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spelling todo:paper_03008177_v102_n2_p155_Ulloa2023-10-03T15:17:40Z Ca2+ calmodulin-dependent protein kinase activity in the ascomycetes Neurospora crassa Ulloa, R.M. Torres, H.N. Ochatt, C.M. Téllez-Iñón, M.T. autophosphorylation Ca2+ calmodulin kinase Neurospora crassa protein kinase (calcium,calmodulin) Ca(2+) Calmodulin Dependent Protein Kinase calcium calmodulin cyclic AMP egtazic acid fungal protein protein kinase protein kinase (calcium,calmodulin) article autophosphorylation neurospora crassa nonhuman priority journal enzymology gel chromatography ion exchange chromatography isolation and purification Neurospora crassa phosphorylation polyacrylamide gel electrophoresis protein processing Ascomycota Neurospora Neurospora crassa Ca(2+)-Calmodulin Dependent Protein Kinase Calcium Calmodulin Chromatography, DEAE-Cellulose Chromatography, Gel Cyclic AMP Egtazic Acid Electrophoresis, Polyacrylamide Gel Fungal Proteins Neurospora crassa Phosphorylation Protein Kinases Protein Processing, Post-Translational Support, Non-U.S. Gov't DEAE-cellulose column chromatography of Neurospora crassa soluble mycelial extracts leads to the resolution of three major protein kinase activity peaks designated PKI, PKII, and PKIII. PKII activity is stimulated by Ca2+ and Neurospora or brain calmodulin. Maximal stimulation was observed at 2 μM-free Ca2+ and 1 μg/ml of the modulator. The stimulatory effect of the Ca2+-calmodulin complex was blocked by EGTA and by some calmodulin antagonists such as phenothiazine drugs or compound 48/80. PKII phosphorylates different proteins, among which histone II-A at a low concentration and CDPKS, the synthetic peptide specific for Ca2+-calmodulin dependent protein kinases, are the best substrates. Some phosphorylation can be detected in the absence of any exogenous acceptor. PKII activity assayed in the presence of histone II-A or in the absence of exogenous phosphate acceptor (autophosphorylation) co-elute in a DEAE-cellulose column at 0.28 M NaCl. As result of the autophosphorylation reaction of the purified enzyme a main phosphorylated component of 70 kDa was resolved by SDS-polyacrylamide gel electrophoresis. It is possible that this component is an active part of this enzyme. © 1991 Kluwer Academic Publishers. Fil:Torres, H.N. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Ochatt, C.M. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_03008177_v102_n2_p155_Ulloa
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic autophosphorylation
Ca2+
calmodulin
kinase
Neurospora crassa
protein kinase (calcium,calmodulin)
Ca(2+) Calmodulin Dependent Protein Kinase
calcium
calmodulin
cyclic AMP
egtazic acid
fungal protein
protein kinase
protein kinase (calcium,calmodulin)
article
autophosphorylation
neurospora crassa
nonhuman
priority journal
enzymology
gel chromatography
ion exchange chromatography
isolation and purification
Neurospora crassa
phosphorylation
polyacrylamide gel electrophoresis
protein processing
Ascomycota
Neurospora
Neurospora crassa
Ca(2+)-Calmodulin Dependent Protein Kinase
Calcium
Calmodulin
Chromatography, DEAE-Cellulose
Chromatography, Gel
Cyclic AMP
Egtazic Acid
Electrophoresis, Polyacrylamide Gel
Fungal Proteins
Neurospora crassa
Phosphorylation
Protein Kinases
Protein Processing, Post-Translational
Support, Non-U.S. Gov't
spellingShingle autophosphorylation
Ca2+
calmodulin
kinase
Neurospora crassa
protein kinase (calcium,calmodulin)
Ca(2+) Calmodulin Dependent Protein Kinase
calcium
calmodulin
cyclic AMP
egtazic acid
fungal protein
protein kinase
protein kinase (calcium,calmodulin)
article
autophosphorylation
neurospora crassa
nonhuman
priority journal
enzymology
gel chromatography
ion exchange chromatography
isolation and purification
Neurospora crassa
phosphorylation
polyacrylamide gel electrophoresis
protein processing
Ascomycota
Neurospora
Neurospora crassa
Ca(2+)-Calmodulin Dependent Protein Kinase
Calcium
Calmodulin
Chromatography, DEAE-Cellulose
Chromatography, Gel
Cyclic AMP
Egtazic Acid
Electrophoresis, Polyacrylamide Gel
Fungal Proteins
Neurospora crassa
Phosphorylation
Protein Kinases
Protein Processing, Post-Translational
Support, Non-U.S. Gov't
Ulloa, R.M.
Torres, H.N.
Ochatt, C.M.
Téllez-Iñón, M.T.
Ca2+ calmodulin-dependent protein kinase activity in the ascomycetes Neurospora crassa
topic_facet autophosphorylation
Ca2+
calmodulin
kinase
Neurospora crassa
protein kinase (calcium,calmodulin)
Ca(2+) Calmodulin Dependent Protein Kinase
calcium
calmodulin
cyclic AMP
egtazic acid
fungal protein
protein kinase
protein kinase (calcium,calmodulin)
article
autophosphorylation
neurospora crassa
nonhuman
priority journal
enzymology
gel chromatography
ion exchange chromatography
isolation and purification
Neurospora crassa
phosphorylation
polyacrylamide gel electrophoresis
protein processing
Ascomycota
Neurospora
Neurospora crassa
Ca(2+)-Calmodulin Dependent Protein Kinase
Calcium
Calmodulin
Chromatography, DEAE-Cellulose
Chromatography, Gel
Cyclic AMP
Egtazic Acid
Electrophoresis, Polyacrylamide Gel
Fungal Proteins
Neurospora crassa
Phosphorylation
Protein Kinases
Protein Processing, Post-Translational
Support, Non-U.S. Gov't
description DEAE-cellulose column chromatography of Neurospora crassa soluble mycelial extracts leads to the resolution of three major protein kinase activity peaks designated PKI, PKII, and PKIII. PKII activity is stimulated by Ca2+ and Neurospora or brain calmodulin. Maximal stimulation was observed at 2 μM-free Ca2+ and 1 μg/ml of the modulator. The stimulatory effect of the Ca2+-calmodulin complex was blocked by EGTA and by some calmodulin antagonists such as phenothiazine drugs or compound 48/80. PKII phosphorylates different proteins, among which histone II-A at a low concentration and CDPKS, the synthetic peptide specific for Ca2+-calmodulin dependent protein kinases, are the best substrates. Some phosphorylation can be detected in the absence of any exogenous acceptor. PKII activity assayed in the presence of histone II-A or in the absence of exogenous phosphate acceptor (autophosphorylation) co-elute in a DEAE-cellulose column at 0.28 M NaCl. As result of the autophosphorylation reaction of the purified enzyme a main phosphorylated component of 70 kDa was resolved by SDS-polyacrylamide gel electrophoresis. It is possible that this component is an active part of this enzyme. © 1991 Kluwer Academic Publishers.
format JOUR
author Ulloa, R.M.
Torres, H.N.
Ochatt, C.M.
Téllez-Iñón, M.T.
author_facet Ulloa, R.M.
Torres, H.N.
Ochatt, C.M.
Téllez-Iñón, M.T.
author_sort Ulloa, R.M.
title Ca2+ calmodulin-dependent protein kinase activity in the ascomycetes Neurospora crassa
title_short Ca2+ calmodulin-dependent protein kinase activity in the ascomycetes Neurospora crassa
title_full Ca2+ calmodulin-dependent protein kinase activity in the ascomycetes Neurospora crassa
title_fullStr Ca2+ calmodulin-dependent protein kinase activity in the ascomycetes Neurospora crassa
title_full_unstemmed Ca2+ calmodulin-dependent protein kinase activity in the ascomycetes Neurospora crassa
title_sort ca2+ calmodulin-dependent protein kinase activity in the ascomycetes neurospora crassa
url http://hdl.handle.net/20.500.12110/paper_03008177_v102_n2_p155_Ulloa
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