| タイトル | Design, synthesis, and X-ray structural studies of a series of highly potent, selective, and drug-like G protein-coupled receptor kinase 5 inhibitors. |
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| ジャーナル・号・ページ | Eur. J. Med. Chem., Vol. 282, Page 117024-117024, Year 2025 |
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| 掲載日 | 2024年5月11日 (構造データの登録日) |
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著者 | Ghosh, A.K. / Chen, Y. / Gadi, R.K. / Sonawane, A. / Gamage, S.P. / Tesmer, J.G. |
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リンク | Eur. J. Med. Chem. / PubMed:39549325 |
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| 手法 | X線回折 |
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| 解像度 | 2.7 - 3.69 Å |
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| 構造データ | PDB-9bre: Crystal Structure of Human G Protein-Coupled Receptor Kinase 5 in Complex with GRL019-21 手法: X-RAY DIFFRACTION / 解像度: 2.8 Å PDB-9brg: Crystal Structure of Human G Protein-Coupled Receptor Kinase 5 in Complex with GRL055-22 手法: X-RAY DIFFRACTION / 解像度: 2.7 Å PDB-9brh: Crystal Structure of Human G Protein-Coupled Receptor Kinase 5 in Complex with GRL056-21 手法: X-RAY DIFFRACTION / 解像度: 3.69 Å PDB-9bri: Crystal Structure of Human G Protein-Coupled Receptor Kinase 5 in Complex with GRL064-22 手法: X-RAY DIFFRACTION / 解像度: 2.9 Å PDB-9brj: Crystal Structure of Human G Protein-Coupled Receptor Kinase 5 in Complex with GRL093-22 手法: X-RAY DIFFRACTION / 解像度: 2.8 Å |
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| 化合物 | ChemComp-W3F: (3Z)-N-[(1R)-1-(4-fluorophenyl)ethyl]-3-[(4-{[(2S)-2-(furan-2-yl)-2-hydroxyacetyl]amino}-3,5-dimethyl-1H-pyrrol-2-yl)methylidene]-2-oxo-2,3-dihydro-1H-indole-5-carboxamide
PDB-1aq6: STRUCTURE OF L-2-HALOACID DEHALOGENASE FROM XANTHOBACTER AUTOTROPHICUS
PDB-1aq7: TRYPSIN WITH INHIBITOR AERUGINOSIN 98-B
PDB-1aq8: STRUCTURE OF ALCALIGENES FAECALIS NITRITE REDUCTASE REDUCED WITH ASCORBATE
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| 由来 | homo sapiens (ヒト)
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キーワード | SIGNALING PROTEIN/INHIBITOR / G protein-coupled receptor / GPCR G protein-coupled receptor kinase / GRK kinase / SIGNALING PROTEIN-INHIBITOR complex |
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