Target intelligence / Profile preview

Guanylate-binding protein 7 (GBP7)

Target
GBP7
Molecular classification
Enzyme (GTPase), Interferon-inducible protein, Other (innate immunity regulator)
01

Overview

Guanylate-binding protein 7 (GBP7) is a member of the GBP family of interferon-inducible large GTPases involved in the innate immune response. GBP7 hydrolyzes GTP to GDP and GMP and is upregulated in response to interferon signaling, particularly during infection. It plays a critical regulatory role in host defense against intracellular pathogens—including viruses, bacteria, and protozoa—by modulating cytokine-mediated immune signaling. Notably, in the context of influenza A virus infection, GBP7 expression is increased, and it acts as a negative regulator of host antiviral cytokine responses by suppressing type I and III interferon expression as well as proinflammatory cytokines through inhibition of the NF-κB and JAK-STAT signaling pathways. GBP7 may also facilitate assembly of NADPH oxidase on phagosomal membranes, supporting a role in oxidative burst responses to pathogens. GBP7 is encoded by the GBP7 gene (Gene ID: 388646) in humans. There are currently no clinically approved drugs known to target GBP7 directly, nor is it a validated biomarker, but its role in viral pathogenesis and innate immune regulation suggests potential as a host-directed therapeutic target.

Other names
Guanylate-binding protein 7GBP7GBP4LGBP-7FLJ38822GTP-binding protein 7Guanine nucleotide-binding protein 7Guanylate-binding protein 4-like
02

Biological functions

Immune responseHost defense against pathogens (viruses, bacteria, protozoa)Regulation of cytokine signalingNegative regulator of type I and III interferon expressionSuppression of NF-κB and JAK-STAT pathways during infection
03

Disease associations

Infection (notably viral, such as influenza A virus)Osteogenesis imperfecta, type XVII (association reported, but not a classical disease gene)
04

Safety considerations

Potential for enhancing viral replication due to suppression of host interferon response during infection

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