SETMAR, also known as SET Nuclear Proto-Oncogene and Transposase MARiner 1, is a bifunctional enzyme that possesses both histone methyltransferase (HMT) and DNA transposase activities. This unique dual functionality allows SETMAR to participate in various cellular processes, including chromatin remodeling, DNA repair, and genome stability. SETMAR inhibitors interact with the active sites or binding domains of this enzyme, thereby disrupting its normal functions and potentially impacting critical cellular processes dependent on SETMAR activity.
By inhibiting SETMAR, these compounds have the potential to interfere with its HMT and DNA transposase activities, which can result in alterations to chromatin structure and genome stability. The study of SETMAR inhibitors is of significant interest to researchers as it provides insights into the regulatory mechanisms governing these essential cellular functions. This knowledge contributes to our understanding of basic cell biology and may have implications in various research areas, such as epigenetics, DNA repair mechanisms, and genome integrity.
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