+データを開く
-基本情報
登録情報 | データベース: PDB / ID: 1uma | ||||||
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タイトル | ALPHA-THROMBIN (HIRUGEN) COMPLEXED WITH NA-(N,N-DIMETHYLCARBAMOYL)-ALPHA-AZALYSINE | ||||||
要素 |
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キーワード | HYDROLASE/HYDROLASE INHIBITOR / HYDROLASE-HYDROLASE INHIBITOR COMPLEX / SERINE PROTEASE / KRINGLE / ALPHA-THROMBIN- HIRUGEN COMPLEX | ||||||
機能・相同性 | 機能・相同性情報 negative regulation of serine-type peptidase activity / positive regulation of lipid kinase activity / cytolysis by host of symbiont cells / positive regulation of phospholipase C-activating G protein-coupled receptor signaling pathway / thrombospondin receptor activity / Defective factor XII causes hereditary angioedema / thrombin / regulation of blood coagulation / neutrophil-mediated killing of gram-negative bacterium / ligand-gated ion channel signaling pathway ...negative regulation of serine-type peptidase activity / positive regulation of lipid kinase activity / cytolysis by host of symbiont cells / positive regulation of phospholipase C-activating G protein-coupled receptor signaling pathway / thrombospondin receptor activity / Defective factor XII causes hereditary angioedema / thrombin / regulation of blood coagulation / neutrophil-mediated killing of gram-negative bacterium / ligand-gated ion channel signaling pathway / Defective F8 cleavage by thrombin / Platelet Aggregation (Plug Formation) / negative regulation of astrocyte differentiation / negative regulation of platelet activation / positive regulation of collagen biosynthetic process / negative regulation of cytokine production involved in inflammatory response / positive regulation of blood coagulation / negative regulation of fibrinolysis / Gamma-carboxylation of protein precursors / Transport of gamma-carboxylated protein precursors from the endoplasmic reticulum to the Golgi apparatus / Common Pathway of Fibrin Clot Formation / Removal of aminoterminal propeptides from gamma-carboxylated proteins / fibrinolysis / regulation of cytosolic calcium ion concentration / Intrinsic Pathway of Fibrin Clot Formation / Peptide ligand-binding receptors / positive regulation of release of sequestered calcium ion into cytosol / acute-phase response / Regulation of Complement cascade / negative regulation of proteolysis / Cell surface interactions at the vascular wall / lipopolysaccharide binding / positive regulation of receptor signaling pathway via JAK-STAT / growth factor activity / serine-type endopeptidase inhibitor activity / positive regulation of insulin secretion / platelet activation / response to wounding / positive regulation of protein localization to nucleus / Golgi lumen / Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs) / positive regulation of reactive oxygen species metabolic process / blood coagulation / antimicrobial humoral immune response mediated by antimicrobial peptide / Thrombin signalling through proteinase activated receptors (PARs) / heparin binding / regulation of cell shape / positive regulation of cell growth / G alpha (q) signalling events / collagen-containing extracellular matrix / blood microparticle / positive regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction / cell surface receptor signaling pathway / positive regulation of protein phosphorylation / G protein-coupled receptor signaling pathway / endoplasmic reticulum lumen / serine-type endopeptidase activity / signaling receptor binding / positive regulation of cell population proliferation / calcium ion binding / proteolysis / extracellular space / extracellular exosome / extracellular region / plasma membrane 類似検索 - 分子機能 | ||||||
生物種 | Homo sapiens (ヒト) Hirudo medicinalis (医用ビル) | ||||||
手法 | X線回折 / 解像度: 2 Å | ||||||
データ登録者 | Nardini, M. / Pesce, A. / Rizzi, M. / Casale, E. / Ferraccioli, R. / Balliano, G. / Milla, P. / Ascenzi, P. / Bolognesi, M. | ||||||
引用 | ジャーナル: J.Mol.Biol. / 年: 1996 タイトル: Human alpha-thrombin inhibition by the active site titrant N alpha-(N,N-dimethylcarbamoyl)-alpha-azalysine p-nitrophenyl ester: a comparative kinetic and X-ray crystallographic study. 著者: Nardini, M. / Pesce, A. / Rizzi, M. / Casale, E. / Ferraccioli, R. / Balliano, G. / Milla, P. / Ascenzi, P. / Bolognesi, M. #1: ジャーナル: Biochem.Biophys.Res.Commun. / 年: 1993 タイトル: Inhibition of Serine Proteinases Belonging to the Chymotrypsin Superfamily by the Cyclic Thiolic Compound Ys3025: A Comparative Crystallographic Study 著者: Carugo, K.D. / Rizzi, M. / Fasano, M. / Luisetti, M. / La Rosa, C. / Ascenzi, P. / Bolognesi, M. #2: ジャーナル: J.Mol.Biol. / 年: 1991 タイトル: Refined Structure of the Hirudin-Thrombin Complex 著者: Rydel, T.J. / Tulinsky, A. / Bode, W. / Huber, R. | ||||||
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 | 1uma.cif.gz | 81.9 KB | 表示 | PDBx/mmCIF形式 |
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PDB形式 | pdb1uma.ent.gz | 59.9 KB | 表示 | PDB形式 |
PDBx/mmJSON形式 | 1uma.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 | 1uma_validation.pdf.gz | 477.5 KB | 表示 | wwPDB検証レポート |
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文書・詳細版 | 1uma_full_validation.pdf.gz | 490.4 KB | 表示 | |
XML形式データ | 1uma_validation.xml.gz | 20.4 KB | 表示 | |
CIF形式データ | 1uma_validation.cif.gz | 26.9 KB | 表示 | |
アーカイブディレクトリ | https://data.pdbj.org/pub/pdb/validation_reports/um/1uma ftp://data.pdbj.org/pub/pdb/validation_reports/um/1uma | HTTPS FTP |
-関連構造データ
類似構造データ |
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-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
-タンパク質・ペプチド , 2種, 2分子 LI
#1: タンパク質・ペプチド | 分子量: 4096.534 Da / 分子数: 1 / 由来タイプ: 天然 / 由来: (天然) Homo sapiens (ヒト) / 組織: PLASMA / 参照: UniProt: P00734, thrombin |
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#3: タンパク質・ペプチド | 分子量: 1363.399 Da / 分子数: 1 / 由来タイプ: 天然 / 由来: (天然) Hirudo medicinalis (医用ビル) / 組織: PLASMA / 参照: UniProt: P28501, UniProt: P01050*PLUS |
-タンパク質 / 糖 , 2種, 2分子 H
#2: タンパク質 | 分子量: 29780.219 Da / 分子数: 1 / 由来タイプ: 天然 / 由来: (天然) Homo sapiens (ヒト) / 組織: PLASMA / 参照: UniProt: P00734, thrombin |
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#4: 糖 | ChemComp-NAG / |
-非ポリマー , 2種, 182分子
#5: 化合物 | #6: 水 | ChemComp-HOH / | |
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-詳細
構成要素の詳細 | THROMBIN IS CLEAVED BETWEEN RESIDUES 15 AND 16. CHAIN IDENTIFIER *L* IS USED FOR RESIDUES 1 - 15 ...THROMBIN IS CLEAVED BETWEEN RESIDUES 15 AND 16. CHAIN IDENTIFIER |
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Has protein modification | Y |
非ポリマーの詳細 | N-ACTYL-D-GLUCOSAMINE OF THE CARBOHYDRATE IS COVALENTLY LINKED TO ASN E 60G. TWO MOLECULES OF ...N-ACTYL-D-GLUCOSAMIN |
-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: 2.58 Å3/Da / 溶媒含有率: 52.3 % | ||||||||||||||||||||||||||||||||||||||||||||||||
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結晶化 | *PLUS pH: 7.3 / 手法: 蒸気拡散法, ハンギングドロップ法 / 詳細: Skrzypczak, J., (1991) J. Mol. Biol., 221, 1379. | ||||||||||||||||||||||||||||||||||||||||||||||||
溶液の組成 | *PLUS
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-データ収集
放射光源 | 波長: 1.5418 |
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検出器 | タイプ: RIGAKU / 検出器: IMAGE PLATE / 日付: 1995年8月19日 |
放射 | 単色(M)・ラウエ(L): M / 散乱光タイプ: x-ray |
放射波長 | 波長: 1.5418 Å / 相対比: 1 |
反射 | Num. obs: 22811 / % possible obs: 94.1 % / Observed criterion σ(I): 0 / 冗長度: 2.9 % / Rmerge(I) obs: 0.056 |
反射 | *PLUS 最高解像度: 2 Å / Num. measured all: 64587 |
-解析
ソフトウェア |
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精密化 | 解像度: 2→20 Å / Num. reflection obs: 22799 / σ(F): 0 | ||||||||||||||||||||||||||||||
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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