+データを開く
-基本情報
登録情報 | データベース: PDB / ID: 4j9e | ||||||
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タイトル | Crystal structure of the N114A mutant of the Abl-SH3 domain complexed with the high affinity peptide P17 | ||||||
要素 |
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キーワード | Transferase/unknown function / beta shandwich / SH3 domain / kinase / poly proline rich motifs / Transferase-unknown function complex | ||||||
機能・相同性 | 機能・相同性情報 positive regulation of actin filament binding / phospholipase C-inhibiting G protein-coupled receptor signaling pathway / positive regulation of oxidoreductase activity / protein localization to cytoplasmic microtubule plus-end / DN4 thymocyte differentiation / response to epinephrine / podocyte apoptotic process / transitional one stage B cell differentiation / Role of ABL in ROBO-SLIT signaling / activation of protein kinase C activity ...positive regulation of actin filament binding / phospholipase C-inhibiting G protein-coupled receptor signaling pathway / positive regulation of oxidoreductase activity / protein localization to cytoplasmic microtubule plus-end / DN4 thymocyte differentiation / response to epinephrine / podocyte apoptotic process / transitional one stage B cell differentiation / Role of ABL in ROBO-SLIT signaling / activation of protein kinase C activity / nicotinate-nucleotide adenylyltransferase activity / regulation of modification of synaptic structure / positive regulation of microtubule binding / delta-catenin binding / DNA conformation change / microspike assembly / neuroepithelial cell differentiation / B cell proliferation involved in immune response / positive regulation of Wnt signaling pathway, planar cell polarity pathway / positive regulation of extracellular matrix organization / cerebellum morphogenesis / positive regulation of blood vessel branching / B-1 B cell homeostasis / negative regulation of ubiquitin-protein transferase activity / neuropilin signaling pathway / neuropilin binding / mitochondrial depolarization / bubble DNA binding / negative regulation of protein serine/threonine kinase activity / activated T cell proliferation / cellular response to dopamine / regulation of hematopoietic stem cell differentiation / regulation of cell motility / regulation of Cdc42 protein signal transduction / proline-rich region binding / mitogen-activated protein kinase binding / positive regulation of dendrite development / myoblast proliferation / syntaxin binding / alpha-beta T cell differentiation / regulation of T cell differentiation / cardiac muscle cell proliferation / regulation of axon extension / Fc-gamma receptor signaling pathway involved in phagocytosis / HDR through Single Strand Annealing (SSA) / positive regulation of cell migration involved in sprouting angiogenesis / negative regulation of cell-cell adhesion / Myogenesis / positive regulation of osteoblast proliferation / regulation of microtubule polymerization / RUNX2 regulates osteoblast differentiation / platelet-derived growth factor receptor-beta signaling pathway / negative regulation of cellular senescence / positive regulation of focal adhesion assembly / associative learning / Bergmann glial cell differentiation / regulation of endocytosis / neuromuscular process controlling balance / negative regulation of mitotic cell cycle / actin monomer binding / negative regulation of long-term synaptic potentiation / negative regulation of BMP signaling pathway / negative regulation of double-strand break repair via homologous recombination / endothelial cell migration / signal transduction in response to DNA damage / RHO GTPases Activate WASPs and WAVEs / positive regulation of T cell migration / mismatch repair / regulation of cell adhesion / BMP signaling pathway / negative regulation of endothelial cell apoptotic process / canonical NF-kappaB signal transduction / peptidyl-tyrosine autophosphorylation / positive regulation of substrate adhesion-dependent cell spreading / four-way junction DNA binding / spleen development / cellular response to transforming growth factor beta stimulus / positive regulation of vasoconstriction / positive regulation of stress fiber assembly / ruffle / positive regulation of establishment of T cell polarity / phosphotyrosine residue binding / response to endoplasmic reticulum stress / positive regulation of interleukin-2 production / ephrin receptor binding / actin filament polymerization / ERK1 and ERK2 cascade / positive regulation of endothelial cell migration / post-embryonic development / SH2 domain binding / positive regulation of mitotic cell cycle / substrate adhesion-dependent cell spreading / thymus development / positive regulation of release of sequestered calcium ion into cytosol / regulation of autophagy / integrin-mediated signaling pathway / neural tube closure / establishment of localization in cell / regulation of actin cytoskeleton organization / non-specific protein-tyrosine kinase 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: 1.4 Å | ||||||
データ登録者 | Camara-Artigas, A. | ||||||
引用 | ジャーナル: To be Published タイトル: Crystal structure of the N114A mutant of the Abl-SH3 domain complexed with the high affinity peptide P17 著者: Camara-Artigas, A. #1: ジャーナル: Acta Crystallogr.,Sect.D / 年: 2007 タイトル: Crystallization by capillary counter-diffusion and structure determination of the N114A mutant of the SH3 domain of Abl tyrosine kinase complexed with a high-affinity peptide ligand. 著者: Camara-Artigas, A. / Palencia, A. / Martinez, J.C. / Luque, I. / Gavira, J.A. / Garcia-Ruiz, J.M. #2: ジャーナル: J.Biol.Chem. / 年: 2010 タイトル: Role of interfacial water molecules in proline-rich ligand recognition by the Src homology 3 domain of Abl. 著者: Palencia, A. / Camara-Artigas, A. / Pisabarro, M.T. / Martinez, J.C. / Luque, I. | ||||||
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 | 4j9e.cif.gz | 126.8 KB | 表示 | PDBx/mmCIF形式 |
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PDB形式 | pdb4j9e.ent.gz | 100.6 KB | 表示 | PDB形式 |
PDBx/mmJSON形式 | 4j9e.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 | 4j9e_validation.pdf.gz | 475.8 KB | 表示 | wwPDB検証レポート |
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文書・詳細版 | 4j9e_full_validation.pdf.gz | 477 KB | 表示 | |
XML形式データ | 4j9e_validation.xml.gz | 11.6 KB | 表示 | |
CIF形式データ | 4j9e_validation.cif.gz | 16.5 KB | 表示 | |
アーカイブディレクトリ | https://data.pdbj.org/pub/pdb/validation_reports/j9/4j9e ftp://data.pdbj.org/pub/pdb/validation_reports/j9/4j9e | HTTPS FTP |
-関連構造データ
関連構造データ | 2o88S S: 精密化の開始モデル |
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類似構造データ |
-リンク
-集合体
登録構造単位 |
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単位格子 |
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Components on special symmetry positions |
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-要素
#1: タンパク質 | 分子量: 6966.669 Da / 分子数: 3 / 断片: SH3 domain (unp residues 60-121) / 変異: N114A / 由来タイプ: 組換発現 / 由来: (組換発現) Homo sapiens (ヒト) / 遺伝子: ABL, ABL1, JTK7 / プラスミド: pET15b / 発現宿主: Escherichia coli (大腸菌) / 株 (発現宿主): BL21(DE3) 参照: UniProt: P00519, non-specific protein-tyrosine kinase #2: タンパク質・ペプチド | 分子量: 1065.218 Da / 分子数: 3 / 由来タイプ: 合成 詳細: This sequence has been optimized to increase the affinity #3: 化合物 | ChemComp-SO4 / | #4: 水 | ChemComp-HOH / | |
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-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: 2.01 Å3/Da / 溶媒含有率: 38.7 % |
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結晶化 | 温度: 298 K / 手法: 蒸気拡散法, ハンギングドロップ法 / pH: 7 詳細: 2M Ammonium sulphate, 5% PEG300 , 0.05M LiCl, 0.1M Hepes , pH 7, VAPOR DIFFUSION, HANGING DROP, temperature 298K |
-データ収集
回折 | 平均測定温度: 100 K | |||||||||||||||||||||
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放射光源 | 由来: シンクロトロン / サイト: ESRF / ビームライン: ID14-4 / 波長: 0.97 Å | |||||||||||||||||||||
検出器 | タイプ: ADSC QUANTUM 315r / 検出器: CCD / 日付: 2011年4月8日 | |||||||||||||||||||||
放射 | モノクロメーター: Channel cut ESRF monochromator and torodial focusing mirror 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: 0.97 Å / 相対比: 1 | |||||||||||||||||||||
反射 | 解像度: 1.4→74.677 Å / Num. all: 36431 / Num. obs: 36431 / % possible obs: 95.7 % / Observed criterion σ(F): 0 / Observed criterion σ(I): 0 / 冗長度: 9.6 % / Biso Wilson estimate: 14.697 Å2 / Rmerge(I) obs: 0.055 / Rsym value: 0.055 / Net I/σ(I): 22 | |||||||||||||||||||||
反射 シェル |
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-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: 2O88 解像度: 1.4→19.287 Å / Occupancy max: 1 / Occupancy min: 0.1 / SU ML: 0.12 / σ(F): 0 / σ(I): 0 / 位相誤差: 18.39 / 立体化学のターゲット値: ML
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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 max: 60.15 Å2 / Biso mean: 19.167 Å2 / Biso min: 5.75 Å2 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
精密化ステップ | サイクル: LAST / 解像度: 1.4→19.287 Å
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拘束条件 |
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LS精密化 シェル | Refine-ID: X-RAY DIFFRACTION / Total num. of bins used: 13
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