Vac17p Inhibitors predominantly target vesicle trafficking and the cytoskeletal dynamics, providing a pathway-centric avenue to indirectly modulate the activity or function of Vac17p. One of the notable features of these chemicals is their interference with pivotal cellular processes. For instance, Wortmannin and LY294002 target PI3K, a linchpin in various cellular pathways including vesicle trafficking. Similarly, Dynasore, which inhibits the GTPase activity of dynamin, has profound effects on vesicle scission, a step integral to vesicle formation and transport.
Another avenue that these inhibitors employ to potentially regulate Vac17p-associated processes is by modulating the cellular cytoskeleton. Compounds like Nocodazole and Cytochalasin D interfere with the dynamics of microtubules and actin filaments, respectively. Given the significance of the cytoskeleton in vesicle transport, it's plausible that altering its dynamics can indirectly affect proteins involved in the vesicle transport machinery, such as Vac17p.
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