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                        "count": 0
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                        "field": "n_linked_glycan_sites",
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                    {
                        "field": "n_linked_glycans",
                        "count": 0
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                    {
                        "field": "o_linked_glycans",
                        "count": 0
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                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
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                        "field": "total",
                        "count": 0
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                    {
                        "field": "total_sites",
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                ],
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            {
                "table_id": "glycosylation_reported",
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                        "field": "total",
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                        "field": "total_sites",
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                    {
                        "field": "o_linked_sites",
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                    {
                        "field": "n_linked_glycan_sites",
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                    {
                        "field": "o_linked_glycan_sites",
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                    {
                        "field": "n_linked_glycans",
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                    {
                        "field": "o_linked_glycans",
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                ],
                "sort_fields": []
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            {
                "table_id": "glycosylation_reported_with_glycan",
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                        "field": "total",
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                        "field": "o_linked_glycans",
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            {
                "table_id": "glycosylation_automatic_literature_mining",
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    },
    {
        "title": "Phosphorylation of the human ubiquitin-conjugating enzyme, CDC34, by casein kinase 2.",
        "journal": "The Journal of biological chemistry",
        "date": "2001",
        "authors": "Block K, Boyer TG, Yew PR",
        "reference": {
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            "id": "11546811",
            "url": "https://pubmed.ncbi.nlm.nih.gov/11546811"
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                "name": "Homo sapiens",
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                        "url": "https://www.uniprot.org/uniprotkb/P49427"
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                ],
                "common_name": "Human",
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                "reference_species": "Homo sapiens [9606]"
            }
        ],
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            {
                "start_pos": 203,
                "end_pos": 203,
                "sequence_org": "S",
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                "comment": "Abolishes phosphorylation by CK2. Impairs nuclear localization; when associated with A-222; A-231; A-233 and A-236.",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P49427",
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                    {
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                        "id": "11546811",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/11546811"
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                ],
                "uniprot_canonical_ac": "P49427-1"
            },
            {
                "start_pos": 222,
                "end_pos": 222,
                "sequence_org": "S",
                "sequence_mut": "A",
                "comment": "Abolishes phosphorylation by CK2. Impairs nuclear localization; when associated with A-203; A-231; A-233 and A-236.",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P49427",
                        "url": "https://www.uniprot.org/uniprotkb/P49427"
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                    {
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                        "url": "https://pubmed.ncbi.nlm.nih.gov/11546811"
                    }
                ],
                "uniprot_canonical_ac": "P49427-1"
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            {
                "start_pos": 231,
                "end_pos": 231,
                "sequence_org": "S",
                "sequence_mut": "A",
                "comment": "Abolishes phosphorylation by CK2. Impairs nuclear localization; when associated with A-203; A-222; A-233 and A-236.",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P49427",
                        "url": "https://www.uniprot.org/uniprotkb/P49427"
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                    {
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                        "id": "12037680",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/12037680"
                    },
                    {
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                        "id": "11546811",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/11546811"
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                ],
                "uniprot_canonical_ac": "P49427-1"
            },
            {
                "start_pos": 233,
                "end_pos": 233,
                "sequence_org": "T",
                "sequence_mut": "A",
                "comment": "Abolishes phosphorylation by CK2. Impairs nuclear localization; when associated with A-203; A-222; A-231 and A-236.",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P49427",
                        "url": "https://www.uniprot.org/uniprotkb/P49427"
                    },
                    {
                        "database": "PubMed",
                        "id": "11546811",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/11546811"
                    }
                ],
                "uniprot_canonical_ac": "P49427-1"
            },
            {
                "start_pos": 236,
                "end_pos": 236,
                "sequence_org": "S",
                "sequence_mut": "A",
                "comment": "Abolishes phosphorylation by CK2. Impairs nuclear localization; when associated with A-203; A-222; A-231 and A-233.",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P49427",
                        "url": "https://www.uniprot.org/uniprotkb/P49427"
                    },
                    {
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                        "id": "11546811",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/11546811"
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                ],
                "uniprot_canonical_ac": "P49427-1"
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                        "id": "P49427",
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                        "id": "11546811",
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                ],
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                "uniprot_canonical_ac": "P49427-1"
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            {
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                    {
                        "database": "iPTMnet",
                        "id": "P49427",
                        "url": "http://research.bioinformatics.udel.edu/iptmnet/entry/P49427"
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                    {
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                        "id": "11546811",
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                ],
                "site_lbl": "Ser203",
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            {
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                    {
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                    {
                        "database": "PubMed",
                        "id": "11546811",
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                        "id": "17461777",
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                ],
                "site_lbl": "Ser203",
                "uniprot_canonical_ac": "P49427-1"
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            {
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                "kinase_uniprot_canonical_ac": "P67870-1",
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                        "id": "P49427",
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                    {
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                        "id": "11546811",
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                ],
                "site_lbl": "Ser222",
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            {
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                        "id": "P49427",
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                    {
                        "database": "PubMed",
                        "id": "11546811",
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                ],
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                "uniprot_canonical_ac": "P49427-1"
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            {
                "start_pos": 222,
                "end_pos": 222,
                "kinase_uniprot_canonical_ac": "",
                "kinase_gene_name": "",
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                        "id": "P49427",
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                    {
                        "database": "iPTMnet",
                        "id": "P49427",
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                    {
                        "database": "PubMed",
                        "id": "11546811",
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                    {
                        "database": "PubMed",
                        "id": "16123592",
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                    {
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                ],
                "site_lbl": "Ser222",
                "uniprot_canonical_ac": "P49427-1"
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            {
                "start_pos": 231,
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                        "id": "P49427",
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                    {
                        "database": "PubMed",
                        "id": "11546811",
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                ],
                "site_lbl": "Ser231",
                "uniprot_canonical_ac": "P49427-1"
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            {
                "start_pos": 231,
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                "kinase_uniprot_canonical_ac": "P68400-1",
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                "evidence": [
                    {
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                        "id": "P49427",
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                    {
                        "database": "PubMed",
                        "id": "11546811",
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                ],
                "site_lbl": "Ser231",
                "uniprot_canonical_ac": "P49427-1"
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            {
                "start_pos": 231,
                "end_pos": 231,
                "kinase_uniprot_canonical_ac": "",
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                "residue": "Ser",
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                        "id": "P49427",
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                    {
                        "database": "iPTMnet",
                        "id": "P49427",
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                    {
                        "database": "PubMed",
                        "id": "11546811",
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                    {
                        "database": "PubMed",
                        "id": "16123592",
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                    {
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                        "id": "12037680",
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                    {
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                        "id": "17461777",
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                "uniprot_canonical_ac": "P49427-1"
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            {
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                "kinase_uniprot_canonical_ac": "P67870-1",
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                        "id": "11546811",
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                "start_pos": 233,
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        "record_id": "pubmed.11546811",
        "abstract": "",
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    {
        "title": "let-7 Overexpression leads to an increased fraction of cells in G2/M, direct down-regulation of Cdc34, and stabilization of Wee1 kinase in primary fibroblasts.",
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                                "url": "https://monarchinitiative.org/disease/MONDO:0009929",
                                "name": "SMDP1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009929",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009929",
                                "name": "interstitial lung disease due to SP-B dysfunction",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009929",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009929",
                                "name": "interstitial lung disease due to surfactant Protein B deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009929",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009929",
                                "name": "neonatal acute respiratory distress due to SP-B deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009929",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009929",
                                "name": "neonatal acute respiratory distress due to surfactant protein B deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009929",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009929",
                                "name": "pulmonary alveolar proteinosis, congenital, 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009929",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009929",
                                "name": "surfactant metabolism dysfunction, pulmonary, 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009929",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009929",
                                "name": "surfactant metabolism dysfunction, pulmonary, type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009929",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009929",
                                "name": "pulmonary surfactant protein B, deficiency of",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010424",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010424",
                                "name": "surfactant metabolism dysfunction, pulmonary, 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010424",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010424",
                                "name": "surfactant metabolism dysfunction, pulmonary, 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010424",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010424",
                                "name": "surfactant metabolism dysfunction, pulmonary, type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010424",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010424",
                                "name": "SMDP4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012582",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012582",
                                "name": "interstitial lung disease due to ABCA3 deficiency",
                                "description": "Interstitial lung disease due to ABCA3 deficiency is a rare genetic respiratory disease characterized by a variable clinical outcome ranging from a fatal respiratory distress syndrome in the neonatal period to chronic interstitial lung disease developing in infancy or childhood with chronic cough, rapid breathing, shortness of breath and recurrent pulmonary infections. Clinical manifestations of respiratory failure include grunting, intercostal retractions, nasal flaring, cyanosis, and progressive dyspnea."
                            },
                            {
                                "id": "MONDO:0012582",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012582",
                                "name": "interstitial lung disease due to ABCA3 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012582",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012582",
                                "name": "interstitial lung disease due to ATP-binding cassette subfamily A member 3 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012582",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012582",
                                "name": "surfactant metabolism dysfunction, pulmonary, type 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012582",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012582",
                                "name": "SMDP3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012582",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012582",
                                "name": "surfactant metabolism dysfunction, pulmonary, 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013712",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013712",
                                "name": "surfactant metabolism dysfunction, pulmonary, 5",
                                "description": "Any hereditary pulmonary alveolar proteinosis in which the cause of the disease is a mutation in the CSF2RB gene."
                            },
                            {
                                "id": "MONDO:0013712",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013712",
                                "name": "CSF2RB hereditary pulmonary alveolar proteinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013712",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013712",
                                "name": "hereditary pulmonary alveolar proteinosis caused by mutation in CSF2RB",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013712",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013712",
                                "name": "surfactant metabolism dysfunction, pulmonary, 5",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013712",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013712",
                                "name": "surfactant metabolism dysfunction, pulmonary, type 5",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013712",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013712",
                                "name": "SMDP5",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0024465",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0024465",
                                "name": "surfactant metabolism dysfunction, pulmonary, 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0024465",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0024465",
                                "name": "SMDP2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0024465",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0024465",
                                "name": "desquamative interstitial pneumonitis due to surfactant Protein C deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0024465",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0024465",
                                "name": "interstitial lung disease due to surfactant Protein C deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0024465",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0024465",
                                "name": "pulmonary alveolar proteinosis, congenital, 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0024465",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0024465",
                                "name": "surfactant metabolism dysfunction, pulmonary, 2",
                                "description": ""
                            },
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                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/265120",
                                "name": "Pulmonary surfactant metabolism dysfunction 1",
                                "description": "Pulmonary surfactant metabolism dysfunction 1"
                            },
                            {
                                "id": "MIM:300770",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/300770",
                                "name": "Pulmonary surfactant metabolism dysfunction 4",
                                "description": "Pulmonary surfactant metabolism dysfunction 4"
                            },
                            {
                                "id": "MIM:610921",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/610921",
                                "name": "Pulmonary surfactant metabolism dysfunction 3",
                                "description": "Pulmonary surfactant metabolism dysfunction 3"
                            },
                            {
                                "id": "MIM:614370",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/614370",
                                "name": "Pulmonary surfactant metabolism dysfunction 5",
                                "description": "Pulmonary surfactant metabolism dysfunction 5"
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                                "id": "MIM:610913",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/610913",
                                "name": "Pulmonary surfactant metabolism dysfunction 2",
                                "description": "Pulmonary surfactant metabolism dysfunction 2"
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