| Gene Symbol | PM20D1 |
| Full Name | Peptidase M20 Domain Containing 1 |
| Protein Family | M20 peptidase family |
| Function | is a mitochondrial peptidase that has emerged as a significant player in Parkinson's disease (PD) pathogenesis. |
| Subcellular Localization | Mitochondria, Cytoplasm |
| Molecular Weight | 58 kDa |
| Amino Acids | 400 aa |
| UniProt ID | Q9NWU1 |
| GeneCards | PM20D1 |
| Human Protein Atlas | PM20D1 |
| Mitochondrial Targeting Sequence | An N-terminal targeting sequence directs PM20D1 to mitochondria. This sequence is cleaved upon mitochondrial import, yielding the mature protein. |
| Dimerization Interface | PM20D1 likely functions as a homodimer, with dimerization mediated by residues in the C-terminal region. Dimer formation may be required for enzymatic activity. |
| Protein Interaction Domains | Regions outside the catalytic domain likely mediate interactions with other proteins, including components of the mitochondrial protein quality control machinery. |
| Peptidase Activity | As a member of the M20 peptidase family, PM20D1 may hydrolyze peptide bonds. Substrates could include mitochondrial peptides generated during protein turnover or imported from the cytosol. |
| Amino Acid Metabolism | PM20D1 may participate in amino acid catabolism or synthesis, particularly in mitochondria where it could process intermediates of the urea cycle or related pathways. |
| Associated Diseases | neurodegeneration |
| Databases | GeneCardsNCBI GeneHPASTRING |
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