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Row Type | Variable Name | Attribute Name | Data Type | Value |
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attribute | NC_GLOBAL | access_formats | String | .htmlTable,.csv,.json,.mat,.nc,.tsv,.esriCsv,.geoJson |
attribute | NC_GLOBAL | acquisition_description | String | Seawater (~180 L) was collected from the stable hydrothermal vent plume\nissuing from the black smoker chimney Inferno (CTD17, 1 450 m). Whole water\nwas transferred to clean 50 L polystyrene reservoirs and concentrated to ~230\nml with a Pellicon 2 tangential flow filtration system equipped with a 30 kDa\nBiomax Polyethersulfone cassette (Millipore Corporation, Billerica, MA) as\ndescribed previously (Morris et al 2010). Cells were collected and\nconcentrated in approximately 2 hours. Concentrated cells were flash frozen in\nliquid nitrogen and stored at -80 \\u00baC until further processing at the\nUniversity of Washington.Cell counts before and after filtration (6.9 x 1010\nand 2.9 x 1010, respectively) indicate that we recovered 42% of the cells\npresent in 180 L of hydrothermal vent plume water. Cells in the concentrated\nsample were divided into replicate samples (Av1 and Av2, ~115 ml each) and\nharvested by centrifuging at 4\\u00b0C for 60 min (17,000 x g). The supernatant\nwas discarded and cell pellets were rinsed with 100 uL of 20 mM Tris buffer pH\n7.4 and stored -80\\u00b0C.\n \nCells were lysed using a titanium sonicating micro-probe (20 sec, 10\nrepetitions) in a 6M urea and 50 \\u03bcM ammonium bicarbonate solution.\nDisulfide bonds were reduced with dithiothreitol and alkylated with iodo-\nacetic acid. After additions of ammonium bicarbonate and methanol, 2 \\u03bcg\nof sequence grade trypsin (Promega, Madison, WI) were added to each sample.\nEnzymatic digestions were incubated for 12 h at 37 oC. Resulting peptides were\ndesalted using a macro-spin C18 column (NestGroup) following the manufacturers\nguidelines prior to analysis by mass spectrometry (MS).\n \nPeptide concentrations from Axial volcano hydrothermal vent plume proteome\nreplicates Av1 and Av2 were measured using the Thermo Scientific Nanodrop\n2000/2000c, which measures the peptide bond absorbance at wavelength of 205\nnm. Approximately 1 \\u03bcg of peptide digest was used for each injection into\nthe mass spectrometer. Each sample consisted of a complex mixture of peptides\nthat were introduced into the mass spectrometer by reverse-phase\nchromatography using a brand new 15 cm long, 75 \\u03bcm i.d. fused silica\ncapillary column packed with C18 particles (Magic C18AQ, 100 \\u00c5, 5\n\\u03bcm; Michrom, Bioresources, Inc., CA) fitted with a 2 cm long, 100 \\u03bcm\ni.d. pre-column (Magic C18AQ, 200 \\u00c5, 5\\u03bcm; Michrom). Peptides were\nfirst trapped on the pre-column (5% ACN; 4 ml min-1; 7 min). Chromatographic\nseparations were performed using an acidified (formic acid, 0.1% v/v) water-\nacetonitrile gradient (5-35% acetonitrile in 60 min) with a total run-time of\n95 minutes.\n \nMass spectrometry was performed on replicates Av1 and Av2 independently using\nthe Thermo Fisher (San Jose, Ca) linear ion trap \\u2013Orbitrap (LTQ-OT)\nhybrid tandem mass spectrometer. Peptides were analyzed using the data-\nindependent Precursor Acquisition Independent from Ion Count (PAcIFIC) method\n(Panchaud et al 2009). Rather than requiring the mass spectrometer to select\nions for fragmentation based on MS1 data, the PAcIFIC method systematically\nfragments ions at all m/z channels (Panchaud et al 2011). Each method file\nincludes the full 95 minute linear HPLC gradient of 5-35% ACN over 60 minutes\n(see above) and covers a 21.5 m/z range using 14 contiguous, unique channels\nthat span 2.5 m/z in the mass spectrometer. This results in a total of 45\nmethod files per PAcIFIC analytical cycle to cover a full m/z range of\n400-1400. |
attribute | NC_GLOBAL | awards_0_award_nid | String | 529021 |
attribute | NC_GLOBAL | awards_0_award_number | String | OCE-1232840 |
attribute | NC_GLOBAL | awards_0_data_url | String | http://www.nsf.gov/awardsearch/showAward.do?AwardNumber=1232840 |
attribute | NC_GLOBAL | awards_0_funder_name | String | NSF Division of Ocean Sciences |
attribute | NC_GLOBAL | awards_0_funding_acronym | String | NSF OCE |
attribute | NC_GLOBAL | awards_0_funding_source_nid | String | 355 |
attribute | NC_GLOBAL | awards_0_program_manager | String | David L. Garrison |
attribute | NC_GLOBAL | awards_0_program_manager_nid | String | 50534 |
attribute | NC_GLOBAL | cdm_data_type | String | Other |
attribute | NC_GLOBAL | comment | String | Inferno Plume Proteins \n replicate Av1 \n (Supplementary Table 3) \n only protein probability > .9 reported \n location and depth added by DMO \n R.Morris, PI |
attribute | NC_GLOBAL | Conventions | String | COARDS, CF-1.6, ACDD-1.3 |
attribute | NC_GLOBAL | creator_email | String | info at bco-dmo.org |
attribute | NC_GLOBAL | creator_name | String | BCO-DMO |
attribute | NC_GLOBAL | creator_type | String | institution |
attribute | NC_GLOBAL | creator_url | String | https://www.bco-dmo.org/ |
attribute | NC_GLOBAL | data_source | String | extract_data_as_tsv version 2.3 19 Dec 2019 |
attribute | NC_GLOBAL | date_created | String | 2015-11-25T16:24:25Z |
attribute | NC_GLOBAL | date_modified | String | 2017-11-12T19:58:17Z |
attribute | NC_GLOBAL | defaultDataQuery | String | &time<now |
attribute | NC_GLOBAL | doi | String | 10.1575/1912/bco-dmo.643630 |
attribute | NC_GLOBAL | Easternmost_Easting | double | -130.0138 |
attribute | NC_GLOBAL | geospatial_lat_max | double | 45.934 |
attribute | NC_GLOBAL | geospatial_lat_min | double | 45.934 |
attribute | NC_GLOBAL | geospatial_lat_units | String | degrees_north |
attribute | NC_GLOBAL | geospatial_lon_max | double | -130.0138 |
attribute | NC_GLOBAL | geospatial_lon_min | double | -130.0138 |
attribute | NC_GLOBAL | geospatial_lon_units | String | degrees_east |
attribute | NC_GLOBAL | geospatial_vertical_max | double | 1450.0 |
attribute | NC_GLOBAL | geospatial_vertical_min | double | 1450.0 |
attribute | NC_GLOBAL | geospatial_vertical_positive | String | down |
attribute | NC_GLOBAL | geospatial_vertical_units | String | m |
attribute | NC_GLOBAL | infoUrl | String | https://www.bco-dmo.org/dataset/627835 |
attribute | NC_GLOBAL | institution | String | BCO-DMO |
attribute | NC_GLOBAL | instruments_0_acronym | String | CTD SBE 9 |
attribute | NC_GLOBAL | instruments_0_dataset_instrument_description | String | Seabird 9plus CTD with temperature and conductivity sensors. |
attribute | NC_GLOBAL | instruments_0_dataset_instrument_nid | String | 637597 |
attribute | NC_GLOBAL | instruments_0_description | String | The Sea-Bird SBE 9 is a type of CTD instrument package. The SBE 9 is the Underwater Unit and is most often combined with the SBE 11 Deck Unit (for real-time readout using conductive wire) when deployed from a research vessel. The combination of the SBE 9 and SBE 11 is called a SBE 911. The SBE 9 uses Sea-Bird's standard modular temperature and conductivity sensors (SBE 3 and SBE 4). The SBE 9 CTD can be configured with auxiliary sensors to measure other parameters including dissolved oxygen, pH, turbidity, fluorometer, altimeter, etc.). Note that in most cases, it is more accurate to specify SBE 911 than SBE 9 since it is likely a SBE 11 deck unit was used. more information from Sea-Bird Electronics |
attribute | NC_GLOBAL | instruments_0_instrument_external_identifier | String | https://vocab.nerc.ac.uk/collection/L05/current/130/ |
attribute | NC_GLOBAL | instruments_0_instrument_name | String | CTD Sea-Bird 9 |
attribute | NC_GLOBAL | instruments_0_instrument_nid | String | 488 |
attribute | NC_GLOBAL | instruments_0_supplied_name | String | CTD Seabird 9 plus |
attribute | NC_GLOBAL | instruments_1_acronym | String | Mass Spec |
attribute | NC_GLOBAL | instruments_1_dataset_instrument_description | String | \"The hybrid Fourier Transform (FT) mass spectrometer(MS) combines a linear ion trap\nMS and the Orbitrap mass analyzer. Ions generated by API\nare collected in the LTQ XL followed by axial ejection to the\nC-shaped storage trap which is used to store and collisionally\ncool ions before injection into the orbital trap. The ions\ntransferred from the C-Trap are captured in the orbital trap\nby rapidly increasing the electric field and the detection of\nthe image current from coherent ion packets takes place\nafter the voltages have stabilized. Signals from each of the\norbital trap outer electrodes are amplified and transformed\ninto a frequency spectrum by fast Fourier transformation\nwhich is finally converted into a mass spectrum.\" (From Fisher Scientific) |
attribute | NC_GLOBAL | instruments_1_dataset_instrument_nid | String | 627987 |
attribute | NC_GLOBAL | instruments_1_description | String | General term for instruments used to measure the mass-to-charge ratio of ions; generally used to find the composition of a sample by generating a mass spectrum representing the masses of sample components. |
attribute | NC_GLOBAL | instruments_1_instrument_external_identifier | String | https://vocab.nerc.ac.uk/collection/L05/current/LAB16/ |
attribute | NC_GLOBAL | instruments_1_instrument_name | String | Mass Spectrometer |
attribute | NC_GLOBAL | instruments_1_instrument_nid | String | 685 |
attribute | NC_GLOBAL | instruments_1_supplied_name | String | Thermo Fisher (San Jose, Ca) linear ion trap –Orbitrap (LTQ-OT) hybrid tandem mass spectrometer |
attribute | NC_GLOBAL | instruments_2_acronym | String | Spectrophotometer |
attribute | NC_GLOBAL | instruments_2_dataset_instrument_description | String | Measured peptide bond absorbance at wavelength 205nm |
attribute | NC_GLOBAL | instruments_2_dataset_instrument_nid | String | 637598 |
attribute | NC_GLOBAL | instruments_2_description | String | An instrument used to measure the relative absorption of electromagnetic radiation of different wavelengths in the near infra-red, visible and ultraviolet wavebands by samples. |
attribute | NC_GLOBAL | instruments_2_instrument_external_identifier | String | https://vocab.nerc.ac.uk/collection/L05/current/LAB20/ |
attribute | NC_GLOBAL | instruments_2_instrument_name | String | Spectrophotometer |
attribute | NC_GLOBAL | instruments_2_instrument_nid | String | 707 |
attribute | NC_GLOBAL | instruments_2_supplied_name | String | Thermo Scientific Nanodrop 2000/2000c Spectrophotometer |
attribute | NC_GLOBAL | keywords | String | annotation, bco, bco-dmo, biological, category, chemical, consensus, consensus_annotation, data, dataset, depth, dmo, entry, erddap, fasta, indep, indep_spectra_tot, kegg, KEGG_category, latitude, link, longitude, management, ncbi, NCBI_FASTA_link, num, num_unique_peptide, oceanography, office, peptide, peptide_seq, preliminary, probability, protein, protein_probability, seq, spectra, tot, unique |
attribute | NC_GLOBAL | license | String | https://www.bco-dmo.org/dataset/627835/license |
attribute | NC_GLOBAL | metadata_source | String | https://www.bco-dmo.org/api/dataset/627835 |
attribute | NC_GLOBAL | Northernmost_Northing | double | 45.934 |
attribute | NC_GLOBAL | param_mapping | String | {'627835': {'lat': 'master - latitude', 'depth': 'flag - depth', 'lon': 'master - longitude'}} |
attribute | NC_GLOBAL | parameter_source | String | https://www.bco-dmo.org/mapserver/dataset/627835/parameters |
attribute | NC_GLOBAL | people_0_affiliation | String | University of Washington |
attribute | NC_GLOBAL | people_0_affiliation_acronym | String | UW |
attribute | NC_GLOBAL | people_0_person_name | String | Robert Morris |
attribute | NC_GLOBAL | people_0_person_nid | String | 51295 |
attribute | NC_GLOBAL | people_0_role | String | Principal Investigator |
attribute | NC_GLOBAL | people_0_role_type | String | originator |
attribute | NC_GLOBAL | people_1_affiliation | String | University of Washington |
attribute | NC_GLOBAL | people_1_affiliation_acronym | String | UW |
attribute | NC_GLOBAL | people_1_person_name | String | Robert Morris |
attribute | NC_GLOBAL | people_1_person_nid | String | 51295 |
attribute | NC_GLOBAL | people_1_role | String | Contact |
attribute | NC_GLOBAL | people_1_role_type | String | related |
attribute | NC_GLOBAL | people_2_affiliation | String | Woods Hole Oceanographic Institution |
attribute | NC_GLOBAL | people_2_affiliation_acronym | String | WHOI BCO-DMO |
attribute | NC_GLOBAL | people_2_person_name | String | Ms Dicky Allison |
attribute | NC_GLOBAL | people_2_person_nid | String | 50382 |
attribute | NC_GLOBAL | people_2_role | String | BCO-DMO Data Manager |
attribute | NC_GLOBAL | people_2_role_type | String | related |
attribute | NC_GLOBAL | project | String | Sulfur Oxidizers |
attribute | NC_GLOBAL | projects_0_acronym | String | Sulfur Oxidizers |
attribute | NC_GLOBAL | projects_0_description | String | Description from NSF award abstract:\nThe ocean serves an immense reservoir of carbon, nitrogen, phosphorus, sulfur, and other elements required for all life. The active and diverse microbial populations that inhabit the oceans are responsible for mediating nutrient transformations that maintain the chemistry of seawater. A recent study identified a ubiquitous group of marine bacteria from the Arctic96BD-19 gamma-proteobacterial sulfur oxidizer (GSO) lineage that is closely related to known sulfur oxidizing species that fix inorganic carbon and oxidize sulfide in low-oxygen waters. The potential for GSOs to use reduced forms of sulfur in oxygenated waters suggests that they are a keystone species that link the marine carbon and sulfur cycles. The only known isolates from the Arctic96BD-19 lineage of GSOs are now in culture, allowing fundamental questions about their roles in carbon and sulfur cycling to be investigated. Preliminary data suggest that they use energy from the oxidation of sulfur to assimilate carbon. This project seek to address the overarching hypothesis that sulfur transformations provide the Arctic96BD- 19 lineage of GSOs with energy for organic and inorganic carbon cycling throughout the water column.\nThree specific hypotheses will be tested.\n1. Arctic96BD-19 cells assimilate either organic carbon or fixes inorganic carbon, depending on environmental conditions.\n2. Arctic96BD-19 cells oxidize thiosulfate via formation of a tetrathionate intermediate, or using the branched thiosulfate oxidation pathway.\n3. Arctic96BD-19 cells are ubiquitous sulfur oxidizers that assimilate organic and inorganic carbon through the Pacific Northwest.\nA combination of laboratory growth studies of the investigator's pure cultures and comparative genomic analyses will be used. The genomic data will be used to determine whether the Arctic96BD-19 cultures possess the genetic potential to oxidize reduced sulfur to sulfate (based on possession of known core and ancillary sulfur oxidation genes), which potential oxidation pathways are used, and whether they can fix inorganic carbon. These data will help guide the physiology studies by determining the most likely forms of inorganic and organic compounds that can be utilized.\nMarine bacteria are critical players in global nutrient cycles, but many of their individual and community functions in the ecosystem are not well understood. Future oceanographers will need to use cultivation-dependent and cultivation-independent methods to identify metabolic process that shape microbial communities and impact biogeochemical cycles. Student education, scientific advancement, and public awareness are all important components of this project. |
attribute | NC_GLOBAL | projects_0_end_date | String | 2015-09 |
attribute | NC_GLOBAL | projects_0_geolocation | String | North Pacific Ocean |
attribute | NC_GLOBAL | projects_0_name | String | Mixotrophic bacteria and the cryptic marine sulfur cycle: Mechanisms of carbon assimilation and sulfur oxidation in the Arctic96BD-19 GSO clade |
attribute | NC_GLOBAL | projects_0_project_nid | String | 529022 |
attribute | NC_GLOBAL | projects_0_project_website | String | http://morrislab.ocean.washington.edu/ |
attribute | NC_GLOBAL | projects_0_start_date | String | 2012-10 |
attribute | NC_GLOBAL | publisher_name | String | Biological and Chemical Oceanographic Data Management Office (BCO-DMO) |
attribute | NC_GLOBAL | publisher_type | String | institution |
attribute | NC_GLOBAL | sourceUrl | String | (local files) |
attribute | NC_GLOBAL | Southernmost_Northing | double | 45.934 |
attribute | NC_GLOBAL | standard_name_vocabulary | String | CF Standard Name Table v55 |
attribute | NC_GLOBAL | subsetVariables | String | latitude,longitude,depth |
attribute | NC_GLOBAL | summary | String | Proteins identified in the Inferno hydrothermal vent plume meta-proteome\n(replicate Av1).\\u00a0 Only proteins identified by peptides with a protein\nprobability >0.9 are listed.\\u00a0\n \nThese data are reported as Supplementary Table 3 and discussed in [Mattes et\nal., 2013](\\\\http://dmoserv3.bco-\ndmo.org/data_docs/SulfurOxidizers/Mattes_2013_PlumeProt.pdf\\\\).\n(doi:10.1038/ismej.2013.113)\n \nThe FASTA information in the data was expanded to include the metadata when\nthose FASTA headers were linked to GenBank.\\u00a0\n \nProteins that were identified in biological replicate Av2 that were not\nidentified in biological replicate Av1. (GSO: Gamma Sulfur Oxidizer)\n \n \n \\u00a0\n \n\\u00a0\n \n\\u00a0\n \n\\u00a0\n \n\\u00a0\n \n\\Although fewer proteins were identified in Av2, nearly all (94%) of the\nproteins identified in Av2 were also identified in Av1.\\u00a0 Differences in\nthe total number of proteins identified in replicate samples may result from\ndifferences in the amount of biomass obtained during sample processing.\\\n \nDMO notes: \n Put multiple FASTA entries on separate lines \n Split out one number in FASTA header for linking \n Left it sorted by Total Independent Spectra column \n Added linkage column \n Removed commas in 'consensus annotation' column (signals database to put in\nnew column) \n Reordered columns to put KEGG last -- much longer than any other column |
attribute | NC_GLOBAL | title | String | [Inferno vent plume proteins-Av1] - Proteins identified from the black smoker chimney Inferno hydrothermal vent plume meta-proteome - replicate Av1 - on the Axial seamount off the coast of Washington in 2011. (Mixotrophic bacteria and the cryptic marine sulfur cycle: Mechanisms of carbon assimilation and sulfur oxidation in the Arctic96BD-19 GSO clade) |
attribute | NC_GLOBAL | version | String | 1 |
attribute | NC_GLOBAL | Westernmost_Easting | double | -130.0138 |
attribute | NC_GLOBAL | xml_source | String | osprey2erddap.update_xml() v1.3 |
variable | entry | String | ||
attribute | entry | bcodmo_name | String | sample |
attribute | entry | description | String | data entry number; each entry number is a unit and all columns of information with the same entry number should be considered together |
attribute | entry | long_name | String | Entry |
attribute | entry | nerc_identifier | String | https://vocab.nerc.ac.uk/collection/P02/current/ACYC/ |
attribute | entry | units | String | number |
variable | latitude | double | ||
attribute | latitude | _CoordinateAxisType | String | Lat |
attribute | latitude | _FillValue | double | NaN |
attribute | latitude | actual_range | double | 45.934, 45.934 |
attribute | latitude | axis | String | Y |
attribute | latitude | bcodmo_name | String | latitude |
attribute | latitude | colorBarMaximum | double | 90.0 |
attribute | latitude | colorBarMinimum | double | -90.0 |
attribute | latitude | description | String | latitude of sample collection |
attribute | latitude | ioos_category | String | Location |
attribute | latitude | long_name | String | Latitude |
attribute | latitude | nerc_identifier | String | https://vocab.nerc.ac.uk/collection/P09/current/LATX/ |
attribute | latitude | standard_name | String | latitude |
attribute | latitude | units | String | degrees_north |
variable | longitude | double | ||
attribute | longitude | _CoordinateAxisType | String | Lon |
attribute | longitude | _FillValue | double | NaN |
attribute | longitude | actual_range | double | -130.0138, -130.0138 |
attribute | longitude | axis | String | X |
attribute | longitude | bcodmo_name | String | longitude |
attribute | longitude | colorBarMaximum | double | 180.0 |
attribute | longitude | colorBarMinimum | double | -180.0 |
attribute | longitude | description | String | longitude of sample collection; West is negative |
attribute | longitude | ioos_category | String | Location |
attribute | longitude | long_name | String | Longitude |
attribute | longitude | nerc_identifier | String | https://vocab.nerc.ac.uk/collection/P09/current/LONX/ |
attribute | longitude | standard_name | String | longitude |
attribute | longitude | units | String | degrees_east |
variable | depth | double | ||
attribute | depth | _CoordinateAxisType | String | Height |
attribute | depth | _CoordinateZisPositive | String | down |
attribute | depth | _FillValue | double | NaN |
attribute | depth | actual_range | double | 1450.0, 1450.0 |
attribute | depth | axis | String | Z |
attribute | depth | bcodmo_name | String | depth |
attribute | depth | colorBarMaximum | double | 8000.0 |
attribute | depth | colorBarMinimum | double | -8000.0 |
attribute | depth | colorBarPalette | String | TopographyDepth |
attribute | depth | description | String | depth of sample collection |
attribute | depth | ioos_category | String | Location |
attribute | depth | long_name | String | Depth |
attribute | depth | nerc_identifier | String | https://vocab.nerc.ac.uk/collection/P09/current/DEPH/ |
attribute | depth | positive | String | down |
attribute | depth | standard_name | String | depth |
attribute | depth | units | String | m |
variable | NCBI_FASTA_link | String | ||
attribute | NCBI_FASTA_link | bcodmo_name | String | external_link |
attribute | NCBI_FASTA_link | description | String | FASTA header with embedded NCBI reference number; link is to protein page in that database; several entries with multiple links separated by commas had to be put on separate lines to enable multiple links |
attribute | NCBI_FASTA_link | long_name | String | NCBI FASTA Link |
attribute | NCBI_FASTA_link | units | String | link |
variable | protein_probability | float | ||
attribute | protein_probability | _FillValue | float | NaN |
attribute | protein_probability | actual_range | float | 0.9052, 1.0 |
attribute | protein_probability | bcodmo_name | String | unknown |
attribute | protein_probability | description | String | the probability that the protein identified from the peptide sequences is correct. Only proteins identified by peptides with a protein probability of >0.9 are listed |
attribute | protein_probability | long_name | String | Protein Probability |
attribute | protein_probability | units | String | decimal number |
variable | num_unique_peptide | byte | ||
attribute | num_unique_peptide | _FillValue | byte | 127 |
attribute | num_unique_peptide | actual_range | byte | 1, 20 |
attribute | num_unique_peptide | bcodmo_name | String | unknown |
attribute | num_unique_peptide | description | String | the number of unique peptide sequences identified; unique peptide is defined as a peptide -- irrespective of its length -- that exists only in one protein of a proteome of interest. The peptide sequences themselves are in the peptide sequence column |
attribute | num_unique_peptide | long_name | String | Num Unique Peptide |
attribute | num_unique_peptide | units | String | number |
variable | indep_spectra_tot | short | ||
attribute | indep_spectra_tot | _FillValue | short | 32767 |
attribute | indep_spectra_tot | actual_range | short | 1, 218 |
attribute | indep_spectra_tot | bcodmo_name | String | unknown |
attribute | indep_spectra_tot | description | String | number of identifying peaks from the tandem mass spectrometer |
attribute | indep_spectra_tot | long_name | String | Indep Spectra Tot |
attribute | indep_spectra_tot | units | String | number |
variable | peptide_seq | String | ||
attribute | peptide_seq | bcodmo_name | String | unknown |
attribute | peptide_seq | description | String | amino acids identified in the peptide; A=Alanine; G=Glycine; etc |
attribute | peptide_seq | long_name | String | Peptide Seq |
attribute | peptide_seq | units | String | text |
variable | consensus_annotation | String | ||
attribute | consensus_annotation | bcodmo_name | String | unknown |
attribute | consensus_annotation | description | String | describing protein X in terms of topic Y; these dominant active bacterial groups are determined by consensus annotation of identified proteins |
attribute | consensus_annotation | long_name | String | Consensus Annotation |
attribute | consensus_annotation | units | String | text |
variable | KEGG_category | String | ||
attribute | KEGG_category | bcodmo_name | String | unknown |
attribute | KEGG_category | description | String | Kyoto Encyclopedia of Genes and Genomes; used to identify dominant functional classifications like metabolism or genetic information processing |
attribute | KEGG_category | long_name | String | KEGG Category |
attribute | KEGG_category | units | String | text |