{
    "uniprot_canonical_ac": "A2APY7-1", 
    "publication_count": 0, 
    "reported_interactions": 0, 
    "record_type": "protein", 
    "predicted_glycosites": 0, 
    "protein_names_refseq": "arginine-hydroxylase NDUFAF5, mitochondrial precursor; probable methyltransferase C20orf7 homolog, mitochondrial; NADH dehydrogenase [ubiquinone] 1 alpha subcomplex assembly factor 5; putative methyltransferase NDUFAF5; arginine-hydroxylase NDUFAF5, mitochondrial; NADH dehydrogenase (ubiquinone) complex I, assembly factor 5", 
    "refseq_ac": "NP_081369.2", 
    "reported_n_glycosites": 0, 
    "refseq_name": "arginine-hydroxylase NDUFAF5, mitochondrial precursor", 
    "record_id": "A2APY7-1", 
    "protein_names_uniprotkb": "Arginine-hydroxylase NDUFAF5, mitochondrial; 1.-.-.-; 2.1.1.-; NADH dehydrogenase [ubiquinone] 1 alpha subcomplex assembly factor 5; Putative methyltransferase NDUFAF5", 
    "pathway": " (mmu:69487); Complex I biogenesis (R-MMU-6799198)", 
    "function": "Arginine hydroxylase involved in the assembly of mitochondrial NADH:ubiquinone oxidoreductase complex (complex I, MT-ND1) at early stages. Acts by mediating hydroxylation of 'Arg-111' of NDUFS7. May also have methyltransferase activity., [UniProtKB]", 
    "protein_name": "Arginine-hydroxylase NDUFAF5, mitochondrial", 
    "reported_mutagensis": 0, 
    "reported_phosphosites": 0, 
    "reported_o_glycosites_with_glycan": 0, 
    "tax_id": 10090, 
    "organism": "Mus musculus", 
    "disease": "mitochondrial complex I deficiency (Disease Ontology:DOID:0060536)", 
    "reported_glycation": 0, 
    "reported_snv": 0, 
    "mass": 38405.0, 
    "gene_names_uniprotkb": "Ndufaf5", 
    "reported_n_glycosites_with_glycan": 0, 
    "reported_o_glycosites": 0, 
    "gene_names_refseq": "2310003L22Rik; Ndufaf5", 
    "gene_name": "Ndufaf5"
}