Target intelligence / Profile preview

Azurocidin 1 (AZU1)

Target
AZU1
Molecular classification
Antimicrobial protein, Chemotactic glycoprotein, Pseudoenzyme (member of serine protease gene family, but lacking serine proteinase activity), Other (azurophil granule protein)
01

Overview

Azurocidin 1 (AZU1) is a neutrophil granule-derived glycoprotein serving both as an antimicrobial molecule and as a chemotactic agent for monocytes and fibroblasts[1][2][3][4][8]. Although it belongs to the serine protease gene family, it is classified as a *pseudoenzyme* because it lacks protease activity, due to substitutions in key catalytic residues[1][2]. AZU1 has potent antibacterial properties, especially against Gram-negative bacteria, attributed to its strong affinity for negatively charged bacterial lipopolysaccharides[2][5][8]. In addition, it is a multifunctional inflammatory mediator that recruits monocytes to sites of infection and inflammation, and binds heparin. Its clinical significance is highlighted by its role as a plasma biomarker for sepsis risk, and emerging data implicate it in tumor cell biology[1][7]. The protein is encoded by the AZU1 gene, located on chromosome 19 in a cluster with other neutrophil granule proteins[1][2].

Other names
Cationic antimicrobial protein CAP37Heparin-binding protein (HBP)CAP37AZAMPNAZCHUMAZURhHBPAzurocidinNeutrophil azurocidinCationic antimicrobial protein 37
02

Mechanism of action

Not applicable (no direct drug interaction information available, but biological function includes antibacterial activity mediated by strong heparin/lipopolysaccharide binding)

03

Biological functions

Antimicrobial activity (especially against Gram-negative bacteria)Monocyte chemotactic activityFibroblast chemotactic activityMediating inflammationHeparin bindingRecruitment of monocytes during inflammationFacilitator of intravasation of renal cell carcinoma cells via N-linked glycosylation
04

Disease associations

Infection (antimicrobial immune response)Inflammation (multifunctional inflammatory mediator)Sepsis (high plasma HBP/AZU1 linked to risk of sepsis with circulatory collapse)ErysipelasCamptodactyly-Arthropathy-Coxa Vara-Pericarditis SyndromeCancer (promotes intravasation of renal cell carcinoma cells)
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Safety considerations

Elevated plasma levels associated with increased risk of sepsis and circulatory collapse in clinical contextNo major therapeutic safety concerns directly identified in current search results
06

Interacting drugs

None identified in current search results
07

Biomarkers

Heparin-binding protein (HBP/AZU1) as a biomarker for high risk of sepsis with circulatory collapse in febrile patientsPossible use in monitoring inflammation or infection status

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