Target Name: CERS2
NCBI ID: G29956
Review Report on CERS2 Target / Biomarker Content of Review Report on CERS2 Target / Biomarker
CERS2
Other Name(s): Ceramide synthase 2 | LASS2 variant 1 | OTTHUMP00000033029 | Longevity assurance (LAG1, S. cerevisiae) homolog 2 | OTTHUMP00000033030 | LASS2 | tumor metastasis-suppressor gene 1 protein | Sphingosine N-acyltransferase CERS2 | FLJ10243 | Very-long-chain ceramide synthase CERS2 | LAG1 longevity assurance 2 | Ceramide synthase 2, transcript variant 2 | Tumor metastasis-suppressor gene 1 protein | OTTHUMP00000033031 | L3 | CERS2_HUMAN | SP260 | very-long-chain ceramide synthase CERS2 | LAG1 homolog, ceramide synthase 2, transcript variant 1 | longevity assurance (LAG1, S. cerevisiae) homolog 2 | MGC987 | CERS2 variant 2 | TMSG1 | CerS2 | LAG1 homolog, ceramide synthase 2 | ceramide synthase 2 | LAG1 longevity assurance homolog 2 | sphingosine N-acyltransferase CERS2

CERS2: A Potential Drug Target for Alzheimer's and Parkinson's Diseases

Ceramide synthase 2 (CERS2) is a protein that is expressed in various tissues throughout the body, including the brain, heart, and kidneys. It is a key enzyme in the synthesis of ceramides, which are a type of lipid molecule that play a crucial role in cellular signaling and memory. Therefore, CERS2 has been identified as a potential drug target or biomarker for various diseases, including Alzheimer's disease, Parkinson's disease, and metabolic disorders.

The synthesis of ceramides is a complex process that involves multiple enzymes, including CERS2. CERS2 is responsible for the synthesis of the first step in the synthesis pathway, which involves the conversion of an acetyl group from the amino acid leucine into a more stable ester form. This conversion is critical for the subsequent steps in the synthesis pathway, and any defects in the process can result in the accumulation of ceramides that can contribute to the development of various diseases.

One of the challenges in the synthesis of ceramides is the high levels of ceramides that can be generated during the synthesis process. These high levels can make the ceramides unstable and prone to aggregation, which can contribute to the development of diseases. Therefore, it is important to identify mechanisms that can regulate the synthesis of ceramides to prevent the accumulation of these molecules.

CERS2 is a key enzyme in the synthesis of ceramides, and its activity can be inhibited by various drugs. For example, inhibitors of CERS2 have been shown to be effective in reducing the production of ceramides in animal models of Alzheimer's disease. These inhibitors work by binding to the active site of CERS2 and inhibiting its activity. By reducing the production of ceramides, these drugs can prevent the accumulation of these molecules in the brain and potentially slow the development of Alzheimer's disease.

Another potential mechanism by which CERS2 may contribute to the development of diseases is its role in cellular signaling. Ceramides have been shown to play a critical role in cellular signaling, particularly in the regulation of inflammation and stress responses. Therefore, alterations in the levels of ceramides in the body can affect the balance of cellular signaling that occurs in the body.

CERS2 is also involved in the regulation of cellular processes that are important for maintaining the structure and function of tissues. For example, ceramides have been shown to play a critical role in the regulation of cell adhesion, which is important for maintaining the integrity of tissues and is critical for various biological processes, including embryonic development and tissue repair.

In conclusion, CERS2 is a protein that is involved in the synthesis of ceramides, which are important molecules that play a critical role in cellular signaling and regulation. Its activity can be inhibited by various drugs, and it is also involved in the regulation of cellular processes that are important for maintaining the structure and function of tissues. Therefore, CERS2 is a potential drug target or biomarker for various diseases, including Alzheimer's disease, Parkinson's disease, and metabolic disorders. Further research is needed to fully understand the role of CERS2 in disease development and to develop effective treatments.

Protein Name: Ceramide Synthase 2

Functions: Ceramide synthase that catalyzes the transfer of the acyl chain from acyl-CoA to a sphingoid base, with high selectivity toward very-long-chain fatty acyl-CoA (chain length C22-C27) (PubMed:17977534, PubMed:18165233, PubMed:18541923, PubMed:19728861, PubMed:20937905, PubMed:22144673, PubMed:22661289, PubMed:26887952, PubMed:29632068). N-acylates sphinganine and sphingosine bases to form dihydroceramides and ceramides in de novo synthesis and salvage pathways, respectively (By similarity) (PubMed:17977534, PubMed:18165233, PubMed:18541923, PubMed:19728861, PubMed:20937905, PubMed:22144673, PubMed:22661289, PubMed:26887952, PubMed:29632068). Plays a non-redundant role in the synthesis of ceramides with very-long-chain fatty acids in kidney, liver and brain. Regulates the abundance of myelin-specific sphingolipids galactosylceramide and sulfatide that affects myelin sheath architecture and motor neuron functions (By similarity)

The "CERS2 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 CERS2 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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