MassIVEapplication/xmlftp://massive.ucsd.edu/MSV000083422primaryOK20000900OtherAnna EdlundGCMSRothia Spp.https://massive.ucsd.edu/ProteoSAFe/dataset.jsp?task=be55b24e6c104d9a88ac0d2929dbba38aedlund@jcvi.orgJ. Craig Venter InstituteMassIVE25MS:1002864 - No post-translational-modifications are included in the identified peptides of this datasetprogeroid syndrome, dental and eye anomalies, Petty syndrome, DmelCG6525, T18E12_21, FPS, craniofacial dysostosis-genital, dental and eye anomalies-patent ductus arteriosus-normal intelligence syndrome, signal peptide peptidase, Rothia <eudicots>, Fontaine progeroid syndrome, PSL3, SPPL1, Gorlin-Chaudhry-Moss syndrome, IMPAS-1, SPP, Spp, Petty type, cranofacial dysostosis-hypertrichosis-hypoplasia of labia majora syndrome, dental, and normal intelligence, Petty Laxova Wiedemann syndrome, patent ductus arteriosus, craniofacial dysostosis, FBgn0082831, progeroid syndrome congenital Petty type, ATSPP., GCMS, Hypoplasia of labia majora, PSENL3, IMP1, GCM syndrome, Stomatococcus, MSTP086, progeroid syndrome Petty type, congenital, H13, hypoplasia of labia majora, Rothia <high GC Gram+>, CG6525, hypertrichosis, dJ324O17.1, T18E12.21, spp, Petty-Laxova-Wiedemann syndrome, IMPAS, cardiac anomalies syndrome, Gorlin Chaudhry Moss syndromeprogeroid syndrome, dental and eye anomalies, Petty syndrome, DmelCG6525, T18E12_21, FPS, signal peptide peptidase, craniofacial dysostosis-genital, dental and eye anomalies-patent ductus arteriosus-normal intelligence syndrome, Rothia <eudicots>, Fontaine progeroid syndrome, PSL3, SPPL1, IMPAS-1, Gorlin-Chaudhry-Moss syndrome, SPP, Spp, Petty type, cranofacial dysostosis-hypertrichosis-hypoplasia of labia majora syndrome, dental, and normal intelligence, Petty Laxova Wiedemann syndrome, patent ductus arteriosus, craniofacial dysostosis, FBgn0082831, GCMS, PSENL3, Hypoplasia of labia majora, IMP1, GCM syndrome, Stomatococcus, MSTP086, H13, progeroid syndrome Petty type, congenital, hypoplasia of labia majora, Rothia <high GC Gram+>, CG6525, dJ324O17.1, T18E12.21, hypertrichosis, spp, IMPAS, Petty-Laxova-Wiedemann syndrome, cardiac anomalies syndrome, Gorlin Chaudhry Moss syndrome, ATSPP, progeroid syndrome congenital Petty type.0.00.00.0277606415792720530.000dbgap_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~0human_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~0lineage-covid19~0gpmdb~0metagenomics~0pfam~0varsite~0true901.0trueRothia spp. GCMSGCMS of Rothia spp. in minimal media, incubated with a variety of substrates.Fri Feb 08 09:36:00 GMT 2019MSV000083422