1XLZ

Catalytic Domain Of Human Phosphodiesterase 4B In Complex With Filaminast

1XLZ の概要

• エントリーDOI: 10.2210/pdb1xlz/pdb
• 関連するPDBエントリー: 1XLX 1XM4 1XM6 1XMU 1XMY 1XN0 1XOM 1XON 1XOQ 1XOR 1XOS 1XOT 1XOZ 1XP0
• 分子名称: cAMP-specific 3',5'-cyclic phosphodiesterase 4B, ZINC ION, MAGNESIUM ION, ... (5 entities in total)
• 機能のキーワード: pde4b, filaminast, hydrolase
• 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: 92378.99

構造登録者

Card, G.L.,England, B.P.,Suzuki, Y.,Fong, D.,Powell, B.,Lee, B.,Luu, C.,Tabrizizad, M.,Gillette, S.,Ibrahim, P.N.,Artis, D.R.,Bollag, G.,Milburn, M.V.,Kim, S.-H.,Schlessinger, J.,Zhang, K.Y.J. (登録日: 2004-09-30, 公開日: 2004-12-14, 最終更新日: 2024-10-30)

主引用文献

Card, G.L.,England, B.P.,Suzuki, Y.,Fong, D.,Powell, B.,Lee, B.,Luu, C.,Tabrizizad, M.,Gillette, S.,Ibrahim, P.N.,Artis, D.R.,Bollag, G.,Milburn, M.V.,Kim, S.-H.,Schlessinger, J.,Zhang, K.Y.J.
Structural Basis for the Activity of Drugs that Inhibit Phosphodiesterases.
STRUCTURE, 12:2233-2247, 2004

PubMed Abstract: Phosphodiesterases (PDEs) comprise a large family of enzymes that catalyze the hydrolysis of cAMP or cGMP and are implicated in various diseases. We describe the high-resolution crystal structures of the catalytic domains of PDE4B, PDE4D, and PDE5A with ten different inhibitors, including the drug candidates cilomilast and roflumilast, for respiratory diseases. These cocrystal structures reveal a common scheme of inhibitor binding to the PDEs: (i) a hydrophobic clamp formed by highly conserved hydrophobic residues that sandwich the inhibitor in the active site; (ii) hydrogen bonding to an invariant glutamine that controls the orientation of inhibitor binding. A scaffold can be readily identified for any given inhibitor based on the formation of these two types of conserved interactions. These structural insights will enable the design of isoform-selective inhibitors with improved binding affinity and should facilitate the discovery of more potent and selective PDE inhibitors for the treatment of a variety of diseases.

PubMed: 15576036
DOI: 10.1016/j.str.2004.10.004

実験手法

X-RAY DIFFRACTION (2.06 Å)