3NHT

Crystal structure of the AnSt-D7L1-U46619 complex

3NHT の概要

• エントリーDOI: 10.2210/pdb3nht/pdb
• 関連するPDBエントリー: 3NHI
• 分子名称: D7 protein, (5E)-7-{6-[(1E)-3-HYDROXYOCT-1-ENYL]-2-OXABICYCLO[2.2.1]HEPT-5-YL}HEPT-5-ENOIC ACID, SULFATE ION, ... (4 entities in total)
• 機能のキーワード: all-helical, odorant-binding protein, ligand-binding protein, d7, transport protein
• 由来する生物種: Anopheles stephensi (Indo-Pakistan malaria mosquito)
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 34898.64

構造登録者

Andersen, J.F.,Alvarenga, P.H.,Francischetti, I.M.,Calvo, E.,Sa-Nunes, A.,Ribeiro, J.M. (登録日: 2010-06-14, 公開日: 2010-12-29, 最終更新日: 2024-11-06)

主引用文献

Alvarenga, P.H.,Francischetti, I.M.,Calvo, E.,Sa-Nunes, A.,Ribeiro, J.M.,Andersen, J.F.
The function and three-dimensional structure of a thromboxane a(2)/cysteinyl leukotriene-binding protein from the saliva of a mosquito vector of the malaria parasite.
Plos Biol., 8:e1000547-e1000547, 2010

PubMed Abstract: The highly expressed D7 protein family of mosquito saliva has previously been shown to act as an anti-inflammatory mediator by binding host biogenic amines and cysteinyl leukotrienes (CysLTs). In this study we demonstrate that AnSt-D7L1, a two-domain member of this group from Anopheles stephensi, retains the CysLT binding function seen in the homolog AeD7 from Aedes aegypti but has lost the ability to bind biogenic amines. Unlike any previously characterized members of the D7 family, AnSt-D7L1 has acquired the important function of binding thromboxane A(2) (TXA(2)) and its analogs with high affinity. When administered to tissue preparations, AnSt-D7L1 abrogated Leukotriene C(4) (LTC(4))-induced contraction of guinea pig ileum and contraction of rat aorta by the TXA(2) analog U46619. The protein also inhibited platelet aggregation induced by both collagen and U46619 when administered to stirred platelets. The crystal structure of AnSt-D7L1 contains two OBP-like domains and has a structure similar to AeD7. In AnSt-D7L1, the binding pocket of the C-terminal domain has been rearranged relative to AeD7, making the protein unable to bind biogenic amines. Structures of the ligand complexes show that CysLTs and TXA(2) analogs both bind in the same hydrophobic pocket of the N-terminal domain. The TXA(2) analog U46619 is stabilized by hydrogen bonding interactions of the ω-5 hydroxyl group with the phenolic hydroxyl group of Tyr 52. LTC(4) and occupies a very similar position to LTE(4) in the previously determined structure of its complex with AeD7. As yet, it is not known what, if any, new function has been acquired by the rearranged C-terminal domain. This article presents, to our knowledge, the first structural characterization of a protein from mosquito saliva that inhibits collagen mediated platelet activation.

PubMed: 21152418
DOI: 10.1371/journal.pbio.1000547

実験手法

X-RAY DIFFRACTION (1.45 Å)