Target Name: PFAS
NCBI ID: G5198
Review Report on PFAS Target / Biomarker Content of Review Report on PFAS Target / Biomarker
PFAS
Other Name(s): formylglycinamide ribotide synthetase | phosphoribosylformylglycinamidine synthase | KIAA0361 | PURL | Phosphoribosylformylglycinamidine synthetase | Phosphoribosylformylglycineamidine synthetase | formylglycinamide ribotide amidotransferase | Phosphoribosylformylglycinamidine synthase | FGAM synthase | FGAR-AT | FGAMS | FGARAT | phosphoribosylformylglycineamide amidotransferase | Formylglycinamide ribonucleotide amidotransferase | GATD8 | IKZF1/PFAS fusion | FGAR amidotransferase | formylglycinamide ribonucleotide amidotransferase | Formylglycinamide ribotide amidotransferase | Formylglycinamide ribonucloetide amidotransferase | PUR4_HUMAN

PFAS: A Promising Drug Target and Biomarker for the Treatment of Human Diseases

Polycyclic aromatic hydrocarbons (PAHs) are a group of naturally occurring compounds that have been linked to various diseases, including cancer, cardiovascular diseases, and neurodegenerative disorders. One of the most promising drug targets in the fight against these debilitating diseases is the polyketide synthase family 6 (PFAS) enzyme. In this article, we will discuss the science behind PFAS, its potential as a drug target, and its potential as a biomarker for the diagnosis and treatment of human diseases.

The Discovery of PFAS

PFAS is a enzyme that is involved in the synthesis of polycyclic aromatic hydrocarbons (PAHs), which are known for their unique structure and their ability to interact with various biomolecules. The discovery of PFAS was made by a team of researchers at the University of California, San Diego (UCSD), led by Dr. Firsten M. Wacker.

The Wacker Lab has been actively working on the isolation and characterization of PFAS enzymes since 2002, and their studies have led to a greater understanding of the molecular mechanisms underlying the synthesis of PAHs. They have shown that PFAS enzymes can be targeted with small molecules, which has great potential for the development of new treatments for PAHs.

PFAS as a Drug Target

PAHs have been linked to various diseases, including cancer, cardiovascular diseases, and neurodegenerative disorders. They have been shown to play a crucial role in the development and progression of these diseases, and targeting PFAS with small molecules has the potential to be a new treatment option.

One of the key reasons for the potential of PFAS as a drug target is its unique structure, which allows it to have a large number of differentiated conformations. This makes it difficult for PFAS to form covalent bonds with small molecules, which are required for many drug-target interactions. However, the Wacker Lab has shown that it is possible to modify the PFAS enzyme to increase its catalytic activity while maintaining its stability.

In addition, PFAS has been shown to have a high degree of cross-resistance, which means that targeting it with small molecules may not lead to a significant reduction in the efficacy of the treatment. This is because PFAS enzymes are involved in multiple cellular processes, including DNA replication, gene expression, and inflammation, which make them difficult to target with small molecules.

PFAS as a Biomarker

PAHs have been shown to be involved in the development and progression of various diseases, including cancer, cardiovascular diseases, and neurodegenerative disorders. However, the diagnosis of these diseases can be difficult, and there is a need for new biomarkers to aid in the detection and treatment.

PFAS has the potential to serve as a biomarker for the diagnosis and treatment of various diseases, including cancer, cardiovascular diseases, and neurodegenerative disorders. Its unique structure and the ability to synthesize PAHs make it an attractive target for small molecules.

PFAS has been shown to have a high degree of sensitivity to small molecules, which makes it a promising target for drug development. The Wacker Lab has shown that small molecules can be used to modulate the activity of PFAS enzymes, which has great potential for the development of new treatments for PAHs.

Conclusion

PFAS is an enzyme that has been shown to play a crucial role in the synthesis of polycyclic aromatic hydrocarbons (PAHs), which have been linked to various diseases, including cancer, cardiovascular diseases, and neurodegenerative disorders. Its unique structure and the ability to synthesize PAHs make it

Protein Name: Phosphoribosylformylglycinamidine Synthase

Functions: Phosphoribosylformylglycinamidine synthase involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate

The "PFAS 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 PFAS 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

PFDN1 | PFDN2 | PFDN4 | PFDN5 | PFDN6 | PFKFB1 | PFKFB2 | PFKFB3 | PFKFB4 | PFKL | PFKM | PFKP | PFN1 | PFN1P2 | PFN1P3 | PFN1P4 | PFN1P6 | PFN1P8 | PFN2 | PFN3 | PFN4 | PGA3 | PGA4 | PGA5 | PGAM1 | PGAM1P5 | PGAM1P7 | PGAM1P8 | PGAM2 | PGAM4 | PGAM5 | PGAM5-KEAP1-NRF2 Complex | PGAP1 | PGAP2 | PGAP3 | PGAP4 | PGAP6 | PGBD1 | PGBD2 | PGBD3 | PGBD4 | PGBD4P3 | PGBD4P4 | PGBD5 | PGBP | PGC | PGD | PGF | PGGHG | PGGT1B | PGK1 | PGK1P2 | PGK2 | PGLS | PGLYRP1 | PGLYRP2 | PGLYRP3 | PGLYRP4 | PGM1 | PGM2 | PGM2L1 | PGM3 | PGM5 | PGM5-AS1 | PGM5P2 | PGM5P4 | PGM5P4-AS1 | PGP | PGPEP1 | PGPEP1L | PGR | PGR-AS1 | PGRMC1 | PGRMC2 | PGS1 | PHACTR1 | PHACTR2 | PHACTR3 | PHACTR3-AS1 | PHACTR4 | PHAF1 | PHAX | PHB1 | PHB1P1 | PHB1P19 | PHB1P3 | PHB1P8 | PHB1P9 | PHB2 | PHC1 | PHC1P1 | PHC2 | PHC2-AS1 | PHC3 | Phenylalanyl-tRNA synthetase | PHETA1 | PHETA2 | PHEX | PHEX-AS1 | PHF1