6NQ9

Crystal structure of YetJ mutant from Bacillus Subtilis - D195E

6NQ9 の概要

• エントリーDOI: 10.2210/pdb6nq9/pdb
• 分子名称: Uncharacterized protein YetJ (1 entity in total)
• 機能のキーワード: ca2+ channel structure, open conformation, ph sensor, membrane protein
• 由来する生物種: Bacillus subtilis (strain 168)
• タンパク質・核酸の鎖数: 4
• 化学式量合計: 95434.31

構造登録者

Guo, G.,Chang, Y.,Liu, Q. (登録日: 2019-01-19, 公開日: 2019-04-17, 最終更新日: 2023-10-11)

主引用文献

Guo, G.,Xu, M.,Chang, Y.,Luyten, T.,Seitaj, B.,Liu, W.,Zhu, P.,Bultynck, G.,Shi, L.,Quick, M.,Liu, Q.
Ion and pH Sensitivity of a TMBIM Ca2+Channel.
Structure, 27:1013-1021.e3, 2019

PubMed Abstract: The anti-apoptotic transmembrane Bax inhibitor motif (TMBIM) containing protein family regulates Ca homeostasis, cell death, and the progression of diseases including cancers. The recent crystal structures of the TMBIM homolog BsYetJ reveal a conserved Asp171-Asp195 dyad that is proposed in regulating a pH-dependent Ca translocation. Here we show that BsYetJ mediates Ca fluxes in permeabilized mammalian cells, and its interaction with Ca is sensitive to protons and other cations. We report crystal structures of BsYetJ in additional states, revealing the flexibility of the dyad in a closed state and a pore-opening mechanism. Functional studies show that the dyad is responsible for both Ca affinity and pH dependence. Computational simulations suggest that protonation of Asp171 weakens its interaction with Arg60, leading to an open state. Our integrated analysis provides insights into the regulation of the BsYetJ Ca channel that may inform understanding of human TMBIM proteins regarding their roles in cell death and diseases.

PubMed: 30930064
DOI: 10.1016/j.str.2019.03.003

実験手法

X-RAY DIFFRACTION (3.1 Å)