1ROR

CRYSTAL STRUCTURES OF THE CATALYTIC DOMAIN OF PHOSPHODIESTERASE 4B2B COMPLEXED WITH AMP

1ROR の概要

• エントリーDOI: 10.2210/pdb1ror/pdb
• 関連するPDBエントリー: 1RO6 1RO9
• 分子名称: cAMP-specific 3',5'-cyclic phosphodiesterase 4B, ZINC ION, ADENOSINE MONOPHOSPHATE, ... (4 entities in total)
• 機能のキーワード: pde, amp, 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: 87859.78

構造登録者

Xu, R.X.,Rocque, W.J.,Lambert, M.H.,Vanderwall, D.E.,Nolte, R.T. (登録日: 2003-12-02, 公開日: 2004-12-07, 最終更新日: 2023-08-23)

主引用文献

Xu, R.X.,Rocque, W.J.,Lambert, M.H.,Vanderwall, D.E.,Luther, M.A.,Nolte, R.T.
Crystal structures of the catalytic domain of phosphodiesterase 4B complexed with AMP, 8-Br-AMP, and rolipram.
J.Mol.Biol., 337:355-365, 2004

PubMed Abstract: Phosphodiesterase catalyzes the hydrolysis of the intracellular second messenger 3',5'-cyclic AMP (cAMP) into the corresponding 5'-nucleotide. Phosphodiesterase 4 (PDE4), the major cAMP-specific PDE in inflammatory and immune cells, is an attractive target for the treatment of asthma and COPD. We have determined crystal structures of the catalytic domain of PDE4B complexed with AMP (2.0 A), 8-Br-AMP (2.13 A) and the potent inhibitor rolipram (2.0 A). All the ligands bind in the same hydrophobic pocket and can interact directly with the active site metal ions. The identity of these metal ions was examined using X-ray anomalous difference data. The structure of the AMP complex confirms the location of the catalytic site and allowed us to speculate about the detailed mechanism of catalysis. The high-resolution structures provided the experimental insight into the nucleotide selectivity of phosphodiesterase. 8-Br-AMP binds in the syn conformation to the enzyme and demonstrates an alternative nucleotide-binding mode. Rolipram occupies much of the AMP-binding site and forms two hydrogen bonds with Gln443 similar to the nucleotides.

PubMed: 15003452
DOI: 10.1016/j.jmb.2004.01.040

実験手法

X-RAY DIFFRACTION (2 Å)