Target Name: TRAJ40
NCBI ID: G28715
Review Report on TRAJ40 Target / Biomarker Content of Review Report on TRAJ40 Target / Biomarker
TRAJ40
Other Name(s): T cell receptor alpha joining 40

T Cell Receptor Alpha Joining 40: A Potential Drug Target

T cell receptor alpha joining 40 (TRAJ40) is a protein that is expressed in T cells, a type of white blood cell that plays a crucial role in the immune system. T cells are responsible for recognizing and responding to foreign substances in the body, and their activity is closely regulated by the T cell receptor alpha joining 40.

The T cell receptor alpha joining 40 is a protein that is made up of two heavy chains and two light chains. The heavy chains contain the extracellular domain of the protein, while the light chains contain the intracellular domain. The protein is expressed in T cells and other immune cells, and it plays a critical role in the development and regulation of T cell responses.

One of the functions of the T cell receptor alpha joining 40 is to regulate the activation and proliferation of T cells. T cells are activated when they recognize an foreign substance, such as a virus or a cancer cell, and the T cell receptor alpha joining 40 helps to ensure that these cells are properly regulated and that they do not continue to divide and proliferate.

Another function of the T cell receptor alpha joining 40 is to regulate the death of T cells. T cells have a limited lifespan and are replaced by new T cells through a process called apoptosis. The T cell receptor alpha joining 40 helps to ensure that properly programmed T cells are apoptosed, while improperly programmed T cells are allowed to divide and proliferate.

The T cell receptor alpha joining 40 is also involved in the regulation of inflammation. When T cells are activated, they produce a variety of cytokines, which are proteins that help to recruit and activate other immune cells. The T cell receptor alpha joining 40 helps to regulate the production of these cytokines and is therefore important for the regulation of inflammatory responses.

In addition to its role in T cell regulation, the T cell receptor alpha joining 40 is also a potential drug target. Many studies have suggested that the T cell receptor alpha joining 40 may be a useful target for new therapies for a variety of diseases, including cancer, autoimmune disorders, and respiratory infections.

One approach to targeting the T cell receptor alpha joining 40 is to use small molecules, such as drugs that bind to the protein. Many of these drugs are currently in clinical trials and have been shown to be effective in treating a variety of diseases. For example, studies have shown that the drug ipilimumab, which is a monoclonal antibody targeting the T cell receptor alpha joining 40, has the potential to be a useful treatment for cancer.

Another approach to targeting the T cell receptor alpha joining 40 is to use genetic modifiers, such as CRISPR/Cas9 genome editing tools. These tools can be used to modify the genes responsible for the production of the T cell receptor alpha joining 40, allowing researchers to specifically target this protein.

Overall, the T cell receptor alpha joining 40 is a protein that plays a critical role in the immune system and is therefore an attractive target for new therapies. Further research is needed to fully understand the functions of this protein and to develop effective treatments for diseases that are caused by its dysfunction.

Protein Name: T Cell Receptor Alpha Joining 40

The "TRAJ40 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 TRAJ40 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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TRAJ41 | TRAJ42 | TRAJ43 | TRAJ44 | TRAJ45 | TRAJ46 | TRAJ47 | TRAJ48 | TRAJ49 | TRAJ5 | TRAJ50 | TRAJ52 | TRAJ53 | TRAJ54 | TRAJ56 | TRAJ57 | TRAJ58 | TRAJ59 | TRAJ6 | TRAJ61 | TRAJ7 | TRAJ8 | TRAJ9 | TRAK1 | TRAK2 | TRAM1 | TRAM1L1 | TRAM2 | TRAM2-AS1 | TRANK1 | Transcription factor AP-2 | Transcription factor GATA | Transcription factor Maf | Transcription factor NF-E2 | Transcription factor SOX | Transcription Factor TCF | Transcription factor TFIIIB complex | Transcriptional Enhancer Factor (TEAD) (nonspecified subype) | Transfer RNA methionine (anticodon CAU) | Transforming growth factor | Transforming growth factor (TGF)-beta receptor | Transforming growth factor beta | Transglutaminase | Transient Receptor Potential Cation Channel (TRP) | Transient receptor potential cation channel subfamily V | Translation initiation factor IF-2-like, transcript variant X1 | Translocase of inner mitochondrial membrane 23 homolog B (yeast), transcript variant X1 | Translocon-associated protein (TRAP) complex | Transmembrane protein FLJ37396 | TRAP1 | TRAPP complex | TRAPPC1 | TRAPPC10 | TRAPPC11 | TRAPPC12 | TRAPPC13 | TRAPPC14 | TRAPPC2 | TRAPPC2L | TRAPPC3 | TRAPPC3L | TRAPPC4 | TRAPPC5 | TRAPPC6A | TRAPPC6B | TRAPPC8 | TRAPPC9 | TRARG1 | TRAT1 | TRAV1-2 | TRAV10 | TRAV11 | TRAV12-1 | TRAV12-2 | TRAV13-2 | TRAV14DV4 | TRAV19 | TRAV2 | TRAV20 | TRAV21 | TRAV22 | TRAV24 | TRAV25 | TRAV26-1 | TRAV26-2 | TRAV27 | TRAV3 | TRAV34 | TRAV38-2DV8 | TRAV39 | TRAV4 | TRAV41 | TRAV8-1 | TRAV8-2 | TRAV8-3 | TRAV8-4 | TRAV8-6 | TRAV9-1 | TRBC1 | TRBC2