1. Signaling Pathways
  2. Neuronal Signaling
  3. AAK1

AAK1 

Adaptor-associated Kinase 1; AP2-associated kinase 1

衔接子相关激酶 1 (AAK1),也称为 AP2 相关激酶 1,是一种 104 kDa 丝氨酸/苏氨酸激酶。AAK1 在细胞膜和细胞质中表达。它是一种关键的内吞激酶,已知具有两种生理底物。AAK1 结合并磷酸化 Numb 蛋白 102 位的苏氨酸残基。AAK1 介导的磷酸化已被证明对 Numb 的内吞活性很重要。AAK1 也是衔接子蛋白 2 (AP2) 复合物的相互作用伙伴,AAK1 将 AP-2 募集到质膜。AAK1 对 AP2 (AP2M1) µ 亚基中苏氨酸残基的磷酸化增加了其对某些膜受体的特定酪氨酸或二亮氨酸分类信号的结合亲和力。它可增强货物募集、囊泡组装和有效内化。AAK1 还参与调节各种信号通路,例如 Notch 通路。研究表明,AAK1 可直接与配体激活的 Notch 相互作用,但不与无活性的全长受体相互作用。

Adaptor-associated kinase 1 (AAK1), also known as AP2-associated kinase 1, is a 104 kDa serine/threonine kinase. AAK1 is expressed within the cell in the membrane and cytoplasm. It is a key endocytic kinase that is known to have two physiological substrates. AAK1 binds and phosphorylates the threonine residue at position 102 of the Numb protein. AAK1-mediated phosphorylation has been shown to be important for the endocytic activity of Numb. AAK1 is also an interacting partner of the adaptor protein 2 (AP2) complex and AAK1 recruits AP-2 to the plasma membrane. Phosphorylation of the threonine residue in the µ–subunit of AP2 (AP2M1) by AAK1 increases its binding affinity for specific tyrosine- or dileucine-based sorting signals of certain membrane receptors. It enhances cargo recruitment, vesicle assembly, and efficient internalization. AAK1 is also implicated in the regulation of various signaling pathways, such as the Notch pathway. It has been shown that AAK1 directly interacts with ligand activated Notch, but not with the inactive fulllength receptor.

Cat. No. Product Name Effect Purity Chemical Structure
  • HY-147083
    SGC-AAK1-1N Inhibitor
    SGC-AAK1-1N 是一种有效且选择性的 AAK1 (AP2 相关激酶 1) 抑制剂,其 IC50 值为 1.8 μM。
    SGC-AAK1-1N
  • HY-161261
    SARS-CoV-2-IN-81 Inhibitor
    SARS-CoV-2-IN-81 (compound 12e) 是一种有效的 AAK1 抑制剂,IC50 值为 9.38 nM。SARS-CoV-2-IN-81 显示出针对 SARS-CoV-2 的抗病毒特性。SARS-CoV-2-IN-81 减弱 AAK1 诱导的 AP2M1 苏氨酸 156 磷酸化,并破坏 AP2M1 和 ACE2 之间的直接相互作用,最终抑制 SARS-CoV-2 感染。
    SARS-CoV-2-IN-81
  • HY-144301A
    AAK1-IN-2 TFA
    AAK1-IN-2 TFA (compound (S)-31) 是一种有效的、选择性的和可透过血脑屏障的 AAK1 抑制剂,IC50 值为 5.8 nM。AAK1-IN-2 TFA 可用于神经性疼痛的研究。
    AAK1-IN-2 TFA
  • HY-144301
    AAK1-IN-2
    AAK1-IN-2 (compound (S)-31) 是一种有效的、选择性的和可透过血脑屏障的 AAK1 抑制剂,IC50 值为 5.8 nM。AAK1-IN-2 可用于神经性疼痛的研究。
    AAK1-IN-2
  • HY-145838
    AAK1-IN-4
    AAK1-IN-4 是一种具有高选择性、可透过血脑屏障以及口服活性的接头蛋白2相关激酶1 (adaptor protein-2-associated kinase 1, AAK1) 抑制剂 (AAK1 IC50=4.6 nM, Filt Ki=0.9 nM, cell IC50=8.6 nM)。AAK1-IN-4 具有研究神经性疼痛的潜力。
    AAK1-IN-4
  • HY-159879
    AAK1-IN-6 Inhibitor
    AAK1-IN-6 (化合物 23) 是 AP-2 相关蛋白激酶 1 的抑制剂 (AAK1, IC50 = 12 nM),对登革病毒 (DNEV2, EC50 = 0.24 μM) 和委内瑞拉马脑炎病毒 (VEEV, EC50 = 0.30 μM) 具有抗病毒活性。AAK1-IN-6 可用于抗病毒研究。
    AAK1-IN-6
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