Target intelligence / Profile preview

Peroxidasin (PXDN)

Target
PXDN
Molecular classification
Enzyme, Heme peroxidase, Extracellular matrix protein, Other (multidomain oxidase with structural, catalytic and binding features)
01

Overview

Peroxidasin (PXDN) is a multidomain, heme-containing peroxidase enzyme that catalyzes the cross-linking of collagen IV molecules in basement membranes, crucial for providing mechanical stability to tissues during development, homeostasis, and repair. PXDN processes hydrogen peroxide and halides to generate hypohalous acids, particularly hypobromous acid, which drives the formation of unique sulfilimine bonds between collagen IV monomers and stabilizes extracellular matrix structure. PXDN is highly glycosylated and secreted primarily as a homotrimer. In addition to its structural role, PXDN participates in host defense through oxidative protein cross-linking, and its dysregulation has been implicated in cancer progression, fibrosis, vascular remodeling, and inherited basement membrane disorders such as congenital eye defects. Select inhibitors such as ABAH block its peroxidase activity in vitro, but no approved drugs selectively target PXDN in clinical medicine as of 2025.

Other names
Peroxidasin homologPXDN active fragmentKIAA0230MG50PRG2PXD01VPOVPO1hsPxd01D2S448D2S448EPXNMelanoma-associated antigen MG50Peroxidasin 1Vascular peroxidase 1p53-responsive gene 2 proteinASGD7COPOA
02

Mechanism of action

Inhibition of peroxidase activity (e.g., via compounds like ABAH). Hypothetical: Blockade of collagen IV cross-linking by targeting peroxidase or Ig domains (theoretical, not established clinically).

03

Biological functions

Cross-linking of collagen IV in basement membranesGeneration of hypohalous acids (immune defense)Extracellular matrix organization and stabilizationOxidative protein cross-linking (di-tyrosine, sulfilimine)Regulation of tissue development, homeostasis, wound healingSignal transduction in matrix remodeling
04

Disease associations

Cancer (notably solid cancer progression and metastasis)Fibrosis (kidney, heart, general fibrogenesis)Vascular disease (atherosclerosis, vascular remodeling)Congenital eye disorders (PXDN mutation)Other (potential roles in inflammation and immune defense)
05

Safety considerations

Loss of PXDN activity can lead to basement membrane fragility and developmental defects (particularly in the eye)Aberrant or excessive PXDN activity may contribute to fibrosis and tissue stiffening in disease statesPotential for unintended tissue remodeling or immune dysfunction if therapeutically targeted
06

Interacting drugs

4-Aminobenzoic acid hydrazide (ABAH) (PXDN inhibitor)

1 more in the full profile.

07

Biomarkers

PXDN protein expression (tissue biomarker for fibrotic disease, cancer progression)Collagen IV sulfilimine cross-link status (matrix stability marker)Di-tyrosine content as oxidative stress marker

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