Ste11 activators are a class of chemical compounds known for their ability to selectively activate Ste11, a kinase enzyme that plays a pivotal role in various cellular signaling pathways. These activators are recognized for their specificity in targeting and modulating the activity of Ste11, which is crucial for the regulation of cell growth, differentiation, and stress response mechanisms in eukaryotic cells. The interaction between Ste11 activators and their target enzyme is a subject of intense research focus, as understanding the molecular details of this interaction can provide insights into the fundamental processes governing cellular behavior. These activators bind to Ste11 in a manner that alters its conformation, thereby enhancing its kinase activity. This modulation is achieved through the direct interaction of the activator with specific domains of the enzyme, leading to an increase in its catalytic efficiency towards downstream substrates.
The identification and development of Ste11 activators involve sophisticated methodologies that span both computational and experimental approaches. Following this, computational modeling and molecular docking techniques are employed to predict the binding affinity and orientation of these compounds to the Ste11 enzyme. This in silico analysis is crucial for understanding the interaction dynamics and for guiding the chemical modification of candidate compounds to improve their efficacy and specificity. Subsequently, detailed biochemical assays are conducted to validate the activator's function, including kinase assays to measure the increase in Ste11 activity in the presence of the compound. Additionally, structural biology techniques such as X-ray crystallography and nuclear magnetic resonance (NMR) spectroscopy are utilized to elucidate the atomic-level details of the activator-Ste11 interaction. This comprehensive approach ensures a deep understanding of how Ste11 activators engage with their target, paving the way for the exploration of their biological significance in cellular signaling networks.
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Sodium Chloride | 7647-14-5 | sc-203274 sc-203274A sc-203274B sc-203274C | 500 g 2 kg 5 kg 10 kg | $18.00 $23.00 $35.00 $65.00 | 15 | |
High concentrations of salt can cause osmotic stress, possibly leading to the activation of Ste11 in osmoregulatory pathways. | ||||||
D-Sorbitol | 50-70-4 | sc-203278A sc-203278 | 100 g 1 kg | $28.00 $68.00 | ||
Sorbitol can induce osmotic pressure changes in yeast, potentially affecting the expression of Ste11. | ||||||
Hydrogen Peroxide | 7722-84-1 | sc-203336 sc-203336A sc-203336B | 100 ml 500 ml 3.8 L | $30.00 $60.00 $93.00 | 27 | |
As an oxidative stressor, hydrogen peroxide may indirectly upregulate stress response pathways involving Ste11. | ||||||
Methylglyoxal solution | 78-98-8 | sc-250394 sc-250394A sc-250394B sc-250394C sc-250394D | 25 ml 100 ml 250 ml 500 ml 1 L | $143.00 $428.00 $469.00 $739.00 $1418.00 | 3 | |
A byproduct of glycolysis that can cause glycation damage and stress responses, potentially influencing Ste11 expression. | ||||||
Lithium | 7439-93-2 | sc-252954 | 50 g | $214.00 | ||
Lithium salts are known to affect yeast MAP kinase pathways and could therefore impact Ste11 expression. | ||||||
Congo Red | 573-58-0 | sc-359843 sc-359843A sc-359843B sc-359843C | 25 g 100 g 250 g 1 kg | $36.00 $87.00 $178.00 $495.00 | 4 | |
Similar to Calcofluor white, Congo red affects cell wall integrity and may influence Ste11-related pathways. |