タイトル | Effects of NVP-BHG712 chemical modifications on EPHA2 binding and affinity |
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ジャーナル・号・ページ | To Be Published |
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掲載日 | 2018年8月20日 (構造データの登録日) |
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著者 | Troester, A. / Kudlinzki, D. / Saxena, K. / Gande, S. / Schwalbe, H. |
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リンク | PubMedで検索 |
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手法 | X線回折 |
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解像度 | 0.978 - 1.719 Å |
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構造データ | PDB-6hes: Crystal Structure of Ephrin A2 (EphA2) Receptor Protein Kinase with the NVP-BHG712 derivative AT050 手法: X-RAY DIFFRACTION / 解像度: 1.128 Å PDB-6het: Crystal Structure of Ephrin A2 (EphA2) Receptor Protein Kinase with the NVP-BHG712 derivative AT055 手法: X-RAY DIFFRACTION / 解像度: 1.208 Å PDB-6heu: Crystal Structure of Ephrin A2 (EphA2) Receptor Protein Kinase with the NVP-BHG712 derivative AT058 手法: X-RAY DIFFRACTION / 解像度: 1.719 Å PDB-6hev: Crystal Structure of Ephrin A2 (EphA2) Receptor Protein Kinase with the NVP-BHG712 derivative AT061 手法: X-RAY DIFFRACTION / 解像度: 1.28 Å PDB-6hew: Crystal Structure of Ephrin A2 (EphA2) Receptor Protein Kinase with the NVP-BHG712 derivative AT069 手法: X-RAY DIFFRACTION / 解像度: 1.268 Å PDB-6hex: Crystal Structure of Ephrin A2 (EphA2) Receptor Protein Kinase with the NVP-BHG712 derivative ATMM006 手法: X-RAY DIFFRACTION / 解像度: 1.413 Å PDB-6hey: Crystal Structure of Ephrin A2 (EphA2) Receptor Protein Kinase with the NVP-BHG712 derivative ATNK002 手法: X-RAY DIFFRACTION / 解像度: 1.367 Å PDB-6q7b: Crystal Structure of Ephrin A2 (EphA2) Receptor Protein Kinase with the NVP-BHG712 derivative ATDL09 手法: X-RAY DIFFRACTION / 解像度: 1.009 Å PDB-6q7c: Crystal Structure of Ephrin A2 (EphA2) Receptor Protein Kinase with the NVP-BHG712 derivative ATDL11 手法: X-RAY DIFFRACTION / 解像度: 1.049 Å PDB-6q7d: Crystal Structure of Ephrin A2 (EphA2) Receptor Protein Kinase with the NVP-BHG712 derivative ATDL13 手法: X-RAY DIFFRACTION / 解像度: 0.978 Å PDB-6q7e: Crystal Structure of Ephrin A2 (EphA2) Receptor Protein Kinase with the NVP-BHG712 derivative ATDL14 手法: X-RAY DIFFRACTION / 解像度: 1.059 Å PDB-6q7f: Crystal Structure of Ephrin A2 (EphA2) Receptor Protein Kinase with the NVP-BHG712 derivative ATDL18 手法: X-RAY DIFFRACTION / 解像度: 1.204 Å PDB-6q7g: Crystal Structure of Ephrin A2 (EphA2) Receptor Protein Kinase with the NVP-BHG712 derivative ATHA01 手法: X-RAY DIFFRACTION / 解像度: 1.047 Å |
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化合物 | ChemComp-G0H: 4-methyl-3-[(2-pyridin-3-ylquinazolin-4-yl)amino]-~{N}-[3-(trifluoromethyl)phenyl]benzamide
ChemComp-G0Q: ~{N}-(3-chlorophenyl)-4-methyl-3-[(1-methyl-6-pyridin-3-yl-pyrazolo[3,4-d]pyrimidin-4-yl)amino]benzamide
ChemComp-G0N: 3-[(4,6-dipyridin-4-yl-1,3,5-triazin-2-yl)amino]-4-methyl-~{N}-[3-(trifluoromethyl)phenyl]benzamide
ChemComp-G0K: 4-methyl-3-[(2-pyridin-3-ylpyrido[2,3-d]pyrimidin-4-yl)amino]-~{N}-[3-(trifluoromethyl)phenyl]benzamide
ChemComp-G0E: 4-methyl-3-[(1-methyl-6-pyrimidin-5-yl-pyrazolo[3,4-d]pyrimidin-4-yl)amino]-~{N}-[3-(trifluoromethyl)phenyl]benzamide
ChemComp-G02: 4-methyl-3-[(1-methyl-6-pyrazin-2-yl-pyrazolo[3,4-d]pyrimidin-4-yl)amino]-~{N}-[3-(trifluoromethyl)phenyl]benzamide
ChemComp-FZW: 3-[(4,6-dipyridin-3-yl-1,3,5-triazin-2-yl)amino]-4-methyl-~{N}-[3-(trifluoromethyl)phenyl]benzamide
ChemComp-HO5: 3-[[4-imidazol-1-yl-6-[(3~{S})-3-oxidanylpyrrolidin-1-yl]-1,3,5-triazin-2-yl]amino]-4-methyl-~{N}-[3-(trifluoromethyl)phenyl]benzamide
ChemComp-HOK: 3-[[4-imidazol-1-yl-6-[(3~{S})-3-oxidanylpiperidin-1-yl]-1,3,5-triazin-2-yl]amino]-4-methyl-~{N}-[3-(trifluoromethyl)phenyl]benzamide
ChemComp-HOT: 3-[[4-imidazol-1-yl-6-(4-oxidanylpiperidin-1-yl)-1,3,5-triazin-2-yl]amino]-4-methyl-~{N}-[3-(trifluoromethyl)phenyl]benzamide
ChemComp-HMW: 3-[[4-imidazol-1-yl-6-[(3~{R})-3-oxidanylpyrrolidin-1-yl]-1,3,5-triazin-2-yl]amino]-4-methyl-~{N}-[3-(trifluoromethyl)phenyl]benzamide
ChemComp-HNZ: 3-[(4-imidazol-1-yl-6-piperazin-1-yl-1,3,5-triazin-2-yl)amino]-4-methyl-~{N}-[3-(trifluoromethyl)phenyl]benzamide
ChemComp-HO8: 3-[(4-imidazol-1-yl-6-morpholin-4-yl-1,3,5-triazin-2-yl)amino]-4-methyl-~{N}-[3-(trifluoromethyl)phenyl]benzamide
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由来 | - homo sapiens (ヒト)
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キーワード | TRANSFERASE / Inhibitor / Complex / Protein Tyrosine Kinase |
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