9D40
Crystal structure of the catalytic region of human MASP-2 with specific inhibitor Analog 20
これはPDB形式変換不可エントリーです。
9D40 の概要
| エントリーDOI | 10.2210/pdb9d40/pdb |
| 関連するPDBエントリー | 9D17 9D3Y |
| 分子名称 | Mannan-binding lectin serine protease 2 B chain, GLYCEROL, N-{[4-(2-amino-1H-imidazol-4-yl)phenyl]methyl}-2-[4-(benzenesulfonamido)phenyl]acetamide, ... (4 entities in total) |
| 機能のキーワード | inhibitor, masp2, hydrolase, hydrolase-inhibitor complex, hydrolase/inhibitor |
| 由来する生物種 | Homo sapiens (human) |
| タンパク質・核酸の鎖数 | 1 |
| 化学式量合計 | 36011.58 |
| 構造登録者 | |
| 主引用文献 | Nakhla, M.C.,Comita, J.,Shapiro, A.B.,Moussa, S.H.,Chen, A.,Eyermann, C.J.,O'Donnell, J.P.,Miller, A.A.,Granger, B.A. Small molecule inhibitors of mannan-binding lectin-associated serine Proteases-2 and-3. Eur.J.Med.Chem., 289:117238-117238, 2025 Cited by PubMed Abstract: The complement system of innate immunity recognizes, opsonizes, and kills invading pathogens and damaged cells, and stimulates an inflammatory response. Inappropriate or excessive complement activity is associated with a wide variety of pathological conditions, and several drugs targeting complement components have been approved. Here we describe the discovery and structure-activity relationships of a novel class of 2-aminoimidazole-containing inhibitors of mannan-binding lectin-associated serine proteases -2 and -3 (MASP-2 and MASP-3), essential enzymes for activation of the lectin and alternative pathways of complement, respectively. With a high degree of target selectivity and favorable in vitro pharmacological properties, this inhibitor series has the potential to be developed as treatments for numerous diseases and pathological conditions. PubMed: 40010268DOI: 10.1016/j.ejmech.2025.117238 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (1.76 Å) |
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