+データを開く
-基本情報
登録情報 | データベース: EMDB / ID: EMD-26067 | ||||||||||||
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タイトル | CryoEM structure of the human 40S small ribosomal subunit in complex with translation initiation factors eIF1A and eIF5B. | ||||||||||||
マップデータ | Sharpened map | ||||||||||||
試料 |
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キーワード | eIF5B / translation / initiation / eIF1A / RIBOSOME | ||||||||||||
機能・相同性 | 機能・相同性情報 protein-synthesizing GTPase / : / negative regulation of endoplasmic reticulum unfolded protein response / oxidized pyrimidine DNA binding / response to TNF agonist / positive regulation of base-excision repair / protein tyrosine kinase inhibitor activity / positive regulation of respiratory burst involved in inflammatory response / positive regulation of intrinsic apoptotic signaling pathway in response to DNA damage / positive regulation of gastrulation ...protein-synthesizing GTPase / : / negative regulation of endoplasmic reticulum unfolded protein response / oxidized pyrimidine DNA binding / response to TNF agonist / positive regulation of base-excision repair / protein tyrosine kinase inhibitor activity / positive regulation of respiratory burst involved in inflammatory response / positive regulation of intrinsic apoptotic signaling pathway in response to DNA damage / positive regulation of gastrulation / nucleolus organization / regulation of adenylate cyclase-activating G protein-coupled receptor signaling pathway / IRE1-RACK1-PP2A complex / positive regulation of endodeoxyribonuclease activity / positive regulation of Golgi to plasma membrane protein transport / TNFR1-mediated ceramide production / negative regulation of RNA splicing / negative regulation of DNA repair / negative regulation of intrinsic apoptotic signaling pathway in response to hydrogen peroxide / supercoiled DNA binding / oxidized purine DNA binding / neural crest cell differentiation / NF-kappaB complex / ubiquitin-like protein conjugating enzyme binding / regulation of translational initiation / regulation of establishment of cell polarity / positive regulation of ubiquitin-protein transferase activity / negative regulation of phagocytosis / rRNA modification in the nucleus and cytosol / erythrocyte homeostasis / Formation of the ternary complex, and subsequently, the 43S complex / cytoplasmic side of rough endoplasmic reticulum membrane / pigmentation / protein kinase A binding / negative regulation of ubiquitin protein ligase activity / Ribosomal scanning and start codon recognition / ion channel inhibitor activity / Translation initiation complex formation / mammalian oogenesis stage / fibroblast growth factor binding / positive regulation of mitochondrial depolarization / activation-induced cell death of T cells / positive regulation of T cell receptor signaling pathway / negative regulation of peptidyl-serine phosphorylation / iron-sulfur cluster binding / negative regulation of Wnt signaling pathway / positive regulation of activated T cell proliferation / monocyte chemotaxis / Protein hydroxylation / regulation of cell division / BH3 domain binding / cysteine-type endopeptidase activator activity involved in apoptotic process / mTORC1-mediated signalling / SARS-CoV-1 modulates host translation machinery / Peptide chain elongation / positive regulation of intrinsic apoptotic signaling pathway by p53 class mediator / Selenocysteine synthesis / positive regulation of signal transduction by p53 class mediator / Formation of a pool of free 40S subunits / ubiquitin ligase inhibitor activity / Eukaryotic Translation Termination / phagocytic cup / negative regulation of respiratory burst involved in inflammatory response / Response of EIF2AK4 (GCN2) to amino acid deficiency / SRP-dependent cotranslational protein targeting to membrane / Viral mRNA Translation / negative regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction / Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) / GTP hydrolysis and joining of the 60S ribosomal subunit / L13a-mediated translational silencing of Ceruloplasmin expression / TOR signaling / endonucleolytic cleavage to generate mature 3'-end of SSU-rRNA from (SSU-rRNA, 5.8S rRNA, LSU-rRNA) / T cell proliferation involved in immune response / regulation of translational fidelity / spindle assembly / positive regulation of cell cycle / Major pathway of rRNA processing in the nucleolus and cytosol / erythrocyte development / Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC) / negative regulation of ubiquitin-dependent protein catabolic process / Amplification of signal from unattached kinetochores via a MAD2 inhibitory signal / Protein methylation / positive regulation of intrinsic apoptotic signaling pathway / ribosomal small subunit export from nucleus / Nuclear events stimulated by ALK signaling in cancer / translation regulator activity / signaling adaptor activity / negative regulation of smoothened signaling pathway / stress granule assembly / Mitotic Prometaphase / rough endoplasmic reticulum / endonucleolytic cleavage in ITS1 to separate SSU-rRNA from 5.8S rRNA and LSU-rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA) / positive regulation of JUN kinase activity / EML4 and NUDC in mitotic spindle formation / gastrulation / MDM2/MDM4 family protein binding / Maturation of protein E / Maturation of protein E / ER Quality Control Compartment (ERQC) / DNA-(apurinic or apyrimidinic site) endonuclease activity 類似検索 - 分子機能 | ||||||||||||
生物種 | Homo sapiens (ヒト) | ||||||||||||
手法 | 単粒子再構成法 / クライオ電子顕微鏡法 / 解像度: 3.2 Å | ||||||||||||
データ登録者 | Lapointe CP / Grosely R | ||||||||||||
資金援助 | 米国, スウェーデン, 3件
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引用 | ジャーナル: Nature / 年: 2022 タイトル: eIF5B and eIF1A reorient initiator tRNA to allow ribosomal subunit joining. 著者: Christopher P Lapointe / Rosslyn Grosely / Masaaki Sokabe / Carlos Alvarado / Jinfan Wang / Elizabeth Montabana / Nancy Villa / Byung-Sik Shin / Thomas E Dever / Christopher S Fraser / Israel ...著者: Christopher P Lapointe / Rosslyn Grosely / Masaaki Sokabe / Carlos Alvarado / Jinfan Wang / Elizabeth Montabana / Nancy Villa / Byung-Sik Shin / Thomas E Dever / Christopher S Fraser / Israel S Fernández / Joseph D Puglisi / 要旨: Translation initiation defines the identity and quantity of a synthesized protein. The process is dysregulated in many human diseases. A key commitment step is when the ribosomal subunits join at a ...Translation initiation defines the identity and quantity of a synthesized protein. The process is dysregulated in many human diseases. A key commitment step is when the ribosomal subunits join at a translation start site on a messenger RNA to form a functional ribosome. Here, we combined single-molecule spectroscopy and structural methods using an in vitro reconstituted system to examine how the human ribosomal subunits join. Single-molecule fluorescence revealed when the universally conserved eukaryotic initiation factors eIF1A and eIF5B associate with and depart from initiation complexes. Guided by single-molecule dynamics, we visualized initiation complexes that contained both eIF1A and eIF5B using single-particle cryo-electron microscopy. The resulting structure revealed how eukaryote-specific contacts between the two proteins remodel the initiation complex to orient the initiator aminoacyl-tRNA in a conformation compatible with ribosomal subunit joining. Collectively, our findings provide a quantitative and architectural framework for the molecular choreography orchestrated by eIF1A and eIF5B during translation initiation in humans. | ||||||||||||
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_26067.map.gz | 381.3 MB | EMDBマップデータ形式 | |
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ヘッダ (付随情報) | emd-26067-v30.xml emd-26067.xml | 59.5 KB 59.5 KB | 表示 表示 | EMDBヘッダ |
画像 | emd_26067.png | 98.3 KB | ||
マスクデータ | emd_26067_msk_1.map | 421.9 MB | マスクマップ | |
Filedesc metadata | emd-26067.cif.gz | 11.8 KB | ||
その他 | emd_26067_additional_1.map.gz emd_26067_half_map_1.map.gz emd_26067_half_map_2.map.gz | 370.1 MB 375.2 MB 369.1 MB | ||
アーカイブディレクトリ | http://ftp.pdbj.org/pub/emdb/structures/EMD-26067 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-26067 | HTTPS FTP |
-検証レポート
文書・要旨 | emd_26067_validation.pdf.gz | 994.1 KB | 表示 | EMDB検証レポート |
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文書・詳細版 | emd_26067_full_validation.pdf.gz | 993.7 KB | 表示 | |
XML形式データ | emd_26067_validation.xml.gz | 17.9 KB | 表示 | |
CIF形式データ | emd_26067_validation.cif.gz | 21.6 KB | 表示 | |
アーカイブディレクトリ | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-26067 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-26067 | HTTPS FTP |
-関連構造データ
関連構造データ | 7tqlMC 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_26067.map.gz / 形式: CCP4 / 大きさ: 421.9 MB / タイプ: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||
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注釈 | Sharpened map | ||||||||||||||||||||||||||||||||||||
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: 1.31 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
-マスク #1
ファイル | emd_26067_msk_1.map | ||||||||||||
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投影像・断面図 |
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密度ヒストグラム |
-追加マップ: Unsharpened map
ファイル | emd_26067_additional_1.map | ||||||||||||
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注釈 | Unsharpened map | ||||||||||||
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_26067_half_map_1.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 |
-ハーフマップ: Half map 2
ファイル | emd_26067_half_map_2.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 |
-試料の構成要素
+全体 : human 40S ribosomal subunit in complex with eIF1A and eIF5B
+超分子 #1: human 40S ribosomal subunit in complex with eIF1A and eIF5B
+分子 #1: Eukaryotic translation initiation factor 5B
+分子 #4: Translation initiation factor eIF1A
+分子 #5: ribosomal protein uS2
+分子 #6: 40S ribosomal protein S2
+分子 #7: 40S ribosomal protein S4, X isoform
+分子 #8: 40S ribosomal protein S3
+分子 #9: 40S ribosomal protein S6
+分子 #10: 40S ribosomal protein S7
+分子 #11: 40S ribosomal protein S8
+分子 #12: 40S ribosomal protein S9
+分子 #13: 40S ribosomal protein S5
+分子 #14: 40S ribosomal protein S11
+分子 #15: 40S ribosomal protein S10
+分子 #16: ribosomal protein uS15
+分子 #17: ribosomal protein eS12
+分子 #18: ribosomal protein uS11
+分子 #19: 40S ribosomal protein S15
+分子 #20: 40S ribosomal protein S16
+分子 #21: ribosomal protein eS17
+分子 #22: ribosomal protein uS13
+分子 #23: 40S ribosomal protein S19
+分子 #24: ribosomal protein uS10
+分子 #25: 40S ribosomal protein S15a
+分子 #26: 40S ribosomal protein S23
+分子 #27: Isoform 3 of 40S ribosomal protein S24
+分子 #28: 40S ribosomal protein S21
+分子 #29: ribosomal protein eS25
+分子 #30: 40S ribosomal protein S27
+分子 #31: 40S ribosomal protein S26
+分子 #32: ribosomal protein eS28
+分子 #33: ribosomal protein eS30
+分子 #34: ribosomal protein uS14
+分子 #35: 40S ribosomal protein S27a
+分子 #36: ribosomal protein eL41
+分子 #37: Receptor of activated protein C kinase 1
+分子 #2: 18S ribosomal RNA
+分子 #3: Human Met-tRNAiMet
+分子 #38: PHOSPHOAMINOPHOSPHONIC ACID-GUANYLATE ESTER
+分子 #39: GUANOSINE-5'-MONOPHOSPHATE
+分子 #40: 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: 7.2 |
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グリッド | モデル: Quantifoil R2/2 / 材質: COPPER / メッシュ: 300 |
凍結 | 凍結剤: ETHANE |
-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 K3 (6k x 4k) / 平均電子線量: 70.0 e/Å2 |
電子線 | 加速電圧: 300 kV / 電子線源: FIELD EMISSION GUN |
電子光学系 | C2レンズ絞り径: 50.0 µm / 照射モード: OTHER / 撮影モード: BRIGHT FIELD / Cs: 2.7 mm / 最大 デフォーカス(公称値): 2.0 µm / 最小 デフォーカス(公称値): 0.5 µm |
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 |
-画像解析
初期モデル | モデルのタイプ: INSILICO MODEL |
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最終 再構成 | 解像度のタイプ: BY AUTHOR / 解像度: 3.2 Å / 解像度の算出法: FSC 0.143 CUT-OFF / 使用した粒子像数: 190000 |
初期 角度割当 | タイプ: MAXIMUM LIKELIHOOD |
最終 角度割当 | タイプ: PROJECTION MATCHING |