V1RH2 inhibitors are a class of chemical compounds specifically targeting the V1RH2 protein, which is a part of the vacuolar-type H+-ATPase (V-ATPase) complex. The V-ATPase complex is crucial for acidifying various intracellular compartments such as lysosomes, endosomes, and vacuoles by using energy from ATP hydrolysis to pump protons across membranes. The V1RH2 protein is located in the V1 domain of this complex and is involved in the ATP hydrolysis process that drives the proton pump mechanism. Inhibitors of V1RH2 are designed to interact with this protein and disrupt its function, thereby impacting the overall activity of the V-ATPase.
The mechanism of action of V1RH2 inhibitors involves binding to the V1RH2 protein, which can interfere with the protein's ability to participate in ATP hydrolysis. By doing so, these inhibitors can affect the assembly and stability of the V1 domain of the V-ATPase complex. This disruption hinders the enzyme's function in proton transport and intracellular compartment acidification. The impact of these inhibitors on V1RH2 provides valuable insights into the role of this protein within the V-ATPase complex, shedding light on the broader implications of V-ATPase activity in cellular functions such as pH regulation and vesicular trafficking. Through their specific interaction with V1RH2, these compounds offer a way to explore and understand the functional contributions of V1RH2 to the V-ATPase machinery.
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