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Hepatitis C virus nonstructural protein 5B RNA-dependent RNA polymerase (Thumb-1 allosteric site) (HCV NS5B Thumb-1 site)

Target
HCV NS5B Thumb-1 site
Molecular classification
Enzyme, RNA-dependent RNA polymerase, Viral nonstructural protein
01

Overview

The Thumb-1 allosteric site is a regulatory pocket located on the thumb domain of the Hepatitis C virus (HCV) nonstructural protein 5B (NS5B), which functions as the RNA-dependent RNA polymerase (RdRp) responsible for replicating the viral genome (Tomei et al., 2005, PubMed: 16135246). This site is a primary target for non-nucleoside inhibitors (NNIs), which bind to the enzyme at a location distal to the catalytic active site. Binding at the Thumb-1 site stabilizes the polymerase in an inactive conformation, preventing the essential structural transition from the initiation phase to the elongation phase of RNA synthesis (Beaulieu, 2009, PubMed: 19450130). This mechanism effectively blocks the production of new viral RNA strands, making it a key component in direct-acting antiviral (DAA) strategies for treating chronic Hepatitis C. While potent, inhibitors targeting this site often face challenges such as a low genetic barrier to resistance and high specificity for certain HCV genotypes, particularly genotype 1 (Di Marco et al., 2005, PubMed: 15939857). Consequently, these drugs are typically developed for use in combination therapy to ensure sustained virologic response and prevent the selection of resistant viral variants.

Other names
NS5B Thumb-1 pocketAllosteric site 1HCV NS5B polymerase Thumb-1 domainNon-nucleoside inhibitor site 1Thumb-I allosteric pocket
02

Mechanism of action

Non-nucleoside inhibition (NNI) through binding to the Thumb-1 allosteric pocket, which stabilizes the polymerase in an inactive conformation and prevents the transition from the initiation to the elongation phase of RNA synthesis.

03

Biological functions

Viral RNA replicationRNA-directed RNA polymerase activityDe novo RNA synthesis
04

Disease associations

Hepatitis C infectionChronic Hepatitis C
05

Safety considerations

Rapid emergence of drug resistance due to low genetic barrierGenotype-specific efficacy (primarily active against genotype 1)Potential for hepatotoxicity (observed in some clinical candidates)Drug-drug interactions via CYP450 metabolism
06

Interacting drugs

Deleobuvir (BI 207127)

4 more in the full profile.

07

Biomarkers

HCV RNA viral loadHCV genotype (specifically Genotype 1)NS5B resistance-associated substitutions (e.g., P495, P496, V499)

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