<HashMap><database>MetaboLights</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Tabular>ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS14573/m_MTBLS14573_LC-MS_negative_reverse-phase_v2_maf.tsv</Tabular><Tabular>ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS14573/m_MTBLS14573_LC-MS_positive_reverse-phase_v2_maf.tsv</Tabular><Txt>ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS14573/a_MTBLS14573_LC-MS_negative_reverse-phase.txt</Txt><Txt>ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS14573/s_MTBLS14573.txt</Txt><Txt>ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS14573/a_MTBLS14573_LC-MS_positive_reverse-phase.txt</Txt><Txt>ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS14573/i_Investigation.txt</Txt></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><ftp_download_link>ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS14573</ftp_download_link><metabolite_identification_protocol>&lt;p>Metabolites were annotated by matching accurate mass-to-charge ratios, MS/MS fragmentation spectra, and chromatographic retention times against public databases (HMDB, METLIN, KEGG) and in-house spectral libraries.&lt;/p></metabolite_identification_protocol><repository>MetaboLights</repository><study_status>Public</study_status><ptm_modification></ptm_modification><instrument_platform>Liquid Chromatography MS - negative - reverse-phase</instrument_platform><instrument_platform>Liquid Chromatography MS - positive - reverse-phase</instrument_platform><chromatography_protocol>&lt;p>Parameter Value[Chromatography Instrument]: Thermo Fisher Scientific UHPLC system (coupled to Q Exactive Orbitrap MS)Parameter Value[Autosampler model]: Thermo Fisher Scientific Vanquish or Dionex series autosampler (matching Q Exactive platform)Parameter Value[Column model]: ACQUITY UPLC HSS T3 column (100 mm × 2.1 mm, 1.8 μm)Parameter Value[Guard column]: ACQUITY UPLC HSS T3 VanGuard guard column (2.1 mm × 5 mm, 1.8 μm)&lt;/p></chromatography_protocol><publication>Energy-translation coupling limits yeast anaerobic growth.</publication><submitter_name>Yongbo Wang</submitter_name><submitter_affiliation>East China University of Science and Technology</submitter_affiliation><organism_part>Cell pellets</organism_part><technology_type>mass spectrometry assay</technology_type><disease></disease><extraction_protocol>&lt;p>Cell pellets were extracted with pre-chilled 80% (v/v) methanol and disrupted by ultrasonication in an ice-water bath. After incubation at −40 °C to precipitate proteins, the mixture was centrifuged at 12,000 × g for 10 min at 4 °C. The supernatant for LC-MS analysis was collected, lyophilized, reconstituted in 20% methanol, briefly sonicated, centrifuged again, and filtered through a 0.22 μm membrane prior to analysis.&lt;/p></extraction_protocol><organism>Saccharomyces cerevisiae</organism><full_dataset_link>https://www.ebi.ac.uk/metabolights/MTBLS14573</full_dataset_link><author>Yongbo Wang. School of Biotechnology, East China University of Science and Technology. y12222081@mail.ecust.edu.cn.</author><data_transformation_protocol>&lt;p>LC-MS raw data were processed using Progenesis QI (Waters Corporation) for peak picking, alignment, retention time correction, and signal intensity normalization.&lt;/p></data_transformation_protocol><study_factor>Treatment</study_factor><submitter_email>y12222081@mail.ecust.edu.cn</submitter_email><sample_collection_protocol>&lt;p>Saccharomyces cerevisiae cell pellets were collected for untargeted metabolomics analysis via LC-MS.&lt;/p></sample_collection_protocol><omics_type>Metabolomics</omics_type><study_design>Thermo Scientific Orbitrap Fusion</study_design><study_design>Cell pellets</study_design><study_design>Metabolomics</study_design><study_design>Thermo Fisher Scientific</study_design><study_design>Energy</study_design><study_design>untargeted analysis</study_design><study_design>untargeted metabolites</study_design><study_design>experimental blank</study_design><study_design>Saccharomyces cerevisiae</study_design><curator_keywords>Thermo Scientific Orbitrap Fusion</curator_keywords><curator_keywords>Cell pellets</curator_keywords><curator_keywords>Metabolomics</curator_keywords><curator_keywords>Thermo Fisher Scientific</curator_keywords><curator_keywords>Energy</curator_keywords><curator_keywords>untargeted analysis</curator_keywords><curator_keywords>untargeted metabolites</curator_keywords><curator_keywords>experimental blank</curator_keywords><curator_keywords>Saccharomyces cerevisiae</curator_keywords><mass_spectrometry_protocol>&lt;p>Parameter Value[Scan m/z range]: 70–1000 m/zParameter Value[Instrument]: Thermo Fisher Scientific Q Exactive Orbitrap mass spectrometerParameter Value[Ion source]: Electrospray ionization (ESI), operated in both positive and negative ion modesParameter Value[Mass analyzer]: Orbitrap high-resolution mass analyzer&lt;/p></mass_spectrometry_protocol><metabolite_name>D-Hexose 6-Phosphate</metabolite_name><metabolite_name>Sorbitol</metabolite_name><metabolite_name>Zymosterol</metabolite_name><metabolite_name>D-Fructose</metabolite_name><metabolite_name>Monolaurin</metabolite_name><metabolite_name>Mg(18:0/0:0/0:0)</metabolite_name><metabolite_name>1-Tricosanol</metabolite_name><metabolite_name>Lophenol</metabolite_name><metabolite_name>Deoxycholic Acid</metabolite_name><metabolite_name>L-Histidine</metabolite_name><metabolite_name>4alpha-Methylzymosterol</metabolite_name><metabolite_name>Edetic Acid</metabolite_name><metabolite_name>Biotin</metabolite_name><metabolite_name>Citrulline</metabolite_name><metabolite_name>3-Hydroxyanthranilic Acid</metabolite_name><metabolite_name>17alpha-Hydroxypregnenolone</metabolite_name><metabolite_name>D-Glucuronic Acid 1-Phosphate</metabolite_name><metabolite_name>1-Kestose</metabolite_name><metabolite_name>Arachidic Acid</metabolite_name><metabolite_name>Phenylsuccinic Acid</metabolite_name><metabolite_name>Dehydroascorbic Acid</metabolite_name><metabolite_name>2,4-Dihydroxypentanedioic Acid</metabolite_name><metabolite_name>Glucosamine</metabolite_name><metabolite_name>Pantothenic Acid</metabolite_name><metabolite_name>1,5-Anhydrohexitol</metabolite_name><metabolite_name>Fructose 1-Phosphate</metabolite_name><metabolite_name>16beta,17beta-Estriol</metabolite_name><metabolite_name>2,3-Diphosphoglycerin</metabolite_name><metabolite_name>L-Tryptophan</metabolite_name><metabolite_name>Glutathione</metabolite_name><metabolite_name>Sorbitol-6-Phosphate</metabolite_name><metabolite_name>Glycyl-Glycine</metabolite_name><metabolite_name>Palatinitol</metabolite_name><metabolite_name>N-Acetyl-D-Glucosamine</metabolite_name><metabolite_name>Myo-Inositol</metabolite_name><metabolite_name>Galactinol</metabolite_name><metabolite_name>Pseudouridine</metabolite_name><metabolite_name>Cystathione</metabolite_name><metabolite_name>Adenosine Monophosphate</metabolite_name><metabolite_name>Cholesterol</metabolite_name><metabolite_name>Ginkgolide B</metabolite_name><metabolite_name>Myo-Inositol 1-Phosphate</metabolite_name><metabolite_name>Ginkgolide A</metabolite_name><metabolite_name>Inosinic Acid</metabolite_name><metabolite_name>N-Acetylmannosamine</metabolite_name><metabolite_name>Nicotianamine</metabolite_name><metabolite_name>Hydroxyphenyllactic Acid</metabolite_name><metabolite_name>3,4-Dimethoxyphenylethylamine</metabolite_name><metabolite_name>Guanosine</metabolite_name><metabolite_name>Morphine</metabolite_name><metabolite_name>Dodecanedioic Acid</metabolite_name><metabolite_name>Alizarin</metabolite_name><metabolite_name>Phytosphingosine</metabolite_name><metabolite_name>Chenodeoxycholic Acid</metabolite_name><metabolite_name>Salbutamol</metabolite_name><metabolite_name>Citric Acid</metabolite_name><metabolite_name>Fructose 6-Phosphate</metabolite_name><metabolite_name>Myristic Acid</metabolite_name><metabolite_name>Cyclic Amp</metabolite_name><metabolite_name>Clioquinol</metabolite_name><metabolite_name>D-Ribofuranose</metabolite_name><metabolite_name>Levan</metabolite_name><metabolite_name>1,25-Dihydroxyvitamin D3</metabolite_name><metabolite_name>Ht-2 Toxin</metabolite_name><metabolite_name>3-Deoxyhexonic Acid</metabolite_name><metabolite_name>Palmitic Acid(D3)</metabolite_name><metabolite_name>Uridine</metabolite_name><metabolite_name>Hypoxanthine</metabolite_name><metabolite_name>Galactofuranose-6-Phosphate</metabolite_name><metabolite_name>Pentadecylic Acid</metabolite_name><metabolite_name>D-(-)-Ribofuranose</metabolite_name><metabolite_name>2-Hydroxydecanedioic Acid</metabolite_name><metabolite_name>D-Glucose</metabolite_name><metabolite_name>Bilobol C15:1</metabolite_name><metabolite_name>Desmosterol</metabolite_name><metabolite_name>N-Alpha-Acetyl-L-Lysine</metabolite_name><metabolite_name>2-Hydroxyadenine</metabolite_name><metabolite_name>2-Hydroxy-N'-(1-(2-Thienyl)Ethylidene)Benzohydrazide</metabolite_name><metabolite_name>Monocyclohexyl Phthalate</metabolite_name><metabolite_name>1-(Sn-Glycero-3-Phospho)-1d-Myo-Inositol</metabolite_name><metabolite_name>11alpha-Hydroxyprogesterone</metabolite_name><metabolite_name>Octaethylene Glycol</metabolite_name><metabolite_name>Beta-Estradiol</metabolite_name><metabolite_name>Allocholic Acid</metabolite_name><metabolite_name>Mannitol 1-Phosphate</metabolite_name><metabolite_name>D-Mannonic Acid</metabolite_name><metabolite_name>Putreanine</metabolite_name><metabolite_name>5-Methyluridine</metabolite_name><metabolite_name>D-Gulose</metabolite_name><metabolite_name>Adenosine</metabolite_name><metabolite_name>Galactitol</metabolite_name><metabolite_name>Beta-Lactose</metabolite_name><metabolite_name>Adenine</metabolite_name><metabolite_name>Pterostilbene</metabolite_name><metabolite_name>Allose</metabolite_name><metabolite_name>Ergosta-7,22-Dien-3beta-Ol</metabolite_name><metabolite_name>L-3-Hydroxykynurenine</metabolite_name><metabolite_name>L-Tyrosine</metabolite_name><metabolite_name>Linoleic Acid</metabolite_name><metabolite_name>17-Octadecynoic Acid</metabolite_name><metabolite_name>Inosine</metabolite_name><metabolite_name>Norepinephrine</metabolite_name><metabolite_name>1d-Myo-Inositol 3-Phosphate</metabolite_name><metabolite_name>Melatonin</metabolite_name><metabolite_name>Sucrose</metabolite_name><metabolite_name>1-Methylindole-2-Carboxylic Acid</metabolite_name><metabolite_name>Ebericol</metabolite_name><metabolite_name>Glucose 6-Phosphate</metabolite_name><metabolite_name>Glucose</metabolite_name><metabolite_name>Mannobiose</metabolite_name><metabolite_name>Glycylproline</metabolite_name><metabolite_name>Galactose 1-Phosphate</metabolite_name><metabolite_name>D-(+)-Mannose</metabolite_name><metabolite_name>Cellobiose</metabolite_name><metabolite_name>Melibiose</metabolite_name><metabolite_name>Spermidine</metabolite_name><metabolite_name>Sphingosine</metabolite_name><metabolite_name>Methyl-Beta-Galactopyranoside</metabolite_name><metabolite_name>L-(-)-Sorbose</metabolite_name><metabolite_name>Saccharopine</metabolite_name><metabolite_name>Oxymorphone</metabolite_name><metabolite_name>D-Iditol</metabolite_name><metabolite_name>Carglumic Acid</metabolite_name><metabolite_name>Bisphenol A Monomethyl Ether</metabolite_name><metabolite_name>Galactonic Acid</metabolite_name><metabolite_name>Maltotriose</metabolite_name><metabolite_name>Arbutin</metabolite_name><metabolite_name>Deoxyadenosine</metabolite_name><metabolite_name>O-Succinyl-L-Homoserine</metabolite_name><metabolite_name>Obtusifoliol</metabolite_name><metabolite_name>L-Iditol</metabolite_name><metabolite_name>L-Cystathionine</metabolite_name><metabolite_name>Amoxicillin</metabolite_name><metabolite_name>Cysteinylglycine</metabolite_name><metabolite_name>Mannose 1-Phosphate</metabolite_name><metabolite_name>Arachidonic Acid</metabolite_name><metabolite_name>Hyenic Acid</metabolite_name><metabolite_name>Psicose</metabolite_name><metabolite_name>D-Galactose 6-Phosphate</metabolite_name><metabolite_name>Stearyl Alcohol</metabolite_name><metabolite_name>Leucrose</metabolite_name><metabolite_name>Isovalerylglucuronide</metabolite_name><metabolite_name>Cannabidiol</metabolite_name><metabolite_name>Glycyltyrosine</metabolite_name><metabolite_name>Beta-D-Glucopyranuronic Acid</metabolite_name><metabolite_name>9-Tetradecenoic Acid</metabolite_name><metabolite_name>5'-Methylthioadenosine</metabolite_name><metabolite_name>Kynurenine</metabolite_name><metabolite_name>D-Galactose</metabolite_name><metabolite_name>Ergosterol</metabolite_name><metabolite_name>Coniferin</metabolite_name><metabolite_name>Mg(16:0/0:0/0:0)</metabolite_name><metabolite_name>Xanthine</metabolite_name><metabolite_name>Deoxyguanosine</metabolite_name><metabolite_name>3-Beta-D-Galactosyl-Sn-Glycerol</metabolite_name><metabolite_name>Dihydrophytol</metabolite_name><metabolite_name>Norcodeine</metabolite_name><metabolite_name>Petroselinic Acid</metabolite_name><metabolite_name>Linoelaidic Acid</metabolite_name><metabolite_name>6-Phosphogluconic Acid</metabolite_name><metabolite_name>Ethyl Gallate</metabolite_name><metabolite_name>Alpha-D-Lactose</metabolite_name><metabolite_name>Oleic Acid</metabolite_name><metabolite_name>Gorgosterol</metabolite_name><metabolite_name>2-Methoxytyramine</metabolite_name><metabolite_name>Thymidine</metabolite_name><metabolite_name>Tranexamic Acid</metabolite_name><metabolite_name>D-Myoinositol 4-Phosphate</metabolite_name><metabolite_name>Gluconic Acid</metabolite_name><metabolite_name>D-Ribulose 5-Phosphate</metabolite_name><metabolite_name>Lactitol</metabolite_name><metabolite_name>Quinic Acid</metabolite_name><metabolite_name>Beta-D-Fructose 6-Phosphate</metabolite_name><metabolite_name>3-Hydroxy-Tetradecanoic Acid</metabolite_name><metabolite_name>Udp-N-Acetylglucosamine</metabolite_name><metabolite_name>(2-Hydroxy-3-Phosphonooxypropyl) Dihydrogen Phosphate</metabolite_name><metabolite_name>Fructose 1,6-Bisphosphate</metabolite_name><metabolite_name>Simvastatin</metabolite_name><metabolite_name>Squalene</metabolite_name><metabolite_name>Maltose</metabolite_name><metabolite_name>Chimyl Alcohol</metabolite_name><metabolite_name>L-Gluconic Acid</metabolite_name><metabolite_name>D-Fructose 2,6-Bisphosphate</metabolite_name><metabolite_name>L-Lysine</metabolite_name><metabolite_name>Sedoheptulose</metabolite_name><metabolite_name>Phosphoserine</metabolite_name><metabolite_name>Cis-Gondoic Acid</metabolite_name><metabolite_name>4-Hydroxy-3-Methylnaphthalene-1,2-Dione</metabolite_name><metabolite_name>Cytidine Monophosphate</metabolite_name><metabolite_name>5-Methoxyindoleacetate</metabolite_name><metabolite_name>Estrogen</metabolite_name><metabolite_name>Ethyl Beta-D-Galactofuranoside</metabolite_name><metabolite_name>2-Methylcitric Acid</metabolite_name><metabolite_name>L-Gulonic??Acid</metabolite_name><metabolite_name>2,5-Diaminopentanoic Acid</metabolite_name><metabolite_name>17-Hydroxy-6-Methylpregn-4-Ene-3,20-Dione</metabolite_name><metabolite_name>1-Hydroxy-3-Methoxy-6-Methylanthraquinone</metabolite_name><metabolite_name>Cis-Piceid</metabolite_name><metabolite_name>Nabilone</metabolite_name><metabolite_name>Palmitic Acid</metabolite_name><metabolite_name>Ursodeoxycholic Acid</metabolite_name><metabolite_name>Cadaverine</metabolite_name><metabolite_name>Beta-Mannosylglycerate</metabolite_name><metabolite_name>D-Tagatose</metabolite_name><metabolite_name>Stearic Acid</metabolite_name><metabolite_name>L-Altrose</metabolite_name><metabolite_name>Maltotriitol</metabolite_name><metabolite_name>Uridine 5'-Monophosphate</metabolite_name><metabolite_name>Beta-D-Glucose 6-Phosphate</metabolite_name><metabolite_name>Mg(0:0/16:0/0:0)</metabolite_name><metabolite_name>D-Mannose 6-Phosphate</metabolite_name><metabolite_name>Chrysin</metabolite_name><metabolite_name>Cis-9-Palmitoleic Acid</metabolite_name><metabolite_name>Estrone</metabolite_name><metabolite_name>3-Ethyl-3,4-Dihydro-2(1h)-Quinoxalinone</metabolite_name></additional><is_claimable>false</is_claimable><name>Energy-translation coupling limits yeast anaerobic growth</name><description>&lt;p> This study employs yeast as a model system to thoroughly investigate the differences in regulatory mechanisms under various nutrient limitation conditions, utilizing a systems biology approach integrated with techniques such as multi-omics analysis.To obtain a comprehensive quantitative landscape of protein expression in (human lung adenocarcinoma), we performed TMT 6-plex–based comparative proteomic analysis. Tumour and adjacent non-tumour tissues (n = 6 pairs) were pulverised under liquid nitrogen and total proteins extracted by phenol–ammonium acetate/methanol precipitation. After reduction, alkylation and acetone precipitation, 50 µg proteins per sample were digested in-solution with trypsin (1:50, w/w, 37 °C, 16 h). Peptides were labelled with TMT 6-plex reagents, pooled and fractionated by high-pH reversed-phase chromatography on an Agilent 1100 HPLC (Zorbax Extend-C18, 15 fractions). LC-MS/MS was carried out on a Q Exactive HF-X (Thermo) in DDA mode. Quantitative analysis was performed with Proteome Discoverer 2.4 using a 1 % FDR threshold at PSM and protein levels. The dataset provides relative abundance information for &amp;gt; 6 000 protein groups across tumour and control tissues, serving as a resource for biomarker and pathway studies in lung adenocarcinoma. 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