{
    "uniprot_canonical_ac": "A0A0R4IZE6-1",
    "uniprot_id": [
        {
            "id": "A0A0R4IZE6_DANRE",
            "url": "https://www.uniprot.org/uniprot/A0A0R4IZE6_DANRE",
            "type": "external"
        }
    ],
    "mass": 38040.0,
    "length": 338,
    "protein_name": "D-aspartate oxidase",
    "gene_name": "ddo",
    "organism": "Zebrafish",
    "refseq_name": "D-aspartate oxidase",
    "refseq_ac": [
        {
            "id": "NP_001274017",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001274017",
            "type": "external"
        }
    ],
    "gene_names_uniprotkb": "ddo; zgc:172341",
    "gene_names_refseq": "ddo; zgc:172341",
    "protein_names_uniprotkb": "D-aspartate oxidase; 1.4.3.1",
    "protein_names_refseq": "D-aspartate oxidase",
    "tax_id": 7955,
    "disease": "",
    "pathway": " (dre:565385)",
    "pathway_count": 1,
    "publication_count": 4,
    "publication_id_list": "23594743;27189481;34481069;35295584",
    "function": "##Evidence-Data-START## Transcript exon combination :: GDQH01008552.1, GFIL01046314.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMEA898401, SAMEA898404 [ECO:0000348] ##Evidence-Data-END## VALIDATED REFSEQ: This record has undergone validation or preliminary review. The reference sequence was derived from CU469532.14. On Nov 26, 2013 this sequence version replaced XP_002665184.1. Sequence Note: The RefSeq transcript and protein were derived from genomic sequence to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on alignments., [RefSeq]; Selectively catalyzes the oxidative deamination of acidic amino acids. Suppresses the level of D-aspartate in the brain, an amino acid that can act as an agonist for glutamate receptors. Protects the organism from the toxicity of D-amino acids. May also function in the intestine., [UniProtKB, UniProtKB]",
    "predicted_glycosites": 0,
    "predicted_n_glycosites": 0,
    "predicted_o_glycosites": 0,
    "mined_glycosites": 0,
    "mined_n_glycosites": 0,
    "mined_o_glycosites": 0,
    "reported_n_glycosites": 0,
    "reported_o_glycosites": 0,
    "reported_n_glycosites_with_glycan": 0,
    "reported_o_glycosites_with_glycan": 0,
    "total_reported_n_glycosites": 0,
    "total_reported_o_glycosites": 0,
    "total_n_glycosites": 0,
    "total_o_glycosites": 0,
    "reported_fully_resolved_glycans": 0,
    "reported_phosphosites": 0,
    "reported_mutagensis": 0,
    "reported_glycation": 0,
    "reported_snv": 0,
    "reported_interactions": 0,
    "missing_score": 10000,
    "biomarker_type": "",
    "glycan_count": 0,
    "disease_count": 0,
    "glyco_site_count": 0,
    "binding_glycan_count": 0,
    "secondary_ac_list": "",
    "ec_number_list": [
        {
            "id": "1.4.3.1",
            "url": "https://www.rhea-db.org/rhea/?query=ec:1.4.3.1",
            "type": "external"
        }
    ],
    "go_molecular_function": "GO:0008445 D-aspartate oxidase activity;GO:0071949 FAD binding",
    "go_cellular_component": "GO:0005737 cytoplasm;GO:0005782 peroxisomal matrix",
    "go_biological_process": "GO:0019478 D-amino acid catabolic process",
    "synthesized_glycan_count": 0,
    "record_id": "A0A0R4IZE6-1",
    "record_type": "protein",
    "filter_code": "0000000.0000101.100000.0000000000000001.00000.000"
}