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upftp://ftp.pride.ebi.ac.uk/pride/data/archive/2020/01/PXD017171/T863_20140614_del_rlm_C_1_1_5-40_120min_200cpsTh_3uLinj_1.groupftp://ftp.pride.ebi.ac.uk/pride/data/archive/2020/01/PXD017171/T872_20140620_del_rsm_F_1_2_5-40_120min_200cpsTh_3uLinj_1.groupftp://ftp.pride.ebi.ac.uk/pride/data/archive/2020/01/PXD017171/T865_20140614_del_rlm_C_2_1_5-40_120min_200cpsTh_3uLinj_1.groupftp://ftp.pride.ebi.ac.uk/pride/data/archive/2020/01/PXD017171/T873_20140620_del_rsm_F_2_1_5-40_120min_200cpsTh_3uLinj_1.groupftp://ftp.pride.ebi.ac.uk/pride/data/archive/2020/01/PXD017171/T868_20140618_del_rlm_E_1_2_5-40_120min_200cpsTh_3uLinj_1.groupftp://ftp.pride.ebi.ac.uk/pride/data/archive/2020/01/PXD017171/T869_20140618_del_rlm_E_2_1_5-40_120min_200cpsTh_3uLinj_1.groupftp://ftp.pride.ebi.ac.uk/pride/data/archive/2020/01/PXD017171/T862_20140606_WT2_2_5-40_120min_200cpsTh_3uLinj_1.groupftp://ftp.pride.ebi.ac.uk/pride/data/archive/2020/01/PXD017171/T871_20140620_del_rsm_F_1_1_5-40_120min_200cpsTh_3uLinj_1.groupprimaryOK200petya@belozersky.msu.ruOlga BukatoMass SpectrometryShotgun proteomicsNot availableLc-msmsEscherichia coliIdahttp://www.ebi.ac.uk/pride/archive/projects/PXD017171Shotgun comparative proteome analysis was performed in the following way. Briefly, cells resuspended in 0,75% w/w RapiGest SF (Waters) were lysed by sonication. After debris removal protein cysteine bonds were reduced with 10 mM dithiothreitol and alkylated with 30 mM iodoacetamide. Trypsin was added in a 1/50 w/w ratio trypsin/protein and incubated at 37°C overnight. To stop trypsinolysis, trifluoroacetic (TFA) acid was added to the final concentration of 0,5% v/v. Peptides were desalted and resuspended in 3% acetonitrile (ACN), 0.1% TFA to a final concentration of 2 μg/μL. Mass-spectrometry analysis was performed on a TripleTOF 5600+ mass‐spectrometer with a NanoSpray III ion source (ABSciex, Canada) coupled to a NanoLC Ultra 2D+ nano‐HPLC system (Eksigent).PrideNot availableNo PTMs are included in the datasetFor protein identification, .wiff data files were analyzed with ProteinPilot 4.5 revision 1656 (ABSciex) using the Paragon 4.5.0.0 revision 1654 (ABSciex)search algorithm and a standard set of identification settingsto search against SwissProt database,species Escherichia coli.ProteomicsPetr SergievTripleTOF 5600Lomonosov Moscow State University, Moscow, RussiaPARTIALEscherichia Coliolya.bukato@gmail.comNot availableFederal Research and Clinical Center of Physical-Chemical Medicine of Federal Medical Biological AgencyRussian FederationCleland Reagent, Cysteine Hydrochloride, MeCN, NCMe, determination, Reagent, FBN, 4-dimercapto-, protein, ACINUS, R*)-, protein-containing complex, peptide, Polypeptides, protein polypeptide chains, STOP, Stable tubule-only polypeptide, peptido, polypeptide chain, reduced, BANF, subnumerary, ECTOL1, CH3-C#N, 1, 2, system, Half-Cystine, tiny, Analysis, protein aggregate, present in fewer numbers in organism, WMS, (R*, proportion, anatomical systems, C79325, peptides, STOP145, Acinus, L Cysteine, weight-weight percentage, 2610036I19Rik, Spectrum, beta-Trypsin, 2610510L13Rik, hypoplasia, proteins, decreased number, acinusL, OCTD, fSAP152, decreased, Sputolysin, acinusS, ACN, Acn, peptidos, Half Cystine, Saeure, GPHYSD2, 2-iodo-, SGS, ratio, small, 2810411E12Rik, mass percentage, 1-(14)C-labeled, 3H-labeled, Zinc Cysteinate, protein complex, Map-6, acid, total expressed protein, Clelands Reagent, acetonitrile, Cell, Peptide, mKIAA0670, ACMICD, Spectroscopy, polypeptide, native protein, natural protein, Cleland, body system., chemical analysis, Protein, Mtap6, 145-kDa STOP, MFS1, connected anatomical system, ACETONITRILE, cyanomethane, WMS2, MAP-6, Cleland's, Acid, underdeveloped, Saeuren, acide, Sonications, proportionality, Tripcellim, Spectrometry, acids, rate, L-Cysteine, 3-Butanediol, acido, ethanenitrile, MASS, beta Trypsin, w/w, organ system, Cleland's Reagent, Trypure, nanospray, concentration, Acetamide, SSKS, quotient, Peptid, assay, Polypeptide, methyl cyanide, SCH, ProteomesAlkalescens-Dispar Group, phapii, data, IPP2A2, Bacterium coli, protein complex, igaad, StF-IT-1, bacterium E3, protein, EAggEC, protein-containing complex, Enteroaggregative E. coli, PHAPII, 5730420M11Rik, protein polypeptide chains, native protein, natural protein, polypeptide chain, template-activating factor I, I-2PP2A, Diffusely Adherent E. coli, Bacillus coli, Algorithm, Escherchia coli, Protein, Dm I-2, I2PP2A, Enteroinvasive Escherichia coli, Enterococcus coli, protein aggregate, Data Base, SET, Diffusely Adherent Escherichia coli, HLA-DR-associated protein II, Escherichia/Shigella coli, Enteroinvasive E. coli, DI-2, TAF-I, I-2Dm, phosphatase 2A inhibitor I2PP2A, ipp2a2, 2pp2a, E coli, proteins, CG4299, inhibitor of granzyme A-activated DNase, E. coli., CG10574, DmelCG4299, I-2PP1, Eschericia coli, Enteroaggregative Escherichia coli, set, dSET/TAF-Ibeta, IGAAD, 2610030F17Rik, 2PP2A, TAF-IBETA, Bacterium coli commune, DmelCG10574, taf-ibeta, dSET, dSet, TAF-Ibeta, species, AA407739, i2pp2aAlkalescens-Dispar Group, Data Set., data, Bacterium coli, Ida, IDA, Sprain, Proteins, total expressed protein, A4, bacterium E3, Gene, EAggEC, Enteroaggregative E. coli, body system, TYPE, LGMD2C, DAGA4, Diffusely Adherent E. coli, Bacillus coli, Escherchia coli, Protein, Strain, Gene Products, l(3)63Fb, system, Enteroinvasive Escherichia coli, Enterococcus coli, connected anatomical system, MAM, Sprains, SCG3, CG10850, Diffusely Adherent Escherichia coli, anatomical systems, Escherichia/Shigella coli, Enteroinvasive E. coli, DMDA1, E coli, INSDC_feature:gene, proteins, DmelCG10850, E. coli, Apc5, APC5, Protein Gene Products, organ system, Eschericia coli, Enteroaggregative Escherichia coli, Gene Proteins, nanospray, DMDA, Bacterium coli commune, SCARMD2, Strains, l(3)SH7, Strains and Sprains, ProteomesAlkalescens-Dispar Group, Diffusely Adherent Escherichia coli, Bacterium coli, Escherichia/Shigella coli, Enteroinvasive E. coli, determination, ribosomal protein, bacterium E3, E coli, INSDC_qualifier:unknown, ribosomal RNA, EAggEC, Enteroaggregative E. coli, E. coli, ribosomal ribonucleic acid, Eschericia coli, Enteroaggregative Escherichia coli, Bacterium coli commune, INSDC_feature:rRNA, Diffusely Adherent E. coli, Bacillus coli, Escherchia coli, chemical analysis, assay, Enteroinvasive Escherichia coli, Enterococcus coli, membrane bound ribosome, Methyltransferase., free ribosomefalseComprehensive functional analysis of Escherichia coli ribosomal RNA methyltransferasesWe analyzed total proteome of three methyltransferase gene knockouts strains of Escherichia coli: ΔrsmF (JW5301), ΔrlmC (JW2756), ΔrlmE (JW3146) from Keio collection and wild type (WT). Proteins were assessed using IDA approach (i.e. Information Dependent Acquisition) and SWATH (Data-Independent Acquisition) on Sciex TripleTof 5600+ mass‐spectrometer with a NanoSpray III ion source (ABSciex, Canada) coupled to a NanoLC Ultra 2D+ nano‐HPLC system (Eksigent). 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