3NJ4
Fluoro-neplanocin A in Human S-Adenosylhomocysteine Hydrolase
3NJ4 の概要
| エントリーDOI | 10.2210/pdb3nj4/pdb |
| 分子名称 | Adenosylhomocysteinase, NICOTINAMIDE-ADENINE-DINUCLEOTIDE, (4S,5S)-4-(6-amino-9H-purin-9-yl)-3-fluoro-5-hydroxy-2-(hydroxymethyl)cyclopent-2-en-1-one, ... (4 entities in total) |
| 機能のキーワード | s-adenosylhomocystein, hydrolase, nad |
| 由来する生物種 | Homo sapiens (human) |
| 細胞内の位置 | Cytoplasm: P23526 |
| タンパク質・核酸の鎖数 | 4 |
| 化学式量合計 | 195991.52 |
| 構造登録者 | Jeong, L.S.,Lee, K.M.,Hwang, K.Y.,Choi, S.,Heo, Y.S. (登録日: 2010-06-17, 公開日: 2011-05-04, 最終更新日: 2024-03-20) |
| 主引用文献 | Lee, K.M.,Choi, W.J.,Lee, Y.,Lee, H.J.,Zhao, L.X.,Lee, H.W.,Park, J.G.,Kim, H.O.,Hwang, K.Y.,Heo, Y.S.,Choi, S.,Jeong, L.S. X-ray crystal structure and binding mode analysis of human S-adenosylhomocysteine hydrolase complexed with novel mechanism-based inhibitors, haloneplanocin A analogues. J.Med.Chem., 54:930-938, 2011 Cited by PubMed Abstract: The X-ray crystal structure of human S-adenosylhomocysteine (AdoHcy) hydrolase was first determined as a tetrameric form bound with the novel mechanism-based inhibitor fluoroneplanocin A (4b). The crystallized enzyme complex showed the closed conformation and turned out to be the intermediate of mechanism-based inhibition. It confirmed that the cofactor depletion by 3'-oxidation of fluoroneplanocin A contributes to the enzyme inhibition along with the irreversible covalent modification of AdoHcy hydrolase. In addition, a series of haloneplanocin A analogues (4b-e and 5b-e) were designed and synthesized to characterize the binding role and reactivity of the halogen substituents and the 4'-CH(2)OH group. The biological evaluation and molecular modeling studies identified the key pharmacophores and structural requirements for the inhibitor binding of AdoHcy hydrolase. The inhibitory activity was decreased as the size of the halogen atom increased and/or if the 4'-CH(2)OH group was absent. These results could be utilized to design new therapeutic agents operating via AdoHcy hydrolase inhibition. PubMed: 21226494DOI: 10.1021/jm1010836 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (2.5 Å) |
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