{
    "uniprot_canonical_ac": "A0A0B4LGG8-1",
    "uniprot_ac": "A0A0B4LGG8",
    "uniprot_id": "A0A0B4LGG8_DROME",
    "mass": {
        "chemical_mass": 155860.0,
        "monoisotopic_mass": 155860.0
    },
    "refseq": {
        "ac": "NP_001286829",
        "name": "uncharacterized protein, isoform B",
        "summary": "",
        "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001286829"
    },
    "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-PB",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001286829",
            "id": "NP_001286829"
        },
        {
            "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": "",
            "id": "A0A0B4LGG8"
        },
        {
            "name": "uncharacterized protein, isoform B",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001286829",
            "id": "NP_001286829"
        },
        {
            "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"
        }
    ],
    "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.ensembl.org/id/FBgn0034985"
                    }
                ]
            }
        }
    ],
    "crossref": [
        {
            "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": "dme:Dmel_CG3328",
            "url": "https://www.genome.jp/dbget-bin/get_linkdb?-t+pathway+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": "2880761at2759",
            "url": "http://www.orthodb.org/?query=2880761at2759",
            "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": "http://pfam.xfam.org/family/PF05224",
            "database": "Pfam",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PF13884",
            "url": "http://pfam.xfam.org/family/PF13884",
            "database": "Pfam",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PF13887",
            "url": "http://pfam.xfam.org/family/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": "",
            "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.ensembl.org/id/FBtr0343435"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "FBpp0310079",
                        "url": "https://www.ensembl.org/id/FBpp0310079"
                    }
                ]
            }
        },
        {
            "isoform_ac": "Q9W1A0-1",
            "url": "",
            "sequence": {
                "sequence": "MDLDFFELSPQDLDDINSDGMDHLDLLVQGAFDDGIQLGHNGHLSAGGGVHSHMESPHTSPMNGLDAHLTNSGRVGSTPVAAQAQSHVHPQLPESPPDSQPAYSPLGEAHGMAMPLQRELIYPGLAPMQHQANMLQTDLGQYASPPQQQHHFAAPQADVRIKHESELIINPSNLLGQQQPQQQQMQQQQQQLNEQMFAQHHQQHQDSILQDQMLYYDNGAGAGMYATGSYQNLSTCTLTSALGLGDRVQVIGTSQLSLNRVSAPSTPVHSLSRKRKMSTQLDCPEFPSAPKVDAGLQMSPLRASHHSLATPTPAPSHCSASVSPALSAVNSQADNSLDGQPGGVVTGSGSGSGSGSGSGSEAGDPAGGQCIRFNAFQPENWHKLFDQSLQELSVIYYRVDADKGFNFSVSDDAYVCQKKNHFQVTCHARLQGDAKFVKTPSGFEKIKSFHLHFYGVKFEAPNQTIRVEQSQSDRSKKAFHPVPIDLQKHIVSKITVGRLHFSETTNNNMRKKGRPNPEQRFFQLVVGLHVHTISGNFPVVSHGSEKIIVRASNPGQFESDVDLCWQRGLTPESVFHTGRVGINTDRPDESLVVHGNLKVSGHIVQPSDSRAKQEIGELDTSVQLRNLQKIRIVRYRYMPEFAVHSGLRRESDTREIEDTGVIAQEVREVIPDAVQEAGSVVLPNGNVIEKFLLVNKDRILMENIGAVKELCKVTCSLETRIEHLERANIGQNSQQLRAKDLLEPRCILPERAAITSYGSRRDGYEVCSSRSLQIVIFLLIIVMAACLAAVSTLYFVEHNKQQQADGFFGAGMFRQEAGPTHLSDEERHYFHNLHTLFKNKTHGPWPMRQMYATSTSRPPGSRQAEEEAEDLAAVLTKPQVSSGQQQLSLKHGVITTTAPRFSNKTISSKKGKWPPTQEVLRQAAGQKLHLPQPVHVVPAAPAKVPPAALNDTVASTEKPPQAIPLPQDFENNSIDIDAQQKQSQLKLDEHIVVVGTIASPASDAYDSNSPSVAAHPIRKFNPGTVYTHVYKTVSPPTANLALTTNKVSTEPAQSPLTHALDVPPPALPVRNSSDNPDALDLQNLSNTNESVDNPITQVFGFEYQESGLRESNLGRRSANQRSLEWIRQKDIKTAIFGQPAECNGDESVSDNCQSVCFEELPPTHPQPDNVDANVKEQHVEDDLQSAEEQEHDPDIVETQPAVSIGNETSAALEAQPGFLGKSSHGTDALTKKQTEPVVAAKDDPVYRLLQSASGQDQGPKADESVLPPFQLDCWSVASCVLAAQYNHTIDVEQFCPTSGSSLNVSYVVPVSRYLQASSLELHLSSNKPLQWSICVDEDQAKPSANGQLNEDDEAESTSGVKILKQQGKNKLSLALDLPARGYFLREFMLRASHDLEQQKLCDDNAHPANPILQYNFRIVRDCD",
                "length": 1423,
                "header": "tr|Q9W1A0-1|Q9W1A0_DROME Computationally mapped isoform of Uncharacterized protein, isoform A  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": "FBtr0343434",
                        "url": "https://www.ensembl.org/id/FBtr0343434"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "FBpp0310078",
                        "url": "https://www.ensembl.org/id/FBpp0310078"
                    }
                ]
            }
        }
    ],
    "glycosylation": [],
    "phosphorylation": [],
    "glycation": [],
    "keywords": [],
    "publication": [],
    "pathway": [
        {
            "id": "dme:Dmel_CG3328",
            "name": "",
            "url": "https://www.genome.jp/dbget-bin/get_linkdb?-t+pathway+dme:Dmel_CG3328",
            "resource": "KEGG Pathway"
        }
    ],
    "orthologs": [],
    "go_annotation": {
        "categories": [
            {
                "name": "Molecular Function",
                "total": 2,
                "go_terms": [
                    {
                        "name": "DNA-binding transcription factor activity",
                        "id": "GO:0003700",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003700",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0B4LGG8",
                                "url": "https://www.uniprot.org/uniprot/A0A0B4LGG8"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "sequence-specific DNA binding",
                        "id": "GO:0043565",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043565",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0B4LGG8",
                                "url": "https://www.uniprot.org/uniprot/A0A0B4LGG8"
                            }
                        ],
                        "pmid": ""
                    }
                ]
            },
            {
                "name": "Cellular Component",
                "total": 2,
                "go_terms": [
                    {
                        "name": "nucleus",
                        "id": "GO:0005634",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005634",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0B4LGG8",
                                "url": "https://www.uniprot.org/uniprot/A0A0B4LGG8"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "endoplasmic reticulum membrane",
                        "id": "GO:0005789",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005789",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0B4LGG8",
                                "url": "https://www.uniprot.org/uniprot/A0A0B4LGG8"
                            }
                        ],
                        "pmid": ""
                    }
                ]
            },
            {
                "name": "Biological Process",
                "total": 3,
                "go_terms": [
                    {
                        "name": "regulation of transcription by RNA polymerase II",
                        "id": "GO:0006357",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006357",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0B4LGG8",
                                "url": "https://www.uniprot.org/uniprot/A0A0B4LGG8"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "positive regulation of DNA-templated transcription",
                        "id": "GO:0045893",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045893",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0B4LGG8",
                                "url": "https://www.uniprot.org/uniprot/A0A0B4LGG8"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "protein autoprocessing",
                        "id": "GO:0016540",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016540",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0B4LGG8",
                                "url": "https://www.uniprot.org/uniprot/A0A0B4LGG8"
                            }
                        ],
                        "pmid": ""
                    }
                ]
            }
        ]
    },
    "pro_annotation": [],
    "site_annotation": [
        {
            "start_pos": 1071,
            "end_pos": 1073,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 1083,
            "end_pos": 1085,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 1088,
            "end_pos": 1090,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 1206,
            "end_pos": 1208,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 1286,
            "end_pos": 1288,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 1303,
            "end_pos": 1305,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 232,
            "end_pos": 234,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 406,
            "end_pos": 408,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 462,
            "end_pos": 464,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 6,
            "end_pos": 8,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 839,
            "end_pos": 841,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 903,
            "end_pos": 905,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 950,
            "end_pos": 952,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 971,
            "end_pos": 973,
            "annotation": "n_glycosylation_sequon"
        }
    ],
    "ptm_annotation": [],
    "interactions": [],
    "reactions": [],
    "reaction_participants": [],
    "reaction_enzymes": [],
    "biomarkers": [],
    "synthesized_glycans": [],
    "cluster_types": [
        {
            "name": "isoformset.uniprotkb",
            "label": "Isoforms"
        }
    ],
    "section_stats": [
        {
            "table_id": "glycosylation",
            "table_stats": [
                {
                    "field": "total",
                    "count": 0
                },
                {
                    "field": "total_sites",
                    "count": 0
                },
                {
                    "field": "n_linked_glycans",
                    "count": 0
                },
                {
                    "field": "n_linked_glycan_sites",
                    "count": 0
                },
                {
                    "field": "o_linked_glycans",
                    "count": 0
                },
                {
                    "field": "o_linked_glycan_sites",
                    "count": 0
                }
            ],
            "sort_fields": []
        },
        {
            "table_id": "glycosylation_reported",
            "table_stats": [
                {
                    "field": "total",
                    "count": 0
                },
                {
                    "field": "total_sites",
                    "count": 0
                },
                {
                    "field": "n_linked_glycans",
                    "count": 0
                },
                {
                    "field": "n_linked_glycan_sites",
                    "count": 0
                },
                {
                    "field": "o_linked_glycans",
                    "count": 0
                },
                {
                    "field": "o_linked_glycan_sites",
                    "count": 0
                }
            ],
            "sort_fields": []
        },
        {
            "table_id": "glycosylation_reported_with_glycan",
            "table_stats": [
                {
                    "field": "total",
                    "count": 0
                },
                {
                    "field": "total_sites",
                    "count": 0
                },
                {
                    "field": "n_linked_glycans",
                    "count": 0
                },
                {
                    "field": "n_linked_glycan_sites",
                    "count": 0
                },
                {
                    "field": "o_linked_glycans",
                    "count": 0
                },
                {
                    "field": "o_linked_glycan_sites",
                    "count": 0
                }
            ],
            "sort_fields": []
        },
        {
            "table_id": "glycosylation_predicted",
            "table_stats": [
                {
                    "field": "total",
                    "count": 0
                },
                {
                    "field": "total_sites",
                    "count": 0
                },
                {
                    "field": "n_linked_glycans",
                    "count": 0
                },
                {
                    "field": "n_linked_glycan_sites",
                    "count": 0
                },
                {
                    "field": "o_linked_glycans",
                    "count": 0
                },
                {
                    "field": "o_linked_glycan_sites",
                    "count": 0
                }
            ],
            "sort_fields": []
        },
        {
            "table_id": "glycosylation_automatic_literature_mining",
            "table_stats": [
                {
                    "field": "total",
                    "count": 0
                },
                {
                    "field": "total_sites",
                    "count": 0
                },
                {
                    "field": "n_linked_glycans",
                    "count": 0
                },
                {
                    "field": "n_linked_glycan_sites",
                    "count": 0
                },
                {
                    "field": "o_linked_glycans",
                    "count": 0
                },
                {
                    "field": "o_linked_glycan_sites",
                    "count": 0
                }
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