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PLoS Pathogens, ISSN 1553-7366, 07/2013, Volume 9, Issue 7, p. e1003508
Bacterial populations co-ordinate gene expression collectively through quorum sensing (QS), a cell-to-cell communication mechanism employing diffusible signal... 
ANALYSIS REVEALS | CRYSTALLIZATION | MICROBIOLOGY | QUINOLONE SIGNAL SYNTHESIS | VIRULENCE | MOLECULES | TRANSCRIPTIONAL REGULATOR | VIROLOGY | GENES | LYSR-TYPE REGULATOR | BENM | CELL | PARASITOLOGY | Virulence - drug effects | Transcription Factors - chemistry | Molecular Conformation | Bacterial Proteins - chemistry | Pseudomonas aeruginosa - physiology | Quinolones - pharmacology | Structure-Activity Relationship | Alkylation | Quinolones - chemistry | Pseudomonas aeruginosa - pathogenicity | Anti-Bacterial Agents - chemistry | Drug Design | Protein Interaction Domains and Motifs | Binding Sites | Mutant Proteins - antagonists & inhibitors | Biofilms - drug effects | Recombinant Proteins - metabolism | Bacterial Proteins - antagonists & inhibitors | Peptide Fragments - metabolism | Quorum Sensing - drug effects | Quinolones - metabolism | Recombinant Proteins - chemistry | Anti-Bacterial Agents - metabolism | Mutant Proteins - metabolism | Transcription Factors - antagonists & inhibitors | Pseudomonas aeruginosa - drug effects | Bacterial Proteins - agonists | Transcription Factors - metabolism | Peptide Fragments - chemistry | Signal Transduction - drug effects | Peptide Fragments - agonists | Peptide Fragments - antagonists & inhibitors | Mutant Proteins - chemistry | Bacterial Proteins - metabolism | Ligands | Anti-Bacterial Agents - pharmacology | Transcription Factors - agonists | Gene Expression Regulation, Bacterial | Mutant Proteins - agonists | Pseudomonas aeruginosa | Genetic aspects | Quorum sensing | Research | Bacterial genetics | Gene expression | Health aspects | Microbiology | Population | Bacteria | Antimicrobial agents | Biosynthesis | Nosocomial infections | Bacteriology
Journal Article
Molecular Cell, ISSN 1097-2765, 09/2016, Volume 63, Issue 5, pp. 768 - 780
Polyphosphate (polyP), a several billion-year-old biopolymer, is produced in every cell, tissue, and organism studied. Structurally extremely simple, polyP... 
INORGANIC POLYPHOSPHATE | CELLS | APOPTOSIS | PROTEIN | GLYCOSAMINOGLYCANS | A-BETA(1-42) | MECHANISM | ALZHEIMERS-DISEASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | ALPHA-SYNUCLEIN | OLIGOMERS | CELL BIOLOGY | Polyphosphates - pharmacology | Neurons - pathology | Escherichia coli - drug effects | Humans | Biofilms - growth & development | tau Proteins - metabolism | tau Proteins - chemistry | tau Proteins - genetics | Amyloid beta-Peptides - genetics | Protein Folding - drug effects | Amyloid beta-Peptides - metabolism | Escherichia coli - metabolism | Escherichia coli Proteins - agonists | Neurons - metabolism | alpha-Synuclein - genetics | Neurons - drug effects | Peptide Fragments - genetics | Biofilms - drug effects | Gene Expression | Peptide Fragments - metabolism | Caenorhabditis elegans - metabolism | Animals, Genetically Modified | Caenorhabditis elegans - genetics | Escherichia coli Proteins - metabolism | alpha-Synuclein - chemistry | Peptide Fragments - chemistry | Animals | Caenorhabditis elegans - drug effects | tau Proteins - agonists | Escherichia coli - genetics | Peptide Fragments - agonists | Cell Line, Tumor | Escherichia coli Proteins - genetics | alpha-Synuclein - agonists | Amyloid beta-Peptides - chemistry | Kinetics | Escherichia coli Proteins - chemistry | Amyloid beta-Peptides - agonists | alpha-Synuclein - metabolism | Polyphosphates - chemistry | Phosphates | Physiological aspects | Bacteria | Glycoproteins | Developmental biology | Analysis
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 02/2016, Volume 291, Issue 7, pp. 3385 - 3394
The adhesion G protein-coupled receptors (aGPCRs) are a large yet poorly understood family of seven-transmembrane proteins. A defining characteristic of the... 
MIGRATION | ACTIVATION | COLLAGEN | signal transduction | BIOCHEMISTRY & MOLECULAR BIOLOGY | TRAFFICKING | TETHERED AGONIST | SUBUNITS | arrestin | MYOBLAST FUSION | receptor structure-function | ubiquitylation (ubiquitination) | APOPTOTIC CELLS | G protein-coupled receptor (GPCR) | GPCR | NUCLEAR FACTOR | proteolysis | Angiogenic Proteins - agonists | Angiogenic Proteins - genetics | Arrestins - chemistry | Receptors, G-Protein-Coupled - metabolism | Allosteric Regulation | Humans | NFATC Transcription Factors - agonists | Arrestins - genetics | Receptors, G-Protein-Coupled - agonists | Arrestins - metabolism | Recombinant Fusion Proteins - metabolism | Ubiquitination | Proteolysis | HEK293 Cells | Conserved Sequence | Protein Interaction Domains and Motifs | Transforming Growth Factor alpha - metabolism | Peptide Fragments - genetics | Genes, Reporter | Recombinant Proteins - metabolism | Peptide Fragments - metabolism | Signal Transduction | Transforming Growth Factor alpha - chemistry | NFATC Transcription Factors - metabolism | Models, Molecular | Recombinant Proteins - chemistry | NFATC Transcription Factors - chemistry | Recombinant Fusion Proteins - chemistry | Transforming Growth Factor alpha - genetics | Angiogenic Proteins - chemistry | Point Mutation | Peptide Fragments - chemistry | Peptide Fragments - agonists | beta-Arrestins | Ligands | Protein Conformation | Receptors, G-Protein-Coupled - genetics | Angiogenic Proteins - metabolism | Receptors, G-Protein-Coupled - chemistry | Amino Acid Substitution | NFATC Transcription Factors - genetics
Journal Article
JOURNAL OF BIOLOGICAL CHEMISTRY, ISSN 0021-9258, 03/2018, Volume 293, Issue 10, pp. 3477 - 3489
CD16a/Fc gamma receptor IIIa is the most abundant antibody Fc receptor expressed on human natural killer (NK) cells and activates a protective cytotoxic... 
NATURAL-KILLER-CELLS | BIOCHEMISTRY & MOLECULAR BIOLOGY | GLYCOFORMS | THERAPEUTIC ANTIBODIES | CARBOHYDRATE | HIGH-AFFINITY BINDING | GLYCOSYLATION | TISSUES | EXPRESSION | CANCER | RIIIA | Immunoglobulin Fc Fragments - metabolism | Humans | Receptors, IgG - chemistry | Male | Recombinant Fusion Proteins - metabolism | Receptors, IgG - metabolism | Receptors, IgG - agonists | Receptors, IgG - genetics | HEK293 Cells | Killer Cells, Natural - immunology | Polysaccharides - chemistry | Protein Interaction Domains and Motifs | Peptide Fragments - genetics | Antibodies, Monoclonal - chemistry | Carbohydrate Sequence | Recombinant Proteins - metabolism | Peptide Fragments - metabolism | Antibodies, Monoclonal - pharmacology | Cells, Cultured | Solubility | Models, Molecular | Recombinant Proteins - chemistry | Immunoglobulin Fc Fragments - chemistry | Glycosylation | Recombinant Fusion Proteins - chemistry | Polysaccharides - metabolism | Antibodies, Monoclonal - genetics | Cell Lineage | Killer Cells, Natural - cytology | Peptide Fragments - chemistry | Peptide Fragments - agonists | Ligands | Protein Conformation | Aged | Killer Cells, Natural - drug effects | Protein Processing, Post-Translational | Antibodies, Monoclonal - metabolism | Killer Cells, Natural - metabolism | Immunoglobulin Fc Fragments - genetics | Editors' Picks | post-translational modification (PTM) | Fc γ receptors IIIa | antibody | glycomics | protein glycosylation | glycosylation | N-glycan | Fc γ receptor | protein secretion
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 2017, Volume 292, Issue 44, pp. 18178 - 18191
Unlike age-matched men, premenopausal women benefit from cardiovascular protection. Estrogens protect against apoptosis of endothelial cells (ECs), one of the... 
Endothelium, Vascular - cytology | Tumor Necrosis Factor-alpha - metabolism | Apoptosis - drug effects | Humans | Receptor, Notch1 - chemistry | Endothelium, Vascular - drug effects | Estrogen Receptor beta - metabolism | Protease Inhibitors - pharmacology | Estrogen Receptor alpha - agonists | Estrogen Receptor beta - agonists | Estrogen Receptor beta - genetics | Protein Processing, Post-Translational - drug effects | RNA Interference | Receptor, Notch1 - agonists | Human Umbilical Vein Endothelial Cells - cytology | Estrogen Receptor alpha - metabolism | Protein Interaction Domains and Motifs | Phosphorylation - drug effects | Proto-Oncogene Proteins c-akt - metabolism | Estrogen Receptor beta - antagonists & inhibitors | Peptide Fragments - genetics | Endothelium, Vascular - immunology | Recombinant Proteins - metabolism | Estradiol - metabolism | Peptide Fragments - metabolism | Cells, Cultured | Recombinant Proteins - chemistry | Estrogen Receptor alpha - antagonists & inhibitors | Receptor, Notch1 - metabolism | Amyloid Precursor Protein Secretases - metabolism | Peptide Fragments - chemistry | Estrogen Receptor alpha - genetics | Signal Transduction - drug effects | Endothelium, Vascular - metabolism | Peptide Fragments - agonists | Proto-Oncogene Proteins c-akt - agonists | Protein Kinase Inhibitors - pharmacology | Amyloid Precursor Protein Secretases - antagonists & inhibitors | Receptor, Notch1 - genetics | Tumor Necrosis Factor-alpha - antagonists & inhibitors | estrogen | Notch pathway | tumor necrosis factor (TNF) | ERβ | estrogen receptor | Notch1 | apoptosis | Akt | endothelial dysfunction | Cell Biology
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 06/2017, Volume 292, Issue 24, pp. 9865 - 9881
The glucagon receptor (GCGR) belongs to the secretin-like (class B) family of G protein-coupled receptors (GPCRs) and is activated by the peptide hormone... 
BETA ADRENERGIC-RECEPTOR | LIGAND-BINDING | GLUCAGON RECEPTOR | IONIC LOCK | CRYSTAL-STRUCTURE | BIOCHEMISTRY & MOLECULAR BIOLOGY | CROSS-LINKING STRATEGY | METAPHYSEAL CHONDRODYSPLASIA | BETA-ADRENERGIC RECEPTOR | PEPTIDE | MUSCARINIC ACETYLCHOLINE-RECEPTOR | Receptor, Parathyroid Hormone, Type 1 - chemistry | Receptors, Corticotropin-Releasing Hormone - metabolism | Receptor, Parathyroid Hormone, Type 1 - metabolism | Humans | Receptors, Corticotropin-Releasing Hormone - agonists | Receptors, Corticotropin-Releasing Hormone - genetics | Receptor, Parathyroid Hormone, Type 1 - agonists | Recombinant Fusion Proteins - metabolism | Receptors, Vasoactive Intestinal Polypeptide, Type I - agonists | Receptors, Pituitary Adenylate Cyclase-Activating Polypeptide, Type I - chemistry | Conserved Sequence | Protein Interaction Domains and Motifs | Receptors, Pituitary Adenylate Cyclase-Activating Polypeptide, Type I - agonists | Receptors, Pituitary Adenylate Cyclase-Activating Polypeptide, Type I - metabolism | Receptors, Vasoactive Intestinal Polypeptide, Type I - metabolism | Protein Stability | Binding Sites | Peptide Fragments - genetics | Second Messenger Systems | Receptors, Glucagon - agonists | Receptors, Glucagon - genetics | Receptors, Vasoactive Intestinal Polypeptide, Type I - chemistry | Recombinant Proteins - metabolism | Amino Acid Sequence | Cell Line | Peptide Fragments - metabolism | Mutagenesis, Site-Directed | Models, Molecular | Receptors, Glucagon - metabolism | Recombinant Proteins - chemistry | Recombinant Fusion Proteins - chemistry | Receptors, Vasoactive Intestinal Polypeptide, Type I - genetics | Peptide Fragments - chemistry | Peptide Fragments - agonists | Receptors, Glucagon - chemistry | Hydrophobic and Hydrophilic Interactions | Receptor, Parathyroid Hormone, Type 1 - genetics | Ligands | Protein Conformation | Structural Homology, Protein | Mutation | Receptors, Pituitary Adenylate Cyclase-Activating Polypeptide, Type I - genetics | Receptors, Corticotropin-Releasing Hormone - chemistry | Amino Acid Substitution | Index Medicus | Editors' Picks | 7-helix receptor | G protein-coupled receptor (GPCR) | parathyroid hormone | glucagon | arrestin
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 2017, Volume 292, Issue 50, pp. 20354 - 20361
In the yeast Saccharomyces cerevisiae, the exposure to mating pheromone activates a prototypic mitogen-activated protein kinase (MAPK) cascade and triggers a... 
differentiation | SPECIFICITY | PHOSPHORYLATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | mitogen-activated protein kinase (MAPK) | PROLIFERATION | SIGNALING DYNAMICS | yeast mating response | imaging | SACCHAROMYCES-CEREVISIAE | cell fate decision | PATHWAY | cell signaling | GROWTH | GENE-EXPRESSION | pheromone | FEEDBACK | single-cell analysis | Cytoskeletal Proteins - genetics | Mating Factor - agonists | Saccharomyces cerevisiae - drug effects | Green Fluorescent Proteins - genetics | Mating Factor - metabolism | Protein Transport - drug effects | Cytoskeletal Proteins - agonists | Recombinant Fusion Proteins - metabolism | Mitogen-Activated Protein Kinases - chemistry | Gene Deletion | Cytoskeletal Proteins - metabolism | Membrane Proteins - metabolism | Green Fluorescent Proteins - chemistry | Single-Cell Analysis | Peptide Fragments - genetics | Recombinant Proteins - metabolism | Green Fluorescent Proteins - metabolism | Peptide Fragments - metabolism | Saccharomyces cerevisiae - physiology | Pheromones - pharmacology | Membrane Proteins - genetics | Recombinant Proteins - chemistry | Cytoskeletal Proteins - chemistry | Recombinant Fusion Proteins - chemistry | Saccharomyces cerevisiae Proteins - genetics | Enzyme Activation - drug effects | Membrane Proteins - agonists | Gene Expression Regulation, Bacterial - drug effects | Peptide Fragments - chemistry | MAP Kinase Signaling System - drug effects | Membrane Proteins - chemistry | Peptide Fragments - agonists | Saccharomyces cerevisiae Proteins - metabolism | Saccharomyces cerevisiae - enzymology | Genes, Reporter - drug effects | Mitogen-Activated Protein Kinases - genetics | Kinetics | Mutation | Saccharomyces cerevisiae Proteins - agonists | Saccharomyces cerevisiae - growth & development | Amino Acid Substitution | Mitogen-Activated Protein Kinases - metabolism | Saccharomyces cerevisiae Proteins - chemistry | Accelerated Communications
Journal Article