Target intelligence / Profile preview

Human immunodeficiency virus group-specific antigen (HIV Gag)

Target
HIV Gag
Molecular classification
Structural polyprotein, Viral core structural protein, Polyprotein precursor
01

Overview

The **human immunodeficiency virus group-specific antigen (HIV Gag)** is a polyprotein precursor that forms the major structural component of the HIV-1 virion core[1][2][7]. Gag comprises multiple domains including matrix (MA, p17), capsid (CA, p24), nucleocapsid (NC, p7), spacer peptides (SP1 and SP2), and p6, each crucial for different steps in the viral life cycle[4][6][7]. During virus assembly, Gag is targeted to the plasma membrane, where it multimerizes, encapsidates the viral RNA, and directs budding of new viral particles. After budding, the viral protease cleaves Gag at specific sites, rearranging the virion structure to form a mature, infectious virus[2][6]. Inhibiting Gag cleavage disrupts maturation and renders virus particles non-infectious. Gag, particularly the p24 capsid fragment, serves as an important clinical biomarker for HIV infection, and the Gag polyprotein is a validated target for antiretroviral drug development, notably for maturation inhibitors[3][7][9].

Other names
Gaggroup-specific antigenHIV-1 GagHIV Gag polyproteinPr55Gag
02

Mechanism of action

Maturation inhibitors: block cleavage of Gag at specific sites, preventing virion maturation and infectivity[3] - Some compounds target the CA|SP1 cleavage site in Gag[3]

03

Biological functions

Viral particle assemblyViral maturationMembrane targetingRNA encapsidationProtein multimerization
04

Disease associations

Infection (HIV/AIDS)
05

Safety considerations

High variability and emergence of drug resistance mutations, particularly at Gag cleavage and maturation inhibitor binding sites[3]Natural polymorphisms in Gag (e.g., V370A in SP1) confer resistance to certain inhibitors[3]
06

Interacting drugs

Bevirimat

2 more in the full profile.

07

Biomarkers

Gag p24 antigen (used as biomarker for HIV infection and disease progression)

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