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{
    "metadata": {
        "accession": "IPR052006",
        "entry_id": null,
        "type": "family",
        "go_terms": null,
        "source_database": "interpro",
        "member_databases": {
            "panther": {
                "PTHR31338": "Major Latex-like"
            }
        },
        "integrated": null,
        "hierarchy": {
            "accession": "IPR052006",
            "name": "Major Latex-like",
            "type": "Family",
            "children": []
        },
        "name": {
            "name": "Major Latex-like",
            "short": "MLP-like"
        },
        "description": [
            {
                "text": "<p>This family of proteins includes members with a yet undefined role, which are known to be abundant in latex, constituting a significant portion of its soluble protein content. Some members of this family have been characterized to catalyze the formation of thebaine from its precursors, indicating a role in alkaloid biosynthesis. These enzymes function by facilitating the conversion of (7S)-salutaridinol 7-O-acetate into thebaine while minimizing the production of hydroxylated by-products through spontaneous allylic elimination. The activity of these enzymes can be slightly inhibited by certain substrates, suggesting a regulatory mechanism in the biosynthetic pathway. The diverse functions within this family reflect a range of biological roles, from enzymatic activity in secondary metabolism to yet-to-be-determined functions in plant physiology.</p>",
                "llm": true,
                "checked": false,
                "updated": false
            }
        ],
        "wikipedia": null,
        "literature": null,
        "set_info": null,
        "overlaps_with": [
            {
                "accession": "IPR023393",
                "name": "START-like domain superfamily",
                "type": "homologous_superfamily"
            }
        ],
        "counters": {
            "subfamilies": 0,
            "domain_architectures": 0,
            "interactions": 0,
            "matches": 2480,
            "pathways": 0,
            "proteins": 2480,
            "proteomes": 222,
            "sets": 0,
            "structural_models": {
                "alphafold": 2135,
                "bfvd": 0
            },
            "structures": 9,
            "taxa": 665
        },
        "entry_annotations": {},
        "cross_references": {},
        "is_llm": true,
        "is_reviewed_llm": false,
        "is_updated_llm": false,
        "representative_structure": {
            "accession": "8vo1",
            "name": "Pathogenesis related 10-10 C155S mutant"
        }
    }
}