The Importance of Protein Phosphorylation for Signaling and Metabolism in Response to Diel Light Cycling and Nutrient Availability in a Marine Diatom
暂无分享,去创建一个
Sarah R. Smith | K. Hixson | Justin Tan | A. Allen | A. Kustka | Maxine Tan | James K. McCarthy | Maxine H. Tan | Adam B Kustka
[1] M. Sachs,et al. Circadian clock control of eIF2α phosphorylation is necessary for rhythmic translation initiation , 2020, Proceedings of the National Academy of Sciences.
[2] A. Horák,et al. Reduction-dependent siderophore assimilation in a model pennate diatom , 2019, Proceedings of the National Academy of Sciences.
[3] Sarah R. Smith,et al. Evolution and regulation of nitrogen flux through compartmentalized metabolic networks in a marine diatom , 2019, Nature Communications.
[4] C. Duarte,et al. Silicic acid limitation drives bloom termination and potential carbon sequestration in an Arctic bloom , 2019, Scientific Reports.
[5] Nitrate and ammonium fluxes to diatoms and dinoflagellates at a single cell level in mixed field communities in the sea , 2019, Scientific Reports.
[6] A. Barkan,et al. Correction: Multilevel effects of light on ribosome dynamics in chloroplasts program genome-wide and psbA-specific changes in translation , 2019, PLoS genetics.
[7] Linda V. Bakker,et al. Orchestration of transcriptome, proteome and metabolome in the diatom Phaeodactylum tricornutum during nitrogen limitation , 2018, Algal Research.
[8] A. Barkan,et al. Multilevel effects of light on ribosome dynamics in chloroplasts program genome-wide and psbA-specific changes in translation , 2018, PLoS genetics.
[9] France Lam,et al. Endocytosis-mediated siderophore uptake as a strategy for Fe acquisition in diatoms , 2018, Science Advances.
[10] Bogumil J. Karas,et al. Carbonate-sensitive phytotransferrin controls high-affinity iron uptake in diatoms , 2018, Nature.
[11] Gerald A Tuskan,et al. Classification of Complete Proteomes of Different Organisms and Protein Sets Based on Their Protein Distributions in Terms of Some Key Attributes of Proteins , 2018, International journal of genomics.
[12] M. Brzezinski,et al. Diatom Transcriptional and Physiological Responses to Changes in Iron Bioavailability across Ocean Provinces , 2017, Front. Mar. Sci..
[13] Sarah R. Smith,et al. Nitrate Reductase Knockout Uncouples Nitrate Transport from Nitrate Assimilation and Drives Repartitioning of Carbon Flux in a Model Pennate Diatom[OPEN] , 2017, Plant Cell.
[14] J. Franco-Zorrilla,et al. The transcription factor bZIP14 regulates the TCA cycle in the diatom Phaeodactylum tricornutum , 2017, The EMBO journal.
[15] A. Gojon,et al. Post-translational regulation of nitrogen transporters in plants and microorganisms , 2017, Journal of experimental botany.
[16] W. Miller,et al. Eukaryotic translation initiation factor 4G (eIF4G) coordinates interactions with eIF4A, eIF4B, and eIF4E in binding and translation of the barley yellow dwarf virus 3′ cap-independent translation element (BTE)* , 2017, The Journal of Biological Chemistry.
[17] S. Oliver,et al. Estimating the total number of phosphoproteins and phosphorylation sites in eukaryotic proteomes , 2017, GigaScience.
[18] T. Kaoud,et al. Signal Integration at Elongation Factor 2 Kinase , 2016, The Journal of Biological Chemistry.
[19] Sarah R. Smith,et al. Transcriptional Orchestration of the Global Cellular Response of a Model Pennate Diatom to Diel Light Cycling under Iron Limitation , 2016, PLoS genetics.
[20] T. Kwon,et al. Depletion of vacuolar protein sorting-associated protein 35 is associated with increased lysosomal degradation of aquaporin-2. , 2016, American journal of physiology. Renal physiology.
[21] S. Vaidyanathan,et al. Proteome response of Phaeodactylum tricornutum, during lipid accumulation induced by nitrogen depletion , 2016, Algal research.
[22] Hong Ma,et al. Abundant protein phosphorylation potentially regulates Arabidopsis anther development , 2016, Journal of experimental botany.
[23] A. Vardi,et al. Chronic Iron Limitation Confers Transient Resistance to Oxidative Stress in Marine Diatoms1 , 2016, Plant Physiology.
[24] Z. Fu,et al. Proteomic analyses bring new insights into the effect of a dark stress on lipid biosynthesis in Phaeodactylum tricornutum , 2016, Scientific Reports.
[25] P. Falkowski,et al. An RNA interference knock-down of nitrate reductase enhances lipid biosynthesis in the diatom Phaeodactylum tricornutum. , 2015, The Plant journal : for cell and molecular biology.
[26] Z. Fu,et al. Analysis of the Proteome of the Marine Diatom Phaeodactylum tricornutum Exposed to Aluminum Providing Insights into Aluminum Toxicity Mechanisms. , 2015, Environmental science & technology.
[27] Tom O. Delmont,et al. Phytoplankton–bacterial interactions mediate micronutrient colimitation at the coastal Antarctic sea ice edge , 2015, Proceedings of the National Academy of Sciences.
[28] E. Virginia Armbrust,et al. Diversity and Evolutionary History of Iron Metabolism Genes in Diatoms , 2015, PloS one.
[29] Alaguraj Veluchamy,et al. A Novel Protein, Ubiquitous in Marine Phytoplankton, Concentrates Iron at the Cell Surface and Facilitates Uptake , 2015, Current Biology.
[30] N. Sonenberg,et al. Targeting the eIF4F translation initiation complex: a critical nexus for cancer development. , 2015, Cancer research.
[31] S. Huang,et al. Phosphorylation of the translation initiation factor eIF2α at serine 51 determines the cell fate decisions of Akt in response to oxidative stress , 2015, Cell Death and Disease.
[32] M. Helm,et al. Phosphorylation of Elp1 by Hrr25 Is Required for Elongator-Dependent tRNA Modification in Yeast , 2015, PLoS genetics.
[33] LeAnn P. Whitney,et al. Genetic indicators of iron limitation in wild populations of Thalassiosira oceanica from the northeast Pacific Ocean , 2014, The ISME Journal.
[34] Pavel A. Pevzner,et al. Universal database search tool for proteomics , 2014, Nature Communications.
[35] L. Hicks,et al. The Global Phosphoproteome of Chlamydomonas reinhardtii Reveals Complex Organellar Phosphorylation in the Flagella and Thylakoid Membrane * , 2014, Molecular & Cellular Proteomics.
[36] Mingkun Yang,et al. Phosphoproteomic analysis provides novel insights into stress responses in Phaeodactylum tricornutum, a model diatom. , 2014, Journal of proteome research.
[37] Xinguang Zhu,et al. Posttranslational Modification of Maize Chloroplast Pyruvate Orthophosphate Dikinase Reveals the Precise Regulatory Mechanism of Its Enzymatic Activity1[C][W][OPEN] , 2014, Plant Physiology.
[38] Thomas J. Begley,et al. A System of RNA Modifications and Biased Codon Use Controls Cellular Stress Response at the Level of Translation , 2014, Chemical research in toxicology.
[39] M. Marletta,et al. Phosphorylation-dependent derepression by the response regulator HnoC in the Shewanella oneidensis nitric oxide signaling network , 2013, Proceedings of the National Academy of Sciences.
[40] J. Dyck,et al. Single phosphorylation sites in Acc1 and Acc2 regulate lipid homeostasis and the insulin–sensitizing effects of metformin , 2013, Nature Medicine.
[41] B. Nunn,et al. Diatom Proteomics Reveals Unique Acclimation Strategies to Mitigate Fe Limitation , 2013, PloS one.
[42] T. Romeis,et al. Calcium-Dependent Protein Kinases: Hubs in Plant Stress Signaling and Development1 , 2013, Plant Physiology.
[43] K. Arrigo,et al. Processes and patterns of oceanic nutrient limitation , 2013 .
[44] A. Vaughan,et al. CyclinB1/Cdk1 phosphorylates mitochondrial antioxidant MnSOD in cell adaptive response to radiation stress. , 2013, Journal of molecular cell biology.
[45] Kara Dolinski,et al. The PhosphoGRID Saccharomyces cerevisiae protein phosphorylation site database: version 2.0 update , 2013, Database J. Biol. Databases Curation.
[46] M. Peng,et al. Toward a comprehensive characterization of a human cancer cell phosphoproteome. , 2013, Journal of proteome research.
[47] M. Petter,et al. The Role of Bromodomain Proteins in Regulating Gene Expression , 2012, Genes.
[48] V. Quesada,et al. Deubiquitinases in cancer: new functions and therapeutic options , 2012, Oncogene.
[49] M. Parker,et al. Coupled effects of light and nitrogen source on the urea cycle and nitrogen metabolism over a diel cycle in the marine diatom Thalassiosira pseudonana. , 2012, Protist.
[50] J. Buchner,et al. Conformational switching of the molecular chaperone Hsp90 via regulated phosphorylation. , 2012, Molecular cell.
[51] Kathryn S. Lilley,et al. Evaluation and Properties of the Budding Yeast Phosphoproteome , 2012, Molecular & Cellular Proteomics.
[52] David M Schruth,et al. Comparative metatranscriptomics identifies molecular bases for the physiological responses of phytoplankton to varying iron availability , 2012, Proceedings of the National Academy of Sciences.
[53] Ulrich C. Klostermeier,et al. Genome and low-iron response of an oceanic diatom adapted to chronic iron limitation , 2012, Genome Biology.
[54] E. Cabrera,et al. Npr1 Ser/Thr Protein Kinase Links Nitrogen Source Quality and Carbon Availability with the Yeast Nitrate Transporter (Ynt1) Levels* , 2011, The Journal of Biological Chemistry.
[55] Edward L. Huttlin,et al. A Tissue-Specific Atlas of Mouse Protein Phosphorylation and Expression , 2010, Cell.
[56] M. Wickens,et al. Translational Repression by Deadenylases* , 2010, The Journal of Biological Chemistry.
[57] T. Pawson,et al. Post-translational modifications in signal integration , 2010, Nature Structural &Molecular Biology.
[58] A. Byström,et al. Elongator function in tRNA wobble uridine modification is conserved between yeast and plants , 2010, Molecular microbiology.
[59] J. Belasco,et al. CCR4-NOT Deadenylates mRNA Associated with RNA-Induced Silencing Complexes in Human Cells , 2010, Molecular and Cellular Biology.
[60] Robert Schmidt,et al. PhosPhAt: the Arabidopsis thaliana phosphorylation site database. An update , 2009, Nucleic Acids Res..
[61] J. Blenis,et al. mTORC1-Mediated Control of Protein Translation , 2010 .
[62] B. Usadel,et al. Ribosome and transcript copy numbers, polysome occupancy and enzyme dynamics in Arabidopsis , 2009, Molecular systems biology.
[63] Zhiguo Zhang,et al. The Elongator Complex Interacts with PCNA and Modulates Transcriptional Silencing and Sensitivity to DNA Damage Agents , 2009, PLoS genetics.
[64] Y. Tsay,et al. CHL1 Functions as a Nitrate Sensor in Plants , 2009, Cell.
[65] S. Ficarro,et al. Magnetic bead processor for rapid evaluation and optimization of parameters for phosphopeptide enrichment. , 2009, Analytical chemistry.
[66] W. Gruissem,et al. Large-Scale Arabidopsis Phosphoproteome Profiling Reveals Novel Chloroplast Kinase Substrates and Phosphorylation Networks1[W] , 2009, Plant Physiology.
[67] Francisco J. Navarro,et al. Phosphorylation of the Yeast Nitrate Transporter Ynt1 Is Essential for Delivery to the Plasma Membrane during Nitrogen Limitation* , 2008, Journal of Biological Chemistry.
[68] A. Fernie,et al. Whole-cell response of the pennate diatom Phaeodactylum tricornutum to iron starvation , 2008, Proceedings of the National Academy of Sciences.
[69] Ling Zhu,et al. Light-Induced Phosphorylation and Degradation of the Negative Regulator PHYTOCHROME-INTERACTING FACTOR1 from Arabidopsis Depend upon Its Direct Physical Interactions with Photoactivated Phytochromes[W] , 2008, The Plant Cell Online.
[70] Hideyuki Takahashi,et al. Arabidopsis VPS35, a retromer component, is required for vacuolar protein sorting and involved in plant growth and leaf senescence. , 2008, Plant & cell physiology.
[71] T. Hunter. The age of crosstalk: phosphorylation, ubiquitination, and beyond. , 2007, Molecular cell.
[72] Elena Litchman,et al. The role of functional traits and trade-offs in structuring phytoplankton communities: scaling from cellular to ecosystem level. , 2007, Ecology letters.
[73] J. Gray,et al. Coordinate Regulation of Phosphoenolpyruvate Carboxylase and Phosphoenolpyruvate Carboxykinase by Light and CO2 during C4 Photosynthesis1[OA] , 2007, Plant Physiology.
[74] Steven P Gygi,et al. A probability-based approach for high-throughput protein phosphorylation analysis and site localization , 2006, Nature Biotechnology.
[75] O. Meyuhas,et al. Ribosomal protein S6 phosphorylation: from protein synthesis to cell size. , 2006, Trends in biochemical sciences.
[76] Min Gao,et al. Activation of the E3 ubiquitin ligase Itch through a phosphorylation-induced conformational change. , 2006, Proceedings of the National Academy of Sciences of the United States of America.
[77] Uwe Sauer,et al. The PEP-pyruvate-oxaloacetate node as the switch point for carbon flux distribution in bacteria. , 2005, FEMS microbiology reviews.
[78] S. Shimada,et al. 14-3-3 Proteins Modulate the Expression of Epithelial Na+ Channels by Phosphorylation-dependent Interaction with Nedd4-2 Ubiquitin Ligase* , 2005, Journal of Biological Chemistry.
[79] Chris Bowler,et al. Prospects in diatom research. , 2005, Current opinion in biotechnology.
[80] John D. Scott,et al. CK2 Phosphorylates SSRP1 and Inhibits Its DNA-binding Activity* , 2005, Journal of Biological Chemistry.
[81] K. Bruland,et al. Iron, macronutrients and diatom blooms in the Peru upwelling regime: Brown and blue waters of Peru , 2005 .
[82] Keith Lindsay,et al. Upper ocean ecosystem dynamics and iron cycling in a global three‐dimensional model , 2004 .
[83] N. Sonenberg,et al. Upstream and downstream of mTOR. , 2004, Genes & development.
[84] N. Krogan,et al. Bromodomain Factor 1 (Bdf1) Is Phosphorylated by Protein Kinase CK2 , 2004, Molecular and Cellular Biology.
[85] W. Gieskes,et al. Effects of iron limitation on photosynthesis and carbohydrate metabolism in the Antarctic diatom Chaetoceros brevis (Bacillariophyceae) , 2004 .
[86] C. Proud,et al. Stimulation of the AMP-activated Protein Kinase Leads to Activation of Eukaryotic Elongation Factor 2 Kinase and to Its Phosphorylation at a Novel Site, Serine 398* , 2004, Journal of Biological Chemistry.
[87] D. Nowara,et al. Cloning, functional expression and expression studies of the nitrate transporter gene from Chlorella sorokiniana (strain 211-8k) , 2003, Plant Molecular Biology.
[88] M. Tuite,et al. Translation elongation factor-3 (EF-3): An evolving eukaryotic ribosomal protein? , 1995, Journal of Molecular Evolution.
[89] A. Iglesias,et al. Phosphorylated Non-Phosphorylating Glyceraldehyde-3-Phosphate Dehydrogenase from Heterotrophic Cells of Wheat Interacts with 14-3-3 Proteins1 , 2003, Plant Physiology.
[90] T. Kieselbach,et al. A novel plant protein undergoing light-induced phosphorylation and release from the photosynthetic thylakoid membranes , 2003, Proceedings of the National Academy of Sciences of the United States of America.
[91] P. Cohen,et al. The origins of protein phosphorylation , 2002, Nature Cell Biology.
[92] R. Leegood,et al. Effects of phosphorylation on phosphoenolpyruvate carboxykinase from the C4 plant Guinea grass. , 2002, Plant physiology.
[93] Kenneth W. Bruland,et al. Iron and macronutrients in California coastal upwelling regimes: Implications for diatom blooms , 2001 .
[94] M. Clemens. Initiation Factor eIF2α Phosphorylation in Stress Responses and Apoptosis , 2001 .
[95] M. Clemens. Initiation factor eIF2 alpha phosphorylation in stress responses and apoptosis. , 2001, Progress in molecular and subcellular biology.
[96] S. Doney,et al. Iron cycling and nutrient-limitation patterns in surface waters of the World Ocean , 2001 .
[97] M. Lomas,et al. COMPARISONS OF NITRATE UPTAKE, STORAGE, AND REDUCTION IN MARINE DIATOMS AND FLAGELLATES , 2000 .
[98] S. Snyder,et al. The Inositol Hexakisphosphate Kinase Family , 2000, Journal of Biological Chemistry.
[99] S. Buratowski,et al. Bromodomain factor 1 corresponds to a missing piece of yeast TFIID. , 2000, Genes & development.
[100] G. Sarath,et al. Further analysis of maize C(4) pyruvate,orthophosphate dikinase phosphorylation by its bifunctional regulatory protein using selective substitutions of the regulatory Thr-456 and catalytic His-458 residues. , 2000, Archives of biochemistry and biophysics.
[101] I. Kudo,et al. Exhaustion of nitrate terminates a phytoplankton bloom in Funka Bay, Japan: change in SiO4:NO3 consumption rate during the bloom , 2000 .
[102] E. Knapp,et al. Structural alignment of ferredoxin and flavodoxin based on electrostatic potentials: Implications for their interactions with photosystem I and ferredoxin‐NADP reductase , 2000, Proteins.
[103] L. Graves,et al. Regulation of carbamoyl phosphate synthetase by MAP kinase , 2000, Nature.
[104] J. Ballesta,et al. Phosphorylation of the yeast ribosomal stalk. Functional effects and enzymes involved in the process. , 1999, FEMS microbiology reviews.
[105] H. Bonkovsky,et al. Heme oxygenase: recent advances in understanding its regulation and role. , 1999, Proceedings of the Association of American Physicians.
[106] R. Gunsalus,et al. Signal-Dependent Phosphorylation of the Membrane-Bound NarX Two-Component Sensor-Transmitter Protein ofEscherichia coli: Nitrate Elicits a Superior Anion Ligand Response Compared to Nitrite , 1999, Journal of bacteriology.
[107] K D Wilkinson,et al. Substrate specificity of deubiquitinating enzymes: ubiquitin C-terminal hydrolases. , 1998, Biochemistry.
[108] R. Pearson,et al. Rapamycin suppresses 5′TOP mRNA translation through inhibition of p70s6k , 1997, The EMBO journal.
[109] L. Pinna,et al. How do protein kinases recognize their substrates? , 1996, Biochimica et biophysica acta.
[110] J. Ballesta,et al. Proteins P1, P2, and P0, components of the eukaryotic ribosome stalk. New structural and functional aspects. , 1995, Biochemistry and cell biology = Biochimie et biologie cellulaire.
[111] D. M. Nelson,et al. Production and dissolution of biogenic silica in the ocean: Revised global estimates, comparison with regional data and relationship to biogenic sedimentation , 1995 .
[112] L. McAlister-Henn,et al. Glucose-induced phosphorylation of the MDH2 isozyme of malate dehydrogenase in Saccharomyces cerevisiae. , 1994, Archives of biochemistry and biophysics.
[113] J. Yates,et al. An approach to correlate tandem mass spectral data of peptides with amino acid sequences in a protein database , 1994, Journal of the American Society for Mass Spectrometry.
[114] M. Tuite,et al. Translation elongation factor 3: a fungus‐specific translation factor? , 1993, Molecular microbiology.
[115] E. Carrey,et al. Regulation of the mammalian carbamoyl-phosphate synthetase II by effectors and phosphorylation. Altered affinity for ATP and magnesium ions measured using the ammonia-dependent part reaction. , 1992, European journal of biochemistry.
[116] D. Hardie,et al. Identification by amino acid sequencing of three major regulatory phosphorylation sites on rat acetyl-CoA carboxylase. , 1988, European journal of biochemistry.
[117] R. Kisilevsky,et al. Ribosome conformational changes associated with protein S6 phosphorylation. , 1984, The Journal of biological chemistry.
[118] P. J. Syrett,et al. Uptake of Nitrate by the Diatom Phaeodactylum tricornutum , 1981 .
[119] P. J. Syrett,et al. Ammonium inhibition of nitrate uptake by the diatom, Phaeodactylum tricornutum , 1979 .
[120] B. Hemmings. Phosphorylation of NAD-dependent glutamate dehydrogenase from yeast. , 1978, The Journal of biological chemistry.
[121] J. Mcdowell,et al. Light-induced phosphorylation of rhodopsin in cattle photoreceptor membranes: substrate activation and inactivation. , 1977, Biochemistry.
[122] S. Nakanishi,et al. Role of acetyl coenzyme A carboxylase in the control of fatty acid synthesis. , 1970, Vitamins and hormones.
[123] A. Frenkel. LIGHT INDUCED PHOSPHORYLATION BY CELL-FREE PREPARATIONS OF PHOTOSYNTHETIC BACTERIA1 , 1954 .