{"database":"PAXDB","file_versions":[{"headers":{"Content-Type":["application/json"]},"body":{"files":{"Other":["http://pax-db.org/downloads/latest/datasets/bioprojects-abundance-files-v4.0.zip"]},"type":"primary"},"statusCode":"OK","statusCodeValue":200}],"scores":{"citationCount":0,"reanalysisCount":0,"viewCount":0,"searchCount":0},"additional":{"omics_type":["Proteomics"],"submitter":["Christian von Mering"],"species":["83332"],"full_dataset_link":["https://pax-db.org/dataset/83332/4068500525"],"submitter_email":["mering@imls.uzh.ch"],"submitter_affiliation":["University of Zurich"],"sample_protocol":[""],"repository":["PAXDB"],"data_protocol":["For the rescaling, the\ndatasets are first parsed or processed such that the data reflect\nproportional abundances of whole protein molecules\n(i.e. proportionality to counts of complete, individual protein\nmolecules, not to molecular weights, protein volumes, or digested\npeptides). In the case of spectral counting data protein. The proportional abundances are rescaled linearly to add up\nto one million; this means the abundance of each protein of\ninterest is finally expressed in (parts per million,) relative to\nall other proteins in a sample. \nFor a given protein abundance dataset, we then compute\nthe absolute log abundance ratios of all pairs of proteins\nannotated to be functionally linked. The median of these absolute\nlog abundance ratios represents an indirect quality\nmetric: the closer it is to zero, the better (i.e. the more there\nis consistency between abundance values and functional annotations\nsuch as protein complexes or pathways). We then\ncompute a background expectation for this metric, by permuting\nthe abundance values in a given dataset randomly,\nand recomputing the median log abundance ratios. The permutation\nis repeated several times, yielding a distribution of\nmedians. The actually observed median is then expressed as a\nZ-score distance to the random distribution ofmedians—this\ndistance is termed the interaction consistency score."],"pubmed_abstract":["In order to successfully enter the latent stage, Mycobacterium tuberculosis must adapt to conditions such as nutrient limitation and hypoxia. In vitro models that mimic latent infection are valuable tools for describing the changes in metabolism that occur when the bacterium exists in a non-growing form. We used two complementary proteomic approaches, label-free LC-MS/MS analysis and two-dimensional difference gel electrophoresis, to determine the proteome profile of extracellular proteins from M. tuberculosis cultured under nutrient starvation. Through the label-free LC-MS/MS analysis of fractionated samples, 1176 proteins were identified from culture filtrates of log phase and nutrient-starved cultures, and the protein levels of 230 proteins were increased in nutrient-starved culture filtrates, whereas those of 208 proteins were decreased. By means of Gene Ontology clustering analysis, significant differences in the overall metabolism during nutrient starvation were detected. Notably, members of the toxin-antitoxin systems were present in larger quantities in nutrient-starved cultures, supporting a role for these global modules as M. tuberculosis switches its metabolism into dormancy. Decreased abundance of proteins involved in amino acid and protein synthesis was apparent, as well as changes in the lipid metabolism. Further analysis of the dataset identified increased abundance of lipoproteins and decreased abundance of ESAT-6 family proteins. Results from the two-dimensional difference gel electrophoresis proteomics demonstrated overall agreement with the LC-MS/MS data and added complementary insights about protein degradation and modification."],"pubmed_title":["Proteomic profiling of Mycobacterium tuberculosis identifies nutrient-starvation-responsive toxin-antitoxin systems."],"pubmed_authors":["Albrethsen Jakob J, Agner Jeppe J, Piersma Sander R SR, Højrup Peter P, Pham Thang V TV, Weldingh Karin K, Jimenez Connie R CR, Andersen Peter P, Rosenkrands Ida I"],"data_synonyms":["Add, DmelCG43443, ADD, ADD-87, Hts-RC, data, AU023367, Data Set, protein complex, supply, Proteins, Ovhts, Gene, HtsRC, CG9325, protein, neutral molecular compounds, protein-containing complex, Dmel_CG9325, Xt, Peptide, 1B1, add, Polypeptides, anon-EST:Posey9, protein polypeptide chains, native protein, peptido, htsRC, GLI3-190, natural protein, polypeptide chain, Add-hts, Protein, CG43443, Gene Products, l(2)k14523, Dmel_CG34197, l(2)00634, median, Ovhts-RC, background, supply and distribution, protein aggregate, all_pairs, molecule, Bph, molecula, Random selection by shearing, oligonucleotide random primer, proportion, HTS-R1, HTS, Hts, molecules, peptides, l(2)k06121, adducin, GLI3FL, distribution, AI854843, proportionality, add-like, HTS-RC, rate, proteins, Molekuel, Pdn, sample population, introduction, Protein Gene Products, Gene Proteins, Adducin, RANDOM, 10^[-6], ppm, sample, supply., quotient, Peptid, peptidos, Polypeptide, Attention Deficit Hyperactivity Disorder, l(2)01103, EST D, CG34197, HtsF, ratio"],"pubmed_title_synonyms":["Bacillus tuberculosis, Macronutrients, Bacterium tuberculosis, nutrient, Toxin-Antitoxin, Toxin-Antitoxin System, Mycobacterium tuberculosis (Zopf 1883) Lehmann and Neumann 1896 (Approved Lists 1980), Mycobacterium tuberculosis var. hominis, Mycobacterium tuberculosis H37Rv, Systems, System, nutrients, Toxin Antitoxin Systems., Nutrient, Macronutrient, Mycobacterium tuberculosis typus humanus"],"name_synonyms":["l(3)Ca, multi-cellular organism, Kochs Disease, body, mCRY, titin, whole body, 26S protease, l(3)62Ca, d-titin, 0020/01, threonine endopeptidase activity, Mbh1, SLS, Sls, ingensin, kettin, organism, large multicatalytic protease, CFU-MC, HEL-S-66, Infection, DmelCG1915, Tuberculosis, Titin, prosome, Crry, Tuberculoses, multicatalytic endopeptidase complex, animal, anon-CREST, Ket, CFU-Mast, tricorn proteinase, D-titin, l(3)j1D7, Koch's Disease, Koch Disease, whole organism, Infections, AFCP, colony forming unit mast cell, D-Titin, Mycobacterium tuberculosis Infections, CG18857, MIC10, ket, sam, sal, TLX, l(3)dre8, lens neutral proteinase, CG1915, CT41299, multicatalytic proteinase (complex), Koerper, proteasome endopeptidase complex., KZ, polyhedral organelle, l(3)S002001, l(3)rL182, CG18242, tricorn protease, Mycobacterium tuberculosis, Mycobacterium tuberculosis Infection, AHUS2, TRA2.10, Mcp, MCP, alkaline protease, active tuberculosis, multicatalytic proteinase, CG18245"],"pubmed_abstract_synonyms":["biochemical pathways, liquid chromatography tandem mass spectroscopy, Forms, protein translation, Networks, Metabolic Process, Gene Ontology Projects, Kinship, determination, latent infection, Aminosaeure, Metabolic Concepts, Amino acid, Protein Digestions., dormancy, Circulating, Oxygen Deficiencies, Techniques, Background, Roles, Mycobacterium tuberculosis var. hominis, Cultural, Latent, Concepts, Project, Life Cycle, Tuberculosis, Reactivated Infection, Analysis, Metabolism Concept, Nutrient, Phenomenon, Family Life Cycle, Koch's Disease, Bacillus tuberculosis, Bacterium tuberculosis, Koch Disease, ethnicity, LCMSMS, amino acids, Kinship Network, Circulating Lipoproteins, Analyses, catabolism, metabolic process resulting in cell growth, proteins, Protein Degradation, Oxygen, Role Concepts, biotransformation, stage, Family Life Cycles, Catabolism, LC-MS2, Two Dimensional Difference Gel Electrophoresis, protein anabolism, 2-Dimensional Difference Gel Electrophoresis, Toxin-Antitoxin System, Degradations, protein biosynthetic process, Mycobacterium tuberculosis (Zopf 1883) Lehmann and Neumann 1896 (Approved Lists 1980), Data Set, Process, Toxin Antitoxin Systems, Aminokarbonsaeure, metabolism resulting in cell growth, LC-MS/MS, Test, alpha-amino carboxylic acids, Reactivation Infections, Cultural Background, Role Concept, Cultures, Digestion, Lipid, Role, protein formation, secretion, Ontology Projects, Reactivated, Reactivation Infection, diapause, Filiation, Gene Ontologies, Amino Acid, Acid, Clusterings, Ontology, In Vitro, Ontologies, Cultural Beliefs, Projects, Amino acids, Tests, System, Hypoxemia, Latent Infections, Life Cycles, multicellular organismal protein catabolic process, Cluster, protein synthesis, label, liquid chromatography-tandem mass spectroscopy, Clustering, Lipoproteins, Acids, Mycobacterium tuberculosis Infection, Anoxemia, Proteomes, active tuberculosis, protein levels, Family Member, In Vitro as Topic, Testings, Peptidomics, Processes, developmental stage, Deficiencies, Degradation, Aminocarbonsaeure, Gene, Network, alpha-amino acid, Metabolic Processes, Gene Ontology Project, Gene Ontology, LC-MS-MS, Oxygen Deficiency, In Vitro Testing, 2D-DIGE, Metabolism, LC-MSMS, Gene Products, 2 Dimensional Difference Gel Electrophoresis, Hypoxia, Infection Reactivations, Metabolism Phenomena, Technique, In Vitro Tests, Backgrounds, In, lipid metabolism, pheromone catabolism, Infections, Research, nutrients, Metabolic Concept, Cultural Relativisms, Mycobacterium tuberculosis Infections, Protein Degradations, Reactivation, Customs, Mycobacterium tuberculosis, culture, Kinship Networks, Family, Macronutrient, nutrient, data, Family Research, degradation, Kochs Disease, Lipoprotein, Proteins, total expressed protein, Infection Reactivation, alpha-amino acids, Cultural Backgrounds, Protein Digestion, Digestions, Testing, Concept, Metabolic Phenomena, Macronutrients, Family Members, Anoxia, Metabolism Concepts, LC/MS/MS, In Vitro Test, native protein, Proteolyses, chemical analysis, Protein, Systems, Phenomena, In Vitro Testings, Infection, protein biosynthesis, Tuberculoses, Vitro Testing, metabolism, Cluster Analyses, Metabolic Phenomenon, Ontology Project, Toxin-Antitoxin, pheromone catabolic process, multicellular organism metabolic process, biodegradation, Metabolic, Mycobacterium tuberculosis H37Rv, Amino, Protein Gene Products, extracellular, Gene Proteins, single-organism metabolic process, Deficiency, lethargus, Families, In Vitro Technique, liquid chromatography tandem mass spectrometry, Relativisms, assay, Relativism, Cultural Relativism, Relatives, Mycobacterium tuberculosis typus humanus, Anabolism"],"citation_count":["0"],"additional_accession":[]},"is_claimable":false,"name":"M.tuberculosis - Whole organism, SC (Albrethsen,mcp,2013)","description":"abundance based on Spectral counting, Interaction consistency score: 5.5, Coverage: 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