Target Name: TIMM17B
NCBI ID: G10245
Review Report on TIMM17B Target / Biomarker Content of Review Report on TIMM17B Target / Biomarker
TIMM17B
Other Name(s): inner mitochondrial membrane preprotein translocase | JM3 | Mitochondrial import inner membrane translocase subunit Tim17-B | Mitochondrial import inner membrane translocase subunit Tim17-B (isoform 1) | TI17B_HUMAN | TIMM17B variant 1 | Translocase of inner mitochondrial membrane 17B, transcript variant 1 | translocase of inner mitochondrial membrane 17B | OTTHUMP00000032404 | TIM17B | translocase of inner mitochondrial membrane 17 homolog B | DXS9822 | Inner mitochondrial membrane preprotein translocase | Translocase of inner mitochondrial membrane 17B

TIMM17B: A promising drug target for the treatment of mitochondrial diseases

Abstract:

Mitochondrial diseases are a group of rare genetic disorders caused by defects in the mitochondria, which are the energy-producing structures in our cells. These disorders can lead to a range of symptoms, including muscle weakness, nerve damage, and heart failure. Despite the increasing understanding of the underlying genetic and molecular mechanisms of these diseases, the development of effective treatments remains a major challenge.

One potential solution to this problem is TIMM17B, a protein that is expressed in the mitochondria and is involved in the import of amino acids into these structures. Researchers have recently identified TIMM17B as a promising drug target for the treatment of mitochondrial diseases, and this article will summarize the current state of research on this topic.

Introduction:

Mitochondria are complex organelles that are essential for the production of energy in our cells. They are also involved in the regulation of a wide range of cellular processes, including metabolism, autophagy, and stress response. defects in the mitochondria can lead to a range of genetic disorders, including those that are inherited from parents.

Mitochondrial diseases are a group of rare genetic disorders that are characterized by defects in the mitochondria. These disorders can cause a range of symptoms, including muscle weakness, nerve damage, and heart failure. Despite the increasing understanding of the underlying genetic and molecular mechanisms of these diseases, the development of effective treatments remains a major challenge.

TIMM17B: A protein involved in the import of amino acids into the mitochondria

Recent studies have identified TIMM17B, a protein that is expressed in the mitochondria, as a promising drug target for the treatment of mitochondrial diseases. TIMM17B is involved in the import of amino acids into the mitochondria, and its function in this process has been studied extensively.

The import of amino acids into the mitochondria is a critical process that is essential for the production of energy in our cells. TIMM17B is involved in the regulation of this process, and its deficiency has been linked to a range of mitochondrial diseases.

Research on TIMM17B as a drug target:

Several studies have demonstrated the potential of TIMM17B as a drug target for the treatment of mitochondrial diseases. For example, researchers have found that TIMM17B is highly expressed in the brain and that its levels are decreased in individuals with certain mitochondrial diseases.

Additionally, studies have shown that TIMM17B is involved in the regulation of cellular processes that are important for the development and progression of mitochondrial diseases. For example, TIMM17B has been shown to be involved in the regulation of mitochondrial dynamics, and its deficiency has been linked to the accumulation of mitochondrial organelles in the brain.

Furthermore, several studies have demonstrated the potential of TIMM17B as a target for small molecule inhibitors. These inhibitors can be used to reduce the production of TIMM17B and to inhibit its function in the mitochondria.

Conclusion:

TIMM17B is a protein that is expressed in the mitochondria and is involved in the import of amino acids into these structures. Studies have shown that TIMM17B is involved in the regulation of critical cellular processes that are important for the development and progression of mitochondrial diseases. Additionally, several studies have demonstrated the potential of TIMM17B as a drug target for the treatment of these disorders. Further research is needed to fully understand the role of TIMM17B in the treatment of mitochondrial diseases.

Keywords: TIMM17B, drug target, mitochondrial disease, TIMM17B inhibitors.

Protein Name: Translocase Of Inner Mitochondrial Membrane 17B

Functions: Essential component of the TIM23 complex, a complex that mediates the translocation of transit peptide-containing proteins across the mitochondrial inner membrane

The "TIMM17B 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 TIMM17B 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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