NBK544286). These drugs disrupt bacterial growth by binding to specific regions of the rRNA, such as the peptidyl transferase center, to inhibit protein synthesis (Nature, doi:10.1038/s41586-020-2110-2). H. pylori infections are a leading cause of chronic gastritis and peptic ulcers, and they are strongly associated with the development of gastric adenocarcinoma and MALT lymphoma (WHO). However, the clinical efficacy of ribosome-targeting drugs is increasingly compromised by the emergence of antibiotic resistance, primarily driven by point mutations in the ribosomal RNA genes (PubMed, PMID: 31434354). Understanding the structural nuances of the H. pylori ribosome is essential for developing next-generation antimicrobial agents that can overcome existing resistance mechanisms.
Inhibition of bacterial protein synthesis by binding to the 30S or 50S ribosomal subunits, which prevents translation initiation, aminoacyl-tRNA binding, or peptidyl transfer (StatPearls, NBK544286).
5 more in the full profile.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Explore the programs pursuing this target and their development progress.
Follow the clinical studies evaluating therapies directed at this target.
Compare approaches across drug candidates, modalities, and indications.
Investigate the research and source evidence behind target biology and development.
Explore patent activity around therapies and technologies addressing this target.
Connect target biology, drug development, and emerging evidence in your research.
See how Gosset can support your research on Helicobacter pylori 70S ribosome (H. pylori ribosome).