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{
    "metadata": {
        "accession": "IPR038505",
        "entry_id": null,
        "type": "homologous_superfamily",
        "go_terms": null,
        "source_database": "interpro",
        "member_databases": {
            "cathgene3d": {
                "G3DSA:1.25.40.490": "G3DSA:1.25.40.490"
            }
        },
        "integrated": null,
        "hierarchy": {
            "accession": "IPR038505",
            "name": "FANCF, C-terminal domain superfamily",
            "type": "Homologous_superfamily",
            "children": []
        },
        "name": {
            "name": "FANCF, C-terminal domain superfamily",
            "short": "FANCF_C_sf"
        },
        "description": [
            {
                "text": "<p>Fanconi anemia (FA) is a genomic instability syndrome caused by mutations in at least 13 distinct genes whose products function in a common DNA repair signaling pathway, the FA pathway. The FA pathway cooperates with other DNA repair proteins for resolving DNA interstrand cross-links during replication [[cite:PUB00073778]].</p>\r\n\r\n<p>Fanconi anemia group F protein (FANCF) is a component of the FA core complex [[cite:PUB00073779], [cite:PUB00042632]]. FANCF regulates its own expression by methylation at both mRNA and protein levels. Methylation-induced inactivation of FANCF has an important role on the occurrence of ovarian cancers by disrupting the FA-BRCA pathway [[cite:PUB00058153]].</p>",
                "llm": false,
                "checked": false,
                "updated": false
            },
            {
                "text": "<p>This entry represents the C-terminal region of the FANCF protein found in metazoa. The C-terminal domain has an helical repeat structure and is necessary for the proper assembly of the FA core complex [[cite:PUB00041761]].</p>",
                "llm": false,
                "checked": false,
                "updated": false
            }
        ],
        "wikipedia": null,
        "literature": {
            "PUB00073779": {
                "PMID": 16357213,
                "ISBN": null,
                "volume": "19",
                "issue": "24",
                "year": 2005,
                "title": "The Fanconi Anemia/BRCA pathway: new faces in the crowd.",
                "URL": null,
                "raw_pages": "2925-40",
                "medline_journal": "Genes Dev",
                "ISO_journal": "Genes Dev.",
                "authors": [
                    "Kennedy RD",
                    "D'Andrea AD."
                ],
                "DOI_URL": "http://dx.doi.org/10.1101/gad.1370505"
            },
            "PUB00073778": {
                "PMID": 20713514,
                "ISBN": null,
                "volume": "24",
                "issue": "16",
                "year": 2010,
                "title": "Expanded roles of the Fanconi anemia pathway in preserving genomic stability.",
                "URL": null,
                "raw_pages": "1680-94",
                "medline_journal": "Genes Dev",
                "ISO_journal": "Genes Dev.",
                "authors": [
                    "Kee Y",
                    "D'Andrea AD."
                ],
                "DOI_URL": "http://dx.doi.org/10.1101/gad.1955310"
            },
            "PUB00058153": {
                "PMID": 16418574,
                "ISBN": null,
                "volume": "5",
                "issue": "3",
                "year": 2006,
                "title": "Promoter hypermethylation of FANCF plays an important role in the occurrence of ovarian cancer through disrupting Fanconi anemia-BRCA pathway.",
                "URL": null,
                "raw_pages": "256-60",
                "medline_journal": "Cancer Biol Ther",
                "ISO_journal": "Cancer Biol. Ther.",
                "authors": [
                    "Wang Z",
                    "Li M",
                    "Lu S",
                    "Zhang Y",
                    "Wang H."
                ],
                "DOI_URL": null
            },
            "PUB00042632": {
                "PMID": 17768402,
                "ISBN": null,
                "volume": "8",
                "issue": "10",
                "year": 2007,
                "title": "Emergence of a DNA-damage response network consisting of Fanconi anaemia and BRCA proteins.",
                "URL": null,
                "raw_pages": "735-48",
                "medline_journal": "Nat Rev Genet",
                "ISO_journal": "Nat. Rev. Genet.",
                "authors": [
                    "Wang W."
                ],
                "DOI_URL": "http://dx.doi.org/10.1038/nrg2159"
            },
            "PUB00041761": {
                "PMID": 17082180,
                "ISBN": null,
                "volume": "282",
                "issue": "3",
                "year": 2007,
                "title": "Structural determinants of human FANCF protein that function in the assembly of a DNA damage signaling complex.",
                "URL": null,
                "raw_pages": "2047-55",
                "medline_journal": "J Biol Chem",
                "ISO_journal": "J. Biol. Chem.",
                "authors": [
                    "Kowal P",
                    "Gurtan AM",
                    "Stuckert P",
                    "D'Andrea AD",
                    "Ellenberger T."
                ],
                "DOI_URL": "http://dx.doi.org/10.1074/jbc.M608356200"
            }
        },
        "set_info": null,
        "overlaps_with": [
            {
                "accession": "IPR035428",
                "name": "Fanconi anemia group F protein",
                "type": "family"
            }
        ],
        "counters": {
            "subfamilies": 0,
            "domain_architectures": 0,
            "interactions": 0,
            "matches": 643,
            "pathways": 4,
            "proteins": 642,
            "proteomes": 531,
            "sets": 0,
            "structural_models": {
                "alphafold": 561,
                "bfvd": 0
            },
            "structures": 7,
            "taxa": 1934
        },
        "entry_annotations": {},
        "cross_references": {},
        "is_llm": false,
        "is_reviewed_llm": false,
        "is_updated_llm": false,
        "representative_structure": null
    }
}