Target intelligence / Profile preview

Influenza virus RNA polymerase subunit PA (PA) (PA)

Target
PA
Molecular classification
Enzyme, Endonuclease, RNA-dependent RNA polymerase complex subunit
01

Overview

The Influenza virus RNA polymerase subunit PA is an essential component of the viral replication machinery, forming a heterotrimeric complex with the PB1 and PB2 subunits (UniProt P03433). Its primary role involves the "cap-snatching" mechanism, where its N-terminal domain acts as a manganese-dependent endonuclease to cleave the 5' cap from host pre-mRNAs (PubMed PMC6466057). These capped fragments then serve as primers for the synthesis of viral mRNAs by the PB1 subunit. Because this process is unique to the virus and critical for its life cycle, the PA subunit is a high-value therapeutic target. Baloxavir marboxil, a small-molecule inhibitor, specifically targets the PA endonuclease site to prevent viral transcription and replication (FDA Xofluza Label). Clinical use of such inhibitors requires monitoring for resistance-associated substitutions, particularly at position I38 of the PA protein, which can significantly reduce drug susceptibility (PubMed PMC7107411).

Other names
Polymerase acidic proteinPA proteinRNA-directed RNA polymerase subunit PAP3 protein
02

Mechanism of action

Cap-dependent endonuclease inhibitor

03

Biological functions

Viral transcriptionViral replicationCap-snatchingEndonuclease activityProteolysis
04

Disease associations

InfectionInfluenza
05

Safety considerations

Emergence of drug resistance (e.g., I38T mutation)Limited clinical benefit if administered more than 48 hours after symptom onset
06

Interacting drugs

Baloxavir marboxil

1 more in the full profile.

07

Biomarkers

PA I38T mutationPA I38M mutationPA I38F mutationViral RNA load

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