Evidence map›Paper›PMID 33847559›Full record

ArticleeLife2021

Allosteric communication in DNA polymerase clamp loaders relies on a critical hydrogen-bonded junction.

Subu Subramanian, Kent Gorday, Kendra Marcus, Matthew R Orellana, Peter Ren, Xiao Ran Luo, Michael E O'Donnell, John Kuriyan

Open access · goldAbstract read
In one paragraph

Article in eLife, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
3.4field-weighted citation impact, top 8% 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

13 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Differences in clamp loader mechanism between bacteria and eukaryotes.bioRxiv : the preprint server for biology · 2023
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Design and engineering of allosteric communications in proteins.Current opinion in structural biology · 2022
    Review
  13. 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

8 authors at 2 institutions in 1 country.

Subu SubramanianDepartment of Molecular and Cell Biology, University of California, Berkeley, Berkeley, United States.ORCID 0000-0001-6095-7021
Kent GordayDepartment of Molecular and Cell Biology, University of California, Berkeley, Berkeley, United States.
Kendra MarcusDepartment of Molecular and Cell Biology, University of California, Berkeley, Berkeley, United States.
Matthew R OrellanaDepartment of Molecular and Cell Biology, University of California, Berkeley, Berkeley, United States.
Peter RenDepartment of Molecular and Cell Biology, University of California, Berkeley, Berkeley, United States.
Xiao Ran LuoDepartment of Molecular and Cell Biology, University of California, Berkeley, Berkeley, United States.
Michael E O'DonnellHoward Hughes Medical Institute, Rockefeller University, New York, United States.
John KuriyanDepartment of Molecular and Cell Biology, University of California, Berkeley, Berkeley, United States.ORCID 0000-0002-4414-5477
QB3 · USHoward Hughes Medical Institute · US

Funding

MOLECULAR BIOPHYSICS TRAINING GRANTT32GM008295 · NIGMS · UNIVERSITY OF CALIFORNIA BERKELEY · PI HURLEY, JAMES H, WEMMER, DAVID E · 1989 to 2022
$8.1M
Immunology & Pathogenesis Program Training GrantT32AI100829 · NIAID · UNIVERSITY OF CALIFORNIA BERKELEY · PI Gregory M Barton, ELLEN A ROBEY · 2012 to 2026
$4.7M
Biochemical Mechanism and Structure of the Eukaryotic Replication ForkR01GM115809 · NIGMS · ROCKEFELLER UNIVERSITY · PI O'DONNELL, MICHAEL E · 2015 to 2022
$2.6M
Howard Hughes Medical InstituteNIAID NIH HHS T32 AI100829
6 · The paper itself

Abstract

Clamp loaders are AAA+ ATPases that load sliding clamps onto DNA. We mapped the mutational sensitivity of the T4 bacteriophage sliding clamp and clamp loader by deep mutagenesis, and found that residues not involved in catalysis or binding display remarkable tolerance to mutation. An exception is a glutamine residue in the AAA+ module (Gln 118) that is not located at a catalytic or interfacial site. Gln 118 forms a hydrogen-bonded junction in a helical unit that we term the central coupler, because it connects the catalytic centers to DNA and the sliding clamp. A suppressor mutation indicates that hydrogen bonding in the junction is important, and molecular dynamics simulations reveal that it maintains rigidity in the central coupler. The glutamine-mediated junction is preserved in diverse AAA+ ATPases, suggesting that a connected network of hydrogen bonds that links ATP molecules is an essential aspect of allosteric communication in these proteins.

Indexed as

Adenosine TriphosphateAllosteric RegulationATPases Associated with Diverse Cellular ActivitiesBacteriophage T4CatalysisDNA-Directed DNA PolymeraseDNA ReplicationGlutamineHydrogen BondingMolecular Dynamics SimulationMutationProtein ConformationStructure-Activity RelationshipVirus ReplicationAdenosine TriphosphateATPases Associated with Diverse Cellular ActivitiesDNA-Directed DNA PolymeraseGlutamineAAA+ proteinsallosteric communicationbacteriophage T4molecular biophysicsreplisomestructural biologyvirus

Identifiers

PMID33847559
PMCPMC8121543
OpenAlexW3156954219

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.