{"database":"Pride","file_versions":[{"headers":{"Content-Type":["application/json"]},"body":{"files":{"Xlsx":["ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2023/01/PXD039148/shenbang29-34-phos.xlsx"],"Txt":["ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2023/01/PXD039148/proteinGroups.txt"],"Xml":["ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2023/01/PXD039148/mqpar.xml","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2023/01/PXD039148/mqpar-phos-.xml"],"Raw":["ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2023/01/PXD039148/shenbangTMT-29-34-6.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2023/01/PXD039148/shenbangTMT-29-34-8-2.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2023/01/PXD039148/shenbang29-34-100C.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2023/01/PXD039148/shenbangTMT-29-34-2.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2023/01/PXD039148/shenbangTMT-29-34-8-1.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2023/01/PXD039148/shenbangTMT-29-34-7.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2023/01/PXD039148/shenbangTMT-29-34-9.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2023/01/PXD039148/shenbang29-34-phos-singlephase-2.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2023/01/PXD039148/shenbang29-34-50C.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2023/01/PXD039148/shenbang29-34-0C.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2023/01/PXD039148/shenbangTMT-29-34-3.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2023/01/PXD039148/shenbangTMT-29-34-12.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2023/01/PXD039148/shenbang29-34-25C.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2023/01/PXD039148/shenbang29-34-phos-singlephase-1.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2023/01/PXD039148/shenbang29-34-5C.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2023/01/PXD039148/shenbangTMT-29-34-4.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2023/01/PXD039148/shenbangTMT-29-34-10.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2023/01/PXD039148/shenbang29-34-30C.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2023/01/PXD039148/shenbangTMT-29-34-11.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2023/01/PXD039148/shenbang29-34-20C.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2023/01/PXD039148/shenbang29-34-15C.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2023/01/PXD039148/shenbangTMT-29-34-5.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2023/01/PXD039148/shenbangTMT-29-34-wash.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2023/01/PXD039148/shenbangTMT-29-34-1.raw"]},"type":"primary"},"statusCode":"OK","statusCodeValue":200}],"scores":null,"additional":{"labhead_mail":["shenbang@mail.hzau.edu.cn"],"submitter":["Yaqiong Li"],"technology_type":["Affinity purification coupled with mass spectrometry proteomics","Mass Spectrometry"],"software":[""],"submitter_keywords":["Toxoplasma","Ampk"],"full_dataset_link":["https://www.ebi.ac.uk/pride/archive/projects/PXD039148"],"sample_protocol":["The AMPKγ-mAID strain was pretreated with or without IAA for 48 hours, followed by needle passage to break host cells and release parasites. Tachyzoites were then collected, purified by filtration, and lysed in 8 M urea (0.1M Tris-Cl, pH 8.5) with the protease inhibitor cocktail (Merk, USA) and phosphatase inhibitor cocktail (Roche Applied Science, Germany). Three samples were prepared independently for each strain under each condition. The lysate was sonicated and centrifuged for 15 minutes at 4 ℃ to collect supernatant for protein concentration assessment using the BCA assay (Thermo Scientific, USA). Then 500 μg protein of each sample was used for digestion. TCEP (Tris(2-carboxyethyl) phosphine, final concentration is 5 mM) (Thermo Scientific, USA) and iodoacetamide (final concentration is 10 mM) (Sigma-Aldrich, USA) for reduction and alkylation were added to protein samples and incubated at room temperature for 30 minutes, respectively. The protein mixture was diluted four times (to reduce the concentration of urea to 2M) and digested at 37 ℃ with Lys-C at 1:100 (w/w) (Wako, Japan) for 2 hours, and then with trypsin at 1:50 (w/w) (Promega, USA) overnight. Then the reaction was stopped by adding formic acid to pH less than 2.Digested samples were desalted by a SepPak tC18 3cc Vac cartridge (Waters Corporation, USA) and dried out by lyophilization. The samples were then resolved in 100 mM HEPES (pH = 8.0), and the peptide concentration was measured using the Quantitative Colorimetric Peptide Assay (Thermo Scientific, USA). 100 μg peptide of each sample (six samples in total, three with IAA treatment and three without) was labeled using the six-plex TMT kit (Thermo Scientific, USA) following the manufacturer’s manual. Sample labeling efficiency of each channel was checked as previously described. The labeling reaction was quenched by hydroxylamine and then desalted by the tC18 Vac cartridge as described above. After TMT labeling, all peptides from the six samples were mixed (600 μg in total) and 30 μg was used for proteomic analysis. The samples were subject to high pH reversed-phase peptide fractionation (Pierce, USA) and 13 fractions were acquired for LC-MS analyses. The rest of labeled peptides (570 μg in total) were used for phospho-peptide enrichment using a SMOAC workflow, which enriched phospho-peptides sequentially by TiO2 and IMAC (Thermo Scientific, USA)."],"repository":["Pride"],"modification":[""],"quantification_method":[""],"data_protocol":["The acquired MS/MS data were analyzed against a Toxoplasma gondii database (ToxoDB.org) by Maxquant V1.6.10.43 using the default settings. Tolerance of precursor mass and fragment mass were set to 20 ppm. The main search peptides tolerance was set at 4.5 ppm according to the feature of the instrument used in the study. Carbamidomethylation of cysteine (+57.021 Da) was set as static modifications. The quantification search type chose the reporter ion ms2 using the TMT 6plex method. Oxidation of methionine (+15.995 Da) and acetylation of protein N terminus were set as variable modifications for the proteomic data analysis, and phosphorylation of Serine/Threonine/Tyrosine (+79.9663 Da) for the phospho-proteomic data. Trypsin was defined as cleavage enzyme at full specific mode, and the maximum missing cleavage was set at 2. FDR of the identified proteins was set at 1%, which was calculated at the peptide level."],"omics_type":["Proteomics"],"labhead":["Bang Shen"],"instrument_platform":[""],"submission_type":["PARTIAL"],"labhead_affiliation":["Huazhong Agricultural University"],"species":["Toxoplasma Gondii Rh"],"publication":["Not available"],"submitter_mail":["liyaqiong624@163.com"],"submitter_affiliation":["Huazhong Agricultural University"],"submitter_country":["China"],"name_synonyms":["Regulations, 3-hydroxy-3-methylglutaryl-CoA reductase kinase activity, AMPKalpha, protein kinase A activity, ampk, Formal Social Control, beta-hydroxy-beta-methylglutaryl-CoA reductase kinase activity, postnatal development, AMPKa2, growth and development, AMPKa1, ATP:hydroxymethylglutaryl-CoA reductase (NADPH) phosphotransferase activity, 3-hydroxy-3-methylglutaryl coenzyme A reductase kinase activity, Social Controls, acetyl coenzyme A carboxylase kinase (phosphorylating) activity, gondius, hydroxymethylglutaryl-CoA reductase (NADPH) kinase activity, development, I-peptide kinase activity, acetyl-coenzyme A carboxylase kinase activity, cyclic AMP-dependent protein kinase activity, PKA, Social Control, cAMP-dependent protein kinase, Gprk-4, intrinsic catalyst activity, AMPK, Formal Social Controls, acetyl-CoA carboxylase kinase (AMP-activated) activity, acetyl-CoA carboxylase kinase (cAMP-independent) activity, ampkalpha, acetyl-CoA carboxylase kinase-2 activity, PKA C, HAMPKb, CG3051, hydroxymethylglutaryl-CoA reductase (NADPH2) kinase activity, EG:132E8.2, STK5, DmAMPK alpha, postnatal growth, Control, ATP:acetyl-CoA carboxylase phosphotransferase activity, AMPK2, 3', prkaa, acetyl-CoA carboxylase kinase-3 (AMP-activated) activity, Toxoplasma gondius, acetyl-CoA carboxylase bound kinase activity, Ampk, Controls, hydroxymethylglutaryl coenzyme A reductase kinase (phosphorylating) activity, hydroxymethylglutaryl-CoA reductase kinase activity, hydroxymethylglutaryl coenzyme A reductase kinase activity, prkaa1, DmelCG3051, Social, ampk2, reductase kinase activity, 5'-cyclophosphate-dependent protein kinase activity, PRKAA, 5' cAMP-dependent protein kinase activity, ATP:protein phosphotransferase (cAMP-dependent) activity, Ampka2, Development and Growth, STK29, dAMPKa, ampka1, Gprk4, Toxoplasma, acetyl-CoA carboxylase kinase 2 activity, dAMPKalpha, STK22, Toxoplasma gondii, snf1a, regulation, Toxoplasmas, ACK3, acetyl-CoA carboxylase kinase activity, 5'-cAMP-dependent protein kinase activity., ACK2, Regulation, growth, adenosine 3', HMG-CoA reductase kinase activity, FBgn0023169"],"data_synonyms":["IPP2A2, para Tyrosine, E 920, ion, Feature, instrument configuration, cleavage, L-Threonine, protein, phosphorylation, 2-Amino-3-hydroxypropionic acid, 5730420M11Rik, peptide, Polypeptides, Techniques, L-Isomer Methionine, protein polypeptide chains, Methionine, peptido, Method, 2-amino-3-mercaptopropanoic acid, Cystein, Analysis, Gpi-1, protein aggregate, WMS, Threonin, SET, C, peptides, Analyses, TAF-I, Nlk, cisteina, M, 2-amino-3-(4-hydroxyphenyl)propanoic acid, 3-(p-Hydroxyphenyl)alanine, E430039A18Rik, HardwareType, proteins, Y, DmelCG4299, IGAAD, set, Methodological Studies, 2-amino-3-hydroxypropanoic acid, DmelCG10574, ppm, Tyr, Toxoplasmas, Half Cystine, GPHYSD2, Racemethionine, SGS, NK/GPI, Gpi, phapii, Zinc Cysteinate, acetylation, 2-Amino-4-(methylthio)butyric acid, 2-Amino-3-(p-hydroxyphenyl)propionic acid, StF-IT-1, para-Tyrosine, Procedure, not genetically inherited, Cys, ACMICD, Tyrosine, TPSG1, S-adenosyl-L-methionine:thiol S-methyltransferase activity, mOC-X, Ionen, 3-Hydroxyalanine, Methionin, NK|GPI, Hmet, (2R)-2-amino-3-sulfanylpropanoic acid, parent ion, Org, ORG, HLA-DR-associated protein II, DI-2, instrument, MS/MS, I-2Dm, L-isomer, Gpi1-r, Gpi1-s, L-Cysteine, MASS, CG4299, Methodological, Toxoplasma gondius, Gpi1-t, Features, Methodological Study, beta Trypsin, L-Cystein, L isomer, I-2PP1, data analysis, TAF-IBETA, precursor ion, PRSS31, Biocatalyst, Toxoplasma, L Serine, TAF-Ibeta, L-Tyrosine, Polypeptide, L-Serine, i2pp2a, TMT, Liquimeth, Bglap-rs1, Gpi1s, Cysteine Hydrochloride, 2-amino-4-(methylsulfanyl)butanoic acid, Procedures, AI461847, Biocatalysts, L-Zystein, L Isomer, FBN, Gene, precursor, protein-containing complex, PHAPII, hardware, gondius, method, polypeptide chain, ECTOL1, method used in an experiment, Studies, Gene Products, L-Methionine, Pgi, Half-Cystine, Technique, Pedameth, study, Gpi-1r, MS2, Gpi-1s, L Cysteine, iones, E-920, Phi, ipp2a2, beta-Trypsin, Gpi-1t, Acetylations, 2pp2a, Hcys, L Threonine, ions, CG10574, CD156, OCTD, Study, Enzyme, 2PP2A, 2-amino-4-(methylthio)butanoic acid, data processing, 10^[-6], CYSTEINE, L Tyrosine, taf-ibeta, dSET, dSet, FREE CYSTEINE, Toxoplasma gondii, peptidos, Characteristics, Tyrosin, (2R)-2-amino-3-mercaptopropanoic acid, metionina, thiol methyltransferase activity, DL-Methionine, protein complex, Proteins, igaad, Phosphorylations, MF, L-Isomer, Amf, Peptide, group, polypeptide, Serin, Characteristic, native protein, natural protein, I-2PP2A, tirosina, Dm I-2, Protein, I2PP2A, MFS1, tandem MS, Zystein, Data Base, NK, WMS2, Met, PRSS, ensemble, 2-amino-3-sulfanylpropanoic acid, Tripcellim, L-2-Amino-3-mercaptopropionic acid, (R)-2-amino-3-mercaptopropanoic acid, CD156a, 2-Amino-3-mercaptopropionic acid, plan specification, Protein Gene Products, Gene Proteins, Trypure, dSET/TAF-Ibeta, 2610030F17Rik, Ion, Data, SSKS, alpha-amino-gamma-methylmercaptobutyric acid, E920, Peptid, variable, AA407739, Peptide., Data Analyses"],"description_synonyms":["Regulations, 3-hydroxy-3-methylglutaryl-CoA reductase kinase activity, AMPKalpha, protein kinase A activity, ampk, Formal Social Control, beta-hydroxy-beta-methylglutaryl-CoA reductase kinase activity, postnatal development, AMPKa2, growth and development, AMPKa1, ATP:hydroxymethylglutaryl-CoA reductase (NADPH) phosphotransferase activity, 3-hydroxy-3-methylglutaryl coenzyme A reductase kinase activity, Social Controls, acetyl coenzyme A carboxylase kinase (phosphorylating) activity, gondius, hydroxymethylglutaryl-CoA reductase (NADPH) kinase activity, development, I-peptide kinase activity, acetyl-coenzyme A carboxylase kinase activity, cyclic AMP-dependent protein kinase activity, PKA, Social Control, cAMP-dependent protein kinase, Gprk-4, intrinsic catalyst activity, AMPK, Formal Social Controls, acetyl-CoA carboxylase kinase (AMP-activated) activity, acetyl-CoA carboxylase kinase (cAMP-independent) activity, ampkalpha, acetyl-CoA carboxylase kinase-2 activity, PKA C, HAMPKb, CG3051, hydroxymethylglutaryl-CoA reductase (NADPH2) kinase activity, EG:132E8.2, STK5, DmAMPK alpha, postnatal growth, Control, ATP:acetyl-CoA carboxylase phosphotransferase activity, AMPK2, 3', prkaa, acetyl-CoA carboxylase kinase-3 (AMP-activated) activity, Toxoplasma gondius, acetyl-CoA carboxylase bound kinase activity, Ampk, Controls, hydroxymethylglutaryl coenzyme A reductase kinase (phosphorylating) activity, hydroxymethylglutaryl-CoA reductase kinase activity, hydroxymethylglutaryl coenzyme A reductase kinase activity, prkaa1, DmelCG3051, Social, ampk2, reductase kinase activity, 5'-cyclophosphate-dependent protein kinase activity, PRKAA, 5' cAMP-dependent protein kinase activity, ATP:protein phosphotransferase (cAMP-dependent) activity, Ampka2, Development and Growth, STK29, dAMPKa, ampka1, Gprk4, Toxoplasma, acetyl-CoA carboxylase kinase 2 activity, dAMPKalpha, STK22, Toxoplasma gondii, snf1a, regulation, Toxoplasmas, ACK3, acetyl-CoA carboxylase kinase activity, 5'-cAMP-dependent protein kinase activity., ACK2, Regulation, growth, adenosine 3', HMG-CoA reductase kinase activity, FBgn0023169"],"sample_synonyms":["sodium salt, host organism, Hypodermic Needles, Endopeptidase Inhibitor, ammonium formate, DmelCG8566, 13C-labeled, cadmium salt, determination, Phosphatase, Liquid Chromatography Mass Spectrometry, Peptide Hydrolase Inhibitor, zinc formate, High Performance Liquid Chromatography Mass Spectrometry, lead salt, HEPES Monosodium Salt, 2-(indol-3-yl)ethanoic acid, Basodexan, protein, magnesium formate, Xkl-1, Ultra Performance Liquid Chromatography-Mass Spectrometry, DmKlp53D, Cahp, zinc salt, High Performance Liquid Chromatography-Mass Spectrometry, Productivity, Bca, Alkylations, peptide, Phosphatases, Polypeptides, DmelCG11081, Hydrolase, protein polypeptide chains, KL receptor activity, 1H-imidazoleacetic acid, ammonium tetraformate, Gsfsco1, HPLC-MS, IAA, peptido, Liquid Chromatography-Mass, diseases, cobalt(II) formate dihydrate, Protease Inhibitor, DPlexA, SCO5, Inhibitors, diseases and disorders, AGM4, SCO1, Hydrolase Inhibitors, protein aggregate, Work Flow, Gsfsow3, Gsfsco5, SOW3, bca, treatment, HEPES Monosodium, Ultra Performance Liquid Chromatography Mass Spectrometry, human disease, Hypodermic, peptides, Rests, E927b, weight-weight percentage, Salt, proteins, W, copper, Phosphomonoesterases, ecotype, CG17245, reaction, Hydroxylammonium Chloride, IMAC, Peptidohydrolase Inhibitor, lithium salt, 1-Piperazineethanesulfonic acid, scientific observation, Liquid Chromatography-Mass Spectrometries, sample, disease management, Therapies, Bs, Homo sapiens disease, Strains, Lyw-57, Needle, imac, Sl, phosphatase, ammonium (2:1) salt, nickel salt, Hypodermic Needle, Therapy, Bonin Islands, Peptidase Inhibitor, Chp, cobalt (+2) salt, Trypsin/K, TSC-1, helminthology, Tr-kit, Peptide Peptidohydrolase, KIF1B, Thermo Scientific, not genetically inherited, ur, SLP65, PBT, carbamide, Ly-57, TPSG1, (Indol-3-yl)acetate, S-adenosyl-L-methionine:thiol S-methyltransferase activity, Workflows, sodium (4:1:1) salt, magnesium salt, XBR, Hydrolase Inhibitor, kl1-A, p24, cultivar, IES, CG8566, KIT, nickel (+2) salt, PlexA1, BcDNA:GM05237, tyrosine-protein kinase Kit, imidazole-4-acetic acid hydrochloride, SLP-65, ammonium salt, pbt, Antagonists, BASH, PlexB, PlexA, LY57, High Pressure Liquid Chromatography Mass Spectrometry, Xylella fastidiosa str. Temecula1, formate, cobaltous formate, Spectrometry, SECC-8, cromium (+3), kit, Sid470p, beta Trypsin, Plex1, Treatments, w/w, disease, H2NC(O)NH2, DmCG8566, Phosphohydrolase, Peptidase Inhibitors, heteroauxin, SCYA26, Parasite, Thermo Scientific., Acetamide, Phosphoric, copper salt, PRSS31, Antiproteases, ammonium (4:1) salt, Liquid, Polypeptide, Endopeptidase, Peptide Peptidohydrolase Inhibitor, HEPES, AI046351, parasites, Hydrolases, lead (+2) salt, PLEXB, Strains and Sprains, Inhibitor, TMT, 1728, glutamic acid side-chain, Work Flows, Gruppe, krk1, AA407358, Hydroxylamine Hydrochloride, other disease, Dunc104, DIP1, nickel formate dihydrate, lead formate, Endopeptidase Inhibitors, aluminum salt, cesium salt, number, SCF receptor activity, Pierce, Gene, Protease, Carbamide, CG11081, Monoester Hydrolase, vac, protein-containing complex, presence, formic acid, GCIP, Karbamid, potassium salt, polypeptide chain, scfr, Filtrations, Ly57, 14C-labeled, Harnstoff, Gene Products, disease or disorder, NRSF, Protease Antagonist, D-Plex A, Peptide Hydrolase, Carmol, Sprains, PH3, SCFR, Pro-Mega, UPLC-MS, Fdc, Ultra-Performance Liquid Chromatography-Mass Spectrometry, thallium (+1) salt, plex A, beta-Trypsin, rubidium salt, Monosodium Salt, plex B, phosphane, imidazolyl-4-acetic acid, inhibiteur, Sciences, Spectrometries, Indoleacetic acid, labeling, calcium formate, methanoic acid, Antagonist, Phosphoric Monoester Hydrolase, non-neoplastic, DmelCG17245, Xylella fastidiosa (strain Temecula1 / ATCC 700964), lysate, inhibidor, (indol-3-yl)acetic acid, MIP-4a, Protease Antagonists, grupos, Peptide Peptidohydrolase Inhibitors, disorder, peptidos, cromium (+3) salt, N-2-Hydroxyethylpiperazine-N'-2'-ethanesulfonic Acid, Chromatography-Mass Spectrometries, 4-(2-hydroxyethyl)-, 2-iodo-, sodium formate, SSEC-8, TCEP, thiol methyltransferase activity, BLNK-S, inhibitors, measuring, proto-oncogene c-Kit, mass percentage, AA960066, grupo, nickel formate, 1500003O03Rik, protein complex, Sprain, Proteins, imidazole-4-acetic acid, disorders, 2610008J04Rik, strontium formate, inhibitor, TelN, medical condition, potassium formate, High Pressure Liquid Chromatography-Mass Spectrometry, Mischung, copper (+2) salt, Needles, backward, strontium salt, plex, Cell, Peptide, group, strain, polypeptide, Phosphomonoesterase, count in organism, native protein, Temperatures, natural protein, carbonyldiamide, KIT ligand receptor activity, Unc104, cupric formate, chemical analysis, Protein, Strain, proteomic analysis, condition, aluminum formate, XKrk1, Phosphoric Monoester, c-KIT, lithium formate, PRSS, uree, 3-Indolylessigsaeure, Tripcellim, Rest, N 2 Hydroxyethylpiperazine N' 2' ethanesulfonic Acid, hydrogen phosphorus, phosphoric monoester hydrolase activity, MIP-4alpha, Klp53D, Peptidohydrolase Inhibitors, CD117, protozoology, sample population, chromic formate, Unc-104, Phosphohydrolases, Protein Gene Products, Gene Proteins, Trypure, Peptidase, AU022347, c-kit, Antiprotease, hydrogen phosphide, Therapeutic, C-Kit, concentration, Maid, 2-carboxyethyl, Ssm, protozoa, Chromatography-Mass Spectrometry, calcium salt, xkl-1, LC-MS, ResT, Peptid, Treatment, Peptide Hydrolase Inhibitors, assay, groupe, reversed"],"additional_accession":[]},"is_claimable":false,"name":"Regulation of Toxoplasma growth and development by AMPK","description":"Regulation of Toxoplasma growth and development by 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