PheRS inhibitors are a class of chemical compounds designed to target and inhibit the activity of phenylalanyl-tRNA synthetase (PheRS), an enzyme essential for protein synthesis in cells. PheRS is responsible for catalyzing the attachment of the amino acid phenylalanine to its corresponding tRNA molecule during translation. This process, known as aminoacylation, is a critical step in ensuring that phenylalanine is incorporated accurately into the growing polypeptide chain according to the mRNA sequence. By inhibiting PheRS, these compounds interfere with the aminoacylation process, disrupting the proper incorporation of phenylalanine into proteins, which can lead to errors in protein synthesis and cellular dysfunction.
PheRS inhibitors are widely used in research to explore the fundamental mechanisms of protein synthesis and to understand the broader effects of disrupted amino acid incorporation on cellular processes. By blocking PheRS activity, researchers can study how phenylalanine deficiency at the translational level impacts cellular metabolism, protein folding, and overall protein homeostasis. These inhibitors also provide insights into the specificity of aminoacyl-tRNA synthetases and the importance of precise amino acid-tRNA pairing for maintaining the fidelity of the genetic code. PheRS inhibitors serve as valuable tools for studying the critical role of aminoacyl-tRNA synthetases in translation, as well as the consequences of disrupting protein synthesis on cellular functions such as growth, division, and response to environmental cues. Through these studies, scientists can gain a deeper understanding of the intricate processes that govern gene expression and protein biosynthesis.
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