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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: 6n4p | ||||||
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| タイトル | RQEFEV, crystal structure of the N-terminal segment RQEFEV from protein tau | ||||||
要素 | Microtubule-associated protein tau | ||||||
キーワード | PROTEIN FIBRIL / Amyloid / tau / Alzheimer's Disease / tauopathy / MAPT | ||||||
| 機能・相同性 | 機能・相同性情報plus-end-directed organelle transport along microtubule / histone-dependent DNA binding / negative regulation of establishment of protein localization to mitochondrion / neurofibrillary tangle / microtubule lateral binding / axonal transport / tubulin complex / positive regulation of protein localization to synapse / negative regulation of tubulin deacetylation / phosphatidylinositol bisphosphate binding ...plus-end-directed organelle transport along microtubule / histone-dependent DNA binding / negative regulation of establishment of protein localization to mitochondrion / neurofibrillary tangle / microtubule lateral binding / axonal transport / tubulin complex / positive regulation of protein localization to synapse / negative regulation of tubulin deacetylation / phosphatidylinositol bisphosphate binding / generation of neurons / rRNA metabolic process / axonal transport of mitochondrion / regulation of mitochondrial fission / axon development / regulation of chromosome organization / central nervous system neuron development / intracellular distribution of mitochondria / minor groove of adenine-thymine-rich DNA binding / lipoprotein particle binding / microtubule polymerization / negative regulation of mitochondrial membrane potential / dynactin binding / regulation of microtubule polymerization / apolipoprotein binding / main axon / protein polymerization / axolemma / glial cell projection / Caspase-mediated cleavage of cytoskeletal proteins / regulation of microtubule polymerization or depolymerization / negative regulation of mitochondrial fission / neurofibrillary tangle assembly / positive regulation of axon extension / regulation of cellular response to heat / Activation of AMPK downstream of NMDARs / synapse assembly / positive regulation of superoxide anion generation / regulation of long-term synaptic depression / positive regulation of protein localization / supramolecular fiber organization / cellular response to brain-derived neurotrophic factor stimulus / cytoplasmic microtubule organization / regulation of calcium-mediated signaling / positive regulation of microtubule polymerization / somatodendritic compartment / axon cytoplasm / astrocyte activation / stress granule assembly / phosphatidylinositol binding / nuclear periphery / regulation of microtubule cytoskeleton organization / protein phosphatase 2A binding / cellular response to reactive oxygen species / Hsp90 protein binding / microglial cell activation / cellular response to nerve growth factor stimulus / synapse organization / protein homooligomerization / PKR-mediated signaling / regulation of synaptic plasticity / SH3 domain binding / response to lead ion / microtubule cytoskeleton organization / memory / cytoplasmic ribonucleoprotein granule / neuron projection development / cell-cell signaling / single-stranded DNA binding / protein-folding chaperone binding / cellular response to heat / actin binding / microtubule cytoskeleton / cell body / growth cone / double-stranded DNA binding / protein-macromolecule adaptor activity / microtubule binding / dendritic spine / sequence-specific DNA binding / amyloid fibril formation / microtubule / learning or memory / neuron projection / regulation of autophagy / membrane raft / axon / negative regulation of gene expression / neuronal cell body / dendrite / DNA damage response / protein kinase binding / enzyme binding / mitochondrion / DNA binding / RNA binding / extracellular region / identical protein binding / nucleus / 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: 1.851 Å | ||||||
データ登録者 | Eisenberg, D.S. / Boyer, D.R. | ||||||
| 資金援助 | 米国, 1件
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引用 | ジャーナル: Biorxiv / 年: 2021タイトル: A structure-based model for the electrostatic interaction of the N-terminus of protein tau with the fibril core of Alzheimer's Disease filaments 著者: Boyer, D.R. / Eisenberg, D.S. | ||||||
| 履歴 |
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構造の表示
| 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 | 6n4p.cif.gz | 11.6 KB | 表示 | PDBx/mmCIF形式 |
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| PDB形式 | pdb6n4p.ent.gz | 5.9 KB | 表示 | PDB形式 |
| PDBx/mmJSON形式 | 6n4p.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 | 6n4p_validation.pdf.gz | 401.7 KB | 表示 | wwPDB検証レポート |
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| 文書・詳細版 | 6n4p_full_validation.pdf.gz | 401.7 KB | 表示 | |
| XML形式データ | 6n4p_validation.xml.gz | 2.6 KB | 表示 | |
| CIF形式データ | 6n4p_validation.cif.gz | 2.8 KB | 表示 | |
| アーカイブディレクトリ | https://data.pdbj.org/pub/pdb/validation_reports/n4/6n4p ftp://data.pdbj.org/pub/pdb/validation_reports/n4/6n4p | HTTPS FTP |
-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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| 1 | ![]()
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| 単位格子 |
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要素
| #1: タンパク質・ペプチド | 分子量: 807.870 Da / 分子数: 2 / 断片: UNP residues 5-10 / 由来タイプ: 合成 / 由来: (合成) Homo sapiens (ヒト) / 参照: UniProt: P10636#2: 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
| 結晶化 | 温度: 291 K / 手法: 蒸気拡散法, ハンギングドロップ法 / 詳細: 0.2 M ammonium citrate dibasic, 30% PEG3350 |
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-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: APS / ビームライン: 24-ID-E / 波長: 0.97 Å | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 検出器 | タイプ: DECTRIS EIGER X 16M / 検出器: PIXEL / 日付: 2017年7月18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: 0.97 Å / 相対比: 1 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 反射 | 解像度: 1.85→24.639 Å / Num. obs: 843 / % possible obs: 97.8 % / 冗長度: 2.868 % / Biso Wilson estimate: 14.78 Å2 / CC1/2: 0.971 / Rmerge(I) obs: 0.16 / Rrim(I) all: 0.196 / Χ2: 0.92 / Net I/σ(I): 4.16 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 反射 シェル | Diffraction-ID: 1
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解析
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| 精密化 | 構造決定の手法: 分子置換開始モデル: 6-residue idealized beta sheet 解像度: 1.851→24.639 Å / SU ML: 0.15 / 交差検証法: THROUGHOUT / σ(F): 1.39 / 位相誤差: 19.28
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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 | ||||||||||||||||||||||||
| 原子変位パラメータ | Biso max: 54.33 Å2 / Biso mean: 21.9015 Å2 / Biso min: 10.28 Å2 | ||||||||||||||||||||||||
| 精密化ステップ | サイクル: final / 解像度: 1.851→24.639 Å
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| LS精密化 シェル | 解像度: 1.8515→1.918 Å / Rfactor Rfree error: 0 / Total num. of bins used: 1 /
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万見について




Homo sapiens (ヒト)
X線回折
米国, 1件
引用







PDBj








