ANKAR inhibitors represent a distinct class of chemical compounds that target specific protein-protein interactions within cellular signaling pathways. The name ANKAR is derived from the ankyrin repeat (ANK) domains, which are structural motifs commonly found in a variety of proteins. Ankyrin repeats are known for their role in mediating protein-protein interactions, as they form stacked helical arrays that create a stable interface for binding. ANKAR inhibitors are designed to disrupt these interactions by binding to the ankyrin repeats or their binding partners, thereby preventing the formation of larger protein complexes that rely on these domains for assembly or function. By interfering with the structural integrity of these complexes, ANKAR inhibitors can modulate key cellular processes such as signaling cascades, gene expression regulation, or cell cycle progression.
The chemical diversity of ANKAR inhibitors is wide, with structures ranging from small molecules to larger peptides or peptidomimetics, reflecting the versatility required to target different types of ankyrin repeat-containing proteins. These inhibitors often exploit specific hydrophobic or electrostatic interactions within the ankyrin repeat domains to achieve high specificity and affinity. In some cases, ANKAR inhibitors are designed to mimic the natural binding partners of ankyrin repeats, while in others, they take advantage of induced conformational changes that disrupt the structural stability of the repeat arrays. The ability of ANKAR inhibitors to selectively modulate protein-protein interactions at the molecular level makes them valuable tools for studying the functional roles of ankyrin repeat-containing proteins in cellular systems.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
ZM-447439 | 331771-20-1 | sc-200696 sc-200696A | 1 mg 10 mg | $150.00 $349.00 | 15 | |
An Aurora kinase inhibitor, ZM-447439 can prevent the phosphorylation of substrates of Aurora kinases, affecting cell division processes. | ||||||
Thapsigargin | 67526-95-8 | sc-24017 sc-24017A | 1 mg 5 mg | $94.00 $349.00 | 114 | |
An inhibitor of the sarcoplasmic/endoplasmic reticulum Ca2+ ATPase (SERCA), thapsigargin can disrupt calcium homeostasis and affect proteins regulated by calcium signaling. | ||||||