Nature Reviews Cancer, ISSN 1474-175X, 07/2007, Volume 7, Issue 7, pp. 554 - 562
Protein kinase C (PKC) comprises a family of serine/ threonine kinases that are involved in the transduction of signals for cell proliferation,...
SIGNAL-TRANSDUCTION PATHWAYS | ANTISENSE OLIGONUCLEOTIDE APRINOCARSEN | ONCOLOGY | PHASE-I TRIAL | GLYCOGEN-SYNTHASE KINASE-3 | COLON CARCINOGENESIS | NECROSIS-FACTOR-ALPHA | BETA-II | BREAST-CANCER-CELLS | MULTIDRUG-RESISTANCE | PHORBOL ESTERS | Signal Transduction | Humans | Neovascularization, Pathologic | Protein Kinase C - antagonists & inhibitors | Enzyme Inhibitors - therapeutic use | Protein Kinase C - classification | Neoplasms - drug therapy | Isoenzymes - metabolism | Protein Kinase C - metabolism | Cell Division | Cell Differentiation | Kinetics | Neovascularization, Physiologic | Apoptosis | Antimitotic agents | Care and treatment | Physiological aspects | Dosage and administration | Genetic aspects | Cellular signal transduction | Research | Antineoplastic agents | Protein kinases | Health aspects | Cancer
SIGNAL-TRANSDUCTION PATHWAYS | ANTISENSE OLIGONUCLEOTIDE APRINOCARSEN | ONCOLOGY | PHASE-I TRIAL | GLYCOGEN-SYNTHASE KINASE-3 | COLON CARCINOGENESIS | NECROSIS-FACTOR-ALPHA | BETA-II | BREAST-CANCER-CELLS | MULTIDRUG-RESISTANCE | PHORBOL ESTERS | Signal Transduction | Humans | Neovascularization, Pathologic | Protein Kinase C - antagonists & inhibitors | Enzyme Inhibitors - therapeutic use | Protein Kinase C - classification | Neoplasms - drug therapy | Isoenzymes - metabolism | Protein Kinase C - metabolism | Cell Division | Cell Differentiation | Kinetics | Neovascularization, Physiologic | Apoptosis | Antimitotic agents | Care and treatment | Physiological aspects | Dosage and administration | Genetic aspects | Cellular signal transduction | Research | Antineoplastic agents | Protein kinases | Health aspects | Cancer
Journal Article
FASEB Journal, ISSN 0892-6638, 1999, Volume 13, Issue 13, pp. 1658 - 1676
Protein kinase C (PKC), a family of related serine-threonine kinases, is a key player in the cellular responses mediated by the second messenger diacylglycerol...
Signal transduction | PKC | Chimaerin | Anchoring proteins | Phorbol ester | TYROSINE PHOSPHORYLATION | signal transduction | phorbol ester | BIOCHEMISTRY & MOLECULAR BIOLOGY | BINDING-PROTEIN | chimaerin | GTPASE-ACTIVATING PROTEIN | CYSTEINE-RICH REGION | CELL BIOLOGY | HIGH-AFFINITY RECEPTOR | CAENORHABDITIS-ELEGANS | anchoring proteins | IN-VIVO | BIOLOGY | PLECKSTRIN HOMOLOGY DOMAIN | SIGNAL-TRANSDUCTION PATHWAY | N-CHIMAERIN
Signal transduction | PKC | Chimaerin | Anchoring proteins | Phorbol ester | TYROSINE PHOSPHORYLATION | signal transduction | phorbol ester | BIOCHEMISTRY & MOLECULAR BIOLOGY | BINDING-PROTEIN | chimaerin | GTPASE-ACTIVATING PROTEIN | CYSTEINE-RICH REGION | CELL BIOLOGY | HIGH-AFFINITY RECEPTOR | CAENORHABDITIS-ELEGANS | anchoring proteins | IN-VIVO | BIOLOGY | PLECKSTRIN HOMOLOGY DOMAIN | SIGNAL-TRANSDUCTION PATHWAY | N-CHIMAERIN
Journal Article
PLoS ONE, ISSN 1932-6203, 03/2017, Volume 12, Issue 3, p. e0174386
Protein classification is one of the critical problems in bioinformatics. Early studies used geometric distances and polygenetic-tree to classify proteins....
SPACE | ORIGIN | MULTIDISCIPLINARY SCIENCES | GENOME | Influenza A virus - chemistry | Multivariate Analysis | Viral Proteins - chemistry | HIV Infections - virology | Humans | Mitochondrial Proteins - classification | Protein Kinase C - classification | Viral Proteins - classification | Algorithms | Animals | HIV - chemistry | Protein Kinase C - chemistry | Mitochondrial Proteins - chemistry | Protein Conformation | Proteins - classification | beta-Globins - classification | Proteins - chemistry | Proteomics - methods | beta-Globins - chemistry | Orthomyxoviridae Infections - virology | Proteins | Phylogenetic trees | Protein biosynthesis | Research | Identification and classification | Analysis | Mean square errors | Time series | Universe | Amino acids | Genomes | Genetic algorithms | Classification | Bioinformatics | Artificial intelligence | Deoxyribonucleic acid--DNA | Methods | Information theory | Deoxyribonucleic acid | DNA
SPACE | ORIGIN | MULTIDISCIPLINARY SCIENCES | GENOME | Influenza A virus - chemistry | Multivariate Analysis | Viral Proteins - chemistry | HIV Infections - virology | Humans | Mitochondrial Proteins - classification | Protein Kinase C - classification | Viral Proteins - classification | Algorithms | Animals | HIV - chemistry | Protein Kinase C - chemistry | Mitochondrial Proteins - chemistry | Protein Conformation | Proteins - classification | beta-Globins - classification | Proteins - chemistry | Proteomics - methods | beta-Globins - chemistry | Orthomyxoviridae Infections - virology | Proteins | Phylogenetic trees | Protein biosynthesis | Research | Identification and classification | Analysis | Mean square errors | Time series | Universe | Amino acids | Genomes | Genetic algorithms | Classification | Bioinformatics | Artificial intelligence | Deoxyribonucleic acid--DNA | Methods | Information theory | Deoxyribonucleic acid | DNA
Journal Article
Journal of Neurochemistry, ISSN 0022-3042, 03/2012, Volume 120, Issue 5, pp. 830 - 841
J. Neurochem. (2012) 120, 830–841. We previously reported the involvement of conventional protein kinase C (cPKC) βII, γ, novel PKC (nPKC) ε and their...
gene ontology | Kyoto encyclopedia of genes and genomes | miRNA microarray | middle cerebral artery occlusion | hypoxic pre‐conditioning | hypoxic pre-conditioning | TARGET | PROTEIN-KINASE-C | ISCHEMIA/REPERFUSION INJURY | ACTIVATION | MEMBRANE TRANSLOCATION | NITRIC-OXIDE SYNTHASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | REPERFUSION | NEUROSCIENCES | HEPATIC STELLATE CELL | UP-REGULATION | BRAIN | Protein Kinase C - genetics | Computational Biology - methods | Gene Regulatory Networks - genetics | Cell Survival | Oligonucleotide Array Sequence Analysis - methods | Brain Ischemia - genetics | Gene Expression Regulation - physiology | Male | MicroRNAs - metabolism | Brain Ischemia - physiopathology | Gene Expression Profiling | Neuroblastoma | Protein Kinase C - classification | Ischemic Preconditioning - methods | Animals | Protein Isoforms - metabolism | Transfection | Protein Kinase C - metabolism | Mice | Mice, Inbred BALB C | Cell Line, Transformed | Cluster Analysis | Disease Models, Animal | Protein Isoforms - genetics | Proteins | MicroRNA | Ischemia | Analysis | Genes | Gene expression | Neurochemistry | Brain | Rodents | Hypoxia | Ribonucleic acid--RNA | Neuroprotection | Oxygen | Protein kinase C | Cortex | Genomes | Glucose | Computer programs | Cell injury | DNA microarrays | Databases | Cerebral blood flow | miRNA | Bioinformatics
gene ontology | Kyoto encyclopedia of genes and genomes | miRNA microarray | middle cerebral artery occlusion | hypoxic pre‐conditioning | hypoxic pre-conditioning | TARGET | PROTEIN-KINASE-C | ISCHEMIA/REPERFUSION INJURY | ACTIVATION | MEMBRANE TRANSLOCATION | NITRIC-OXIDE SYNTHASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | REPERFUSION | NEUROSCIENCES | HEPATIC STELLATE CELL | UP-REGULATION | BRAIN | Protein Kinase C - genetics | Computational Biology - methods | Gene Regulatory Networks - genetics | Cell Survival | Oligonucleotide Array Sequence Analysis - methods | Brain Ischemia - genetics | Gene Expression Regulation - physiology | Male | MicroRNAs - metabolism | Brain Ischemia - physiopathology | Gene Expression Profiling | Neuroblastoma | Protein Kinase C - classification | Ischemic Preconditioning - methods | Animals | Protein Isoforms - metabolism | Transfection | Protein Kinase C - metabolism | Mice | Mice, Inbred BALB C | Cell Line, Transformed | Cluster Analysis | Disease Models, Animal | Protein Isoforms - genetics | Proteins | MicroRNA | Ischemia | Analysis | Genes | Gene expression | Neurochemistry | Brain | Rodents | Hypoxia | Ribonucleic acid--RNA | Neuroprotection | Oxygen | Protein kinase C | Cortex | Genomes | Glucose | Computer programs | Cell injury | DNA microarrays | Databases | Cerebral blood flow | miRNA | Bioinformatics
Journal Article
Molecular Phylogenetics and Evolution, ISSN 1055-7903, 09/2017, Volume 114, pp. 49 - 62
Understanding the role of geography and climatic cycles in determining patterns of biodiversity is important in comparative and evolutionary biology and...
Isolation-with-migration | Vicariance | Coalescence | Afrotheria | Saxicolous mammal | Distribution modelling | NUMBER | MITOCHONDRIAL | BIOCHEMISTRY & MOLECULAR BIOLOGY | SIZE | POPULATION-GROWTH | SOFTWARE | AGAMA-ATRA | EVOLUTIONARY BIOLOGY | EVOLUTION | GENETICS & HEREDITY | DYNAMICS | DIVERSITY | CYTOCHROME-B GENE | Haplotypes | Protein Kinase C - genetics | Gene Flow | Isoenzymes - genetics | Phylogeography | Cytochromes b - classification | Genotype | Hyraxes - classification | Phylogeny | Africa, Southern | Protein Kinase C - classification | Tartrate-Resistant Acid Phosphatase - classification | Isoenzymes - classification | Microsatellite Repeats - genetics | Biological Evolution | Genetic Variation | Hyraxes - genetics | Animals | Climate Change | Mitochondria - genetics | Cytochromes b - genetics | Tartrate-Resistant Acid Phosphatase - genetics | Climate cycles | Cytochrome b | Zoology | Analysis
Isolation-with-migration | Vicariance | Coalescence | Afrotheria | Saxicolous mammal | Distribution modelling | NUMBER | MITOCHONDRIAL | BIOCHEMISTRY & MOLECULAR BIOLOGY | SIZE | POPULATION-GROWTH | SOFTWARE | AGAMA-ATRA | EVOLUTIONARY BIOLOGY | EVOLUTION | GENETICS & HEREDITY | DYNAMICS | DIVERSITY | CYTOCHROME-B GENE | Haplotypes | Protein Kinase C - genetics | Gene Flow | Isoenzymes - genetics | Phylogeography | Cytochromes b - classification | Genotype | Hyraxes - classification | Phylogeny | Africa, Southern | Protein Kinase C - classification | Tartrate-Resistant Acid Phosphatase - classification | Isoenzymes - classification | Microsatellite Repeats - genetics | Biological Evolution | Genetic Variation | Hyraxes - genetics | Animals | Climate Change | Mitochondria - genetics | Cytochromes b - genetics | Tartrate-Resistant Acid Phosphatase - genetics | Climate cycles | Cytochrome b | Zoology | Analysis
Journal Article
European Journal of Neuroscience, ISSN 0953-816X, 09/2003, Volume 18, Issue 6, pp. 1387 - 1401
1‐Methyl‐4‐phenylpyridinium (MPP+), the neurotoxic metabolite of MPTP (1‐methyl‐4‐phenyl‐1,2,3,6‐tetrahydropyridine), induces apoptosis in dopaminergic...
Parkinson's disease | MPTP | feedback regulation | environmental factors | phosphorylation | Feedback regulation | Phosphorylation | Environmental factors | POLY(ADP-RIBOSE) POLYMERASE | METHYLCYCLOPENTADIENYL MANGANESE TRICARBONYL | SH-SY5Y NEUROBLASTOMA-CELLS | NECROSIS-FACTOR-ALPHA | ICE-LIKE PROTEASE | NEUROSCIENCES | MITOCHONDRIAL PERMEABILITY TRANSITION | DISTINCT MECHANISMS | PKC-DELTA | HYDROGEN-PEROXIDE | PARKINSONS-DISEASE | Free Radical Scavengers - pharmacology | Coumarins - metabolism | Protein Kinase C - genetics | Caspase 9 | Flow Cytometry - methods | Mesencephalon - cytology | Reactive Oxygen Species - metabolism | Gene Expression - drug effects | Apoptosis - drug effects | Mesencephalon - metabolism | Oxidative Stress - physiology | Nerve Degeneration - physiopathology | Metalloporphyrins - pharmacology | Protein Kinase C - classification | Nerve Degeneration - chemically induced | Dose-Response Relationship, Drug | Organometallic Compounds | Caspases - metabolism | Drug Interactions | Transfection - methods | Time Factors | Protein Kinase C - metabolism | DNA Fragmentation | Caspase 3 | Dopamine - metabolism | Protein Kinase C-delta | Flow Cytometry - instrumentation | Cell Line | Cytochromes c - metabolism | Enzyme Inhibitors - pharmacology | Rats | Herbicides - toxicity | Caspase Inhibitors | Precipitin Tests | Animals | Benzimidazoles - metabolism | 1-Methyl-4-phenylpyridinium - toxicity | Oxidative Stress - drug effects | In Vitro Techniques | Manganese Compounds - pharmacology
Parkinson's disease | MPTP | feedback regulation | environmental factors | phosphorylation | Feedback regulation | Phosphorylation | Environmental factors | POLY(ADP-RIBOSE) POLYMERASE | METHYLCYCLOPENTADIENYL MANGANESE TRICARBONYL | SH-SY5Y NEUROBLASTOMA-CELLS | NECROSIS-FACTOR-ALPHA | ICE-LIKE PROTEASE | NEUROSCIENCES | MITOCHONDRIAL PERMEABILITY TRANSITION | DISTINCT MECHANISMS | PKC-DELTA | HYDROGEN-PEROXIDE | PARKINSONS-DISEASE | Free Radical Scavengers - pharmacology | Coumarins - metabolism | Protein Kinase C - genetics | Caspase 9 | Flow Cytometry - methods | Mesencephalon - cytology | Reactive Oxygen Species - metabolism | Gene Expression - drug effects | Apoptosis - drug effects | Mesencephalon - metabolism | Oxidative Stress - physiology | Nerve Degeneration - physiopathology | Metalloporphyrins - pharmacology | Protein Kinase C - classification | Nerve Degeneration - chemically induced | Dose-Response Relationship, Drug | Organometallic Compounds | Caspases - metabolism | Drug Interactions | Transfection - methods | Time Factors | Protein Kinase C - metabolism | DNA Fragmentation | Caspase 3 | Dopamine - metabolism | Protein Kinase C-delta | Flow Cytometry - instrumentation | Cell Line | Cytochromes c - metabolism | Enzyme Inhibitors - pharmacology | Rats | Herbicides - toxicity | Caspase Inhibitors | Precipitin Tests | Animals | Benzimidazoles - metabolism | 1-Methyl-4-phenylpyridinium - toxicity | Oxidative Stress - drug effects | In Vitro Techniques | Manganese Compounds - pharmacology
Journal Article
Endocrinology, ISSN 0013-7227, 01/2011, Volume 152, Issue 1, pp. 313 - 325
Protein kinase C (PKC) is a multigene family of serine/threonine kinases. PKC is involved in regulating adrenal and gonadal steroidogenesis; however, the...
KINASE-D ACTIVATION | SIGNALING PATHWAYS | ELEMENT BINDING-PROTEIN | C-DELTA | ENDOCRINOLOGY & METABOLISM | PLECKSTRIN HOMOLOGY DOMAIN | GENE-EXPRESSION | TUMOR-CELLS | GONADAL STEROIDOGENESIS | RESPONSE-ELEMENT | TRANSCRIPTIONAL REGULATION | Protein Kinase C - genetics | Signal Transduction | Isoenzymes | Gene Expression Regulation - physiology | Male | Phosphoproteins - genetics | Phosphoproteins - metabolism | Protein Kinase C - classification | Proto-Oncogene Proteins c-fos | Cyclic AMP Response Element-Binding Protein - genetics | Phorbol Esters - metabolism | Animals | Leydig Cells - metabolism | Protein Kinase C - metabolism | Cyclic AMP Response Element-Binding Protein - metabolism | Cell Line, Tumor | Mice | Proto-Oncogene Proteins c-jun
KINASE-D ACTIVATION | SIGNALING PATHWAYS | ELEMENT BINDING-PROTEIN | C-DELTA | ENDOCRINOLOGY & METABOLISM | PLECKSTRIN HOMOLOGY DOMAIN | GENE-EXPRESSION | TUMOR-CELLS | GONADAL STEROIDOGENESIS | RESPONSE-ELEMENT | TRANSCRIPTIONAL REGULATION | Protein Kinase C - genetics | Signal Transduction | Isoenzymes | Gene Expression Regulation - physiology | Male | Phosphoproteins - genetics | Phosphoproteins - metabolism | Protein Kinase C - classification | Proto-Oncogene Proteins c-fos | Cyclic AMP Response Element-Binding Protein - genetics | Phorbol Esters - metabolism | Animals | Leydig Cells - metabolism | Protein Kinase C - metabolism | Cyclic AMP Response Element-Binding Protein - metabolism | Cell Line, Tumor | Mice | Proto-Oncogene Proteins c-jun
Journal Article
Immunological Reviews, ISSN 0105-2896, 04/2003, Volume 192, Issue 1, pp. 64 - 79
The distinct protein kinase C (PKC) multigene family (PKC gene module) is known to be the ‘classic’ intracellular receptor for mitogenic phorbol esters, and it...
SIGNAL-TRANSDUCTION | PROTEIN-KINASE-C | DEPENDENT PHOSPHORYLATION | INTERLEUKIN-2 PRODUCTION | TYROSINE PHOSPHORYLATION | SYNERGISTIC ACTIVATION | NECROSIS-FACTOR-ALPHA | ACTIN CYTOSKELETON | IMMUNOLOGY | IMMUNOLOGICAL SYNAPSE | NF-KAPPA-B | Protein Kinase C - genetics | Liver - enzymology | Protein Kinase C - physiology | Signal Transduction | T-Lymphocytes - enzymology | Isoenzymes - genetics | Lymphocyte Activation | Humans | Phylogeny | Thymus Gland - enzymology | Protein Kinase C - classification | Isoenzymes - classification | Mice, Knockout | Animals | Models, Biological | T-Lymphocytes - immunology | Mice | Isoenzymes - physiology
SIGNAL-TRANSDUCTION | PROTEIN-KINASE-C | DEPENDENT PHOSPHORYLATION | INTERLEUKIN-2 PRODUCTION | TYROSINE PHOSPHORYLATION | SYNERGISTIC ACTIVATION | NECROSIS-FACTOR-ALPHA | ACTIN CYTOSKELETON | IMMUNOLOGY | IMMUNOLOGICAL SYNAPSE | NF-KAPPA-B | Protein Kinase C - genetics | Liver - enzymology | Protein Kinase C - physiology | Signal Transduction | T-Lymphocytes - enzymology | Isoenzymes - genetics | Lymphocyte Activation | Humans | Phylogeny | Thymus Gland - enzymology | Protein Kinase C - classification | Isoenzymes - classification | Mice, Knockout | Animals | Models, Biological | T-Lymphocytes - immunology | Mice | Isoenzymes - physiology
Journal Article
Protein Science, ISSN 0961-8368, 02/1997, Volume 6, Issue 2, pp. 477 - 480
C1 domains are compact α/β structural units of about 50 amino acids which tightly bind two zinc ions. These domains were first discovered as the loci of...
unc‐13 | phorbol ester | Raf | diacylglycerol kinase | Vav | kinase suppressor of Ras | n‐chimaerin | GTPase activating protein | gua‐nine nucleotide exchange factor | guanine nucleotide exchange factor | n-chimaerin | unc- 13 | TARGET | ACTIVATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | unc-13 | ZINC | kinase suppressor of Pas | PHORBOL ESTER BINDING | CYSTEINE-RICH DOMAIN | PROTOONCOGENE
unc‐13 | phorbol ester | Raf | diacylglycerol kinase | Vav | kinase suppressor of Ras | n‐chimaerin | GTPase activating protein | gua‐nine nucleotide exchange factor | guanine nucleotide exchange factor | n-chimaerin | unc- 13 | TARGET | ACTIVATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | unc-13 | ZINC | kinase suppressor of Pas | PHORBOL ESTER BINDING | CYSTEINE-RICH DOMAIN | PROTOONCOGENE
Journal Article
The Journal of Immunology, ISSN 0022-1767, 08/2008, Volume 181, Issue 3, pp. 2044 - 2055
Protein kinase D1 (PKD1) is expressed ubiquitously and regulates diverse cellular processes such as oxidative stress, gene expression, cell survival, and...
RECEPTOR-ASSOCIATED FACTOR-6 | B-LYMPHOCYTES | DENDRITIC CELLS | PROTEIN-KINASE-D | CELL ANTIGEN RECEPTOR | INNATE IMMUNE-RESPONSE | D ACTIVATION | IMMUNOLOGY | CPG DNA | C-MU | BACTERIAL-DNA | Interleukin-1 Receptor-Associated Kinases - metabolism | Protein Kinase C - genetics | Humans | Toll-Like Receptor 9 - genetics | Protein Kinase C - classification | Protein Kinase C - metabolism | src-Family Kinases - metabolism | Signal Transduction | Toll-Like Receptor 9 - deficiency | Cells, Cultured | Myeloid Differentiation Factor 88 - genetics | Protein Kinase C - antagonists & inhibitors | Macrophages - enzymology | Mice, Knockout | DNA - genetics | Transcription Factors - metabolism | Animals | Myeloid Differentiation Factor 88 - deficiency | CpG Islands | Protein Binding | Mice | Protein Kinase Inhibitors - pharmacology | Enzyme Activation | Toll-Like Receptor 9 - metabolism | Myeloid Differentiation Factor 88 - metabolism | Cytokines - biosynthesis | Mitogen-Activated Protein Kinases - metabolism
RECEPTOR-ASSOCIATED FACTOR-6 | B-LYMPHOCYTES | DENDRITIC CELLS | PROTEIN-KINASE-D | CELL ANTIGEN RECEPTOR | INNATE IMMUNE-RESPONSE | D ACTIVATION | IMMUNOLOGY | CPG DNA | C-MU | BACTERIAL-DNA | Interleukin-1 Receptor-Associated Kinases - metabolism | Protein Kinase C - genetics | Humans | Toll-Like Receptor 9 - genetics | Protein Kinase C - classification | Protein Kinase C - metabolism | src-Family Kinases - metabolism | Signal Transduction | Toll-Like Receptor 9 - deficiency | Cells, Cultured | Myeloid Differentiation Factor 88 - genetics | Protein Kinase C - antagonists & inhibitors | Macrophages - enzymology | Mice, Knockout | DNA - genetics | Transcription Factors - metabolism | Animals | Myeloid Differentiation Factor 88 - deficiency | CpG Islands | Protein Binding | Mice | Protein Kinase Inhibitors - pharmacology | Enzyme Activation | Toll-Like Receptor 9 - metabolism | Myeloid Differentiation Factor 88 - metabolism | Cytokines - biosynthesis | Mitogen-Activated Protein Kinases - metabolism
Journal Article