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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
39
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pubmed:dateCreated |
1997-10-23
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pubmed:abstractText |
To investigate the role of serine/threonine autophosphorylation of protein kinase C-delta (PKC-delta), we mutated serine 643 of PKC-delta to an alanine residue (PKC-deltaS643A). Two different expression vectors containing PKC-deltaS643A mutant cDNAs were transfected and expressed in 32D myeloid progenitor cells. In vitro autophosphorylation assays demonstrated 65-83% reduction in autophosphorylation of PKC-deltaS643A in comparison to wild type PKC-delta (PKC-deltaWT). The enzymatic activity of PKC-deltaS643A mutant as measured by phosphorylating the PKC-delta pseudosubstrate region-derived substrate was also reduced more than 70% in comparison to that of PKC-deltaWT. In vivo labeling and subsequent two-dimensional phosphopeptide analysis demonstrated that at least one phosphopeptide was absent in PKC-deltaS643A when compared with PKC-deltaWT, further substantiating that serine 643 is phosphorylated in vivo. Localization and 12-O-tetradecanoylphorbol-13-acetate-dependent translocation and tyrosine phosphorylation of PKC-deltaS643A were not altered in comparison to PKC-deltaWT, indicating that mutagenesis did not affect the structural integrity of the mutant protein. 12-O-Tetradecanoylphorbol-13-acetate-mediated monocytic differentiation of 32D cells overexpressing PKC-deltaS643A mutant protein was impaired in comparison to that of PKC-deltaWT transfectant. Taken together, our results demonstrate that serine 643 of PKC-delta is a major autophosphorylation site, and phosphorylation of this site plays an important role in controlling its enzymatic activity and biological function.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/DNA, Complementary,
http://linkedlifedata.com/resource/pubmed/chemical/Isoenzymes,
http://linkedlifedata.com/resource/pubmed/chemical/Prkcd protein, mouse,
http://linkedlifedata.com/resource/pubmed/chemical/Protein Kinase C,
http://linkedlifedata.com/resource/pubmed/chemical/Protein Kinase C-delta,
http://linkedlifedata.com/resource/pubmed/chemical/Serine,
http://linkedlifedata.com/resource/pubmed/chemical/Tetradecanoylphorbol Acetate
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pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
0021-9258
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
26
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pubmed:volume |
272
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
24550-5
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:9305920-Amino Acid Sequence,
pubmed-meshheading:9305920-Animals,
pubmed-meshheading:9305920-Biological Transport,
pubmed-meshheading:9305920-Cell Differentiation,
pubmed-meshheading:9305920-DNA, Complementary,
pubmed-meshheading:9305920-Isoenzymes,
pubmed-meshheading:9305920-Mice,
pubmed-meshheading:9305920-Molecular Sequence Data,
pubmed-meshheading:9305920-Monocytes,
pubmed-meshheading:9305920-Mutagenesis, Site-Directed,
pubmed-meshheading:9305920-Phosphorylation,
pubmed-meshheading:9305920-Protein Kinase C,
pubmed-meshheading:9305920-Protein Kinase C-delta,
pubmed-meshheading:9305920-Sequence Alignment,
pubmed-meshheading:9305920-Serine,
pubmed-meshheading:9305920-Substrate Specificity,
pubmed-meshheading:9305920-Tetradecanoylphorbol Acetate
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pubmed:year |
1997
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pubmed:articleTitle |
Identification of serine 643 of protein kinase C-delta as an important autophosphorylation site for its enzymatic activity.
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pubmed:affiliation |
Laboratory of Cellular and Molecular Biology, NCI, National Institutes of Health, Bethesda, Maryland 20892, USA. Liwe@dc37a.nci.nih.gov
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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