Journal article
The ups and downs of elevator-type di-/tricarboxylate membrane transporters
- Abstract:
- The divalent anion sodium symporter (DASS) family contains both sodium-driven anion cotransporters and anion/anion exchangers. The family belongs to a broader ion transporter superfamily (ITS), which comprises 24 families of transporters, including those of AbgT antibiotic efflux transporters. The human proteins in the DASS family play major physiological roles and are drug targets. We recently determined multiple structures of the human sodium-dependent citrate transporter (NaCT) and the succinate/dicarboxylate transporter from Lactobacillus acidophilus (LaINDY). Structures of both proteins show high degrees of structural similarity to the previously determined VcINDY fold. Conservation between these DASS protein structures and those from the AbgT family indicates that the VcINDY fold represents the overall protein structure for the entire ITS. The new structures of NaCT and LaINDY are captured in the inward- or outward-facing conformations, respectively. The domain arrangements in these structures agree with a rigid body elevator-type transport mechanism for substrate translocation across the membrane. Two separate NaCT structures in complex with a substrate or an inhibitor allowed us to explain the inhibition mechanism and propose a detailed classification scheme for grouping disease-causing mutations in the human protein. Structural understanding of multiple kinetic states of DASS proteins is a first step toward the detailed characterization of their entire transport cycle.
- Publication status:
- Published
- Peer review status:
- Peer reviewed
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- Files:
-
-
(Preview, Accepted manuscript, pdf, 1.4MB, Terms of use)
-
- Publisher copy:
- 10.1111/febs.16158
Authors
+ National Institute of General Medical Sciences
More from this funder
- Funder identifier:
- https://ror.org/04q48ey07
- Publisher:
- Wiley
- Journal:
- FEBS Journal More from this journal
- Volume:
- 289
- Issue:
- 6
- Pages:
- 1515-1523
- Publication date:
- 2021-08-24
- Acceptance date:
- 2021-08-16
- DOI:
- EISSN:
-
1742-4658
- ISSN:
-
1742-464X
- Pmid:
-
34403567
- Language:
-
English
- Keywords:
- Pubs id:
-
1192691
- UUID:
-
uuid_1eae8b0c-acb6-4b95-b6f3-7b0c7676eb11
- Local pid:
-
pubs:1192691
- Source identifiers:
-
W3196159109
- Deposit date:
-
2025-12-17
- ARK identifier:
Terms of use
- Copyright holder:
- Federation of European Biochemical Societies
- Copyright date:
- 2021
- Rights statement:
- © 2021 Federation of European Biochemical Societies
- Notes:
- This is the accepted manuscript version of the article. The final version is available online from Wiley at https://dx.doi.org/10.1111/febs.16158
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