{"database":"Pride","file_versions":[{"headers":{"Content-Type":["application/json"]},"body":{"files":{"Txt":["ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2024/08/PXD053507/checksum.txt"],"Raw":["ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2024/08/PXD053507/XB03952PI_isonico_Fr1.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2024/08/PXD053507/XB03952PI_isonico_Fr2.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2024/08/PXD053507/XB03952PI_isonico_Fr4.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2024/08/PXD053507/XB03952PI_isonico_Fr3.raw"],"Other":["ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2024/08/PXD053507/txt.zip"]},"type":"primary"},"statusCode":"OK","statusCodeValue":200}],"scores":null,"additional":{"labhead_mail":["yixiaoli@bjmu.edu.cn"],"submitter":["li yixiao"],"technology_type":["Mass Spectrometry","Bottom-up proteomics"],"software":[""],"submitter_keywords":["Isonicotinylation proteomic"],"full_dataset_link":["https://www.ebi.ac.uk/pride/archive/projects/PXD053507"],"tissue":["Cell Culture"],"sample_protocol":["HepG2 cells were lysed by ultrasound with lysis buffer (8 M urea 1% protease inhibitor cocktail, 3 μM TSA, 50 mM NAM). After centrifugation the supernatant was collected for protein concentration using BCA kit. The peptide was dissolved in IP buffer solution (100 mM NaCl, 1 mM EDTA, 50 mM Tris-HCl, 0.5% NP-40, pH 8.0) and the supernatant was transferred to pre-washed isonicotinylation modified resin incubated overnight at 4℃. The resin was washed with IP buffer solution and deionized water.The resin-bound peptide was eluted off with 0.1% trifluoroacetic acid eluent and the eluent was collected. After vacuum freezing and drying, the liquid was used for mass spectrometry analysis"],"repository":["Pride"],"modification":[""],"quantification_method":["Not available"],"data_protocol":["The MaxQuant search engine (v.1.6.15.0) was used to processed the resulting MS/MS data. Tandem mass spectra were searched against the human SwissProt database concatenated with reverse decoy database. The mass tolerance for precursor ions was set as 20 ppm in first search and 5 ppm in main search, and the mass tolerance for fragment ions was set as 0.02 Da. FDR was adjusted to < 1%."],"omics_type":["Proteomics"],"labhead":["Yixiao Li"],"instrument_platform":[""],"labhead_affiliation":["Program for Cancer and Cell Biology, Department of Human Anatomy, Histology and Embryology, School of Basic Medical Sciences; Peking University International Cancer Institute; State Key Laboratory of Molecular Oncology, Peking University Health Science Center, Beijing 100191, China."],"species":["Homo Sapiens (human)"],"submission_type":["PARTIAL"],"publication":["Not available"],"submitter_mail":["yixiaoli@bjmu.edu.cn"],"curator_keywords":["Human proteome project"],"submitter_affiliation":["peking university"],"submitter_country":["China"],"name_synonyms":["Human, Cell Line, human being, Hep G2, Man (Taxonomy), HepG2 Cell., Homo sapiens, Modern Man, HepG2 Cells, Hepatoblastoma G2 Cell Line, HepG2 cell, Cells, Modern, Hepatoblastoma G2, HepG2, Hep-G2, Man, Hep G2 Cell, Hep G2 Cell Line, human, humans, Cell"],"data_synonyms":["phapii, IPP2A2, human being, ion, T5E21.12, Modern, igaad, FBN, StF-IT-1, Search, precursor, Engine, PHAPII, group, ACMICD, Human, 5730420M11Rik, Homo sapiens, Ionen, I-2PP2A, ECTOL1, Dm I-2, I2PP2A, MFS1, Man, tandem MS, WMS, WMS2, Data Base, T5E21_12, parent ion, Search Engines, SET, Man (Taxonomy), HLA-DR-associated protein II, i2pp2a., ensemble, DI-2, TAF-I, MS/MS, MS2, iones, I-2Dm, ipp2a2, 2pp2a, MASS, CG4299, ions, human, CG10574, OCTD, DmelCG4299, I-2PP1, IGAAD, set, dSET/TAF-Ibeta, 2610030F17Rik, TAF-IBETA, 2PP2A, precursor ion, 10^[-6], Ion, DmelCG10574, taf-ibeta, ppm, Modern Man, SSKS, dSET, dSet, TAF-Ibeta, GPHYSD2, AA407739, i2pp2a, humans, SGS"],"sample_synonyms":["Water, Endopeptidase Inhibitor, TDPX1, F14G24.15, NKEF-B, PhrB photolyase activity, HepG2 cell, Thioredoxin peroxidase 1, classic hairy cell leukaemia, H(2)O, Peptide Hydrolase Inhibitor, Natural killer cell-enhancing factor B, BOUND WATER, F14G24_15, Basodexan, Xkl-1, Hydrogenchlorid, NP-40, pigmented epithelium, oxidane, WATER, HOH, Bca, peptide, Trifluoroacetate, Thiol-specific antioxidant protein, Polypeptides, KL receptor activity, Gsfsco1, halite, hydrogen chloride, peptido, congenital, Protease Inhibitor, indoleglycerolphosphate aldolase activity, SCO5, Inhibitors, AGM4, 3, SCO1, NUP96, Hydrolase Inhibitors, Gsfsow3, Arabidopsis NAC domain containing protein 18, Gsfsco5, epithelium, SOW3, bca, peptides, E927b, Torin, pigmented retina, Tdpx1, W, ATNAM, DNA cyclobutane dipyrimidine photolyase activity, SUPPRESSOR OF AUXIN RESISTANCE 3, 6-dimethyl-7-oxo-2, cloruro sodico, indole-3-glycerolphosphate D-glyceraldehyde-3-phosphate-lyase activity, salt, Wasserstoffchlorid, Peptidohydrolase Inhibitor, Non-Idet P-40, (1S, trifluoro-, Bs, dihydridooxygen, TPX1, autolysin activity, necrosis, Lyw-57, with cleft palate and malignant hyperthermia, dihydrogen oxide, PRX2, Sl, (2E, TR, PRE, rock salt, TX-144 surfactant, Peptidase Inhibitor, NKEFB, PRP, 1.11.1.15, indole glycerol phosphate hydrolase activity, ORF 3617, deoxyribonucleic cyclobutane dipyrimidine photolyase activity, 4E, aqua, Tr-kit, classic hairy cell leukemia, Peptide Peptidohydrolase, BX1, ur, SLP65, PBT, carbamide, Ly-57, H2O, common salt, retinal pigment, PrxII, NO APICAL MERISTEM, Hydrolase Inhibitor, Chlorwasserstoff, kl1-A, dipyrimidine photolyase (photosensitive), bacteriocin activity, KIT, NkefB, PRXII, retinal pigment layer, Triton X-114, Acetic acid, Hydrogen Oxide, congenital myopathy cleft palate and malignant hyperthermia, tyrosine-protein kinase Kit, Acid, SLP-65, pbt, NAC DOMAIN PROTEIN NAM, Antagonists, BASH, LY57, liquid., HCl, Trifluoroacetic, hydrogen hydroxide, kit, HepG2, natrii chloridum, acqua, indole-3-glycerol phosphate lyase activity, H2NC(O)NH2, phr A photolyase activity, lysin activity, Peptidase Inhibitors, DNA-photoreactivating enzyme, HEPG2, Cesium, Band-8, Antiproteases, IGL, bacteriolytic toxin activity, tryptophan synthase alpha activity, TPx-B, Polypeptide, Wasser, Endopeptidase, Peptide Peptidohydrolase Inhibitor, chlorane, Inhibitor, 1728, NAM, krk1, Endopeptidase Inhibitors, chlorure d'hydrogene, SCF receptor activity, Protease, Carbamide, NARS2, photoreactivating enzyme activity, 2R)-1-C-(indol-3-yl)glycerol 3-phosphate D-glyceraldehyde-3-phosphate-lyase (indole-forming) activity, agua, Buffer, Karbamid, potassium salt, scfr, HEP-G2, Ly57, Harnstoff, 6R)-7-(4-(dimethylamino)phenyl)-N-hydroxy-4, Protease Antagonist, stratum pigmentosa retinae, Peptide Hydrolase, Carmol, SCFR, cloruro de hidrogeno, tryptophan synthase alpha subunit activity, Cesium Trifluoroacetate, Fdc, MOS3, deoxyribocyclobutadipyrimidine pyrimidine-lyase activity, PRECOCIOUS, Hydrogen chloride, chlorure de sodium, F23A5.3, eau, Antagonist, Thioredoxin-dependent peroxide reductase 1, Solution, AL022839, Melting, Protease Antagonists, TDX1, Kochsalz, Peptide Peptidohydrolase Inhibitors, peptidos, Hep-G2, F23A5_3, TPx, BLNK-S, proto-oncogene c-Kit, Hep G2, Igepal CA-630, chloridohydrogen, buffer, Cell, Peptide, 4-heptadienamide, polypeptide, TSA, [HCl], MODIFIER OF SNC1, Natriumchlorid, carbonyldiamide, ANAC018, KIT ligand receptor activity, water, deoxyribonucleic photolyase activity, Hydrochloride, table salt, Vacuums, 2R)-1-C-(indol-3-yl)glycerol 3-phosphate D-glyceraldehyde-3-phosphate-lyase activity, NaCl, indole synthase activity, XKrk1, congenital myopathy - cleft palate - malignant hyperthermia, c-KIT, RPE, holin, uree, photolyase activity, HEP G2, Peptidohydrolase Inhibitors, CD117, p. pigmentosa retinae, Peptidase, myopathy, c-kit, Antiprotease, C-Kit, Ssm, Nonidet P-40, xkl-1, Peptid, HEL-S-2a, deoxyribonucleate pyrimidine dimer lyase (photosensitive), Peptide Hydrolase Inhibitors, PTX1, [OH2], NAC-REGULATED SEED MORPHOLOGY 2, hydrochloric acid"],"description_synonyms":["Activity, Procedures, determination, Laboratory, Peptidomics, taxonomy, Liquid Chromatography Mass Spectrometry, Proteins, Systematics, High Performance Liquid Chromatography Mass Spectrometry, Research Priorities, Gene, Ultra Performance Liquid Chromatography-Mass Spectrometry, High Pressure Liquid Chromatography-Mass Spectrometry, Procedure, motif, High Performance Liquid Chromatography-Mass Spectrometry, Classifications, Taxonomies, Techniques, method, hierarchies, Priority, HPLC-MS, hierarchy, Liquid Chromatography-Mass, Method, systematics, method used in an experiment, Protein, chemical analysis, Research Activities, Studies, Gene Products, Research Activity, Laboratory Research, Technique, Research and Development, Priorities, UPLC-MS, study, Ultra Performance Liquid Chromatography Mass Spectrometry, Ultra-Performance Liquid Chromatography-Mass Spectrometry, Taxonomy, Research, High Pressure Liquid Chromatography Mass Spectrometry, Spectrometry, chemical analysis., Spectrometries, Methodological, Methodological Study, Activities, plan specification, Protein Gene Products, Study, Gene Proteins, Methodological Studies, Liquid Chromatography-Mass Spectrometries, Chromatography-Mass Spectrometry, Liquid, LC-MS, Development and Research, assay, Research Priority, Chromatography-Mass Spectrometries"],"additional_accession":[]},"is_claimable":false,"name":"Human HepG2 cell isonicotinylation proteomic","description":"Qualitative proteomic research by isonicoacylation enrichment technique and high resolution liquid chromatography-mass spectrometry.In this project, a qualitative study of isonicotinylation proteomics was carried out. A total of 35 were identified in this study 44 isonicotinylation sites on individual proteins. We conducted a systematic bioinformatics analysis of the modified proteins,It includes Motif analysis, annotation of modified proteins, functional classification and functional enrichment 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