Target Name: GRAMD1A
NCBI ID: G57655
Review Report on GRAMD1A Target / Biomarker Content of Review Report on GRAMD1A Target / Biomarker
GRAMD1A
Other Name(s): GRAM domain-containing protein 1A | GRAMD1A variant 5 | ASTRA_HUMAN | KIAA1533 | GRAM domain containing 1A, transcript variant 1 | GRAMD1A variant 1 | Protein Aster-A (isoform 5) | Protein Aster-A (isoform 1) | GRAM domain containing 1A | Protein Aster-A | GRAM domain containing 1A, transcript variant 5

Targeting GRAMD1A: A Promising Approach To Treating Neurodegenerative Disorders

Gram domain-containing protein 1A (GRAMD1A) is a protein that is expressed in various tissues of the body, including the brain, heart, and kidneys. It is a key regulator of cellular processes that are essential for the proper functioning of these organs. Unfortunately, GRAMD1A has also been implicated in the development and progression of several diseases, including neurodegenerative disorders, diabetes, and cancer. As a result, targeting this protein has become an attractive research topic, with the goal of developing new treatments for a variety of diseases.

TheGRAMD1A gene

TheGRAMD1A gene is located on chromosome 19q34 and encodes a protein that is composed of 154 amino acid residues. The protein has a GRAM domain, which is a unique structural feature that is found in a variety of proteins that play important roles in cellular processes. The GRAM domain is composed of a specific sequence of amino acids that is unique among proteins and gives the protein its unique structure and function.

TheGRAMD1A protein

GRAMD1A is a protein that is involved in a variety of cellular processes that are essential for the proper functioning of the brain and other organs. It is a key regulator of the axon, which is the structure that transmits electrical signals along the length of the neuron. In addition, GRAMD1A is involved in the regulation of the cytoskeleton, which is the structure that gives shape to the cell and helps maintain its integrity.

GRAMD1A has also been shown to play an important role in the development and progression of neurodegenerative disorders. For example, studies have shown that GRAMD1A is overexpressed in the brains of individuals with Alzheimer's disease, which is a leading cause of neurodegenerative disorder. In addition,GRAMD1A has also been shown to be involved in the development of other neurodegenerative disorders, including Parkinson's disease and Huntington's disease.

GRAMD1A is also involved in the regulation of cellular processes that are essential for the proper functioning of the heart and kidneys. Studies have shown that GRAMD1A is involved in the regulation of the contractions of the heart muscle and the regulation of the production of urine in the kidneys. In addition,GRAMD1A has also been shown to play an important role in the regulation of the immune system, which is essential for maintaining the health and integrity of the body.

Targeting GRAMD1A

Targeting GRAMD1A is an attractive research topic, as it has the potential to lead to the development of new treatments for a variety of diseases. One approach to targeting GRAMD1A is to develop small molecules that can inhibit its activity. This can be done by using a variety of techniques, including chemical screening, high-throughput screening, and biochemical assays.

Another approach to targeting GRAMD1A is to develop antibodies that can specifically recognize and bind to the protein. This can be done using techniques such as monoclonal antibodies, which are antibodies that are produced by a single cell and can be used to detect and bind to specific proteins.

GRAMD1A as a drug target

Targeting GRAMD1A as a drug target is an attractive research topic, as it has the potential to lead to the development of new treatments for a variety of diseases. By inhibiting the activity of GRAMD1A, researchers may be able to treat a variety of conditions, including neurodegenerative disorders, diabetes, and cancer.

One potential approach to targeting GRAMD1A as a drug

Protein Name: GRAM Domain Containing 1A

Functions: Cholesterol transporter that mediates non-vesicular transport of cholesterol from the plasma membrane (PM) to the endoplasmic reticulum (ER) (By similarity). Contains unique domains for binding cholesterol and the PM, thereby serving as a molecular bridge for the transfer of cholesterol from the PM to the ER (By similarity). Plays a crucial role in cholesterol homeostasis and has the unique ability to localize to the PM based on the level of membrane cholesterol (By similarity). In lipid-poor conditions localizes to the ER membrane and in response to excess cholesterol in the PM is recruited to the endoplasmic reticulum-plasma membrane contact sites (EPCS) which is mediated by the GRAM domain (By similarity). At the EPCS, the sterol-binding VASt/ASTER domain binds to the cholesterol in the PM and facilitates its transfer from the PM to ER (By similarity). May play a role in tumor progression (By similarity). Plays a role in autophagy regulation and is required for biogenesis of the autophagosome (PubMed:31222192). This function in autophagy requires its cholesterol-transfer activity (PubMed:31222192)

The "GRAMD1A 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 GRAMD1A 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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GRAMD1B | GRAMD1C | GRAMD2A | GRAMD2B | GRAMD4 | GRAMD4P2 | GRAMD4P5 | GRAMD4P7 | Granzyme | GRAP | GRAP2 | GRAPL | GRAPL-AS1 | GRASLND | GRB10 | GRB14 | GRB2 | GRB7 | GREB1 | GREB1L | GREM1 | GREM1-AS1 | GREM2 | GREP1 | GRHL1 | GRHL2 | GRHL3 | GRHL3-AS1 | GRHPR | GRIA1 | GRIA2 | GRIA3 | GRIA4 | GRID1 | GRID2 | GRID2IP | GRIFIN | GRIK1 | GRIK1-AS1 | GRIK1-AS2 | GRIK2 | GRIK3 | GRIK4 | GRIK5 | GRIN1 | GRIN2A | GRIN2B | GRIN2C | GRIN2D | GRIN3A | GRIN3B | GRINA | GRIP1 | GRIP2 | GRIPAP1 | GRK1 | GRK2 | GRK3 | GRK4 | GRK5 | GRK6 | GRK7 | GRM1 | GRM2 | GRM3 | GRM4 | GRM5 | GRM5-AS1 | GRM5P1 | GRM6 | GRM7 | GRM7-AS3 | GRM8 | GRM8-AS1 | GRN | Growth Factor Receptor-Bound Protein | GRP | GRPEL1 | GRPEL2 | GRPEL2-AS1 | GRPR | GRSF1 | GRTP1 | GRTP1-AS1 | GRWD1 | GRXCR1 | GRXCR2 | GS1-24F4.2 | GS1-600G8.3 | GSAP | GSC | GSC2 | GSDMA | GSDMB | GSDMC | GSDMD | GSDME | GSE1 | GSEC | GSG1