Literature DB >> 7839144

Independent human MAP-kinase signal transduction pathways defined by MEK and MKK isoforms.

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.

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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


  396 in total

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8.  NIK is a new Ste20-related kinase that binds NCK and MEKK1 and activates the SAPK/JNK cascade via a conserved regulatory domain.

Authors:  Y C Su; J Han; S Xu; M Cobb; E Y Skolnik
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9.  Inhibition of pancreatic cancer Panc1 cell migration by omeprazole is dependent on aryl hydrocarbon receptor activation of JNK.

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10.  c-Jun N-terminal protein kinase 1 (JNK1), but not JNK2, is essential for tumor necrosis factor alpha-induced c-Jun kinase activation and apoptosis.

Authors:  Jing Liu; Yuzuru Minemoto; Anning Lin
Journal:  Mol Cell Biol       Date:  2004-12       Impact factor: 4.272

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