Target Name: TRAPPC4
NCBI ID: G51399
Review Report on TRAPPC4 Target / Biomarker Content of Review Report on TRAPPC4 Target / Biomarker
TRAPPC4
Other Name(s): hematopoietic stem/progenitor cell protein 172 | HSPC172 | TRAPPC4 variant 1 | TRS23 | CGI-104 | SBDN | SYNBINDIN | trafficking protein particle complex subunit 4 | Trafficking protein particle complex subunit 4 | Synbindin | PTD009 | TPPC4_HUMAN | TRS23 homolog | NEDESBA | Trafficking protein particle complex subunit 4, transcript variant 1 | Trafficking protein particle complex subunit 4 (isoform 1) | trafficking protein particle complex 4 | Hematopoietic stem/progenitor cell protein 172

TRAPPC4: A Potential Drug Target and Biomarker for Hematopoietic Stem/Progenitor Cell Proliferation

Hematopoietic stem/progenitor cells (HSCs) are a vital component of the immune system, responsible for the production of all blood cells. They are found in the bone marrow and have the ability to develop into any type of blood cell. This property makes them a promising target for cancer therapies, as cancer cells often arise from stem cells that have gone rogue and begin to divide uncontrollably. The TRAPPC4 protein is one such potential drug target that has been identified by researchers for its role in the proliferation of HSCs.

TRAPPC4 is a transmembrane protein that is expressed in a variety of tissues, including the bone marrow, where it is involved in the development and maintenance of HSCs. It is a member of the TRAPC family, which includes several other proteins that are involved in cell signaling and division. The TRAPPC4 protein is characterized by a unique domain that consists of a long extracellular domain, a transmembrane region, and a short intracellular domain. This unique structure allows it to interact with various signaling molecules and to participate in a wide range of cellular processes.

One of the key functions of TRAPPC4 is its role in the proliferation of HSCs. HSCs are known for their ability to self-renew and to differentiate into different types of blood cells. This process is controlled by a complex set of genes, including the master regulator TAL1. TRAPPC4 is a key regulator of TAL1 activity, and it has been shown to play a critical role in the self-renewal and proliferation of HSCs.

In addition to its role in HSC proliferation, TRAPPC4 has also been shown to be involved in the regulation of stem cell differentiation. HSCs have the ability to differentiate into any type of blood cell, and this process is controlled by the genes that are present in the stem cells. TRAPPC4 is involved in the regulation of these genes, and it has been shown to play a critical role in the differentiation of HSCs into mature blood cells.

The potential implications of TRAPPC4 as a drug target are significant. If TRAPPC4 is found to be a reliable drug target, it could be used to treat a wide range of diseases that are characterized by the over-production or dysfunction of HSCs. For example, TRAPPC4 has been shown to be involved in the development of leukemia, and it is possible that targeting TRAPPC4 could be a effective way to treat this disease. Additionally, TRAPPC4 has also been shown to be involved in the development of multiple myeloma, a type of cancer that is characterized by the over-production of a type of white blood cell called a plasma cell. Targeting TRAPPC4 in these cases could be a promising new approach to cancer treatment.

Another potential application of TRAPPC4 as a drug target is its role in the regulation of regenerative medicine. HSCs have the ability to regenerate and differentiate into different types of cells, and this process is critical for the development of tissues and organs. TRAPPC4 plays a critical role in the regulation of this process, and it is possible that targeting TRAPPC4 could be a useful approach to regenerative medicine.

In conclusion, TRAPPC4 is a protein that has significant potential as a drug target. Its role in the proliferation and differentiation of HSCs makes it an attractive target for cancer therapies. Additionally, TRAPPC4 has also been shown to play a critical role in the regulation of stem cell differentiation, which makes it a promising target for regenerative medicine. Further research is needed to fully understand the role of TRAPPC4 in these processes and to determine its potential as a drug target.

Protein Name: Trafficking Protein Particle Complex Subunit 4

Functions: Core component of the TRAPP complexes which has a function of guanine nucleotide exchange factor activity for Rab1 GTPase (Probable). Plays a role in vesicular transport from endoplasmic reticulum to Golgi and autophagy (PubMed:31794024). May play a role in dendrite postsynaptic membrane trafficking (By similarity)

The "TRAPPC4 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 TRAPPC4 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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