登録情報 データベース : PDB / ID : 5fv7 構造の表示 ダウンロードとリンクタイトル Human Fen1 in complex with an N-hydroxyurea compound 要素FLAP ENDONUCLEASE 1 詳細 キーワード HYDROLASE機能・相同性 機能・相同性情報分子機能 ドメイン・相同性 構成要素
flap endonuclease activity / positive regulation of sister chromatid cohesion / double-stranded DNA exodeoxyribonuclease activity / telomere maintenance via semi-conservative replication / 5'-flap endonuclease activity / DNA replication, removal of RNA primer / Removal of the Flap Intermediate / UV protection / HDR through MMEJ (alt-NHEJ) / 5'-3' exonuclease activity ... flap endonuclease activity / positive regulation of sister chromatid cohesion / double-stranded DNA exodeoxyribonuclease activity / telomere maintenance via semi-conservative replication / 5'-flap endonuclease activity / DNA replication, removal of RNA primer / Removal of the Flap Intermediate / UV protection / HDR through MMEJ (alt-NHEJ) / 5'-3' exonuclease activity / Removal of the Flap Intermediate from the C-strand / exonuclease activity / Early Phase of HIV Life Cycle / POLB-Dependent Long Patch Base Excision Repair / PCNA-Dependent Long Patch Base Excision Repair / base-excision repair, gap-filling / double-strand break repair via homologous recombination / memory / RNA-DNA hybrid ribonuclease activity / double-strand break repair / manganese ion binding / double-stranded DNA binding / endonuclease activity / damaged DNA binding / 加水分解酵素; エステル加水分解酵素 / DNA replication / chromosome, telomeric region / DNA repair / nucleolus / magnesium ion binding / protein-containing complex / mitochondrion / DNA binding / nucleoplasm / membrane / nucleus 類似検索 - 分子機能 Flap endonuclease 1 / XPG protein signature 2. / XPG conserved site / XPG protein signature 1. / XPG/Rad2 endonuclease / XPG, N-terminal / XPG-I domain / XPG N-terminal domain / XPG I-region / Xeroderma pigmentosum G I-region ... Flap endonuclease 1 / XPG protein signature 2. / XPG conserved site / XPG protein signature 1. / XPG/Rad2 endonuclease / XPG, N-terminal / XPG-I domain / XPG N-terminal domain / XPG I-region / Xeroderma pigmentosum G I-region / Xeroderma pigmentosum G N-region / Helix-hairpin-helix motif, class 2 / Helix-hairpin-helix class 2 (Pol1 family) motifs / 5'-3' exonuclease, C-terminal domain superfamily / PIN-like domain superfamily 類似検索 - ドメイン・相同性生物種 HOMO SAPIENS (ヒト)手法 X線回折 / シンクロトロン / 分子置換 / 解像度 : 2.84 Å 詳細データ登録者 Exell, J.C. / Thompson, M.J. / Finger, L.D. / Shaw, S.K. / Abbott, W.M. / McWhirter, C. / Debreczeni, J.E. / Jones, C.D. / Nissink, J.W.M. / Ward, T.A. ...Exell, J.C. / Thompson, M.J. / Finger, L.D. / Shaw, S.K. / Abbott, W.M. / McWhirter, C. / Debreczeni, J.E. / Jones, C.D. / Nissink, J.W.M. / Ward, T.A. / Sioberg, C.W.L. / Molina, D.M. / Durant, S.T. / Grasby, J.A. 引用ジャーナル : Nat.Chem.Biol. / 年 : 2016タイトル : Cellular Active N-Hydroxyurea Fen1 Inhibitors Block Substrate Entry to the Active Site著者: Exell, J.C. / Thompson, M.J. / Finger, L.D. / Shaw, S.K. / Abbott, W.M. / Mcwhirter, C. / Debreczeni, J.E. / Jones, C.D. / Nissink, J.W.M. / Ward, T.A. / Sioberg, C.W.L. / Molina, D.M. / ... 著者 : Exell, J.C. / Thompson, M.J. / Finger, L.D. / Shaw, S.K. / Abbott, W.M. / Mcwhirter, C. / Debreczeni, J.E. / Jones, C.D. / Nissink, J.W.M. / Ward, T.A. / Sioberg, C.W.L. / Molina, D.M. / Durant, S.T. / Grasby, J.A. 履歴 登録 2016年2月3日 登録サイト : PDBE / 処理サイト : PDBE改定 1.0 2016年8月17日 Provider : repository / タイプ : Initial release改定 1.1 2016年8月24日 Group : Database references改定 1.2 2016年10月5日 Group : Database references改定 1.3 2017年8月23日 Group : Data collection / カテゴリ : diffrn_detector / Item : _diffrn_detector.type改定 1.4 2024年5月8日 Group : Data collection / Database references ... Data collection / Database references / Derived calculations / Other カテゴリ : chem_comp_atom / chem_comp_bond ... chem_comp_atom / chem_comp_bond / database_2 / pdbx_database_status / pdbx_struct_conn_angle / struct_conn / struct_site Item : _database_2.pdbx_DOI / _database_2.pdbx_database_accession ... _database_2.pdbx_DOI / _database_2.pdbx_database_accession / _pdbx_database_status.status_code_sf / _pdbx_struct_conn_angle.ptnr1_auth_comp_id / _pdbx_struct_conn_angle.ptnr1_auth_seq_id / _pdbx_struct_conn_angle.ptnr1_label_asym_id / _pdbx_struct_conn_angle.ptnr1_label_atom_id / _pdbx_struct_conn_angle.ptnr1_label_comp_id / _pdbx_struct_conn_angle.ptnr1_label_seq_id / _pdbx_struct_conn_angle.ptnr3_auth_comp_id / _pdbx_struct_conn_angle.ptnr3_auth_seq_id / _pdbx_struct_conn_angle.ptnr3_label_asym_id / _pdbx_struct_conn_angle.ptnr3_label_atom_id / _pdbx_struct_conn_angle.ptnr3_label_comp_id / _pdbx_struct_conn_angle.ptnr3_label_seq_id / _pdbx_struct_conn_angle.value / _struct_conn.pdbx_dist_value / _struct_conn.ptnr1_auth_comp_id / _struct_conn.ptnr1_auth_seq_id / _struct_conn.ptnr1_label_asym_id / _struct_conn.ptnr1_label_atom_id / _struct_conn.ptnr1_label_comp_id / _struct_conn.ptnr1_label_seq_id / _struct_conn.ptnr2_auth_comp_id / _struct_conn.ptnr2_auth_seq_id / _struct_conn.ptnr2_label_asym_id / _struct_conn.ptnr2_label_atom_id / _struct_conn.ptnr2_label_comp_id / _struct_conn.ptnr2_label_seq_id / _struct_site.pdbx_auth_asym_id / _struct_site.pdbx_auth_comp_id / _struct_site.pdbx_auth_seq_id
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