Evidence map›Paper›PMID 33711341›Full record

ArticleThe Journal of biological chemistry

Peptidoglycan binding by a pocket on the accessory NTF2-domain of Pgp2 directs helical cell shape of Campylobacter jejuni.

Chang Sheng-Huei Lin, Anson C K Chan, Jenny Vermeulen, Jacob Brockerman, Arvind S Soni, Martin E Tanner, Erin C Gaynor, Lawrence P McIntosh, Jean-Pierre Simorre, Michael E P Murphy

Open access · goldAbstract read
In one paragraph

Article in The Journal of biological chemistry. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

10 authors at 2 institutions in 2 countries.

Chang Sheng-Huei LinDepartment of Microbiology and Immunology, University of British Columbia, Vancouver, British Columbia, Canada.
Anson C K ChanDepartment of Microbiology and Immunology, University of British Columbia, Vancouver, British Columbia, Canada.
Jenny VermeulenDepartment of Microbiology and Immunology, University of British Columbia, Vancouver, British Columbia, Canada.
Jacob BrockermanDepartment of Biochemistry and Molecular Biology, University of British Columbia, Vancouver, British Columbia, Canada.
Arvind S SoniDepartment of Chemistry, University of British Columbia, Vancouver, British Columbia, Canada.
Martin E TannerDepartment of Chemistry, University of British Columbia, Vancouver, British Columbia, Canada.
Erin C GaynorDepartment of Microbiology and Immunology, University of British Columbia, Vancouver, British Columbia, Canada.
Lawrence P McIntoshDepartment of Biochemistry and Molecular Biology, University of British Columbia, Vancouver, British Columbia, Canada; Department of Chemistry, University of British Columbia, Vancouver, British Columbia, Canada.
Jean-Pierre SimorreUniversity of Grenoble Alpes, CNRS, CEA, IBS, Grenoble, France.
Michael E P MurphyDepartment of Microbiology and Immunology, University of British Columbia, Vancouver, British Columbia, Canada. Electronic address: michael.murphy@ubc.ca.
University of British Columbia · CACentre National de la Recherche Scientifique · FR

Funding

X-ray Absorption Spectroscopy (XAS) pp.711-759P41GM103393 · NIGMS · STANFORD UNIVERSITY · PI HODGSON, KEITH O · 2012 to 2019
$30.6M
NIGMS NIH HHS P41 GM103393
6 · The paper itself

Abstract

The helical morphology of Campylobacter jejuni, a bacterium involved in host gut colonization and pathogenesis in humans, is determined by the structure of the peptidoglycan (PG) layer. This structure is dictated by trimming of peptide stems by the LD-carboxypeptidase Pgp2 within the periplasm. The interaction interface between Pgp2 and PG to select sites for peptide trimming is unknown. We determined a 1.6 Å resolution crystal structure of Pgp2, which contains a conserved LD-carboxypeptidase domain and a previously uncharacterized domain with an NTF2-like fold (NTF2). We identified a pocket in the NTF2 domain formed by conserved residues and located ∼40 Å from the LD-carboxypeptidase active site. Expression of pgp2 in trans with substitutions of charged (Lys257, Lys307, Glu324) and hydrophobic residues (Phe242 and Tyr233) within the pocket did not restore helical morphology to a pgp2 deletion strain. Muropeptide analysis indicated a decrease of murotripeptides in the deletion strain expressing these mutants, suggesting reduced Pgp2 catalytic activity. Pgp2 but not the K307A mutant was pulled down by C. jejuni Δpgp2 PG sacculi, supporting a role for the pocket in PG binding. NMR spectroscopy was used to define the interaction interfaces of Pgp2 with several PG fragments, which bound to the active site within the LD-carboxypeptidase domain and the pocket of the NTF2 domain. We propose a model for Pgp2 binding to PG strands involving both the LD-carboxypeptidase domain and the accessory NTF2 domain to induce a helical cell shape.

Indexed as

Bacterial ProteinsCampylobacter jejuniCarboxypeptidasesCatalytic DomainHumansNucleocytoplasmic Transport ProteinsPeptidoglycanProtein ConformationBacterial ProteinsCarboxypeptidasesLD-carboxypeptidaseNucleocytoplasmic Transport ProteinsPeptidoglycanbacterial cell shapeCampylobactercarboxypeptidasecrystal structuredockingNTF2 domainnuclear magnetic resonance (NMR)peptidoglycan

Identifiers

PMID33711341
PMCPMC8038945
OpenAlexW3134225298

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.