+データを開く
-基本情報
登録情報 | データベース: PDB / ID: 7zaw | ||||||
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タイトル | GPC3-Unc5D octamer structure and role in cell migration | ||||||
要素 | Glypican-3 | ||||||
キーワード | SIGNALING PROTEIN / Glycoprotein / Migration | ||||||
機能・相同性 | 機能・相同性情報 peptidyl-dipeptidase inhibitor activity / mesonephric duct morphogenesis / body morphogenesis / cell proliferation involved in kidney development / regulation of protein localization to membrane / regulation of non-canonical Wnt signaling pathway / mesenchymal cell proliferation involved in ureteric bud development / Defective B3GALT6 causes EDSP2 and SEMDJL1 / Defective B4GALT7 causes EDS, progeroid type / Defective B3GAT3 causes JDSSDHD ...peptidyl-dipeptidase inhibitor activity / mesonephric duct morphogenesis / body morphogenesis / cell proliferation involved in kidney development / regulation of protein localization to membrane / regulation of non-canonical Wnt signaling pathway / mesenchymal cell proliferation involved in ureteric bud development / Defective B3GALT6 causes EDSP2 and SEMDJL1 / Defective B4GALT7 causes EDS, progeroid type / Defective B3GAT3 causes JDSSDHD / Defective EXT2 causes exostoses 2 / Defective EXT1 causes exostoses 1, TRPS2 and CHDS / cell proliferation involved in metanephros development / A tetrasaccharide linker sequence is required for GAG synthesis / cell migration involved in gastrulation / HS-GAG biosynthesis / HS-GAG degradation / negative regulation of growth / positive regulation of Wnt signaling pathway, planar cell polarity pathway / coronary vasculature development / positive regulation of BMP signaling pathway / positive regulation of smoothened signaling pathway / embryonic hindlimb morphogenesis / regulation of canonical Wnt signaling pathway / anterior/posterior axis specification / Wnt signaling pathway, planar cell polarity pathway / branching involved in ureteric bud morphogenesis / smoothened signaling pathway / bone mineralization / RSV-host interactions / positive regulation of endocytosis / Respiratory syncytial virus (RSV) attachment and entry / anatomical structure morphogenesis / canonical Wnt signaling pathway / Retinoid metabolism and transport / side of membrane / negative regulation of smoothened signaling pathway / lysosomal lumen / osteoclast differentiation / epithelial cell proliferation / positive regulation of D-glucose import / Post-translational protein phosphorylation / response to bacterium / lung development / negative regulation of canonical Wnt signaling pathway / Golgi lumen / Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs) / positive regulation of protein catabolic process / negative regulation of epithelial cell proliferation / positive regulation of canonical Wnt signaling pathway / cell migration / collagen-containing extracellular matrix / Attachment and Entry / endoplasmic reticulum lumen / cell surface / plasma membrane 類似検索 - 分子機能 | ||||||
生物種 | Homo sapiens (ヒト) | ||||||
手法 | X線回折 / シンクロトロン / 分子置換 / 解像度: 2.58 Å | ||||||
データ登録者 | Akkermans, O. / Delloye-Bourgeois, C. / Peregrina, C. / Carrasquero, M. / Kokolaki, M. / Berbeira-Santana, M. / Chavent, M. / Reynaud, F. / Ritu, R. / Agirre, J. ...Akkermans, O. / Delloye-Bourgeois, C. / Peregrina, C. / Carrasquero, M. / Kokolaki, M. / Berbeira-Santana, M. / Chavent, M. / Reynaud, F. / Ritu, R. / Agirre, J. / Aksu, M. / White, E. / Lowe, E. / Ben Amar, D. / Zaballa, S. / Huo, J. / Pakos, I. / McCubbin, P. / Comoletti, D. / Owens, R. / Robinson, C. / Castellani, V. / del Toro, D. / Seiradake, E. | ||||||
資金援助 | 英国, 1件
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引用 | ジャーナル: Cell / 年: 2022 タイトル: GPC3-Unc5 receptor complex structure and role in cell migration. 著者: Akkermans, O. / Delloye-Bourgeois, C. / Peregrina, C. / Carrasquero-Ordaz, M. / Kokolaki, M. / Berbeira-Santana, M. / Chavent, M. / Reynaud, F. / Raj, R. / Agirre, J. / Aksu, M. / White, E.S. ...著者: Akkermans, O. / Delloye-Bourgeois, C. / Peregrina, C. / Carrasquero-Ordaz, M. / Kokolaki, M. / Berbeira-Santana, M. / Chavent, M. / Reynaud, F. / Raj, R. / Agirre, J. / Aksu, M. / White, E.S. / Lowe, E. / Ben Amar, D. / Zaballa, S. / Huo, J. / Pakos, I. / McCubbin, P.T.N. / Comoletti, D. / Owens, R.J. / Robinson, C.V. / Castellani, V. / Del Toro, D. / Seiradake, E. #1: ジャーナル: Acta Crystallogr., Sect. D: Biol. Crystallogr. 年: 2012 タイトル: Towards automated crystallographic structure refinement with phenix.refine. 著者: Afonine, P.V. #2: ジャーナル: Acta Crystallogr D Struct Biol / 年: 2019 タイトル: Macromolecular structure determination using X-rays, neutrons and electrons: recent developments in Phenix. 著者: Dorothee Liebschner / Pavel V Afonine / Matthew L Baker / Gábor Bunkóczi / Vincent B Chen / Tristan I Croll / Bradley Hintze / Li Wei Hung / Swati Jain / Airlie J McCoy / Nigel W Moriarty / ...著者: Dorothee Liebschner / Pavel V Afonine / Matthew L Baker / Gábor Bunkóczi / Vincent B Chen / Tristan I Croll / Bradley Hintze / Li Wei Hung / Swati Jain / Airlie J McCoy / Nigel W Moriarty / Robert D Oeffner / Billy K Poon / Michael G Prisant / Randy J Read / Jane S Richardson / David C Richardson / Massimo D Sammito / Oleg V Sobolev / Duncan H Stockwell / Thomas C Terwilliger / Alexandre G Urzhumtsev / Lizbeth L Videau / Christopher J Williams / Paul D Adams / 要旨: Diffraction (X-ray, neutron and electron) and electron cryo-microscopy are powerful methods to determine three-dimensional macromolecular structures, which are required to understand biological ...Diffraction (X-ray, neutron and electron) and electron cryo-microscopy are powerful methods to determine three-dimensional macromolecular structures, which are required to understand biological processes and to develop new therapeutics against diseases. The overall structure-solution workflow is similar for these techniques, but nuances exist because the properties of the reduced experimental data are different. Software tools for structure determination should therefore be tailored for each method. Phenix is a comprehensive software package for macromolecular structure determination that handles data from any of these techniques. Tasks performed with Phenix include data-quality assessment, map improvement, model building, the validation/rebuilding/refinement cycle and deposition. Each tool caters to the type of experimental data. The design of Phenix emphasizes the automation of procedures, where possible, to minimize repetitive and time-consuming manual tasks, while default parameters are chosen to encourage best practice. A graphical user interface provides access to many command-line features of Phenix and streamlines the transition between programs, project tracking and re-running of previous tasks. | ||||||
履歴 |
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-構造の表示
構造ビューア | 分子: MolmilJmol/JSmol |
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-ダウンロードとリンク
-ダウンロード
PDBx/mmCIF形式 | 7zaw.cif.gz | 192.7 KB | 表示 | PDBx/mmCIF形式 |
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PDB形式 | pdb7zaw.ent.gz | 127.2 KB | 表示 | PDB形式 |
PDBx/mmJSON形式 | 7zaw.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
文書・要旨 | 7zaw_validation.pdf.gz | 455.6 KB | 表示 | wwPDB検証レポート |
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文書・詳細版 | 7zaw_full_validation.pdf.gz | 459.2 KB | 表示 | |
XML形式データ | 7zaw_validation.xml.gz | 14.4 KB | 表示 | |
CIF形式データ | 7zaw_validation.cif.gz | 18.7 KB | 表示 | |
アーカイブディレクトリ | https://data.pdbj.org/pub/pdb/validation_reports/za/7zaw ftp://data.pdbj.org/pub/pdb/validation_reports/za/7zaw | HTTPS FTP |
-関連構造データ
-リンク
-集合体
登録構造単位 |
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1 |
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単位格子 |
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-要素
#1: タンパク質 | 分子量: 53383.656 Da / 分子数: 1 / 由来タイプ: 組換発現 / 由来: (組換発現) Homo sapiens (ヒト) / 遺伝子: GPC3, OCI5 / 細胞株 (発現宿主): HEK293S GnTI- / 発現宿主: Homo sapiens (ヒト) / 参照: UniProt: P51654 | ||||
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#2: 糖 | 研究の焦点であるリガンドがあるか | N | Has protein modification | Y | |
-実験情報
-実験
実験 | 手法: X線回折 / 使用した結晶の数: 1 |
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-試料調製
結晶 | マシュー密度: 2.45 Å3/Da / 溶媒含有率: 49.76 % |
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結晶化 | 温度: 291.15 K / 手法: 蒸気拡散法, シッティングドロップ法 / pH: 8.5 詳細: 20% ethylene glycol, 10% w/v PEG 8000, 0.1 M Tris/BICINE (pH 8.5) and 0.02 M of amino acids (L-Na-glutamate, alanine, glycine, lysine-HCl, and serine) |
-データ収集
回折 | 平均測定温度: 100 K / Serial crystal experiment: N |
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放射光源 | 由来: シンクロトロン / サイト: Diamond / ビームライン: I03 / 波長: 0.9201 Å |
検出器 | タイプ: DECTRIS EIGER2 S 16M / 検出器: PIXEL / 日付: 2018年9月8日 |
放射 | プロトコル: SINGLE WAVELENGTH / 単色(M)・ラウエ(L): M / 散乱光タイプ: x-ray |
放射波長 | 波長: 0.9201 Å / 相対比: 1 |
反射 | 解像度: 2.58→86.86 Å / Num. obs: 16895 / % possible obs: 100 % / 冗長度: 15.5 % / Biso Wilson estimate: 87.61 Å2 / CC1/2: 0.999 / Rmerge(I) obs: 0.075 / Rpim(I) all: 0.02 / Rrim(I) all: 0.079 / Net I/σ(I): 16 |
反射 シェル | 解像度: 2.58→2.65 Å / 冗長度: 6.9 % / Mean I/σ(I) obs: 0.9 / Num. unique obs: 1239 / CC1/2: 0.324 / Rpim(I) all: 1.39 / % possible all: 100 |
-解析
ソフトウェア |
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精密化 | 構造決定の手法: 分子置換 開始モデル: 4YWT 解像度: 2.58→50.09 Å / SU ML: 0.5552 / 交差検証法: FREE R-VALUE / σ(F): 1.34 / 位相誤差: 39.5576 立体化学のターゲット値: GeoStd + Monomer Library + CDL v1.2
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溶媒の処理 | 減衰半径: 0.9 Å / VDWプローブ半径: 1.11 Å / 溶媒モデル: FLAT BULK SOLVENT MODEL | |||||||||||||||||||||||||||||||||||||||||||||||||
原子変位パラメータ | Biso mean: 100.43 Å2 | |||||||||||||||||||||||||||||||||||||||||||||||||
精密化ステップ | サイクル: LAST / 解像度: 2.58→50.09 Å
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拘束条件 |
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LS精密化 シェル |
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精密化 TLS | 手法: refined / Origin x: -19.0789262058 Å / Origin y: -23.9386677376 Å / Origin z: 11.8014785731 Å
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精密化 TLSグループ | Selection details: all |