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データを開く
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基本情報
登録情報 | データベース: EMDB / ID: EMD-8279 | ||||||||||||
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タイトル | Structure of RelA bound to ribosome in absence of A/R tRNA (Structure I) | ||||||||||||
![]() | Ribosome*RelA structures reveal the mechanism of stringent response activation (Structure I) | ||||||||||||
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![]() | ribosome / RelA | ||||||||||||
機能・相同性 | ![]() guanosine tetraphosphate metabolic process / guanosine-3',5'-bis(diphosphate) 3'-diphosphatase activity / GTP diphosphokinase / GTP diphosphokinase activity / guanosine tetraphosphate biosynthetic process / nucleobase-containing small molecule interconversion / response to starvation / negative regulation of cytoplasmic translational initiation / stringent response / ornithine decarboxylase inhibitor activity ...guanosine tetraphosphate metabolic process / guanosine-3',5'-bis(diphosphate) 3'-diphosphatase activity / GTP diphosphokinase / GTP diphosphokinase activity / guanosine tetraphosphate biosynthetic process / nucleobase-containing small molecule interconversion / response to starvation / negative regulation of cytoplasmic translational initiation / stringent response / ornithine decarboxylase inhibitor activity / transcription antitermination factor activity, RNA binding / misfolded RNA binding / Group I intron splicing / RNA folding / transcriptional attenuation / endoribonuclease inhibitor activity / RNA-binding transcription regulator activity / positive regulation of ribosome biogenesis / translational termination / negative regulation of cytoplasmic translation / four-way junction DNA binding / DnaA-L2 complex / translation repressor activity / negative regulation of translational initiation / regulation of mRNA stability / negative regulation of DNA-templated DNA replication initiation / mRNA regulatory element binding translation repressor activity / assembly of large subunit precursor of preribosome / positive regulation of RNA splicing / ribosome assembly / transcription elongation factor complex / regulation of DNA-templated transcription elongation / cytosolic ribosome assembly / response to reactive oxygen species / DNA endonuclease activity / transcription antitermination / translational initiation / regulation of cell growth / DNA-templated transcription termination / response to radiation / maintenance of translational fidelity / mRNA 5'-UTR binding / kinase activity / ribosome biogenesis / large ribosomal subunit / regulation of translation / ribosome binding / transferase activity / ribosomal small subunit biogenesis / ribosomal small subunit assembly / small ribosomal subunit / 5S rRNA binding / small ribosomal subunit rRNA binding / ribosomal large subunit assembly / cytosolic small ribosomal subunit / large ribosomal subunit rRNA binding / cytosolic large ribosomal subunit / cytoplasmic translation / tRNA binding / negative regulation of translation / rRNA binding / structural constituent of ribosome / ribosome / translation / response to antibiotic / negative regulation of DNA-templated transcription / mRNA binding / GTP binding / DNA binding / RNA binding / zinc ion binding / ATP binding / membrane / cytosol / cytoplasm 類似検索 - 分子機能 | ||||||||||||
生物種 | ![]() ![]() ![]() ![]() | ||||||||||||
手法 | 単粒子再構成法 / クライオ電子顕微鏡法 / 解像度: 3.9 Å | ||||||||||||
![]() | Loveland AB / Bah E | ||||||||||||
資金援助 | ![]()
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![]() | ![]() タイトル: Ribosome•RelA structures reveal the mechanism of stringent response activation. 著者: Anna B Loveland / Eugene Bah / Rohini Madireddy / Ying Zhang / Axel F Brilot / Nikolaus Grigorieff / Andrei A Korostelev / ![]() 要旨: Stringent response is a conserved bacterial stress response underlying virulence and antibiotic resistance. RelA/SpoT-homolog proteins synthesize transcriptional modulators (p)ppGpp, allowing ...Stringent response is a conserved bacterial stress response underlying virulence and antibiotic resistance. RelA/SpoT-homolog proteins synthesize transcriptional modulators (p)ppGpp, allowing bacteria to adapt to stress. RelA is activated during amino-acid starvation, when cognate deacyl-tRNA binds to the ribosomal A (aminoacyl-tRNA) site. We report four cryo-EM structures of E. coli RelA bound to the 70S ribosome, in the absence and presence of deacyl-tRNA accommodating in the 30S A site. The boomerang-shaped RelA with a wingspan of more than 100 Å wraps around the A/R (30S A-site/RelA-bound) tRNA. The CCA end of the A/R tRNA pins the central TGS domain against the 30S subunit, presenting the (p)ppGpp-synthetase domain near the 30S spur. The ribosome and A/R tRNA are captured in three conformations, revealing hitherto elusive states of tRNA engagement with the ribosomal decoding center. Decoding-center rearrangements are coupled with the step-wise 30S-subunit 'closure', providing insights into the dynamics of high-fidelity tRNA decoding. | ||||||||||||
履歴 |
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構造の表示
ムービー |
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構造ビューア | EMマップ: ![]() ![]() ![]() |
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マップデータ | ![]() | 137.6 MB | ![]() | |
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ヘッダ (付随情報) | ![]() ![]() | 82.3 KB 82.3 KB | 表示 表示 | ![]() |
画像 | ![]() | 148.4 KB | ||
Filedesc metadata | ![]() | 14.6 KB | ||
その他 | ![]() ![]() ![]() | 139.7 MB 139.3 MB 139.3 MB | ||
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-検証レポート
文書・要旨 | ![]() | 994.9 KB | 表示 | ![]() |
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文書・詳細版 | ![]() | 994.5 KB | 表示 | |
XML形式データ | ![]() | 18.3 KB | 表示 | |
CIF形式データ | ![]() | 21.7 KB | 表示 | |
アーカイブディレクトリ | ![]() ![]() | HTTPS FTP |
-関連構造データ
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リンク
EMDBのページ | ![]() ![]() |
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「今月の分子」の関連する項目 |
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マップ
ファイル | ![]() | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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注釈 | Ribosome*RelA structures reveal the mechanism of stringent response activation (Structure I) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
ボクセルのサイズ | X=Y=Z: 0.82 Å | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
密度 |
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対称性 | 空間群: 1 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
詳細 | EMDB XML:
CCP4マップ ヘッダ情報:
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-添付データ
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試料の構成要素
+全体 : RelA bound to 70S ribosome in the absence of A/R tRNA
+超分子 #1: RelA bound to 70S ribosome in the absence of A/R tRNA
+分子 #1: GTP pyrophosphokinase
+分子 #2: 50S ribosomal protein L2
+分子 #3: 50S ribosomal protein L3
+分子 #4: 50S ribosomal protein L4
+分子 #5: 50S ribosomal protein L5
+分子 #6: 50S ribosomal protein L6
+分子 #7: 50S ribosomal protein L9
+分子 #8: 50S ribosomal protein L10
+分子 #9: 50S ribosomal protein L11
+分子 #10: 50S ribosomal protein L13
+分子 #11: 50S ribosomal protein L14
+分子 #12: 50S ribosomal protein L15
+分子 #13: 50S ribosomal protein L16
+分子 #14: 50S ribosomal protein L17
+分子 #15: 50S ribosomal protein L18
+分子 #16: 50S ribosomal protein L19
+分子 #17: 50S ribosomal protein L20
+分子 #18: 50S ribosomal protein L21
+分子 #19: 50S ribosomal protein L22
+分子 #20: 50S ribosomal protein L23
+分子 #21: 50S ribosomal protein L24
+分子 #22: 50S ribosomal protein L25
+分子 #23: 50S ribosomal protein L27
+分子 #24: 50S ribosomal protein L28
+分子 #25: 50S ribosomal protein L29
+分子 #26: 50S ribosomal protein L30
+分子 #27: 50S ribosomal protein L31
+分子 #28: 50S ribosomal protein L32
+分子 #29: 50S ribosomal protein L33
+分子 #30: 50S ribosomal protein L34
+分子 #31: 50S ribosomal protein L35
+分子 #32: 50S ribosomal protein L36
+分子 #33: 30S ribosomal protein S2
+分子 #34: 30S ribosomal protein S3
+分子 #35: 30S ribosomal protein S4
+分子 #36: 30S ribosomal protein S5
+分子 #37: 30S ribosomal protein S6
+分子 #38: 30S ribosomal protein S7
+分子 #39: 30S ribosomal protein S8
+分子 #40: 30S ribosomal protein S9
+分子 #41: 30S ribosomal protein S10
+分子 #42: 30S ribosomal protein S11
+分子 #43: 30S ribosomal protein S12
+分子 #44: 30S ribosomal protein S13
+分子 #45: 30S ribosomal protein S14
+分子 #46: 30S ribosomal protein S15
+分子 #47: 30S ribosomal protein S16
+分子 #48: 30S ribosomal protein S17
+分子 #49: 30S ribosomal protein S18
+分子 #50: 30S ribosomal protein S19
+分子 #51: 30S ribosomal protein S20
+分子 #52: 30S ribosomal protein S21
+分子 #53: 16S ribosomal RNA
+分子 #54: 23S ribosomal RNA
+分子 #55: 5S ribosomal RNA
+分子 #56: mRNA
+分子 #57: P site tRNAfmet
+分子 #58: E-site tRNAfMet
-実験情報
-構造解析
手法 | クライオ電子顕微鏡法 |
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![]() | 単粒子再構成法 |
試料の集合状態 | particle |
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試料調製
濃度 | 0.1 mg/mL |
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緩衝液 | pH: 7.4 |
グリッド | モデル: C-flat-1.2/1.3 / 材質: COPPER / メッシュ: 400 / 支持フィルム - 材質: CARBON / 支持フィルム - トポロジー: CONTINUOUS / 前処理 - タイプ: GLOW DISCHARGE / 前処理 - 時間: 45 sec. / 前処理 - 雰囲気: AIR |
凍結 | 凍結剤: ETHANE / チャンバー内湿度: 75 % / チャンバー内温度: 295 K / 装置: GATAN CRYOPLUNGE 3 詳細: Apply 2 uL sample and blot 4 seconds before plunging into liquid ethane (GATAN CRYOPLUNGE 3).. |
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電子顕微鏡法
顕微鏡 | FEI TITAN KRIOS |
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撮影 | フィルム・検出器のモデル: GATAN K2 SUMMIT (4k x 4k) 検出モード: SUPER-RESOLUTION / デジタル化 - 画像ごとのフレーム数: 1-25 / 撮影したグリッド数: 5 / 実像数: 5763 / 平均露光時間: 0.4 sec. / 平均電子線量: 1.6 e/Å2 |
電子線 | 加速電圧: 300 kV / 電子線源: ![]() |
電子光学系 | C2レンズ絞り径: 100.0 µm / 最大 デフォーカス(補正後): 2.2 µm / 最小 デフォーカス(補正後): 0.5 µm / 倍率(補正後): 30488 / 照射モード: FLOOD BEAM / 撮影モード: BRIGHT FIELD / Cs: 2.7 mm / 最大 デフォーカス(公称値): 2.2 µm / 最小 デフォーカス(公称値): 0.5 µm / 倍率(公称値): 30488 |
試料ステージ | 試料ホルダーモデル: FEI TITAN KRIOS AUTOGRID HOLDER ホルダー冷却材: NITROGEN |
実験機器 | ![]() モデル: Titan Krios / 画像提供: FEI Company |