5X9H

Crystal structure of the Mg2+ channel MgtE in complex with ATP

Summary for 5X9H

• Entry DOI: 10.2210/pdb5x9h/pdb
• Related: 5X9G
• Descriptor: Magnesium transporter MgtE, ADENOSINE-5'-TRIPHOSPHATE, MAGNESIUM ION (3 entities in total)
• Functional Keywords: channels, metal transport
• Biological source: Thermus thermophilus (strain HB8 / ATCC 27634 / DSM 579)
• Cellular location: Cell membrane ; Multi-pass membrane protein : Q5SMG8
• Total number of polymer chains: 2
• Total formula weight: 106313.26

Authors

Tomita, A.,Hattori, M.,Nureki, O. (deposition date: 2017-03-07, release date: 2017-08-16, Last modification date: 2024-03-27)

Primary citation

Tomita, A.,Zhang, M.,Jin, F.,Zhuang, W.,Takeda, H.,Maruyama, T.,Osawa, M.,Hashimoto, K.I.,Kawasaki, H.,Ito, K.,Dohmae, N.,Ishitani, R.,Shimada, I.,Yan, Z.,Hattori, M.,Nureki, O.
ATP-dependent modulation of MgtE in Mg(2+) homeostasis
Nat Commun, 8:148-148, 2017

PubMed Abstract: Magnesium is an essential ion for numerous physiological processes. MgtE is a Mg selective channel involved in the maintenance of intracellular Mg homeostasis, whose gating is regulated by intracellular Mg levels. Here, we report that ATP binds to MgtE, regulating its Mg-dependent gating. Crystal structures of MgtE-ATP complex show that ATP binds to the intracellular CBS domain of MgtE. Functional studies support that ATP binding to MgtE enhances the intracellular domain affinity for Mg within physiological concentrations of this divalent cation, enabling MgtE to function as an in vivo Mg sensor. ATP dissociation from MgtE upregulates Mg influx at both high and low intracellular Mg concentrations. Using site-directed mutagenesis and structure based-electrophysiological and biochemical analyses, we identify key residues and main structural changes involved in the process. This work provides the molecular basis of ATP-dependent modulation of MgtE in Mg homeostasis.MgtE is an Mg transporter involved in Mg homeostasis. Here, the authors report that ATP regulates the Mg-dependent gating of MgtE and use X-ray crystallography combined with functional studies to propose the molecular mechanisms involved in this process.

PubMed: 28747715
DOI: 10.1038/s41467-017-00082-w

Experimental method

X-RAY DIFFRACTION (3.598 Å)