ATP13A3 activators are a category of compounds known for their ability to modulate the activity of ATP13A3, a type of P-type ATPase that is integral to cellular physiology. ATP13A3 is a transmembrane protein that plays a crucial role in the transport of ions across cellular membranes, utilizing ATP hydrolysis to drive these processes. The activators of ATP13A3 are diverse in their chemical composition, ranging from small organic molecules to larger biomolecular entities. These compounds interact with ATP13A3 in a manner that enhances its ATPase activity, thereby potentially affecting ion homeostasis and membrane potential within cells. The interaction between these activators and ATP13A3 can occur through various mechanisms, including direct binding to the protein, which may induce conformational changes that enhance its enzymatic activity, or through indirect pathways that modulate the protein's environment or its regulatory factors, thereby influencing its activity.
The exploration of ATP13A3 activators encompasses detailed biochemical and biophysical studies aimed at understanding the precise mechanisms by which these compounds influence ATP13A3 function. This involves investigations into the binding affinity, specificity, and the resultant structural alterations in ATP13A3 upon activator interaction. Such studies are critical for elucidating the molecular dynamics at play, including how activators impact ATP hydrolysis and ion transport processes mediated by ATP13A3. Researchers employ a variety of techniques, including crystallography, spectroscopy, and computational modeling, to gain insights into the interactions between ATP13A3 and its activators. This research not only deepens our understanding of ATP13A3's role in cellular physiology but also contributes to the broader field of membrane transport and the complex regulatory networks that maintain cellular function. Through these studies, the scientific community aims to unravel the intricate balance of ion transport and its regulation, shedding light on the fundamental processes that underpin cellular life.
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Spironolactone | 52-01-7 | sc-204294 | 50 mg | $107.00 | 3 | |
A potassium-sparing diuretic that may indirectly affect ion transport gene expression through its interaction with aldosterone receptors. | ||||||
Amiloride • HCl | 2016-88-8 | sc-3578 sc-3578A | 25 mg 100 mg | $22.00 $56.00 | 6 | |
Functions as a diuretic, potentially altering the expression of ion channels and transporters by modulating cellular ion balance. | ||||||
Ouabain-d3 (Major) | sc-478417 | 1 mg | $506.00 | |||
Known as a cardiac glycoside inhibiting the Na+/K+ ATPase pump which may influence the expression of other ion transporters. | ||||||
12β-Hydroxydigitoxin | 20830-75-5 | sc-213604 sc-213604A | 1 g 5 g | $140.00 $680.00 | ||
Another cardiac glycoside that inhibits Na+/K+ ATPase activity, possibly leading to compensatory effects on the expression of ion transport genes. | ||||||
Verapamil | 52-53-9 | sc-507373 | 1 g | $367.00 | ||
A calcium channel blocker that might affect calcium homeostasis, potentially influencing the expression of genes that regulate ion transport. | ||||||
Nifedipine | 21829-25-4 | sc-3589 sc-3589A | 1 g 5 g | $58.00 $170.00 | 15 | |
Also a calcium channel blocker that may have effects on the expression of calcium transporters and channels in cells. | ||||||
Diazoxide | 364-98-7 | sc-200980 | 1 g | $300.00 | 5 | |
Opens KATP channels, which could subsequently modulate the expression of genes related to ion transport in response to K+ flux changes. | ||||||
Nicorandil | 65141-46-0 | sc-200995 sc-200995B sc-200995A sc-200995C | 50 mg 100 mg 250 mg 1 g | $57.00 $98.00 $240.00 $500.00 | 4 | |
Acts as a KATP channel opener and a nitric oxide donor, which might affect gene expression related to ion channels. | ||||||
Hydrochlorothiazide | 58-93-5 | sc-207738 sc-207738A sc-207738B sc-207738C sc-207738D | 5 g 25 g 50 g 100 g 250 g | $54.00 $235.00 $326.00 $551.00 $969.00 | ||
A thiazide diuretic that could indirectly influence the expression of various ion transporters due to its diuretic action. | ||||||
Captopril | 62571-86-2 | sc-200566 sc-200566A | 1 g 5 g | $48.00 $89.00 | 21 | |
An ACE inhibitor that may alter the regulation of genes involved in electrolyte balance as a result of its effects on the renin-angiotensin system. |