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Structures in multiple conformations reveal distinct transition metal and proton pathways in an Nramp transporter.


ABSTRACT: Nramp family transporters-expressed in organisms from bacteria to humans-enable uptake of essential divalent transition metals via an alternating-access mechanism that also involves proton transport. We present high-resolution structures of Deinococcus radiodurans (Dra)Nramp in multiple conformations to provide a thorough description of the Nramp transport cycle by identifying the key intramolecular rearrangements and changes to the metal coordination sphere. Strikingly, while metal transport requires cycling from outward- to inward-open states, efficient proton transport still occurs in outward-locked (but not inward-locked) DraNramp. We propose a model in which metal and proton enter the transporter via the same external pathway to the binding site, but follow separate routes to the cytoplasm, which could facilitate the co-transport of two cationic species. Our results illustrate the flexibility of the LeuT fold to support a broad range of substrate transport and conformational change mechanisms.

SUBMITTER: Bozzi AT 

PROVIDER: S-EPMC6398981 | biostudies-literature | 2019 Feb

REPOSITORIES: biostudies-literature

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Structures in multiple conformations reveal distinct transition metal and proton pathways in an Nramp transporter.

Bozzi Aaron T AT   Zimanyi Christina M CM   Nicoludis John M JM   Lee Brandon K BK   Zhang Casey H CH   Gaudet Rachelle R  

eLife 20190204


Nramp family transporters-expressed in organisms from bacteria to humans-enable uptake of essential divalent transition metals via an alternating-access mechanism that also involves proton transport. We present high-resolution structures of <i>Deinococcus radiodurans</i> (Dra)Nramp in multiple conformations to provide a thorough description of the Nramp transport cycle by identifying the key intramolecular rearrangements and changes to the metal coordination sphere. Strikingly, while metal trans  ...[more]

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