[ { "title": "Evaluation of the human arrestin gene in patients with retinitis pigmentosa and stationary night blindness.", "journal": "Invest. Ophthalmol. Vis. Sci.", "date": "1998", "authors": "Sippel K C, DeStefano J D, Berson E L, Dryja T P", "reference": { "type": "PubMed", "id": "9501883", "url": "https://pubmed.ncbi.nlm.nih.gov/9501883" }, "referenced_glycans": [], "referenced_proteins": [ { "uniprot_canonical_ac": "P10523-1", "protein_name": "S-arrestin", "gene_name": "SAG", "tax_name": "Human" } ], "species": [ { "name": "Homo sapiens", "taxid": 9606, "evidence": [ { "database": "UniProtKB", "id": "P10523", "url": "https://www.uniprot.org/uniprotkb/P10523" } ], "common_name": "Human", "glygen_name": "Human", "reference_species": "Homo sapiens [9606]" } ], "record_id": "pubmed.9501883", "abstract": "", "glycosylation": [], "mutagenesis": [], "snv": [], "phosphorylation": [], "glycation": [], "section_stats": [ { "table_id": "referenced_proteins", "table_stats": [ { "field": "total", "count": 1 } ], "sort_fields": [ "uniprot_canonical_ac", "protein_name", "gene_name", "tax_name" ] }, { "table_id": "referenced_glycans", "table_stats": [ 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genotype-phenotype association in pseudoachondroplasia and multiple epiphyseal dysplasia.", "journal": "Human genetics", "date": "2003", "authors": "Mabuchi A, Manabe N, Haga N, Kitoh H, Ikeda T, Kawaji H, Tamai K, Hamada J, Nakamura S, Brunetti-Pierri N, Kimizuka M, Takatori Y, Nakamura K, Nishimura G, Ohashi H, Ikegawa S", "reference": { "type": "PubMed", "id": "12483304", "url": "https://pubmed.ncbi.nlm.nih.gov/12483304" }, "referenced_glycans": [], "referenced_proteins": [ { "uniprot_canonical_ac": "P49747-1", "protein_name": "Cartilage oligomeric matrix protein", "gene_name": "COMP", "tax_name": "Human" } ], "species": [ { "name": "Homo sapiens", "taxid": 9606, "evidence": [ { "database": "UniProtKB", "id": "P49747", "url": "https://www.uniprot.org/uniprotkb/P49747" } ], "common_name": "Human", "glygen_name": "Human", "reference_species": "Homo sapiens [9606]" } ], "snv": [ { "evidence": [ { "id": "rs869320730", "database": "dbSNP", "url": 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"description": "" }, { "id": "DOID:0070303", "resource": "Disease Ontology", "url": "https://disease-ontology.org/term/DOID:0070303", "name": "MED1", "description": "" }, { "id": "DOID:0070303", "resource": "Disease Ontology", "url": "https://disease-ontology.org/term/DOID:0070303", "name": "multiple epiphyseal dysplasia COMP-related", "description": "" }, { "id": "DOID:0070303", "resource": "Disease Ontology", "url": "https://disease-ontology.org/term/DOID:0070303", "name": "polyepiphyseal dysplasia type 1", "description": "" }, { "id": "MONDO:0007561", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0007561", "name": "multiple epiphyseal dysplasia type 1", "description": "Multiple epiphyseal dysplasia type 1 (MED 1) is a form of multiple epiphyseal dysplasia that is characterized by normal or mild short stature, pain in the hips and/or knees, progressive deformity of extremities and early-onset osteoarthrosis. Specific features to MED 1 include a more pronounced involvement of hip joints and gait abnormality and a shorter adult height. MED1 is allelic to pseudoachondroplasia with which it shares clinical and radiological features. 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Leroy JG, Biesecker L, Lipson M, Wilcox WR, Lachman RS, Rimoin DL, Knowlton RG, Cohn DH", "reference": { "type": "PubMed", "id": "9463320", "url": "https://pubmed.ncbi.nlm.nih.gov/9463320" }, "referenced_glycans": [], "referenced_proteins": [ { "uniprot_canonical_ac": "P49747-1", "protein_name": "Cartilage oligomeric matrix protein", "gene_name": "COMP", "tax_name": "Human" } ], "species": [ { "name": "Homo sapiens", "taxid": 9606, "evidence": [ { "database": "UniProtKB", "id": "P49747", "url": "https://www.uniprot.org/uniprotkb/P49747" } ], "common_name": "Human", "glygen_name": "Human", "reference_species": "Homo sapiens [9606]" } ], "record_id": "pubmed.9463320", "abstract": "", "glycosylation": [], "mutagenesis": [], "snv": [], "phosphorylation": [], "glycation": [], "section_stats": [ { "table_id": "referenced_proteins", "table_stats": [ { "field": "total", "count": 1 } ], "sort_fields": [ "uniprot_canonical_ac", "protein_name", "gene_name", "tax_name" ] }, { "table_id": 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Part A", "date": "2015", "authors": "Pons L, Cordier MP, Labalme A, Till M, Louvrier C, Schluth-Bolard C, Lesca G, Edery P, Sanlaville D", "reference": { "type": "PubMed", "id": "25425123", "url": "https://pubmed.ncbi.nlm.nih.gov/25425123" }, "referenced_glycans": [], "referenced_proteins": [ { "uniprot_canonical_ac": "Q9BZK7-1", "protein_name": "F-box-like/WD repeat-containing protein TBL1XR1", "gene_name": "TBL1XR1", "tax_name": "Human" } ], "species": [ { "name": "Homo sapiens", "taxid": 9606, "evidence": [ { "database": "UniProtKB", "id": "Q9BZK7", "url": "https://www.uniprot.org/uniprotkb/Q9BZK7" } ], "common_name": "Human", "glygen_name": "Human", "reference_species": "Homo sapiens [9606]" } ], "record_id": "pubmed.25425123", "abstract": "", "glycosylation": [], "mutagenesis": [], "snv": [], "phosphorylation": [], "glycation": [], "section_stats": [ { "table_id": "referenced_proteins", "table_stats": [ { "field": "total", "count": 1 } ], "sort_fields": [ "uniprot_canonical_ac", 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], "sort_fields": [] }, { "table_id": "glycosylation_automatic_literature_mining", "table_stats": [ { "field": "total", "count": 0 }, { "field": "total_sites", "count": 0 }, { "field": "n_linked_sites", "count": 0 }, { "field": "o_linked_sites", "count": 0 }, { "field": "n_linked_glycan_sites", "count": 0 }, { "field": "o_linked_glycan_sites", "count": 0 }, { "field": "n_linked_glycans", "count": 0 }, { "field": "o_linked_glycans", "count": 0 } ], "sort_fields": [] } ] }, { "title": "A specific mutation in TBL1XR1 causes Pierpont syndrome.", "journal": "Journal of medical genetics", "date": "2016", "authors": "Heinen CA, Jongejan A, Watson PJ, Redeker B, Boelen A, Boudzovitch-Surovtseva O, Forzano F, Hordijk R, Kelley R, Olney AH, Pierpont ME, Schaefer GB, Stewart F, van Trotsenburg AS, Fliers E, Schwabe JW, Hennekam RC", "reference": { "type": "PubMed", "id": "26769062", "url": "https://pubmed.ncbi.nlm.nih.gov/26769062" }, "referenced_glycans": [], "referenced_proteins": [ { 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Tifft Cynthia, Becker Catherine, Melo De Gusmao Claudio, Khurana Vikram, Neumeyer Ann M, Eichler Florian S", "reference": { "type": "PubMed", "id": "38378692", "url": "https://pubmed.ncbi.nlm.nih.gov/38378692" }, "referenced_glycans": [], "referenced_proteins": [ { "uniprot_canonical_ac": "Q9BZK7-1", "protein_name": "F-box-like/WD repeat-containing protein TBL1XR1", "gene_name": "TBL1XR1", "tax_name": "Human" } ], "species": [ { "name": "Homo sapiens", "taxid": 9606, "evidence": [ { "database": "UniProtKB", "id": "Q9BZK7", "url": "https://www.uniprot.org/uniprotkb/Q9BZK7" } ], "common_name": "Human", "glygen_name": "Human", "reference_species": "Homo sapiens [9606]" } ], "record_id": "pubmed.38378692", "abstract": "", "glycosylation": [], "mutagenesis": [], "snv": [], "phosphorylation": [], "glycation": [], "section_stats": [ { "table_id": "referenced_proteins", "table_stats": [ { "field": "total", "count": 1 } ], "sort_fields": [ "uniprot_canonical_ac", "protein_name", "gene_name", 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No effect on interaction with P4HB; when associated with S-109 and S-332.", "evidence": [ { "database": "UniProtKB", "id": "O75460", "url": "https://www.uniprot.org/uniprotkb/O75460" }, { "database": "PubMed", "id": "32149426", "url": "https://pubmed.ncbi.nlm.nih.gov/32149426" }, { "database": "PubMed", "id": "12637535", "url": "https://pubmed.ncbi.nlm.nih.gov/12637535" }, { "database": "PubMed", "id": "24508390", "url": "https://pubmed.ncbi.nlm.nih.gov/24508390" } ], "uniprot_canonical_ac": "O75460-1" }, { "start_pos": 332, "end_pos": 332, "sequence_org": "C", "sequence_mut": "S", "comment": "No effect on dimerization. Weakens dimer; when associated with S-148. 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with the transmembrane domain. Abolishes normal maturation. Impairs trafficking to the apical cell membrane.", "evidence": [ { "database": "UniProtKB", "id": "P26361", "url": "https://www.uniprot.org/uniprotkb/P26361" }, { "database": "PubMed", "id": "22265409", "url": "https://pubmed.ncbi.nlm.nih.gov/22265409" }, { "database": "PubMed", "id": "15619636", "url": "https://pubmed.ncbi.nlm.nih.gov/15619636" }, { "database": "PubMed", "id": "21884936", "url": "https://pubmed.ncbi.nlm.nih.gov/21884936" } ], "uniprot_canonical_ac": "P26361-1" }, { "start_pos": 2, "end_pos": 2, "sequence_org": "G", "sequence_mut": "A", "comment": "Abolishes myristoylation. Loss of its ability to mediate unconventional (ER/Golgi-independent) trafficking of CFTR to the cell membrane. No effect on ER stress-induced relocalization from Golgi to ER.", "evidence": [ { "database": "UniProtKB", "id": "Q9H8Y8", "url": "https://www.uniprot.org/uniprotkb/Q9H8Y8" }, { "database": "PubMed", "id": "27062250", "url": "https://pubmed.ncbi.nlm.nih.gov/27062250" }, { "database": "PubMed", "id": "21884936", "url": "https://pubmed.ncbi.nlm.nih.gov/21884936" } ], "uniprot_canonical_ac": "Q9H8Y8-1" }, { "start_pos": 441, "end_pos": 441, "sequence_org": "S", "sequence_mut": "A", "comment": "Loss of phosphorylation and its ability to mediate unconventional (ER/Golgi-independent) trafficking of CFTR to the cell membrane. Inhibits ER stress-mediated disruption of homodimerization. Loss of ER stress-induced relocalization from Golgi to ER.", "evidence": [ { "database": "UniProtKB", "id": "Q9H8Y8", "url": "https://www.uniprot.org/uniprotkb/Q9H8Y8" }, { "database": "PubMed", "id": "27062250", "url": "https://pubmed.ncbi.nlm.nih.gov/27062250" }, { "database": "PubMed", "id": "21884936", "url": "https://pubmed.ncbi.nlm.nih.gov/21884936" } ], "uniprot_canonical_ac": "Q9H8Y8-1" }, { "start_pos": 441, "end_pos": 441, "sequence_org": "S", "sequence_mut": "D", "comment": "Phosphomimetic mutant. No loss of its ability to mediate unconventional (ER/Golgi-independent) trafficking of CFTR to the cell membrane. Disrupts homodimerization. No loss of ER stress-induced relocalization from Golgi to ER.", "evidence": [ { "database": "UniProtKB", "id": "Q9H8Y8", "url": "https://www.uniprot.org/uniprotkb/Q9H8Y8" }, { "database": "PubMed", "id": "27062250", "url": "https://pubmed.ncbi.nlm.nih.gov/27062250" }, { "database": "PubMed", "id": "21884936", "url": "https://pubmed.ncbi.nlm.nih.gov/21884936" } ], "uniprot_canonical_ac": "Q9H8Y8-1" } ], "phosphorylation": [ { "start_pos": 441, "end_pos": 441, "kinase_uniprot_canonical_ac": "", "kinase_gene_name": "", "residue": "Ser", "comment": "Phosphoserine", "evidence": [ { "database": "UniProtKB", "id": "Q9H8Y8", "url": "https://www.uniprot.org/uniprotkb/Q9H8Y8" }, { "database": "PubMed", "id": "27062250", "url": "https://pubmed.ncbi.nlm.nih.gov/27062250" }, { "database": "PubMed", "id": "21884936", "url": "https://pubmed.ncbi.nlm.nih.gov/21884936" }, { "database": "iPTMnet", "id": "Q9H8Y8", "url": "http://research.bioinformatics.udel.edu/iptmnet/entry/Q9H8Y8" } ], "site_lbl": 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} ], "sort_fields": [] }, { "table_id": "glycosylation_predicted", "table_stats": [ { "field": "total", "count": 0 }, { "field": "total_sites", "count": 0 }, { "field": "n_linked_sites", "count": 0 }, { "field": "o_linked_sites", "count": 0 }, { "field": "n_linked_glycan_sites", "count": 0 }, { "field": "o_linked_glycan_sites", "count": 0 }, { "field": "n_linked_glycans", "count": 0 }, { "field": "o_linked_glycans", "count": 0 } ], "sort_fields": [] }, { "table_id": "glycosylation_automatic_literature_mining", "table_stats": [ { "field": "total", "count": 0 }, { "field": "total_sites", "count": 0 }, { "field": "n_linked_sites", "count": 0 }, { "field": "o_linked_sites", "count": 0 }, { "field": "n_linked_glycan_sites", "count": 0 }, { "field": "o_linked_glycan_sites", "count": 0 }, { "field": "n_linked_glycans", "count": 0 }, { "field": "o_linked_glycans", "count": 0 } ], "sort_fields": [] } ] }, { "title": "Protein disulfide isomerase A6 controls the decay of IRE1alpha signaling via disulfide-dependent association.", "journal": "Molecular cell", "date": "2014", "authors": "Eletto D, Eletto D, Dersh D, Gidalevitz T, Argon Y", "reference": { "type": "PubMed", "id": "24508390", "url": "https://pubmed.ncbi.nlm.nih.gov/24508390" }, "referenced_glycans": [], "referenced_proteins": [ { "uniprot_canonical_ac": "O75460-1", "protein_name": "Serine/threonine-protein kinase/endoribonuclease IRE1", "gene_name": "ERN1", "tax_name": "Human" }, { "uniprot_canonical_ac": "Q9NZJ5-1", "protein_name": "Eukaryotic translation initiation factor 2-alpha kinase 3", "gene_name": "EIF2AK3", "tax_name": "Human" }, { "uniprot_canonical_ac": "Q922R8-1", "protein_name": "Protein disulfide-isomerase A6", "gene_name": "Pdia6", "tax_name": "Mouse" }, { "uniprot_canonical_ac": "Q15084-1", "protein_name": "Protein disulfide-isomerase A6", "gene_name": "PDIA6", "tax_name": "Human" } ], "species": [ { "name": "Homo sapiens", "taxid": 9606, "evidence": [ { "database": "UniProtKB", "id": "O75460", "url": "https://www.uniprot.org/uniprotkb/O75460" } ], "common_name": "Human", "glygen_name": "Human", "reference_species": "Homo sapiens [9606]" } ], "mutagenesis": [ { "start_pos": 148, "end_pos": 148, "sequence_org": "C", "sequence_mut": "S", "comment": "No effect on dimerization. Weakens dimer; when associated with S-332. Abolishes interaction with PDIA6. Prolonged splicing of XBP1, probably due to prolonged activation of PDIA6. Inhibits formation of oxidized multimeric forms of ERN1 in response to ER stress. No effect on interaction with P4HB; when associated with S-109 and S-332.", "evidence": [ { "database": "UniProtKB", "id": "O75460", "url": "https://www.uniprot.org/uniprotkb/O75460" }, { "database": "PubMed", "id": "32149426", "url": "https://pubmed.ncbi.nlm.nih.gov/32149426" }, { "database": "PubMed", "id": "12637535", "url": "https://pubmed.ncbi.nlm.nih.gov/12637535" }, { "database": "PubMed", "id": "24508390", "url": "https://pubmed.ncbi.nlm.nih.gov/24508390" } ], "uniprot_canonical_ac": "O75460-1" }, { "start_pos": 193, "end_pos": 193, "sequence_org": "C", "sequence_mut": "A", "comment": "Accelerates dephosphorylation of ERN1; when associated with A-58.", "evidence": [ { "database": "UniProtKB", "id": "Q15084", "url": "https://www.uniprot.org/uniprotkb/Q15084" }, { "database": "PubMed", "id": "24508390", "url": "https://pubmed.ncbi.nlm.nih.gov/24508390" } ], "uniprot_canonical_ac": "Q15084-1" }, { "start_pos": 58, "end_pos": 58, "sequence_org": "C", "sequence_mut": "A", "comment": 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Med.", "date": "2005", "authors": "Hibbert Richard G, Teriete Peter, Grundy Gabrielle J, Beavil Rebecca L, Reljic Rajko, Holers V Michael, Hannan Jonathan P, Sutton Brian J, Gould Hannah J, McDonnell James M", "reference": { "type": "PubMed", "id": "16172256", "url": "https://pubmed.ncbi.nlm.nih.gov/16172256" }, "referenced_glycans": [], "referenced_proteins": [ { "uniprot_canonical_ac": "P06734-1", "protein_name": "Low affinity immunoglobulin epsilon Fc receptor", "gene_name": "FCER2", "tax_name": "Human" }, { "uniprot_canonical_ac": "P20023-1", "protein_name": "Complement receptor type 2", "gene_name": "CR2", "tax_name": "Human" }, { "uniprot_canonical_ac": "P01854-2", "protein_name": "Immunoglobulin heavy constant epsilon", "gene_name": "IGHE", "tax_name": "Human" } ], "species": [ { "name": "Homo sapiens", "taxid": 9606, "evidence": [ { "database": "UniProtKB", "id": "P06734", "url": "https://www.uniprot.org/uniprotkb/P06734" } ], "common_name": "Human", "glygen_name": "Human", 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"count": 0 }, { "field": "o_linked_glycans", "count": 0 } ], "sort_fields": [] } ] }, { "title": "Identification of new phosphorylation sites of CD23 in B-cells of patients with chronic lymphocytic leukemia.", "journal": "Leukemia research", "date": "2018", "authors": "Madarova M, Mucha R, Hresko S, Makarova Z, Gdovinova Z, Szilasiova J, Vitkova M, Guman T, Stecova N, Dobransky T", "reference": { "type": "PubMed", "id": "29763855", "url": "https://pubmed.ncbi.nlm.nih.gov/29763855" }, "referenced_glycans": [], "referenced_proteins": [ { "uniprot_canonical_ac": "P06734-1", "protein_name": "Low affinity immunoglobulin epsilon Fc receptor", "gene_name": "FCER2", "tax_name": "Human" } ], "species": [ { "name": "Homo sapiens", "taxid": 9606, "evidence": [ { "database": "UniProtKB", "id": "P06734", "url": "https://www.uniprot.org/uniprotkb/P06734" } ], "common_name": "Human", "glygen_name": "Human", "reference_species": "Homo sapiens [9606]" } ], "phosphorylation": [ { "start_pos": 314, 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calcium-binding site transitions between human and murine CD23.", "journal": "FEBS open bio", "date": "2021", "authors": "Ilkow VF, Davies AM, Dhaliwal B, Beavil AJ, Sutton BJ, McDonnell JM", "reference": { "type": "PubMed", "id": "34075727", "url": "https://pubmed.ncbi.nlm.nih.gov/34075727" }, "referenced_glycans": [], "referenced_proteins": [ { "uniprot_canonical_ac": "P06734-1", "protein_name": "Low affinity immunoglobulin epsilon Fc receptor", "gene_name": "FCER2", "tax_name": "Human" } ], "species": [ { "name": "Homo sapiens", "taxid": 9606, "evidence": [ { "database": "UniProtKB", "id": "P06734", "url": "https://www.uniprot.org/uniprotkb/P06734" } ], "common_name": "Human", "glygen_name": "Human", "reference_species": "Homo sapiens [9606]" } ], "record_id": "pubmed.34075727", "abstract": "", "glycosylation": [], "mutagenesis": [], "snv": [], "phosphorylation": [], "glycation": [], "section_stats": [ { "table_id": "referenced_proteins", "table_stats": [ { "field": "total", 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Leishmania major by human macrophages is mediated by nitric oxide induced after ligation of the Fc epsilon RII/CD23 surface antigen.", "journal": "Proceedings of the National Academy of Sciences of the United States of America", "date": "1995", "authors": "Vouldoukis I, Riveros-Moreno V, Dugas B, Ouaaz F, Becherel P, Debre P, Moncada S, Mossalayi MD", "reference": { "type": "PubMed", "id": "7544003", "url": "https://pubmed.ncbi.nlm.nih.gov/7544003" }, "referenced_glycans": [], "referenced_proteins": [ { "uniprot_canonical_ac": "P06734-1", "protein_name": "Low affinity immunoglobulin epsilon Fc receptor", "gene_name": "FCER2", "tax_name": "Human" }, { "uniprot_canonical_ac": "P01854-2", "protein_name": "Immunoglobulin heavy constant epsilon", "gene_name": "IGHE", "tax_name": "Human" } ], "species": [ { "name": "Homo sapiens", "taxid": 9606, "evidence": [ { "database": "UniProtKB", "id": "P06734", "url": "https://www.uniprot.org/uniprotkb/P06734" } ], "common_name": "Human", 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"table_stats": [ { "field": "total", "count": 0 }, { "field": "total_sites", "count": 0 }, { "field": "n_linked_sites", "count": 0 }, { "field": "o_linked_sites", "count": 0 }, { "field": "n_linked_glycan_sites", "count": 0 }, { "field": "o_linked_glycan_sites", "count": 0 }, { "field": "n_linked_glycans", "count": 0 }, { "field": "o_linked_glycans", "count": 0 } ], "sort_fields": [] }, { "table_id": "glycosylation_automatic_literature_mining", "table_stats": [ { "field": "total", "count": 0 }, { "field": "total_sites", "count": 0 }, { "field": "n_linked_sites", "count": 0 }, { "field": "o_linked_sites", "count": 0 }, { "field": "n_linked_glycan_sites", "count": 0 }, { "field": "o_linked_glycan_sites", "count": 0 }, { "field": "n_linked_glycans", "count": 0 }, { "field": "o_linked_glycans", "count": 0 } ], "sort_fields": [] } ] }, { "title": "Modeling of the lectin-homology domains of the human and murine low-affinity Fc epsilon receptor (Fc epsilon RII/CD23).", "journal": "Receptor", "date": "1993", "authors": "Padlan E A, Helm B A", "reference": { "type": "PubMed", "id": "8142907", "url": "https://pubmed.ncbi.nlm.nih.gov/8142907" }, "referenced_glycans": [], "referenced_proteins": [ { "uniprot_canonical_ac": "P06734-1", "protein_name": "Low affinity immunoglobulin epsilon Fc receptor", "gene_name": "FCER2", "tax_name": "Human" }, { "uniprot_canonical_ac": "P20693-1", "protein_name": "Low affinity immunoglobulin epsilon Fc receptor", "gene_name": "Fcer2a; Fcer2", "tax_name": "Mouse" } ], "species": [ { "name": "Homo sapiens", "taxid": 9606, "evidence": [ { "database": "UniProtKB", "id": "P06734", "url": "https://www.uniprot.org/uniprotkb/P06734" } ], "common_name": "Human", "glygen_name": "Human", "reference_species": "Homo sapiens [9606]" } ], "record_id": "pubmed.8142907", "abstract": "", "glycosylation": [], "mutagenesis": [], "snv": [], "phosphorylation": [], "glycation": [], "section_stats": [ { "table_id": "referenced_proteins", "table_stats": [ { "field": 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"protein_name": "Low affinity immunoglobulin epsilon Fc receptor", "gene_name": "FCER2", "tax_name": "Human" } ], "species": [ { "name": "Homo sapiens", "taxid": 9606, "evidence": [ { "database": "UniProtKB", "id": "P06734", "url": "https://www.uniprot.org/uniprotkb/P06734" } ], "common_name": "Human", "glygen_name": "Human", "reference_species": "Homo sapiens [9606]" } ], "record_id": "pubmed.8745401", "abstract": "", "glycosylation": [], "mutagenesis": [], "snv": [], "phosphorylation": [], "glycation": [], "section_stats": [ { "table_id": "referenced_proteins", "table_stats": [ { "field": "total", "count": 1 } ], "sort_fields": [ "uniprot_canonical_ac", "protein_name", "gene_name", "tax_name" ] }, { "table_id": "referenced_glycans", "table_stats": [ { "field": "total", "count": 0 } ], "sort_fields": [] }, { "table_id": "glycosylation", "table_stats": [ { "field": "total", "count": 0 }, { "field": "total_sites", "count": 0 }, { "field": "n_linked_sites", "count": 0 }, { "field": 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"count": 0 }, { "field": "o_linked_sites", "count": 0 }, { "field": "n_linked_glycan_sites", "count": 0 }, { "field": "o_linked_glycan_sites", "count": 0 }, { "field": "n_linked_glycans", "count": 0 }, { "field": "o_linked_glycans", "count": 0 } ], "sort_fields": [] }, { "table_id": "glycosylation_predicted", "table_stats": [ { "field": "total", "count": 0 }, { "field": "total_sites", "count": 0 }, { "field": "n_linked_sites", "count": 0 }, { "field": "o_linked_sites", "count": 0 }, { "field": "n_linked_glycan_sites", "count": 0 }, { "field": "o_linked_glycan_sites", "count": 0 }, { "field": "n_linked_glycans", "count": 0 }, { "field": "o_linked_glycans", "count": 0 } ], "sort_fields": [] }, { "table_id": "glycosylation_automatic_literature_mining", "table_stats": [ { "field": "total", "count": 0 }, { "field": "total_sites", "count": 0 }, { "field": "n_linked_sites", "count": 0 }, { "field": "o_linked_sites", "count": 0 }, { "field": "n_linked_glycan_sites", "count": 0 }, { "field": 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