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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: 1i1b | ||||||
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| タイトル | CRYSTAL STRUCTURE OF RECOMBINANT HUMAN INTERLEUKIN-1BETA AT 2.0 ANGSTROMS RESOLUTION | ||||||
要素 | INTERLEUKIN-1 BETA | ||||||
キーワード | CYTOKINE | ||||||
| 機能・相同性 | 機能・相同性情報positive regulation of T cell mediated immunity / positive regulation of cell adhesion molecule production / negative regulation of adiponectin secretion / monocyte aggregation / negative regulation of lipid metabolic process / smooth muscle adaptation / positive regulation of lipid catabolic process / negative regulation of D-glucose transmembrane transport / regulation of nitric-oxide synthase activity / hyaluronan biosynthetic process ...positive regulation of T cell mediated immunity / positive regulation of cell adhesion molecule production / negative regulation of adiponectin secretion / monocyte aggregation / negative regulation of lipid metabolic process / smooth muscle adaptation / positive regulation of lipid catabolic process / negative regulation of D-glucose transmembrane transport / regulation of nitric-oxide synthase activity / hyaluronan biosynthetic process / positive regulation of T-helper 1 cell cytokine production / positive regulation of complement activation / cellular response to interleukin-17 / positive regulation of RNA biosynthetic process / positive regulation of tight junction disassembly / positive regulation of prostaglandin biosynthetic process / negative regulation of gap junction assembly / positive regulation of prostaglandin secretion / positive regulation of immature T cell proliferation in thymus / vascular endothelial growth factor production / positive regulation of fever generation / positive regulation of neuroinflammatory response / regulation of defense response to virus by host / positive regulation of platelet-derived growth factor receptor signaling pathway / fever generation / CLEC7A/inflammasome pathway / regulation of establishment of endothelial barrier / Interleukin-1 processing / response to carbohydrate / interleukin-1 receptor binding / positive regulation of heterotypic cell-cell adhesion / positive regulation of monocyte chemotactic protein-1 production / positive regulation of p38MAPK cascade / positive regulation of macrophage derived foam cell differentiation / negative regulation of synaptic transmission / positive regulation of granulocyte macrophage colony-stimulating factor production / positive regulation of membrane protein ectodomain proteolysis / positive regulation of vascular endothelial growth factor receptor signaling pathway / regulation of canonical NF-kappaB signal transduction / interleukin-1-mediated signaling pathway / response to ATP / Interleukin-10 signaling / positive regulation of vascular endothelial growth factor production / positive regulation of cell division / positive regulation of glial cell proliferation / Pyroptosis / regulation of neurogenesis / negative regulation of extrinsic apoptotic signaling pathway in absence of ligand / ectopic germ cell programmed cell death / positive regulation of epithelial to mesenchymal transition / negative regulation of lipid catabolic process / regulation of ERK1 and ERK2 cascade / Purinergic signaling in leishmaniasis infection / negative regulation of MAPK cascade / JNK cascade / positive regulation of T cell proliferation / neutrophil chemotaxis / extrinsic apoptotic signaling pathway in absence of ligand / embryo implantation / positive regulation of interleukin-2 production / astrocyte activation / regulation of insulin secretion / positive regulation of mitotic nuclear division / negative regulation of insulin receptor signaling pathway / response to interleukin-1 / secretory granule / positive regulation of protein export from nucleus / cytokine activity / positive regulation of interleukin-8 production / positive regulation of JNK cascade / cellular response to mechanical stimulus / positive regulation of non-canonical NF-kappaB signal transduction / negative regulation of neurogenesis / positive regulation of interleukin-6 production / integrin binding / cellular response to xenobiotic stimulus / positive regulation of type II interferon production / Interleukin-1 signaling / cytokine-mediated signaling pathway / positive regulation of angiogenesis / positive regulation of inflammatory response / positive regulation of nitric oxide biosynthetic process / cell-cell signaling / cellular response to lipopolysaccharide / Interleukin-4 and Interleukin-13 signaling / response to lipopolysaccharide / positive regulation of ERK1 and ERK2 cascade / lysosome / positive regulation of canonical NF-kappaB signal transduction / positive regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction / positive regulation of MAPK cascade / defense response to Gram-positive bacterium / immune response / positive regulation of cell migration / inflammatory response / protein domain specific binding / negative regulation of cell population proliferation / positive regulation of cell population proliferation / apoptotic process / positive regulation of gene expression 類似検索 - 分子機能 | ||||||
| 生物種 | Homo sapiens (ヒト) | ||||||
| 手法 | X線回折 / 解像度: 2 Å | ||||||
データ登録者 | Finzel, B.C. / Watenpaugh, K.D. / Einspahr, H.M. | ||||||
引用 | ジャーナル: J.Mol.Biol. / 年: 1989タイトル: Crystal structure of recombinant human interleukin-1 beta at 2.0 A resolution. 著者: Finzel, B.C. / Clancy, L.L. / Holland, D.R. / Muchmore, S.W. / Watenpaugh, K.D. / Einspahr, H.M. #1: ジャーナル: Proteins: Struct.,Funct.,Genet. / 年: 1988タイトル: Crystallization of Purified Recombinant Human Interleukin-1Beta 著者: Carter, D.B. / Curry, K.A. / Tomich, C.-S.C. / Yem, A.W. / Deibel, M.R. / Tracey, D.E. / Paslay, J.W. / Carter, J.B. / Theriault, N.Y. / Harris, P.K.W. / Reardon, I.M. / Zurcher-Neely, H.A. / ...著者: Carter, D.B. / Curry, K.A. / Tomich, C.-S.C. / Yem, A.W. / Deibel, M.R. / Tracey, D.E. / Paslay, J.W. / Carter, J.B. / Theriault, N.Y. / Harris, P.K.W. / Reardon, I.M. / Zurcher-Neely, H.A. / Heinrikson, R.L. / Clancy, L.L. / Muchmore, S.W. / Watenpaugh, K.D. / Einspahr, H.M. #2: ジャーナル: J.Cryst.Growth / 年: 1988タイトル: Crystallization of Recombinant Human Interleukin 1Beta 著者: Einspahr, H. / Clancy, L.L. / Muchmore, S.W. / Watenpaugh, K.D. / Harris, P.K.W. / Carter, D.B. / Curry, K.A. / Tomich, C.-S.C. / Yem, A.W. / Deibeljunior, M.R. / Tracey, D.E. / Pasley, J.W. ...著者: Einspahr, H. / Clancy, L.L. / Muchmore, S.W. / Watenpaugh, K.D. / Harris, P.K.W. / Carter, D.B. / Curry, K.A. / Tomich, C.-S.C. / Yem, A.W. / Deibeljunior, M.R. / Tracey, D.E. / Pasley, J.W. / Staite, N.D. / Carter, J.B. / Theriault, N.Y. / Reardon, I.M. / Zurcher-Neely, H.A. / Heinrikson, R.L. #3: ジャーナル: Embo J. / 年: 1988タイトル: Crystal Structure of the Cytokine Interleukin-1Beta 著者: Priestle, J.P. / Schaer, H.-P. / Gruetter, M.G. | ||||||
| 履歴 |
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| Remark 700 | SHEET THE SHEET PRESENTED AS *BRL* ON SHEET RECORDS BELOW IS ACTUALLY A SIX-STRANDED BETA-BARREL. ...SHEET THE SHEET PRESENTED AS *BRL* ON SHEET RECORDS BELOW IS ACTUALLY A SIX-STRANDED BETA-BARREL. THIS IS REPRESENTED BY A SEVEN-STRANDED SHEET IN WHICH THE FIRST AND LAST STRANDS ARE IDENTICAL. |
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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 | 1i1b.cif.gz | 44.3 KB | 表示 | PDBx/mmCIF形式 |
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| PDB形式 | pdb1i1b.ent.gz | 31.4 KB | 表示 | PDB形式 |
| PDBx/mmJSON形式 | 1i1b.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 | 1i1b_validation.pdf.gz | 368.5 KB | 表示 | wwPDB検証レポート |
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| 文書・詳細版 | 1i1b_full_validation.pdf.gz | 376 KB | 表示 | |
| XML形式データ | 1i1b_validation.xml.gz | 5.7 KB | 表示 | |
| CIF形式データ | 1i1b_validation.cif.gz | 8.1 KB | 表示 | |
| アーカイブディレクトリ | https://data.pdbj.org/pub/pdb/validation_reports/i1/1i1b ftp://data.pdbj.org/pub/pdb/validation_reports/i1/1i1b | 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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| Atom site foot note | 1: RESIDUE 91 IS A CIS PROLINE. 2: THE SIDE CHAIN ATOMS OF RESIDUES 93 AND 94 ARE DISORDERED AND ARE NOT INCLUDED IN THIS ENTRY. 3: THERE ARE TWO CONFORMATIONS PRESENTED IN THIS ENTRY FOR RESIDUES 63 - 65. |
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要素
| #1: タンパク質 | 分子量: 17395.832 Da / 分子数: 1 / 由来タイプ: 組換発現 / 由来: (組換発現) Homo sapiens (ヒト) / Cell: SK-HEP-1 HEMATOMA CELLS / 発現宿主: ![]() |
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| #2: 水 | ChemComp-HOH / |
-実験情報
-実験
| 実験 | 手法: X線回折 |
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試料調製
| 結晶 | マシュー密度: 3.33 Å3/Da / 溶媒含有率: 63.06 % | |||||||||||||||||||||||||
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| 結晶化 | *PLUS 手法: 蒸気拡散法, ハンギングドロップ法 / pH: 7 | |||||||||||||||||||||||||
| 溶液の組成 | *PLUS
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-データ収集
| 放射 | 散乱光タイプ: x-ray |
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| 放射波長 | 相対比: 1 |
| 反射 | *PLUS 最高解像度: 2 Å / 最低解像度: 40 Å / Num. obs: 12333 / % possible obs: 84 % / Num. measured all: 44483 / Rmerge(I) obs: 0.0423 |
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解析
| ソフトウェア | 名称: PROLSQ / 分類: 精密化 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| 精密化 | 解像度: 2→20 Å /
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| 精密化ステップ | サイクル: LAST / 解像度: 2→20 Å
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| 拘束条件 |
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| ソフトウェア | *PLUS 名称: PROLSQ / 分類: refinement | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 精密化 | *PLUS Rfactor obs: 0.189 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 溶媒の処理 | *PLUS | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 原子変位パラメータ | *PLUS |
ムービー
コントローラー
万見について




Homo sapiens (ヒト)
X線回折
引用









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