Target Name: HBS1L
NCBI ID: G10767
Review Report on HBS1L Target / Biomarker Content of Review Report on HBS1L Target / Biomarker
HBS1L
Other Name(s): HSPC276 | eRF3 family member | Hsp70 subfamily B suppressor 1-like protein | ERFS | HBS1L_HUMAN | KIAA1038 | HBS1L variant 1 | HBS1-like protein | HBS1-like protein (isoform 1) | OTTHUMP00000017253 | HBS1L variant 2 | EF-1a | OTTHUMP00000017254 | DKFZp686L13262 | HBS1-like protein (isoform 2) | ERF3-similar protein | eRF3c | HBS1 like translational GTPase, transcript variant 2 | HBS1 like translational GTPase, transcript variant 1 | HBS1 like translational GTPase | HBS1

Understanding The Role of HSPC276 in Cellular Homeostasis

HBS1L (HSPC276) is a protein that is expressed in various tissues throughout the body. It is a member of the heat shock protein (HSP) family, which are proteins that are expressed in high levels in response to an increase in temperature. HSPs are known for their ability to withstand and recover from temperatures that are too high for most cells to survive.

One of the functions of HSPs is to help cells maintain a stable internal environment, even in the face of extreme temperatures. This is achieved through a process called \"proteostasis,\" which involves the regulation of protein synthesis and degradation. HSPs can interact with other proteins to help maintain a stable level of protein synthesis and degradation, which is critical for maintaining cellular homeostasis.

HSPs have also been shown to play a role in various cellular processes, including the regulation of cell growth, apoptosis (programmed cell death), and inflammation. For example, HSPs have been shown to help regulate the growth of cancer cells and to play a role in the development of neurodegenerative diseases.

Despite the importance of HSPs in various cellular processes, the majority of HSPs have not yet been identified, and many potential drug targets have not been identified either. This is because HSPs are difficult to study, due to their complex cellular and molecular mechanisms of function.

One potential drug target for HSPs is the protein HSPC276, which is a key component of the HSP family. HSPC276 is a 27-kDa protein that is expressed in various tissues throughout the body, including the brain, heart, and liver. HSPC276 has been shown to play a role in a variety of cellular processes, including the regulation of protein synthesis and degradation, DNA replication, and cell survival.

Studies have shown that HSPC276 is involved in the regulation of cellular homeostasis, and that it plays a role in the development of various diseases, including cancer. For example, HSPC276 has been shown to be involved in the regulation of the growth and survival of cancer cells, and has been shown to interact with other proteins that are involved in the development of cancer.

In addition to its potential role in cancer, HSPC276 may also be involved in the regulation of other cellular processes that are important for maintaining cellular homeostasis. For example, HSPC276 has been shown to play a role in the regulation of protein synthesis and degradation, which is critical for maintaining cellular homeostasis. Additionally, HSPC276 may be involved in the regulation of cell apoptosis, which is a critical process for maintaining cellular homeostasis and for eliminating damaged or dysfunctional cells.

Despite the potential importance of HSPC276, the majority of its functions have not yet been identified. This is due to the complexity of its cellular and molecular mechanisms of function, as well as the difficulty of studying HSPs in general. To further understand the functions of HSPC276 and its potential as a drug target, it is important to continue research into its biology and the mechanisms of its function. This research will be important for the development of new treatments for a variety of diseases.

Protein Name: HBS1 Like Translational GTPase

Functions: Cotranslational quality control factor involved in the No-Go Decay (NGD) pathway (PubMed:21448132). In the presence of ABCE1 and PELO, is required for 48S complex formation from 80S ribosomes and dissociation of vacant 80S ribosomes (PubMed:21448132). Together with PELO and in presence of ABCE1, recognizes stalled ribosomes and promotes dissociation of elongation complexes assembled on non-stop mRNAs; this triggers endonucleolytic cleavage of the mRNA, a mechanism to release non-functional ribosomes and to degrade damaged mRNAs as part of the No-Go Decay (NGD) pathway (PubMed:21448132)

The "HBS1L 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 HBS1L 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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