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Zhang"],"technology_type":["Mass Spectrometry","Shotgun proteomics"],"software":[""],"submitter_keywords":["Yeast","Cell cycle","Phosphoproteome"],"full_dataset_link":["https://www.ebi.ac.uk/pride/archive/projects/PXD015235"],"tissue":["Whole Body"],"sample_protocol":["Proteins were extracted from yeasts at different time points in the cell cycle and digested to peptides. A small part of the resulting peptides were labeled with TMT, combined, fractionated and desalted for mass spectrometry analysis of the proteome. The majority of the peptides were enriched for phosphopeptides using TiO2, labeled with TMT, combined, fractionated and desalted for mass spectrometry analysis of the phosphoproteome."],"repository":["Pride"],"quantification_method":[""],"modification":[""],"data_protocol":["Raw data were searched using SEQUEST in Proteome Discoverer 2.2 against a sequence database of yeast (strain W303, NCBI taxonomy ID 559292, downloaded on July 28, 2016).  Trypsin was selected as the enzyme with at most two missed cleavage sites.  Precursor mass tolerance was set to +/- 10 ppm and fragment mass tolerance was set to +/- 0.6 Da.  At most three dynamic modifications were allowed per peptide.  Carbamidomethylation of cysteine (+57.021 Da) and TMT-labeled N-terminus and lysine (+229.163) were set as static modification. Oxidation of methionine (+15.995 Da) and acetylation of protein N-terminus (+42.011 Da) were set as differential modification. For phosphoenriched dataset, phosphorylation of Serine, Tyrosine and Tyrosine was also set as differential modification. Percolator was applied to filter out the false MS2 assignments at a false discovery rate of 1% for both peptides and proteins.  For quantification, a mass tolerance of +/-20 ppm window was applied to the integration of report ions using the most confident centroid method and S/N values were reported as reporter abundances.  The threshold for average reporter S/N was set to 5 and the threshold for co-isolation was set to 30%. Quantification results were rejected with missing channels.  The data normalization mode was set to “total peptide amount” and scaling mode was set to “on channels average”."],"omics_type":["Proteomics"],"labhead":["Jennifer Ewald"],"instrument_platform":[""],"labhead_affiliation":["Molecular Cell Biology Interfaculty Institute of Cell Biology (IFIZ) University of Tübingen"],"submission_type":["PARTIAL"],"species":["Saccharomyces Cerevisiae (baker's Yeast)"],"publication":["31921850 Zhang L, Winkler S, Schlottmann FP, Kohlbacher O, Elias JE, Skotheim JM, Ewald JC. Multiple Layers of Phospho-Regulation Coordinate Metabolism and the Cell Cycle in Budding Yeast. Front Cell Dev Biol. 2019 7:338 10.3389/fcell.2019.00338"],"submitter_mail":["lichao.zhang@czbiohub.org"],"submitter_affiliation":["Chan Zuckerberg Biohub"],"submitter_country":["United States"],"pubmed_abstract":["The coordination of metabolism and growth with cell division is crucial for proliferation. While it has long been known that cell metabolism regulates the cell division cycle, it is becoming increasingly clear that the cell division cycle also regulates metabolism. In budding yeast, we previously showed that over half of all measured metabolites change concentration through the cell cycle indicating that metabolic fluxes are extensively regulated during cell cycle progression. However, how this regulation is achieved still remains poorly understood. Since both the cell cycle and metabolism are regulated to a large extent by protein phosphorylation, we here decided to measure the phosphoproteome through the budding yeast cell cycle. Specifically, we chose a cell cycle synchronization strategy that avoids stress and nutrient-related perturbations of metabolism, and we grew the yeast on ethanol minimal medium to force cells to utilize their full biosynthetic repertoire. Using a tandem-mass-tagging approach, we found over 200 sites on metabolic enzymes and transporters to be phospho-regulated. These sites were distributed among many pathways including carbohydrate catabolism, lipid metabolism, and amino acid synthesis and therefore likely contribute to changing metabolic fluxes through the cell cycle. Among all one thousand sites whose phosphorylation increases through the cell cycle, the CDK consensus motif and an arginine-directed motif were highly enriched. This arginine-directed R-R-x-S motif is associated with protein-kinase A, which regulates metabolism and promotes growth. Finally, we also found over one thousand sites that are dephosphorylated through the G1/S transition. We speculate that the phosphatase Glc7/PP1, known to regulate both the cell cycle and carbon metabolism, may play an important role because its regulatory subunits are phospho-regulated in our data. In summary, our results identify extensive cell cycle dependent phosphorylation and dephosphorylation of metabolic enzymes and suggest multiple mechanisms through which the cell division cycle regulates metabolic signaling pathways to temporally coordinate biosynthesis with distinct phases of the cell division cycle."],"pubmed_title":["Multiple Layers of Phospho-Regulation Coordinate Metabolism and the Cell Cycle in Budding Yeast."],"pubmed_authors":["Zhang Lichao L, Winkler Sebastian S, Schlottmann Fabian P FP, Kohlbacher Oliver O, Elias Josh E JE, Skotheim Jan M JM, Ewald Jennifer C JC"],"sample_synonyms":["small, yeasts, Effects, Proteins, Longterm Effect, total expressed protein, Gene, Cell, Peptide, Long Term, Division Cycles, Polypeptides, TPSG1, S-adenosyl-L-methionine:thiol S-methyltransferase activity, Phosphopeptide, peptido, reduced, Protein, Long Term Effects, Cycle, Gene Products, tiny, Effect, Cell Division Cycles, Cycles, Yeast, peptides, Division Cycle, underdeveloped, Longterm, Cell Division Cycle, cell-division cycle, hypoplasia, Cell Division, Long-Term, Longterm Effects, Protein Gene Products, Gene Proteins, Cell Cycles, PRSS31, Peptid, peptidos, Long-Term Effect, Polypeptide, PRSS31., TMT, Long-Term Effects, Proteomes, thiol methyltransferase activity"],"name_synonyms":["Saccharomyces oviformis, Cell Division Cycles, Cycles, Sccharomyces cerevisiae, Yeast, Candida robusta, Saccharomyces capensis, Division Cycle, yeast, Cycle, Cell Division Cycle, cell-division cycle, Saccharomyes cerevisiae, baker's yeast, Cell Division, brewer's yeast, Cell Cycles., Saccharomyces uvarum var. melibiosus, Saccharomyces italicus, Saccaromyces cerevisiae, lager beer yeast, Cell, Division Cycles"],"data_synonyms":["Bru, IPP2A2, para Tyrosine, E 920, Raw, ion, Lysine Hydrochloride, cleavage, protein, Progress Reports, phosphorylation, 2-Amino-3-hydroxypropionic acid, 5730420M11Rik, peptide, Polypeptides, L-Isomer Methionine, Techniques, Lysine Acetate, Drug Tolerance, Methionine, peptido, Method, Summary Report, 2, 2-amino-3-mercaptopropanoic acid, Cystein, protein aggregate, Summary Reports, WMS, L Lysine, Svc, average, SET, C, F, i2pp2a., peptides, Progress Report, TAF-I, K, cisteina, M, 2-amino-3-(4-hydroxyphenyl)propanoic acid, 3-(p-Hydroxyphenyl)alanine, E430039A18Rik, epsilon-diaminocaproic acid, Saccharomyes cerevisiae, purification, Y, Saccharomyces uvarum var. melibiosus, ecotype, DmelCG4299, isolation and purification, Progress, IGAAD, set, LYS, Field Reports, 2-amino-3-hydroxypropanoic acid, Methodological Studies, DmelCG10574, Saccharomyces capensis, ppm, Lysin, Tyr, Strains, Half Cystine, brewer's yeast, GPHYSD2, Racemethionine, drug tolerance, SGS, phapii, Data Set, Zinc Cysteinate, immune system tolerance, acetylation, 2-Amino-4-(methylthio)butyric acid, 2-Amino-3-(p-hydroxyphenyl)propionic acid, StF-IT-1, para-Tyrosine, Procedure, Cys, results, ACMICD, Tyrosine, TPSG1, S-adenosyl-L-methionine:thiol S-methyltransferase activity, 3-Hydroxyalanine, Investigative Report, Ionen, 163, lysine, Immunologic Tolerance, Methionin, cultivar, Hmet, (2R)-2-amino-3-sulfanylpropanoic acid, parent ion, Yeast, HLA-DR-associated protein II, DI-2, MS/MS, I-2Dm, L-isomer, Field, L-Cysteine, MASS, CG4299, alpha, Methodological, beta Trypsin, Methodological Study, L-Cystein, L isomer, I-2PP1, Report, Self Tolerance, TAF-IBETA, precursor ion, Tolerance, PRSS31, Biocatalyst, L Serine, TAF-Ibeta, L-Tyrosine, Polypeptide, L-Serine, Strains and Sprains, i2pp2a, TMT, Liquimeth, Cysteine Hydrochloride, 2-amino-4-(methylsulfanyl)butanoic acid, Procedures, False, Biocatalysts, L-Zystein, L Isomer, FBN, baker's yeast, Gene, precursor, protein-containing complex, Saccharomyces italicus, PHAPII, method, Investigative, isolation, ECTOL1, method used in an experiment, yeast, Gene Products, Studies, L-Methionine, Del(8)44H, Lysine, Half-Cystine, Sprains, Technique, Pedameth, lager beer yeast, L Cysteine, MS2, iones, E-920, ipp2a2, beta-Trypsin, Acetylations, 2pp2a, Hcys, ions, CG10574, CD156, OCTD, Study, Enzyme, Candida robusta, 2PP2A, 2-amino-4-(methylthio)butanoic acid, 10^[-6], CYSTEINE, L Tyrosine, taf-ibeta, dSET, dSet, FREE CYSTEINE, peptidos, Tyrosin, (2R)-2-amino-3-mercaptopropanoic acid, Investigative Reports, metionina, thiol methyltransferase activity, DL-Methionine, protein complex, Sprain, Proteins, igaad, Phosphorylations, L-Isomer, Saccaromyces cerevisiae, Peptide, group, strain, Sccharomyces cerevisiae, polypeptide, Serin, Immune Tolerance, native protein, I-2PP2A, tirosina, Acetate, Dm I-2, Protein, Research Reports, Strain, I2PP2A, sequence, MFS1, L-Lysine, Zystein, tandem MS, Data Base, WMS2, Met, Saccharomyces oviformis, Col4a-1, PRSS, ensemble, 2-amino-3-sulfanylpropanoic acid, Tripcellim, L-2-Amino-3-mercaptopropionic acid, (R)-2-amino-3-mercaptopropanoic acid, CD156a, primary structure of sequence macromolecule, 2-Amino-3-mercaptopropionic acid, Protein Gene Products, plan specification, Trypure, Gene Proteins, dSET/TAF-Ibeta, 2610030F17Rik, Reports, Ion, SSKS, alpha-amino-gamma-methylmercaptobutyric acid, E920, Peptid, AA407739, 6-diaminohexanoic acid, Summary, Enisyl, Field Report, Immunological Tolerance"],"description_synonyms":["biochemical pathways, Regulations, Metabolic Process, degradation, Process, Formal Social Control, Processes, metabolism resulting in cell growth, Metabolic Concepts, baker's yeast, Metabolic Processes, Saccharomyces italicus, Saccaromyces cerevisiae, Cell, Social Controls, Division Cycles, Concept, Metabolic Phenomena, Sccharomyces cerevisiae, Metabolism Concepts, Social Control, Metabolism, yeast, Cycle, Phenomena, Concepts, secretion, Metabolism Concept, Phenomenon, Metabolism Phenomena, metabolism, Formal Social Controls, lager beer yeast, Metabolic Phenomenon, Saccharomyces oviformis, Cell Division Cycles, Cycles, Yeast, multicellular organism metabolic process, biodegradation, Metabolic, Division Cycle, catabolism, Cell Division Cycle, Control, cell-division cycle, Metabolic Concept, Saccharomyes cerevisiae, metabolic process resulting in cell growth, Cell Division, Controls, Cell Cycles., Saccharomyces uvarum var. melibiosus, Social, Candida robusta, Saccharomyces capensis, biotransformation, regulation, brewer's yeast, Regulation, Catabolism, Anabolism"],"pubmed_abstract_synonyms":["extent, l(1)d norm-12, l(2)k06503, EG:17A9.1, CDK, BR_C, neuronal cdc2-like kinase activity, Phosphatase, Su(var)(3)6, CG3938., fond, Metabolic Concepts, catalytic subunit activity, Phases, 2Bc, growth and development, pp1alpha96A, CG32505, CycEI, Divisions, phosphorylation, Social Controls, multicellular organismal carbohydrate catabolic process, dmTAF[[II]]230, l(1)2Bad, l(1)2Bab, Carbon-12, cdk, br-Z1, br-Z3, FLW/PP1B, Kinase, Metabolism Concept, myd, Nutrient, l(1)dn1, WMS, cyclin-dependent protein kinase, CG1459, Cell Division Cycles, rbp, C, (S)-2-amino-5-guanidinopentanoic acid, Suvar(3)6, Grain, M Phases, amino acids, TFIID TAF250, Su(Var)3-6, CG9156, cel, catabolism, M, PP4 19C, l(3)ck19, anabolism, PP187B, FLW, BR, R, Mbp-1, Saccharomyes cerevisiae, Arginine, metabolic process resulting in cell growth, Monohydrate DL-Arginine Acetate, CG18339, Saccharomyces uvarum var. melibiosus, Phosphomonoesterases, Br-C-Z3, SID6-8061, Social, HEL-S-66p, Dehydrated ethanol, Budding Yeast, Role Concepts, Br, BRC-Z2, BRC-Z3, PPP4c, BRC-Z1, BRC-Z4, PP1c, ATP Phosphotransferases, DmPp1-87B, phosphatase, SGS, DmelCG6593, single organism signaling, spiritus vini, rdp, Budding Yeasts, rds, dTAF[[II]]230, PP1c 96A, PP1alpha13C, completeness, metabolism resulting in cell growth, l(1)d.norm.1, TAF200, Pp1-87Bb, arginine, DmPpp4-19C, dephosphorylation, l(1)npr-1, Cyc E, Cell Divisions, l(1)npr1, Absolute Alcohol, ACMICD, Cdk-activating protein kinase activity, Vitreous, cdk-activating kinase activity, Role Concept, BG:DS07108.3, PP4C, Playthings and Play, mKIAA0609, Role, secretion, PP1alpha-87B, l(2)05206, PP1-87B, [OEtH], ck19, DmelCG2096, fg, Acid, 96A, PP1 13C, PP1 beta87b, expanded, Cdk4/6, Controls, DmPp1-96A, alcohol etilico, Methylcarbinol, MDC1D, cyclin-dependent kinase 6 activity, Phosphohydrolase, hyaline, enr, Taf250, Proliferation, Phosphoric, PP13C, l(2)0671, CG1596, l(1)pp-2, l(1)pp-1, Acids, PP1beta, TAF230, Regulations, big, cyclin D-cdk6 kinase activity, cycline, Processes, Biocatalysts, DmcyclinE, etanol, 2-Amino-5-guanidinovaleric acid, DmelCG32505, PP1 beta13c, Metabolic Processes, protein-containing complex, Saccharomyces italicus, cdi7, CG11511, 87B, large, pp1-87B, CG11514, cyclinE, PP1alpha[[1]], Harg, yeast, Consensus, Cdi7, CDI7, Gene Products, CG5650, DmPp1-13C, lager beer yeast, Toy, Cycles, dTAF[[II]]250, lipid metabolism, Cell Division Phase, Playthings, cell, MDDGB6, ethanol, proliferating, nutrients, Cell Division Cycle, cell-division cycle, Metabolic Concept, DmcycE, Division, PP-1alpha, Phosphoric Monoester Hydrolase, dTAF250, C2H5OH, cdk4, Enzyme, Puppets, dis2m1, PP1 96A, L-Arg, l(1)PP1, l(1)pp1, CDK4, l(1)pp2, l(2)05428, Macronutrient, Puppet, Su-var(3)6, EG:123F11.1, DmelCG5650, degradation, PP1 87B, Proteins, Phosphorylations, BG:DS00004.13, PP19C, L-Isomer, l(1)G0284a, carbone, Cell, Saccaromyces cerevisiae, single-organism carbohydrate catabolic process, Pp-1alpha, Concept, dTAF230, Macronutrients, carbono, Sccharomyces cerevisiae, l(2)k02514, catabolic carbohydrate metabolic process, DmCycE, native protein, Social Control, L-Isomer Arginine, PP1beta-9C, PP-1G, alcool ethylique, TAF[[II]]250/230, MFS1, PP1A87B, cyclin-A associated kinase activity, intrinsic catalyst activity, metabolism, Metabolic Phenomenon, Saccharomyces oviformis, Taf[[II]]250, Phase, multicellular organism metabolic process, l(2)k02602, PP1alpha87B, cdc2 kinase activity, (2S)-2-amino-5-guanidinopentanoic acid, postnatal growth, D-CycE, Gene Proteins, signalling process, PP1alpha[[2]], l(1)G0401, Pk53C, BRC, regulation, carbohydrate catabolism, CDK activity, Anabolism, biochemical pathways, PP, Metabolic Process, Grain Alcohol, carbohydrate breakdown, DL-Arginine Acetate, postnatal development, Aminosaeure, Pp1, Mbp1, cdk4/6, Monohydrate, protein, BR-C, 1-hydroxyethane, alcohol, Endomycetale, Phosphatases, Ethanol, Hydrolase, Ccne, A18, br-C, Roles, CG6593, PP1alpha96A, Alkohol, PP1, Concepts, PP2, PP4, pp4, Arg, protein aggregate, Phenomenon, PpX, BR-c, Br-C, Formal Social Controls, multicellular organismal biosynthetic process, PP1 beta9c, Br-Z4, l(3)j6E7, single-organism biosynthetic process, enzymes, l(1)G0318, de12, long, Ethyl, (S)-2-Amino-5-guanidinovaleric acid, l(1)n34, BrC-Z1, Aethanol, PPX, PP1beta9C, [CH2Me(OH)], Division Phase, 13C, reaction, pp1-13C, Endomycopses, Saccharomyces capensis, CG2096, su-var(3)6, Cell Cycles, Carbon, dCdk4, biotransformation, Consensus Development, brewer's yeast, PP1 9C, GPHYSD2, Catabolism, CG11491, Budding, ATP, L-Arginin, Saccharomycetale, anon-WO03040301.120, PP1B_DROME, Alcohol, Process, gyltl1b-b, Aminokarbonsaeure, BR-C Z1, Arginine Hydrochloride, D-type cyclin kinase activity, Ethyl alcohol, TAFII-250, TAF250/230, br37, Arginin, uq, results, Division Cycles, TAFII250, MDDGA6, Lipid, Plaything, nrp1, KIAA0609, ETHANOL, cyclin-dependent kinase-2 activity, L-Arginine, Yeasts, Amino Acid, Yeast, Transphosphorylases, cyclin-dependent kinase activity, CG15305, gyltl1b, EtOH, growth pattern, Division Cycle, non-developmental growth, 6C, mdc1d, Pp1-96A, Control, ATP:cyclin phosphotransferase activity, Toys, DmPp1-9C, npr-1, MASS, DmelCG9156, CG17603, TAF[[II]], cyclin D-dependent kinase activity, CDK4/6, Vitreous Carbon, l35Dd, enlarged, SR3-5, Endomycopsis, carbonium, Biocatalyst, npr, Hydrolases, Regulation, Endomycetales, Pp1beta-9C, Proliferating, d230, Plays, bioformation, l(1)G0018, DmelCG11491, Su(var)3-6, Aminocarbonsaeure, L Isomer, FBN, l(1)ts144, baker's yeast, Gene, dTAFII250, l(1)2Ba, cycE, Pk?7, l(1)2Bb, carbon, Z1, l(1)2Bc, Development, Z2, Monoester Hydrolase, Z3, Z4, EfW1, l(2)br37, froggy, CYCLE, Gyltl1a, L-(+)-arginine, protein amino acid phosphorylation, Aethylalkohol, PP1c 87B, EG:25D2.1, (2S)-2-amino-5-(carbamimidamido)pentanoic acid, dmTAF1, Taf230, ECTOL1, Metabolism, nrp, Cycle, Br-C Z2, l(1)ts132, l(1)ts376, Metabolism Phenomena, Ppl-87B, Phosphotransferase, TAF250, l(1)ESHS5, IOPPP, Taf200, carbohydrate degradation, CYCE, Absolute, CG5072, DmelCG3938, CyclE, cyclin E kinase activity, cyclin-dependent protein kinase activity, nprl, 3938, Taf1p, Cell Division, LARGE, Transphosphorylase, OCTD, l(2)k05007, BPFD#36, cyclin-dependent kinase-4 activity, dm-cycE, Kohlenstoff, l(1)G0042, l(1)G0284, Candida robusta, Pp1alpha-87B, l(1)2Bd, great, l(3)87Bg, Play, npr1, TAF, 2-amino-5-(carbamimidamido)pentanoic acid, dPP4, PP-1, nutrient, TAF[[II]]250, Formal Social Control, protein complex, synthesize, l(3)84Ab, ecs, enzyme activity, BrZ3, 2-amino-5-guanidinopentanoic acid, DL Arginine Acetate, l(1)G0172, Phosphotransferases, Metabolic Phenomena, l(2)s4639, development, Metabolism Concepts, Phosphomonoesterase, PP1 b9C, o.c.c., p230, Protein, Phenomena, Hydrochloride, TFIID, L Arginine, CyeE, catabolic carbohydrate metabolism, M Phase, DmCdk4, WMS2, Ethyl Alcohol, Phosphoric Monoester, PP1 alpha96a, TAF[[II]]230, biodegradation, distinct, Metabolic, Kinases, l(1)ts358, l(2)35Dd, phosphoric monoester hydrolase activity, TAF[II]250, Amino, DmelCG5072, Carbon 12, Protein Gene Products, Phosphohydrolases, 8-6, hydroxyethane, 2B5, DmelCG17603, clear, concentration, SSKS, PP1alpha-13C, PP1-13C, growth, CG3938, l(2)sh0671, TAF1"],"pubmed_title_synonyms":["biochemical pathways, Budding Yeasts, Regulations, Saccharomycetale, Metabolic Process, degradation, Process, Formal Social Control, Processes, metabolism resulting in cell growth, Metabolic Concepts, Metabolic Processes, Cell, Social Controls, Division Cycles, Concept, Metabolic Phenomena, Endomycetale, Budding., Metabolism Concepts, Social Control, Metabolism, Cycle, Phenomena, Concepts, secretion, Metabolism Concept, Phenomenon, Metabolism Phenomena, metabolism, Formal Social Controls, Metabolic Phenomenon, Cell Division Cycles, Cycles, Yeasts, Yeast, multicellular organism metabolic process, biodegradation, Metabolic, Division Cycle, catabolism, Cell Division Cycle, Control, cell-division cycle, Metabolic Concept, metabolic process resulting in cell growth, Cell Division, Controls, Social, Budding Yeast, Endomycopses, Endomycopsis, Cell Cycles, biotransformation, regulation, Regulation, Catabolism, Endomycetales, Budding, Anabolism"],"additional_accession":[]},"is_claimable":false,"name":"Phosphoproteomic analyses of yeast cell cycle","description":"This is to provide phosphoproteomic analyses to support multiple layers of phospho-regulation coordinate metabolism in yeast cell 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