{
    "uniprot_canonical_ac": "A0A0B4LGG8-1",
    "uniprot_ac": "A0A0B4LGG8",
    "uniprot_id": "A0A0B4LGG8_DROME",
    "mass": {
        "chemical_mass": 155860.0,
        "monoisotopic_mass": 155860.0
    },
    "refseq": {
        "ac": "NP_001286830",
        "name": "uncharacterized protein, isoform C",
        "summary": "",
        "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001286830"
    },
    "gene_names": [
        {
            "name": "Dmel\\CG3328",
            "resource": "UniProtKB",
            "type": "recommended",
            "url": "https://www.uniprot.org/uniprot/A0A0B4LGG8",
            "id": "A0A0B4LGG8"
        },
        {
            "name": "CG3328-RA",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/A0A0B4LGG8",
            "id": "A0A0B4LGG8"
        },
        {
            "name": "CG3328",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001286830",
            "id": "NP_001286830"
        },
        {
            "name": "CG3328",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/A0A0B4LGG8",
            "id": "A0A0B4LGG8"
        },
        {
            "name": "Dmel\\CG3328",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001286830",
            "id": "NP_001286830"
        },
        {
            "name": "Dmel_CG3328",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/A0A0B4LGG8",
            "id": "A0A0B4LGG8"
        }
    ],
    "protein_names": [
        {
            "name": "CG3328-PC",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001286830",
            "id": "NP_001286830"
        },
        {
            "name": "Uncharacterized protein, isoform C",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprotkb/A0A0B4LGG8/entry#names_and_taxonomy",
            "id": "A0A0B4LGG8"
        },
        {
            "name": "uncharacterized protein, isoform C",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001286830",
            "id": "NP_001286830"
        }
    ],
    "function": [],
    "disease": [
        {
            "disease_id": "DOID:0080634",
            "recommended_name": {
                "id": "DOID:0080634",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:0080634",
                "name": "nanophthalmos",
                "description": "A microphthalmia that is characterized by a small eye with a short axial length, severe hyperopia, an elevated lens/eye ratio, and a high incidence of angle-closure glaucoma."
            },
            "synonyms": [
                {
                    "id": "MONDO:0010836",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010836",
                    "name": "nanophthalmos 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0010836",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010836",
                    "name": "NNO1",
                    "description": ""
                },
                {
                    "id": "MONDO:0010836",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010836",
                    "name": "nanophthalmos 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0010836",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010836",
                    "name": "nanophthalmos-1",
                    "description": ""
                },
                {
                    "id": "MONDO:0010836",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010836",
                    "name": "Nanophthalmia 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0010836",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010836",
                    "name": "microphthalmos, simple, autosomal dominant",
                    "description": ""
                },
                {
                    "id": "MONDO:0010836",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010836",
                    "name": "nanophthalmos with high hyperopia and angle-closure glaucoma",
                    "description": ""
                },
                {
                    "id": "MONDO:0010836",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010836",
                    "name": "nanophthalmos, autosomal dominant",
                    "description": ""
                },
                {
                    "id": "MONDO:0012754",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012754",
                    "name": "nanophthalmos 3",
                    "description": ""
                },
                {
                    "id": "MONDO:0012754",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012754",
                    "name": "NNO3",
                    "description": ""
                },
                {
                    "id": "MONDO:0012754",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012754",
                    "name": "nanophthalmos 3",
                    "description": ""
                },
                {
                    "id": "MONDO:0012754",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012754",
                    "name": "Nanophthalmia 3",
                    "description": ""
                },
                {
                    "id": "MONDO:0012299",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012299",
                    "name": "nanophthalmos 2",
                    "description": "Any nanophthalmia in which the cause of the disease is a mutation in the MFRP gene."
                },
                {
                    "id": "MONDO:0012299",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012299",
                    "name": "MFRP nanophthalmia",
                    "description": ""
                },
                {
                    "id": "MONDO:0012299",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012299",
                    "name": "nanophthalmia caused by mutation in MFRP",
                    "description": ""
                },
                {
                    "id": "MONDO:0012299",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012299",
                    "name": "nanophthalmos 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0012299",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012299",
                    "name": "nanophthalmos type 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0012299",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012299",
                    "name": "NNO2",
                    "description": ""
                },
                {
                    "id": "MONDO:0012299",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012299",
                    "name": "Nanophthalmia 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0012299",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012299",
                    "name": "nanophthalmos, autosomal recessive",
                    "description": ""
                },
                {
                    "id": "MONDO:0014426",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014426",
                    "name": "nanophthalmos 4",
                    "description": "Any nanophthalmia in which the cause of the disease is a mutation in the TMEM98 gene."
                },
                {
                    "id": "MONDO:0014426",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014426",
                    "name": "TMEM98 nanophthalmia",
                    "description": ""
                },
                {
                    "id": "MONDO:0014426",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014426",
                    "name": "nanophthalmia caused by mutation in TMEM98",
                    "description": ""
                },
                {
                    "id": "MONDO:0014426",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014426",
                    "name": "nanophthalmos 4",
                    "description": ""
                },
                {
                    "id": "MONDO:0014426",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014426",
                    "name": "nanophthalmos type 4",
                    "description": ""
                },
                {
                    "id": "MONDO:0014426",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014426",
                    "name": "NNO4",
                    "description": ""
                },
                {
                    "id": "MONDO:0014426",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014426",
                    "name": "Nanophthalmia 4",
                    "description": ""
                },
                {
                    "id": "MIM:609549",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/609549",
                    "name": "Nanophthalmos 2",
                    "description": "Nanophthalmos 2"
                },
                {
                    "id": "MIM:615972",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/615972",
                    "name": "Nanophthalmos 4",
                    "description": "Nanophthalmos 4"
                }
            ],
            "evidence": [
                {
                    "id": "0080634",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:0080634"
                }
            ]
        },
        {
            "disease_id": "DOID:1405",
            "recommended_name": {
                "id": "DOID:1405",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:1405",
                "name": "primary angle-closure glaucoma",
                "description": "An angle-closure glaucoma characterized by closure of the anterior chamber angle by an intrinsic defect such that aqueous outflow is blocked and the intraocular pressure becomes inappropriately elevated leading to optic nerve damage and visual field loss. Primary angle-closure glaucoma has_symptom progressive peripheral vision loss, decreased vision, and pain, redness, and headache in acute cases. Primary angle closure glaucoma can be caused by anatomically narrow angle, defects in the trabecular meshwork, and iris abnormalities. Primary angle-closure glaucoma has a strong genetic component."
            },
            "synonyms": [
                {
                    "id": "DOID:1405",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:1405",
                    "name": "primary Angle Closure Glaucoma",
                    "description": ""
                }
            ],
            "evidence": [
                {
                    "id": "1405",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:1405"
                }
            ]
        },
        {
            "disease_id": "DOID:3526",
            "recommended_name": {
                "id": "DOID:3526",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:3526",
                "name": "cerebral infarction",
                "description": "A cerebrovascular disease that is characterized by an area of necrotic tissue in the brain resulting from a blockage or narrowing in the arteries supplying blood and oxygen to the brain."
            },
            "synonyms": [
                {
                    "id": "DOID:3526",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:3526",
                    "name": "CVA - Cerebral infarction",
                    "description": ""
                },
                {
                    "id": "DOID:3526",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:3526",
                    "name": "Cerebral infarct",
                    "description": ""
                },
                {
                    "id": "MONDO:0020671",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0020671",
                    "name": "obsolete susceptibility to ischemic stroke",
                    "description": ""
                },
                {
                    "id": "MONDO:0020671",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0020671",
                    "name": "cerebral infarction, susceptibility to",
                    "description": ""
                },
                {
                    "id": "MONDO:0020671",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0020671",
                    "name": "ischemic stroke, susceptibility to",
                    "description": ""
                },
                {
                    "id": "MONDO:0020671",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0020671",
                    "name": "stroke, ischemic, susceptibility to",
                    "description": ""
                },
                {
                    "id": "MONDO:0020671",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0020671",
                    "name": "stroke, susceptibility to",
                    "description": ""
                },
                {
                    "id": "MONDO:0020671",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0020671",
                    "name": "cerebral infarction",
                    "description": ""
                },
                {
                    "id": "MONDO:0020671",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0020671",
                    "name": "cerebrovascular accident",
                    "description": ""
                },
                {
                    "id": "MONDO:0020671",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0020671",
                    "name": "stroke, ischemic",
                    "description": ""
                },
                {
                    "id": "MIM:601367",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/601367",
                    "name": "Ischemic stroke",
                    "description": "Ischemic stroke"
                }
            ],
            "evidence": [
                {
                    "id": "3526",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:3526"
                }
            ]
        },
        {
            "disease_id": "DOID:3827",
            "recommended_name": {
                "id": "DOID:3827",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:3827",
                "name": "congenital diaphragmatic hernia",
                "description": "A diaphragm disease characterized by the lack of development of all or part of the diaphragm, which results in an abnormal opening that allows the stomach and intestines to move into the chest cavity and crowd the heart and lungs."
            },
            "synonyms": [
                {
                    "id": "DOID:3827",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:3827",
                    "name": "Diaphragmatic Hernia",
                    "description": ""
                },
                {
                    "id": "MONDO:0007719",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007719",
                    "name": "diaphragmatic hernia 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0007719",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007719",
                    "name": "diaphragmatic hernia, congenital 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0007719",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007719",
                    "name": "hernia, congenital diaphragmatic 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0007719",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007719",
                    "name": "DIH1",
                    "description": ""
                },
                {
                    "id": "MONDO:0007719",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007719",
                    "name": "diaphragm, complete agenesis of",
                    "description": ""
                },
                {
                    "id": "MONDO:0007719",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007719",
                    "name": "diaphragm, unilateral agenesis of",
                    "description": ""
                },
                {
                    "id": "MONDO:0007719",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007719",
                    "name": "diaphragmatic defect, congenital",
                    "description": ""
                },
                {
                    "id": "MONDO:0007719",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007719",
                    "name": "diaphragmatic hernia, congenital",
                    "description": ""
                },
                {
                    "id": "MONDO:0007719",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007719",
                    "name": "hemidiaphragm, agenesis of",
                    "description": ""
                },
                {
                    "id": "MONDO:0007719",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007719",
                    "name": "hernia, congenital diaphragmatic",
                    "description": ""
                },
                {
                    "id": "MONDO:0009103",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009103",
                    "name": "diaphragmatic hernia 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0009103",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009103",
                    "name": "diaphragmatic hernia 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0009103",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009103",
                    "name": "hernia, congenital diaphragmatic 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0009103",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009103",
                    "name": "DIH2",
                    "description": ""
                },
                {
                    "id": "MONDO:0012431",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012431",
                    "name": "diaphragmatic hernia 3",
                    "description": "Any congenital diaphragmatic hernia in which the cause of the disease is a mutation in the ZFPM2 gene."
                },
                {
                    "id": "MONDO:0012431",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012431",
                    "name": "ZFPM2 congenital diaphragmatic hernia",
                    "description": ""
                },
                {
                    "id": "MONDO:0012431",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012431",
                    "name": "congenital diaphragmatic hernia caused by mutation in ZFPM2",
                    "description": ""
                },
                {
                    "id": "MONDO:0012431",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012431",
                    "name": "diaphragmatic hernia 3",
                    "description": ""
                },
                {
                    "id": "MONDO:0012431",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012431",
                    "name": "diaphragmatic hernia type 3",
                    "description": ""
                },
                {
                    "id": "MONDO:0012431",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012431",
                    "name": "DIH3",
                    "description": ""
                },
                {
                    "id": "MIM:610187",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/610187",
                    "name": "Diaphragmatic hernia 3",
                    "description": "Diaphragmatic hernia 3"
                }
            ],
            "evidence": [
                {
                    "id": "3827",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:3827"
                }
            ]
        },
        {
            "disease_id": "DOID:5614",
            "recommended_name": {
                "id": "DOID:5614",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:5614",
                "name": "eye disease",
                "description": "An eye and adnexa disease that is located_in the eye."
            },
            "synonyms": [],
            "evidence": [
                {
                    "id": "5614",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:5614"
                }
            ]
        },
        {
            "disease_id": "DOID:9834",
            "recommended_name": {
                "id": "DOID:9834",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:9834",
                "name": "hyperopia",
                "description": "A refractive error that is characterized by rays of light entering the eye parallel to the optic axis are brought to a focus behind the retina, as a result of the eyeball being too short from front to back."
            },
            "synonyms": [
                {
                    "id": "DOID:9834",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:9834",
                    "name": "Far-sightedness",
                    "description": ""
                },
                {
                    "id": "DOID:9834",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:9834",
                    "name": "hypermetropia",
                    "description": ""
                },
                {
                    "id": "DOID:9834",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:9834",
                    "name": "farsightedness",
                    "description": ""
                }
            ],
            "evidence": [
                {
                    "id": "9834",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:9834"
                }
            ]
        }
    ],
    "snv": [],
    "mutagenesis": [],
    "expression_tissue": [],
    "expression_disease": [],
    "species": [
        {
            "name": "Drosophila melanogaster",
            "taxid": 7227,
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "A0A0B4LGG8",
                    "url": "https://www.uniprot.org/uniprot/A0A0B4LGG8"
                }
            ],
            "common_name": "Fruit fly",
            "glygen_name": "Fruit fly",
            "reference_species": "Drosophila melanogaster [7227]"
        }
    ],
    "gene": [
        {
            "name": "Dmel\\CG3328",
            "url": "https://www.uniprot.org/uniprot/A0A0B4LGG8",
            "locus": {
                "chromosome": "2R",
                "start_pos": 24173660,
                "end_pos": 24162489,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Gene",
                        "id": "FBgn0034985",
                        "url": "https://www.ensemblgenomes.org/id/FBgn0034985"
                    }
                ]
            }
        }
    ],
    "crossref": [
        {
            "id": "A0A0B4LGG8",
            "url": "https://alphafold.ebi.ac.uk/entry/A0A0B4LGG8",
            "database": "AlphaFoldDB",
            "categories": []
        },
        {
            "id": "FBgn0034985",
            "url": "https://bgee.org/?page=gene&gene_id=FBgn0034985",
            "database": "Bgee",
            "categories": [
                "Gene Expression"
            ]
        },
        {
            "id": "cd10144",
            "url": "https://www.ncbi.nlm.nih.gov/Structure/cdd/cddsrv.cgi?uid=cd10144",
            "database": "CDD",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "FBgn0034985",
            "url": "https://flybase.org/reports/FBgn0034985",
            "database": "FlyBase",
            "categories": [
                "Organism-specific"
            ]
        },
        {
            "id": "37871",
            "url": "https://www.ncbi.nlm.nih.gov/gene/37871",
            "database": "GeneID",
            "categories": [
                "Genome Annotation"
            ]
        },
        {
            "id": "Q9W1A0",
            "url": "https://www.ebi.ac.uk/intact/interactors/id:Q9W1A0*",
            "database": "IntAct",
            "categories": [
                "Other"
            ]
        },
        {
            "id": "IPR008967",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR008967",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR024061",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR024061",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR026932",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR026932",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR030392",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR030392",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR051577",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR051577",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "dme:Dmel_CG3328",
            "url": "https://www.genome.jp/dbget-bin/www_bget?dme:Dmel_CG3328",
            "database": "KEGG Pathway",
            "categories": [
                "Enzyme and Pathway"
            ]
        },
        {
            "id": "LDCWSIS",
            "url": "https://omabrowser.org/oma/group/LDCWSIS/",
            "database": "OMA",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "A0A0B4LGG8",
            "url": "https://www.orthodb.org/?gene=A0A0B4LGG8",
            "database": "OrthoDB",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "Q9W1A0",
            "url": "https://www.orthodb.org/?gene=Q9W1A0",
            "database": "OrthoDB",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PTHR13029",
            "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR13029",
            "database": "PANTHER",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PTHR13029:SF18",
            "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR13029:SF18",
            "database": "PANTHER",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PF05224",
            "url": "https://www.ebi.ac.uk/interpro/entry/pfam/PF05224",
            "database": "Pfam",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PF13884",
            "url": "https://www.ebi.ac.uk/interpro/entry/pfam/PF13884",
            "database": "Pfam",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PF13887",
            "url": "https://www.ebi.ac.uk/interpro/entry/pfam/PF13887",
            "database": "Pfam",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "NP_001286830",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001286830",
            "database": "RefSeq",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "A0A0B4LGG8",
            "url": "https://www.uniprot.org/uniprot/A0A0B4LGG8",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "A0A0B4LGG8-1",
            "url": "https://www.uniprot.org/uniprot/A0A0B4LGG8-1",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "Q9W1A0",
            "url": "https://www.uniprot.org/uniprot/Q9W1A0",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "Q9W1A0-1",
            "url": "https://www.uniprot.org/uniprot/Q9W1A0-1",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        }
    ],
    "sequence": {
        "sequence": "MDYPKNLSAPQDLDDINSDGMDHLDLLVQGAFDDGIQLGHNGHLSAGGGVHSHMESPHTSPMNGLDAHLTNSGRVGSTPVAAQAQSHVHPQLPESPPDSQPAYSPLGEAHGMAMPLQRELIYPGLAPMQHQANMLQTDLGQYASPPQQQHHFAAPQADVRIKHESELIINPSNLLGQQQPQQQQMQQQQQQLNEQMFAQHHQQHQDSILQDQMLYYDNGAGAGMYATGSYQNLSTCTLTSALGLGDRVQVIGTSQLSLNRVSAPSTPVHSLSRKRKMSTQLDCPEFPSAPKVDAGLQMSPLRASHHSLATPTPAPSHCSASVSPALSAVNSQADNSLDGQPGGVVTGSGSGSGSGSGSGSEAGDPAGGQCIRFNAFQPENWHKLFDQSLQELSVIYYRVDADKGFNFSVSDDAYVCQKKNHFQVTCHARLQGDAKFVKTPSGFEKIKSFHLHFYGVKFEAPNQTIRVEQSQSDRSKKAFHPVPIDLQKHIVSKITVGRLHFSETTNNNMRKKGRPNPEQRFFQLVVGLHVHTISGNFPVVSHGSEKIIVRASNPGQFESDVDLCWQRGLTPESVFHTGRVGINTDRPDESLVVHGNLKVSGHIVQPSDSRAKQEIGELDTSVQLRNLQKIRIVRYRYMPEFAVHSGLRRESDTREIEDTGVIAQEVREVIPDAVQEAGSVVLPNGNVIEKFLLVNKDRILMENIGAVKELCKVTCSLETRIEHLERANIGQNSQQLRAKDLLEPRCILPERAAITSYGSRRDGYEVCSSRSLQIVIFLLIIVMAACLAAVSTLYFVEHNKQQQADGFFGAGMFRQEAGPTHLSDEERHYFHNLHTLFKNKTHGPWPMRQMYATSTSRPPGSRQAEEEAEDLAAVLTKPQVSSGQQQLSLKHGVITTTAPRFSNKTISSKKGKWPPTQEVLRQAAGQKLHLPQPVHVVPAAPAKVPPAALNDTVASTEKPPQAIPLPQDFENNSIDIDAQQKQSQLKLDEHIVVVGTIASPASDAYDSNSPSVAAHPIRKFNPGTVYTHVYKTVSPPTANLALTTNKVSTEPAQSPLTHALDVPPPALPVRNSSDNPDALDLQNLSNTNESVDNPITQVFGFEYQESGLRESNLGRRSANQRSLEWIRQKDIKTAIFGQPAECNGDESVSDNCQSVCFEELPPTHPQPDNVDANVKEQHVEDDLQSAEEQEHDPDIVETQPAVSIGNETSAALEAQPGFLGKSSHGTDALTKKQTEPVVAAKDDPVYRLLQSASGQDQGPKADESVLPPFQLDCWSVASCVLAAQYNHTIDVEQFCPTSGSSLNVSYVVPVSRYLQASSLELHLSSNKPLQWSICVDEDQAKPSANGQLNEDDEAESTSGVKILKQQGKNKLSLALDLPARGYFLREFMLRASHDLEQQKLCDDNAHPANPILQYNFRIVRDCD",
        "length": 1423,
        "header": "tr|A0A0B4LGG8-1|A0A0B4LGG8_DROME Isoform 1 of Uncharacterized protein, isoform C  OS=Drosophila melanogaster OX=7227 GN=Dmel\\CG3328 PE=4 SV=1 CANONICAL=A0A0B4LGG8-1"
    },
    "isoforms": [
        {
            "isoform_ac": "A0A0B4LGG8-1",
            "url": "https://www.uniprot.org/uniprotkb/A0A0B4LGG8/entry#A0A0B4LGG8-1",
            "sequence": {
                "sequence": "MDYPKNLSAPQDLDDINSDGMDHLDLLVQGAFDDGIQLGHNGHLSAGGGVHSHMESPHTSPMNGLDAHLTNSGRVGSTPVAAQAQSHVHPQLPESPPDSQPAYSPLGEAHGMAMPLQRELIYPGLAPMQHQANMLQTDLGQYASPPQQQHHFAAPQADVRIKHESELIINPSNLLGQQQPQQQQMQQQQQQLNEQMFAQHHQQHQDSILQDQMLYYDNGAGAGMYATGSYQNLSTCTLTSALGLGDRVQVIGTSQLSLNRVSAPSTPVHSLSRKRKMSTQLDCPEFPSAPKVDAGLQMSPLRASHHSLATPTPAPSHCSASVSPALSAVNSQADNSLDGQPGGVVTGSGSGSGSGSGSGSEAGDPAGGQCIRFNAFQPENWHKLFDQSLQELSVIYYRVDADKGFNFSVSDDAYVCQKKNHFQVTCHARLQGDAKFVKTPSGFEKIKSFHLHFYGVKFEAPNQTIRVEQSQSDRSKKAFHPVPIDLQKHIVSKITVGRLHFSETTNNNMRKKGRPNPEQRFFQLVVGLHVHTISGNFPVVSHGSEKIIVRASNPGQFESDVDLCWQRGLTPESVFHTGRVGINTDRPDESLVVHGNLKVSGHIVQPSDSRAKQEIGELDTSVQLRNLQKIRIVRYRYMPEFAVHSGLRRESDTREIEDTGVIAQEVREVIPDAVQEAGSVVLPNGNVIEKFLLVNKDRILMENIGAVKELCKVTCSLETRIEHLERANIGQNSQQLRAKDLLEPRCILPERAAITSYGSRRDGYEVCSSRSLQIVIFLLIIVMAACLAAVSTLYFVEHNKQQQADGFFGAGMFRQEAGPTHLSDEERHYFHNLHTLFKNKTHGPWPMRQMYATSTSRPPGSRQAEEEAEDLAAVLTKPQVSSGQQQLSLKHGVITTTAPRFSNKTISSKKGKWPPTQEVLRQAAGQKLHLPQPVHVVPAAPAKVPPAALNDTVASTEKPPQAIPLPQDFENNSIDIDAQQKQSQLKLDEHIVVVGTIASPASDAYDSNSPSVAAHPIRKFNPGTVYTHVYKTVSPPTANLALTTNKVSTEPAQSPLTHALDVPPPALPVRNSSDNPDALDLQNLSNTNESVDNPITQVFGFEYQESGLRESNLGRRSANQRSLEWIRQKDIKTAIFGQPAECNGDESVSDNCQSVCFEELPPTHPQPDNVDANVKEQHVEDDLQSAEEQEHDPDIVETQPAVSIGNETSAALEAQPGFLGKSSHGTDALTKKQTEPVVAAKDDPVYRLLQSASGQDQGPKADESVLPPFQLDCWSVASCVLAAQYNHTIDVEQFCPTSGSSLNVSYVVPVSRYLQASSLELHLSSNKPLQWSICVDEDQAKPSANGQLNEDDEAESTSGVKILKQQGKNKLSLALDLPARGYFLREFMLRASHDLEQQKLCDDNAHPANPILQYNFRIVRDCD",
                "length": 1423,
                "header": "tr|A0A0B4LGG8-1|A0A0B4LGG8_DROME Isoform 1 of Uncharacterized protein, isoform C  OS=Drosophila melanogaster OX=7227 GN=Dmel\\CG3328 PE=4 SV=1 CANONICAL=A0A0B4LGG8-1"
            },
            "locus": {
                "chromosome": "2R",
                "start_pos": 24173393,
                "end_pos": 24167772,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "FBtr0343435",
                        "url": "https://www.ensemblgenomes.org/id/FBtr0343435"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "FBpp0310079",
                        "url": "https://www.ensemblgenomes.org/id/FBpp0310079"
                    }
                ]
            }
        },
        {
            "isoform_ac": "Q9W1A0-1",
            "url": "https://www.uniprot.org/uniprotkb/A0A0B4LGG8/entry#Q9W1A0-1",
            "sequence": {
                "sequence": "MDLDFFELSPQDLDDINSDGMDHLDLLVQGAFDDGIQLGHNGHLSAGGGVHSHMESPHTSPMNGLDAHLTNSGRVGSTPVAAQAQSHVHPQLPESPPDSQPAYSPLGEAHGMAMPLQRELIYPGLAPMQHQANMLQTDLGQYASPPQQQHHFAAPQADVRIKHESELIINPSNLLGQQQPQQQQMQQQQQQLNEQMFAQHHQQHQDSILQDQMLYYDNGAGAGMYATGSYQNLSTCTLTSALGLGDRVQVIGTSQLSLNRVSAPSTPVHSLSRKRKMSTQLDCPEFPSAPKVDAGLQMSPLRASHHSLATPTPAPSHCSASVSPALSAVNSQADNSLDGQPGGVVTGSGSGSGSGSGSGSEAGDPAGGQCIRFNAFQPENWHKLFDQSLQELSVIYYRVDADKGFNFSVSDDAYVCQKKNHFQVTCHARLQGDAKFVKTPSGFEKIKSFHLHFYGVKFEAPNQTIRVEQSQSDRSKKAFHPVPIDLQKHIVSKITVGRLHFSETTNNNMRKKGRPNPEQRFFQLVVGLHVHTISGNFPVVSHGSEKIIVRASNPGQFESDVDLCWQRGLTPESVFHTGRVGINTDRPDESLVVHGNLKVSGHIVQPSDSRAKQEIGELDTSVQLRNLQKIRIVRYRYMPEFAVHSGLRRESDTREIEDTGVIAQEVREVIPDAVQEAGSVVLPNGNVIEKFLLVNKDRILMENIGAVKELCKVTCSLETRIEHLERANIGQNSQQLRAKDLLEPRCILPERAAITSYGSRRDGYEVCSSRSLQIVIFLLIIVMAACLAAVSTLYFVEHNKQQQADGFFGAGMFRQEAGPTHLSDEERHYFHNLHTLFKNKTHGPWPMRQMYATSTSRPPGSRQAEEEAEDLAAVLTKPQVSSGQQQLSLKHGVITTTAPRFSNKTISSKKGKWPPTQEVLRQAAGQKLHLPQPVHVVPAAPAKVPPAALNDTVASTEKPPQAIPLPQDFENNSIDIDAQQKQSQLKLDEHIVVVGTIASPASDAYDSNSPSVAAHPIRKFNPGTVYTHVYKTVSPPTANLALTTNKVSTEPAQSPLTHALDVPPPALPVRNSSDNPDALDLQNLSNTNESVDNPITQVFGFEYQESGLRESNLGRRSANQRSLEWIRQKDIKTAIFGQPAECNGDESVSDNCQSVCFEELPPTHPQPDNVDANVKEQHVEDDLQSAEEQEHDPDIVETQPAVSIGNETSAALEAQPGFLGKSSHGTDALTKKQTEPVVAAKDDPVYRLLQSASGQDQGPKADESVLPPFQLDCWSVASCVLAAQYNHTIDVEQFCPTSGSSLNVSYVVPVSRYLQASSLELHLSSNKPLQWSICVDEDQAKPSANGQLNEDDEAESTSGVKILKQQGKNKLSLALDLPARGYFLREFMLRASHDLEQQKLCDDNAHPANPILQYNFRIVRDCD",
                "length": 1423,
                "header": "tr|Q9W1A0-1|Q9W1A0_DROME Computationally mapped isoform of FI22703p1  OS=Drosophila melanogaster OX=7227 GN=Dmel\\CG3328 PE=2 SV=3 CANONICAL=A0A0B4LGG8-1"
            },
            "locus": {
                "chromosome": "2R",
                "start_pos": 24173393,
                "end_pos": 24166474,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "FBtr0072257",
                        "url": "https://www.ensemblgenomes.org/id/FBtr0072257"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "FBpp0072165",
                        "url": "https://www.ensemblgenomes.org/id/FBpp0072165"
                    }
                ]
            }
        }
    ],
    "glycosylation": [
        {
            "glytoucan_ac": "",
            "type": "O-linked",
            "subtype": "other",
            "prediction_tool": "isoglyp",
            "mining_tool": "",
            "site_category": "predicted",
            "site_category_dict": {
                "predicted": true
            },
            "site_seq": "",
            "relation": "attached",
            "comment": "",
            "start_pos": 312,
            "start_aa": "T",
            "end_pos": 312,
            "end_aa": "T",
            "residue": "Thr",
            "site_lbl": "Thr312",
            "evidence": [
                {
                    "id": "GLY_001163",
                    "database": "GlyGen",
                    "url": "https://data.glygen.org/GLY_001163"
                }
            ],
            "filter_code": "00000000000000001000.00000000001000.1.01000"
        }
    ],
    "phosphorylation": [],
    "glycation": [],
    "keywords": [
        "glycoprotein",
        "glycoprotein_predicted"
    ],
    "publication": [
        {
            "title": "The genome sequence of Drosophila melanogaster.",
            "journal": "Science",
            "date": "2000",
            "authors": "Adams MD, Celniker SE, Holt RA, Evans CA, Gocayne JD, Amanatides PG, Scherer SE, Li PW, Hoskins RA, Galle RF, George RA, Lewis SE, Richards S, Ashburner M, Henderson SN, Sutton GG, Wortman JR, Yandell MD, Zhang Q, Chen LX, Brandon RC, Rogers YH, Blazej RG, Champe M, Pfeiffer BD, Wan KH, Doyle C, Baxter EG, Helt G, Nelson CR, Gabor GL, Abril JF, Agbayani A, An HJ, Andrews-Pfannkoch C, Baldwin D, Ballew RM, Basu A, Baxendale J, Bayraktaroglu L, Beasley EM, Beeson KY, Benos PV, Berman BP, Bhandari D, Bolshakov S, Borkova D, Botchan MR, Bouck J, Brokstein P, Brottier P, Burtis KC, Busam DA, Butler H, Cadieu E, Center A, Chandra I, Cherry JM, Cawley S, Dahlke C, Davenport LB, Davies P, de Pablos B, Delcher A, Deng Z, Mays AD, Dew I, Dietz SM, Dodson K, Doup LE, Downes M, Dugan-Rocha S, Dunkov BC, Dunn P, Durbin KJ, Evangelista CC, Ferraz C, Ferriera S, Fleischmann W, Fosler C, Gabrielian AE, Garg NS, Gelbart WM, Glasser K, Glodek A, Gong F, Gorrell JH, Gu Z, Guan P, Harris M, Harris NL, Harvey D, Heiman TJ, Hernandez JR, Houck J, Hostin D, Houston KA, Howland TJ, Wei MH, Ibegwam C, Jalali M, Kalush F, Karpen GH, Ke Z, Kennison JA, Ketchum KA, Kimmel BE, Kodira CD, Kraft C, Kravitz S, Kulp D, Lai Z, Lasko P, Lei Y, Levitsky AA, Li J, Li Z, Liang Y, Lin X, Liu X, Mattei B, McIntosh TC, McLeod MP, McPherson D, Merkulov G, Milshina NV, Mobarry C, Morris J, Moshrefi A, Mount SM, Moy M, Murphy B, Murphy L, Muzny DM, Nelson DL, Nelson DR, Nelson KA, Nixon K, Nusskern DR, Pacleb JM, Palazzolo M, Pittman GS, Pan S, Pollard J, Puri V, Reese MG, Reinert K, Remington K, Saunders RD, Scheeler F, Shen H, Shue BC, Siden-Kiamos I, Simpson M, Skupski MP, Smith T, Spier E, Spradling AC, Stapleton M, Strong R, Sun E, Svirskas R, Tector C, Turner R, Venter E, Wang AH, Wang X, Wang ZY, Wassarman DA, Weinstock GM, Weissenbach J, Williams SM, WoodageT, Worley KC, Wu D, Yang S, Yao QA, Ye J, Yeh RF, Zaveri JS, Zhan M, Zhang G, Zhao Q, Zheng L, Zheng XH, Zhong FN, Zhong W, Zhou X, Zhu S, Zhu X, Smith HO, Gibbs RA, Myers EW, Rubin GM, Venter JC",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "A0A0B4LGG8",
                    "url": "https://www.uniprot.org/uniprot/A0A0B4LGG8"
                }
            ],
            "reference": [
                {
                    "type": "PubMed",
                    "id": "10731132",
                    "url": "https://glygen.org/publication/PubMed/10731132"
                }
            ]
        },
        {
            "title": "Finishing a whole-genome shotgun: release 3 of the Drosophila melanogaster euchromatic genome sequence.",
            "journal": "Genome Biol.",
            "date": "2002",
            "authors": "Celniker SE, Wheeler DA, Kronmiller B, Carlson JW, Halpern A, Patel S, Adams M, Champe M, Dugan SP, Frise E, Hodgson A, George RA, Hoskins RA, Laverty T, Muzny DM, Nelson CR, Pacleb JM, Park S, Pfeiffer BD, Richards S, Sodergren EJ, Svirskas R, Tabor PE, Wan K, Stapleton M, Sutton GG, Venter C, Weinstock G, Scherer SE, Myers EW, Gibbs RA, Rubin GM",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "A0A0B4LGG8",
                    "url": "https://www.uniprot.org/uniprot/A0A0B4LGG8"
                }
            ],
            "reference": [
                {
                    "type": "PubMed",
                    "id": "12537568",
                    "url": "https://glygen.org/publication/PubMed/12537568"
                }
            ]
        },
        {
            "title": "Annotation of the Drosophila melanogaster euchromatic genome: a systematic review.",
            "journal": "Genome Biol.",
            "date": "2002",
            "authors": "Misra S, Crosby MA, Mungall CJ, Matthews BB, Campbell KS, Hradecky P, Huang Y, Kaminker JS, Millburn GH, Prochnik SE, Smith CD, Tupy JL, Whitfied EJ, Bayraktaroglu L, Berman BP, Bettencourt BR, Celniker SE, de Grey AD, Drysdale RA, Harris NL, Richter J, Russo S, Schroeder AJ, Shu SQ, Stapleton M, Yamada C, Ashburner M, Gelbart WM, Rubin GM, Lewis SE",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "A0A0B4LGG8",
                    "url": "https://www.uniprot.org/uniprot/A0A0B4LGG8"
                }
            ],
            "reference": [
                {
                    "type": "PubMed",
                    "id": "12537572",
                    "url": "https://glygen.org/publication/PubMed/12537572"
                }
            ]
        },
        {
            "title": "The transposable elements of the Drosophila melanogaster euchromatin: a genomics perspective.",
            "journal": "Genome Biol.",
            "date": "2002",
            "authors": "Kaminker JS, Bergman CM, Kronmiller B, Carlson J, Svirskas R, Patel S, Frise E, Wheeler DA, Lewis SE, Rubin GM, Ashburner M, Celniker SE",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "A0A0B4LGG8",
                    "url": "https://www.uniprot.org/uniprot/A0A0B4LGG8"
                }
            ],
            "reference": [
                {
                    "type": "PubMed",
                    "id": "12537573",
                    "url": "https://glygen.org/publication/PubMed/12537573"
                }
            ]
        },
        {
            "title": "Heterochromatic sequences in a Drosophila whole-genome shotgun assembly.",
            "journal": "Genome Biol.",
            "date": "2002",
            "authors": "Hoskins RA, Smith CD, Carlson JW, Carvalho AB, Halpern A, Kaminker JS, Kennedy C, Mungall CJ, Sullivan BA, Sutton GG, Yasuhara JC, Wakimoto BT, Myers EW, Celniker SE, Rubin GM, Karpen GH",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "A0A0B4LGG8",
                    "url": "https://www.uniprot.org/uniprot/A0A0B4LGG8"
                }
            ],
            "reference": [
                {
                    "type": "PubMed",
                    "id": "12537574",
                    "url": "https://glygen.org/publication/PubMed/12537574"
                }
            ]
        },
        {
            "title": "Combined evidence annotation of transposable elements in genome sequences.",
            "journal": "PLoS Comput. Biol.",
            "date": "2005",
            "authors": "Quesneville H, Bergman CM, Andrieu O, Autard D, Nouaud D, Ashburner M, Anxolabehere D",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "A0A0B4LGG8",
                    "url": "https://www.uniprot.org/uniprot/A0A0B4LGG8"
                }
            ],
            "reference": [
                {
                    "type": "PubMed",
                    "id": "16110336",
                    "url": "https://glygen.org/publication/PubMed/16110336"
                }
            ]
        },
        {
            "title": "The Release 5.1 annotation of Drosophila melanogaster heterochromatin.",
            "journal": "Science",
            "date": "2007",
            "authors": "Smith CD, Shu S, Mungall CJ, Karpen GH",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "A0A0B4LGG8",
                    "url": "https://www.uniprot.org/uniprot/A0A0B4LGG8"
                }
            ],
            "reference": [
                {
                    "type": "PubMed",
                    "id": "17569856",
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