1UDT
Crystal structure of Human Phosphodiesterase 5 complexed with Sildenafil(Viagra)
1UDT の概要
| エントリーDOI | 10.2210/pdb1udt/pdb |
| 関連するPDBエントリー | 1UDU |
| 分子名称 | cGMP-specific 3',5'-cyclic phosphodiesterase, ZINC ION, MAGNESIUM ION, ... (5 entities in total) |
| 機能のキーワード | cgmp-specific phosphodiesterase 5, sildenafil, selective inhibitor, hydrolase |
| 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 | 38094.60 |
| 構造登録者 | Sung, B.-J.,Lee, J.I.,Heo, Y.-S.,Kim, J.H.,Moon, J.,Yoon, J.M.,Hyun, Y.-L.,Kim, E.,Eum, S.J.,Lee, T.G.,Cho, J.M.,Park, S.-Y.,Lee, J.-O.,Jeon, Y.H.,Hwang, K.Y.,Ro, S. (登録日: 2003-05-06, 公開日: 2004-05-11, 最終更新日: 2023-12-27) |
| 主引用文献 | Sung, B.-J.,Hwang, K.Y.,Jeon, Y.H.,Lee, J.I.,Heo, Y.-S.,Kim, J.H.,Moon, J.,Yoon, J.M.,Hyun, Y.-L.,Kim, E.,Eum, S.J.,Park, S.-Y.,Lee, J.-O.,Lee, T.G.,Ro, S.,Cho, J.M. Structure of the catalytic domain of human phosphodiesterase 5 with bound drug molecules Nature, 425:98-102, 2003 Cited by PubMed Abstract: Phosphodiesterases (PDEs) are a superfamily of enzymes that degrade the intracellular second messengers cyclic AMP and cyclic GMP. As essential regulators of cyclic nucleotide signalling with diverse physiological functions, PDEs are drug targets for the treatment of various diseases, including heart failure, depression, asthma, inflammation and erectile dysfunction. Of the 12 PDE gene families, cGMP-specific PDE5 carries out the principal cGMP-hydrolysing activity in human corpus cavernosum tissue. It is well known as the target of sildenafil citrate (Viagra) and other similar drugs for the treatment of erectile dysfunction. Despite the pressing need to develop selective PDE inhibitors as therapeutic drugs, only the cAMP-specific PDE4 structures are currently available. Here we present the three-dimensional structures of the catalytic domain (residues 537-860) of human PDE5 complexed with the three drug molecules sildenafil, tadalafil (Cialis) and vardenafil (Levitra). These structures will provide opportunities to design potent and selective PDE inhibitors with improved pharmacological profiles. PubMed: 12955149DOI: 10.1038/nature01914 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (2.3 Å) |
構造検証レポート
検証レポート(詳細版)
をダウンロード






