| Literature DB >> 7839144 |
B Dérijard1, J Raingeaud, T Barrett, I H Wu, J Han, R J Ulevitch, R J Davis.
Abstract
Mammalian mitogen-activated protein (MAP) kinases include extracellular signal-regulated protein kinase (ERK), c-Jun amino-terminal kinase (JNK), and p38 subgroups. These MAP kinase isoforms are activated by dual phosphorylation on threonine and tyrosine. Two human MAP kinase kinases (MKK3 and MKK4) were cloned that phosphorylate and activate p38 MAP kinase. These MKK isoforms did not activate the ERK subgroup of MAP kinases, but MKK4 did activate JNK. These data demonstrate that the activators of p38 (MKK3 and MKK4), JNK (MKK4), and ERK (MEK1 and MEK2) define independent MAP kinase signal transduction pathways.Entities:
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Year: 1995 PMID: 7839144 DOI: 10.1126/science.7839144
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728