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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: PDB / ID: 5fz5 | ||||||
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| タイトル | Transcription initiation complex structures elucidate DNA opening (CC) | ||||||
要素 |
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キーワード | TRANSCRIPTION / GENE EXPRESSION / TRANSCRIPTION INITIATION | ||||||
| 機能・相同性 | 機能・相同性情報: / transcription open complex formation at RNA polymerase II promoter / TFIIA-class transcription factor complex binding / RNA polymerase III transcription regulatory region sequence-specific DNA binding / RNA polymerase III preinitiation complex assembly / transcription factor TFIIIB complex / transcription factor TFIIE complex / regulation of transcription by RNA polymerase III / TFIIF-class transcription factor complex binding / RNA polymerase I general transcription initiation factor binding ...: / transcription open complex formation at RNA polymerase II promoter / TFIIA-class transcription factor complex binding / RNA polymerase III transcription regulatory region sequence-specific DNA binding / RNA polymerase III preinitiation complex assembly / transcription factor TFIIIB complex / transcription factor TFIIE complex / regulation of transcription by RNA polymerase III / TFIIF-class transcription factor complex binding / RNA polymerase I general transcription initiation factor binding / transcriptional start site selection at RNA polymerase II promoter / transcription factor TFIIF complex / RPB4-RPB7 complex / transcription factor TFIIA complex / RNA polymerase I preinitiation complex assembly / nuclear-transcribed mRNA catabolic process, deadenylation-dependent decay / RNA Polymerase I Transcription Initiation / transcription preinitiation complex / DNA binding, bending / Processing of Capped Intron-Containing Pre-mRNA / RNA Polymerase III Transcription Initiation From Type 2 Promoter / RNA Pol II CTD phosphorylation and interaction with CE / Formation of the Early Elongation Complex / mRNA Capping / RNA polymerase II transcribes snRNA genes / TP53 Regulates Transcription of DNA Repair Genes / RNA Polymerase II Promoter Escape / RNA Polymerase II Transcription Pre-Initiation And Promoter Opening / RNA Polymerase II Transcription Initiation / RNA Polymerase II Transcription Initiation And Promoter Clearance / termination of RNA polymerase II transcription / RNA Polymerase II Pre-transcription Events / termination of RNA polymerase III transcription / transcription factor TFIID complex / RNA-templated transcription / RNA polymerase II general transcription initiation factor activity / Formation of TC-NER Pre-Incision Complex / positive regulation of nuclear-transcribed mRNA poly(A) tail shortening / RNA Polymerase I Promoter Escape / transcription initiation at RNA polymerase III promoter / termination of RNA polymerase I transcription / Gap-filling DNA repair synthesis and ligation in TC-NER / transcription initiation at RNA polymerase I promoter / nucleolar large rRNA transcription by RNA polymerase I / Estrogen-dependent gene expression / RNA polymerase II complex binding / transcription by RNA polymerase III / maintenance of transcriptional fidelity during transcription elongation by RNA polymerase II / Dual incision in TC-NER / positive regulation of translational initiation / protein phosphatase activator activity / nuclear-transcribed mRNA catabolic process / positive regulation of transcription initiation by RNA polymerase II / RNA polymerase II core promoter sequence-specific DNA binding / RNA polymerase I complex / RNA polymerase III complex / transcription elongation by RNA polymerase I / RNA polymerase II preinitiation complex assembly / RNA polymerase II, core complex / tRNA transcription by RNA polymerase III / translesion synthesis / transcription by RNA polymerase I / transcription-coupled nucleotide-excision repair / translation initiation factor binding / TBP-class protein binding / transcription coregulator activity / transcription initiation at RNA polymerase II promoter / DNA-templated transcription initiation / P-body / transcription elongation by RNA polymerase II / positive regulation of transcription elongation by RNA polymerase II / mRNA transcription by RNA polymerase II / ribonucleoside binding / mRNA processing / DNA-directed RNA polymerase / cytoplasmic stress granule / disordered domain specific binding / DNA-directed RNA polymerase activity / peroxisome / single-stranded DNA binding / ribosome biogenesis / transcription regulator complex / transcription by RNA polymerase II / DNA-binding transcription factor binding / nucleic acid binding / RNA polymerase II-specific DNA-binding transcription factor binding / protein dimerization activity / single-stranded RNA binding / nucleotide binding / negative regulation of DNA-templated transcription / mRNA binding / chromatin binding / regulation of DNA-templated transcription / nucleolus / positive regulation of transcription by RNA polymerase II / protein-containing complex / mitochondrion / DNA binding / zinc ion binding / nucleoplasm 類似検索 - 分子機能 | ||||||
| 生物種 | ![]() SYNTHETIC (人工物) | ||||||
| 手法 | 電子顕微鏡法 / 単粒子再構成法 / クライオ電子顕微鏡法 / 解像度: 8.8 Å | ||||||
データ登録者 | Plaschka, C. / Hantsche, M. / Dienemann, C. / Burzinski, C. / Plitzko, J. / Cramer, P. | ||||||
引用 | ジャーナル: Nature / 年: 2016タイトル: Transcription initiation complex structures elucidate DNA opening. 著者: C Plaschka / M Hantsche / C Dienemann / C Burzinski / J Plitzko / P Cramer / ![]() 要旨: Transcription of eukaryotic protein-coding genes begins with assembly of the RNA polymerase (Pol) II initiation complex and promoter DNA opening. Here we report cryo-electron microscopy (cryo-EM) ...Transcription of eukaryotic protein-coding genes begins with assembly of the RNA polymerase (Pol) II initiation complex and promoter DNA opening. Here we report cryo-electron microscopy (cryo-EM) structures of yeast initiation complexes containing closed and open DNA at resolutions of 8.8 Å and 3.6 Å, respectively. DNA is positioned and retained over the Pol II cleft by a network of interactions between the TATA-box-binding protein TBP and transcription factors TFIIA, TFIIB, TFIIE, and TFIIF. DNA opening occurs around the tip of the Pol II clamp and the TFIIE 'extended winged helix' domain, and can occur in the absence of TFIIH. Loading of the DNA template strand into the active centre may be facilitated by movements of obstructing protein elements triggered by allosteric binding of the TFIIE 'E-ribbon' domain. The results suggest a unified model for transcription initiation with a key event, the trapping of open promoter DNA by extended protein-protein and protein-DNA contacts. | ||||||
| 履歴 |
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| Remark 700 | SHEET DETERMINATION METHOD: DSSP THE SHEETS PRESENTED AS "AM" IN EACH CHAIN ON SHEET RECORDS BELOW ... SHEET DETERMINATION METHOD: DSSP THE SHEETS PRESENTED AS "AM" IN EACH CHAIN ON SHEET RECORDS BELOW IS ACTUALLY AN 9-STRANDED BARREL THIS IS REPRESENTED BY A 10-STRANDED SHEET IN WHICH THE FIRST AND LAST STRANDS ARE IDENTICAL. THE SHEETS PRESENTED AS "GB" IN EACH CHAIN ON SHEET RECORDS BELOW IS ACTUALLY AN 5-STRANDED BARREL THIS IS REPRESENTED BY A 6-STRANDED SHEET IN WHICH THE FIRST AND LAST STRANDS ARE IDENTICAL. THE SHEETS PRESENTED AS "QC" IN EACH CHAIN ON SHEET RECORDS BELOW IS ACTUALLY AN 8-STRANDED BARREL THIS IS REPRESENTED BY A 9-STRANDED SHEET IN WHICH THE FIRST AND LAST STRANDS ARE IDENTICAL. THE SHEETS PRESENTED AS "UA" IN EACH CHAIN ON SHEET RECORDS BELOW IS ACTUALLY AN 6-STRANDED BARREL THIS IS REPRESENTED BY A 7-STRANDED SHEET IN WHICH THE FIRST AND LAST STRANDS ARE IDENTICAL. |
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構造の表示
| ムービー |
ムービービューア |
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| 構造ビューア | 分子: Molmil Jmol/JSmol |
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ダウンロードとリンク
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ダウンロード
| PDBx/mmCIF形式 | 5fz5.cif.gz | 1.1 MB | 表示 | PDBx/mmCIF形式 |
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| PDB形式 | pdb5fz5.ent.gz | 856.7 KB | 表示 | PDB形式 |
| PDBx/mmJSON形式 | 5fz5.json.gz | ツリー表示 | PDBx/mmJSON形式 | |
| その他 | その他のダウンロード |
-検証レポート
| アーカイブディレクトリ | https://data.pdbj.org/pub/pdb/validation_reports/fz/5fz5 ftp://data.pdbj.org/pub/pdb/validation_reports/fz/5fz5 | HTTPS FTP |
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-関連構造データ
| 関連構造データ | ![]() 3383MC ![]() 3375C ![]() 3376C ![]() 3377C ![]() 3378C ![]() 3379C ![]() 3380C ![]() 3381C ![]() 3382C ![]() 5fywC ![]() 5ip7C ![]() 5ip9C C: 同じ文献を引用 ( M: このデータのモデリングに利用したマップデータ |
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| 類似構造データ |
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リンク
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集合体
| 登録構造単位 | ![]()
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要素
-DNA-DIRECTED RNA POLYMERASE II SUBUNIT ... , 7種, 7分子 ABCDGIK
| #1: タンパク質 | 分子量: 191821.578 Da / 分子数: 1 / 由来タイプ: 天然 / 由来: (天然) ![]() |
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| #2: タンパク質 | 分子量: 138937.297 Da / 分子数: 1 / 由来タイプ: 天然 / 由来: (天然) ![]() |
| #3: タンパク質 | 分子量: 35330.457 Da / 分子数: 1 / 由来タイプ: 天然 / 由来: (天然) ![]() |
| #4: タンパク質 | 分子量: 25451.191 Da / 分子数: 1 / 由来タイプ: 天然 / 由来: (天然) ![]() |
| #7: タンパク質 | 分子量: 19081.053 Da / 分子数: 1 / 由来タイプ: 天然 / 由来: (天然) ![]() |
| #9: タンパク質 | 分子量: 14308.161 Da / 分子数: 1 / 由来タイプ: 天然 / 由来: (天然) ![]() |
| #11: タンパク質 | 分子量: 13633.493 Da / 分子数: 1 / 由来タイプ: 天然 / 由来: (天然) ![]() |
-DNA-DIRECTED RNA POLYMERASES I, II, AND III SUBUNIT RPABC ... , 5種, 5分子 EFHJL
| #5: タンパク質 | 分子量: 25117.094 Da / 分子数: 1 / 由来タイプ: 天然 / 由来: (天然) ![]() |
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| #6: タンパク質 | 分子量: 17931.834 Da / 分子数: 1 / 由来タイプ: 天然 / 由来: (天然) ![]() |
| #8: タンパク質 | 分子量: 16525.363 Da / 分子数: 1 / 由来タイプ: 天然 / 由来: (天然) ![]() |
| #10: タンパク質 | 分子量: 8290.732 Da / 分子数: 1 / 由来タイプ: 天然 / 由来: (天然) ![]() |
| #12: タンパク質 | 分子量: 7729.969 Da / 分子数: 1 / 由来タイプ: 天然 / 由来: (天然) ![]() |
-タンパク質 , 2種, 2分子 MO
| #13: タンパク質 | 分子量: 38257.340 Da / 分子数: 1 / 由来タイプ: 組換発現 由来: (組換発現) ![]() プラスミド: POPINE / 発現宿主: ![]() |
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| #15: タンパク質 | 分子量: 27042.275 Da / 分子数: 1 / 由来タイプ: 組換発現 由来: (組換発現) ![]() プラスミド: PET21B / 発現宿主: ![]() |
-SYNTHETIC CLOSED PROMOTER DNA ... , 2種, 2分子 NT
| #14: DNA鎖 | 分子量: 17254.084 Da / 分子数: 1 / 由来タイプ: 天然 / 詳細: NON-TEMPLATE STRAND / 由来: (天然) ![]() |
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| #18: DNA鎖 | 分子量: 26172.779 Da / 分子数: 1 / 由来タイプ: 合成 / 詳細: TEMPLATE STRAND / 由来: (合成) SYNTHETIC (人工物) |
-TRANSCRIPTION INITIATION FACTOR IIF SUBUNIT ... , 2種, 2分子 QR
| #16: タンパク質 | 分子量: 82320.570 Da / 分子数: 1 / 由来タイプ: 組換発現 由来: (組換発現) ![]() プラスミド: PET21 / 発現宿主: ![]() |
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| #17: タンパク質 | 分子量: 46684.492 Da / 分子数: 1 / 由来タイプ: 組換発現 由来: (組換発現) ![]() プラスミド: PETDUET-1 / 発現宿主: ![]() |
-TRANSCRIPTION INITIATION FACTOR IIA ... , 2種, 2分子 UV
| #19: タンパク質 | 分子量: 32230.805 Da / 分子数: 1 / 由来タイプ: 組換発現 由来: (組換発現) ![]() 株: BJ5464 RPB3 HIS-BIO / 発現宿主: ![]() |
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| #20: タンパク質 | 分子量: 13473.070 Da / 分子数: 1 / 由来タイプ: 組換発現 由来: (組換発現) ![]() プラスミド: POPINE / 発現宿主: ![]() |
-TRANSCRIPTION INITIATION FACTOR IIE SUBUNIT ... , 2種, 2分子 WX
| #21: タンパク質 | 分子量: 54804.809 Da / 分子数: 1 / 由来タイプ: 組換発現 由来: (組換発現) ![]() プラスミド: POPINE / 発現宿主: ![]() |
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| #22: タンパク質 | 分子量: 37050.434 Da / 分子数: 1 / 由来タイプ: 組換発現 由来: (組換発現) ![]() プラスミド: PET21 / 発現宿主: ![]() |
-非ポリマー , 2種, 11分子 


| #23: 化合物 | ChemComp-ZN / #24: 化合物 | ChemComp-MG / | |
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-実験情報
-実験
| 実験 | 手法: 電子顕微鏡法 |
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| EM実験 | 試料の集合状態: PARTICLE / 3次元再構成法: 単粒子再構成法 |
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試料調製
| 構成要素 | 名称: YEAST POL II TRANSCRIPTION INITIATION COMPLEX (CLOSED DNA) タイプ: COMPLEX |
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| 緩衝液 | 名称: 25 MM HEPES-KOH PH 7.5, 150 MM POTASSIUM ACETATE, 2 MM MGCL2, 5 MM DTT pH: 7.5 詳細: 25 MM HEPES-KOH PH 7.5, 150 MM POTASSIUM ACETATE, 2 MM MGCL2, 5 MM DTT |
| 試料 | 濃度: 0.3 mg/ml / 包埋: NO / シャドウイング: NO / 染色: NO / 凍結: YES |
| 試料支持 | 詳細: HOLEY CARBON |
| 急速凍結 | 装置: FEI VITROBOT MARK IV / 凍結剤: ETHANE / 詳細: LIQUID ETHANE |
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電子顕微鏡撮影
| 実験機器 | ![]() モデル: Titan Krios / 画像提供: FEI Company |
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| 顕微鏡 | モデル: FEI TITAN KRIOS / 日付: 2016年6月20日 |
| 電子銃 | 電子線源: FIELD EMISSION GUN / 加速電圧: 300 kV / 照射モード: FLOOD BEAM |
| 電子レンズ | モード: BRIGHT FIELD / 倍率(公称値): 37000 X / 倍率(補正後): 37037 X / 最大 デフォーカス(公称値): 5000 nm / 最小 デフォーカス(公称値): 800 nm |
| 撮影 | 電子線照射量: 40 e/Å2 フィルム・検出器のモデル: GATAN K2 SUMMIT (4k x 4k) |
| 画像スキャン | デジタル画像の数: 959 |
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解析
| EMソフトウェア | 名称: RELION / カテゴリ: 3次元再構成 | ||||||||||||
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| CTF補正 | 詳細: EACH PARTICLE | ||||||||||||
| 対称性 | 点対称性: C1 (非対称) | ||||||||||||
| 3次元再構成 | 手法: RELION 1.3 / 解像度: 8.8 Å / 粒子像の数: 5690 詳細: THE MODEL FOR THE CLOSED COMPLEX WAS DERIVED FROM THE OPEN COMPLEX MODEL (5FYW). THREE RIGID-BODY GROUPS (1. POL II, TFIIA, TFIIB, TBP, TFIIE E-RIBBON AND TFIIF DIMERIZATION DOMAIN, 2. TFIIE ...詳細: THE MODEL FOR THE CLOSED COMPLEX WAS DERIVED FROM THE OPEN COMPLEX MODEL (5FYW). THREE RIGID-BODY GROUPS (1. POL II, TFIIA, TFIIB, TBP, TFIIE E-RIBBON AND TFIIF DIMERIZATION DOMAIN, 2. TFIIE DOMAINS TFA1 AND TFA2 WH, 3.TFIIE TFA2 WH1 AND TFIIF TFG2 WH) WERE INDIVIDUALLY FITTED INTO THE CLOSED COMPLEX EM DENSITY BY AN AUTOMATED CORRELATION SEARCH IN SITUS. TO MODEL CLOSED PROMOTER DNA, UPSTREAM DNA WAS EXTENDED WITH CANONICAL DUPLEX B-FORM DNA IN COOT AND RIGID-BODY FITTED IN UCSF CHIMERA TO REFLECT THE DENSITY. SUBMISSION BASED ON EXPERIMENTAL DATA FROM EMDB EMD-3383. (DEPOSITION ID: 14367). 対称性のタイプ: POINT | ||||||||||||
| 精密化 | 最高解像度: 8.8 Å | ||||||||||||
| 精密化ステップ | サイクル: LAST / 最高解像度: 8.8 Å
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万見について






引用
UCSF Chimera




















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