{
    "uniprot_canonical_ac": "A0A0G2JUB4-1",
    "uniprot_ac": "A0A0G2JUB4",
    "uniprot_id": "A0A0G2JUB4_RAT",
    "mass": {
        "chemical_mass": 41319.0,
        "monoisotopic_mass": 41319.0
    },
    "refseq": {},
    "gene_names": [
        {
            "name": "Acat2l1",
            "resource": "UniProtKB",
            "type": "recommended",
            "url": "https://www.uniprot.org/uniprot/A0A0G2JUB4",
            "id": "A0A0G2JUB4"
        },
        {
            "name": "RGD1562948",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/A0A0G2JUB4",
            "id": "A0A0G2JUB4"
        }
    ],
    "protein_names": [
        {
            "name": "Acetyl-CoA acetyltransferase 2-like 1",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "A0A0G2JUB4"
        }
    ],
    "function": [],
    "disease": [
        {
            "disease_id": "DOID:3393",
            "recommended_name": {
                "id": "DOID:3393",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:3393",
                "name": "coronary artery disease",
                "description": "An artery disease that is characterized by plaque building up along the inner walls of the arteries of the heart resulting in a narrowing of the arteries and a reduced blood supply to the cardiac muscles."
            },
            "synonyms": [
                {
                    "id": "DOID:3393",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:3393",
                    "name": "CHD",
                    "description": ""
                },
                {
                    "id": "DOID:3393",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:3393",
                    "name": "Coronary disease",
                    "description": ""
                },
                {
                    "id": "DOID:3393",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:3393",
                    "name": "coronary arteriosclerosis",
                    "description": ""
                },
                {
                    "id": "DOID:3393",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:3393",
                    "name": "coronary heart disease",
                    "description": ""
                },
                {
                    "id": "MONDO:0012010",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012010",
                    "name": "coronary heart disease, susceptibility to, 4",
                    "description": ""
                },
                {
                    "id": "MONDO:0012010",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012010",
                    "name": "coronary heart disease, susceptibility to, 4",
                    "description": ""
                },
                {
                    "id": "MONDO:0012010",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012010",
                    "name": "coronary heart disease, susceptibility to, type 4",
                    "description": ""
                },
                {
                    "id": "MONDO:0012010",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012010",
                    "name": "Chds4",
                    "description": ""
                },
                {
                    "id": "MONDO:0012009",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012009",
                    "name": "coronary heart disease, susceptibility to, 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0012009",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012009",
                    "name": "coronary heart disease, susceptibility to, 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0012009",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012009",
                    "name": "coronary heart disease, susceptibility to, type 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0012009",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012009",
                    "name": "Chds2",
                    "description": ""
                },
                {
                    "id": "MONDO:0013671",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013671",
                    "name": "hydatidiform mole, recurrent, 2",
                    "description": "Any complete hydatidiform mole in which the cause of the disease is a mutation in the KHDC3L gene."
                },
                {
                    "id": "MONDO:0013671",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013671",
                    "name": "KHDC3L complete hydatidiform mole",
                    "description": ""
                },
                {
                    "id": "MONDO:0013671",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013671",
                    "name": "complete hydatidiform mole caused by mutation in KHDC3L",
                    "description": ""
                },
                {
                    "id": "MONDO:0013671",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013671",
                    "name": "hydatidiform Mole, recurrent, type 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0013671",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013671",
                    "name": "hydatidiform mole, recurrent, 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0013671",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013671",
                    "name": "HYDM2",
                    "description": ""
                },
                {
                    "id": "MONDO:0013671",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013671",
                    "name": "hydatidiform MOLE, recurrent, 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0013671",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013671",
                    "name": "hydatidiform Mole, complete",
                    "description": ""
                },
                {
                    "id": "MONDO:0011817",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011817",
                    "name": "coronary heart disease, susceptibility to, 1",
                    "description": "Any coronary artery disease in which the cause of the disease is a mutation in the CX3CR1 gene."
                },
                {
                    "id": "MONDO:0011817",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011817",
                    "name": "CX3CR1 coronary artery disease",
                    "description": ""
                },
                {
                    "id": "MONDO:0011817",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011817",
                    "name": "coronary artery disease caused by mutation in CX3CR1",
                    "description": ""
                },
                {
                    "id": "MONDO:0011817",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011817",
                    "name": "coronary artery disease, resistance to",
                    "description": ""
                },
                {
                    "id": "MONDO:0011817",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011817",
                    "name": "coronary heart disease, susceptibility to",
                    "description": ""
                },
                {
                    "id": "MONDO:0011817",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011817",
                    "name": "coronary heart disease, susceptibility to, 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0011817",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011817",
                    "name": "coronary heart disease, susceptibility to, type 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0011817",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011817",
                    "name": "Chds1",
                    "description": ""
                },
                {
                    "id": "MONDO:0012011",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012011",
                    "name": "coronary artery disease, autosomal dominant, 1",
                    "description": "Any coronary artery disease in which the cause of the disease is a mutation in the MEF2A gene."
                },
                {
                    "id": "MONDO:0012011",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012011",
                    "name": "MEF2A coronary artery disease",
                    "description": ""
                },
                {
                    "id": "MONDO:0012011",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012011",
                    "name": "coronary artery disease caused by mutation in MEF2A",
                    "description": ""
                },
                {
                    "id": "MONDO:0012011",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012011",
                    "name": "coronary artery disease, autosomal dominant, 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0012011",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012011",
                    "name": "coronary artery disease, autosomal dominant, type 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0012011",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012011",
                    "name": "ADCAD1",
                    "description": ""
                },
                {
                    "id": "MONDO:0012011",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012011",
                    "name": "coronary artery disease with myocardial infarction",
                    "description": ""
                },
                {
                    "id": "MONDO:0012586",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012586",
                    "name": "coronary artery disease, autosomal dominant 2",
                    "description": "Any coronary artery disease in which the cause of the disease is a mutation in the LRP6 gene."
                },
                {
                    "id": "MONDO:0012586",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012586",
                    "name": "LRP6 coronary artery disease",
                    "description": ""
                },
                {
                    "id": "MONDO:0012586",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012586",
                    "name": "coronary artery disease caused by mutation in LRP6",
                    "description": ""
                },
                {
                    "id": "MONDO:0012586",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012586",
                    "name": "coronary artery disease, autosomal dominant 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0012586",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012586",
                    "name": "coronary artery disease, autosomal dominant type 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0012586",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012586",
                    "name": "coronary artery disease, autosomal dominant, 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0012586",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012586",
                    "name": "ADCAD2",
                    "description": ""
                },
                {
                    "id": "MONDO:0012788",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012788",
                    "name": "coronary heart disease, susceptibility to, 9",
                    "description": ""
                },
                {
                    "id": "MONDO:0012788",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012788",
                    "name": "CHDS9",
                    "description": ""
                },
                {
                    "id": "MONDO:0012788",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012788",
                    "name": "coronary heart disease, susceptibility to, 9",
                    "description": ""
                },
                {
                    "id": "MONDO:0010331",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010331",
                    "name": "coronary heart disease, susceptibility to, 3",
                    "description": ""
                },
                {
                    "id": "MONDO:0010331",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010331",
                    "name": "coronary heart disease, susceptibility to, 3",
                    "description": ""
                },
                {
                    "id": "MONDO:0010331",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010331",
                    "name": "coronary heart disease, susceptibility to, type 3",
                    "description": ""
                },
                {
                    "id": "MONDO:0010331",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010331",
                    "name": "Chds3",
                    "description": ""
                },
                {
                    "id": "MONDO:0012628",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012628",
                    "name": "coronary heart disease, susceptibility to, 8",
                    "description": ""
                },
                {
                    "id": "MONDO:0012628",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012628",
                    "name": "CHDS8",
                    "description": ""
                },
                {
                    "id": "MONDO:0012628",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012628",
                    "name": "coronary heart disease, susceptibility to, 8",
                    "description": ""
                },
                {
                    "id": "MIM:614293",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/614293",
                    "name": "Hydatidiform mole, recurrent, 2",
                    "description": "Hydatidiform mole, recurrent, 2"
                },
                {
                    "id": "MIM:608320",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/608320",
                    "name": "Coronary artery disease, autosomal dominant, 1",
                    "description": "Coronary artery disease, autosomal dominant, 1"
                },
                {
                    "id": "MIM:610947",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/610947",
                    "name": "Coronary artery disease, autosomal dominant, 2",
                    "description": "Coronary artery disease, autosomal dominant, 2"
                }
            ],
            "evidence": [
                {
                    "id": "3393",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:3393"
                }
            ]
        }
    ],
    "snv": [],
    "mutagenesis": [],
    "expression_tissue": [],
    "expression_disease": [],
    "species": [
        {
            "name": "Rattus norvegicus",
            "taxid": 10116,
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "A0A0G2JUB4",
                    "url": "https://www.uniprot.org/uniprot/A0A0G2JUB4"
                }
            ],
            "common_name": "Rat"
        }
    ],
    "gene": [
        {
            "name": "Acat2l1",
            "url": "https://www.uniprot.org/uniprot/A0A0G2JUB4",
            "locus": {
                "chromosome": "1",
                "start_pos": 47829151,
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                        "database": "Ensembl Gene",
                        "id": "ENSRNOG00000013975",
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                ]
            }
        }
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    "crossref": [
        {
            "id": "ENSRNOG00000013975",
            "url": "https://bgee.org/?page=gene&gene_id=ENSRNOG00000013975",
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            "categories": [
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            ]
        },
        {
            "id": "ENSRNOG00000019189",
            "url": "https://bgee.org/?page=gene&gene_id=ENSRNOG00000019189",
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            "categories": [
                "Gene Expression"
            ]
        },
        {
            "id": "cd00751",
            "url": "https://www.ncbi.nlm.nih.gov/Structure/cdd/cddsrv.cgi?uid=cd00751",
            "database": "CDD",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR002155",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR002155",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR016039",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR016039",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR020610",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR020610",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR020613",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR020613",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR020616",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR020616",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR020617",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR020617",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "MSQAEFY",
            "url": "https://omabrowser.org/oma/group/MSQAEFY/",
            "database": "OMA",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PTHR18919",
            "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR18919",
            "database": "PANTHER",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PTHR18919:SF81",
            "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR18919:SF81",
            "database": "PANTHER",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PF00108",
            "url": "http://pfam.xfam.org/family/PF00108",
            "database": "Pfam",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PF02803",
            "url": "http://pfam.xfam.org/family/PF02803",
            "database": "Pfam",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "1562948",
            "url": "http://rgd.mcw.edu/tools/genes/genes_view.cgi?id=1562948",
            "database": "RGD",
            "categories": [
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            ]
        },
        {
            "id": "A0A0G2JUB4",
            "url": "https://www.uniprot.org/uniprot/A0A0G2JUB4",
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            "categories": [
                "Protein"
            ]
        },
        {
            "id": "A0A0G2JUB4-1",
            "url": "https://www.uniprot.org/uniprot/A0A0G2JUB4-1",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "D3ZKB6",
            "url": "https://www.uniprot.org/uniprot/D3ZKB6",
            "database": "UniProtKB",
            "categories": [
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            ]
        },
        {
            "id": "D3ZKB6-1",
            "url": "https://www.uniprot.org/uniprot/D3ZKB6-1",
            "database": "UniProtKB",
            "categories": [
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            ]
        }
    ],
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        "sequence": "MNRSSDPEVTVSAARSSIGSFSGALFTVPVHDLGTTVIKEVLQRAKVAPEEVSEVIFGHVLTAGCGQNPTRQASVGAGIPYSVPAWSCQMICGSGLKAVCLAAQSIAMGDSTIVVAGGMENMSKAPHLAHLRSGVKMGEVPLADSILCDGLTDAFHNYHMGITAENVAKKWQVSREAQDRVAVVSQNRAEHAQKAGHFDKEIVPVHVSSRKGLAEVKIDEFPRHGSNLEAMSKLKPYFLTDGTGTVTSANATGMNDGAAAVVLMKKTEAESRMLKPLAQVVSWSQAGVEPSVMGVGPIPAIKQAVAKAGWSLPDVDVFEINEAYAALSVAIAKELGLNPEKVNIDGGAIALGHPLGASGCRILVTLLHTLERVGGTRGVAALCIGGGMGIAMCVQRG",
        "length": 397,
        "header": "tr|A0A0G2JUB4-1|A0A0G2JUB4_RAT Isoform 1 of Acetyl-CoA acetyltransferase 2-like 1  OS=Rattus norvegicus OX=10116 GN=Acat2l1 PE=3 SV=2 CANONICAL=A0A0G2JUB4-1"
    },
    "isoforms": [
        {
            "isoform_ac": "A0A0G2JUB4-1",
            "url": "",
            "sequence": {
                "sequence": "MNRSSDPEVTVSAARSSIGSFSGALFTVPVHDLGTTVIKEVLQRAKVAPEEVSEVIFGHVLTAGCGQNPTRQASVGAGIPYSVPAWSCQMICGSGLKAVCLAAQSIAMGDSTIVVAGGMENMSKAPHLAHLRSGVKMGEVPLADSILCDGLTDAFHNYHMGITAENVAKKWQVSREAQDRVAVVSQNRAEHAQKAGHFDKEIVPVHVSSRKGLAEVKIDEFPRHGSNLEAMSKLKPYFLTDGTGTVTSANATGMNDGAAAVVLMKKTEAESRMLKPLAQVVSWSQAGVEPSVMGVGPIPAIKQAVAKAGWSLPDVDVFEINEAYAALSVAIAKELGLNPEKVNIDGGAIALGHPLGASGCRILVTLLHTLERVGGTRGVAALCIGGGMGIAMCVQRG",
                "length": 397,
                "header": "tr|A0A0G2JUB4-1|A0A0G2JUB4_RAT Isoform 1 of Acetyl-CoA acetyltransferase 2-like 1  OS=Rattus norvegicus OX=10116 GN=Acat2l1 PE=3 SV=2 CANONICAL=A0A0G2JUB4-1"
            },
            "locus": {
                "chromosome": "1",
                "start_pos": 47828974,
                "end_pos": 47803947,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "ENSRNOT00000077707.2",
                        "url": "https://www.ensembl.org/id/ENSRNOT00000077707.2"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSRNOP00000069035.2",
                        "url": "https://www.ensembl.org/id/ENSRNOP00000069035.2"
                    }
                ]
            }
        },
        {
            "isoform_ac": "D3ZKB6-1",
            "url": "",
            "sequence": {
                "sequence": "MNRRSNQVIIVLAARTAIGSFSGALFTVPVHDLGTTVIKEVLQRAKVAPEEVSEVIFGHVLTAGCGQNPTRQASVGAGIPYSVPAWSCQMICGSGLKAVCLAAQSIAMGDSTIVVAGGMENMSKAPHLAHLRSGVKMGEVPLADSILCDGLTDAFHNYHMGITAENVAKKWQVSREAQDRVAVVSQNRAEHAQKAGHFDKEIVPVHVSSRKGLAEVKIDEFPRHGSNLEAMSKLKPYFLTDGTGTVTSANATGMNDGAAAVVLMKKTEAESRMLKPLAQVVSWSQAGVEPSVMGVGPIPAIKQAVAKAGWSLPDVDVFEINEAYAALSVAIAKELGLNPEKVNIDGGAIALGHPLGASGCRILVTLLHTLERVGGTRGVAALCIGGGMGIAMCVQRG",
                "length": 397,
                "header": "tr|D3ZKB6-1|D3ZKB6_RAT Computationally mapped isoform of Acetyl-CoA acetyltransferase 2-like 1  OS=Rattus norvegicus OX=10116 GN=Acat2l1 PE=3 SV=3 CANONICAL=A0A0G2JUB4-1"
            },
            "locus": {
                "chromosome": "1",
                "start_pos": 47828974,
                "end_pos": 47812083,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "ENSRNOT00000018934.7",
                        "url": "https://www.ensembl.org/id/ENSRNOT00000018934.7"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSRNOP00000018934.6",
                        "url": "https://www.ensembl.org/id/ENSRNOP00000018934.6"
                    }
                ]
            }
        }
    ],
    "glycosylation": [],
    "phosphorylation": [],
    "glycation": [],
    "keywords": [],
    "publication": [],
    "pathway": [],
    "orthologs": [],
    "go_annotation": {
        "categories": [
            {
                "name": "Cellular Component",
                "total": 1,
                "go_terms": [
                    {
                        "name": "mitochondrion",
                        "id": "GO:0005739",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005739",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2JUB4",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2JUB4"
                            }
                        ],
                        "pmid": ""
                    }
                ]
            },
            {
                "name": "Biological Process",
                "total": 1,
                "go_terms": [
                    {
                        "name": "fatty acid beta-oxidation",
                        "id": "GO:0006635",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006635",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2JUB4",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2JUB4"
                            }
                        ],
                        "pmid": ""
                    }
                ]
            },
            {
                "name": "Molecular Function",
                "total": 1,
                "go_terms": [
                    {
                        "name": "acetyl-CoA C-acetyltransferase activity",
                        "id": "GO:0003985",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003985",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2JUB4",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2JUB4"
                            }
                        ],
                        "pmid": ""
                    }
                ]
            }
        ]
    },
    "pro_annotation": [],
    "site_annotation": [
        {
            "start_pos": 121,
            "end_pos": 123,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 250,
            "end_pos": 252,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 2,
            "end_pos": 4,
            "annotation": "n_glycosylation_sequon"
        }
    ],
    "ptm_annotation": [],
    "interactions": [],
    "reactions": [],
    "reaction_participants": [],
    "reaction_enzymes": [],
    "biomarkers": [],
    "synthesized_glycans": [],
    "cluster_types": [
        {
            "name": "isoformset.uniprotkb",
            "label": "Isoforms"
        }
    ],
    "section_stats": [
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                {
                    "field": "total_sites",
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                    "field": "n_linked_glycans",
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                },
                {
                    "field": "n_linked_glycan_sites",
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                },
                {
                    "field": "o_linked_glycans",
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                    "field": "o_linked_glycan_sites",
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            ],
            "sort_fields": []
        },
        {
            "table_id": "glycosylation_reported",
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        {
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        {
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                {
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            ],
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        {
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        {
            "table_id": "snv_disease",
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}