2ARM

Crystal Structure of the Complex of Phospholipase A2 with a natural compound atropine at 1.2 A resolution

2ARM の概要

• エントリーDOI: 10.2210/pdb2arm/pdb
• 関連するPDBエントリー: 1FVO 1Q7A
• 分子名称: Phospholipase A2 VRV-PL-VIIIa, (1R,5S)-8-METHYL-8-AZABICYCLO[3.2.1]OCT-3-YL (2R)-3-HYDROXY-2-PHENYLPROPANOATE, SULFATE ION, ... (4 entities in total)
• 機能のキーワード: enzyme, complex, hydrolase
• 由来する生物種: Daboia russellii pulchella
• 細胞内の位置: Secreted: P59071
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 14303.39

構造登録者

Singh, N.,Pal, A.,Jabeen, T.,Sharma, S.,Perbandt, M.,Betzel, C.,Singh, T.P. (登録日: 2005-08-20, 公開日: 2005-09-20, 最終更新日: 2024-10-30)

主引用文献

Singh, N.,Jabeen, T.,Pal, A.,Sharma, S.,Perbandt, M.,Betzel, C.,Singh, T.P.
Crystal structures of the complexes of a group IIA phospholipase A2 with two natural anti-inflammatory agents, anisic acid, and atropine reveal a similar mode of binding
Proteins, 64:89-100, 2006

PubMed Abstract: Secretory low molecular weight phospholipase A(2)s (PLA(2)s) are believed to be involved in the release of arachidonic acid, a precursor for the biosynthesis of pro-inflammatory eicosanoids. Therefore, the specific inhibitors of these enzymes may act as potent anti-inflammatory agents. Similarly, the compounds with known anti-inflammatory properties should act as specific inhibitors. Two plant compounds, (a) anisic acid (4-methoxy benzoic acid) and (b) atropine (8-methyl-8-azabicyclo oct-3-hydroxy-2-phenylpropanoate), have been used in various inflammatory disorders. Both compounds (a) and (b) have been found to inhibit PLA(2) activity having binding constants of 4.5 x 10(-5) M and 2.1 x 10(-8) M, respectively. A group IIA PLA(2) was isolated and purified from the venom of Daboia russelli pulchella (DRP) and its complexes were made with anisic acid and atropine. The crystal structures of the two complexes (i) and (ii) of PLA(2) with compounds (a) and (b) have been determined at 1.3 and 1.2 A resolutions, respectively. The high-quality observed electron densities for the two compounds allowed the accurate determinations of their atomic positions. The structures revealed that these compounds bound to the enzyme at the substrate - binding cleft and their positions were stabilized by networks of hydrogen bonds and hydrophobic interactions. The most characteristic interactions involving Asp 49 and His 48 were clearly observed in both complexes, although the residues that formed hydrophobic interactions with these compounds were not identical because their positions did not exactly superimpose in the large substrate-binding hydrophobic channel. Owing to a relatively small size, the structure of anisic acid did not alter upon binding to PLA(2), while that of atropine changed significantly when compared with its native crystal structure. The conformation of the protein also did not show notable changes upon the bindings of these ligands. The mode of binding of anisic acid to the present group II PLA(2) is almost identical to its binding with bovine pancreatic PLA(2) of group I. On the other hand, the binding of atropine to PLA(2) is similar to that of another plant alkaloid aristolochic acid.

PubMed: 16596639
DOI: 10.1002/prot.20970

実験手法

X-RAY DIFFRACTION (1.23 Å)