Title : Tumor necrosis factor-alpha-induced IKK phosphorylation of NF-kappaB p65 on serine 536 is mediated through the TRAF2, TRAF5, and TAK1 signaling pathway.

Pub. Date : 2003 Sep 19

PMID : 12842894






6 Functional Relationships(s)
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1 Tumor necrosis factor-alpha-induced IKK phosphorylation of NF-kappaB p65 on serine 536 is mediated through the TRAF2, TRAF5, and TAK1 signaling pathway. Serine v-rel reticuloendotheliosis viral oncogene homolog A (avian) Mus musculus
2 Here, we characterized the intracellular signaling pathway leading to phosphorylation of p65 on Ser-536 using a novel anti-phospho-p65 (Ser-536) antibody. Serine v-rel reticuloendotheliosis viral oncogene homolog A (avian) Mus musculus
3 Here, we characterized the intracellular signaling pathway leading to phosphorylation of p65 on Ser-536 using a novel anti-phospho-p65 (Ser-536) antibody. Serine v-rel reticuloendotheliosis viral oncogene homolog A (avian) Mus musculus
4 Here, we characterized the intracellular signaling pathway leading to phosphorylation of p65 on Ser-536 using a novel anti-phospho-p65 (Ser-536) antibody. Serine v-rel reticuloendotheliosis viral oncogene homolog A (avian) Mus musculus
5 Here, we characterized the intracellular signaling pathway leading to phosphorylation of p65 on Ser-536 using a novel anti-phospho-p65 (Ser-536) antibody. Serine v-rel reticuloendotheliosis viral oncogene homolog A (avian) Mus musculus
6 The Ser-536 of endogenous p65 was rapidly phosphorylated in response to a wide variety of NF-kappaB stimulants including TNF-alpha in the cytoplasm and rapidly dephosphorylated in the nucleus. Serine v-rel reticuloendotheliosis viral oncogene homolog A (avian) Mus musculus