4Q6X

Structure of phospholipase D Beta1B1i from Sicarius terrosus venom at 2.14 A resolution

4Q6X の概要

• エントリーDOI: 10.2210/pdb4q6x/pdb
• 分子名称: Phospholipase D StSicTox-betaIC1, MAGNESIUM ION (3 entities in total)
• 機能のキーワード: tim barrel, venom gland secretion of sicarius terrosus, lyase
• 由来する生物種: Sicarius terrosus (Cave spider)
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 34310.68

構造登録者

Lajoie, D.M.,Roberts, S.A.,Zobel-Thropp, P.A.,Binford, G.J.,Cordes, M.H. (登録日: 2014-04-23, 公開日: 2015-03-18, 最終更新日: 2023-09-20)

主引用文献

Lajoie, D.M.,Roberts, S.A.,Zobel-Thropp, P.A.,Delahaye, J.L.,Bandarian, V.,Binford, G.J.,Cordes, M.H.
Variable Substrate Preference among Phospholipase D Toxins from Sicariid Spiders.
J.Biol.Chem., 290:10994-11007, 2015

PubMed Abstract: Venoms of the sicariid spiders contain phospholipase D enzyme toxins that can cause severe dermonecrosis and even death in humans. These enzymes convert sphingolipid and lysolipid substrates to cyclic phosphates by activating a hydroxyl nucleophile present in both classes of lipid. The most medically relevant substrates are thought to be sphingomyelin and/or lysophosphatidylcholine. To better understand the substrate preference of these toxins, we used (31)P NMR to compare the activity of three related but phylogenetically diverse sicariid toxins against a diverse panel of sphingolipid and lysolipid substrates. Two of the three showed significantly faster turnover of sphingolipids over lysolipids, and all three showed a strong preference for positively charged (choline and/or ethanolamine) over neutral (glycerol and serine) headgroups. Strikingly, however, the enzymes vary widely in their preference for choline, the headgroup of both sphingomyelin and lysophosphatidylcholine, versus ethanolamine. An enzyme from Sicarius terrosus showed a strong preference for ethanolamine over choline, whereas two paralogous enzymes from Loxosceles arizonica either preferred choline or showed no significant preference. Intrigued by the novel substrate preference of the Sicarius enzyme, we solved its crystal structure at 2.1 Å resolution. The evolution of variable substrate specificity may help explain the reduced dermonecrotic potential of some natural toxin variants, because mammalian sphingolipids use primarily choline as a positively charged headgroup; it may also be relevant for sicariid predatory behavior, because ethanolamine-containing sphingolipids are common in insect prey.

PubMed: 25752604
DOI: 10.1074/jbc.M115.636951

実験手法

X-RAY DIFFRACTION (2.14 Å)