Target Name: PDF
NCBI ID: G64146
Review Report on PDF Target / Biomarker Content of Review Report on PDF Target / Biomarker
PDF
Other Name(s): peptide deformylase, mitochondrial | polypeptide deformylase | peptide deformylase-like protein | Peptide deformylase, mitochondrial | Peptide deformylase-like protein | Polypeptide deformylase | DEFM_HUMAN

PDF: A Protein Linked To Parkinsons and Myopathies

PDF (Peptide Deformylase) is a protein that is expressed in high levels in the mitochondria, and is involved in the breaking down of peptides, which are the building blocks of proteins. Mutations in the PDF gene have been linked to a variety of diseases, including Parkinsons disease and myopathies. As a result, PDF has become a promising drug target and a biomarker for a variety of diseases.

PDF is a 26kDa protein that is expressed in the mitochondria and is involved in the breakdown of peptides. It is a key enzyme in the mitochondrial proteasome system, which is responsible for breaking down and removing damaged or unnecessary proteins. In addition to its role in protein degradation, PDF is also involved in the regulation of mitochondrial fission and fusion.

Mutations in the PDF gene have been linked to a variety of diseases, including Parkinsons disease, a neurodegenerative disorder that is characterized by symptoms such as tremors, rigidity, and difficulty with movement. In Parkinsons disease, the level of PDF is often reduced, and this reduction is thought to contribute to the progression of the disease.

PDF has also been linked to a variety of other diseases, including myopathies, which are conditions that affect muscles and other soft tissue. Myopathies can be caused by a variety of factors, including genetic mutations, infections, and exposure to toxins. The levels of PDF in myopathies are often increased, and this increase is thought to contribute to the severity of the disease.

In addition to its role in disease, PDF is also a potential drug target. The PDF gene has been shown to be involved in a variety of cellular processes, including cell signaling, DNA replication, and protein synthesis. As a result, compounds that can inhibit the activity of PDF may be effective in treating a variety of diseases, including those related to protein synthesis and degradation.

One approach to targeting PDF as a drug target is to use small molecules that can inhibit the activity of the PDF enzyme. These small molecules can be found in a variety of natural compounds, including herbs, berries, and other plants. For example, a compound called curcumin, which is an active compound in turmeric, has been shown to inhibit the activity of PDF and may be a potential drug for the treatment of various diseases.

Another approach to targeting PDF as a drug target is to use antibodies that can bind to the PDF protein and prevent it from interacting with its target. These antibodies can be used to treat a variety of diseases, including those related to protein synthesis and degradation. For example, an antibody called peptide-conjugated scFv has been shown to be able to bind to PDF and prevent it from interacting with its target, making it a potential candidate for the treatment of various diseases.

In addition to its potential as a drug target, PDF is also a potential biomarker for a variety of diseases. The levels of PDF in certain diseases, such as myopathies, are often increased, which can be used as a biomarker for the disease. Additionally , the levels of PDF in certain diseases, such as Parkinsons disease, are often reduced, which can also be used as a biomarker for the disease.

Overall, PDF is a protein that is expressed in the mitochondria and is involved in the breakdown of peptides. Mutations in the PDF gene have been linked to a variety of diseases, including Parkinsons disease and myopathies. As a result, PDF has become a promising drug target and a biomarker for a variety of diseases. Further research is needed to fully understand the role of PDF in disease and to develop effective treatments.

Protein Name: Peptide Deformylase, Mitochondrial

Functions: Removes the formyl group from the N-terminal Met of newly synthesized proteins

The "PDF Target / Biomarker Review Report" is a customizable review of hundreds up to thousends of related scientific research literature by AI technology, covering specific information about PDF comprehensively, including but not limited to:
•   general information;
•   protein structure and compound binding;
•   protein biological mechanisms;
•   its importance;
•   the target screening and validation;
•   expression level;
•   disease relevance;
•   drug resistance;
•   related combination drugs;
•   pharmacochemistry experiments;
•   related patent analysis;
•   advantages and risks of development, etc.
The report is helpful for project application, drug molecule design, research progress updates, publication of research papers, patent applications, etc. If you are interested to get a full version of this report, please feel free to contact us at BD@silexon.ai

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