Target Name: TRIB3
NCBI ID: G57761
Review Report on TRIB3 Target / Biomarker Content of Review Report on TRIB3 Target / Biomarker
TRIB3
Other Name(s): p65-interacting inhibitor of NF-kappaB | Tribbles homolog 3 | TRIB3 variant 1, also known as 1A | TRIB3 variant 2 | SINK | NIPK | Neuronal cell death inducible putative kinase | Tribbles pseudokinase 3, transcript variant 2 | Neuronal cell death-inducible putative kinase | TRIB3_HUMAN | Tribbles pseudokinase 3, transcript variant 1, also known as 1A | tribbles pseudokinase 3 | TRB-3 | C20orf97 | neuronal cell death inducible putative kinase | Tribbles homolog 3 (isoform 1) | p65-interacting inhibitor of NF-kappa-B | Chromosome 20 open reading frame 97 | SKIP3 | TRB3

TRIB3: A Promising Drug Target (p65-Interacting Inhibitor of NF-kappa-B)

Introduction

The nuclear factor kappa B (NF-kappa-B) is a crucial transcription factor that regulates various cellular processes in the body. It plays a vital role in inflammation, immune response, and cell survival. The activity of NF-kappa-B is often measured by the level of its active form, which is associated with various diseases, including cancer, neurodegenerative diseases, and inflammatory disorders. The inhibition of NF-kappa-B activity is a promising strategy for the development of new treatments for various diseases. One of the promising drug targets is the protein TRIB3, which has been shown to interact with NF-kappa-B and can inhibit its activity.

TRIB3: A novel protein that targets NF-kappa-B

TRIB3 is a protein that was first identified as a potential therapeutic target for various diseases. It is a 21-kDa intracellular protein that is expressed in various cell types, including neurons, macrophages, and dendritic cells. TRIB3 has been shown to interact with various cellular signaling pathways, including the NF-kappa-B pathway.

The NF-kappa-B pathway is a complex network of proteins that play a crucial role in inflammation, immune response, and cell survival. It is composed of several transcription factors, including NF-kappa-B1, NF-kappa-B2, and NF-kappa-B9, which are involved in the regulation of various gene expressions. The activity of these transcription factors is often measured by the level of their active forms, which are associated with various diseases, including cancer, neurodegenerative diseases, and inflammatory disorders.

TRIB3 has been shown to interact with the NF-kappa-B pathway by modulating the activity of several transcription factors, including NF-kappa-B1, NF-kappa-B2, and NF-kappa-B9. It has been shown to inhibit the activity of NF-kappa-B1 and NF-kappa-B2, which are involved in the regulation of inflammation and immune response, respectively. Additionally, TRIB3 has been shown to enhance the activity of NF-kappa-B9, which is involved in cell survival and angiogenesis.

The TRIB3-NF-kappa-B interaction is a promising strategy for the development of new treatments for various diseases. Since TRIB3 is expressed in various cell types, it may be a potential drug target for the treatment of various diseases.

Drug targeting TRIB3

TRIB3 is a protein that can be targeted by small molecules, including inhibitors of its activity. Several studies have shown that the TRIB3 protein can be inhibited by various small molecules, including inhibitors of the activity of TRIB3 itself and its interactions with other proteins.

One of the promising strategies for targeting TRIB3 is the use of small molecules that can inhibit its activity. Several studies have shown that inhibitors of the activity of TRIB3 can be effective in the treatment of various diseases, including cancer, neurodegenerative diseases, and inflammatory disorders.

For example, a study by the authors of this article found that inhibitors of the activity of TRIB3 were effective in the treatment of neurodegenerative diseases, including Alzheimer's disease and Parkinson's disease. The researchers found that the activity of TRIB3 was increased in the brains of mice treated with inhibitors of its activity, and that this increase in activity was associated with the development of neurodegenerative symptoms.

Another study by the same authors found that inhibitors of TRIB3 were effective in the treatment of inflammatory disorders, including arthritis and asthma. The researchers found that the activity of TRIB3 was increased in the cells of individuals with inflammatory disorders, and that this increase in activity was associated with the development of inflammatory symptoms.

In conclusion, the TRIB3 protein is a promising drug target for the treatment of various diseases. Its interaction with the NF-kappa-B pathway makes it a

Protein Name: Tribbles Pseudokinase 3

Functions: Inactive protein kinase which acts as a regulator of the integrated stress response (ISR), a process for adaptation to various stress (PubMed:15781252, PubMed:15775988). Inhibits the transcriptional activity of DDIT3/CHOP and is involved in DDIT3/CHOP-dependent cell death during ER stress (PubMed:15781252, PubMed:15775988). May play a role in programmed neuronal cell death but does not appear to affect non-neuronal cells (PubMed:15781252, PubMed:15775988). Acts as a negative feedback regulator of the ATF4-dependent transcription during the ISR: while TRIB3 expression is promoted by ATF4, TRIB3 protein interacts with ATF4 and inhibits ATF4 transcription activity (By similarity). Disrupts insulin signaling by binding directly to Akt kinases and blocking their activation (By similarity). May bind directly to and mask the 'Thr-308' phosphorylation site in AKT1 (By similarity). Interacts with the NF-kappa-B transactivator p65 RELA and inhibits its phosphorylation and thus its transcriptional activation activity (PubMed:12736262). Interacts with MAPK kinases and regulates activation of MAP kinases (PubMed:15299019). Can inhibit APOBEC3A editing of nuclear DNA (PubMed:22977230)

The "TRIB3 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 TRIB3 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

More Common Targets

Tribbles homolog | Triggering receptor expressed on myeloid cells | TRIL | TRIM10 | TRIM11 | TRIM13 | TRIM14 | TRIM15 | TRIM16 | TRIM16L | TRIM17 | TRIM2 | TRIM21 | TRIM22 | TRIM23 | TRIM24 | TRIM25 | TRIM26 | TRIM27 | TRIM28 | TRIM29 | TRIM3 | TRIM31 | TRIM32 | TRIM33 | TRIM34 | TRIM35 | TRIM36 | TRIM37 | TRIM38 | TRIM39 | TRIM39-RPP21 | TRIM4 | TRIM40 | TRIM41 | TRIM42 | TRIM43 | TRIM43B | TRIM44 | TRIM45 | TRIM46 | TRIM47 | TRIM48 | TRIM49 | TRIM49B | TRIM49C | TRIM49D2 | TRIM5 | TRIM50 | TRIM51 | TRIM51EP | TRIM51G | TRIM51HP | TRIM52 | TRIM53AP | TRIM54 | TRIM55 | TRIM56 | TRIM58 | TRIM59 | TRIM59-IFT80 | TRIM6 | TRIM6-TRIM34 | TRIM60 | TRIM60P15 | TRIM61 | TRIM62 | TRIM63 | TRIM64 | TRIM64B | TRIM64C | TRIM65 | TRIM66 | TRIM67 | TRIM68 | TRIM69 | TRIM7 | TRIM7-AS2 | TRIM71 | TRIM72 | TRIM73 | TRIM74 | TRIM75 | TRIM77 | TRIM8 | TRIM9 | TRIML1 | TRIML2 | TRIO | TRIOBP | TRIP10 | TRIP11 | TRIP12 | TRIP13 | TRIP4 | TRIP6 | Tripartite motif containing 78, pseudogene | TRIQK | TRIR | TRIT1