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rdf:type |
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lifeskim:mentions |
umls-concept:C0015744,
umls-concept:C0031715,
umls-concept:C0109317,
umls-concept:C0205145,
umls-concept:C0752312,
umls-concept:C1150579,
umls-concept:C1333340,
umls-concept:C1334474,
umls-concept:C1366882,
umls-concept:C1370600,
umls-concept:C1514873,
umls-concept:C1515655,
umls-concept:C1533691,
umls-concept:C1546857,
umls-concept:C1556066,
umls-concept:C1619636,
umls-concept:C1705767,
umls-concept:C1705791,
umls-concept:C1879547,
umls-concept:C2911691
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pubmed:issue |
48
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pubmed:dateCreated |
1999-12-29
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pubmed:abstractText |
An ERK2-binding site at the N terminus of MEK1 was reported to mediate their stable association. We examined the importance of this binding site in the feedback phosphorylation of MEK1 on Thr(292) and Thr(386) by ERK2, the phosphorylation and activation of ERK2 by MEK1, and the interaction of MEK1 with ERK2 and Raf-1. Deletion of the binding site from MEK1 reduced its phosphorylation by ERK2, but had no effect on its phosphorylation by p21-activated protein kinase-1 (PAK1). A MEK1 N-terminal peptide containing the binding site inhibited MEK1 phosphorylation by ERK2. However, it did not affect MEK1 phosphorylation by p21-activated protein kinase or myelin basic protein phosphorylation by ERK2. Deletion of the N-terminal ERK-binding domain of MEK1 also reduced its ability to phosphorylate ERK2 in vitro, to co-immunoprecipitate with ERK2, and to stimulate ERK2 activation in transfected cells, but it did not alter the association with endogenous Raf-1. Using ERK2-p38 chimeras and an ERK2 deletion mutant, a MEK1-binding site of ERK2 was localized to its N terminus.
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pubmed:grant |
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/MAP Kinase Kinase 1,
http://linkedlifedata.com/resource/pubmed/chemical/MAP2K1 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Mitogen-Activated Protein Kinase 1,
http://linkedlifedata.com/resource/pubmed/chemical/Mitogen-Activated Protein Kinase...,
http://linkedlifedata.com/resource/pubmed/chemical/Mitogen-Activated Protein Kinases,
http://linkedlifedata.com/resource/pubmed/chemical/Oligopeptides,
http://linkedlifedata.com/resource/pubmed/chemical/PAK1 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Protein-Serine-Threonine Kinases,
http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins c-raf,
http://linkedlifedata.com/resource/pubmed/chemical/Threonine,
http://linkedlifedata.com/resource/pubmed/chemical/p21-Activated Kinases
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pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
0021-9258
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:day |
26
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pubmed:volume |
274
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
34029-35
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:10567369-Amino Acid Sequence,
pubmed-meshheading:10567369-Binding, Competitive,
pubmed-meshheading:10567369-Binding Sites,
pubmed-meshheading:10567369-Cell Line,
pubmed-meshheading:10567369-Enzyme Activation,
pubmed-meshheading:10567369-Humans,
pubmed-meshheading:10567369-MAP Kinase Kinase 1,
pubmed-meshheading:10567369-Mitogen-Activated Protein Kinase 1,
pubmed-meshheading:10567369-Mitogen-Activated Protein Kinase Kinases,
pubmed-meshheading:10567369-Mitogen-Activated Protein Kinases,
pubmed-meshheading:10567369-Molecular Sequence Data,
pubmed-meshheading:10567369-Oligopeptides,
pubmed-meshheading:10567369-Phosphorylation,
pubmed-meshheading:10567369-Protein Binding,
pubmed-meshheading:10567369-Protein-Serine-Threonine Kinases,
pubmed-meshheading:10567369-Proto-Oncogene Proteins c-raf,
pubmed-meshheading:10567369-Sequence Deletion,
pubmed-meshheading:10567369-Threonine,
pubmed-meshheading:10567369-Time Factors,
pubmed-meshheading:10567369-p21-Activated Kinases
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pubmed:year |
1999
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pubmed:articleTitle |
The N-terminal ERK-binding site of MEK1 is required for efficient feedback phosphorylation by ERK2 in vitro and ERK activation in vivo.
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pubmed:affiliation |
Department of Pharmacology, University of Texas Southwestern Medical Center, Dallas, Texas 75235-9041, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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