Evidence map›Paper›PMID 35452090›Full record

ArticleThe Journal of general physiology2022

The archaeal glutamate transporter homologue GltPh shows heterogeneous substrate binding.

Krishna D Reddy, Didar Ciftci, Amanda J Scopelliti, Olga Boudker

Open access · hybridAbstract read
In one paragraph

Article in The Journal of general physiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.7field-weighted citation impact, top 15% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Conformational free energy landscape of a glutamate transporter and microscopic details of its transport mechanism.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  3. Article
  4. The Cranefield Awards 2022.The Journal of general physiology · 2023
    Article
  5. Article
  6. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 1 country.

Krishna D ReddyDepartment of Physiology and Biophysics, Weill Cornell Medicine, New York, NY.ORCID 0000-0002-0475-8375
Didar CiftciDepartment of Physiology and Biophysics, Weill Cornell Medicine, New York, NY.ORCID 0000-0001-8079-1022
Amanda J ScopellitiDepartment of Physiology and Biophysics, Weill Cornell Medicine, New York, NY.
Olga BoudkerDepartment of Physiology and Biophysics, Weill Cornell Medicine, New York, NY.
Cornell University · USHoward Hughes Medical Institute · US

Funding

TRD #3: An automated and streamlined pipeline for in-situ molecular microscopyP41GM103310 · NIGMS · SCRIPPS RESEARCH INSTITUTE, THE · PI KIEFT, JEFFREY S · 2012 to 2021
$14.7M
The structural dynamics of a glutamate transporter homologueR37NS085318 · NINDS · WEILL MEDICAL COLL OF CORNELL UNIV · PI BOUDKER, OLGA · 2014 to 2020
$4.3M
Conformational Ensemble of Glutamate Transporters: Structure and IonicModulationR01NS064357 · NINDS · WEILL MEDICAL COLL OF CORNELL UNIV · PI BOUDKER, OLGA · 2009 to 2018
$3.8M
Acquisition of Detector for JEOL 3200 FSC Electron MicroscopeS10OD019994 · OD · NEW YORK STRUCTURAL BIOLOGY CENTER · PI CARRAGHER, BRIDGET OLIVIA · 2015 to 2015
$600k
Evolution of ion specificity in glutamate transportersF32NS102325 · NINDS · WEILL MEDICAL COLL OF CORNELL UNIV · PI REDDY, KRISHNA · 2017 to 2019
$177k
Agouron Institute F00316American Heart Association 19PRE34380215NIGMS NIH HHS GM103310NIGMS NIH HHS P41 GM103310NIH HHS F32 NS102325NIH HHS S10 OD019994NINDS NIH HHS F32 NS102325NINDS NIH HHS R01 NS064357NINDS NIH HHS R37 NS085318NYSTARSimons Foundation 349247
6 · The paper itself

Abstract

Integral membrane glutamate transporters couple the concentrative substrate transport to ion gradients. There is a wealth of structural and mechanistic information about this protein family. Recent studies of an archaeal homologue, GltPh, revealed transport rate heterogeneity, which is inconsistent with simple kinetic models; however, its structural and mechanistic determinants remain undefined. Here, we demonstrate that in a mutant GltPh, which exclusively populates the outward-facing state, at least two substates coexist in slow equilibrium, binding the substrate with different apparent affinities. Wild type GltPh shows similar binding properties, and modulation of the substate equilibrium correlates with transport rates. The low-affinity substate of the mutant is transient following substrate binding. Consistently, cryo-EM on samples frozen within seconds after substrate addition reveals the presence of structural classes with perturbed helical packing of the extracellular half of the transport domain in regions adjacent to the binding site. By contrast, an equilibrated structure does not show such classes. The structure at 2.2-Å resolution details a pattern of waters in the intracellular half of the domain and resolves classes with subtle differences in the substrate-binding site. We hypothesize that the rigid cytoplasmic half of the domain mediates substrate and ion recognition and coupling, whereas the extracellular labile half sets the affinity and dynamic properties.

Indexed as

Amino Acid Transport System X-AGArchaeaBinding SitesGlutamic AcidKineticsSubstrate SpecificityAmino Acid Transport System X-AGGlutamic Acid

Identifiers

PMID35452090
PMCPMC9044058
OpenAlexW4224292125

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.