{ "uniprot_canonical_ac": "Q5XIF2-1", "uniprot_ac": "Q5XIF2", "uniprot_id": "Q5XIF2_RAT", "mass": { "chemical_mass": 28439.0, "monoisotopic_mass": 28439.0 }, "refseq": { "ac": "NP_001012068", "name": "uroporphyrinogen-III synthase", "summary": "", "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001012068" }, "gene_names": [ { "name": "Uros", "resource": "UniProtKB", "type": "recommended", "url": "https://www.uniprot.org/uniprot/Q5XIF2", "id": "Q5XIF2" }, { "name": "Uros", "resource": "RefSeq", "type": "synonym", "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001012068", "id": "NP_001012068" } ], "protein_names": [ { "name": "uroporphyrinogen-III synthase", "resource": "UniProtKB", "type": "recommended", "url": "", "id": "Q5XIF2" }, { "name": "4.2.1.75", "resource": "UniProtKB", "type": "synonym", "url": "", "id": "Q5XIF2" }, { "name": "Hydroxymethylbilane hydrolyase [cyclizing]", "resource": "UniProtKB", "type": "synonym", "url": "", "id": "Q5XIF2" }, { "name": "Uroporphyrinogen-III cosynthase", "resource": "UniProtKB", "type": "synonym", "url": "", "id": "Q5XIF2" }, { "name": "urogen III synthase; uroporphyrinogen III co-synthase", "resource": "RefSeq", "type": "synonym", "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001012068", "id": "NP_001012068" }, { "name": "uroporphyrinogen-III synthase", "resource": "RefSeq", "type": "synonym", "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001012068", "id": "NP_001012068" } ], "function": [], "disease": [ { "disease_id": "DOID:13270", "recommended_name": { "id": "DOID:13270", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:13270", "name": "erythropoietic protoporphyria", "description": "An acute porphyria characterized by a deficiency in the enzyme ferrochelatase, leading to abnormally high levels of protoporphyrin in the tissue." }, "synonyms": [ { "id": "DOID:13270", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:13270", "name": "EPP", "description": "" }, { "id": "DOID:13270", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:13270", "name": "Protoporphyria", "description": "" }, { "id": "MONDO:0008319", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0008319", "name": "protoporphyria, erythropoietic, 1", "description": "Erythropoietic protoporphyria caused by a compound heterozygous or homozygous mutation in the gene encoding ferrochelatase (FECH) on chromosome 18q21." }, { "id": "MONDO:0008319", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0008319", "name": "erythropoietic protoporphyria", "description": "" }, { "id": "MONDO:0008319", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0008319", "name": "protoporphyria, erythropoietic", "description": "" }, { "id": "MONDO:0008319", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0008319", "name": "EPP1", "description": "" }, { "id": "MONDO:0008319", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0008319", "name": "ferrochelatase deficiency", "description": "" }, { "id": "MONDO:0008319", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0008319", "name": "heme synthetase deficiency", "description": "" }, { "id": "MONDO:0008319", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0008319", "name": "protoporphyria, erythropoietic, 1", "description": "" }, { "id": "MONDO:0008319", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0008319", "name": "EPP", "description": "" }, { "id": "MONDO:0008319", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0008319", "name": "erythrohepatic protoporphyria", "description": "" }, { "id": "MONDO:0010420", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010420", "name": "X-linked erythropoietic protoporphyria", "description": "X-linked form of erythropoietic protoporphyria." }, { "id": "MONDO:0010420", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010420", "name": "X-linked dominant erythropoietic protoporphyria", "description": "" }, { "id": "MONDO:0010420", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010420", "name": "X-linked dominant protoporphyria", "description": "" }, { "id": "MONDO:0010420", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010420", "name": "XLDPP", "description": "" }, { "id": "MONDO:0010420", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010420", "name": "XLP", "description": "" }, { "id": "MONDO:0010420", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010420", "name": "XLPP", "description": "" }, { "id": "MONDO:0010420", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010420", "name": "erythropoietic protoporphyria, X-linked", "description": "" }, { "id": "MONDO:0010420", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010420", "name": "Erythrohepatic protoporphyria, X-linked", "description": "" }, { "id": "MONDO:0010420", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010420", "name": "XLEPP", "description": "" }, { "id": "MONDO:0010420", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010420", "name": "protoporphyria, erythropoietic, X-linked", "description": "" }, { "id": "MONDO:0010420", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010420", "name": "protoporphyria, erythropoietic, X-linked dominant", "description": "" }, { "id": "MIM:177000", "resource": "MIM", "url": "https://www.omim.org/entry/177000", "name": "Protoporphyria, erythropoietic, 1", "description": "Protoporphyria, erythropoietic, 1" }, { "id": "MIM:300752", "resource": "MIM", "url": "https://www.omim.org/entry/300752", "name": "Erythropoietic protoporphyria, X-linked dominant", "description": "Erythropoietic protoporphyria, X-linked dominant" } ], "evidence": [ { "id": "13270", "database": "Alliance of Genome Resources", "url": "https://www.alliancegenome.org/disease/DOID:13270" } ] }, { "disease_id": "DOID:13271", "recommended_name": { "id": "DOID:13271", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:13271", "name": "cutaneous porphyria", "description": "" }, "synonyms": [ { "id": "DOID:13271", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:13271", "name": "Erythropoietic porphyria", "description": "" }, { "id": "MONDO:0009902", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009902", "name": "cutaneous porphyria", "description": "Congenital erythropoietic porphyria, or Gnther disease, is a form of erythropoietic porphyria characterized by very severe and mutilating photodermatosis." }, { "id": "MONDO:0009902", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009902", "name": "CEP", "description": "" }, { "id": "MONDO:0009902", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009902", "name": "Gnther disease", "description": "" }, { "id": "MONDO:0009902", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009902", "name": "cutaneous porphyria", "description": "" }, { "id": "MONDO:0009902", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009902", "name": "erythropoietic porphyria", "description": "" }, { "id": "MONDO:0009902", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009902", "name": "Cep", "description": "" }, { "id": "MONDO:0009902", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009902", "name": "Gunther disease", "description": "" }, { "id": "MONDO:0009902", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009902", "name": "Uros deficiency", "description": "" }, { "id": "MONDO:0009902", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009902", "name": "congenital erythropoietic porphyria", "description": "" }, { "id": "MONDO:0009902", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009902", "name": "congenital porphyria", "description": "" }, { "id": "MONDO:0009902", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009902", "name": "porphyria, congenital erythropoietic", "description": "" }, { "id": "MONDO:0009902", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009902", "name": "uroporphyrinogen 3 synthase deficiency", "description": "" }, { "id": "MONDO:0009902", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009902", "name": "uroporphyrinogen III synthase, deficiency of", "description": "" }, { "id": "MIM:263700", "resource": "MIM", "url": "https://www.omim.org/entry/263700", "name": "Congenital erythropoietic porphyria", "description": "Congenital erythropoietic porphyria" } ], "evidence": [ { "id": "13271", "database": "Alliance of Genome Resources", "url": "https://www.alliancegenome.org/disease/DOID:13271" } ] } ], "snv": [], "mutagenesis": [], "expression_tissue": [], "expression_disease": [], "species": [ { "name": "Rattus norvegicus", "taxid": 10116, "evidence": [ { "database": "UniProtKB", "id": "Q5XIF2", "url": "https://www.uniprot.org/uniprot/Q5XIF2" } ], "common_name": "Rat" } ], "gene": [ { "name": "Uros", "url": "https://www.uniprot.org/uniprot/Q5XIF2", "locus": { "chromosome": "1", "start_pos": 188490323, "end_pos": 188512249, "strand": "+", "evidence": [ { "database": "Ensembl Gene", "id": "ENSRNOG00000017810", "url": "https://www.ensembl.org/id/ENSRNOG00000017810" } ] } } ], "crossref": [ { "id": "ENSRNOG00000017810", "url": "https://bgee.org/?page=gene&gene_id=ENSRNOG00000017810", "database": "Bgee", "categories": [ "Gene Expression" ] }, { "id": "cd06578", "url": "https://www.ncbi.nlm.nih.gov/Structure/cdd/cddsrv.cgi?uid=cd06578", "database": "CDD", "categories": [ "Protein Classification" ] }, { "id": "309070", "url": "https://www.ncbi.nlm.nih.gov/gene/309070", "database": "GeneID", "categories": [ "Genome Annotation" ] }, { "id": "IPR003754", "url": "https://www.ebi.ac.uk/interpro/entry/IPR003754", "database": "InterPro", "categories": [ "Protein Classification" ] }, { "id": "IPR036108", "url": "https://www.ebi.ac.uk/interpro/entry/IPR036108", "database": "InterPro", "categories": [ "Protein Classification" ] }, { "id": "IPR039793", "url": "https://www.ebi.ac.uk/interpro/entry/IPR039793", "database": "InterPro", "categories": [ "Protein Classification" ] }, { "id": "rno:309070", "url": "https://www.genome.jp/dbget-bin/get_linkdb?-t+pathway+rno:309070", "database": "KEGG Pathway", "categories": [ "Enzyme and Pathway" ] }, { "id": "IHGADTG", "url": "https://omabrowser.org/oma/group/IHGADTG/", "database": "OMA", "categories": [ "Protein Classification" ] }, { "id": "1472480at2759", "url": "http://www.orthodb.org/?query=1472480at2759", "database": "OrthoDB", "categories": [ "Protein Classification" ] }, { "id": "PTHR12390", "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR12390", "database": "PANTHER", "categories": [ "Protein Classification" ] }, { "id": "PTHR12390:SF0", "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR12390:SF0", "database": "PANTHER", "categories": [ "Protein Classification" ] }, { "id": "PF02602", "url": "http://pfam.xfam.org/family/PF02602", "database": "Pfam", "categories": [ "Protein Classification" ] }, { "id": "R-RNO-189451", "url": "https://www.reactome.org/PathwayBrowser/#R-RNO-189451", "database": "Reactome", "categories": [ "Protein Classification" ] }, { "id": "NP_001012068", "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001012068", "database": "RefSeq", "categories": [ "Protein" ] }, { "id": "1310396", "url": "http://rgd.mcw.edu/tools/genes/genes_view.cgi?id=1310396", "database": "RGD", "categories": [ "Organism-specific" ] }, { "id": "Q5XIF2", "url": "https://www.uniprot.org/uniprot/Q5XIF2", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "Q5XIF2-1", "url": "https://www.uniprot.org/uniprot/Q5XIF2-1", "database": "UniProtKB", "categories": [ "Protein" ] } ], "sequence": { "sequence": "MKVLLLKDAKDDDSGQDPYIQELRLCGLEATLIPVLSFEFMSLPSLSEKLSHPEGFGGLIFTSPRAVEAVKLCLEKDNKTEAWEKSLKDRWNAKSVYVVGSATASLVNKIGLDAEGAGSGNAEKLAEYICSKPSSELPLLFPCGTIKGDTLPKMLRDKGIPMESMHVYQTIPHPGIQGSLESYYENQGIPASITFFSPSGLKYSLEYIQALSGGSFDQIKFVAIGPSTTRAMAAKGLPVSCTAESPTPQALAAGIRKALKPNSCC", "length": 265, "header": "tr|Q5XIF2-1|Q5XIF2_RAT Isoform 1 of uroporphyrinogen-III synthase OS=Rattus norvegicus OX=10116 GN=Uros PE=3 SV=1 CANONICAL=Q5XIF2-1" }, "isoforms": [ { "isoform_ac": "Q5XIF2-1", "url": "", "sequence": { "sequence": "MKVLLLKDAKDDDSGQDPYIQELRLCGLEATLIPVLSFEFMSLPSLSEKLSHPEGFGGLIFTSPRAVEAVKLCLEKDNKTEAWEKSLKDRWNAKSVYVVGSATASLVNKIGLDAEGAGSGNAEKLAEYICSKPSSELPLLFPCGTIKGDTLPKMLRDKGIPMESMHVYQTIPHPGIQGSLESYYENQGIPASITFFSPSGLKYSLEYIQALSGGSFDQIKFVAIGPSTTRAMAAKGLPVSCTAESPTPQALAAGIRKALKPNSCC", "length": 265, "header": "tr|Q5XIF2-1|Q5XIF2_RAT Isoform 1 of uroporphyrinogen-III synthase OS=Rattus norvegicus OX=10116 GN=Uros PE=3 SV=1 CANONICAL=Q5XIF2-1" }, "locus": { "chromosome": "1", "start_pos": 188506132, "end_pos": 188492334, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENSRNOT00000024279.5", "url": "https://www.ensembl.org/id/ENSRNOT00000024279.5" }, { "database": "Ensembl Peptide", "id": "ENSRNOP00000024278.3", "url": "https://www.ensembl.org/id/ENSRNOP00000024278.3" } ] } } ], "glycosylation": [], "phosphorylation": [], "glycation": [], "keywords": [ "enzyme" ], "publication": [], "pathway": [ { "id": "rno:309070", "name": "", "url": "https://www.genome.jp/dbget-bin/get_linkdb?-t+pathway+rno:309070", "resource": "KEGG Pathway" }, { "id": "R-RNO-189451", "name": "Heme biosynthesis", "url": "https://www.reactome.org/PathwayBrowser/#R-RNO-189451", "resource": "Reactome", "description": "Heme biosynthesis" } ], "orthologs": [ { "uniprot_canonical_ac": "P10746-1", "protein_name": "Uroporphyrinogen-III synthase", "gene_name": "UROS", "tax_id": 9606, "organism": "Homo sapiens", "sequence": { "sequence": "MKVLLLKDAKEDDCGQDPYIRELGLYGLEATLIPVLSFEFLSLPSFSEKLSHPEDYGGLIFTSPRAVEAAELCLEQNNKTEVWERSLKEKWNAKSVYVVGNATASLVSKIGLDTEGETCGNAEKLAEYICSRESSALPLLFPCGNLKREILPKALKDKGIAMESITVYQTVAHPGIQGNLNSYYSQQGVPASITFFSPSGLTYSLKHIQELSGDNIDQIKFAAIGPTTARALAAQGLPVSCTAESPTPQALATGIRKALQPHGCC", "length": 265 }, "evidence": [ { "id": "45225716", "url": "http://www.informatics.jax.org/homology/45225716", "database": "MGI" } ], "common_name": "Human" }, { "uniprot_canonical_ac": "P51163-1", "protein_name": "Uroporphyrinogen-III synthase", "gene_name": "Uros", "tax_id": 10090, "organism": "Mus musculus", "sequence": { "sequence": "MKVLLLKDAKEDDSGLDPYIQELRLCGLEATLIPVLSFEFMSLPSLSEKLSHPEGFGGLIFTSPRAVEAVKLCLEKDNKTEAWEKSLKDRWNAKSVYVVGSATASLVNKIGLDAEGAGSGNAEKLAEYICSKPSSELPLLFPCGTIKGDTLPKMLKDKGIPMESMHVYQTVPHPGIQGSLKSYYEDQGIPASITFFSPSGLKYSLEYIQALSGSSFDQIKFIAIGPSTTRAMAAKGLPVSCTAESPTPQALAAGIRNVLKPNHCC", "length": 265 }, "evidence": [ { "id": "45225716", "url": "http://www.informatics.jax.org/homology/45225716", "database": "MGI" } ], "common_name": "Mouse" } ], "go_annotation": { "categories": [ { "name": "Cellular Component", "total": 1, "go_terms": [ { "name": "cytosol", "id": "GO:0005829", "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005829", "evidence": [ { "database": "UniProtKB", "id": "Q5XIF2", "url": "https://www.uniprot.org/uniprot/Q5XIF2" } ], "pmid": "" } ] }, { "name": "Biological Process", "total": 7, "go_terms": [ { "name": "porphyrin-containing compound biosynthetic process", "id": "GO:0006779", "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006779", "evidence": [ { "database": "UniProtKB", "id": "Q5XIF2", "url": "https://www.uniprot.org/uniprot/Q5XIF2" } ], "pmid": "" }, { "name": "heme biosynthetic process", "id": "GO:0006783", "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006783", "evidence": [ { "database": "UniProtKB", "id": "Q5XIF2", "url": "https://www.uniprot.org/uniprot/Q5XIF2" } ], "pmid": "" }, { "name": "protoporphyrinogen IX biosynthetic process", "id": "GO:0006782", "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006782", "evidence": [ { "database": "UniProtKB", "id": "Q5XIF2", "url": "https://www.uniprot.org/uniprot/Q5XIF2" } ], "pmid": "" }, { "name": "response to platinum ion", "id": "GO:0070541", "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0070541", "evidence": [ { "database": "UniProtKB", "id": "Q5XIF2", "url": "https://www.uniprot.org/uniprot/Q5XIF2" } ], "pmid": "" }, { "name": "cellular response to arsenic-containing substance", "id": "GO:0071243", "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0071243", "evidence": [ { "database": "UniProtKB", "id": "Q5XIF2", "url": "https://www.uniprot.org/uniprot/Q5XIF2" } ], "pmid": "" }, { "name": "uroporphyrinogen III biosynthetic process", "id": "GO:0006780", "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006780", "evidence": [ { "database": "UniProtKB", "id": "Q5XIF2", "url": "https://www.uniprot.org/uniprot/Q5XIF2" } ], "pmid": "" }, { "name": "cellular response to amine stimulus", "id": "GO:0071418", "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0071418", "evidence": [ { "database": "UniProtKB", "id": "Q5XIF2", "url": "https://www.uniprot.org/uniprot/Q5XIF2" } ], "pmid": "" } ] }, { "name": "Molecular Function", "total": 2, "go_terms": [ { "name": "folic acid binding", "id": "GO:0005542", "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005542", "evidence": [ { "database": "UniProtKB", "id": "Q5XIF2", "url": "https://www.uniprot.org/uniprot/Q5XIF2" } ], "pmid": "" }, { "name": "uroporphyrinogen-III synthase activity", "id": "GO:0004852", "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004852", "evidence": [ { "database": "UniProtKB", "id": "Q5XIF2", "url": "https://www.uniprot.org/uniprot/Q5XIF2" } ], "pmid": "" } ] } ] }, "pro_annotation": [], "site_annotation": [ { "start_pos": 78, "end_pos": 80, "annotation": "n_glycosylation_sequon" } ], "ptm_annotation": [], "interactions": [], "reactions": [ { "id": "R-RNO-189488", "name": "UROS transforms HMB to URO3", "equation": "", "summary": "This event has been computationally inferred from an event that has been demonstrated in another species.

The inference is based on the homology mapping from PANTHER. Briefly, reactions for which all involved PhysicalEntities (in input, output and catalyst) have a mapped orthologue/paralogue (for complexes at least 75% of components must have a mapping) are inferred to the other species. High level events are also inferred for these events to allow for easier navigation.

More details and caveats of the event inference in Reactome. For details on PANTHER see also: http://www.pantherdb.org/about.jsp", "cellular_location": "cytosol", "input_participant_list": [], "output_participant_list": [], "enzyme_list": [ "Q5XIF2-1" ], "evidence": [ { "id": "R-RNO-189488", "database": "Reactome", "url": "https://www.reactome.org/PathwayBrowser/#R-RNO-189488" } ] } ], "reaction_participants": [], "reaction_enzymes": [ { "uniprot_ac": "Q5XIF2", "gene_name": "Uros", "activity": [ { "ec_number": "4.2.1.75", "activity": "hydroxymethylbilane = H2O + uroporphyrinogen III.", "evidence": [ { "id": "Q5XIF2", "database": "UniProtKB", "url": "https://www.uniprot.org/uniprot/Q5XIF2" } ] }, { "ec_number": "4.2.1.75", "activity": "", "evidence": [ { "id": "Q5XIF2", "database": "UniProtKB", "url": "https://www.uniprot.org/uniprot/Q5XIF2" } ] } ] } ], "biomarkers": [], "synthesized_glycans": [], "cluster_types": [ { "name": "homologset.mgi", "label": "MGI Homologs" } ], "section_stats": [ { "table_id": "glycosylation", "table_stats": [ { "field": "total", "count": 0 }, { "field": "total_sites", "count": 0 }, { "field": "n_linked_glycans", "count": 0 }, { "field": "n_linked_glycan_sites", "count": 0 }, { "field": "o_linked_glycans", "count": 0 }, { "field": "o_linked_glycan_sites", "count": 0 } ], "sort_fields": [] }, { "table_id": "glycosylation_reported", "table_stats": [ { "field": "total", "count": 0 }, { "field": "total_sites", "count": 0 }, { "field": "n_linked_glycans", "count": 0 }, { "field": "n_linked_glycan_sites", "count": 0 }, { "field": "o_linked_glycans", "count": 0 }, { "field": "o_linked_glycan_sites", "count": 0 } ], "sort_fields": [] }, { "table_id": "glycosylation_reported_with_glycan", "table_stats": [ { "field": "total", "count": 0 }, { "field": "total_sites", "count": 0 }, { "field": "n_linked_glycans", "count": 0 }, { "field": "n_linked_glycan_sites", "count": 0 }, { "field": "o_linked_glycans", "count": 0 }, { "field": "o_linked_glycan_sites", "count": 0 } ], "sort_fields": [] }, { "table_id": "glycosylation_predicted", "table_stats": [ { "field": "total", "count": 0 }, { "field": "total_sites", "count": 0 }, { "field": "n_linked_glycans", "count": 0 }, { "field": "n_linked_glycan_sites", "count": 0 }, { "field": "o_linked_glycans", "count": 0 }, { "field": "o_linked_glycan_sites", "count": 0 } ], "sort_fields": [] }, { "table_id": "glycosylation_automatic_literature_mining", "table_stats": [ { "field": "total", "count": 0 }, { "field": "total_sites", "count": 0 }, { "field": "n_linked_glycans", "count": 0 }, { "field": "n_linked_glycan_sites", "count": 0 }, { "field": "o_linked_glycans", "count": 0 }, { "field": "o_linked_glycan_sites", "count": 0 } ], "sort_fields": [] }, { "table_id": "phosphorylation", "table_stats": [ { "field": "total", "count": 0 }, { "field": "total_sites", "count": 0 } ], "sort_fields": [] }, { "table_id": "snv", "table_stats": [ { "field": "total", "count": 0 }, { "field": "total_sites", "count": 0 } ], "sort_fields": [] }, { "table_id": "snv_disease", "table_stats": [ { "field": "total", "count": 0 }, { "field": "total_sites", "count": 0 } ], "sort_fields": [] }, { "table_id": "snv_non_disease", "table_stats": [ { "field": "total", "count": 0 }, { "field": "total_sites", "count": 0 } ], "sort_fields": [] }, { "table_id": "publication", "table_stats": [ { "field": "total", "count": 0 } ], "sort_fields": [] } ] }