| 登録情報 | データベース: PDB / ID: 6mxy |
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| タイトル | Structure of 53BP1 tandem Tudor domains in complex with small molecule UNC3351 |
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要素 | TP53-binding protein 1 |
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キーワード | PROTEIN BINDING / DNA damage response / Tudor domain / 53BP1 / small molecule inhibitor |
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| 機能・相同性 | 機能・相同性情報
ubiquitin-modified histone reader activity / histone H4K20me2 reader activity / positive regulation of isotype switching / cellular response to X-ray / double-strand break repair via classical nonhomologous end joining / protein localization to site of double-strand break / DNA repair complex / : / telomeric DNA binding / SUMOylation of transcription factors ...ubiquitin-modified histone reader activity / histone H4K20me2 reader activity / positive regulation of isotype switching / cellular response to X-ray / double-strand break repair via classical nonhomologous end joining / protein localization to site of double-strand break / DNA repair complex / : / telomeric DNA binding / SUMOylation of transcription factors / histone reader activity / positive regulation of intrinsic apoptotic signaling pathway by p53 class mediator / negative regulation of double-strand break repair via homologous recombination / DNA damage checkpoint signaling / replication fork / transcription coregulator activity / Nonhomologous End-Joining (NHEJ) / protein homooligomerization / G2/M DNA damage checkpoint / kinetochore / double-strand break repair via nonhomologous end joining / p53 binding / Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks / site of double-strand break / Processing of DNA double-strand break ends / histone binding / damaged DNA binding / RNA polymerase II-specific DNA-binding transcription factor binding / transcription coactivator activity / chromosome, telomeric region / nuclear body / DNA damage response / positive regulation of DNA-templated transcription / positive regulation of transcription by RNA polymerase II / nucleoplasm / nucleus / cytoplasm類似検索 - 分子機能 Tumour suppressor p53-binding protein-1 Tudor domain / : / Tumour suppressor p53-binding protein-1 Tudor / BRCA1 C Terminus (BRCT) domain / : / : / SH3 type barrels. - #30 / SH3 type barrels. - #140 / breast cancer carboxy-terminal domain / BRCT domain profile. ...Tumour suppressor p53-binding protein-1 Tudor domain / : / Tumour suppressor p53-binding protein-1 Tudor / BRCA1 C Terminus (BRCT) domain / : / : / SH3 type barrels. - #30 / SH3 type barrels. - #140 / breast cancer carboxy-terminal domain / BRCT domain profile. / BRCT domain / BRCT domain superfamily / SH3 type barrels. / Ribosomal protein L2, domain 2 / Roll / Mainly Beta類似検索 - ドメイン・相同性 Chem-K6M / PHOSPHATE ION / TP53-binding protein 1類似検索 - 構成要素 |
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| 生物種 | Homo sapiens (ヒト) |
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| 手法 | X線回折 / シンクロトロン / 分子置換 / 解像度: 1.624 Å |
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データ登録者 | Cui, G. / Botuyan, M.V. / Mer, G. |
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| 資金援助 | 米国, 2件 | 組織 | 認可番号 | 国 |
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| National Institutes of Health/National Cancer Institute (NIH/NCI) | CA132878 | 米国 | | Other private | W81XWH-16-1-0391 | 米国 |
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引用 | ジャーナル: Nat Commun / 年: 2023 タイトル: An autoinhibited state of 53BP1 revealed by small molecule antagonists and protein engineering. 著者: Cui, G. / Botuyan, M.V. / Drane, P. / Hu, Q. / Bragantini, B. / Thompson, J.R. / Schuller, D.J. / Detappe, A. / Perfetti, M.T. / James, L.I. / Frye, S.V. / Chowdhury, D. / Mer, G. |
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| 履歴 | | 登録 | 2018年10月31日 | 登録サイト: RCSB / 処理サイト: RCSB |
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| 改定 1.0 | 2019年11月27日 | Provider: repository / タイプ: Initial release |
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| 改定 1.1 | 2023年10月11日 | Group: Advisory / Data collection ...Advisory / Data collection / Database references / Refinement description カテゴリ: chem_comp_atom / chem_comp_bond ...chem_comp_atom / chem_comp_bond / citation / citation_author / database_2 / pdbx_initial_refinement_model / pdbx_unobs_or_zero_occ_atoms Item: _citation.country / _citation.journal_abbrev ..._citation.country / _citation.journal_abbrev / _citation.journal_id_CSD / _citation.journal_id_ISSN / _citation.journal_volume / _citation.page_first / _citation.page_last / _citation.pdbx_database_id_DOI / _citation.pdbx_database_id_PubMed / _citation.title / _citation.year / _database_2.pdbx_DOI / _database_2.pdbx_database_accession |
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