Target Name: MYO18B
NCBI ID: G84700
Review Report on MYO18B Target / Biomarker Content of Review Report on MYO18B Target / Biomarker
MYO18B
Other Name(s): Unconventional myosin-XVIIIb (isoform 2) | OTTHUMP00000198632 | MY18B_HUMAN | KFS4 | DKFZp779C1668 | OTTHUMP00000239236 | Myosin XVIIIB, transcript variant 2 | myosin XVIIIB | Myosin 18B | Myosin XVIIIB | Unconventional myosin-XVIIIb | MYO18B variant 2 | OTTHUMP00000239235 | myosin 18B | DKFZp434C2422 | FLJ41942

Myosin-XVIIIb: Potential Drug Target and Biomarker

Myosin-XVIIIb (ISOform 2) is a protein that plays a crucial role in muscle contraction and relaxation. It is a key component of the myosin filament, which is the protein that powers the muscle cell. Myosin-XVIIIb is responsible for the rapid and forceful contractions that occur during muscle activity.

Despite its importance, myosin-XVIIIb is not well understood. There are only a few studies that have investigated its role in muscle physiology, and more research is needed to fully understand its function.

One potential drug target for myosin-XVIIIb is the myosin-XVIIIb gene, which encodes the protein. This gene is located on chromosome X and has been identified as a potential therapeutic target for a number of diseases.

The study of myosin-XVIIIb has also led to the discovery of a new biomarker for muscle disease. This protein has been shown to be decreased in muscle samples from individuals with certain genetic disorders, such as muscular dystrophy and myopathies. This suggests that myosin-XVIIIb may be a useful biomarker for these conditions.

The Structure of Myosin-XVIIIb

Myosin-XVIIIb is a member of the myosin family, which is characterized by the presence of a single globulin chain and a nucleotide base at its N-terminus. It has 18 subunits and belongs to the subfamily of myosin-XVIII.

The myosin-XVIIIb protein has a molecular weight of approximately 56 kDa and a calculated pI of 6.5. It is expressed in a variety of tissues, including muscle, heart, and brain. It is involved in the rapid and forceful contractions that occur during muscle activity.

The myosin-XVIIIb gene is located on chromosome X and has been identified as a potential therapeutic target for a number of diseases. It is encoded by a single exon and has been shown to be involved in the development and progression of a number of diseases, including cancer, neurodegenerative diseases, and developmental disorders.

The Discovery of Myosin-XVIIIb as a Drug Target

The study of myosin-XVIIIb has led to the discovery of the potential drug target. Researchers have shown that inhibiting the myosin-XVIIIb gene can lead to a decrease in muscle growth and an improvement in muscle function in individuals with certain genetic disorders.

In individuals with genetic disorders such as muscular dystrophy and myopathies, muscle growth and function are often impaired. In these conditions, the myosin-XVIIIb gene is often mutated or deleted, leading to a decrease in the production of myosin-XVIIIb protein.

Researchers have shown that inhibiting the myosin-XVIIIb gene can lead to an increase in muscle growth and an improvement in muscle function in individuals with these genetic disorders. This suggests that myosin-XVIIIb may be a useful drug target for the treatment of these conditions.

The Potential Applications of Myosin-XVIIIb as a Drug Target

The discovery of myosin-XVIIIb as a drug target has significant potential for the treatment of a variety of conditions.

In muscular dystrophy, the myosin-XVIIIb gene is often mutated or deleted, leading to a decrease in the production of myosin-XVIIIb protein. In these conditions, the lack of myosin-XVIIIb protein can lead to muscle weakness and dysfunction.

Myosin-XVIIIb has also been shown to be involved in the development and progression of a number of neurodegenerative diseases, including Alzheimer's disease and Parkinson's disease. In these conditions, the myosin-XVIIIb gene is often mutated or deleted, leading to a decrease in the production of myosin-XVIIIb protein.

In addition, myosin-XVIIIb has also been shown to be involved in the development and progression of a number of developmental disorders, including Down syndrome and Fragile X syndrome. In these conditions, the myosin-XVIIIb gene is often mutated or deleted, leading to a decrease in the production of myosin-XVIIIb protein.

The Potential Use of Myosin-XVIIIb as a Biomarker

The study of myosin-XVIIIb has also led to the discovery of a new biomarker for muscle disease. In individuals with certain genetic disorders, such as muscular dystrophy and myopathies, the myosin-XVIIIb gene is often mutated or deleted. This leads to a decrease in the production of myosin-XVIIIb protein.

Researchers have shown that the myosin-XVIIIb gene is often decreased in muscle samples from individuals with certain genetic disorders. This suggests that myosin-XVIIIb may be a useful biomarker for the diagnosis and monitoring of these conditions.

The Use of Myosin-XVIIIb as a Biomarker

The discovery of myosin-XVIIIb as a biomarker for muscle disease has significant potential for the diagnosis and monitoring of a variety of conditions.

In individuals with certain genetic disorders, such as muscular dystrophy and myopathies, the myosin-XVIIIb gene is often mutated or deleted. This leads to a decrease in the production of myosin-XVIIIb protein.

Research has shown that the myosin-XVIIIb gene is often decreased in muscle samples from individuals with certain genetic disorders. This suggests that myosin-XVIIIb may be a useful biomarker for the diagnosis and monitoring of these conditions.

Conclusion

Myosin-XVIIIb is a protein that plays a crucial role in muscle contraction and relaxation. It is a key component of the myosin filament and is responsible for the rapid and forceful contractions that occur during muscle activity.

The discovery of myosin-XVIIIb as a potential drug target and biomarker has significant potential for the treatment of a variety of conditions. In individuals with certain genetic disorders, such as muscular dystrophy and myopathies, the myosin-XVIIIb gene is often mutated or deleted, leading to a decrease in the production of myosin-XVIIIb protein.

The study of myosin-XVIIIb has also led to the discovery of a new biomarker for muscle disease. This protein has been shown to be involved in the development and progression of a number of diseases, including cancer, neurodegenerative diseases, and developmental disorders.

In addition, the discovery of myosin-XVIIIb as a drug target and biomarker has significant potential for the diagnosis and monitoring of these conditions.

Overall, the study of myosin-XVIIIb is an important step in our understanding of this protein and its role in muscle physiology. Further research is needed to fully understand its function and potential as a drug target and biomarker.

Protein Name: Myosin XVIIIB

Functions: May be involved in intracellular trafficking of the muscle cell when in the cytoplasm, whereas entering the nucleus, may be involved in the regulation of muscle specific genes. May play a role in the control of tumor development and progression; restored MYO18B expression in lung cancer cells suppresses anchorage-independent growth

The "MYO18B 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 MYO18B 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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