Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Accept all cookies' we'll assume that you are happy to receive all cookies and you won't see this message again. If you click 'Reject all non-essential cookies' only necessary cookies providing core functionality such as security, network management, and accessibility will be enabled. Click 'Find out more' for information on how to change your cookie settings.

Abstract The divalent anion sodium symporter (DASS) family mediates the uptake of Krebs cycle intermediates and sulfate, and influences adiposity, insulin resistance, and metabolism in mammals. While Na+:substrate stoichiometry is known for several DASS transporters, the location of key Na+ binding sites remains elusive; important information for understanding the mechanism. In VcINDY, a bacterial DASS protein, we visualized a non-protein cryo-EM density in the middle of the transport domain. Its size and coordination suggest it may represent either a third Na+ ion or a structural water molecule. Using a combination of in vitro binding and transport assays, cryo-EM structural determination and molecular dynamic simulations, we show that the density is not a Na+ ion. Instead, the data indicate that the density likely represents a structural water molecule critical for transport domain integrity. Sequence and structural similarities suggest this feature may be conserved across human DASS transporters such as NaCT and NaDC3.

More information Original publication

DOI

10.1093/pnasnexus/pgag242

Type

Journal article

Publisher

Oxford University Press (OUP)

Publication Date

2026-07-16T00:00:00+00:00