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{
    "metadata": {
        "accession": "IPR013177",
        "entry_id": null,
        "type": "domain",
        "go_terms": null,
        "source_database": "interpro",
        "member_databases": {
            "pfam": {
                "PF08213": "Mitochondrial mRNA-processing protein COX24, C-terminal"
            },
            "smart": {
                "SM01155": "Mitochondrial domain of unknown function (DUF1713)"
            }
        },
        "integrated": null,
        "hierarchy": {
            "accession": "IPR013177",
            "name": "Ribosomal protein bS22, C-terminal",
            "type": "Domain",
            "children": []
        },
        "name": {
            "name": "Ribosomal protein bS22, C-terminal",
            "short": "Ribosomal_bS22_C"
        },
        "description": [
            {
                "text": "<p>This domain is found at the C-terminal of small ribosomal subunit protein bS22m (formerly known as mS38; also called COX24 in yeast). The mitochondrial protein bS22m shares sequence homology with bacterial bS22, particularly in the N-terminal region, leading to its renaming to reflect their common evolutionary origin. This domain is also found in the bacterial small ribosomal subunit protein bS22, which occupies a similar position beneath the mRNA channel and interacts with 16S rRNA helix 44 to stabilise the decoding centre [[cite:PUB00163225]]. In some proteins this domain convers the whole length of the protein.</p>",
                "llm": false,
                "checked": false,
                "updated": false
            },
            {
                "text": "<p>bS22m is a component of the mitochondrial ribosome (mitoribosome), responsible for the synthesis of mitochondrial genome-encoded proteins, including essential transmembrane subunits of the mitochondrial respiratory chain. Mitoribosomes are attached to the mitochondrial inner membrane, and translation products are cotranslationally integrated into the membrane [[cite:PUB00089004], [cite:PUB00098057]]. In mammals, bS22m preferentially stimulates translation initiation of COX1, COX2, and COX3 mRNAs [[cite:PUB00163226]]. In yeast, bS22m is also involved in the splicing of the COX1 mRNA [[cite:PUB00076420]].</p>",
                "llm": false,
                "checked": false,
                "updated": false
            }
        ],
        "wikipedia": null,
        "literature": {
            "PUB00163225": {
                "PMID": 37034768,
                "ISBN": null,
                "volume": null,
                "issue": null,
                "year": 2023,
                "title": "The small mycobacterial ribosomal protein, bS22, modulates aminoglycoside accessibility to its 16S rRNA helix-44 binding site.",
                "URL": null,
                "raw_pages": "2023.03.31.535098",
                "medline_journal": "bioRxiv",
                "ISO_journal": "bioRxiv",
                "authors": [
                    "Majumdar S",
                    "Deep A",
                    "Sharma MR",
                    "Canestrari J",
                    "Stone M",
                    "Smith C",
                    "Koripella RK",
                    "Keshavan P",
                    "Banavali NK",
                    "Wade JT",
                    "Gray TA",
                    "Derbyshire KM",
                    "Agrawal RK."
                ],
                "DOI_URL": "https://doi.org/10.1101/2023.03.31.535098"
            },
            "PUB00076420": {
                "PMID": 16339141,
                "ISBN": null,
                "volume": "281",
                "issue": "6",
                "year": 2006,
                "title": "COX24 codes for a mitochondrial protein required for processing of the COX1 transcript.",
                "URL": null,
                "raw_pages": "3743-51",
                "medline_journal": "J Biol Chem",
                "ISO_journal": "J. Biol. Chem.",
                "authors": [
                    "Barros MH",
                    "Myers AM",
                    "Van Driesche S",
                    "Tzagoloff A."
                ],
                "DOI_URL": "http://dx.doi.org/10.1074/jbc.M510778200"
            },
            "PUB00089004": {
                "PMID": 25609543,
                "ISBN": null,
                "volume": "6",
                "issue": null,
                "year": 2015,
                "title": "Organization of the mitochondrial translation machinery studied in situ by cryoelectron tomography.",
                "URL": null,
                "raw_pages": "6019",
                "medline_journal": "Nat Commun",
                "ISO_journal": "Nat Commun",
                "authors": [
                    "Pfeffer S",
                    "Woellhaf MW",
                    "Herrmann JM",
                    "Forster F."
                ],
                "DOI_URL": "https://doi.org/10.1038/ncomms7019"
            },
            "PUB00098057": {
                "PMID": 28154081,
                "ISBN": null,
                "volume": "355",
                "issue": "6324",
                "year": 2017,
                "title": "The structure of the yeast mitochondrial ribosome.",
                "URL": null,
                "raw_pages": "528-531",
                "medline_journal": "Science",
                "ISO_journal": "Science",
                "authors": [
                    "Desai N",
                    "Brown A",
                    "Amunts A",
                    "Ramakrishnan V."
                ],
                "DOI_URL": null
            },
            "PUB00163226": {
                "PMID": 30968120,
                "ISBN": null,
                "volume": "47",
                "issue": "11",
                "year": 2019,
                "title": "The mitoribosome-specific protein mS38 is preferentially required for synthesis of cytochrome c oxidase subunits.",
                "URL": null,
                "raw_pages": "5746-5760",
                "medline_journal": "Nucleic Acids Res",
                "ISO_journal": "Nucleic Acids Res",
                "authors": [
                    "Mays JN",
                    "Camacho-Villasana Y",
                    "Garcia-Villegas R",
                    "Perez-Martinez X",
                    "Barrientos A",
                    "Fontanesi F."
                ],
                "DOI_URL": "https://doi.org/10.1093/nar/gkz266"
            },
            "PUB00078824": {
                "PMID": 17125467,
                "ISBN": null,
                "volume": "403",
                "issue": "1",
                "year": 2007,
                "title": "Aurora-A kinase interacting protein 1 (AURKAIP1) promotes Aurora-A degradation through an alternative ubiquitin-independent pathway.",
                "URL": null,
                "raw_pages": "119-27",
                "medline_journal": "Biochem J",
                "ISO_journal": "Biochem. J.",
                "authors": [
                    "Lim SK",
                    "Gopalan G."
                ],
                "DOI_URL": "http://dx.doi.org/10.1042/BJ20061272"
            }
        },
        "set_info": null,
        "overlaps_with": null,
        "counters": {
            "subfamilies": 0,
            "domain_architectures": 43,
            "interactions": 0,
            "matches": 6671,
            "pathways": 7,
            "proteins": 6670,
            "proteomes": 5397,
            "sets": 0,
            "structural_models": {
                "alphafold": 5136,
                "bfvd": 0
            },
            "structures": 118,
            "taxa": 11352
        },
        "entry_annotations": {
            "alignment:seed": 39,
            "alignment:full": 3583
        },
        "cross_references": {},
        "is_llm": false,
        "is_reviewed_llm": false,
        "is_updated_llm": false,
        "representative_structure": null
    }
}