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1UDT

Crystal structure of Human Phosphodiesterase 5 complexed with Sildenafil(Viagra)

1UDT の概要
エントリーDOI10.2210/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
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: 12955149
DOI: 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
Validation report summary of 1udt
検証レポート(詳細版)ダウンロードをダウンロード

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件を2025-12-31に公開中

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