GPMDB00143OtherSchmitt-Ulms G, et al.InstrumentNot AvailableNot availableHomo_sapiens_viruses, Humang.schmittulms@utoronto.caNot availableUniversity of Torontohttp://gpmdb.thegpm.org/~/dblist_gpmnum/gpmnum=GPM32320017709http://gpmdb.thegpm.org/~/dblist_gpmnum/gpmnum=GPM32320017703http://gpmdb.thegpm.org/~/dblist_gpmnum/gpmnum=GPM32320017704http://gpmdb.thegpm.org/~/dblist_gpmnum/gpmnum=GPM32320017701http://gpmdb.thegpm.org/~/dblist_gpmnum/gpmnum=GPM32320017702http://gpmdb.thegpm.org/~/dblist_gpmnum/gpmnum=GPM32320017707http://gpmdb.thegpm.org/~/dblist_gpmnum/gpmnum=GPM32320017708http://gpmdb.thegpm.org/~/dblist_gpmnum/gpmnum=GPM32320017705http://gpmdb.thegpm.org/~/dblist_gpmnum/gpmnum=GPM32320017706http://gpmdb.thegpm.org/~/dblist_gpmnum/gpmnum=GPM32320017700http://gpmdb.thegpm.org/~/dblist_gpmnum/gpmnum=GPM32320017714http://gpmdb.thegpm.org/~/dblist_gpmnum/gpmnum=GPM32320017715http://gpmdb.thegpm.org/~/dblist_gpmnum/gpmnum=GPM32320017712http://gpmdb.thegpm.org/~/dblist_gpmnum/gpmnum=GPM32320017713http://gpmdb.thegpm.org/~/dblist_gpmnum/gpmnum=GPM32320017718http://gpmdb.thegpm.org/~/dblist_gpmnum/gpmnum=GPM32320017719http://gpmdb.thegpm.org/~/dblist_gpmnum/gpmnum=GPM32320017716http://gpmdb.thegpm.org/~/dblist_gpmnum/gpmnum=GPM32320017717http://gpmdb.thegpm.org/~/dblist_gpmnum/gpmnum=GPM32320017695http://gpmdb.thegpm.org/~/dblist_gpmnum/gpmnum=GPM32320017696http://gpmdb.thegpm.org/~/dblist_gpmnum/gpmnum=GPM32320017694http://gpmdb.thegpm.org/~/dblist_gpmnum/gpmnum=GPM32320017699http://gpmdb.thegpm.org/~/dblist_gpmnum/gpmnum=GPM32320017710http://gpmdb.thegpm.org/~/dblist_gpmnum/gpmnum=GPM32320017711http://gpmdb.thegpm.org/~/dblist_gpmnum/gpmnum=GPM32320017697Not availableGPMDBSH-SY5Y, human being, progressive dementia, Tandem, Steele-Richardson-Olszewski Syndrome, Amentias, Neurologic Diseases, Degenerative Neurologic Disorders, Traumatic Brain Injury, Gene, Neurologic Degenerative Condition, Homo sapiense, Mass Spectrometry Mass Spectrometry, central nervous system degenerative disorder, AW045860, Neurodegenerative Diseases, Progressive supranuclear ophthalmoplegia, Homo spaiens, Homo sapien, Neurologic Disorders, Steele-Richardson-Olszewski Disease, DDPAC, Homo sapians, B1, Gene Products, pathogenesis, Paranoid Dementia, Senile Paranoid Dementias, Nervous System Degenerative Diseases, study, Nervous System, tau Protein, human disease, Homo sapients, Degenerative Condition, Amentia, Familial, proteins, labeling, Mass Spectrometry, causes, CK1epsilon, Neurodegenerative Disorder, man, Neurodegenerative Disorders, AW457082, Neurologic, AI426939, Neurologic Degenerative Diseases, Degenerative Neurologic Disease, Homo sapience, Homo sampiens, D1, causality, Degenerative Neurologic Diseases, PPP1R103, Neurologic Degenerative Disease, KC1epsilon, Homo sapiens disease, Spinal Cord, Familial Dementias, Home sapiens, NBL cell., MTBT1, AI413597, PTHB1, MTBT2, Senile, data, Neurologic Disorder, TAU, Tau, Mtapt, Proteins, PPND, Degenerative Neurologic Disorder, polypeptide, tau, C18, Homo sapian, PSP, AI551861, Protein, Diseases, Steele-Richardson-Olszewski syndrome, MSTD, Homo sapeins, CKIe, Dementia, Senile Paranoid Dementia, Degenerative Conditions, Paranoid Dementias, Degenerative Diseases, Humo sapiens, Dementias, Neurologic Degenerative Conditions, Mass Spectrometry-Mass Spectrometry, FTDP-17, Neurologic Disease, supranuclear palsy, Homo sapines, human, Protein Gene Products, Familial Dementia, Gene Proteins, Homo spiens, "human" EXACT genbank_common_name [], Senile Paranoid, Degenerative, MAPTL, Neurodegenerative Disease, Central Nervous System, Progressive Supranuclear Palsy, progressive, progressive supranuclear ophthalmoplegia (disorder)AW457082, AW045860., AI426939, TAU, tau, Tau, DDPAC, AI551861, Mtapt, MAPTL, PPP1R103, KC1epsilon, MSTD, PPND, FTDP-17, CK1epsilon, CKIe, MTBT1, AI413597, MTBT2140http://gpmdb.thegpm.org/~/dblist_gpmnum/gpmnum=GPM323200177063dbgap_ncbi~0patentfamilies~0rfam~0merops~0complex-portal~0uniprot~0wormbaseparasite~0embl-covid19~0reactome~0emdb~0wgs_masters~0ebiweb_resources~0opentargets_genetics~0biomodels_all~0ipd-mhc~0ebiweb_teams~0taxonomy~0genome_assembly~0sc-experiments~0ebiweb_people~0enzymeportal_enzymes~0ipd-nhkir~0cellosaurus~0pdbe~0chebi~0patentproteins~0interpro7~0uniref~0chembl~0pdbekb~0gpcrdb~0hgnc~0sc-genes~0intact~0rhea~0ebiweb_training~0alphafold~0imgt-hla~0patentnucleotides~0ensemblroot~0eva_studies~0non-coding~0europepmc~0identifiers_registry~0pdbechem~0hpa-covid19~0eva-variants-covid19~0biosamples~0gwas_catalog~0biotools~0tls_masters~0mesh~0coding~0sra~0opentargets~0efo~0embl-pathogen~0project~0pride~1human_diseases~0geo_datasets~0embl~0treefam~0uniparc~0ols~0dgva~0intenz~0go~0tsa_masters~0biosamples-covid19~0ebiweb_corporate~0omim~0lrg~0earlycause-molecular-sequences~0ipd-kir~0empiar~0rnacentral~0orcid_data_claims~0gpmdb~1lineage-covid19~0metagenomics~0pfam~0pride archive~1varsite~00Resource Reanalysis0.00.00.004318322023442320.01.0falseTau interactomeData from ProteomeXchange, PXD ID: PXD002058. File: 3_OF_SH-SY5Y_hTau40_minus_plus_RNase_interactome_6_7_8_9_0_1_C18_2.mzml. From ProteomeXchange: {{i}} The tau protein is central to the etiology of several neurodegenerative diseases, including Alzheimer-s disease, a subset of frontotemporal dementias, progressive supranuclear palsy and dementia following traumatic brain injury, yet the proteins it interacts with have not been studied using a systematic discovery approach. The study employed mild in vivo crosslinking, isobaric labeling and tandem mass spectrometry to characterize molecular interactions of human tau in a neuroblastoma cell model. {{/i}}2015-08-18GPM32320017706PXD002058PXD002058