Target intelligence / Profile preview

Influenza A virus neuraminidase 3 (NA3)

Target
NA3
Molecular classification
Enzyme, Viral protein, Hydrolase (EC 3.2.1.18)
01

Overview

Influenza A virus neuraminidase 3 is a viral surface enzyme belonging to the neuraminidase (NA) family, which are key glycoproteins of the influenza A virus envelope[1][2][5]. NA3 is one of nine major subtypes of neuraminidase (N1–N9) that are divided phylogenetically into two groups, with N3 in group 2[2]. The protein forms a homotetramer that displays exosialidase activity—removing terminal sialic acids from host cell receptors and newly formed viral glycoproteins[1][2][6]. This action is crucial for the release of progeny virions from the infected cell and for successful viral spread[1][5][6]. Neuraminidases are major therapeutic targets for antiviral drugs (notably oseltamivir, zanamivir, peramivir), which act by blocking the active site and thus interfering with virus dissemination[1][3][5]. Drug resistance mutations in the neuraminidase gene are a significant safety and therapeutic challenge[1][5]. NA3, like other neuraminidase subtypes, can also elicit protective antibody responses, making it a relevant immunological target[2][5].

Other names
Influenza neuraminidase N3N3 neuraminidaseNA subtype 3
02

Mechanism of action

Competitive inhibition of neuraminidase active site, preventing sialic acid cleavage and viral release

03

Biological functions

Cleavage of sialic acid from host cell glycoproteins and glycolipidsFacilitation of viral particle release and spreadVirion egress
04

Disease associations

Infection
05

Safety considerations

Development of drug resistance
06

Interacting drugs

Oseltamivir

2 more in the full profile.

07

Biomarkers

Antibody titers to neuraminidase (NA) for immune response assessmentNA gene mutations for drug resistance profiling

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