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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: 1tmt | ||||||
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| タイトル | CHANGES IN INTERACTIONS IN COMPLEXES OF HIRUDIN DERIVATIVES AND HUMAN ALPHA-THROMBIN DUE TO DIFFERENT CRYSTAL FORMS | ||||||
要素 |
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キーワード | HYDROLASE/HYDROLASE INHIBITOR / COMPLEX / SERINE PROTEASE / INHIBITOR / HYDROLASE-HYDROLASE INHIBITOR COMPLEX | ||||||
| 機能・相同性 | 機能・相同性情報: / thrombospondin receptor activity / thrombin / thrombin-activated receptor signaling pathway / Defective factor XII causes hereditary angioedema / negative regulation of astrocyte differentiation / regulation of blood coagulation / neutrophil-mediated killing of gram-negative bacterium / positive regulation of phospholipase C-activating G protein-coupled receptor signaling pathway / Defective F8 cleavage by thrombin ...: / thrombospondin receptor activity / thrombin / thrombin-activated receptor signaling pathway / Defective factor XII causes hereditary angioedema / negative regulation of astrocyte differentiation / regulation of blood coagulation / neutrophil-mediated killing of gram-negative bacterium / positive regulation of phospholipase C-activating G protein-coupled receptor signaling pathway / Defective F8 cleavage by thrombin / Platelet Aggregation (Plug Formation) / ligand-gated ion channel signaling pathway / positive regulation of collagen biosynthetic process / negative regulation of platelet activation / negative regulation of blood coagulation / negative regulation of fibrinolysis / blood coagulation, fibrin clot formation / positive regulation of blood coagulation / Transport of gamma-carboxylated protein precursors from the endoplasmic reticulum to the Golgi apparatus / : / Gamma-carboxylation of protein precursors / Removal of aminoterminal propeptides from gamma-carboxylated proteins / regulation of cytosolic calcium ion concentration / fibrinolysis / : / negative regulation of proteolysis / negative regulation of cytokine production involved in inflammatory response / Regulation of Complement cascade / Peptide ligand-binding receptors / positive regulation of release of sequestered calcium ion into cytosol / acute-phase response / Cell surface interactions at the vascular wall / growth factor activity / positive regulation of receptor signaling pathway via JAK-STAT / serine-type endopeptidase inhibitor activity / lipopolysaccharide binding / 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 / positive regulation of insulin secretion / antimicrobial humoral immune response mediated by antimicrobial peptide / regulation of cell shape / heparin binding / toxin activity / Thrombin signalling through proteinase activated receptors (PARs) / positive regulation of cell growth / blood microparticle / G alpha (q) signalling events / positive regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction / cell surface receptor signaling pathway / endoplasmic reticulum lumen / receptor ligand activity / serine-type endopeptidase activity / signaling receptor binding / calcium ion binding / positive regulation of cell population proliferation / proteolysis / : / extracellular exosome / extracellular region / plasma membrane 類似検索 - 分子機能 | ||||||
| 生物種 | Homo sapiens (ヒト) | ||||||
| 手法 | X線回折 / 解像度: 2.2 Å | ||||||
データ登録者 | Priestle, J.P. / Gruetter, M.G. | ||||||
引用 | ジャーナル: Protein Sci. / 年: 1993タイトル: Changes in interactions in complexes of hirudin derivatives and human alpha-thrombin due to different crystal forms. 著者: Priestle, J.P. / Rahuel, J. / Rink, H. / Tones, M. / Grutter, M.G. #1: ジャーナル: J.Mol.Biol. / 年: 1991タイトル: Structure of the Hirugen and Hirulog Complexes of Alpha-Thrombin 著者: Skrzypczak-Jankun, E. / Carperos, V.E. / Ravichandran, K.G. / Tulinsky, A. #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. #3: ジャーナル: Embo J. / 年: 1990タイトル: Crystal Structure of the Thrombin-Hirudin Complex: A Novel Mode of Serine Protease Inhibition 著者: Gruetter, M.G. / Priestle, J.P. / Rahuel, J. / Grossenbacher, H. / Bode, W. / Hofsteenge, J. / Stone, S.R. #4: ジャーナル: Embo J. / 年: 1989タイトル: The Refined 1.9 Angstrom Crystal Structure of Human Alpha Thrombin: Interaction with D-Phe-Pro-Arg Chloromethylketone and Significance of the Tyr-Pro-Pro-Trp Insertion Segment 著者: Bode, W. / Mayr, I. / Baumann, U. / Huber, R. / Stone, S.R. / Hofsteenge, J. | ||||||
| 履歴 |
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| Remark 700 | SHEET THE SHEET PRESENTED AS *BS1* ON SHEET RECORDS BELOW IS ACTUALLY A SIX-STRANDED BETA-BARREL. ...SHEET THE SHEET PRESENTED AS *BS1* 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. THE SHEET PRESENTED AS *BS2* ON SHEET RECORDS BELOW IS ACTUALLY A SEVEN-STRANDED BETA- BARREL. THIS IS REPRESENTED BY AN EIGHT-STRANDED SHEET IN WHICH THE FIRST AND SECOND TO 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 | 1tmt.cif.gz | 78.6 KB | 表示 | PDBx/mmCIF形式 |
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| PDB形式 | pdb1tmt.ent.gz | 57.3 KB | 表示 | PDB形式 |
| PDBx/mmJSON形式 | 1tmt.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
| アーカイブディレクトリ | https://data.pdbj.org/pub/pdb/validation_reports/tm/1tmt ftp://data.pdbj.org/pub/pdb/validation_reports/tm/1tmt | HTTPS FTP |
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-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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| 単位格子 |
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| Atom site foot note | 1: CIS PROLINE - PRO H 37 / 2: RESIDUE DPN I 1 OF INHIBITOR CGP 50,856 IS A D-PHE. 3: RESIDUE TYR J 63 OF INHIBITOR CGP 50,856 IS NOT SULFATED AS IT IS IN NATIVE HIRUDIN. |
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要素
-ALPHA-THROMBIN ... , 2種, 2分子 LH
| #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: 組換発現 / 由来: (組換発現) Homo sapiens (ヒト) / 発現宿主: ![]() |
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| #2: タンパク質 | 分子量: 29780.219 Da / 分子数: 1 / 由来タイプ: 組換発現 / 由来: (組換発現) Homo sapiens (ヒト) / 発現宿主: ![]() |
-CGP 50,856 INHIBITOR, cleaved ... , 2種, 2分子 IJ
| #3: タンパク質・ペプチド | |
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| #4: タンパク質・ペプチド | 分子量: 1908.927 Da / 分子数: 1 / 由来タイプ: 組換発現 / 参照: UniProt: P28504 |
-糖 / 非ポリマー , 2種, 112分子 


| #5: 糖 | ChemComp-NAG / |
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| #6: 水 | ChemComp-HOH / |
-詳細
| 構成要素の詳細 | RESIDUE DPN I 1 OF INHIBITOR CGP 50,856 IS A D-PHE. THROMBIN IS CLEAVED BETWEEN RESIDUES 15 AND 16. ...RESIDUE DPN I 1 OF INHIBITOR CGP 50,856 IS A D-PHE. 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 | RESIDUE TYR J 63 OF INHIBITOR CGP 50,856 IS NOT SULFATED AS IT IS IN NATIVE HIRUDIN. |
| 配列の詳細 | 1. CHYMOTRYPSIN NUMBERING (RATHER THAN SEQUENTIAL) SYSTEM IS USED, BASED ON THE TOPOLOGICAL ...1. CHYMOTRYPS |
-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: 2.73 Å3/Da / 溶媒含有率: 54.87 % | |||||||||||||||
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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 range low: 5 / PH range high: 4 | |||||||||||||||
| 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 | 解像度: 2.2→15 Å |
| 反射 | *PLUS 最高解像度: 2.2 Å / 最低解像度: 30 Å / Num. obs: 18572 / % possible obs: 89 % / Num. measured all: 43768 / Rmerge(I) obs: 0.086 |
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解析
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| 精密化 | 解像度: 2.2→6 Å / Rfactor Rwork: 0.177 / Rfactor obs: 0.177 / σ(F): 0 | ||||||||||||||||||||||||||||||
| 精密化ステップ | サイクル: LAST / 解像度: 2.2→6 Å
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| 拘束条件 |
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| 精密化 | *PLUS Rfactor obs: 0.177 | ||||||||||||||||||||||||||||||
| 溶媒の処理 | *PLUS | ||||||||||||||||||||||||||||||
| 原子変位パラメータ | *PLUS | ||||||||||||||||||||||||||||||
| 拘束条件 | *PLUS タイプ: t_angle_d / Dev ideal: 3 |
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万見について




Homo sapiens (ヒト)
X線回折
引用

















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