6E2O
ASK1 kinase domain complex with inhibitor
6E2O の概要
エントリーDOI | 10.2210/pdb6e2o/pdb |
分子名称 | Mitogen-activated protein kinase kinase kinase 5, 4-(4-cyclopropyl-1H-imidazol-1-yl)-N-[3-(4-cyclopropyl-4H-1,2,4-triazol-3-yl)phenyl]pyridine-2-carboxamide (3 entities in total) |
機能のキーワード | protein kinase, inhibitor complex, transferase-inhibitor complex, transferase/inhibitor |
由来する生物種 | Homo sapiens (Human) |
タンパク質・核酸の鎖数 | 2 |
化学式量合計 | 67230.36 |
構造登録者 | |
主引用文献 | Liles, J.T.,Corkey, B.K.,Notte, G.T.,Budas, G.R.,Lansdon, E.B.,Hinojosa-Kirschenbaum, F.,Badal, S.S.,Lee, M.,Schultz, B.E.,Wise, S.,Pendem, S.,Graupe, M.,Castonguay, L.,Koch, K.A.,Wong, M.H.,Papalia, G.A.,French, D.M.,Sullivan, T.,Huntzicker, E.G.,Ma, F.Y.,Nikolic-Paterson, D.J.,Altuhaifi, T.,Yang, H.,Fogo, A.B.,Breckenridge, D.G. ASK1 contributes to fibrosis and dysfunction in models of kidney disease. J. Clin. Invest., 128:4485-4500, 2018 Cited by PubMed Abstract: Oxidative stress is an underlying component of acute and chronic kidney disease. Apoptosis signal-regulating kinase 1 (ASK1) is a widely expressed redox-sensitive serine threonine kinase that activates p38 and c-Jun N-terminal kinase (JNK) mitogen-activated protein kinase kinases, and induces apoptotic, inflammatory, and fibrotic signaling in settings of oxidative stress. We describe the discovery and characterization of a potent and selective small-molecule inhibitor of ASK1, GS-444217, and demonstrate the therapeutic potential of ASK1 inhibition to reduce kidney injury and fibrosis. Activation of the ASK1 pathway in glomerular and tubular compartments was confirmed in renal biopsies from patients with diabetic kidney disease (DKD) and was decreased by GS-444217 in several rodent models of kidney injury and fibrosis that collectively represented the hallmarks of DKD pathology. Treatment with GS-444217 reduced progressive inflammation and fibrosis in the kidney and halted glomerular filtration rate decline. Combination of GS-444217 with enalapril, an angiotensin-converting enzyme inhibitor, led to a greater reduction in proteinuria and regression of glomerulosclerosis. These results identify ASK1 as an important target for renal disease and support the clinical development of an ASK1 inhibitor for the treatment of DKD. PubMed: 30024858DOI: 10.1172/JCI99768 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (2.389 Å) |
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