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5JDM

Structural mechanisms of extracellular ion exchange and induced binding-site occlusion in the sodium-calcium exchanger NCX_Mj soaked with 2.5 mM Na+ and 0.1mM Sr2+

Summary for 5JDM
Entry DOI10.2210/pdb5jdm/pdb
Related5HWX 5HWY 5HXC 5HXE 5HXH 5HXR 5HXS 5HYA 5JDF 5JDG 5JDH 5JDL 5JDN 5JDQ
Descriptorsodium-calcium exchanger NCX_Mj, SODIUM ION, STRONTIUM ION, ... (8 entities in total)
Functional Keywordsna+/ca2+ exchange, calcium signalling, membrane transporter, induced conformational change, membrane protein
Biological sourceMethanocaldococcus jannaschii (strain ATCC 43067 / DSM 2661 / JAL-1 / JCM 10045 / NBRC 100440)
Total number of polymer chains1
Total formula weight35702.68
Authors
Liao, J.,Jiang, Y.X.,Faraldo-Gomez, J.D. (deposition date: 2016-04-17, release date: 2016-05-11, Last modification date: 2023-09-27)
Primary citationLiao, J.,Marinelli, F.,Lee, C.,Huang, Y.,Faraldo-Gomez, J.D.,Jiang, Y.
Mechanism of extracellular ion exchange and binding-site occlusion in a sodium/calcium exchanger.
Nat.Struct.Mol.Biol., 23:590-599, 2016
Cited by
PubMed Abstract: Na(+)/Ca(2+) exchangers use the Na(+) electrochemical gradient across the plasma membrane to extrude intracellular Ca(2+) and play a central role in Ca(2+) homeostasis. Here, we elucidate their mechanisms of extracellular ion recognition and exchange through a structural analysis of the exchanger from Methanococcus jannaschii (NCX_Mj) bound to Na(+), Ca(2+) or Sr(2+) in various occupancies and in an apo state. This analysis defines the binding mode and relative affinity of these ions, establishes the structural basis for the anticipated 3:1 Na(+)/Ca(2+)-exchange stoichiometry and reveals the conformational changes at the onset of the alternating-access transport mechanism. An independent analysis of the dynamics and conformational free-energy landscape of NCX_Mj in different ion-occupancy states, based on enhanced-sampling molecular dynamics simulations, demonstrates that the crystal structures reflect mechanistically relevant, interconverting conformations. These calculations also reveal the mechanism by which the outward-to-inward transition is controlled by the ion occupancy, thereby explaining the emergence of strictly coupled Na(+)/Ca(2+) antiport.
PubMed: 27183196
DOI: 10.1038/nsmb.3230
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.558 Å)
Structure validation

226707

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