Target Name: HSPA1B
NCBI ID: G3304
Review Report on HSPA1B Target / Biomarker Content of Review Report on HSPA1B Target / Biomarker
HSPA1B
Other Name(s): heat shock 70kDa protein 1B | HSPA1 | HSP70.2 | Heat shock 70 kDa protein 1 | Heat shock 70 kDa protein 2 | heat shock 70 kDa protein 1/2 | HS71B_HUMAN | Heat shock 70 kDa protein 1A | HSX70 | heat shock protein family A (Hsp70) member 1B | HSP70-2 | HSP72 | heat shock 70 kDa protein 1A/1B | Heat shock 70 kDa protein 1B | heat shock 70 kDa protein 2 | HSP70-1/HSP70-2 | HSP70.1/HSP70.2 | HSP70-1 | heat shock 70kD protein 1B | HSP70-1B | HSP70.1 | Heat shock 70kDa protein 1B

Unlocking The Potential of Heat Shock Protein 1B

Heat shock protein 1B (HSPA1B) is a protein that is expressed in a wide range of tissues and cells in the human body. It is a key regulator of the stress response and has been implicated in a number of cellular processes, including DNA damage repair, cell signaling, and inflammation. Despite its importance, HSPA1B has remained a relatively unstudied protein, and there is currently limited information about potential drug targets or biomarkers that may be associated with its function.

In recent years, researchers have made significant progress in the study of HSPA1B. One of the most significant findings is that HSPA1B plays a key role in the regulation of DNA damage repair. damaged DNA is a common occurrence in aging and can lead to the development of diseases such as cancer. HSPA1B has been shown to help repair damaged DNA by promoting the formation of DNA repair complexes and by inhibiting the activity of enzymes that can cause DNA damage.

Another important function of HSPA1B is its role in cell signaling. HSPA1B has been shown to play a key role in the regulation of cell signaling pathways, including the TGF-β pathway. This pathway is involved in the regulation of cell growth, differentiation, and survival, and is a key factor in the development of many diseases, including cancer. HSPA1B has been shown to regulate the activity of the TGF-β pathway by interacting with its downstream effector, SMAD1.

In addition to its role in cell signaling, HSPA1B is also involved in the regulation of inflammation. HSPA1B has been shown to play a key role in the regulation of the immune response, specifically in the regulation of the production of antibodies. HSPA1B has been shown to interact with the immune receptor PD-1 and to regulate the activity of the T-cells, which are a key component of the immune system.

Despite its importance, HSPA1B has remained a relatively unstudied protein. There are currently limited number of studies that have investigated its role in disease, and there is a lack of clear cut biomarkers that are associated with its function.

In conclusion, HSPA1B is a protein that plays a key role in a wide range of cellular processes, including DNA damage repair, cell signaling, and inflammation. Despite its importance, HSPA1B has remained a relatively unstudied protein. Further research is needed to fully understand its role in disease and to identify potential drug targets or biomarkers that may be associated with its function.

Protein Name: Heat Shock Protein Family A (Hsp70) Member 1B

The "HSPA1B 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 HSPA1B 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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