{
    "uniprot_canonical_ac": "A2VCV8-1", 
    "publication_count": 7, 
    "reported_interactions": 0, 
    "record_type": "protein", 
    "predicted_glycosites": 0, 
    "protein_names_refseq": "max-like factor protein; transcription factor-like 4; MLX, MAX dimerization protein; max-like protein X", 
    "refseq_ac": "NP_001029284.1", 
    "reported_n_glycosites": 0, 
    "refseq_name": "max-like protein X", 
    "record_id": "A2VCV8-1", 
    "protein_names_uniprotkb": "MAX dimerization protein MLX; MAX-like protein X, isoform CRA_a; MAX-like protein X", 
    "pathway": " (rno:360631); ChREBP activates metabolic gene expression (R-RNO-163765)", 
    "function": "ChREBP.Mlx is the principal transcription factor regulating glucose-responsive genes in the liver and coordinately regulates a family of genes required for glucose utilization and energy storage, [RefSeq]; Involved in control of hepatic L-type pyruvate kinase gene transcription, [RefSeq]", 
    "protein_name": "MAX dimerization protein MLX; MAX-like protein X, isoform CRA_a; MAX-like protein X", 
    "reported_mutagensis": 0, 
    "reported_phosphosites": 0, 
    "reported_o_glycosites_with_glycan": 0, 
    "tax_id": 10116, 
    "organism": "Rattus norvegicus", 
    "disease": "", 
    "reported_glycation": 0, 
    "reported_snv": 0, 
    "mass": 33420.0, 
    "gene_names_uniprotkb": "Mlx; rCG_32676", 
    "reported_n_glycosites_with_glycan": 0, 
    "reported_o_glycosites": 0, 
    "gene_names_refseq": "Mlx; Tcfl4", 
    "gene_name": "Mlx"
}