PDK1-IN-RS2 is a mimic of peptide docking motif (PIFtide) and is a substrate-selective PDK1 inhibitor with a K d of 9 μM. PDK1-IN-RS2 suppresses the activation of the downstream kinases S6K1 by PDK1
In Vitro
PDK1-IN-RS2 stimulates the catalytic activity of PDK1 toward a peptide substrate by sixfold. The sulfonyl group of PDK1-IN-RS2 interacts with Arg131 through a salt bridge, because the sulfonamide is likely ionized under the crystallization conditions. MCE has not independently confirmed the accuracy of these methods. They are for reference only.
Form:Solid
IC50& Target:Kd: 9 μM (PDK1)
规格
别名
PDK1-输入-RS2
规格或纯度
≥98%
英文名称
PDK1-IN-RS2
生化机理
PDK1-IN-RS2 是肽对接基序(PIFtide)的模拟物,是一种底物选择性 PDK1 抑制剂,其 K d 为 9 μM。PDK1-IN-RS2 可抑制 PDK1 对下游激酶 S6K1 的激活。