Target Name: Phosphatidylinositol N-acetylglucosaminyltransferase
NCBI ID: P14886
Review Report on Phosphatidylinositol N-acetylglucosaminyltransferase Target / Biomarker Content of Review Report on Phosphatidylinositol N-acetylglucosaminyltransferase Target / Biomarker
Phosphatidylinositol N-acetylglucosaminyltransferase
Other Name(s): None

Understanding P-GALT: Potential Drug Target and Biomarker

Phosphatidylinositol N-acetylglucosaminyltransferase (P-GALT) is a protein that plays a crucial role in cellular signaling. It is a key enzyme in the PI3K/Akt signaling pathway, which is involved in a wide range of cellular processes including cell survival, proliferation, and angiogenesis. P-GALT is also a potential drug target and biomarker for several diseases, including cancer, neurodegenerative diseases, and autoimmune disorders.

P-GALT is a protein that is expressed in most tissues and cells in the body. It is a 21-kDa protein that consists of 214 amino acid residues. P-GALT is localized to the endoplasmic reticulum (ER) and is predominantly expressed in the liver, heart, and pancreas. It is also expressed in other tissues, including the placenta, brain, and testes.

P-GALT is involved in the synthesis of phosphatidylinositol (PI), which is a key signaling molecule in the PI3K/Akt signaling pathway. PI is a hydrophilic molecule that can interact with various signaling molecules, including P-GALT. P-GALT is the first enzyme in the PI3K/Akt pathway, and its activity is essential for the formation of IP3 and the activation of the downstream signaling pathway.

P-GALT is also involved in the synthesis of N-acetylglucosaminyltransferase (NAGL), which is a critical enzyme in the glycosylation of proteins. NAGL is a 22-kDa protein that consists of 208 amino acid residues. It is expressed in most tissues and cells and is responsible for the N-acetylation of the lysine residue on the N-terminus of target proteins. The N-acetylation of proteins is a critical modification that can affect protein stability, localization, and interactions with other molecules.

P-GALT is a potential drug target because of its involvement in the PI3K/Akt signaling pathway. Many diseases, including cancer, neurodegenerative diseases, and autoimmune disorders, are caused by the abnormal activity of the PI3K/Akt signaling pathway. P-GALT is a key enzyme in this pathway, and its activity can be inhibited by small molecules such as inhibitors of the PI3K/Akt signaling pathway. This suggests that P-GALT may be a useful target for the treatment of diseases that are caused by the abnormal activity of the PI3K/Akt signaling pathway.

P-GALT is also a potential biomarker for several diseases. The PI3K/Akt signaling pathway is involved in many cellular processes, including cell survival, angiogenesis, and inflammation. Therefore, changes in the activity of P-GALT may be indicative of the presence of certain diseases. For example, P-GALT activity has been used as a biomarker for cancer, as it has been shown to be increased in the blood of patients with various types of cancer. Additionally, P-GALT has been used as a biomarker for neurodegenerative diseases, as changes in its activity have been observed in the brain in patients with conditions such as Alzheimer's disease and Parkinson's disease.

In conclusion, P-GALT is a protein that is involved in the PI3K/Akt signaling pathway and is expressed in most tissues and cells in the body. It is a potential drug target and biomarker for several diseases, including cancer, neurodegenerative diseases, and autoimmune disorders. Further research is needed to fully understand the role of P-GALT in cellular signaling and its potential as a drug target and biomarker.

Protein Name: Phosphatidylinositol N-acetylglucosaminyltransferase

The "Phosphatidylinositol N-acetylglucosaminyltransferase 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 Phosphatidylinositol N-acetylglucosaminyltransferase 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

Phosphatidylinositol-5-phosphate 4-kinase | PHOSPHO1 | PHOSPHO2 | PHOSPHO2-KLHL23 | Phosphodiesterase | Phosphodiesterase 1 (PDE1) | Phosphodiesterase 6 (PDE6) | Phosphodiesterase 8 (nons | Phosphodiesterase IV (PDE4) | Phosphoglucomutase 5 pseudogene 1 | Phosphoglycerate kinase | Phospholipase A | Phospholipase A2 | Phospholipase A2, Cytosolic | Phospholipase A2, Secretory (sPLA2) | Phospholipase C | Phospholipase D | Phosphorylase kinase | PHOX2A | PHOX2B | PHPT1 | PHRF1 | PHTF1 | PHTF2 | PHYH | PHYHD1 | PHYHIP | PHYHIPL | PHYKPL | PI15 | PI16 | PI3 | PI4K2A | PI4K2B | PI4KA | PI4KAP1 | PI4KAP2 | PI4KB | PIANP | PIAS1 | PIAS2 | PIAS3 | PIAS4 | PIBF1 | PICALM | PICART1 | PICK1 | PICSAR | PID1 | PIDD1 | PIERCE1 | PIERCE2 | PIEZO1 | PIEZO2 | PIF1 | PIFO | PIGA | PIGB | PIGBOS1 | PIGC | PIGF | PIGG | PIGH | PIGK | PIGL | PIGM | PIGN | PIGO | PIGP | PIGQ | PIGR | PIGS | PIGT | PIGU | PIGV | PIGW | PIGX | PIGY | PIGZ | PIH1D1 | PIH1D2 | PIK3AP1 | PIK3C2A | PIK3C2B | PIK3C2G | PIK3C3 | PIK3CA | PIK3CA-DT | PIK3CB | PIK3CD | PIK3CD-AS1 | PIK3CD-AS2 | PIK3CG | PIK3IP1 | PIK3IP1-DT | PIK3R1 | PIK3R2 | PIK3R3 | PIK3R4 | PIK3R5