6IZ5

Crystal Structure Analysis of a Eukaryotic Membrane Protein

Summary for 6IZ5

• Entry DOI: 10.2210/pdb6iz5/pdb
• Descriptor: Trimeric intracellular cation channel type B-B (2 entities in total)
• Functional Keywords: tric, cation channel, membrane protein
• Biological source: Xenopus laevis (African clawed frog)
• Total number of polymer chains: 1
• Total formula weight: 35463.84

Authors

Li, D.,Su, M.,Hendrickson, W.A.,Chen, Y.H. (deposition date: 2018-12-18, release date: 2019-05-01, Last modification date: 2023-11-22)

Primary citation

Wang, X.H.,Su, M.,Gao, F.,Xie, W.,Zeng, Y.,Li, D.L.,Liu, X.L.,Zhao, H.,Qin, L.,Li, F.,Liu, Q.,Clarke, O.B.,Lam, S.M.,Shui, G.H.,Hendrickson, W.A.,Chen, Y.H.
Structural basis for activity of TRIC counter-ion channels in calcium release.
Proc.Natl.Acad.Sci.USA, 116:4238-4243, 2019

PubMed Abstract: Trimeric intracellular cation (TRIC) channels are thought to provide counter-ion currents that facilitate the active release of Ca from intracellular stores. TRIC activity is controlled by voltage and Ca modulation, but underlying mechanisms have remained unknown. Here we describe high-resolution crystal structures of vertebrate TRIC-A and TRIC-B channels, both in Ca-bound and Ca-free states, and we analyze conductance properties in structure-inspired mutagenesis experiments. The TRIC channels are symmetric trimers, wherein we find a pore in each protomer that is gated by a highly conserved lysine residue. In the resting state, Ca binding at the luminal surface of TRIC-A, on its threefold axis, stabilizes lysine blockage of the pores. During active Ca release, luminal Ca depletion removes inhibition to permit the lysine-bearing and voltage-sensing helix to move in response to consequent membrane hyperpolarization. Diacylglycerol is found at interprotomer interfaces, suggesting a role in metabolic control.

PubMed: 30770441
DOI: 10.1073/pnas.1817271116

Experimental method

X-RAY DIFFRACTION (3.701 Å)