| Modification Notes |
Activation of NFkB requires that IkB be phosphorylated on specific serine residues, which results in targeted degradation of IkB. IkB kinase å (IKKå), previously designated CHUK, interacts with IkB-å and specifically phosphorylates IkB-å on the sites that trigger its degradation, serines 32 and 36. IKKå appears to be critical for NFkB activation in response to proinflammatory cytokines. Phosphorylation of IkB by IKKå is stimulated by the NFkB inducing kinase (NIK), which itself is a central regulator for NFkB activation in response to TNF and IL-1. The functional IKK complex contains three subunits, IKKå, IKK∫ and IKK© (also designated NEMO), and each appear to make essential contributions to IkB phosphorylation. The IKK∫ phosphorylates human IKK© at Ser-31, Ser-43, and Ser-376 following the enforced expression of either the Tax oncoprotein or the type 1 TNF receptor. |