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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
3
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pubmed:dateCreated |
1997-3-18
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pubmed:abstractText |
Myosin-associated giant protein kinases of the titin/witchin-like superfamily have previously been implicated in the regulation of muscle function, based on genetic and physiological studies. We find that recombinant constitutively active Caenorhabditis elegans and Aplysia twitchin kinase fragments differ in their catalytic activities and peptide-substrate specificities, as well as in their sensitivities to the naphthalene sulfonamide inhibitors 1-(5-chloronaphthalenesulfonyl)-1H-hexahydro-1,4-diazepine (ML-7) and 1-(5-iodonaphthalenesulfonyl)-1H-hexahydro-1,4-diazepine (ML-9). The constitutively active Aplysia twitchin kinase fragment has a remarkably high activity (Vmax > 100 mumol.min-1.mg-1) towards some substrate peptides. The autoinhibited forms of these twitchin kinases can be activated in a Ca(2+)-dependent manner by the dimeric form of the S100A1 protein (S100A1(2)). The twitchin kinase S100A1(2)-binding site can also bind Ca2+/calmodulin but neither kinase is activated by calmodulin. The data provide a functional basis for the ongoing crystallographic study of twitchin kinase fragments.
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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/Caenorhabditis elegans Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Calcium,
http://linkedlifedata.com/resource/pubmed/chemical/Calcium-Calmodulin-Dependent...,
http://linkedlifedata.com/resource/pubmed/chemical/Calmodulin,
http://linkedlifedata.com/resource/pubmed/chemical/Calmodulin-Binding Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Muscle Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Myosin-Light-Chain Kinase,
http://linkedlifedata.com/resource/pubmed/chemical/Peptides,
http://linkedlifedata.com/resource/pubmed/chemical/S100 Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/unc-22 protein, C elegans
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pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
0014-2956
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
242
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
454-9
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:9022668-Amino Acid Sequence,
pubmed-meshheading:9022668-Animals,
pubmed-meshheading:9022668-Aplysia,
pubmed-meshheading:9022668-Caenorhabditis elegans,
pubmed-meshheading:9022668-Caenorhabditis elegans Proteins,
pubmed-meshheading:9022668-Calcium,
pubmed-meshheading:9022668-Calcium-Calmodulin-Dependent Protein Kinases,
pubmed-meshheading:9022668-Calmodulin,
pubmed-meshheading:9022668-Calmodulin-Binding Proteins,
pubmed-meshheading:9022668-Enzyme Activation,
pubmed-meshheading:9022668-Kinetics,
pubmed-meshheading:9022668-Molecular Sequence Data,
pubmed-meshheading:9022668-Muscle Proteins,
pubmed-meshheading:9022668-Myosin-Light-Chain Kinase,
pubmed-meshheading:9022668-Peptides,
pubmed-meshheading:9022668-Protein Structure, Secondary,
pubmed-meshheading:9022668-S100 Proteins,
pubmed-meshheading:9022668-Substrate Specificity
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pubmed:year |
1996
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pubmed:articleTitle |
Substrate specificity and inhibitor sensitivity of Ca2+/S100-dependent twitchin kinases.
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pubmed:affiliation |
St Vincent's Institute of Medical Research, Fitzroy, Victoria, Australia. j.heierhorst@medicine.unimelb.edu.au
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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