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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: 6ven | ||||||
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| タイトル | Yeast COMPASS in complex with a ubiquitinated nucleosome | ||||||
要素 |
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キーワード | TRANSFERASE/STRUCTURAL PROTEIN/DNA / Methylation / histone / transcription / ubiquitin / gene regulation / TRANSFERASE-STRUCTURAL PROTEIN-DNA complex | ||||||
| 機能・相同性 | 機能・相同性情報positive regulation of synaptonemal complex assembly / regulation of meiotic DNA double-strand break formation / Formation of WDR5-containing histone-modifying complexes / : / sterol homeostasis / meiotic DNA double-strand break formation / [histone H3]-lysine4 N-trimethyltransferase / ascospore formation / synaptonemal complex assembly / histone H3K4 trimethyltransferase activity ...positive regulation of synaptonemal complex assembly / regulation of meiotic DNA double-strand break formation / Formation of WDR5-containing histone-modifying complexes / : / sterol homeostasis / meiotic DNA double-strand break formation / [histone H3]-lysine4 N-trimethyltransferase / ascospore formation / synaptonemal complex assembly / histone H3K4 trimethyltransferase activity / regulation of chromatin organization / rDNA heterochromatin formation / protein methylation / Set1C/COMPASS complex / protein-lysine N-methyltransferase activity / RMTs methylate histone arginines / histone H3K4 methyltransferase activity / histone H3K4me3 reader activity / silent mating-type cassette heterochromatin formation / cellular response to stress / subtelomeric heterochromatin formation / Maturation of protein E / Maturation of protein E / ER Quality Control Compartment (ERQC) / Myoclonic epilepsy of Lafora / FLT3 signaling by CBL mutants / IRAK2 mediated activation of TAK1 complex / Prevention of phagosomal-lysosomal fusion / Alpha-protein kinase 1 signaling pathway / Glycogen synthesis / IRAK1 recruits IKK complex / IRAK1 recruits IKK complex upon TLR7/8 or 9 stimulation / Endosomal Sorting Complex Required For Transport (ESCRT) / Membrane binding and targetting of GAG proteins / Negative regulation of FLT3 / Regulation of TBK1, IKKε (IKBKE)-mediated activation of IRF3, IRF7 / PTK6 Regulates RTKs and Their Effectors AKT1 and DOK1 / Regulation of TBK1, IKKε-mediated activation of IRF3, IRF7 upon TLR3 ligation / IRAK2 mediated activation of TAK1 complex upon TLR7/8 or 9 stimulation / Constitutive Signaling by NOTCH1 HD Domain Mutants / NOTCH2 Activation and Transmission of Signal to the Nucleus / TICAM1,TRAF6-dependent induction of TAK1 complex / TICAM1-dependent activation of IRF3/IRF7 / APC/C:Cdc20 mediated degradation of Cyclin B / Regulation of FZD by ubiquitination / Downregulation of ERBB4 signaling / APC-Cdc20 mediated degradation of Nek2A / telomere maintenance / p75NTR recruits signalling complexes / InlA-mediated entry of Listeria monocytogenes into host cells / TRAF6 mediated IRF7 activation in TLR7/8 or 9 signaling / NF-kB is activated and signals survival / TRAF6-mediated induction of TAK1 complex within TLR4 complex / Regulation of pyruvate metabolism / Pexophagy / Regulation of innate immune responses to cytosolic DNA / NRIF signals cell death from the nucleus / Downregulation of ERBB2:ERBB3 signaling / Regulation of PTEN localization / VLDLR internalisation and degradation / Activated NOTCH1 Transmits Signal to the Nucleus / Synthesis of active ubiquitin: roles of E1 and E2 enzymes / Translesion synthesis by REV1 / TICAM1, RIP1-mediated IKK complex recruitment / Regulation of BACH1 activity / Translesion synthesis by POLK / InlB-mediated entry of Listeria monocytogenes into host cell / JNK (c-Jun kinases) phosphorylation and activation mediated by activated human TAK1 / MAP3K8 (TPL2)-dependent MAPK1/3 activation / Activation of IRF3, IRF7 mediated by TBK1, IKKε (IKBKE) / Downregulation of TGF-beta receptor signaling / Translesion synthesis by POLI / Josephin domain DUBs / IKK complex recruitment mediated by RIP1 / Gap-filling DNA repair synthesis and ligation in GG-NER / PINK1-PRKN Mediated Mitophagy / TGF-beta receptor signaling in EMT (epithelial to mesenchymal transition) / Regulation of activated PAK-2p34 by proteasome mediated degradation / TNFR1-induced NF-kappa-B signaling pathway / TCF dependent signaling in response to WNT / Regulation of NF-kappa B signaling / activated TAK1 mediates p38 MAPK activation / Autodegradation of Cdh1 by Cdh1:APC/C / APC/C:Cdc20 mediated degradation of Securin / Asymmetric localization of PCP proteins / Regulation of signaling by CBL / N-glycan trimming in the ER and Calnexin/Calreticulin cycle / Ubiquitin-dependent degradation of Cyclin D / NOTCH3 Activation and Transmission of Signal to the Nucleus / Negative regulators of DDX58/IFIH1 signaling / Fanconi Anemia Pathway / Peroxisomal protein import / SCF-beta-TrCP mediated degradation of Emi1 / NIK-->noncanonical NF-kB signaling / Negative regulation of FGFR3 signaling / AUF1 (hnRNP D0) binds and destabilizes mRNA / TNFR2 non-canonical NF-kB pathway / Deactivation of the beta-catenin transactivating complex / Stabilization of p53 / Assembly of the pre-replicative complex 類似検索 - 分子機能 | ||||||
| 生物種 | synthetic construct (人工物) Homo sapiens (ヒト)![]() | ||||||
| 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: 3.37 Å | ||||||
データ登録者 | Worden, E.J. / Wolberger, C. | ||||||
| 資金援助 | 米国, 1件
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引用 | ジャーナル: Elife / 年: 2020タイトル: Structural basis for COMPASS recognition of an H2B-ubiquitinated nucleosome. 著者: Evan J Worden / Xiangbin Zhang / Cynthia Wolberger / ![]() 要旨: Methylation of histone H3K4 is a hallmark of actively transcribed genes that depends on mono-ubiquitination of histone H2B (H2B-Ub). H3K4 methylation in yeast is catalyzed by Set1, the ...Methylation of histone H3K4 is a hallmark of actively transcribed genes that depends on mono-ubiquitination of histone H2B (H2B-Ub). H3K4 methylation in yeast is catalyzed by Set1, the methyltransferase subunit of COMPASS. We report here the cryo-EM structure of a six-protein core COMPASS subcomplex, which can methylate H3K4 and be stimulated by H2B-Ub, bound to a ubiquitinated nucleosome. Our structure shows that COMPASS spans the face of the nucleosome, recognizing ubiquitin on one face of the nucleosome and methylating H3 on the opposing face. As compared to the structure of the isolated core complex, Set1 undergoes multiple structural rearrangements to cement interactions with the nucleosome and with ubiquitin. The critical Set1 RxxxRR motif adopts a helix that mediates bridging contacts between the nucleosome, ubiquitin and COMPASS. The structure provides a framework for understanding mechanisms of trans-histone cross-talk and the dynamic role of H2B ubiquitination in stimulating histone methylation. | ||||||
| 履歴 |
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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 | 6ven.cif.gz | 573.3 KB | 表示 | PDBx/mmCIF形式 |
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| PDB形式 | pdb6ven.ent.gz | 435 KB | 表示 | PDB形式 |
| PDBx/mmJSON形式 | 6ven.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/ve/6ven ftp://data.pdbj.org/pub/pdb/validation_reports/ve/6ven | HTTPS FTP |
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-関連構造データ
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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
-タンパク質 , 6種, 10分子 AEBFCGDHKN
| #1: タンパク質 | 分子量: 15251.830 Da / 分子数: 2 / 変異: K4(NLE), M90(NLE), M120(NLE), G102A / 由来タイプ: 組換発現 由来: (組換発現) プラスミド: pQE-81L / 発現宿主: ![]() #2: タンパク質 | 分子量: 11263.231 Da / 分子数: 2 / 由来タイプ: 組換発現 由来: (組換発現) プラスミド: pET3a / 発現宿主: ![]() #3: タンパク質 | 分子量: 13978.241 Da / 分子数: 2 / 変異: G99R, A123S / 由来タイプ: 組換発現 由来: (組換発現) プラスミド: pET3a / 発現宿主: ![]() #4: タンパク質 | 分子量: 13498.715 Da / 分子数: 2 / 変異: K120C, S30T / 由来タイプ: 組換発現 由来: (組換発現) プラスミド: pET3a / 発現宿主: ![]() #7: タンパク質 | | 分子量: 9036.393 Da / 分子数: 1 / 変異: G76C / 由来タイプ: 組換発現 / 由来: (組換発現) Homo sapiens (ヒト) / 遺伝子: UBC / プラスミド: pET3a / 発現宿主: ![]() #10: タンパク質 | | 分子量: 41508.488 Da / 分子数: 1 / Fragment: UNP residues 762-1080 / 由来タイプ: 組換発現 由来: (組換発現) ![]() 遺伝子: SET1, KMT2, YTX1, YHR119W / 発現宿主: Trichoplusia ni (イラクサキンウワバ) / 株 (発現宿主): Hi Five参照: UniProt: P38827, [histone H3]-lysine4 N-trimethyltransferase |
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-601 DNA (146- ... , 2種, 2分子 IJ
| #5: DNA鎖 | 分子量: 44825.559 Da / 分子数: 1 / 由来タイプ: 組換発現 / 由来: (組換発現) synthetic construct (人工物) / 発現宿主: ![]() |
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| #6: DNA鎖 | 分子量: 45305.852 Da / 分子数: 1 / 由来タイプ: 組換発現 / 由来: (組換発現) synthetic construct (人工物) / 発現宿主: ![]() |
-COMPASS component ... , 5種, 6分子 LMOPQR
| #8: タンパク質 | 分子量: 34786.637 Da / 分子数: 1 / 由来タイプ: 組換発現 由来: (組換発現) ![]() 遺伝子: SWD3, CPS30, SAF35, YBR175W, YBR1237 / 発現宿主: Trichoplusia ni (イラクサキンウワバ) / 株 (発現宿主): Hi five / 参照: UniProt: P38123 | ||
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| #9: タンパク質 | 分子量: 48702.574 Da / 分子数: 1 / 由来タイプ: 組換発現 由来: (組換発現) ![]() 遺伝子: SWD1, CPS50, SAF49, YAR003W, FUN16 / 発現宿主: Trichoplusia ni (イラクサキンウワバ) / 株 (発現宿主): Hi five / 参照: UniProt: P39706 | ||
| #11: タンパク質 | 分子量: 58425.301 Da / 分子数: 1 / 由来タイプ: 組換発現 由来: (組換発現) ![]() 遺伝子: BRE2, CPS60, YLR015W / 発現宿主: Trichoplusia ni (イラクサキンウワバ) / 株 (発現宿主): Hi five / 参照: UniProt: P43132 | ||
| #12: タンパク質 | 分子量: 19466.219 Da / 分子数: 2 / 由来タイプ: 組換発現 由来: (組換発現) ![]() 遺伝子: SDC1, CPS25, SAF19, YDR469W / 発現宿主: Trichoplusia ni (イラクサキンウワバ) / 株 (発現宿主): Hi five / 参照: UniProt: Q03323#13: タンパク質 | | 分子量: 45489.457 Da / 分子数: 1 / 由来タイプ: 組換発現 由来: (組換発現) ![]() 遺伝子: SPP1, CPS40, SAF41, YPL138C / 発現宿主: Trichoplusia ni (イラクサキンウワバ) / 株 (発現宿主): Hi five / 参照: UniProt: Q03012 |
-非ポリマー , 2種, 2分子 


| #14: 化合物 | ChemComp-ZN / |
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| #15: 化合物 | ChemComp-SAM / |
-詳細
| 研究の焦点であるリガンドがあるか | N |
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| Has protein modification | Y |
-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
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| 由来(天然) |
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| 由来(組換発現) |
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| 緩衝液 | pH: 7.5 | |||||||||||||||||||||||||
| 緩衝液成分 |
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| 試料 | 濃度: 0.5 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: 15 mA / グリッドの材料: COPPER / グリッドのサイズ: 200 divisions/in. / グリッドのタイプ: Quantifoil R2/2 | |||||||||||||||||||||||||
| 急速凍結 | 装置: FEI VITROBOT MARK III / 凍結剤: ETHANE / 湿度: 100 % / 凍結前の試料温度: 277 K / 詳細: blot force 5 3.5 sec blot time |
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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 |
| 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): 81000 X / 最大 デフォーカス(公称値): 2500 nm / 最小 デフォーカス(公称値): -1000 nm / Cs: 2.7 mm / C2レンズ絞り径: 100 µm |
| 試料ホルダ | 凍結剤: NITROGEN 試料ホルダーモデル: FEI TITAN KRIOS AUTOGRID HOLDER |
| 撮影 | 平均露光時間: 2.96 sec. / 電子線照射量: 50 e/Å2 / フィルム・検出器のモデル: GATAN K3 (6k x 4k) / 撮影したグリッド数: 1 / 実像数: 5784 |
| 電子光学装置 | エネルギーフィルタースリット幅: 20 eV |
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解析
| EMソフトウェア |
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| CTF補正 | タイプ: PHASE FLIPPING AND AMPLITUDE CORRECTION | ||||||||||||||||||||||||||||||||||||
| 粒子像の選択 | 選択した粒子像数: 2036654 / 詳細: Relion template-based picking from 3D model | ||||||||||||||||||||||||||||||||||||
| 対称性 | 点対称性: C1 (非対称) | ||||||||||||||||||||||||||||||||||||
| 3次元再構成 | 解像度: 3.37 Å / 解像度の算出法: FSC 0.143 CUT-OFF / 粒子像の数: 650847 / 対称性のタイプ: POINT | ||||||||||||||||||||||||||||||||||||
| 原子モデル構築 | B value: 110 / プロトコル: OTHER / 空間: REAL | ||||||||||||||||||||||||||||||||||||
| 原子モデル構築 | 3D fitting-ID: 1 / Source name: PDB / タイプ: experimental model
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万見について




Homo sapiens (ヒト)

米国, 1件
引用
UCSF Chimera







PDBj




















































Trichoplusia ni (イラクサキンウワバ)



