登録情報 データベース : PDB / ID : 1gz6 構造の表示 ダウンロードとリンクタイトル (3R)-HYDROXYACYL-COA DEHYDROGENASE FRAGMENT OF RAT PEROXISOMAL MULTIFUNCTIONAL ENZYME TYPE 2 要素ESTRADIOL 17 BETA-DEHYDROGENASE 4 詳細 キーワード DEHYDROGENASE / 17BETA-HSD4 / MFE-2 / BETA-OXIDATION / PEROXISOME / SDR / STEROID BIOSYNTHESIS / OXIDOREDUCTASE / NADP / MULTIGENE FAMIL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
Beta-oxidation of pristanoyl-CoA / alpha-linolenic acid (ALA) metabolism / Synthesis of bile acids and bile salts via 7alpha-hydroxycholesterol / 3alpha,7alpha,12alpha-trihydroxy-5beta-cholest-24-enoyl-CoA hydratase / 3alpha,7alpha,12alpha-trihydroxy-5beta-cholest-24-enoyl-CoA hydratase activity / very long-chain fatty-acyl-CoA metabolic process / medium-chain fatty-acyl-CoA metabolic process / : / (3R)-3-hydroxyacyl-CoA dehydrogenase (NAD+) activity / Beta-oxidation of very long chain fatty acids ... Beta-oxidation of pristanoyl-CoA / alpha-linolenic acid (ALA) metabolism / Synthesis of bile acids and bile salts via 7alpha-hydroxycholesterol / 3alpha,7alpha,12alpha-trihydroxy-5beta-cholest-24-enoyl-CoA hydratase / 3alpha,7alpha,12alpha-trihydroxy-5beta-cholest-24-enoyl-CoA hydratase activity / very long-chain fatty-acyl-CoA metabolic process / medium-chain fatty-acyl-CoA metabolic process / : / (3R)-3-hydroxyacyl-CoA dehydrogenase (NAD+) activity / Beta-oxidation of very long chain fatty acids / enoyl-CoA hydratase 2 / Peroxisomal protein import / 3-hydroxyacyl-CoA dehydratase activity / 17-beta-hydroxysteroid dehydrogenase (NAD+) activity / very long-chain fatty acid metabolic process / (3S)-3-hydroxyacyl-CoA dehydrogenase (NAD+) activity / : / Sertoli cell development / enoyl-CoA hydratase activity / estradiol 17-beta-dehydrogenase [NAD(P)+] activity / response to steroid hormone / estrogen metabolic process / fatty acid beta-oxidation / androgen metabolic process / isomerase activity / cholesterol metabolic process / peroxisome / response to xenobiotic stimulus / protein homodimerization activity / identical protein binding 類似検索 - 分子機能 Helix Hairpins - #4290 / : / MFE-2 hydratase 2 N-terminal domain / : / SCP2 sterol-binding domain / SCP-2 sterol transfer family / SCP2 sterol-binding domain superfamily / MaoC-like dehydratase domain / MaoC like domain / short chain dehydrogenase ... Helix Hairpins - #4290 / : / MFE-2 hydratase 2 N-terminal domain / : / SCP2 sterol-binding domain / SCP-2 sterol transfer family / SCP2 sterol-binding domain superfamily / MaoC-like dehydratase domain / MaoC like domain / short chain dehydrogenase / HotDog domain superfamily / PKS_KR / Short-chain dehydrogenase/reductase SDR / Helix Hairpins / NAD(P)-binding Rossmann-like Domain / NAD(P)-binding domain superfamily / Rossmann fold / Orthogonal Bundle / 3-Layer(aba) Sandwich / Mainly Alpha / Alpha Beta 類似検索 - ドメイン・相同性 1,4-DIHYDRONICOTINAMIDE ADENINE DINUCLEOTIDE / Peroxisomal multifunctional enzyme type 2 類似検索 - 構成要素生物種 RATTUS NORVEGICUS (ドブネズミ)手法 X線回折 / シンクロトロン / 多波長異常分散 / 解像度 : 2.38 Å 詳細データ登録者 Haapalainen, A.M. / Hiltunen, J.K. / Glumoff, T. 引用ジャーナル : Structure / 年 : 2003タイトル : Binary Structure of the Two-Domain (3R)-Hydroxyacyl-Coa Dehydrogenase from Rat Peroxisomal Multifunctional Enzyme Type 2 at 2.38 A Resolution著者 : Haapalainen, A.M. / Koski, M.K. / Qin, Y.M. / Hiltunen, J.K. / Glumoff, T. 履歴 登録 2002年5月16日 登録サイト : PDBE / 処理サイト : PDBE改定 1.0 2003年1月24日 Provider : repository / タイプ : Initial release改定 1.1 2011年5月8日 Group : Version format compliance改定 1.2 2011年7月13日 Group : Version format compliance改定 1.3 2024年11月6日 Group : Data collection / Database references ... Data collection / Database references / Derived calculations / Other / Structure summary カテゴリ : chem_comp_atom / chem_comp_bond ... chem_comp_atom / chem_comp_bond / database_2 / pdbx_database_status / pdbx_entry_details / pdbx_modification_feature / struct_conn 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 / _struct_conn.pdbx_leaving_atom_flag
すべて表示 表示を減らす Remark 700 SHEET THE SHEET STRUCTURE OF THIS MOLECULE IS BIFURCATED. IN ORDER TO REPRESENT THIS FEATURE IN ... SHEET THE SHEET STRUCTURE OF THIS MOLECULE IS BIFURCATED. IN ORDER TO REPRESENT THIS FEATURE IN THE SHEET RECORDS BELOW, TWO SHEETS ARE DEFINED.