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Quantitative Circadian Phosphoproteomic Analysis of Arabidopsis Reveals Extensive Clock Control of Key Components in Physiological, Metabolic, and Signaling Pathways

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Outgoing claims: the papers this work cites, builds on, or argues with.

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Dephosphorylation of photosystem II core proteins is light‐regulated in vivo.
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Prediction of post‐translational glycosylation and phosphorylation of proteins from the amino acid sequence
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Ser/Thr/Tyr phosphoproteome analysis of pathogenic and non‐pathogenic Pseudomonas species
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Proteomics and circadian rhythms: It's all about signaling!
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Identification of the Major Regulatory Phosphorylation Site in Sucrose-Phosphate Synthase
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StageTip-Based HAMMOC, an Efficient and Inexpensive Phosphopeptide Enrichment Method for Plant Shotgun Phosphoproteomics
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Circadian and light-regulated expression of nitrate reductase in Arabidopsis
inferredcites →https://doi.org/10.1007/bf00194005openalex-snapshot
Nitrate-reductase expression is under the control of a circadian rhythm and is light inducible in Nicotiana tabacum leaves
inferredcites →https://doi.org/10.1007/bf00203585openalex-snapshot
Sucrose-phosphate synthase is regulated via metabolites and protein phosphorylation in potato tubers, in a manner analogous to the enzyme in leaves
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Regulation of plant NR activity by reversible phosphorylation, 14-3-3 proteins and proteolysis
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Protein phosphorylation as a mechanism for regulation of spinach leaf sucrose-phosphate synthase activity
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The Circadian Clock of the Fly: A Neurogenetics Journey Through Time
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The Genetics of Circadian Rhythms in Neurospora
inferredcites →https://doi.org/10.1016/b978-0-12-387690-4.00004-0openalex-snapshot
The Genetics of Plant Clocks
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Environmentally modulated phosphorylation and dynamics of proteins in photosynthetic membranes
inferredcites →https://doi.org/10.1016/j.bbabio.2010.08.002openalex-snapshot
Dynamics of reversible protein phosphorylation in thylakoids of flowering plants: The roles of STN7, STN8 and TAP38
inferredcites →https://doi.org/10.1016/j.celrep.2013.02.021openalex-snapshot
ELF4 Regulates GIGANTEA Chromatin Access through Subnuclear Sequestration
inferredcites →https://doi.org/10.1016/j.cub.2006.04.026openalex-snapshot
Circadian Orchestration of the Hepatic Proteome
inferredcites →https://doi.org/10.1016/j.cub.2009.10.024openalex-snapshot
Proteomic Analysis Reveals the Role of Synaptic Vesicle Cycling in Sustaining the Suprachiasmatic Circadian Clock
inferredcites →https://doi.org/10.1016/j.cub.2010.12.013openalex-snapshot
Temporal Repression of Core Circadian Genes Is Mediated through EARLY FLOWERING 3 in Arabidopsis
inferredcites →https://doi.org/10.1016/j.cub.2012.07.025openalex-snapshot
Complexity in the Wiring and Regulation of Plant Circadian Networks
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A previously found thylakoid membrane protein of 14 kDa (TMP14) is a novel subunit of plant photosystem I and is designated PSI‐P
inferredcites →https://doi.org/10.1016/j.febslet.2011.02.038openalex-snapshot
Kinases and phosphatases in the mammalian circadian clock
inferredcites →https://doi.org/10.1016/j.molcel.2009.04.023openalex-snapshot
Quantitative Proteomics Reveals a Dynamic Interactome and Phase-Specific Phosphorylation in the Neurospora Circadian Clock
inferredcites →https://doi.org/10.1016/j.tplants.2010.05.011openalex-snapshot
Singlet oxygen signaling links photosynthesis to translation and plant growth
inferredcites →https://doi.org/10.1016/j.tplants.2012.06.008openalex-snapshot
Phosphorylation in the plant circadian system
inferredcites →https://doi.org/10.1016/j.tplants.2013.11.007openalex-snapshot
Wheels within wheels: the plant circadian system
inferredcites →https://doi.org/10.1016/s0014-5793(97)00698-4openalex-snapshot
Evidence for light‐dependent and light‐independent protein dephosphorylation in chloroplasts
inferredcites →https://doi.org/10.1016/s0076-6879(06)11009-5openalex-snapshot
[9] TM4 Microarray Software Suite
inferredcites →https://doi.org/10.1016/s1357-2725(02)00012-2openalex-snapshot
The acidic ribosomal P proteins
inferredcites →https://doi.org/10.1016/s1387-2656(08)00001-xopenalex-snapshot
The social network of a cell: Recent advances in interactome mapping
inferredcites →https://doi.org/10.1021/ac026117iopenalex-snapshot
Stop and Go Extraction Tips for Matrix-Assisted Laser Desorption/Ionization, Nanoelectrospray, and LC/MS Sample Pretreatment in Proteomics
inferredcites →https://doi.org/10.1021/ac0497104openalex-snapshot
A Neutral Loss Activation Method for Improved Phosphopeptide Sequence Analysis by Quadrupole Ion Trap Mass Spectrometry
inferredcites →https://doi.org/10.1021/cr000230wopenalex-snapshot
Kinetic and Catalytic Mechanisms of Protein Kinases
inferredcites →https://doi.org/10.1034/j.1399-3054.2002.1150216.xopenalex-snapshot
Auxin stimulates S6 ribosomal protein phosphorylation in maize thereby affecting protein synthesis regulation
inferredcites →https://doi.org/10.1038/emboj.2009.297openalex-snapshot
TOC1 functions as a molecular switch connecting the circadian clock with plant responses to drought
inferredcites →https://doi.org/10.1038/emboj.2010.76openalex-snapshot
PRR5 regulates phosphorylation, nuclear import and subnuclear localization of TOC1 in the Arabidopsis circadian clock
inferredcites →https://doi.org/10.1038/msb.2008.32openalex-snapshot
Large‐scale phosphorylation mapping reveals the extent of tyrosine phosphorylation in Arabidopsis
inferredcites →https://doi.org/10.1038/msb.2009.68openalex-snapshot
Ribosome and transcript copy numbers, polysome occupancy and enzyme dynamics in Arabidopsis
inferredcites →https://doi.org/10.1038/nature00954openalex-snapshot
The ELF4 gene controls circadian rhythms and flowering time in Arabidopsis thaliana
inferredcites →https://doi.org/10.1038/nature04316openalex-snapshot
Structural mechanism of plant aquaporin gating
inferredcites →https://doi.org/10.1038/nature05013openalex-snapshot
The nitrate/proton antiporter AtCLCa mediates nitrate accumulation in plant vacuoles
inferredcites →https://doi.org/10.1038/nature06132openalex-snapshot
ZEITLUPE is a circadian photoreceptor stabilized by GIGANTEA in blue light
inferredcites →https://doi.org/10.1038/nature08599openalex-snapshot
In vitro reconstitution of an abscisic acid signalling pathway
inferredcites →https://doi.org/10.1038/nature10182openalex-snapshot
The ELF4–ELF3–LUX complex links the circadian clock to diurnal control of hypocotyl growth
inferredcites →https://doi.org/10.1038/nbt1146openalex-snapshot
An iterative statistical approach to the identification of protein phosphorylation motifs from large-scale data sets
inferredcites →https://doi.org/10.1038/nprot.2007.324openalex-snapshot
Integration of biological networks and gene expression data using Cytoscape
inferredcites →https://doi.org/10.1038/nrg1633openalex-snapshot
Circadian rhythms from multiple oscillators: lessons from diverse organisms
inferredcites →https://doi.org/10.1038/nrg2972openalex-snapshot
Understanding systems-level properties: timely stories from the study of clocks
inferredcites →https://doi.org/10.1038/nrm2106openalex-snapshot
Post-translational modifications regulate the ticking of the circadian clock
inferredcites →https://doi.org/10.1038/nrm2838openalex-snapshot
The mechanism of eukaryotic translation initiation and principles of its regulation
inferredcites →https://doi.org/10.1042/bj20091412openalex-snapshot
Chloroplast DnaJ-like proteins 3 and 4 (CDJ3/4) from Chlamydomonas reinhardtii contain redox-active Fe–S clusters and interact with stromal HSP70B
inferredcites →https://doi.org/10.1046/j.1365-313x.1999.00353.xopenalex-snapshot
Circadian dysfunction causes aberrant hypocotyl elongation patterns in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.0400163101openalex-snapshot
CK2 phosphorylation of CCA1 is necessary for its circadian oscillator function in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.0503029102openalex-snapshot
LUX ARRHYTHMO encodes a Myb domain protein essential for circadian rhythms
inferredcites →https://doi.org/10.1073/pnas.0800788105openalex-snapshot
Precision proteomics: The case for high resolution and high mass accuracy
inferredcites →https://doi.org/10.1073/pnas.0903522106openalex-snapshot
Singlet oxygen-dependent translational control in the tigrina-d.12 mutant of barley
inferredcites →https://doi.org/10.1073/pnas.0914299107openalex-snapshot
Circadian control of carbohydrate availability for growth in Arabidopsis plants at night
inferredcites →https://doi.org/10.1073/pnas.1116590109openalex-snapshot
Reconstitution of abscisic acid activation of SLAC1 anion channel by CPK6 and OST1 kinases and branched ABI1 PP2C phosphatase action
inferredcites →https://doi.org/10.1073/pnas.1314066111openalex-snapshot
Circadian clock-dependent and -independent rhythmic proteomes implement distinct diurnal functions in mouse liver
inferredcites →https://doi.org/10.1073/pnas.190309197openalex-snapshot
Arabidopsis basic leucine zipper transcription factors involved in an abscisic acid-dependent signal transduction pathway under drought and high-salinity conditions
inferredcites →https://doi.org/10.1073/pnas.95.15.8660openalex-snapshot
Resonating circadian clocks enhance fitness in cyanobacteria
inferredcites →https://doi.org/10.1073/pnas.95.18.11020openalex-snapshot
Protein kinase CK2 interacts with and phosphorylates the Arabidopsis circadian clock-associated 1 protein
inferredcites →https://doi.org/10.1073/pnas.95.5.2378openalex-snapshot
Evolutionary analyses of the 12-kDa acidic ribosomal P-proteins reveal a distinct protein of higher plant ribosomes
inferredcites →https://doi.org/10.1073/pnas.96.22.12362openalex-snapshot
The protein kinase CK2 is involved in regulation of circadian rhythms in Arabidopsis
inferredcites →https://doi.org/10.1074/jbc.m803471200openalex-snapshot
Post-translational Regulation of the Arabidopsis Circadian Clock through Selective Proteolysis and Phosphorylation of Pseudo-response Regulator Proteins
inferredcites →https://doi.org/10.1074/mcp.m300050-mcp200openalex-snapshot
Identification of Three Previously Unknown in Vivo Protein Phosphorylation Sites in Thylakoid Membranes of Arabidopsis thaliana
inferredcites →https://doi.org/10.1074/mcp.m500123-mcp200openalex-snapshot
Expression Clustering Reveals Detailed Co-expression Patterns of Functionally Related Proteins during B Cell Differentiation
inferredcites →https://doi.org/10.1074/mcp.m700052-mcp200openalex-snapshot
Analysis of the Arabidopsis Cytosolic Ribosome Proteome Provides Detailed Insights into Its Components and Their Post-translational Modification
inferredcites →https://doi.org/10.1074/mcp.t400003-mcp200openalex-snapshot
Trypsin Cleaves Exclusively C-terminal to Arginine and Lysine Residues
inferredcites →https://doi.org/10.1074/mcp.t500030-mcp200openalex-snapshot
Parts per Million Mass Accuracy on an Orbitrap Mass Spectrometer via Lock Mass Injection into a C-trap
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Label-free Quantitative Proteomics Using Large Peptide Data Sets Generated by Nanoflow Liquid Chromatography and Mass Spectrometry
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A hierarchical unsupervised growing neural network for clustering gene expression patterns
inferredcites →https://doi.org/10.1093/bioinformatics/bti551openalex-snapshot
BiNGO: a Cytoscape plugin to assess overrepresentation of Gene Ontology categories in Biological Networks
inferredcites →https://doi.org/10.1093/jxb/erq288openalex-snapshot
Thioredoxin-regulated β-amylase (BAM1) triggers diurnal starch degradation in guard cells, and in mesophyll cells under osmotic stress
inferredcites →https://doi.org/10.1093/jxb/eru117openalex-snapshot
Connections between circadian clocks and carbon metabolism reveal species-specific effects on growth control
inferredcites →https://doi.org/10.1093/jxb/eru339openalex-snapshot
Light and the circadian clock mediate time-specific changes in sensitivity to UV-B stress under light/dark cycles
inferredcites →https://doi.org/10.1093/nar/gks1094openalex-snapshot
STRING v9.1: protein-protein interaction networks, with increased coverage and integration
inferredcites →https://doi.org/10.1093/pcp/pcd043openalex-snapshot
Circadian Waves of Expression of the APRR1/TOC1 Family of Pseudo-Response Regulators in Arabidopsis thaliana : Insight into the Plant Circadian Clock
inferredcites →https://doi.org/10.1093/pcp/pcf188openalex-snapshot
ABA-Activated SnRK2 Protein Kinase is Required for Dehydration Stress Signaling in Arabidopsis
inferredcites →https://doi.org/10.1093/pcp/pch065openalex-snapshot
Characterization of Circadian-Associated APRR3 Pseudo-Response Regulator Belonging to the APRR1/TOC1 Quintet in Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/pcp/pcn008openalex-snapshot
Comparative Transcriptome of Diurnally Oscillating Genes and Hormone-Responsive Genes in Arabidopsis thaliana: Insight into Circadian Clock-Controlled Daily Responses to Common Ambient Stresses in Plants
inferredcites →https://doi.org/10.1093/pcp/pcq062openalex-snapshot
CLC-b-Mediated NOFormula/H+ Exchange Across the Tonoplast of Arabidopsis Vacuoles
inferredcites →https://doi.org/10.1093/pcp/pcq198openalex-snapshot
The Circadian Clock Modulates Water Dynamics and Aquaporin Expression in Arabidopsis Roots
inferredcites →https://doi.org/10.1093/pcp/pcr148openalex-snapshot
Shotguns in the Front Line: Phosphoproteomics in Plants
inferredcites →https://doi.org/10.1098/rstb.2001.0965openalex-snapshot
Clock-associated genes in Arabidopsis : a family affair
inferredcites →https://doi.org/10.1101/gr.128876.111openalex-snapshot
Deep sequencing the circadian and diurnal transcriptome ofDrosophilabrain
inferredcites →https://doi.org/10.1101/sqb.2007.72.006openalex-snapshot
The Diurnal Project: Diurnal and Circadian Expression Profiling, Model-based Pattern Matching, and Promoter Analysis
inferredcites →https://doi.org/10.1101/sqb.2007.72.010openalex-snapshot
Posttranslational Control of theNeurospora CircadianClock
inferredcites →https://doi.org/10.1101/sqb.2007.72.035openalex-snapshot
Posttranslational Photomodulation of Circadian Amplitude
inferredcites →https://doi.org/10.1101/sqb.2007.72.036openalex-snapshot
Role of Phosphorylation in the Mammalian Circadian Clock
inferredcites →https://doi.org/10.1104/pp.004374openalex-snapshot
Circadian Rhythms Confer a Higher Level of Fitness to Arabidopsis Plants
inferredcites →https://doi.org/10.1104/pp.013441openalex-snapshot
Phosphorylation of the D1 Photosystem II Reaction Center Protein Is Controlled by an Endogenous Circadian Rhythm
inferredcites →https://doi.org/10.1104/pp.021006openalex-snapshot
Enhancer Trapping Reveals Widespread Circadian Clock Transcriptional Control in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.103.022749openalex-snapshot
Regulated Phosphorylation of 40S Ribosomal Protein S6 in Root Tips of Maize
inferredcites →https://doi.org/10.1104/pp.103.035873openalex-snapshot
Phytohormones Participate in an S6 Kinase Signal Transduction Pathway in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.104.044347openalex-snapshot
Diurnal Changes in the Transcriptome Encoding Enzymes of Starch Metabolism Provide Evidence for Both Transcriptional and Posttranscriptional Regulation of Starch Metabolism in Arabidopsis Leaves
inferredcites →https://doi.org/10.1104/pp.107.096206openalex-snapshot
ELF4Is Required for Oscillatory Properties of the Circadian Clock
inferredcites →https://doi.org/10.1104/pp.107.1.225openalex-snapshot
Circadian Oscillation of Nitrate Reductase Activity in Gonyaulax polyedra Is Due to Changes in Cellular Protein Levels
inferredcites →https://doi.org/10.1104/pp.109.138677openalex-snapshot
Large-Scale Arabidopsis Phosphoproteome Profiling Reveals Novel Chloroplast Kinase Substrates and Phosphorylation Networks
inferredcites →https://doi.org/10.1104/pp.110.157347openalex-snapshot
Large-Scale Comparative Phosphoproteomics Identifies Conserved Phosphorylation Sites in Plants
inferredcites →https://doi.org/10.1104/pp.113.4.1167openalex-snapshot
Circadian Regulation of Sucrose Phosphate Synthase Activity in Tomato by Protein Phosphatase Activity
inferredcites →https://doi.org/10.1104/pp.114.3.947openalex-snapshot
Protein Phosphorylation as a Mechanism for Osmotic-Stress Activation of Sucrose-Phosphate Synthase in Spinach Leaves
inferredcites →https://doi.org/10.1104/pp.118.1.149openalex-snapshot
Chilling Delays Circadian Pattern of Sucrose Phosphate Synthase and Nitrate Reductase Activity in Tomato1
inferredcites →https://doi.org/10.1104/pp.73.4.989openalex-snapshot
Regulation of Spinach Leaf Sucrose Phosphate Synthase by Glucose-6-Phosphate, Inorganic Phosphate, and pH
inferredcites →https://doi.org/10.1104/pp.96.1.275openalex-snapshot
Differential Expression of the Two Arabidopsis Nitrate Reductase Genes
inferredcites →https://doi.org/10.1105/tpc.016808openalex-snapshot
The F-Box Protein ZEITLUPE Confers Dosage-Dependent Control on the Circadian Clock, Photomorphogenesis, and Flowering Time[W]
inferredcites →https://doi.org/10.1105/tpc.10.3.451openalex-snapshot
Water Transport Activity of the Plasma Membrane Aquaporin PM28A Is Regulated by Phosphorylation
inferredcites →https://doi.org/10.1105/tpc.105.035659openalex-snapshot
AREB1 Is a Transcription Activator of Novel ABRE-Dependent ABA Signaling That Enhances Drought Stress Tolerance in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.105.038315openalex-snapshot
FLOWERING LOCUS C Mediates Natural Variation in the High-Temperature Response of the Arabidopsis Circadian Clock
inferredcites →https://doi.org/10.1105/tpc.107.054775openalex-snapshot
PRR3 Is a Vascular Regulator of TOC1 Stability in theArabidopsisCircadian Clock
inferredcites →https://doi.org/10.1105/tpc.109.067603openalex-snapshot
The Arabidopsis Nitrate Transporter NRT1.7, Expressed in Phloem, Is Responsible for Source-to-Sink Remobilization of Nitrate
inferredcites →https://doi.org/10.1105/tpc.111.093807openalex-snapshot
EARLY FLOWERING4 Recruitment of EARLY FLOWERING3 in the Nucleus Sustains the Arabidopsis Circadian Clock
inferredcites →https://doi.org/10.1105/tpc.112.108456openalex-snapshot
Regulation of Arabidopsis Leaf Hydraulics Involves Light-Dependent Phosphorylation of Aquaporins in Veins
inferredcites →https://doi.org/10.1105/tpc.113.113118openalex-snapshot
Arabidopsis CURVATURE THYLAKOID1 Proteins Modify Thylakoid Architecture by Inducing Membrane Curvature
inferredcites →https://doi.org/10.1105/tpc.113.119842openalex-snapshot
Multiple Layers of Posttranslational Regulation Refine Circadian Clock Activity in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.114.125815openalex-snapshot
Meta-Analysis of Arabidopsis thaliana Phospho-Proteomics Data Reveals Compartmentalization of Phosphorylation Motifs
inferredcites →https://doi.org/10.1105/tpc.8.3.519openalex-snapshot
Identification in vitro of a post-translational regulatory site in the hinge 1 region of Arabidopsis nitrate reductase.
inferredcites →https://doi.org/10.1111/j.1365-313x.2004.02055.xopenalex-snapshot
ABA activates ADPR cyclase and cADPR induces a subset of ABA‐responsive genes in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02531.xopenalex-snapshot
ELF4 is a phytochrome‐regulated component of a negative‐feedback loop involving the central oscillator components CCA1 and LHY
inferredcites →https://doi.org/10.1111/j.1365-313x.2009.04054.xopenalex-snapshot
PYR/PYL/RCAR family members are major in‐vivo ABI1 protein phosphatase 2C‐interacting proteins in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1399-3054.1984.tb05900.xopenalex-snapshot
Circadian rhythmicity of nitrate reductase activity in barley leaves
inferredcites →https://doi.org/10.1126/science.1082971openalex-snapshot
Enhanced Fitness Conferred by Naturally Occurring Variation in the Circadian Clock
inferredcites →https://doi.org/10.1126/science.1115581openalex-snapshot
Plant Circadian Clocks Increase Photosynthesis, Growth, Survival, and Competitive Advantage
inferredcites →https://doi.org/10.1126/science.1124619openalex-snapshot
Mass Spectrometry and Protein Analysis
inferredcites →https://doi.org/10.1126/science.1146757openalex-snapshot
The Arabidopsis Circadian Clock Incorporates a cADPR-Based Feedback Loop
inferredcites →https://doi.org/10.1126/science.1173041openalex-snapshot
Abscisic Acid Inhibits Type 2C Protein Phosphatases via the PYR/PYL Family of START Proteins
inferredcites →https://doi.org/10.1126/science.1226339openalex-snapshot
Transcriptional Architecture and Chromatin Landscape of the Core Circadian Clock in Mammals
inferredcites →https://doi.org/10.1126/science.290.5499.2110openalex-snapshot
Orchestrated Transcription of Key Pathways in Arabidopsis by the Circadian Clock
inferredcites →https://doi.org/10.1146/annurev-arplant-042110-103741openalex-snapshot
Anion Channels/Transporters in Plants: From Molecular Bases to Regulatory Networks
inferredcites →https://doi.org/10.1146/annurev-biochem-060713-035644openalex-snapshot
Interactive Features of Proteins Composing Eukaryotic Circadian Clocks
inferredcites →https://doi.org/10.1146/annurev.genom.5.061903.175925openalex-snapshot
MAMMALIAN CIRCADIAN BIOLOGY: Elucidating Genome-Wide Levels of Temporal Organization
inferredcites →https://doi.org/10.1177/074873049701200302openalex-snapshot
Quantitative Analysis of Drosophila period Gene Transcription in Living Animals
inferredcites →https://doi.org/10.1186/gb-2008-9-8-r130openalex-snapshot
Global transcriptome analysis reveals circadian regulation of key pathways in plant growth and development
inferredcites →https://doi.org/10.1186/gb-2009-10-2-r17openalex-snapshot
Exploring the transcriptional landscape of plant circadian rhythms using genome tiling arrays
inferredcites →https://doi.org/10.1371/journal.pbio.0040327openalex-snapshot
CDPKs CPK6 and CPK3 Function in ABA Regulation of Guard Cell S-Type Anion- and Ca2+- Permeable Channels and Stomatal Closure
inferredcites →https://doi.org/10.1371/journal.pbio.1001442openalex-snapshot
Genome-Wide RNA Polymerase II Profiles and RNA Accumulation Reveal Kinetics of Transcription and Associated Epigenetic Changes During Diurnal Cycles
inferredcites →https://doi.org/10.1371/journal.pbio.1001455openalex-snapshot
The Circadian Clock Coordinates Ribosome Biogenesis
inferredcites →https://doi.org/10.1371/journal.pgen.1001201openalex-snapshot
The Functional Interplay between Protein Kinase CK2 and CCA1 Transcriptional Activity Is Essential for Clock Temperature Compensation in Arabidopsis
inferredcites →https://doi.org/10.1371/journal.pgen.1001350openalex-snapshot
REVEILLE8 and PSEUDO-REPONSE REGULATOR5 Form a Negative Feedback Loop within the Arabidopsis Circadian Clock
inferredcites →https://doi.org/10.1371/journal.pgen.1004047openalex-snapshot
In-Vivo Quantitative Proteomics Reveals a Key Contribution of Post-Transcriptional Mechanisms to the Circadian Regulation of Liver Metabolism
inferredcites →https://doi.org/10.1371/journal.pone.0003105openalex-snapshot
Systems Biology of the Clock in Neurospora crassa
inferredcites →https://doi.org/10.1371/journal.pone.0029307openalex-snapshot
Differential Phosphorylation of Ribosomal Proteins in Arabidopsis thaliana Plants during Day and Night
inferredcites →https://doi.org/10.2144/03342mt01openalex-snapshot
TM4: A Free, Open-Source System for Microarray Data Management and Analysis
inferredcites →https://doi.org/10.2307/3870329openalex-snapshot
Identification in vitro of a Post-Translational Regulatory Site in the Hinge 1 Region of Arabidopsis Nitrate Reductase
inferredcites →https://doi.org/10.2976/1.3218766openalex-snapshot
Integrating ELF4 into the circadian system through combined structural and functional studies
inferredcites →https://doi.org/10.4161/psb.18766openalex-snapshot
ELF3 recruitment to thePRR9promoter requires other Evening Complex members in the Arabidopsis circadian clock
inferredcites →https://doi.org/10.7554/elife.00011openalex-snapshot
Nascent-Seq reveals novel features of mouse circadian transcriptional regulation

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113489zenodo-depositor-declared
Diurnal accumulation of K+-dependent L-asparaginase in leaf of common bean (Phaseolus vulgaris L.)
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Drought Stress Mediated Changes in Food Crops: Mechanisms and Remediation Strategies
inferred← citeshttps://doi.org/10.1002/bies.202400211openalex-snapshot
A Compensated Clock: Temperature and Nutritional Compensation Mechanisms Across Circadian Systems
inferred← citeshttps://doi.org/10.1002/pld3.566openalex-snapshot
A phosphorylation‐deficient ribosomal protein eS6 is largely functional in Arabidopsis thaliana , rescuing mutant defects from global translation and gene expression to photosynthesis and growth
inferred← citeshttps://doi.org/10.1002/pmic.201500351openalex-snapshot
A year (2014–2015) of plants in Proteomics journal. Progress in wet and dry methodologies, moving from protein catalogs, and the view of classic plant biochemists
inferred← citeshttps://doi.org/10.1002/wrna.1597openalex-snapshot
Translational gene regulation in plants: A green new deal
inferred← citeshttps://doi.org/10.1002/wsbm.1450openalex-snapshot
Circadian rhythms and proteomics: It's all about posttranslational modifications!
inferred← citeshttps://doi.org/10.1007/124_2022_64openalex-snapshot
Photorespiration and Improving Photosynthesis
inferred← citeshttps://doi.org/10.1007/978-1-0716-1370-2_12openalex-snapshot
Uncover the Nuclear Proteomic Landscape with Enriched Nuclei Followed by Label-Free Quantitative Mass Spectrometry
inferred← citeshttps://doi.org/10.1007/978-3-319-33705-0_7openalex-snapshot
The Current Status of Proteomic Studies in Somatic Embryogenesis
inferred← citeshttps://doi.org/10.1007/978-3-319-43589-3_17openalex-snapshot
Plant SnRK1 Kinases: Structure, Regulation, and Function
inferred← citeshttps://doi.org/10.1007/978-3-319-49395-4_4openalex-snapshot
Plant Aquaporin Posttranslational Regulation
inferred← citeshttps://doi.org/10.1007/978-3-319-95315-1_4openalex-snapshot
Interactions Between Circadian Rhythms, ROS and Redox
inferred← citeshttps://doi.org/10.1007/s00726-017-2501-7openalex-snapshot
Long photoperiod affects the maize transition from vegetative to reproductive stages: a proteomic comparison between photoperiod-sensitive inbred line and its recurrent parent
inferred← citeshttps://doi.org/10.1016/j.bpj.2020.09.025openalex-snapshot
Early Detection of Daylengths with a Feedforward Circuit Coregulated by Circadian and Diurnal Cycles
inferred← citeshttps://doi.org/10.1016/j.cub.2021.03.046openalex-snapshot
Layers of crosstalk between circadian regulation and environmental signalling in plants
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2020.104367openalex-snapshot
Dynamic role of aquaporin transport system under drought stress in plants
inferred← citeshttps://doi.org/10.1016/j.jmb.2019.12.004openalex-snapshot
Proteomics in Circadian Biology
inferred← citeshttps://doi.org/10.1016/j.mcpro.2021.100063openalex-snapshot
Quantitative Proteomics and Phosphoproteomics Support a Role for Mut9-Like Kinases in Multiple Metabolic and Signaling Pathways in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.mcpro.2021.100172openalex-snapshot
The Circadian Clock Gene Circuit Controls Protein and Phosphoprotein Rhythms in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1016/j.molp.2025.01.014openalex-snapshot
NTRC mediates the coupling of chloroplast redox rhythm with nuclear circadian clock in plant cells
inferred← citeshttps://doi.org/10.1016/j.plantsci.2020.110786openalex-snapshot
Molecular and functional dissection of EARLY-FLOWERING 3 (ELF3) and ELF4 in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.plantsci.2023.111675openalex-snapshot
Substrate profiling of the Arabidopsis Ca2+-dependent protein kinase AtCPK4 and its Ricinus communis ortholog RcCDPK1
inferred← citeshttps://doi.org/10.1016/j.tplants.2025.07.013openalex-snapshot
Phosphorylation-regulated SEC14-GOLD PATELLIN lipid transfer proteins
inferred← citeshttps://doi.org/10.1021/acs.analchem.5b04123openalex-snapshot
Phosphoproteomics in the Age of Rapid and Deep Proteome Profiling
inferred← citeshttps://doi.org/10.1021/acs.jproteome.6b00348openalex-snapshot
Up-to-Date Workflow for Plant (Phospho)proteomics Identifies Differential Drought-Responsive Phosphorylation Events in Maize Leaves
inferred← citeshttps://doi.org/10.1038/nsmb.3327openalex-snapshot
Molecular mechanisms at the core of the plant circadian oscillator
inferred← citeshttps://doi.org/10.1038/s41438-020-00440-8openalex-snapshot
Protein phosphorylation associated with drought priming-enhanced heat tolerance in a temperate grass species
inferred← citeshttps://doi.org/10.1038/s41477-021-00993-zopenalex-snapshot
Lipid flippases as key players in plant adaptation to their environment
inferred← citeshttps://doi.org/10.1038/s44323-025-00058-wopenalex-snapshot
Temperature compensation of the Arabidopsis circadian clock
inferred← citeshttps://doi.org/10.1042/bcj20190339openalex-snapshot
CBL–CIPK module-mediated phosphoregulation: facts and hypothesis
inferred← citeshttps://doi.org/10.1042/bst20190572openalex-snapshot
The intersection between circadian and heat-responsive regulatory networks controls plant responses to increasing temperatures
inferred← citeshttps://doi.org/10.1042/ebc20210071openalex-snapshot
Activation and turnover of the plant immune signaling kinase BIK1: a fine balance
inferred← citeshttps://doi.org/10.1073/pnas.1819971116openalex-snapshot
Phosphoproteomics of Arabidopsis Highly ABA-Induced1 identifies AT-Hook–Like10 phosphorylation required for stress growth regulation
inferred← citeshttps://doi.org/10.1074/mcp.m115.054064openalex-snapshot
Identification of Evening Complex Associated Proteins in Arabidopsis by Affinity Purification and Mass Spectrometry
inferred← citeshttps://doi.org/10.1080/15476286.2017.1391444openalex-snapshot
What makes ribosomes tick?
inferred← citeshttps://doi.org/10.1080/15592324.2019.1642037openalex-snapshot
Phosphorylation regulates the activity of INDETERMINATE-DOMAIN (IDD/BIRD) proteins in response to diverse environmental conditions
inferred← citeshttps://doi.org/10.1093/hr/uhad258openalex-snapshot
Multi-omics landscape to decrypt the distinct flavonoid biosynthesis of Scutellaria baicalensis across multiple tissues
inferred← citeshttps://doi.org/10.1093/jxb/erad290openalex-snapshot
A phospho-dawn of protein modification anticipates light onset in the picoeukaryoteOstreococcus tauri
inferred← citeshttps://doi.org/10.1093/jxb/eraf509openalex-snapshot
Novel effector proteins of the plant heteromeric acetyl-CoA carboxylase
inferred← citeshttps://doi.org/10.1093/pcp/pcag044openalex-snapshot
The circadian morning complex modulates abscisic acid signaling by transcriptionally repressing PYL4 , PYL5 , and PYL6 at dawn
inferred← citeshttps://doi.org/10.1093/pcp/pcz010openalex-snapshot
Algal Protein Kinase, Triacylglycerol Accumulation Regulator 1, Modulates Cell Viability and Gametogenesis in Carbon/Nitrogen-Imbalanced Conditions
inferred← citeshttps://doi.org/10.1093/pcp/pcz163openalex-snapshot
Comparative Phosphoproteomic Analysis Reveals a Decay of ABA Signaling in Barley Embryos during After-Ripening
inferred← citeshttps://doi.org/10.1093/plcell/koac049openalex-snapshot
Phosphorylation of MdERF17 by MdMPK4 promotes apple fruit peel degreening during light/dark transitions
inferred← citeshttps://doi.org/10.1093/plphys/kiab373openalex-snapshot
Hormonal and environmental signaling pathways target membrane water transport
inferred← citeshttps://doi.org/10.1093/plphys/kiac269openalex-snapshot
Multi-omic analysis showsREVEILLEclock genes are involved in carbohydrate metabolism and proteasome function
inferred← citeshttps://doi.org/10.1093/plphys/kiae254openalex-snapshot
40S Ribosomal protein S6 kinase integrates daylength perception and growth regulation in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1098/rsob.160333openalex-snapshot
Parallel analysis ofArabidopsiscircadian clock mutants reveals different scales of transcriptome and proteome regulation
inferred← citeshttps://doi.org/10.1098/rstb.2023.0346openalex-snapshot
Circadian gating: concepts, processes, and opportunities
inferred← citeshttps://doi.org/10.1101/2020.04.23.057711openalex-snapshot
Early detection of daylengths with a feedforward circuit coregulated by circadian and diurnal cycles
inferred← citeshttps://doi.org/10.1101/2020.05.15.098418openalex-snapshot
Loss of Photosynthetic RhythmThermal Plasticity Under Domestication and Repurposing Drivers of Circadian Clock (DOC) Loci for Adaptive Breeding in Barley
inferred← citeshttps://doi.org/10.1101/2021.06.27.450011openalex-snapshot
GTL1 is required for a robust root hair growth response to avoid nutrient overloading
inferred← citeshttps://doi.org/10.1101/2021.10.25.465654openalex-snapshot
Multi-omic analysis of the Arabidopsis clock activator mutant rve 4 6 8 reveals connections to carbohydrate metabolism and proteasome regulation
inferred← citeshttps://doi.org/10.1101/2025.07.31.667909openalex-snapshot
Temporal dynamics of RNA metabolic enzyme interactome lay the foundation for riboregulation mediated circadian metabolism
inferred← citeshttps://doi.org/10.1101/287862openalex-snapshot
Circadian protein regulation in the green lineage I. A phospho-dawn of protein modification anticipates light onset in the picoeukaryote O. tauri
inferred← citeshttps://doi.org/10.1101/413013openalex-snapshot
Phosphoproteomics of Arabidopsis Highly ABA-Induced1 identifies AT-Hook Like10 phosphorylation required for stress growth regulation
inferred← citeshttps://doi.org/10.1101/760892openalex-snapshot
The circadian clock gene circuit controls protein and phosphoprotein rhythms in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1104/pp.16.01738openalex-snapshot
EARLY FLOWERING3 Redundancy Fine-Tunes Photoperiod Sensitivity
inferred← citeshttps://doi.org/10.1105/tpc.18.00804openalex-snapshot
Oscillating Aquaporin Phosphorylation and 14-3-3 Proteins Mediate the Circadian Regulation of Leaf Hydraulics
inferred← citeshttps://doi.org/10.1111/jipb.13622openalex-snapshot
How plants sense and respond to osmotic stress
inferred← citeshttps://doi.org/10.1111/jnc.13960openalex-snapshot
Actin filament‐associated protein 1 (AFAP‐1) is a key mediator in inflammatory signaling‐induced rapid attenuation of intrinsic P‐gp function in human brain capillary endothelial cells
inferred← citeshttps://doi.org/10.1111/nph.15473openalex-snapshot
ABA signalling is regulated by the circadian clock component LHY
inferred← citeshttps://doi.org/10.1111/nph.16507openalex-snapshot
Changes in ambient temperature are the prevailing cue in determining Brachypodium distachyon diurnal gene regulation
inferred← citeshttps://doi.org/10.1111/nph.18255openalex-snapshot
Trihelix transcription factors GTL1 and DF1 prevent aberrant root hair formation in an excess nutrient condition
inferred← citeshttps://doi.org/10.1111/pce.13346openalex-snapshot
New connections between circadian rhythms, photosynthesis, and environmental adaptation
inferred← citeshttps://doi.org/10.1111/pce.13969openalex-snapshot
Diurnal dynamics of the Arabidopsis rosette proteome and phosphoproteome
inferred← citeshttps://doi.org/10.1111/ppl.70726openalex-snapshot
Dual Phosphorylation of Thr175 and Ser176 Is Essential for SnRK1α1 Activation
inferred← citeshttps://doi.org/10.1111/tpj.14315openalex-snapshot
Diurnal changes in concerted plant protein phosphorylation and acetylation in Arabidopsis organs and seedlings
inferred← citeshttps://doi.org/10.1111/tpj.15254openalex-snapshot
Closing the protein gap in plant chronobiology
inferred← citeshttps://doi.org/10.1111/tpj.15395openalex-snapshot
Arabidopsis thaliana 2,3‐bisphosphoglycerate‐independent phosphoglycerate mutase 2 activity requires serine 82 phosphorylation
inferred← citeshttps://doi.org/10.1111/tpj.16240openalex-snapshot
Regulation of plant carbon assimilation metabolism by post‐translational modifications
inferred← citeshttps://doi.org/10.1111/tpj.16405openalex-snapshot
Circadian regulation of metabolism across photosynthetic organisms
inferred← citeshttps://doi.org/10.1111/tpj.16406openalex-snapshot
The interplay of post‐translational protein modifications in Arabidopsis leaves during photosynthesis induction
inferred← citeshttps://doi.org/10.1111/tpj.70275openalex-snapshot
The time machine: feedback loops, post‐transcriptional regulation, and environmental integration in the plant circadian oscillator
inferred← citeshttps://doi.org/10.1146/annurev-arplant-071720-104814openalex-snapshot
Engineering of Crassulacean Acid Metabolism
inferred← citeshttps://doi.org/10.11606/t.46.2018.tde-19072018-113726openalex-snapshot
Vias de sinalização por auxinas e sua interação com o relógio biológico de cana-de-açúcar
inferred← citeshttps://doi.org/10.1177/0748730417737633openalex-snapshot
Sumoylation Contributes to Timekeeping and Temperature Compensation of the Plant Circadian Clock
inferred← citeshttps://doi.org/10.1371/journal.pgen.1007037openalex-snapshot
The GYF domain protein PSIG1 dampens the induction of cell death during plant-pathogen interactions
inferred← citeshttps://doi.org/10.1371/journal.pgen.1007708openalex-snapshot
The Trihelix transcription factor GT2-like 1 (GTL1) promotes salicylic acid metabolism, and regulates bacterial-triggered immunity
inferred← citeshttps://doi.org/10.1371/journal.pgen.1010947openalex-snapshot
Genome-wide circadian gating of a cold temperature response in bread wheat
inferred← citeshttps://doi.org/10.18632/oncotarget.7065openalex-snapshot
Evolving roles of circadian rhythms in liver homeostasis and pathology
inferred← citeshttps://doi.org/10.2139/ssrn.7507384openalex-snapshot
Phosphorylation of ELF4 by SOS2 protein kinase releases ELF3 to confer salt tolerance in Arabidopsis
inferred← citeshttps://doi.org/10.3389/fmicb.2022.1004074openalex-snapshot
The enigmatic clock of dinoflagellates, is it unique?
inferred← citeshttps://doi.org/10.3389/fpls.2016.00752openalex-snapshot
Comparative Proteomic Analysis of the Response of Maize (Zea mays L.) Leaves to Long Photoperiod Condition
inferred← citeshttps://doi.org/10.3389/fpls.2016.01007openalex-snapshot
Circadian Profiling of the Arabidopsis Proteome Using 2D-DIGE
inferred← citeshttps://doi.org/10.3389/fpls.2017.02210openalex-snapshot
Phosphorylation of Ribosomal Protein RPS6 Integrates Light Signals and Circadian Clock Signals
inferred← citeshttps://doi.org/10.3389/fpls.2019.00667openalex-snapshot
Luciferase-Based Screen for Post-translational Control Factors in the Regulation of the Pseudo-Response Regulator PRR7
inferred← citeshttps://doi.org/10.3389/fpls.2020.00377openalex-snapshot
Protein Phosphorylation Dynamics Under Carbon/Nitrogen-Nutrient Stress and Identification of a Cell Death-Related Receptor-Like Kinase in Arabidopsis
inferred← citeshttps://doi.org/10.3389/fpls.2020.618835openalex-snapshot
Signaling Toward Reactive Oxygen Species-Scavenging Enzymes in Plants
inferred← citeshttps://doi.org/10.3390/biology8010014openalex-snapshot
The Plant Circadian Oscillator
inferred← citeshttps://doi.org/10.3390/genes12030325openalex-snapshot
Post-Translational Mechanisms of Plant Circadian Regulation
inferred← citeshttps://doi.org/10.3390/genes9120567openalex-snapshot
A Functional Connection between the Circadian Clock and Hormonal Timing in Arabidopsis
inferred← citeshttps://doi.org/10.3390/ijms20020451openalex-snapshot
Comparative Phosphoproteomic Analysis of Barley Embryos with Different Dormancy during Imbibition
inferred← citeshttps://doi.org/10.3390/ijms21228631openalex-snapshot
Large-Scale Phosphoproteomic Study of Arabidopsis Membrane Proteins Reveals Early Signaling Events in Response to Cold
inferred← citeshttps://doi.org/10.3390/ijms232214134openalex-snapshot
Phytochromes and Their Role in Diurnal Variations of ROS Metabolism and Plant Proteome
inferred← citeshttps://doi.org/10.3390/ijms241713307openalex-snapshot
The Case for the Target of Rapamycin Pathway as a Candidate Circadian Oscillator
inferred← citeshttps://doi.org/10.3390/plants10102053openalex-snapshot
The Arabidopsis Rho of Plants GTPase ROP1 Is a Potential Calcium-Dependent Protein Kinase (CDPK) Substrate
inferred← citeshttps://doi.org/10.3390/plants9010027openalex-snapshot
Enzymatic Properties of Recombinant Phospho-Mimetic Photorespiratory Glycolate Oxidases from Arabidopsis thaliana and Zea mays
inferred← citeshttps://doi.org/10.3390/stresses2010006openalex-snapshot
Abscisic Acid Machinery Is under Circadian Clock Regulation at Multiple Levels
inferred← citeshttps://doi.org/10.3791/54586openalex-snapshot
Rapid Analysis of Circadian Phenotypes in Arabidopsis Protoplasts Transfected with a Luminescent Clock Reporter
inferred← citeshttps://doi.org/10.64898/2025.12.19.695194openalex-snapshot
The plant circadian clock exerts stronger control over the diel proteome than the transcriptome
inferred← citeshttps://doi.org/10.64898/2026.06.05.730517openalex-snapshot
A co-proteomic view of metabolite-specific interactions in the Botrytis cinerea-Arabidopsis pathosystem
inferred← citeshttps://doi.org/10.70675/6f8b480az9ff0z4ac7z86bcz1635252eca60openalex-snapshot
Phosphoregulation of photorespiratory enzymes in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.70675/a48a46ddze462z471dz9db1zbc87a8c51c41openalex-snapshot
Anchoring mechanism of the plant protein remorin to membrane nanodomains
inferred← citeshttps://doi.org/10.7554/elife.58993openalex-snapshot
Expansion of the circadian transcriptome in Brassica rapa and genome-wide diversification of paralog expression patterns
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