| 登録情報 | データベース: PDB / ID: 9fbo |
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| タイトル | Deletion mutant of chitinase MmChi60 |
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要素 | Chitinase 60 |
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キーワード | HYDROLASE / Chitinase / Psychrophilic / Deletion mutant / Protein engineering |
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| 機能・相同性 | 機能・相同性情報
endochitinase activity / chitinase / chitin binding / carbohydrate binding / carbohydrate metabolic process / extracellular region類似検索 - 分子機能 Pesticidal crystal protein Cry22Aa, Ig-like domain / Bacterial surface protein, Ig-like domain / : / Carbohydrate-binding module family 5/12 / Chitin-binding domain type 3 / Carbohydrate-binding module family 5/12 / Carbohydrate-binding module superfamily 5/12 / Glycosyl hydrolases family 18 (GH18) active site / Glycosyl hydrolases family 18 (GH18) active site signature. / Chitinase II ...Pesticidal crystal protein Cry22Aa, Ig-like domain / Bacterial surface protein, Ig-like domain / : / Carbohydrate-binding module family 5/12 / Chitin-binding domain type 3 / Carbohydrate-binding module family 5/12 / Carbohydrate-binding module superfamily 5/12 / Glycosyl hydrolases family 18 (GH18) active site / Glycosyl hydrolases family 18 (GH18) active site signature. / Chitinase II / Glyco_18 / Glycosyl hydrolases family 18 / Glycosyl hydrolases family 18 (GH18) domain profile. / Glycoside hydrolase family 18, catalytic domain / Glycoside hydrolase superfamily / Immunoglobulin-like fold類似検索 - ドメイン・相同性 |
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| 生物種 | Moritella marina (バクテリア) |
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| 手法 | X線回折 / シンクロトロン / 分子置換 / 解像度: 2.69 Å |
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データ登録者 | Malecki, P.H. / Rypniewski, W. |
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| 資金援助 | ポーランド, 1件 | 組織 | 認可番号 | 国 |
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| Polish National Science Centre | UMO-2017/27/B/NZ1/02201 | ポーランド |
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引用 | ジャーナル: To Be Published タイトル: Probing the structure and thermodynamics of a psychrophilic chitinase 著者: Malecki, P.H. / Bejger, M. / Rypniewski, W. |
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| 履歴 | | 登録 | 2024年5月14日 | 登録サイト: PDBE / 処理サイト: PDBE |
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| 改定 1.0 | 2025年5月28日 | Provider: repository / タイプ: Initial release |
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| 改定 2.0 | 2025年10月22日 | Group: Atomic model / Author supporting evidence ...Atomic model / Author supporting evidence / Data collection / Database references / Derived calculations / Other / Polymer sequence / Refinement description / Structure summary カテゴリ: atom_site / cell ...atom_site / cell / entity / entity_poly / entity_poly_seq / pdbx_contact_author / pdbx_entity_instance_feature / pdbx_entity_nonpoly / pdbx_entry_details / pdbx_nonpoly_scheme / pdbx_poly_seq_scheme / pdbx_struct_conn_angle / pdbx_struct_sheet_hbond / pdbx_validate_torsion / refine / refine_hist / refine_ls_restr / refine_ls_shell / struct_asym / struct_conf / struct_conn / struct_ref / struct_ref_seq / struct_ref_seq_dif / struct_sheet_range Item: _atom_site.B_iso_or_equiv / _atom_site.Cartn_x ..._atom_site.B_iso_or_equiv / _atom_site.Cartn_x / _atom_site.Cartn_y / _atom_site.Cartn_z / _atom_site.auth_atom_id / _atom_site.auth_comp_id / _atom_site.auth_seq_id / _atom_site.label_atom_id / _atom_site.label_comp_id / _atom_site.label_entity_id / _atom_site.occupancy / _atom_site.pdbx_formal_charge / _atom_site.type_symbol / _cell.Z_PDB / _cell.angle_alpha / _cell.angle_beta / _cell.angle_gamma / _pdbx_entity_nonpoly.entity_id / _pdbx_entry_details.has_ligand_of_interest / _pdbx_nonpoly_scheme.auth_seq_num / _pdbx_nonpoly_scheme.entity_id / _pdbx_nonpoly_scheme.pdb_seq_num / _pdbx_poly_seq_scheme.auth_mon_id / _pdbx_poly_seq_scheme.auth_seq_num / _pdbx_poly_seq_scheme.entity_id / _pdbx_poly_seq_scheme.mon_id / _pdbx_poly_seq_scheme.pdb_mon_id / _pdbx_poly_seq_scheme.pdb_seq_num / _pdbx_struct_conn_angle.ptnr2_auth_seq_id / _pdbx_struct_sheet_hbond.range_1_auth_seq_id / _pdbx_struct_sheet_hbond.range_2_auth_seq_id / _pdbx_validate_torsion.auth_seq_id / _pdbx_validate_torsion.phi / _refine.B_iso_mean / _refine.aniso_B[1][3] / _refine.aniso_B[2][3] / _refine.details / _refine.ls_R_factor_R_free / _refine.ls_R_factor_R_work / _refine.ls_R_factor_all / _refine.ls_d_res_low / _refine.ls_number_reflns_R_work / _refine.ls_percent_reflns_R_free / _refine.ls_percent_reflns_obs / _refine.overall_SU_B / _refine.overall_SU_ML / _refine.pdbx_overall_ESU_R / _refine.pdbx_overall_ESU_R_Free / _refine.pdbx_solvent_ion_probe_radii / _refine.pdbx_solvent_shrinkage_radii / _refine.pdbx_solvent_vdw_probe_radii / _refine.solvent_model_details / _refine_hist.d_res_low / _struct_asym.entity_id / _struct_conf.beg_auth_comp_id / _struct_conf.beg_label_comp_id / _struct_conn.ptnr2_auth_seq_id / _struct_ref_seq.pdbx_auth_seq_align_beg / _struct_ref_seq.pdbx_auth_seq_align_end / _struct_ref_seq.ref_id / _struct_sheet_range.beg_auth_seq_id / _struct_sheet_range.end_auth_seq_id 解説: Sequence discrepancy 詳細: The present structure is a deletion mutant with 82 residues missing. An offset of 82 was added to residues 423-468, chains A and B, for consistency with the native structure of this protein. ...詳細: The present structure is a deletion mutant with 82 residues missing. An offset of 82 was added to residues 423-468, chains A and B, for consistency with the native structure of this protein. In addition, an error in sequence was corrected: residue 153, chain B, now is Glu, not Gln. Provider: author / タイプ: Coordinate replacement |
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