Target intelligence / Profile preview

MPN domain-containing protein (MPND)

Target
MPND
Molecular classification
Other (MPN domain-containing protein; within the JAMM metalloisopeptidase superfamily, but not established as a canonical receptor, ion channel, enzyme, transporter, or transcription factor), Predicted metallopeptidase/protease, Protein associated with ubiquitin signaling and m6A DNA recognition
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Overview

MPN domain-containing protein (MPND) is a human protein encoded on chromosome 19, distinguished by possessing an MPN domain often linked to protein complexes that function in isopeptidase and metalloisopeptidase activities, particularly those associated with ubiquitin and protein turnover. MPND acts as a sensor of N6-methyladenosine (m6A) DNA methylation, binding selectively to m6A-modified double-stranded DNA and leading to DNA degradation. It is predicted to have protease/metallopeptidase activity and bind polyubiquitin, and may participate in DNA damage repair steps via association with the BRCA1-A and BRISC complexes. Genetic association studies implicate it in cerebellar ataxia and Machado-Joseph Disease. However, MPND is not currently classified as a direct therapeutic target; there are no drugs or clinical agents known to act on it, nor are there established biomarkers or safety concerns for therapeutic use. If a more specific molecular subclass or canonical role emerges from further research, current classification may be updated from "Other" to, for example, "Enzyme/metallopeptidase," but at present, "Other" is appropriate given the evidence.

Other names
MPNDFLJ14981ENSG00000008382MPN domain-containing protein
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Mechanism of action

Not applicable (no drugs known to act on this protein)

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Biological functions

Sensor of N6-methyladenosine (m6A) DNA methylationRecognizes and binds m6A-modified DNA, leading to its degradationPredicted metalloisopeptidase activity (ubiquitin-related hydrolysis)Predicted role in double-strand DNA break repair (co-complexes: BRCA1-A and BRISC)Polyubiquitin modification-dependent protein bindingPost-translational regulation
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Disease associations

Associated (genetically) with Machado-Joseph DiseaseAssociated with Autosomal Dominant Cerebellar AtaxiaNo direct evidence for a role in cancer, inflammation, neurodegeneration, or infection as a therapeutic target at present
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Safety considerations

None reported in the literature or databases presently
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Interacting drugs

None known (No currently identified drugs targeting MPN domain-containing protein)
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Biomarkers

None established for patient selection or efficacy monitoring

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