| タイトル | Structural Analysis of Protein Kinase A Mutants with Rho-kinase Inhibitor Specificity. |
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| ジャーナル・号・ページ | J. Biol. Chem., Vol. 281, Page 24818-24830, Year 2006 |
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| 掲載日 | 2006年3月21日 (構造データの登録日) |
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著者 | Bonn, S. / Herrero, S. / Breitenlechner, C.B. / Erlbruch, A. / Lehmann, W. / Engh, R.A. / Gassel, M. / Bossemeyer, D. |
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リンク | J. Biol. Chem. / PubMed:16699172 |
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| 手法 | X線回折 |
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| 解像度 | 1.87 - 2.6 Å |
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| 構造データ | PDB-2gfc: cAMP-dependent protein kinase PKA catalytic subunit with PKI-5-24 手法: X-RAY DIFFRACTION / 解像度: 1.87 Å PDB-2gnf: Protein kinase A fivefold mutant model of Rho-kinase with Y-27632 手法: X-RAY DIFFRACTION / 解像度: 2.28 Å PDB-2gng: Protein kinase A fivefold mutant model of Rho-kinase 手法: X-RAY DIFFRACTION / 解像度: 1.87 Å PDB-2gnh: PKA five fold mutant model of Rho-kinase with H1152P 手法: X-RAY DIFFRACTION / 解像度: 2.05 Å PDB-2gni: PKA fivefold mutant model of Rho-kinase with inhibitor Fasudil (HA1077) 手法: X-RAY DIFFRACTION / 解像度: 2.27 Å PDB-2gnj: PKA three fold mutant model of Rho-kinase with Y-27632 手法: X-RAY DIFFRACTION / 解像度: 2.28 Å PDB-2gnl: PKA threefold mutant model of Rho-kinase with inhibitor H-1152P 手法: X-RAY DIFFRACTION / 解像度: 2.6 Å |
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| 化合物 | ChemComp-Y27: (R)-TRANS-4-(1-AMINOETHYL)-N-(4-PYRIDYL) CYCLOHEXANECARBOXAMIDE
ChemComp-H52: (S)-2-METHYL-1-[(4-METHYL-5-ISOQUINOLINE)SULFONYL]-HOMOPIPERAZINE
ChemComp-M77: 5-(1,4-DIAZEPAN-1-SULFONYL)ISOQUINOLINE / 阻害剤*YM
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| 由来 |  bos taurus (ウシ) oryctolagus cuniculus (ウサギ)
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キーワード | TRANSFERASE / binary complex / peptide inhibitor / TRANSFERASE/TRANSFERASE INHIBITOR / PKA / Rho-kinase / surrogate / Y-27632 / TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX / mutant / inhibitor / H1152P / Fasudil / HA1077 / H-1152P |
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