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FEBS Letters, ISSN 0014-5793, 07/2015, Volume 589, Issue 16, pp. 2100 - 2109
...‐tagged ATG9, and increased autophagic flux independent of its transport activity. G6PT negatively regulated mTORC1 activity, demonstrating that G6PT functions upstream of mTORC1 in stimulating autophagy... 
Screening | G6PT | ULK1 | ATG9 | Autophagy modulator | glucose-6-phosphate transporter | N-terminus of Venus vector | chlorogenic acid | BiFC | bimolecular fluorescence complementation | CHA | C-terminus of Venus vector | NEURODEGENERATIVE DISEASE | DISEASE TYPE-IB | BIOCHEMISTRY & MOLECULAR BIOLOGY | CELL-GROWTH | MACROAUTOPHAGY | MTOR | CELL BIOLOGY | MAMMALIAN ATG PROTEINS | FORMATION SITE | BIOPHYSICS | SIGNALING PATHWAY | AMINO-ACIDS | ANTIPORTER DEFICIENT | Up-Regulation | TOR Serine-Threonine Kinases - metabolism | Vesicular Transport Proteins - metabolism | Humans | Intracellular Signaling Peptides and Proteins - metabolism | Multiprotein Complexes - metabolism | RNA Interference | Intracellular Signaling Peptides and Proteins - genetics | Monosaccharide Transport Proteins - metabolism | Peptide Fragments - genetics | Protein-Serine-Threonine Kinases - metabolism | Monosaccharide Transport Proteins - genetics | Membrane Proteins - genetics | Phagosomes - metabolism | Recombinant Proteins - chemistry | Antiporters - metabolism | Recombinant Fusion Proteins - chemistry | Huntingtin Protein | Peptide Fragments - chemistry | Models, Biological | Protein-Serine-Threonine Kinases - chemistry | Antiporters - antagonists & inhibitors | Hepatocytes - enzymology | Autophagy-Related Proteins | Phagosomes - enzymology | Cricetulus | Hepatocytes - metabolism | Autophagy | Recombinant Fusion Proteins - metabolism | Autophagy-Related Protein-1 Homolog | Mechanistic Target of Rapamycin Complex 1 | Multiprotein Complexes - antagonists & inhibitors | TOR Serine-Threonine Kinases - antagonists & inhibitors | Hepatocytes - cytology | Nerve Tissue Proteins - chemistry | Antiporters - genetics | Membrane Proteins - metabolism | Protein Interaction Domains and Motifs | Monosaccharide Transport Proteins - antagonists & inhibitors | Recombinant Proteins - metabolism | Cell Line | Peptide Fragments - metabolism | Vesicular Transport Proteins - genetics | Protein-Serine-Threonine Kinases - genetics | Mutant Proteins - metabolism | Vesicular Transport Proteins - chemistry | Recombinant Proteins - genetics | Nerve Tissue Proteins - genetics | Protein Transport | Nerve Tissue Proteins - metabolism | Animals | Membrane Proteins - chemistry | Intracellular Signaling Peptides and Proteins - chemistry | Mutant Proteins - chemistry | Amino Acid Substitution | Phosphates | Enzymes | Glucose | Analysis | Dextrose
Journal Article
Proceedings of the National Academy of Sciences - PNAS, ISSN 1091-6490, 2011, Volume 108, Issue 23, pp. 9361 - 9366
...) transports galactopyranosides and is specifically inactivated by methanethiosulfonyl-galactopyranosides (MTS-gal... 
Membrane transport proteins | Proteins | Hydroxyls | Escherichia coli | Atoms | Biochemistry | Sugars | Binding sites | Alkylation | Crystal structure | Membrane protein crystal structure | Bioenergetics | Sugar binding | Affinity labeling | MTS reagents | affinity labeling | MECHANISM | VESICLES | MULTIDISCIPLINARY SCIENCES | ESCHERICHIA-COLI | membrane protein crystal structure | sugar binding | MODEL | ACTIVE-TRANSPORT | MEMBRANE-TRANSPORT PROTEIN | bioenergetics | SUBSTRATE-BINDING SITE | Galactose - metabolism | Mesylates - metabolism | Substrate Specificity | Cysteine - genetics | Lactose - metabolism | Biological Transport | Membrane Transport Proteins - genetics | X-Ray Diffraction | Escherichia coli - metabolism | Membrane Transport Proteins - metabolism | Cysteine - metabolism | Monosaccharide Transport Proteins - metabolism | Monosaccharide Transport Proteins - genetics | Protein Structure, Tertiary | Crystallization | Models, Molecular | Escherichia coli Proteins - metabolism | Binding Sites - genetics | Cysteine - chemistry | Mesylates - chemistry | Symporters - chemistry | Symporters - metabolism | Membrane Transport Proteins - chemistry | Galactose - chemistry | Escherichia coli - genetics | Symporters - genetics | Escherichia coli Proteins - genetics | Protein Binding | Lactose - chemistry | Protein Conformation | Monosaccharide Transport Proteins - chemistry | Escherichia coli Proteins - chemistry | Amino Acid Substitution | MEMBRANE PROTEINS | SACCHAROSE | ESCHERICHIA COLI | BASIC BIOLOGICAL SCIENCES | SUBSTRATES | LACTOSE | CRYSTAL STRUCTURE | 60 APPLIED LIFE SCIENCES | DISULFIDES | INACTIVATION | AFFINITY | COORDINATES | RESIDUES | Biological Sciences
Journal Article
BMC plant biology, ISSN 1471-2229, 2010, Volume 10, Issue 1, pp. 245 - 245
.... They are distributed through the plant via sugar transporters, which are involved not only in sugar long-distance transport via the loading and the unloading of the conducting complex, but also... 
HEXOSE TRANSPORTER | MONOSACCHARIDE TRANSPORTER | SUCROSE TRANSPORTER | ARABIDOPSIS-THALIANA | XYLEM PARENCHYMA CELLS | SWEET-POTATO | FUNCTIONAL-CHARACTERIZATION | MEDIATED TRANSCRIPTIONAL REGULATION | GRAPE BERRY | PHYSIOLOGICAL CHARACTERIZATION | PLANT SCIENCES | Arabidopsis Proteins - genetics | Multigene Family | Carbohydrates - pharmacology | Oligonucleotide Array Sequence Analysis | Gene Expression Profiling | Phylogeny | Promoter Regions, Genetic - genetics | Arabidopsis Proteins - metabolism | Plant Proteins - genetics | Blotting, Northern | Gene Expression Regulation, Plant - drug effects | Plant Proteins - classification | Membrane Transport Proteins - classification | Membrane Transport Proteins - genetics | Membrane Transport Proteins - metabolism | Plant Proteins - metabolism | Vitis - metabolism | Arabidopsis Proteins - classification | Monosaccharide Transport Proteins - metabolism | Vitis - genetics | Monosaccharide Transport Proteins - classification | Polymers - metabolism | Monosaccharide Transport Proteins - genetics | Usage | DNA microarrays | Grapes | Physiological aspects | Genetic aspects | Research | Gene expression | Phylogeny (Botany) | Proteins | Membranes | Sucrose | Cloning | Genomes | Hybridization | Manuscripts | Sugar | Promoter Regions, Genetic | Carbohydrates | Vitis | Life Sciences | Arabidopsis Proteins | Membrane Transport Proteins | Monosaccharide Transport Proteins | Gene Expression Regulation, Plant | Plant Proteins | Vegetal Biology | Polymers
Journal Article
Molecular Biology of the Cell, ISSN 1059-1524, 01/2015, Volume 26, Issue 2, pp. 373 - 386
..., is displaced from the nucleus. Its displacement is dependent on Ca2+/calmodulin-dependent kinase kinase, Ssp1, and Sds23 inhibition of PP2A/PP6-like protein phosphatases... 
CELL-DIVISION | SKELETAL-MUSCLE | PROTEIN-KINASE | CATABOLITE REPRESSION | FACILITATED HEXOSE | FAMILY KINASE POM1 | SACCHAROMYCES-CEREVISIAE | PLASMA-MEMBRANE | HEXOSE TRANSPORTERS | SCHIZOSACCHAROMYCES-POMBE | CELL BIOLOGY | Glucose Transport Proteins, Facilitative - metabolism | TOR Serine-Threonine Kinases - metabolism | Humans | Phosphoprotein Phosphatases - metabolism | Immunoblotting | Multiprotein Complexes - genetics | Green Fluorescent Proteins - genetics | Mechanistic Target of Rapamycin Complex 2 | Schizosaccharomyces - genetics | Gene Expression Regulation, Fungal - drug effects | Multiprotein Complexes - metabolism | Cell Nucleus - metabolism | Protein Isoforms - metabolism | TOR Serine-Threonine Kinases - genetics | Schizosaccharomyces pombe Proteins - metabolism | Cell Cycle Proteins - genetics | Time-Lapse Imaging - methods | Glucose Transport Proteins, Facilitative - genetics | Monosaccharide Transport Proteins - metabolism | Monosaccharide Transport Proteins - genetics | Green Fluorescent Proteins - metabolism | Schizosaccharomyces pombe Proteins - genetics | Cell Cycle Proteins - metabolism | HSP70 Heat-Shock Proteins - genetics | Glucose - pharmacology | Calcium-Calmodulin-Dependent Protein Kinase Kinase - genetics | HSP70 Heat-Shock Proteins - metabolism | Schizosaccharomyces - metabolism | Phosphoprotein Phosphatases - genetics | Active Transport, Cell Nucleus - drug effects | Glucose - pharmacokinetics | Calcium-Calmodulin-Dependent Protein Kinase Kinase - metabolism | Glucose - metabolism | Mutation | Microscopy, Fluorescence | Protein Isoforms - genetics
Journal Article
The Journal of cell biology, ISSN 0021-9525, 4/2004, Volume 165, Issue 1, pp. 53 - 62
.... Here, we use as a model the lactose permease (LacY), a membrane transport protein with a known three-dimensional structure, to determine whether YidC plays a role in polytopic membrane protein insertion and/or folding... 
Membrane transport proteins | String theory | Plasmids | Escherichia coli | Fluorescence | Antibodies | Epitopes | Cells | P branes | Membrane proteins | Oxal/Alb3 protein family | Protein folding | SecYEG | Membrane insertion | LacY | RESPIRATORY-CHAIN | INSERTION | Oxa1/Alb3 protein family | ESCHERICHIA-COLI | MONOCLONAL-ANTIBODY | TRANSPORT PROTEINS | CELL BIOLOGY | SIGNAL-RECOGNITION PARTICLE | LACTOSE PERMEASE | NASCENT FTSQ | membrane insertion | protein folding | LAC PERMEASE | COLI INNER MEMBRANE | Protein Binding - genetics | Epitopes - metabolism | Molecular Chaperones - metabolism | Proteolipids - metabolism | Protein Transport - physiology | Epitopes - immunology | Membrane Transport Proteins - genetics | Escherichia coli - metabolism | Membrane Transport Proteins - metabolism | Membrane Proteins - metabolism | Protein Biosynthesis - genetics | Monosaccharide Transport Proteins - metabolism | Antibodies, Monoclonal - immunology | Monosaccharide Transport Proteins - genetics | Molecular Chaperones - genetics | Models, Molecular | Escherichia coli Proteins - metabolism | Protein Binding - immunology | Protein Folding | Symporters - metabolism | Carrier Proteins - metabolism | Symporters - genetics | Escherichia coli Proteins - genetics | Membrane Lipids - metabolism | Antibodies, Monoclonal - metabolism | Escherichia coli - ultrastructure | Intracellular Membranes - metabolism | Research | LacY; membrane insertion; protein folding; SecYEG; Oxa1 | Alb3 protein family
Journal Article
The Journal of biological chemistry, ISSN 1083-351X, 2003, Volume 278, Issue 46, pp. 45777 - 45784
.... This effect of IL-6 was accompanied by a marked reduction in IRS-1, but not IRS-2, protein expression, and insulin-stimulated tyrosine phosphorylation, whereas no inhibitory effect was seen... 
IRS 1 | PROTEIN | LIPOLYSIS | BIOCHEMISTRY & MOLECULAR BIOLOGY | SENSITIVITY | RECEPTOR | GLUCOSE-TRANSPORT | TNF-ALPHA | RELEASE | EXPRESSION | ADIPOSE-TISSUE | Tumor Necrosis Factor-alpha - metabolism | Up-Regulation | Phosphorylation | Humans | Middle Aged | Repressor Proteins | Phosphoproteins - metabolism | RNA, Messenger - metabolism | Suppressor of Cytokine Signaling Proteins | Dose-Response Relationship, Drug | Adipose Tissue - metabolism | Mitogen-Activated Protein Kinase Kinases - metabolism | Muscle Proteins | MAP Kinase Kinase 4 | Biological Transport | Time Factors | Insulin Receptor Substrate Proteins | JNK Mitogen-Activated Protein Kinases | Adult | Transcription, Genetic | Interleukin-8 - metabolism | Interleukin-6 - metabolism | Monosaccharide Transport Proteins - metabolism | Tyrosine - chemistry | RNA - metabolism | Cytokines - metabolism | Glucose Transporter Type 4 | Insulin Resistance | 3T3-L1 Cells | Reverse Transcriptase Polymerase Chain Reaction | Suppressor of Cytokine Signaling 3 Protein | Blotting, Northern | Tyrosine - metabolism | Animals | Proteins - metabolism | Adipocytes - metabolism | Glucose - metabolism | Mice | Transcription Factors | insulin receptors | pS-307 protein | peroxisome proliferator-activated receptors | IRS-1 protein | GLUT-4 protein | JNK protein | insulin-receptor substrate 2 | insulin resistance | glucose transporter GLUT4 | insulin-receptor substrate 1 protein
Journal Article
Diabetes (New York, N.Y.), ISSN 1939-327X, 2018, Volume 67, Issue 2, pp. 265 - 277
Mitophagy is a cellular quality-control pathway, which is essential for elimination of unhealthy mitochondria. While mitophagy is critical to pancreatic... 
PARKIN-MEDIATED MITOPHAGY | INSULIN-SECRETION | GROWTH | ENDOCRINOLOGY & METABOLISM | DOWN-REGULATION | LENALIDOMIDE | RECEPTOR | DEGRADATION | STABILIZES | PROMOTES | CANCER | Tissue Banks | Humans | Endosomal Sorting Complexes Required for Transport - genetics | Ubiquitin-Protein Ligases - antagonists & inhibitors | Lectins, C-Type - genetics | Recombinant Fusion Proteins - metabolism | Lectins, C-Type - chemistry | Lectins, C-Type - metabolism | Endopeptidases - chemistry | Insulin-Secreting Cells - metabolism | Ubiquitination - drug effects | Endosomal Sorting Complexes Required for Transport - antagonists & inhibitors | Ubiquitin Thiolesterase - metabolism | Endosomal Sorting Complexes Required for Transport - chemistry | Insulin-Secreting Cells - cytology | Insulin Secretion | Monosaccharide Transport Proteins - metabolism | Ubiquitin Thiolesterase - antagonists & inhibitors | Monosaccharide Transport Proteins - antagonists & inhibitors | Monosaccharide Transport Proteins - genetics | Cell Line | Endopeptidases - metabolism | Tissue Culture Techniques | Mice, Inbred C57BL | Cells, Cultured | Endosomal Sorting Complexes Required for Transport - metabolism | Enzyme Inhibitors - pharmacology | Ubiquitin-Protein Ligases - metabolism | Angiogenesis Inhibitors - pharmacology | Mice, Transgenic | Recombinant Fusion Proteins - chemistry | Ubiquitin Thiolesterase - genetics | Ubiquitin-Protein Ligases - chemistry | Mice, Knockout | Insulin - metabolism | Animals | Endopeptidases - genetics | Insulin-Secreting Cells - drug effects | Mitophagy - drug effects | Protein Stability - drug effects | Glucose - metabolism | Mice | Monosaccharide Transport Proteins - chemistry | Ubiquitin-Protein Ligases - genetics | Lectins, C-Type - antagonists & inhibitors | Protein Multimerization - drug effects | Ubiquitin Thiolesterase - chemistry | Crosses, Genetic | Ubiquitin | Mitochondria | Pancreatic beta cells | Research | 0711 | Islet Studies
Journal Article
Nature communications, ISSN 2041-1723, 2018, Volume 9, Issue 1, pp. 4151 - 12
Journal Article
Proceedings of the National Academy of Sciences - PNAS, ISSN 1091-6490, 2014, Volume 111, Issue 14, pp. 5159 - 5164
Journal Article