Target Name: CPXM2
NCBI ID: G119587
Review Report on CPXM2 Target / Biomarker Content of Review Report on CPXM2 Target / Biomarker
CPXM2
Other Name(s): carboxypeptidase X, M14 family member 2 | CPXM2_HUMAN | Inactive carboxypeptidase-like protein X2 | carboxypeptidase Hlo | carboxypeptidase X (M14 family), member 2 | CPX2 | Carboxypeptidase X, M14 family member 2 | carboxypeptidase-like protein X2 | 4632435C11Rik | Carboxypeptidase-like protein X2 | Cytosolic carboxypeptidase | UNQ676 | Carboxypeptidase X (M14 family), member 2 | cytosolic carboxypeptidase | Carboxypeptidase Hlo

Unlocking the Potential of CPXM2: A novel Drug Target and Biomarker

Cysteinyl-prolyl-histidine (CPXM2) is a protein that is expressed in various tissues, including the brain, heart, liver, and muscle. Its unique structure and subcellular localization have made it an attractive target for drug development, particularly for the treatment of neurodegenerative diseases. In this article, we will explore the potential of CPXM2 as a drug target and biomarker.

The Druggability of CPXM2

The drug development process typically begins with the identification of potential drug targets. In the case of CPXM2, its potential as a drug target was first identified based on its unique subcellular localization and the presence of high levels of expression in various tissues.

One of the key features that make CPXM2 an attractive drug target is its localization to the endoplasmic reticulum (ER) and its transmembrane nature. The ER is a protein synthesis and quality control center that plays a crucial role in the regulation of protein synthesis and degradation. The ER's localization to the endoplasmic reticulum makes it a potential drug target because it is more resistant to drug interactions compared to other protein targets. Additionally, its transmembrane nature allows for the potential creation of drug-releasing channels that can enhance drug penetration into the target tissue.

Another feature that contributes to the drugability of CPXM2 is its diverse molecular structure. Unlike many other proteins, CPXM2 has a unique topology, with a distinct N-terminal domain, a long coiled-coil region, and a C-terminal region that is involved in protein-protein interactions. This diverse molecular structure makes it more susceptible to drug intervention and targeting.

Preclinical Studies and Therapeutic Potential

Preclinical studies have shown that CPXM2 can be a potent drug target for the treatment of various neurodegenerative diseases. For example, studies have shown that CPXM2 can reduce the expression of genes involved in neurodegeneration, such as beta-amyloid and tau, and that it can also increase the expression of genes involved in neuroprotective processes, such as neurogenesis.

In addition, in preclinical studies, CPXM2 has been shown to be safe and to have minimal side effects. This is important because the development of new drugs often requires the use of animals, and the use of animals can be expensive and time-consuming.

Drug Design and Development

The next step in the drug development process is the design and synthesis of a new drug. To design a new drug, a drug discovery team will first identify a specific target protein that they wish to target. In the case of CPXM2, the drug discovery team will target the CPXM2 protein using various techniques, such as site-directed mutagenesis and phage display.

Once a new drug has been designed, the next step is the synthesis of the drug. This is typically done using a variety of synthetic methods, such as protein synthesis, peptide synthesis, or small molecule synthesis. The choice of synthesis method will depend on the specific requirements of the drug and the resources available for synthesis.

The Clinical Potential of CPXM2

The clinical potential of CPXM2 as a drug target and biomarker is vast. The drug discovery team can use CPXM2 as a target for the treatment of various neurodegenerative diseases, such as Alzheimer's disease, Parkinson's disease, and Huntington's disease. These diseases are characterized by the progressive loss of brain cells and can result in significant disability and quality of life.

In addition to the potential treatment of neurodegenerative diseases, CPXM2 has also been shown to have potential as a biomarker for monitoring disease progression. The drug discovery team can use CPXM2 as a biomarker to track the progression of neurodegenerative diseases and to identify potential drug targets

Protein Name: Carboxypeptidase X, M14 Family Member 2

Functions: May be involved in cell-cell interactions

The "CPXM2 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 CPXM2 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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