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データを開く
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基本情報
登録情報 | ![]() | |||||||||
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タイトル | RpoC2 SI domain of the spinach plastid-encoded RNA polymerase | |||||||||
![]() | Author said This map is a locally refined map of 8XZV/EMD-38799. Author said they masked a flexible domain of the map to get some pose information for model building. Consequently, the density of the unmasked region is fragmented and looks like noise. All the calculations were performed in cryoSPARC, which may have led to an overestimation of the resolution, especially in the case of intrinsic flexibility. Author said they can either adopt the resolution calculated by the EMDB and make corresponding revisions to the article, or we can provide the Auto-tightening mask used during the CryoSPARC refinement. | |||||||||
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![]() | plastid-encoded RNA polymerase / chloroplast / spinach / TRANSCRIPTION | |||||||||
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: 3.24 Å | |||||||||
![]() | Wang G-L / Yu L-J / Lu C | |||||||||
資金援助 | ![]()
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![]() | ![]() タイトル: Architecture of the spinach plastid-encoded RNA polymerase. 著者: Tongtong Wang / Guang-Lei Wang / Ying Fang / Yi Zhang / Wenxin Peng / Yue Zhou / Aihong Zhang / Long-Jiang Yu / Congming Lu / ![]() 要旨: The plastid-encoded RNA polymerase serves as the principal transcription machinery within chloroplasts, transcribing over 80% of all primary plastid transcripts. This polymerase consists of a ...The plastid-encoded RNA polymerase serves as the principal transcription machinery within chloroplasts, transcribing over 80% of all primary plastid transcripts. This polymerase consists of a prokaryotic-like core enzyme known as the plastid-encoded RNA polymerase core, and is supplemented by newly evolved associated proteins known as PAPs. However, the architecture of the plastid-encoded RNA polymerase and the possible functions of PAPs remain unknown. Here, we present the cryo-electron microscopy structure of a 19-subunit plastid-encoded RNA polymerase complex derived from spinach (Spinacia oleracea). The structure shows that the plastid-encoded RNA polymerase core resembles bacterial RNA polymerase. Twelve PAPs and two additional proteins (FLN2 and pTAC18) bind at the periphery of the plastid-encoded RNA polymerase core, forming extensive interactions that may facilitate complex assembly and stability. PAPs may also protect the complex against oxidative damage and has potential functions in transcriptional regulation. This research offers a structural basis for future investigations into the functions and regulatory mechanisms governing the transcription of plastid genes. | |||||||||
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 | ![]() | 484 MB | ![]() | |
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ヘッダ (付随情報) | ![]() ![]() | 15.1 KB 15.1 KB | 表示 表示 | ![]() |
FSC (解像度算出) | ![]() | 16.9 KB | 表示 | ![]() |
画像 | ![]() | 54.6 KB | ||
マスクデータ | ![]() | 512 MB | ![]() | |
Filedesc metadata | ![]() | 5.5 KB | ||
その他 | ![]() ![]() | 475.1 MB 475 MB | ||
アーカイブディレクトリ | ![]() ![]() | HTTPS FTP |
-検証レポート
文書・要旨 | ![]() | 921.2 KB | 表示 | ![]() |
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文書・詳細版 | ![]() | 920.7 KB | 表示 | |
XML形式データ | ![]() | 26.1 KB | 表示 | |
CIF形式データ | ![]() | 34.6 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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マップ
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注釈 | Author said This map is a locally refined map of 8XZV/EMD-38799. Author said they masked a flexible domain of the map to get some pose information for model building. Consequently, the density of the unmasked region is fragmented and looks like noise. All the calculations were performed in cryoSPARC, which may have led to an overestimation of the resolution, especially in the case of intrinsic flexibility. Author said they can either adopt the resolution calculated by the EMDB and make corresponding revisions to the article, or we can provide the Auto-tightening mask used during the CryoSPARC refinement. | ||||||||||||||||||||||||||||||||||||
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: 1.1 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 | ![]() | ||||||||||||
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投影像・断面図 |
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密度ヒストグラム |
-ハーフマップ: #1
ファイル | emd_61149_half_map_1.map | ||||||||||||
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投影像・断面図 |
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密度ヒストグラム |
-ハーフマップ: #2
ファイル | emd_61149_half_map_2.map | ||||||||||||
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投影像・断面図 |
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密度ヒストグラム |
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試料の構成要素
-全体 : DNA-directed RNA polymerase subunit beta''
全体 | 名称: DNA-directed RNA polymerase subunit beta'' |
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要素 |
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-超分子 #1: DNA-directed RNA polymerase subunit beta''
超分子 | 名称: DNA-directed RNA polymerase subunit beta'' / タイプ: complex / ID: 1 / 親要素: 0 / 含まれる分子: all |
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由来(天然) | 生物種: ![]() |
-分子 #1: DNA-directed RNA polymerase subunit beta''
分子 | 名称: DNA-directed RNA polymerase subunit beta'' / タイプ: protein_or_peptide / ID: 1 / 光学異性体: LEVO / EC番号: DNA-directed RNA polymerase |
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由来(天然) | 生物種: ![]() |
配列 | 文字列: MAERANLVFH NKAIDGTAMK RLISRLIDHF GMAYTSHILD QLKTLGFQQA TATSISLGID DLLTIPSKGW LVQDAEQQSL ILEKHHHYG NVHAVEKLRQ SIEIWYSTSE YLRQEMNPNF RMTDPYNPVH IMSFSGARGN VSQVHQLVGM RGLMSDPQGQ M IDLPIQSN ...文字列: MAERANLVFH NKAIDGTAMK RLISRLIDHF GMAYTSHILD QLKTLGFQQA TATSISLGID DLLTIPSKGW LVQDAEQQSL ILEKHHHYG NVHAVEKLRQ SIEIWYSTSE YLRQEMNPNF RMTDPYNPVH IMSFSGARGN VSQVHQLVGM RGLMSDPQGQ M IDLPIQSN LREGLSLTEY IISCYGARKG VVDTAVRTSD AGYLTRRLVE VVQHIVVRRR DCGTIRGISV SPQNSTMPER IL IQTLIGR VLADDIYMGS RCIATRNQDI GVGLVNRFIT LRTQLISIRT PFTCRSASWI CRLCYGRSPT HGGLVELGEA VGI IAGQSI GEPGTQLTLR TFHTGGVFTG GTAEHVRAPS NGKIQFNEDL VHPTRTRHGH PAFLCYIDLY VTIESDDILH NVNI PPKSF LLVQNDQYVE SEQVIAEIRA GTSTLNFKER VRKHIYSDSE GEMHWSTDVY HAPEFTYGNV HLLPKTSHLW VLSGK PYRS SVVPFSLSKD QDQMNTHSLS FEQIYISNPS VTNDQVKDKL SDSFSKKEDR ITDYSELNRI GHCNLIYPAK NLDLLA KKR RNRFIIPFQG SQERKKELMS LSGISIEIPI NGIFRKNSIF AYFDDPRYRR KSSGITKYGT IEMHSIVKKE DLIEYRG VK EFRPKYQMKV DRFFFIPEEV HILAGSSSIM VRNNSIIGVD TWITLNTRSR IGGVVRVERK KKKIELTIFS GDIHFPGE T DKISRHSGIL IPPSRKNSKD SKNLKKWIYV QRITPTKKKY FVLVRPVVPY EITDGINLAT LFPQDLLQER DNVQLRVVN YILYGNGKVT RGISDTSIQL VRTCLVLNWN QDKKGSSIEE ARGSFVEVRT NGMIQDFLKV NLVKPAISYI SKRNDPSSEK KEGSDHTNM NPFYSIYIYP KTKLQKSFNQ NQGTVRTLLG INKECQFFLI LSSSNCFRIG PFKGVKYPKE LIKKDPLIPI R NSFGPLGT ALQIANFFSF YYLITHNQIL VTNYLQLDNL KQTFQPFKFQ YYLMDENGRI YNPDPCSNII FNPFKLNWYF LH YHFCEET STKIDLGQFV CENVCITKKG THLKSGQVLI VQFDSVVIRS AKPYLATPGA TLHGHYGEII YEGDTLVTFI YEK SRSGDI TQGLPKVEQV LEVRSIDSIS INLEKRIDSW NERITRILGS PWGFLIGAEL TIAQSRISLV NKIQKVYRSQ GVQI HNRHI EIIVRQITSK VLVSEDGMSN VFLPGELIGL FRAERTGRAL EEAICYRATL LGITRASLNT QSFISEASFQ ETARV LAKA ALRGRIDWLK GLKENVVLGG MIPVGTGFKG FVHHSSQHKD IPLKTKKQNL FEGEMGDILF YHRELFESCL SKN |
-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 | 2 mg/mL |
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緩衝液 | pH: 7.6 |
凍結 | 凍結剤: ETHANE / チャンバー内湿度: 100 % / チャンバー内温度: 298 K / 装置: FEI VITROBOT MARK IV |
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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 K3 (6k x 4k) / 平均電子線量: 50.0 e/Å2 |
電子線 | 加速電圧: 300 kV / 電子線源: ![]() |
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): 2.0 µm / 最小 デフォーカス(公称値): 0.8 µm |
実験機器 | ![]() モデル: Titan Krios / 画像提供: FEI Company |