2X6F

THE CRYSTAL STRUCTURE OF THE DROSOPHILA CLASS III PI3-KINASE VPS34 IN COMPLEX WITH 3-METHYLADENINE

2X6F の概要

• エントリーDOI: 10.2210/pdb2x6f/pdb
• 関連するPDBエントリー: 2X6H 2X6I 2X6J 2X6K
• 分子名称: PHOSPHOTIDYLINOSITOL 3 KINASE 59F, 6-AMINO-3-METHYLPURINE (2 entities in total)
• 機能のキーワード: transferase
• 由来する生物種: DROSOPHILA MELANOGASTER (FRUIT FLY)
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 157831.26

構造登録者

Miller, S.,Tavshanjian, B.,Oleksy, A.,Perisic, O.,Houseman, B.T.,Shokat, K.M.,Williams, R.L. (登録日: 2010-02-17, 公開日: 2010-04-07, 最終更新日: 2023-12-20)

主引用文献

Miller, S.,Tavshanjian, B.,Oleksy, A.,Perisic, O.,Houseman, B.T.,Shokat, K.M.,Williams, R.L.
Shaping Development of Autophagy Inhibitors with the Structure of the Lipid Kinase Vps34.
Science, 327:1638-, 2010

PubMed Abstract: Phosphoinositide 3-kinases (PI3Ks) are lipid kinases with diverse roles in health and disease. The primordial PI3K, Vps34, is present in all eukaryotes and has essential roles in autophagy, membrane trafficking, and cell signaling. We solved the crystal structure of Vps34 at 2.9 angstrom resolution, which revealed a constricted adenine-binding pocket, suggesting the reason that specific inhibitors of this class of PI3K have proven elusive. Both the phosphoinositide-binding loop and the carboxyl-terminal helix of Vps34 mediate catalysis on membranes and suppress futile adenosine triphosphatase cycles. Vps34 appears to alternate between a closed cytosolic form and an open form on the membrane. Structures of Vps34 complexes with a series of inhibitors reveal the reason that an autophagy inhibitor preferentially inhibits Vps34 and underpin the development of new potent and specific Vps34 inhibitors.

PubMed: 20339072
DOI: 10.1126/SCIENCE.1184429

実験手法

X-RAY DIFFRACTION (3.3 Å)