V1RH21 inhibitors are a class of chemical compounds designed to selectively interact with the V1RH21 protein, a component of the vacuolar-type H+-ATPase (V-ATPase) complex. This complex is integral to various cellular processes, primarily through its role in establishing and maintaining acidic environments within intracellular compartments such as lysosomes, endosomes, and vacuoles. The V1RH21 protein is part of the V1 domain of the V-ATPase, contributing to the ATP hydrolysis mechanism that drives proton transport across membranes. By influencing the function of this protein, V1RH21 inhibitors affect the activity of the entire V-ATPase complex.
The mechanism of action of V1RH21 inhibitors involves binding to the V1RH21 protein and disrupting its interaction with other subunits within the V1 domain. This binding interference impairs the assembly and stability of the V-ATPase complex, thereby affecting its ability to hydrolyze ATP effectively and pump protons. The inhibition of V1RH21 disrupts the acidification processes that are crucial for numerous cellular functions, including protein sorting, receptor-mediated endocytosis, and cellular homeostasis. Through this specific interaction, V1RH21 inhibitors provide valuable insights into the structural and functional dynamics of the V-ATPase complex, as well as the role of V1RH21 in proton transport and intracellular pH regulation.
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