Document
type: Class

Characterization of pI(Cln) phosphorylation state and a pI(Cln)-associated protein kinase
volume: 1381
has funding vehicle: National Institutes of Health, NIH
has funding vehicle: National Institute of Diabetes and Digestive and Kidney Diseases, NIDDK: R01DK051610
type: Generically Dependent Continuant
date time value: article date 616
type: Entity
estado: published
chemicalscas: protein kinase, 9026-43-1; Chloride Channels; Protein Kinases, EC 2.7.1.37
type: Continuant
type: Document
type: Thing
pmid: 9659371
type: Article
e iscopus: 2-s2.0-0032485963
related by: authorship 2917
freetext keyword: Anion channel; Cell swelling; Cell volume regulation anion channel; protein kinase; chloride channel; protein kinase; amino acid sequence; animal cell; article; cell swelling; cell volume; chloride current; controlled study; glioma cell; nonhuman; priority journal; protein phosphorylation; rat; animal; cell culture; metabolism; molecular genetics; peptide mapping; phosphorylation; Amino Acid Sequence; Animals; Chloride Channels; Molecular Sequence Data; Peptide Mapping; Phosphorylation; Protein Kinases; Rats; Tumor Cells, Cultured
has publication venue: Biochimica et Biophysica Acta - General Subjects
abstract: pI(Cln) is a ubiquitous cellular protein that has been proposed to be a volume-sensitive Cl- channel or a channel regulator. Detailed biochemical, cellular and molecular characterization of pI(Cln) is required to understand its function. Our goal in the present investigation was to define further the biochemical properties of pI(Cln) and the proteins that associate with it. Immunoprecipitation of pI(Cln) from 32P-orthophosphoric acid-labeled C6 glioma cells revealed that the protein is phosphorylated constitutively, primarily on serine residues. Protein kinase activity was detected in pI(Cln) immunoprecipitates, revealing that a constitutively active protein kinase co-precipitates with pI(Cln). A specific association between pI(Cln) and a protein kinase was also observed in affinity assays using a recombinant GST-pI(Cln) fusion protein. The pI(Cln)-associated kinase displayed broad substrate specificity and was inhibited in a concentration-dependent manner by heparin, zinc and 5,6-dichloro-1-β-d-ribofuranosylbenose (DRB). These characteristics resembled those of casein kinase I and II. The pI(Cln)-associated kinase was not recognized, however, by antibodies against these two enzymes. Association of the kinase with pI(Cln) was disrupted by increasing concentrations of NaCl in the washing buffer, suggesting that electrostatic interactions are involved in kinase binding. Mutagenesis experiments corroborated this observation. Truncation of pI(Cln) demonstrated that two highly charged clusters of acidic amino acid residues are both necessary and sufficient for kinase binding. Phosphopeptide mapping demonstrated that pI(Cln) contains at least two phosphorylated serine residues that are located on trypsin cleavage fragments rich in acidic amino acid residues. We propose that the kinase or a kinase binding protein binds to acidic amino acids located between D101 and Y156 and phosphorylates nearby serine residues. Copyright (C) 1998 Elsevier Science B.V.
related by: authorship 2919
most specific type: Document
most specific type: Article
has funding vehicle: National Institute of Neurological Disorders and Stroke, NINDS: R01NS030591
type: Information Content Entity
crisid: 616
doi: 10.1016/S0304-4165(98)00009-9
has funding vehicle: American Heart Association, AHA
issue: 1
origen: scopus
page start: 49
related by: authorship 2918
related by: authorship 2920
page end: 60

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RDF description of Characterization of pI(Cln) phosphorylation state and a pI(Cln)-associated protein kinase - http://orbis.uaslp.mx/vivo/individual/scopus615
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date: 2026-08-28T03:39:34
publisher: vivo
type: Document

National Institute of Diabetes and Digestive and Kidney Diseases, NIDDK: R01DK051610
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type: BFO_0000020
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type: Grant
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funding vehicle for: Characterization of pI(Cln) phosphorylation state and a pI(Cln)-associated protein kinase

Article
type: Class

National Institute of Neurological Disorders and Stroke, NINDS: R01NS030591
type: Relationship
type: BFO_0000020
type: Entity
type: Thing
type: Grant
type: Continuant
funding vehicle for: Characterization of pI(Cln) phosphorylation state and a pI(Cln)-associated protein kinase

Information Content Entity
type: Class

American Heart Association, AHA
type: Relationship
type: BFO_0000020
type: Entity
type: Thing
type: Grant
type: Continuant
funding vehicle for: Characterization of pI(Cln) phosphorylation state and a pI(Cln)-associated protein kinase

National Institutes of Health, NIH
type: Relationship
type: BFO_0000020
type: Entity
type: Thing
type: Grant
type: Continuant
funding vehicle for: Characterization of pI(Cln) phosphorylation state and a pI(Cln)-associated protein kinase

Biochimica et Biophysica Acta - General Subjects
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type: Entity
type: Journal
type: Continuant
type: Generically Dependent Continuant
publication venue for: Characterization of pI(Cln) phosphorylation state and a pI(Cln)-associated protein kinase
type: Document
type: Thing
type: Information Content Entity
type: Periodical