+データを開く
-基本情報
登録情報 | データベース: EMDB / ID: EMD-42479 | |||||||||
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タイトル | Escherichia coli transcription-translation coupled complex class B (TTC-B) containing RfaH bound to ops signal, NusA, mRNA with a 24 nt long spacer, and fMet-tRNAs in E-site and P-site of the ribosome | |||||||||
マップデータ | Escherichia coli transcription-translation coupled complex class B (TTC-B) containing RfaH bound to ops signal, NusA, mRNA with a 24 nt long spacer, and fMet-tRNAs in E-site and P-site of the ribosome | |||||||||
試料 |
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キーワード | transcription / translation / RfaH / gene expression / regulation / ops / ribosome / coupling | |||||||||
機能・相同性 | 機能・相同性情報 transcription antitermination factor activity, DNA binding / negative regulation of cytoplasmic translational initiation / transcription elongation-coupled chromatin remodeling / RNA polymerase complex / submerged biofilm formation / stringent response / cellular response to cell envelope stress / bacterial-type RNA polymerase core enzyme binding / cytosolic DNA-directed RNA polymerase complex / regulation of DNA-templated transcription initiation ...transcription antitermination factor activity, DNA binding / negative regulation of cytoplasmic translational initiation / transcription elongation-coupled chromatin remodeling / RNA polymerase complex / submerged biofilm formation / stringent response / cellular response to cell envelope stress / bacterial-type RNA polymerase core enzyme binding / cytosolic DNA-directed RNA polymerase complex / regulation of DNA-templated transcription initiation / bacterial-type flagellum assembly / misfolded RNA binding / Group I intron splicing / RNA folding / bacterial-type flagellum-dependent cell motility / positive regulation of ribosome biogenesis / nitrate assimilation / translational termination / DnaA-L2 complex / negative regulation of translational initiation / negative regulation of DNA-templated DNA replication initiation / mRNA regulatory element binding translation repressor activity / ribosome assembly / assembly of large subunit precursor of preribosome / positive regulation of RNA splicing / cytosolic ribosome assembly / transcription elongation factor complex / regulation of DNA-templated transcription elongation / DNA-templated transcription initiation / transcription antitermination / cell motility / regulation of cell growth / translational initiation / DNA-templated transcription termination / maintenance of translational fidelity / ribonucleoside binding / mRNA 5'-UTR binding / DNA-directed 5'-3' RNA polymerase activity / DNA-directed RNA polymerase / ribosomal small subunit biogenesis / small ribosomal subunit rRNA binding / large ribosomal subunit / ribosome binding / ribosomal small subunit assembly / large ribosomal subunit rRNA binding / 5S rRNA binding / transferase activity / small ribosomal subunit / response to heat / cytosolic small ribosomal subunit / ribosomal large subunit assembly / protein-containing complex assembly / cytoplasmic translation / cytosolic large ribosomal subunit / intracellular iron ion homeostasis / tRNA binding / negative regulation of translation / protein dimerization activity / rRNA binding / ribosome / structural constituent of ribosome / translation / ribonucleoprotein complex / DNA-binding transcription factor activity / response to antibiotic / mRNA binding / nucleotide binding / magnesium ion binding / DNA binding / RNA binding / zinc ion binding / membrane / cytosol / cytoplasm 類似検索 - 分子機能 | |||||||||
生物種 | Escherichia coli (大腸菌) / synthetic construct (人工物) | |||||||||
手法 | 単粒子再構成法 / クライオ電子顕微鏡法 / 解像度: 3.4 Å | |||||||||
データ登録者 | Molodtsov V / Wang C / Ebright RH | |||||||||
資金援助 | 米国, 1件
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引用 | ジャーナル: Nat Struct Mol Biol / 年: 2024 タイトル: Structural basis of RfaH-mediated transcription-translation coupling. 著者: Vadim Molodtsov / Chengyuan Wang / Jing Zhang / Jason T Kaelber / Gregor Blaha / Richard H Ebright / 要旨: The NusG paralog RfaH mediates bacterial transcription-translation coupling in genes that contain a DNA sequence element, termed an ops site, required for pausing RNA polymerase (RNAP) and for ...The NusG paralog RfaH mediates bacterial transcription-translation coupling in genes that contain a DNA sequence element, termed an ops site, required for pausing RNA polymerase (RNAP) and for loading RfaH onto the paused RNAP. Here, we report cryo-electron microscopy structures of transcription-translation complexes (TTCs) containing Escherichia coli RfaH. The results show that RfaH bridges RNAP and the ribosome, with the RfaH N-terminal domain interacting with RNAP and the RfaH C-terminal domain interacting with the ribosome. The results show that the distribution of translational and orientational positions of RNAP relative to the ribosome in RfaH-coupled TTCs is more restricted than in NusG-coupled TTCs because of the more restricted flexibility of the RfaH interdomain linker. The results further suggest that the structural organization of RfaH-coupled TTCs in the 'loading state', in which RNAP and RfaH are located at the ops site during formation of the TTC, is the same as the structural organization of RfaH-coupled TTCs in the 'loaded state', in which RNAP and RfaH are located at positions downstream of the ops site during function of the TTC. The results define the structural organization of RfaH-containing TTCs and set the stage for analysis of functions of RfaH during translation initiation and transcription-translation coupling. | |||||||||
履歴 |
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-構造の表示
添付画像 |
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-ダウンロードとリンク
-EMDBアーカイブ
マップデータ | emd_42479.map.gz | 196.5 MB | EMDBマップデータ形式 | |
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ヘッダ (付随情報) | emd-42479-v30.xml emd-42479.xml | 94.5 KB 94.5 KB | 表示 表示 | EMDBヘッダ |
画像 | emd_42479.png | 37.6 KB | ||
Filedesc metadata | emd-42479.cif.gz | 20.1 KB | ||
その他 | emd_42479_half_map_1.map.gz emd_42479_half_map_2.map.gz | 585.3 MB 588.7 MB | ||
アーカイブディレクトリ | http://ftp.pdbj.org/pub/emdb/structures/EMD-42479 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-42479 | HTTPS FTP |
-検証レポート
文書・要旨 | emd_42479_validation.pdf.gz | 1 MB | 表示 | EMDB検証レポート |
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文書・詳細版 | emd_42479_full_validation.pdf.gz | 1 MB | 表示 | |
XML形式データ | emd_42479_validation.xml.gz | 21 KB | 表示 | |
CIF形式データ | emd_42479_validation.cif.gz | 24 KB | 表示 | |
アーカイブディレクトリ | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-42479 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-42479 | HTTPS FTP |
-関連構造データ
関連構造データ | 8ur0MC 8upoC 8uprC 8uqlC 8uqmC 8uqpC 8urhC 8uriC 8urxC 8uryC M: このマップから作成された原子モデル C: 同じ文献を引用 (文献) |
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類似構造データ | 類似検索 - 機能・相同性F&H 検索 |
-リンク
EMDBのページ | EMDB (EBI/PDBe) / EMDataResource |
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「今月の分子」の関連する項目 |
-マップ
ファイル | ダウンロード / ファイル: emd_42479.map.gz / 形式: CCP4 / 大きさ: 512 MB / タイプ: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||
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注釈 | Escherichia coli transcription-translation coupled complex class B (TTC-B) containing RfaH bound to ops signal, NusA, mRNA with a 24 nt long spacer, and fMet-tRNAs in E-site and P-site of the ribosome | ||||||||||||||||||||||||||||||||||||
投影像・断面図 | 画像のコントロール
画像は Spider により作成 | ||||||||||||||||||||||||||||||||||||
ボクセルのサイズ | X=Y=Z: 1.04 Å | ||||||||||||||||||||||||||||||||||||
密度 |
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対称性 | 空間群: 1 | ||||||||||||||||||||||||||||||||||||
詳細 | EMDB XML:
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-添付データ
-ハーフマップ: half-map 2
ファイル | emd_42479_half_map_1.map | ||||||||||||
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注釈 | half-map 2 | ||||||||||||
投影像・断面図 |
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密度ヒストグラム |
-ハーフマップ: half-map 1
ファイル | emd_42479_half_map_2.map | ||||||||||||
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注釈 | half-map 1 | ||||||||||||
投影像・断面図 |
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密度ヒストグラム |
-試料の構成要素
+全体 : Escherichia coli transcription-translation coupled complex class ...
+超分子 #1: Escherichia coli transcription-translation coupled complex class ...
+分子 #1: Ribosomal protein L21
+分子 #2: 50S ribosomal protein L22
+分子 #3: 50S ribosomal protein L23
+分子 #4: 50S ribosomal protein L24
+分子 #5: 50S ribosomal protein L25
+分子 #9: 50S ribosomal protein L10
+分子 #11: DNA-directed RNA polymerase subunit beta
+分子 #12: Transcription antitermination protein RfaH
+分子 #13: DNA-directed RNA polymerase subunit alpha
+分子 #14: DNA-directed RNA polymerase subunit beta'
+分子 #15: DNA-directed RNA polymerase subunit omega
+分子 #16: Transcription termination/antitermination protein NusA
+分子 #17: 30S ribosomal protein S18
+分子 #19: 30S ribosomal protein S20
+分子 #20: 30S ribosomal protein S21
+分子 #21: 30S ribosomal protein S2
+分子 #22: 30S ribosomal protein S1
+分子 #23: 30S ribosomal protein S3
+分子 #24: 30S ribosomal protein S4
+分子 #25: 30S ribosomal protein S5
+分子 #26: 30S ribosomal protein S6
+分子 #27: 30S ribosomal protein S7
+分子 #28: 30S ribosomal protein S8
+分子 #29: 30S ribosomal protein S9
+分子 #30: 30S ribosomal protein S10
+分子 #31: 30S ribosomal protein S11
+分子 #32: 30S ribosomal protein S12
+分子 #33: 30S ribosomal protein S14
+分子 #34: 30S ribosomal protein S15
+分子 #35: 30S ribosomal protein S16
+分子 #36: 30S ribosomal protein S17
+分子 #37: 30S ribosomal protein S19
+分子 #38: 30S ribosomal protein S13
+分子 #39: 50S ribosomal protein L11
+分子 #40: 50S ribosomal protein L7/L12
+分子 #42: 50S ribosomal protein L27
+分子 #43: 50S ribosomal protein L28
+分子 #45: 50S ribosomal protein L29
+分子 #46: 50S ribosomal protein L30
+分子 #47: 50S ribosomal protein L31
+分子 #48: 50S ribosomal protein L2
+分子 #49: 50S ribosomal protein L32
+分子 #50: 50S ribosomal protein L3
+分子 #51: 50S ribosomal protein L33
+分子 #52: 50S ribosomal protein L4
+分子 #53: 50S ribosomal protein L34
+分子 #54: 50S ribosomal protein L5
+分子 #55: 50S ribosomal protein L35
+分子 #56: 50S ribosomal protein L6
+分子 #57: 50S ribosomal protein L36
+分子 #58: 50S ribosomal protein L9
+分子 #59: 50S ribosomal protein L13
+分子 #60: 50S ribosomal protein L14
+分子 #61: 50S ribosomal protein L15
+分子 #62: 50S ribosomal protein L16
+分子 #63: 50S ribosomal protein L17
+分子 #64: 50S ribosomal protein L18
+分子 #65: 50S ribosomal protein L19
+分子 #66: 50S ribosomal protein L20
+分子 #6: NT DNA ops
+分子 #7: T DNA ops
+分子 #8: mRNA with 24 nt long spacer
+分子 #10: E-site and P-site fMet-tRNA
+分子 #18: 16S rRNA
+分子 #41: 23S rRNA
+分子 #44: 5S rRNA
+分子 #67: MAGNESIUM ION
+分子 #68: ZINC ION
-実験情報
-構造解析
手法 | クライオ電子顕微鏡法 |
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解析 | 単粒子再構成法 |
試料の集合状態 | particle |
-試料調製
緩衝液 | pH: 7.5 |
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凍結 | 凍結剤: ETHANE |
-電子顕微鏡法
顕微鏡 | FEI TALOS ARCTICA |
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撮影 | フィルム・検出器のモデル: GATAN K2 SUMMIT (4k x 4k) 平均電子線量: 28.0 e/Å2 |
電子線 | 加速電圧: 200 kV / 電子線源: FIELD EMISSION GUN |
電子光学系 | 照射モード: FLOOD BEAM / 撮影モード: BRIGHT FIELD / 最大 デフォーカス(公称値): 2.5 µm / 最小 デフォーカス(公称値): 1.25 µm |
実験機器 | モデル: Talos Arctica / 画像提供: FEI Company |
-画像解析
初期モデル | モデルのタイプ: NONE |
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最終 再構成 | 解像度のタイプ: BY AUTHOR / 解像度: 3.4 Å / 解像度の算出法: FSC 0.143 CUT-OFF / 使用した粒子像数: 14614 |
初期 角度割当 | タイプ: COMMON LINE |
最終 角度割当 | タイプ: COMMON LINE |