{
    "uniprot_canonical_ac": "A0A6H2EG45-1",
    "uniprot_ac": "A0A6H2EG45",
    "uniprot_id": "A0A6H2EG45_DROME",
    "mass": {
        "chemical_mass": 45149.0,
        "monoisotopic_mass": 45149.0
    },
    "refseq": {
        "ac": "NP_572758",
        "name": "uncharacterized protein, isoform A",
        "summary": "",
        "url": "https://www.ncbi.nlm.nih.gov/protein/NP_572758"
    },
    "gene_names": [
        {
            "name": "Dmel\\CG1847",
            "resource": "UniProtKB",
            "type": "recommended",
            "url": "https://www.uniprot.org/uniprot/A0A6H2EG45",
            "id": "A0A6H2EG45"
        },
        {
            "name": "CG1847",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_572758",
            "id": "NP_572758"
        },
        {
            "name": "CG1847",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/A0A6H2EG45",
            "id": "A0A6H2EG45"
        },
        {
            "name": "Dmel\\CG1847",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_572758",
            "id": "NP_572758"
        },
        {
            "name": "Dmel_CG1847",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/A0A6H2EG45",
            "id": "A0A6H2EG45"
        }
    ],
    "protein_names": [
        {
            "name": "CG1847-PA",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_572758",
            "id": "NP_572758"
        },
        {
            "name": "CG1847-PC",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_727574",
            "id": "NP_727574"
        },
        {
            "name": "Uncharacterized protein, isoform D",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "A0A6H2EG45"
        },
        {
            "name": "uncharacterized protein, isoform A",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_572758",
            "id": "NP_572758"
        },
        {
            "name": "uncharacterized protein, isoform C",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_727574",
            "id": "NP_727574"
        }
    ],
    "function": [],
    "disease": [
        {
            "disease_id": "DOID:0110332",
            "recommended_name": {
                "id": "DOID:0110332",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:0110332",
                "name": "Leber congenital amaurosis 4",
                "description": "A Leber congenital amaurosis that is characterized by a relatively severe phenotype, with maculopathy and marked bone-spicule pigmentary retinopathy in most and keratoconus and cataract in a large subset and that has_material_basis_in mutation in the AIPL1 gene on chromosome 17p13."
            },
            "synonyms": [
                {
                    "id": "DOID:0110332",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0110332",
                    "name": "LCA4",
                    "description": ""
                },
                {
                    "id": "MONDO:0011458",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011458",
                    "name": "Leber congenital amaurosis 4",
                    "description": "Any Leber congenital amaurosis in which the cause of the disease is a mutation in the AIPL1 gene."
                },
                {
                    "id": "MONDO:0011458",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011458",
                    "name": "cone-rod dystrophy",
                    "description": ""
                },
                {
                    "id": "MONDO:0011458",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011458",
                    "name": "AIPL1 Leber congenital amaurosis",
                    "description": ""
                },
                {
                    "id": "MONDO:0011458",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011458",
                    "name": "LCA4",
                    "description": ""
                },
                {
                    "id": "MONDO:0011458",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011458",
                    "name": "Leber congenital amaurosis 4",
                    "description": ""
                },
                {
                    "id": "MONDO:0011458",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011458",
                    "name": "Leber congenital amaurosis caused by mutation in AIPL1",
                    "description": ""
                },
                {
                    "id": "MONDO:0011458",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011458",
                    "name": "Leber congenital amaurosis type 4",
                    "description": ""
                },
                {
                    "id": "MONDO:0011458",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011458",
                    "name": "amaurosis congenita of Leber, type 4",
                    "description": ""
                },
                {
                    "id": "MONDO:0011458",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011458",
                    "name": "cone-rod dystrophy, Aipl1-related",
                    "description": ""
                },
                {
                    "id": "MONDO:0011458",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011458",
                    "name": "retinitis pigmentosa, juvenile",
                    "description": ""
                },
                {
                    "id": "MONDO:0011458",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011458",
                    "name": "retinitis pigmentosa, juvenile, Aipl1-related",
                    "description": ""
                },
                {
                    "id": "MIM:604393",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/604393",
                    "name": "Leber congenital amaurosis 4",
                    "description": "Leber congenital amaurosis 4"
                }
            ],
            "evidence": [
                {
                    "id": "0110332",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:0110332"
                }
            ]
        },
        {
            "disease_id": "DOID:0112009",
            "recommended_name": {
                "id": "DOID:0112009",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:0112009",
                "name": "pituitary adenoma 1",
                "description": "A pituitary adenoma characterized by different types of familial or sporadic pituitary adenomas that has_material_basis_in heterozygous mutation in AIP on chromosome 11q13.2."
            },
            "synonyms": [
                {
                    "id": "DOID:0112009",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0112009",
                    "name": "PITA1",
                    "description": ""
                },
                {
                    "id": "DOID:0112009",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0112009",
                    "name": "pituitary adenoma 1, multiple types",
                    "description": ""
                },
                {
                    "id": "MONDO:0007052",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007052",
                    "name": "growth hormone secreting pituitary adenoma 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0007052",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007052",
                    "name": "pituitary adenoma 1, multiple types, autosomal dominant, somatic mutation",
                    "description": ""
                },
                {
                    "id": "MONDO:0007052",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007052",
                    "name": "pituitary adenoma predisposition, autosomal dominant, somatic mutation",
                    "description": ""
                },
                {
                    "id": "MONDO:0007052",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007052",
                    "name": "pituitary adenoma, growth hormone-secreting, type 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0007052",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007052",
                    "name": "PAGH1",
                    "description": ""
                },
                {
                    "id": "MONDO:0007052",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007052",
                    "name": "PITA1",
                    "description": ""
                },
                {
                    "id": "MONDO:0007052",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007052",
                    "name": "Somatotrophinoma, familial",
                    "description": ""
                },
                {
                    "id": "MONDO:0007052",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007052",
                    "name": "acromegaly due to pituitary adenoma 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0007052",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007052",
                    "name": "familial isolated pituitary adenoma syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0007052",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007052",
                    "name": "isolated familial somatotropinoma",
                    "description": ""
                },
                {
                    "id": "MONDO:0007052",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007052",
                    "name": "pituitary adenoma 1, multiple types",
                    "description": ""
                },
                {
                    "id": "MONDO:0007052",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007052",
                    "name": "pituitary adenoma predisposition",
                    "description": ""
                },
                {
                    "id": "MONDO:0007052",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007052",
                    "name": "pituitary adenoma, familial isolated",
                    "description": ""
                },
                {
                    "id": "MONDO:0007052",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007052",
                    "name": "pituitary adenoma, growth hormone-secreting, 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0007052",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007052",
                    "name": "somatotropinoma, familial isolated",
                    "description": ""
                },
                {
                    "id": "MIM:102200",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/102200",
                    "name": "Pituitary adenoma 1, multiple types",
                    "description": "Pituitary adenoma 1, multiple types"
                }
            ],
            "evidence": [
                {
                    "id": "0112009",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:0112009"
                }
            ]
        },
        {
            "disease_id": "DOID:10584",
            "recommended_name": {
                "id": "DOID:10584",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:10584",
                "name": "retinitis pigmentosa",
                "description": "A retinal degeneration characterized by the gradual deterioration of the photoreceptors or the retinal pigment epithelium of the retina leading to progressive sight loss."
            },
            "synonyms": [
                {
                    "id": "DOID:10584",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:10584",
                    "name": "pericentral pigmentary retinopathy",
                    "description": ""
                },
                {
                    "id": "MONDO:0019200",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0019200",
                    "name": "retinitis pigmentosa",
                    "description": "Retinitis pigmentosa (RP) is an inherited retinal dystrophy leading to progressive loss of the photoreceptors and retinal pigment epithelium and resulting in blindness usually after several decades."
                },
                {
                    "id": "MONDO:0019200",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0019200",
                    "name": "retinitis pigmentosa",
                    "description": ""
                },
                {
                    "id": "MONDO:0019200",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0019200",
                    "name": "pericentral pigmentary retinopathy",
                    "description": ""
                },
                {
                    "id": "MONDO:0019200",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0019200",
                    "name": "Rod-cone dystrophy",
                    "description": ""
                },
                {
                    "id": "MIM:268000",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/268000",
                    "name": "Retinitis pigmentosa",
                    "description": "Retinitis pigmentosa"
                }
            ],
            "evidence": [
                {
                    "id": "10584",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:10584"
                }
            ]
        },
        {
            "disease_id": "DOID:1432",
            "recommended_name": {
                "id": "DOID:1432",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:1432",
                "name": "blindness",
                "description": "An eye disease characterized by a lack or loss of vision."
            },
            "synonyms": [
                {
                    "id": "DOID:1432",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:1432",
                    "name": "vision impairment",
                    "description": ""
                },
                {
                    "id": "DOID:1432",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:1432",
                    "name": "vision loss",
                    "description": ""
                },
                {
                    "id": "DOID:1432",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:1432",
                    "name": "visual impairment",
                    "description": ""
                }
            ],
            "evidence": [
                {
                    "id": "1432",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:1432"
                }
            ]
        },
        {
            "disease_id": "DOID:14791",
            "recommended_name": {
                "id": "DOID:14791",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:14791",
                "name": "Leber congenital amaurosis",
                "description": "A retinal disease that is characterized by nystagmus, sluggish or no pupillary responses, and severe vision loss or blindness."
            },
            "synonyms": [
                {
                    "id": "DOID:14791",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:14791",
                    "name": "LCA",
                    "description": ""
                },
                {
                    "id": "DOID:14791",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:14791",
                    "name": "Leber's amaurosis",
                    "description": ""
                },
                {
                    "id": "DOID:14791",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:14791",
                    "name": "Leber's congenital amaurosis",
                    "description": ""
                },
                {
                    "id": "DOID:14791",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:14791",
                    "name": "Leber's disease",
                    "description": ""
                },
                {
                    "id": "MONDO:0008764",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008764",
                    "name": "Leber congenital amaurosis 1",
                    "description": "Any Leber congenital amaurosis in which the cause of the disease is a mutation in the GUCY2D gene."
                },
                {
                    "id": "MONDO:0008764",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008764",
                    "name": "GUCY2D Leber congenital amaurosis",
                    "description": ""
                },
                {
                    "id": "MONDO:0008764",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008764",
                    "name": "LCA1",
                    "description": ""
                },
                {
                    "id": "MONDO:0008764",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008764",
                    "name": "Leber congenital amaurosis 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0008764",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008764",
                    "name": "Leber congenital amaurosis caused by mutation in GUCY2D",
                    "description": ""
                },
                {
                    "id": "MONDO:0008764",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008764",
                    "name": "Leber congenital amaurosis type 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0008764",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008764",
                    "name": "amaurosis congenita of Leber I",
                    "description": ""
                },
                {
                    "id": "MONDO:0008764",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008764",
                    "name": "CRB",
                    "description": ""
                },
                {
                    "id": "MONDO:0008764",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008764",
                    "name": "LCA",
                    "description": ""
                },
                {
                    "id": "MONDO:0008764",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008764",
                    "name": "amaurosis congenita of Leber 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0008764",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008764",
                    "name": "amaurosis congenita of Leber, type 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0008764",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008764",
                    "name": "retinal blindness, congenital",
                    "description": ""
                },
                {
                    "id": "MIM:204000",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/204000",
                    "name": "Leber congenital amaurosis 1",
                    "description": "Leber congenital amaurosis 1"
                }
            ],
            "evidence": [
                {
                    "id": "14791",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:14791"
                }
            ]
        }
    ],
    "snv": [],
    "mutagenesis": [],
    "expression_tissue": [],
    "expression_disease": [],
    "species": [
        {
            "name": "Drosophila melanogaster",
            "taxid": 7227,
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "A0A6H2EG45",
                    "url": "https://www.uniprot.org/uniprot/A0A6H2EG45"
                }
            ],
            "common_name": "Fruit fly"
        }
    ],
    "gene": [
        {
            "name": "Dmel\\CG1847",
            "url": "https://www.uniprot.org/uniprot/A0A6H2EG45",
            "locus": {
                "chromosome": "X",
                "start_pos": 11871168,
                "end_pos": 11869170,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Gene",
                        "id": "FBgn0030345",
                        "url": "https://www.ensembl.org/id/FBgn0030345"
                    }
                ]
            }
        }
    ],
    "crossref": [
        {
            "id": "FBgn0030345",
            "url": "https://bgee.org/?page=gene&gene_id=FBgn0030345",
            "database": "Bgee",
            "categories": [
                "Gene Expression"
            ]
        },
        {
            "id": "FBgn0030345",
            "url": "https://flybase.org/reports/FBgn0030345",
            "database": "FlyBase",
            "categories": [
                "Organism-specific"
            ]
        },
        {
            "id": "32144",
            "url": "https://www.ncbi.nlm.nih.gov/gene/32144",
            "database": "GeneID",
            "categories": [
                "Genome Annotation"
            ]
        },
        {
            "id": "Q8IR85",
            "url": "https://www.ebi.ac.uk/intact/interactors/id:Q8IR85*",
            "database": "IntAct",
            "categories": [
                "Other"
            ]
        },
        {
            "id": "Q9VYT2",
            "url": "https://www.ebi.ac.uk/intact/interactors/id:Q9VYT2*",
            "database": "IntAct",
            "categories": [
                "Other"
            ]
        },
        {
            "id": "IPR001179",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR001179",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR011990",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR011990",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR019734",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR019734",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR039663",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR039663",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR046357",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR046357",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "QQHERNV",
            "url": "https://omabrowser.org/oma/group/QQHERNV/",
            "database": "OMA",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "11153at2759",
            "url": "http://www.orthodb.org/?query=11153at2759",
            "database": "OrthoDB",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PTHR11242",
            "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR11242",
            "database": "PANTHER",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PTHR11242:SF0",
            "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR11242:SF0",
            "database": "PANTHER",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PF00254",
            "url": "http://pfam.xfam.org/family/PF00254",
            "database": "Pfam",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "R-DME-8937144",
            "url": "https://www.reactome.org/PathwayBrowser/#R-DME-8937144",
            "database": "Reactome",
            "categories": [
                "Protein Classification"
            ]
        },
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            "id": "A0A6H2EG45",
            "url": "https://www.uniprot.org/uniprot/A0A6H2EG45",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "A0A6H2EG45-1",
            "url": "https://www.uniprot.org/uniprot/A0A6H2EG45-1",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "Q8IR85",
            "url": "https://www.uniprot.org/uniprot/Q8IR85",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "Q8IR85-1",
            "url": "https://www.uniprot.org/uniprot/Q8IR85-1",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "Q9VYT2",
            "url": "https://www.uniprot.org/uniprot/Q9VYT2",
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            "categories": [
                "Protein"
            ]
        },
        {
            "id": "Q9VYT2-1",
            "url": "https://www.uniprot.org/uniprot/Q9VYT2-1",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        }
    ],
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        "sequence": "MQSRSKSDMKPIRKEILNPGNAYIELTPGTRVKFHFQTRRAGDSRIIDDSRKMEKPMELVLGKKFKLEVWELIVQQMSLNEVAKFTVHKSLCAQYPFISKTLRDIGKKPEERRHCCGMTLQNEGIGYTDLDELLQNPSDLEFIIELFSIELPEQYEKERWQMSDDEKMLATSTLRERGNNFYKASRFTEAETCYREAVGIVEQLMLKEKPHDEEWQELAAIKTPLLLNYAQCRLIAGDFYAVIEHCNEVLTLDPRNVKALFRRAKAHAGAWNPAQARRDFLDALALDASLKSTVSKELKSIEDQQQARNVQDRIHMQKLFXNISCVNVLLMLLVYWSSYLQRXQYLSLPSFLSLAVSFAHGLVLLCSMANLFLCCWTLKKLLRAMQGLSW",
        "length": 390,
        "header": "tr|A0A6H2EG45-1|A0A6H2EG45_DROME Isoform 1 of Uncharacterized protein, isoform D  OS=Drosophila melanogaster OX=7227 GN=Dmel\\CG1847 PE=1 SV=1 CANONICAL=A0A6H2EG45-1"
    },
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            "isoform_ac": "A0A6H2EG45-1",
            "url": "",
            "sequence": {
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                "header": "tr|A0A6H2EG45-1|A0A6H2EG45_DROME Isoform 1 of Uncharacterized protein, isoform D  OS=Drosophila melanogaster OX=7227 GN=Dmel\\CG1847 PE=1 SV=1 CANONICAL=A0A6H2EG45-1"
            },
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                        "id": "FBtr0479842",
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                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "FBpp0428178",
                        "url": "https://www.ensembl.org/id/FBpp0428178"
                    }
                ]
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                "length": 342,
                "header": "tr|Q8IR85-1|Q8IR85_DROME Computationally mapped isoform of Uncharacterized protein, isoform C  OS=Drosophila melanogaster OX=7227 GN=Dmel\\CG1847 PE=1 SV=2 CANONICAL=A0A6H2EG45-1"
            },
            "locus": {
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                "end_pos": 11869247,
                "strand": "-",
                "evidence": [
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                        "database": "Ensembl Transcript",
                        "id": "FBtr0330413",
                        "url": "https://www.ensembl.org/id/FBtr0330413"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "FBpp0303439",
                        "url": "https://www.ensembl.org/id/FBpp0303439"
                    }
                ]
            }
        },
        {
            "isoform_ac": "Q9VYT2-1",
            "url": "",
            "sequence": {
                "sequence": "MQSRSKSDMKPIRKEILNPGNAYIELTPGTRVKFHFQTRRAGDSRIIDDSRKMEKPMELVLGKKFKLEVWELIVQQMSLNEVAKFTVHKSLCAQYPFISKTLRDIGKKPEERRHCCGMTLQNEGIGYTDLDELLQNPSDLEFIIELFSIELPEQYEKERWQMSDDEKMLATSTLRERGNNFYKASRFTEAETCYREAVGIVEQLMLKEKPHDEEWQELAAIKTPLLLNYAQCRLIAGDFYAVIEHCNEVLTLDPRNVKALFRRAKAHAGAWNPAQARRDFLDALALDASLKSTVSKELKSIEDQQQARNVQDRIHMQKLF",
                "length": 320,
                "header": "tr|Q9VYT2-1|A0A6H2EG45_DROME Computationally mapped isoform of Uncharacterized protein, isoform D  OS=Drosophila melanogaster OX=7227 GN=Dmel\\CG1847 PE=1 SV=1 CANONICAL=A0A6H2EG45-1"
            },
            "locus": {
                "chromosome": "X",
                "start_pos": 11870429,
                "end_pos": 11869247,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "FBtr0073567",
                        "url": "https://www.ensembl.org/id/FBtr0073567"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "FBpp0073411",
                        "url": "https://www.ensembl.org/id/FBpp0073411"
                    }
                ]
            }
        }
    ],
    "glycosylation": [],
    "phosphorylation": [],
    "glycation": [],
    "keywords": [],
    "publication": [],
    "pathway": [
        {
            "id": "R-DME-8937144",
            "name": "Aryl hydrocarbon receptor signalling",
            "url": "https://www.reactome.org/PathwayBrowser/#R-DME-8937144",
            "resource": "Reactome",
            "description": "Aryl hydrocarbon receptor signalling"
        }
    ],
    "orthologs": [],
    "go_annotation": {
        "categories": [
            {
                "name": "Cellular Component",
                "total": 2,
                "go_terms": [
                    {
                        "name": "membrane",
                        "id": "GO:0016020",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016020",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A6H2EG45",
                                "url": "https://www.uniprot.org/uniprot/A0A6H2EG45"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "cytosol",
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                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005829",
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                                "database": "UniProtKB",
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                            }
                        ],
                        "pmid": ""
                    }
                ]
            },
            {
                "name": "Molecular Function",
                "total": 2,
                "go_terms": [
                    {
                        "name": "peptidyl-prolyl cis-trans isomerase activity",
                        "id": "GO:0003755",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003755",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A6H2EG45",
                                "url": "https://www.uniprot.org/uniprot/A0A6H2EG45"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "unfolded protein binding",
                        "id": "GO:0051082",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0051082",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A6H2EG45",
                                "url": "https://www.uniprot.org/uniprot/A0A6H2EG45"
                            }
                        ],
                        "pmid": ""
                    }
                ]
            },
            {
                "name": "Biological Process",
                "total": 2,
                "go_terms": [
                    {
                        "name": "protein targeting to mitochondrion",
                        "id": "GO:0006626",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006626",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A6H2EG45",
                                "url": "https://www.uniprot.org/uniprot/A0A6H2EG45"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "protein maturation by protein folding",
                        "id": "GO:0022417",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0022417",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A6H2EG45",
                                "url": "https://www.uniprot.org/uniprot/A0A6H2EG45"
                            }
                        ],
                        "pmid": ""
                    }
                ]
            }
        ]
    },
    "pro_annotation": [],
    "site_annotation": [
        {
            "start_pos": 322,
            "end_pos": 324,
            "annotation": "n_glycosylation_sequon"
        }
    ],
    "ptm_annotation": [],
    "interactions": [],
    "reactions": [],
    "reaction_participants": [],
    "reaction_enzymes": [],
    "biomarkers": [],
    "synthesized_glycans": [],
    "cluster_types": [
        {
            "name": "isoformset.uniprotkb",
            "label": "Isoforms"
        }
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