{
    "uniprot_canonical_ac": "Q06836-1",
    "uniprot_ac": "Q06836",
    "uniprot_id": "SYT1_YEAST",
    "mass": {
        "chemical_mass": 137583.0,
        "monoisotopic_mass": 137583.0
    },
    "refseq": {
        "ac": "NP_015420",
        "name": "Arf family guanine nucleotide exchange factor SYT1",
        "summary": "",
        "url": "https://www.ncbi.nlm.nih.gov/protein/NP_015420"
    },
    "gene_names": [
        {
            "name": "SYT1",
            "resource": "UniProtKB",
            "type": "recommended",
            "url": "https://www.uniprot.org/uniprot/Q06836",
            "id": "Q06836"
        },
        {
            "name": "P9513.17",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/Q06836",
            "id": "Q06836"
        },
        {
            "name": "SYT1",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_015420",
            "id": "NP_015420"
        }
    ],
    "protein_names": [
        {
            "name": "Arf guanine nucleotide exchange factor SYT1",
            "resource": "UniProtKB",
            "type": "recommended",
            "url": "",
            "id": "Q06836"
        },
        {
            "name": "Arf family guanine nucleotide exchange factor SYT1",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_015420",
            "id": "NP_015420"
        },
        {
            "name": "Arf-GEF SYT1",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "Q06836"
        },
        {
            "name": "Suppressor of YPT3 protein 1",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "Q06836"
        }
    ],
    "function": [
        {
            "annotation": "Guanine nucleotide exchange factor for Arf GTPases, stimulating the nucleotide exchange from the GDP-bound to the GTP-bound form. Catalyzes both the GDP release by and the GTP binding to ARF2. Has no exchange activity on Rab GTPases. Involved in vesicular transport.",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "Q06836",
                    "url": "https://www.uniprot.org/uniprot/Q06836#function"
                },
                {
                    "database": "PubMed",
                    "id": "10430582",
                    "url": "https://glygen.org/publication/PubMed/10430582"
                }
            ]
        }
    ],
    "disease": [
        {
            "disease_id": "DOID:0050776",
            "recommended_name": {
                "id": "DOID:0050776",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:0050776",
                "name": "non-syndromic X-linked intellectual disability",
                "description": "A non-syndromic intellectual disability characterized by a X-linked inheritance pattern."
            },
            "synonyms": [
                {
                    "id": "DOID:0050776",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0050776",
                    "name": "non-specific X-linked mental retardation",
                    "description": ""
                },
                {
                    "id": "MONDO:0010413",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010413",
                    "name": "intellectual disability, X-linked 95",
                    "description": ""
                },
                {
                    "id": "MONDO:0010413",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010413",
                    "name": "MRX95",
                    "description": ""
                },
                {
                    "id": "MONDO:0010413",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010413",
                    "name": "intellectual disability, X-linked 95",
                    "description": ""
                },
                {
                    "id": "MONDO:0010413",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010413",
                    "name": "mental retardation, X-linked 95, X-linked dominant",
                    "description": ""
                },
                {
                    "id": "MONDO:0010413",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010413",
                    "name": "mental retardation, X-linked 95",
                    "description": ""
                },
                {
                    "id": "MONDO:0010656",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010656",
                    "name": "intellectual disability, X-linked 1",
                    "description": "An X-linked dominant condition caused by mutation(s) in the IQSEC2 gene, encoding IQ motif and SEC7 domain-containing protein 2. It is characterized by substantially impaired intellectual functioning and behavioral abnormalities."
                },
                {
                    "id": "MONDO:0010656",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010656",
                    "name": "MRX",
                    "description": ""
                },
                {
                    "id": "MONDO:0010656",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010656",
                    "name": "MRX1",
                    "description": ""
                },
                {
                    "id": "MONDO:0010656",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010656",
                    "name": "MRX78",
                    "description": ""
                },
                {
                    "id": "MONDO:0010656",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010656",
                    "name": "intellectual developmental disorder, X-linked 1, X-linked dominant",
                    "description": ""
                },
                {
                    "id": "MONDO:0010656",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010656",
                    "name": "intellectual disability, X-linked 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0010656",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010656",
                    "name": "mental retardation, X-linked 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0010656",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010656",
                    "name": "mental retardation, X-linked 18",
                    "description": ""
                },
                {
                    "id": "MONDO:0010656",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010656",
                    "name": "mental retardation, X-linked 78",
                    "description": ""
                },
                {
                    "id": "MONDO:0010656",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010656",
                    "name": "mental retardation, X-linked type 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0010656",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010656",
                    "name": "IQSEC2",
                    "description": ""
                },
                {
                    "id": "MONDO:0010656",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010656",
                    "name": "IQSEC2-related epilepsy",
                    "description": ""
                },
                {
                    "id": "MONDO:0010656",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010656",
                    "name": "IQSEC2-related intellectual disability",
                    "description": ""
                },
                {
                    "id": "MONDO:0010656",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010656",
                    "name": "X-linked intellectual disability 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0010656",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010656",
                    "name": "X-linked intellectual disability 1/78",
                    "description": ""
                },
                {
                    "id": "MONDO:0010656",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010656",
                    "name": "X-linked intellectual disability 78",
                    "description": ""
                },
                {
                    "id": "MIM:309530",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/309530",
                    "name": "Intellectual developmental disorder, X-linked 1",
                    "description": "Intellectual developmental disorder, X-linked 1"
                }
            ],
            "evidence": [
                {
                    "id": "0050776",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:0050776"
                }
            ]
        },
        {
            "disease_id": "DOID:0111674",
            "recommended_name": {
                "id": "DOID:0111674",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:0111674",
                "name": "intellectual developmental disorder with short stature and behavioral abnormalities",
                "description": "A syndrome characterized by intellectual disability, global developmental delay, short stature, aphasia, and hypotonia that has_material_basis_in homozygous or compound heterozygous mutation in the IQSEC1 gene on chromosome 3p25.2-p25.1."
            },
            "synonyms": [
                {
                    "id": "DOID:0111674",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0111674",
                    "name": "IDDSSBA",
                    "description": ""
                },
                {
                    "id": "MONDO:0032870",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0032870",
                    "name": "intellectual developmental disorder with short stature and behavioral abnormalities",
                    "description": ""
                },
                {
                    "id": "MONDO:0032870",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0032870",
                    "name": "IDDSSBA",
                    "description": ""
                },
                {
                    "id": "MONDO:0032870",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0032870",
                    "name": "INTELLECTUAL DEVELOPMENTAL DISORDER WITH SHORT STATURE AND BEHAVIORAL ABNORMALITIES",
                    "description": ""
                },
                {
                    "id": "MIM:618687",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/618687",
                    "name": "Intellectual developmental disorder with short stature and behavioral abnormalities",
                    "description": "Intellectual developmental disorder with short stature and behavioral abnormalities"
                }
            ],
            "evidence": [
                {
                    "id": "0111674",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:0111674"
                }
            ]
        },
        {
            "disease_id": "DOID:0112038",
            "recommended_name": {
                "id": "DOID:0112038",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:0112038",
                "name": "non-syndromic X-linked intellectual disability 1",
                "description": "A non-syndromic X-linked intellectual disability characterized by moderate to severe intellectual disability in males and varying levels of intellectual disability in females that has_material_basis_in hemizygous or heterozygous mutation in the IQSEC2 gene on chromosome Xp11.22."
            },
            "synonyms": [
                {
                    "id": "DOID:0112038",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0112038",
                    "name": "MRX1",
                    "description": ""
                },
                {
                    "id": "DOID:0112038",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0112038",
                    "name": "MRX18",
                    "description": ""
                },
                {
                    "id": "DOID:0112038",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0112038",
                    "name": "MRX78",
                    "description": ""
                },
                {
                    "id": "DOID:0112038",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0112038",
                    "name": "X-linked mental retardation 1",
                    "description": ""
                },
                {
                    "id": "DOID:0112038",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0112038",
                    "name": "X-linked mental retardation 1/78",
                    "description": ""
                },
                {
                    "id": "DOID:0112038",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0112038",
                    "name": "X-linked mental retardation 18",
                    "description": ""
                },
                {
                    "id": "DOID:0112038",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0112038",
                    "name": "X-linked mental retardation 78",
                    "description": ""
                },
                {
                    "id": "MONDO:0010656",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010656",
                    "name": "intellectual disability, X-linked 1",
                    "description": "An X-linked dominant condition caused by mutation(s) in the IQSEC2 gene, encoding IQ motif and SEC7 domain-containing protein 2. It is characterized by substantially impaired intellectual functioning and behavioral abnormalities."
                },
                {
                    "id": "MONDO:0010656",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010656",
                    "name": "MRX",
                    "description": ""
                },
                {
                    "id": "MONDO:0010656",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010656",
                    "name": "MRX1",
                    "description": ""
                },
                {
                    "id": "MONDO:0010656",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010656",
                    "name": "MRX78",
                    "description": ""
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                {
                    "id": "MONDO:0010656",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010656",
                    "name": "intellectual developmental disorder, X-linked 1, X-linked dominant",
                    "description": ""
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                {
                    "id": "MONDO:0010656",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010656",
                    "name": "intellectual disability, X-linked 1",
                    "description": ""
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                {
                    "id": "MONDO:0010656",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010656",
                    "name": "mental retardation, X-linked 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0010656",
                    "resource": "MONDO",
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                    "description": ""
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                {
                    "id": "MONDO:0010656",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010656",
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                    "description": ""
                },
                {
                    "id": "MONDO:0010656",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010656",
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                    "description": ""
                },
                {
                    "id": "MONDO:0010656",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010656",
                    "name": "IQSEC2",
                    "description": ""
                },
                {
                    "id": "MONDO:0010656",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010656",
                    "name": "IQSEC2-related epilepsy",
                    "description": ""
                },
                {
                    "id": "MONDO:0010656",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010656",
                    "name": "IQSEC2-related intellectual disability",
                    "description": ""
                },
                {
                    "id": "MONDO:0010656",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010656",
                    "name": "X-linked intellectual disability 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0010656",
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                    "description": ""
                },
                {
                    "id": "MONDO:0010656",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010656",
                    "name": "X-linked intellectual disability 78",
                    "description": ""
                },
                {
                    "id": "MIM:309530",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/309530",
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                    "description": "Intellectual developmental disorder, X-linked 1"
                }
            ],
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                {
                    "id": "0112038",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:0112038"
                }
            ]
        },
        {
            "disease_id": "DOID:1574",
            "recommended_name": {
                "id": "DOID:1574",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:1574",
                "name": "alcohol use disorder",
                "description": "A substance abuse that involves the recurring use of alcoholic beverages despite negative consequences."
            },
            "synonyms": [
                {
                    "id": "DOID:1574",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:1574",
                    "name": "Ethanol abuse",
                    "description": ""
                },
                {
                    "id": "DOID:1574",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:1574",
                    "name": "alcohol abuse",
                    "description": ""
                }
            ],
            "evidence": [
                {
                    "id": "1574",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:1574"
                }
            ]
        },
        {
            "disease_id": "DOID:3908",
            "recommended_name": {
                "id": "DOID:3908",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:3908",
                "name": "lung non-small cell carcinoma",
                "description": "A lung carcinoma that is characterized as any type of epithelial lung cancer other than small cell lung carcinoma."
            },
            "synonyms": [
                {
                    "id": "DOID:3908",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:3908",
                    "name": "NSCLC",
                    "description": ""
                },
                {
                    "id": "DOID:3908",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:3908",
                    "name": "Non-small cell lung cancer",
                    "description": ""
                },
                {
                    "id": "DOID:3908",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:3908",
                    "name": "non-small cell lung carcinoma",
                    "description": ""
                }
            ],
            "evidence": [
                {
                    "id": "3908",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:3908"
                }
            ]
        },
        {
            "disease_id": "DOID:3910",
            "recommended_name": {
                "id": "DOID:3910",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:3910",
                "name": "lung adenocarcinoma",
                "description": "A lung non-small cell carcinoma that derives_from epithelial cells of glandular origin."
            },
            "synonyms": [
                {
                    "id": "DOID:3910",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:3910",
                    "name": "bronchogenic lung adenocarcinoma",
                    "description": ""
                },
                {
                    "id": "DOID:3910",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:3910",
                    "name": "nonsmall cell adenocarcinoma",
                    "description": ""
                }
            ],
            "evidence": [
                {
                    "id": "3910",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:3910"
                }
            ]
        }
    ],
    "snv": [],
    "mutagenesis": [],
    "expression_tissue": [],
    "expression_disease": [],
    "species": [
        {
            "name": "Saccharomyces cerevisiae S288C",
            "taxid": 559292,
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "Q06836",
                    "url": "https://www.uniprot.org/uniprot/Q06836"
                }
            ],
            "common_name": "Yeast"
        }
    ],
    "gene": [
        {
            "name": "SYT1",
            "url": "https://www.uniprot.org/uniprot/Q06836",
            "locus": {}
        }
    ],
    "crossref": [
        {
            "id": "cd00171",
            "url": "https://www.ncbi.nlm.nih.gov/Structure/cdd/cddsrv.cgi?uid=cd00171",
            "database": "CDD",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "856210",
            "url": "https://www.ncbi.nlm.nih.gov/gene/856210",
            "database": "GeneID",
            "categories": [
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        },
        {
            "id": "Q06836",
            "url": "https://www.ebi.ac.uk/intact/interactors/id:Q06836*",
            "database": "IntAct",
            "categories": [
                "Other"
            ]
        },
        {
            "id": "IPR000904",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR000904",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR001849",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR001849",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR023394",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR023394",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR035999",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR035999",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "sce:YPR095C",
            "url": "https://www.genome.jp/dbget-bin/get_linkdb?-t+pathway+sce:YPR095C",
            "database": "KEGG Pathway",
            "categories": [
                "Enzyme and Pathway"
            ]
        },
        {
            "id": "Q06836",
            "url": "https://oglcnac.org/atlas/detail/Q06836",
            "database": "O-GlcNAc Atlas",
            "categories": [
                "Glycoproteomics"
            ]
        },
        {
            "id": "Q06836",
            "url": "https://www.oglcnac.mcw.edu/search/?query_protein=Q06836",
            "database": "O-GlcNAc Database",
            "categories": [
                "Glycoproteomics"
            ]
        },
        {
            "id": "QENINIY",
            "url": "https://omabrowser.org/oma/group/QENINIY/",
            "database": "OMA",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "4248238at2759",
            "url": "http://www.orthodb.org/?query=4248238at2759",
            "database": "OrthoDB",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PTHR10663",
            "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR10663",
            "database": "PANTHER",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PTHR10663:SF328",
            "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR10663:SF328",
            "database": "PANTHER",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PF01369",
            "url": "http://pfam.xfam.org/family/PF01369",
            "database": "Pfam",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PR_Q06836",
            "url": "http://purl.obolibrary.org/obo/PR_Q06836",
            "database": "PRO",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "NP_015420",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_015420",
            "database": "RefSeq",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "S000006299",
            "url": "https://www.yeastgenome.org/locus/S000006299",
            "database": "SGD",
            "categories": [
                "Organism-specific"
            ]
        },
        {
            "id": "Q06836",
            "url": "https://www.uniprot.org/uniprot/Q06836",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "Q06836-1",
            "url": "https://www.uniprot.org/uniprot/Q06836-1",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        }
    ],
    "sequence": {
        "sequence": "MNQSISSLIKLKFLQSHSNDKNGNKKGGSNVSTGIDKLRESESYRSPFLQLAEIQEHTNNDDDKLDVKECEPTKKHSKLSRIRRKMGRLDLNFRSANEKGSEDDEILVAQHLRNGQDPEEMPFKSENNIDSIEKVPKPDGERVTLTSSGSDNVKRNSKHAPFIPVKPALEKFPSSNRLSRDYRKSQEPTLFNGDRLVPTLPTVSRISTSSSVGSSTAASRYFNPSKRAVVASSSSSSSSIKFNSLHAIPLDATPQIELAKQQDEISKRRFGRRRSRTVDVFDYINKNNTAKNKPPLSPSSFIRTIDEKNTNSLMQDPMGSRGPLLPDDANIISNDTDGAEASHPDHQVLSRSRSQSTSFVQGKGGKRKSIEDEGYHNKLGLPHGSGPTSVYNNKSNANSTITGMSRRSSSIVNALSSFVNLRSSSLSSSRQQHLQQQQQLQQKLDVSLEDLPPVPAPEFSDSCKDFLIKLAPYGKFIGIILTEKDDEFKKNCLNYLLTNCFEFKNDPLDIALRKLLMFLELPKETQQIDRLIMAFSFAYYKAQKSYSKKKGIECPWSNADQVYFIAFSLLMLHTDYFNPNNKSKMTKHDFVDLVHNDKYSGGNEIPMAVLTYFYENVTAKESPKFNYFLMSPMALDDSILDKDAFDTNFAITLSSNSMYSPIDMIKRGSIIPKEASLSPIFYPLTNSISASGIAPSTAASCPPSTSGTINGANLGTANSNSNRPASNSISSYFSYNPSSSSSGNATLVQDDINVYSHIINDTLNEVNLFPEVSKYWNKNALKANLLRNEEHKYEKYYSIMNDTKGGYLRFHKSQLNKLNLPNFEILNDNSRSGCKNSDYKYCKILQMGAIMNLGMPSRKFSIVNSAKIHWKKEFAILTSLGLLICDKMDWINPQMMKDPKSGTTNYIIDFKSGFSFVPGSTIDVYNGLFADRERDSLGKSHFASLVLAYTEHHSTGSHTSNTTAASSSAKHNEGVFEPSSDEEDSITNSTDGTSSVSNGESDNDSVSSSDNQLSSNDSNEDYHSIKDEYPIFEDENADCLLYLHTCHRNFIWKCANKYERDNWIDSINLFSAYDGCYVEIGSIANTICNKRKLTILQRMERLRSIKSAKWEKLKKFESTLMLMGKCVPISTKTKTDMINRIRQLAVRMDWLIYEIKRSELFVSIIKEVTRKQAEKNILEHGKGEEEGQGNNDDSDGIDDIEESFLFNENSLQVCVSDSSYDEYSNE",
        "length": 1226,
        "header": "sp|Q06836-1|SYT1_YEAST Isoform 1 of Arf guanine nucleotide exchange factor SYT1  OS=Saccharomyces cerevisiae S288C OX=559292 GN=SYT1 PE=1 SV=1 CANONICAL=Q06836-1"
    },
    "isoforms": [
        {
            "isoform_ac": "Q06836-1",
            "url": "",
            "sequence": {
                "sequence": "MNQSISSLIKLKFLQSHSNDKNGNKKGGSNVSTGIDKLRESESYRSPFLQLAEIQEHTNNDDDKLDVKECEPTKKHSKLSRIRRKMGRLDLNFRSANEKGSEDDEILVAQHLRNGQDPEEMPFKSENNIDSIEKVPKPDGERVTLTSSGSDNVKRNSKHAPFIPVKPALEKFPSSNRLSRDYRKSQEPTLFNGDRLVPTLPTVSRISTSSSVGSSTAASRYFNPSKRAVVASSSSSSSSIKFNSLHAIPLDATPQIELAKQQDEISKRRFGRRRSRTVDVFDYINKNNTAKNKPPLSPSSFIRTIDEKNTNSLMQDPMGSRGPLLPDDANIISNDTDGAEASHPDHQVLSRSRSQSTSFVQGKGGKRKSIEDEGYHNKLGLPHGSGPTSVYNNKSNANSTITGMSRRSSSIVNALSSFVNLRSSSLSSSRQQHLQQQQQLQQKLDVSLEDLPPVPAPEFSDSCKDFLIKLAPYGKFIGIILTEKDDEFKKNCLNYLLTNCFEFKNDPLDIALRKLLMFLELPKETQQIDRLIMAFSFAYYKAQKSYSKKKGIECPWSNADQVYFIAFSLLMLHTDYFNPNNKSKMTKHDFVDLVHNDKYSGGNEIPMAVLTYFYENVTAKESPKFNYFLMSPMALDDSILDKDAFDTNFAITLSSNSMYSPIDMIKRGSIIPKEASLSPIFYPLTNSISASGIAPSTAASCPPSTSGTINGANLGTANSNSNRPASNSISSYFSYNPSSSSSGNATLVQDDINVYSHIINDTLNEVNLFPEVSKYWNKNALKANLLRNEEHKYEKYYSIMNDTKGGYLRFHKSQLNKLNLPNFEILNDNSRSGCKNSDYKYCKILQMGAIMNLGMPSRKFSIVNSAKIHWKKEFAILTSLGLLICDKMDWINPQMMKDPKSGTTNYIIDFKSGFSFVPGSTIDVYNGLFADRERDSLGKSHFASLVLAYTEHHSTGSHTSNTTAASSSAKHNEGVFEPSSDEEDSITNSTDGTSSVSNGESDNDSVSSSDNQLSSNDSNEDYHSIKDEYPIFEDENADCLLYLHTCHRNFIWKCANKYERDNWIDSINLFSAYDGCYVEIGSIANTICNKRKLTILQRMERLRSIKSAKWEKLKKFESTLMLMGKCVPISTKTKTDMINRIRQLAVRMDWLIYEIKRSELFVSIIKEVTRKQAEKNILEHGKGEEEGQGNNDDSDGIDDIEESFLFNENSLQVCVSDSSYDEYSNE",
                "length": 1226,
                "header": "sp|Q06836-1|SYT1_YEAST Isoform 1 of Arf guanine nucleotide exchange factor SYT1  OS=Saccharomyces cerevisiae S288C OX=559292 GN=SYT1 PE=1 SV=1 CANONICAL=Q06836-1"
            },
            "locus": {
                "chromosome": "XVI",
                "start_pos": 724717,
                "end_pos": 721040,
                "strand": "+",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "YPR095C_mRNA",
                        "url": "https://www.ensembl.org/id/YPR095C_mRNA"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "YPR095C",
                        "url": "https://www.ensembl.org/id/YPR095C"
                    }
                ]
            }
        }
    ],
    "glycosylation": [
        {
            "glytoucan_ac": "G49108TO",
            "type": "O-linked",
            "subtype": "O-GlcNAcylation",
            "site_category": "reported_with_glycan",
            "site_seq": "T",
            "relation": "attached",
            "comment": "O-GlcNAcylation",
            "start_pos": 144,
            "start_aa": "Thr",
            "end_pos": 144,
            "end_aa": "Thr",
            "residue": "Thr",
            "site_lbl": "Thr144",
            "evidence": [
                {
                    "id": "Q06836",
                    "database": "O-GlcNAc Atlas",
                    "url": "https://oglcnac.org/atlas/detail/Q06836"
                },
                {
                    "id": "33229814",
                    "database": "PubMed",
                    "url": "https://glygen.org/publication/PubMed/33229814"
                }
            ]
        },
        {
            "glytoucan_ac": "G49108TO",
            "type": "O-linked",
            "subtype": "O-GlcNAcylation",
            "site_category": "reported_with_glycan",
            "site_seq": "T",
            "relation": "attached",
            "comment": "O-GlcNAcylation",
            "start_pos": 146,
            "start_aa": "Thr",
            "end_pos": 146,
            "end_aa": "Thr",
            "residue": "Thr",
            "site_lbl": "Thr146",
            "evidence": [
                {
                    "id": "Q06836",
                    "database": "O-GlcNAc Atlas",
                    "url": "https://oglcnac.org/atlas/detail/Q06836"
                },
                {
                    "id": "33229814",
                    "database": "PubMed",
                    "url": "https://glygen.org/publication/PubMed/33229814"
                }
            ]
        },
        {
            "glytoucan_ac": "G49108TO",
            "type": "O-linked",
            "subtype": "O-GlcNAcylation",
            "site_category": "reported_with_glycan",
            "site_seq": "S",
            "relation": "attached",
            "comment": "O-GlcNAcylation",
            "start_pos": 147,
            "start_aa": "Ser",
            "end_pos": 147,
            "end_aa": "Ser",
            "residue": "Ser",
            "site_lbl": "Ser147",
            "evidence": [
                {
                    "id": "Q06836",
                    "database": "O-GlcNAc Atlas",
                    "url": "https://oglcnac.org/atlas/detail/Q06836"
                },
                {
                    "id": "33229814",
                    "database": "PubMed",
                    "url": "https://glygen.org/publication/PubMed/33229814"
                }
            ]
        },
        {
            "glytoucan_ac": "G49108TO",
            "type": "O-linked",
            "subtype": "O-GlcNAcylation",
            "site_category": "reported_with_glycan",
            "site_seq": "S",
            "relation": "attached",
            "comment": "O-GlcNAcylation",
            "start_pos": 148,
            "start_aa": "Ser",
            "end_pos": 148,
            "end_aa": "Ser",
            "residue": "Ser",
            "site_lbl": "Ser148",
            "evidence": [
                {
                    "id": "Q06836",
                    "database": "O-GlcNAc Atlas",
                    "url": "https://oglcnac.org/atlas/detail/Q06836"
                },
                {
                    "id": "33229814",
                    "database": "PubMed",
                    "url": "https://glygen.org/publication/PubMed/33229814"
                }
            ]
        },
        {
            "glytoucan_ac": "G49108TO",
            "type": "O-linked",
            "subtype": "O-GlcNAcylation",
            "site_category": "reported_with_glycan",
            "site_seq": "S",
            "relation": "attached",
            "comment": "O-GlcNAcylation",
            "start_pos": 150,
            "start_aa": "Ser",
            "end_pos": 150,
            "end_aa": "Ser",
            "residue": "Ser",
            "site_lbl": "Ser150",
            "evidence": [
                {
                    "id": "Q06836",
                    "database": "O-GlcNAc Atlas",
                    "url": "https://oglcnac.org/atlas/detail/Q06836"
                },
                {
                    "id": "33229814",
                    "database": "PubMed",
                    "url": "https://glygen.org/publication/PubMed/33229814"
                }
            ]
        },
        {
            "glytoucan_ac": "G49108TO",
            "type": "O-linked",
            "subtype": "O-GlcNAcylation",
            "site_category": "reported_with_glycan",
            "site_seq": "S",
            "relation": "attached",
            "comment": "O-GlcNAcylation",
            "start_pos": 207,
            "start_aa": "Ser",
            "end_pos": 207,
            "end_aa": "Ser",
            "residue": "Ser",
            "site_lbl": "Ser207",
            "evidence": [
                {
                    "id": "Q06836",
                    "database": "O-GlcNAc Atlas",
                    "url": "https://oglcnac.org/atlas/detail/Q06836"
                },
                {
                    "id": "33229814",
                    "database": "PubMed",
                    "url": "https://glygen.org/publication/PubMed/33229814"
                }
            ]
        },
        {
            "glytoucan_ac": "G49108TO",
            "type": "O-linked",
            "subtype": "O-GlcNAcylation",
            "site_category": "reported_with_glycan",
            "site_seq": "T",
            "relation": "attached",
            "comment": "O-GlcNAcylation",
            "start_pos": 208,
            "start_aa": "Thr",
            "end_pos": 208,
            "end_aa": "Thr",
            "residue": "Thr",
            "site_lbl": "Thr208",
            "evidence": [
                {
                    "id": "Q06836",
                    "database": "O-GlcNAc Atlas",
                    "url": "https://oglcnac.org/atlas/detail/Q06836"
                },
                {
                    "id": "33229814",
                    "database": "PubMed",
                    "url": "https://glygen.org/publication/PubMed/33229814"
                }
            ]
        },
        {
            "glytoucan_ac": "G49108TO",
            "type": "O-linked",
            "subtype": "O-GlcNAcylation",
            "site_category": "reported_with_glycan",
            "site_seq": "S",
            "relation": "attached",
            "comment": "O-GlcNAcylation",
            "start_pos": 209,
            "start_aa": "Ser",
            "end_pos": 209,
            "end_aa": "Ser",
            "residue": "Ser",
            "site_lbl": "Ser209",
            "evidence": [
                {
                    "id": "Q06836",
                    "database": "O-GlcNAc Atlas",
                    "url": "https://oglcnac.org/atlas/detail/Q06836"
                },
                {
                    "id": "33229814",
                    "database": "PubMed",
                    "url": "https://glygen.org/publication/PubMed/33229814"
                }
            ]
        },
        {
            "glytoucan_ac": "G49108TO",
            "type": "O-linked",
            "subtype": "O-GlcNAcylation",
            "site_category": "reported_with_glycan",
            "site_seq": "S",
            "relation": "attached",
            "comment": "O-GlcNAcylation",
            "start_pos": 210,
            "start_aa": "Ser",
            "end_pos": 210,
            "end_aa": "Ser",
            "residue": "Ser",
            "site_lbl": "Ser210",
            "evidence": [
                {
                    "id": "Q06836",
                    "database": "O-GlcNAc Atlas",
                    "url": "https://oglcnac.org/atlas/detail/Q06836"
                },
                {
                    "id": "33229814",
                    "database": "PubMed",
                    "url": "https://glygen.org/publication/PubMed/33229814"
                }
            ]
        },
        {
            "glytoucan_ac": "G49108TO",
            "type": "O-linked",
            "subtype": "O-GlcNAcylation",
            "site_category": "reported_with_glycan",
            "site_seq": "S",
            "relation": "attached",
            "comment": "O-GlcNAcylation",
            "start_pos": 211,
            "start_aa": "Ser",
            "end_pos": 211,
            "end_aa": "Ser",
            "residue": "Ser",
            "site_lbl": "Ser211",
            "evidence": [
                {
                    "id": "Q06836",
                    "database": "O-GlcNAc Atlas",
                    "url": "https://oglcnac.org/atlas/detail/Q06836"
                },
                {
                    "id": "33229814",
                    "database": "PubMed",
                    "url": "https://glygen.org/publication/PubMed/33229814"
                }
            ]
        },
        {
            "glytoucan_ac": "G49108TO",
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            "site_seq": "S",
            "relation": "attached",
            "comment": "O-GlcNAcylation",
            "start_pos": 214,
            "start_aa": "Ser",
            "end_pos": 214,
            "end_aa": "Ser",
            "residue": "Ser",
            "site_lbl": "Ser214",
            "evidence": [
                {
                    "id": "Q06836",
                    "database": "O-GlcNAc Atlas",
                    "url": "https://oglcnac.org/atlas/detail/Q06836"
                },
                {
                    "id": "33229814",
                    "database": "PubMed",
                    "url": "https://glygen.org/publication/PubMed/33229814"
                }
            ]
        },
        {
            "glytoucan_ac": "G49108TO",
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            "start_pos": 215,
            "start_aa": "Ser",
            "end_pos": 215,
            "end_aa": "Ser",
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                {
                    "id": "Q06836",
                    "database": "O-GlcNAc Atlas",
                    "url": "https://oglcnac.org/atlas/detail/Q06836"
                },
                {
                    "id": "33229814",
                    "database": "PubMed",
                    "url": "https://glygen.org/publication/PubMed/33229814"
                }
            ]
        },
        {
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            "comment": "O-GlcNAcylation",
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            "start_aa": "Ser",
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            "end_aa": "Ser",
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                {
                    "id": "Q06836",
                    "database": "O-GlcNAc Atlas",
                    "url": "https://oglcnac.org/atlas/detail/Q06836"
                },
                {
                    "id": "33229814",
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                    "url": "https://glygen.org/publication/PubMed/33229814"
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            ]
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        {
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            "evidence": [
                {
                    "id": "Q06836",
                    "database": "O-GlcNAc Atlas",
                    "url": "https://oglcnac.org/atlas/detail/Q06836"
                },
                {
                    "id": "33229814",
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                    "url": "https://glygen.org/publication/PubMed/33229814"
                }
            ]
        },
        {
            "glytoucan_ac": "G49108TO",
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            "comment": "O-GlcNAcylation",
            "start_pos": 233,
            "start_aa": "Ser",
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            "end_aa": "Ser",
            "residue": "Ser",
            "site_lbl": "Ser233",
            "evidence": [
                {
                    "id": "Q06836",
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                    "url": "https://oglcnac.org/atlas/detail/Q06836"
                },
                {
                    "id": "33229814",
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                    "url": "https://glygen.org/publication/PubMed/33229814"
                }
            ]
        },
        {
            "glytoucan_ac": "G49108TO",
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                    "id": "Q06836",
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                },
                {
                    "id": "33229814",
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            ]
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        {
            "glytoucan_ac": "G49108TO",
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            "evidence": [
                {
                    "id": "Q06836",
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                },
                {
                    "id": "33229814",
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                }
            ]
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        {
            "glytoucan_ac": "G49108TO",
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                    "id": "Q06836",
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                },
                {
                    "id": "33229814",
                    "database": "PubMed",
                    "url": "https://glygen.org/publication/PubMed/33229814"
                }
            ]
        },
        {
            "glytoucan_ac": "G49108TO",
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            "comment": "O-GlcNAcylation",
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            "start_aa": "Ser",
            "end_pos": 237,
            "end_aa": "Ser",
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            "evidence": [
                {
                    "id": "Q06836",
                    "database": "O-GlcNAc Atlas",
                    "url": "https://oglcnac.org/atlas/detail/Q06836"
                },
                {
                    "id": "33229814",
                    "database": "PubMed",
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                }
            ]
        },
        {
            "glytoucan_ac": "G49108TO",
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            "subtype": "O-GlcNAcylation",
            "site_category": "reported_with_glycan",
            "site_seq": "S",
            "relation": "attached",
            "comment": "O-GlcNAcylation",
            "start_pos": 238,
            "start_aa": "Ser",
            "end_pos": 238,
            "end_aa": "Ser",
            "residue": "Ser",
            "site_lbl": "Ser238",
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            "title": "Genetic interactions in yeast between Ypt GTPases and Arf guanine nucleotide exchangers.",
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