{
    "uniprot_canonical_ac": "Q6Q595-1",
    "uniprot_ac": "Q6Q595",
    "uniprot_id": "SCS22_YEAST",
    "mass": {
        "chemical_mass": 19678.0,
        "monoisotopic_mass": 19678.0
    },
    "refseq": {
        "ac": "NP_009461",
        "name": "phospholipid metabolism-regulating protein SCS22",
        "summary": "",
        "url": "https://www.ncbi.nlm.nih.gov/protein/NP_009461"
    },
    "gene_names": [
        {
            "name": "SCS22",
            "resource": "UniProtKB",
            "type": "recommended",
            "url": "https://www.uniprot.org/uniprot/Q6Q595",
            "id": "Q6Q595"
        },
        {
            "name": "SCS22",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_009461",
            "id": "NP_009461"
        }
    ],
    "protein_names": [
        {
            "name": "Vesicle-associated membrane protein-associated protein SCS22",
            "resource": "UniProtKB",
            "type": "recommended",
            "url": "",
            "id": "Q6Q595"
        },
        {
            "name": "VAMP-associated protein SCS22",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "Q6Q595"
        },
        {
            "name": "VAP homolog 2",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "Q6Q595"
        },
        {
            "name": "phospholipid metabolism-regulating protein SCS22",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_009461",
            "id": "NP_009461"
        }
    ],
    "function": [
        {
            "annotation": "Targets proteins containing a FFAT motif to membranes (By similarity). Involved in regulation of phospholipid metabolism.",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "Q6Q595",
                    "url": "https://www.uniprot.org/uniprot/Q6Q595#function"
                },
                {
                    "database": "PubMed",
                    "id": "15668246",
                    "url": "https://glygen.org/publication/PubMed/15668246"
                }
            ]
        }
    ],
    "disease": [
        {
            "disease_id": "DOID:0050752",
            "recommended_name": {
                "id": "DOID:0050752",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:0050752",
                "name": "amyotrophic lateral sclerosis type 8",
                "description": "An amyotrophic lateral sclerosis that has_material_basis_in mutation in the VAPB gene on chromosome 20."
            },
            "synonyms": [
                {
                    "id": "DOID:0050752",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0050752",
                    "name": "ALS8",
                    "description": ""
                },
                {
                    "id": "DOID:0050752",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0050752",
                    "name": "amyotrophic lateral sclerosis 8",
                    "description": ""
                },
                {
                    "id": "MONDO:0012077",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012077",
                    "name": "amyotrophic lateral sclerosis type 8",
                    "description": "Any amyotrophic lateral sclerosis in which the cause of the disease is a mutation in the VAPB gene."
                },
                {
                    "id": "MONDO:0012077",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012077",
                    "name": "ALS8",
                    "description": ""
                },
                {
                    "id": "MONDO:0012077",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012077",
                    "name": "VAPB amyotrophic lateral sclerosis",
                    "description": ""
                },
                {
                    "id": "MONDO:0012077",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012077",
                    "name": "amyotrophic lateral sclerosis 8",
                    "description": ""
                },
                {
                    "id": "MONDO:0012077",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012077",
                    "name": "amyotrophic lateral sclerosis caused by mutation in VAPB",
                    "description": ""
                },
                {
                    "id": "MONDO:0012077",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012077",
                    "name": "amyotrophic lateral sclerosis type 8",
                    "description": ""
                },
                {
                    "id": "MIM:608627",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/608627",
                    "name": "Amyotrophic lateral sclerosis 8",
                    "description": "Amyotrophic lateral sclerosis 8"
                }
            ],
            "evidence": [
                {
                    "id": "0050752",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:0050752"
                }
            ]
        },
        {
            "disease_id": "DOID:0111194",
            "recommended_name": {
                "id": "DOID:0111194",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:0111194",
                "name": "autosomal dominant adult-onset proximal spinal muscular atrophy",
                "description": "A spinal muscular atrophy characterized by adult-onset of slowly progressive, proximal muscular weakness with fasciculations and absent/hypoactive deep tendon reflexes, without bulbar or pyramidal involvement that has_material_basis_in heterozygous mutation in VAPB on 20q13."
            },
            "synonyms": [
                {
                    "id": "DOID:0111194",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0111194",
                    "name": "Finkel disease",
                    "description": ""
                },
                {
                    "id": "DOID:0111194",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0111194",
                    "name": "Finkel late-adult type SMA",
                    "description": ""
                },
                {
                    "id": "DOID:0111194",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0111194",
                    "name": "SMAFK",
                    "description": ""
                },
                {
                    "id": "DOID:0111194",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0111194",
                    "name": "autosomal dominant adult-onset proximal SMA",
                    "description": ""
                },
                {
                    "id": "DOID:0111194",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0111194",
                    "name": "autosomal dominant late-onset spinal muscular atrophy, Finkel type",
                    "description": ""
                },
                {
                    "id": "DOID:0111194",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0111194",
                    "name": "autosomal dominant adult proximal spinal muscular atrophy",
                    "description": ""
                },
                {
                    "id": "MONDO:0008453",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008453",
                    "name": "adult-onset proximal spinal muscular atrophy, autosomal dominant",
                    "description": ""
                },
                {
                    "id": "MONDO:0008453",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008453",
                    "name": "Finkel disease",
                    "description": ""
                },
                {
                    "id": "MONDO:0008453",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008453",
                    "name": "autosomal dominant adult-onset proximal SMA",
                    "description": ""
                },
                {
                    "id": "MONDO:0008453",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008453",
                    "name": "autosomal dominant late-onset spinal muscular atrophy, Finkel type",
                    "description": ""
                },
                {
                    "id": "MONDO:0008453",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008453",
                    "name": "Finkel late-adult type Sma",
                    "description": ""
                },
                {
                    "id": "MONDO:0008453",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008453",
                    "name": "SMAFK",
                    "description": ""
                },
                {
                    "id": "MONDO:0008453",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008453",
                    "name": "autosomal dominant adult-onset proximal spinal muscular atrophy",
                    "description": ""
                },
                {
                    "id": "MONDO:0008453",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008453",
                    "name": "spinal muscular atrophy, late-onset, FINKEL type",
                    "description": ""
                },
                {
                    "id": "MONDO:0008453",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008453",
                    "name": "spinal muscular atrophy, proximal, adult, autosomal dominant",
                    "description": ""
                },
                {
                    "id": "MIM:182980",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/182980",
                    "name": "Spinal muscular atrophy, proximal, adult, autosomal dominant",
                    "description": "Spinal muscular atrophy, proximal, adult, autosomal dominant"
                }
            ],
            "evidence": [
                {
                    "id": "0111194",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:0111194"
                }
            ]
        },
        {
            "disease_id": "DOID:12377",
            "recommended_name": {
                "id": "DOID:12377",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:12377",
                "name": "spinal muscular atrophy",
                "description": "A motor neuron disease that is a degenerative neuromuscular disease characterized by lower motor neuron degeneration associated with progressive muscle weakness and atrophy."
            },
            "synonyms": [],
            "evidence": [
                {
                    "id": "12377",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:12377"
                }
            ]
        },
        {
            "disease_id": "DOID:1289",
            "recommended_name": {
                "id": "DOID:1289",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:1289",
                "name": "neurodegenerative disease",
                "description": "A central nervous system disease that results in the progressive deterioration of function or structure of neurons."
            },
            "synonyms": [
                {
                    "id": "DOID:1289",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:1289",
                    "name": "degenerative disease",
                    "description": ""
                }
            ],
            "evidence": [
                {
                    "id": "1289",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:1289"
                }
            ]
        },
        {
            "disease_id": "DOID:231",
            "recommended_name": {
                "id": "DOID:231",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:231",
                "name": "motor neuron disease",
                "description": "A neurodegenerative disease that is located_in the motor neurons."
            },
            "synonyms": [],
            "evidence": [
                {
                    "id": "231",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:231"
                }
            ]
        },
        {
            "disease_id": "DOID:332",
            "recommended_name": {
                "id": "DOID:332",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:332",
                "name": "amyotrophic lateral sclerosis",
                "description": "A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing."
            },
            "synonyms": [
                {
                    "id": "DOID:332",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:332",
                    "name": "ALS",
                    "description": ""
                },
                {
                    "id": "DOID:332",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:332",
                    "name": "Lou Gehrig's disease",
                    "description": ""
                },
                {
                    "id": "DOID:332",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:332",
                    "name": "motor neuron disease, bulbar",
                    "description": ""
                },
                {
                    "id": "MONDO:0007103",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007103",
                    "name": "amyotrophic lateral sclerosis type 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0007103",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007103",
                    "name": "ALS1",
                    "description": ""
                },
                {
                    "id": "MONDO:0007103",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007103",
                    "name": "amyotrophic lateral sclerosis 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0007103",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007103",
                    "name": "amyotrophic lateral sclerosis type 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0007103",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007103",
                    "name": "FALS",
                    "description": ""
                },
                {
                    "id": "MONDO:0007103",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007103",
                    "name": "amyotrophic lateral sclerosis 1, autosomal dominant",
                    "description": ""
                },
                {
                    "id": "MONDO:0007103",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007103",
                    "name": "amyotrophic lateral sclerosis 1, autosomal dominant amyotrophic lateral sclerosis 1, autosomal recessive, included",
                    "description": ""
                },
                {
                    "id": "MONDO:0007103",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007103",
                    "name": "amyotrophic lateral sclerosis 1, autosomal recessive",
                    "description": ""
                },
                {
                    "id": "MONDO:0007103",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007103",
                    "name": "amyotrophic lateral sclerosis 1, familial",
                    "description": ""
                },
                {
                    "id": "MONDO:0007103",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007103",
                    "name": "amyotrophic lateral sclerosis, autosomal dominant",
                    "description": ""
                },
                {
                    "id": "MONDO:0007103",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007103",
                    "name": "amyotrophic lateral sclerosis, familial",
                    "description": ""
                },
                {
                    "id": "MONDO:0007103",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007103",
                    "name": "amyotrophic lateral sclerosis, sporadic",
                    "description": ""
                },
                {
                    "id": "MONDO:0007103",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007103",
                    "name": "amyotrophic lateral sclerosis, sporadic, included",
                    "description": ""
                },
                {
                    "id": "MONDO:0007103",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007103",
                    "name": "amyotrophic lateral sclerosis, susceptibility to",
                    "description": ""
                },
                {
                    "id": "MIM:105400",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/105400",
                    "name": "Amyotrophic lateral sclerosis 1",
                    "description": "Amyotrophic lateral sclerosis 1"
                }
            ],
            "evidence": [
                {
                    "id": "332",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:332"
                }
            ]
        }
    ],
    "snv": [],
    "mutagenesis": [],
    "expression_tissue": [],
    "expression_disease": [],
    "species": [
        {
            "name": "Saccharomyces cerevisiae S288C",
            "taxid": 559292,
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "Q6Q595",
                    "url": "https://www.uniprot.org/uniprot/Q6Q595"
                }
            ],
            "common_name": "Yeast"
        }
    ],
    "gene": [
        {
            "name": "SCS22",
            "url": "https://www.uniprot.org/uniprot/Q6Q595",
            "locus": {}
        }
    ],
    "crossref": [
        {
            "id": "852186",
            "url": "https://www.ncbi.nlm.nih.gov/gene/852186",
            "database": "GeneID",
            "categories": [
                "Genome Annotation"
            ]
        },
        {
            "id": "Q6Q595",
            "url": "https://www.ebi.ac.uk/intact/interactors/id:Q6Q595*",
            "database": "IntAct",
            "categories": [
                "Other"
            ]
        },
        {
            "id": "IPR000535",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR000535",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR008962",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR008962",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR013783",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR013783",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR016763",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR016763",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "sce:YBL091C-A",
            "url": "https://www.genome.jp/dbget-bin/get_linkdb?-t+pathway+sce:YBL091C-A",
            "database": "KEGG Pathway",
            "categories": [
                "Enzyme and Pathway"
            ]
        },
        {
            "id": "TAPKIYC",
            "url": "https://omabrowser.org/oma/group/TAPKIYC/",
            "database": "OMA",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "122649at2759",
            "url": "http://www.orthodb.org/?query=122649at2759",
            "database": "OrthoDB",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PTHR10809",
            "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR10809",
            "database": "PANTHER",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PTHR10809:SF6",
            "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR10809:SF6",
            "database": "PANTHER",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PF00635",
            "url": "http://pfam.xfam.org/family/PF00635",
            "database": "Pfam",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PR_Q6Q595",
            "url": "http://purl.obolibrary.org/obo/PR_Q6Q595",
            "database": "PRO",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "NP_009461",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_009461",
            "database": "RefSeq",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "S000007228",
            "url": "https://www.yeastgenome.org/locus/S000007228",
            "database": "SGD",
            "categories": [
                "Organism-specific"
            ]
        },
        {
            "id": "Q6Q595",
            "url": "https://www.uniprot.org/uniprot/Q6Q595",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "Q6Q595-1",
            "url": "https://www.uniprot.org/uniprot/Q6Q595-1",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        }
    ],
    "sequence": {
        "sequence": "MRIVPEKLVFKAPLNKQSTEYIKLENDGEKRVIFKVRTSAPTKYCVRPNVAIIGAHESVNVQIVFLGLPKSTADDEMDQKRDKFLIVTLPIPAAYQNVEDGELLSDWPNLEEQYKDDIVFKKIKIFHSVLPKRKPSGNHDAESARAPSAGNGQSLSSRALLIITVIALLVGWIYY",
        "length": 175,
        "header": "sp|Q6Q595-1|SCS22_YEAST Isoform 1 of Vesicle-associated membrane protein-associated protein SCS22  OS=Saccharomyces cerevisiae S288C OX=559292 GN=SCS22 PE=1 SV=2 CANONICAL=Q6Q595-1"
    },
    "isoforms": [
        {
            "isoform_ac": "Q6Q595-1",
            "url": "",
            "sequence": {
                "sequence": "MRIVPEKLVFKAPLNKQSTEYIKLENDGEKRVIFKVRTSAPTKYCVRPNVAIIGAHESVNVQIVFLGLPKSTADDEMDQKRDKFLIVTLPIPAAYQNVEDGELLSDWPNLEEQYKDDIVFKKIKIFHSVLPKRKPSGNHDAESARAPSAGNGQSLSSRALLIITVIALLVGWIYY",
                "length": 175,
                "header": "sp|Q6Q595-1|SCS22_YEAST Isoform 1 of Vesicle-associated membrane protein-associated protein SCS22  OS=Saccharomyces cerevisiae S288C OX=559292 GN=SCS22 PE=1 SV=2 CANONICAL=Q6Q595-1"
            },
            "locus": {
                "chromosome": "II",
                "start_pos": 47180,
                "end_pos": 46568,
                "strand": "+",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "YBL091C-A_mRNA",
                        "url": "https://www.ensembl.org/id/YBL091C-A_mRNA"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "YBL091C-A",
                        "url": "https://www.ensembl.org/id/YBL091C-A"
                    }
                ]
            }
        }
    ],
    "glycosylation": [],
    "phosphorylation": [],
    "glycation": [],
    "keywords": [],
    "publication": [
        {
            "title": "Reinvestigation of the Saccharomyces cerevisiae genome annotation by comparison to the genome of a related fungus: Ashbya gossypii.",
            "journal": "Genome Biol.",
            "date": "2003",
            "authors": "Zhang Z., Philippsen P., Stuart L., Dietrich F.S., Brachat S., Gaffney T.D., Gates K., Lerch A., Voegeli S.",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "Q6Q595",
                    "url": "https://www.uniprot.org/uniprot/Q6Q595"
                }
            ],
            "reference": [
                {
                    "type": "PubMed",
                    "id": "12844361",
                    "url": "https://glygen.org/publication/PubMed/12844361"
                }
            ]
        },
        {
            "title": "Global analysis of protein expression in yeast.",
            "journal": "Nature",
            "date": "2003",
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