Evidence map›Paper›PMID 22412371›Full record

ArticlePLoS pathogens2012

Differential function of lip residues in the mechanism and biology of an anthrax hemophore.

MarCia T Ekworomadu, Catherine B Poor, Cedric P Owens, Miriam A Balderas, Marian Fabian, John S Olson, Frank Murphy, Erol Bakkalbasi, Erol Balkabasi, Erin S Honsa and 3 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

26 citing papers in PubMed, 43 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Iron and zinc exploitation during bacterial pathogenesis.Metallomics : integrated biometal science · 2015
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Heme uptake in bacterial pathogens.Current opinion in chemical biology · 2014
    Review
  19. Article
  20. Article
4 · The record

Corrections and comments

  • Erratum issued
    Balkabasi, Erol [corrected to Bakkalbasi, Erol]
5 · Who and what money

Authors and funding

13 authors at 5 institutions in 1 country.

MarCia T EkworomaduDepartment of Molecular Virology and Microbiology, Baylor College of Medicine, Houston, Texas, USA.
Catherine B Poor
Cedric P Owens
Miriam A Balderas
Marian Fabian
John S Olson
Frank Murphy
Erol Bakkalbasi
Erol Balkabasi
Erin S Honsa
Chuan He
Celia W Goulding
Anthony W Maresso
Baylor College of Medicine · USRice University · USUniversity of California, Irvine · USUniversity of Chicago · USArgonne National Laboratory · US

Funding

Initiative for Maximizing Student Development (IMSD) ProgramR25GM056929 · NIGMS · BAYLOR COLLEGE OF MEDICINE · PI PEREIRA, FRED A · 1998 to 2023
$12.4M
Tuning Virulence Determinants in Staphylococcus aureusR01AI074658 · NIAID · UNIVERSITY OF CHICAGO · PI HE, CHUAN · 2007 to 2016
$3.8M
Nutrient Uptake during Anthrax DiseaseR01AI097167 · NIAID · BAYLOR COLLEGE OF MEDICINE · PI MARESSO, ANTHONY W · 2012 to 2022
$3.5M
Function Properties of Hemoglobins and MyoglobinsR01GM035649 · NIGMS · RICE UNIVERSITY · PI OLSON, JOHN S. · 1985 to 2010
$3.3M
DESIGN OF HEME-PROTEIN BASED BLOOD SUBSTITUTESR01HL047020 · NHLBI · RICE UNIVERSITY · PI OLSON, JOHN S. · 1991 to 2010
$2.9M
Structural And Biochemical Characterization Of A Novel Mycobacterial Heme UptakeR01AI081161 · NIAID · UNIVERSITY OF CALIFORNIA-IRVINE · PI GOULDING, CELIA · 2009 to 2013
$1.8M
Molecular mechanism of redox driven proton pumpsR01GM084348 · NIGMS · RICE UNIVERSITY · PI FABIAN, MARIAN · 2009 to 2010
$458k
Branched Chain Amino Acid Metabolism During AnthraxR21AI146481 · NIAID · BAYLOR COLLEGE OF MEDICINE · PI MARESSO, ANTHONY W · 2019 to 2020
$440k
Bacterial Heme Transport by non-Isd NEAT ProteinsR21AI096314 · NIAID · BAYLOR COLLEGE OF MEDICINE · PI MARESSO, ANTHONY W · 2012 to 2013
$430k
Characterization of Heme Acquisition in B. anthracisF32AI069697 · NIAID · UNIVERSITY OF CHICAGO · PI MARESSO, ANTHONY W · 2007 to 2008
$58k
NHLBI NIH HHS HL047020NHLBI NIH HHS R01 HL047020NIAID NIH HHS AI069697NIAID NIH HHS AI074658NIAID NIH HHS AI081161NIAID NIH HHS F32 AI069697NIAID NIH HHS R01 AI074658NIAID NIH HHS R01 AI081161NIAID NIH HHS R01 AI097167NIAID NIH HHS R21 AI096314NIAID NIH HHS R21 AI146481NIGMS NIH HHS GM035649NIGMS NIH HHS GM84348NIGMS NIH HHS R01 GM035649NIGMS NIH HHS R01 GM084348NIGMS NIH HHS R25 GM056929
6 · The paper itself

Abstract

To replicate in mammalian hosts, bacterial pathogens must acquire iron. The majority of iron is coordinated to the protoporphyrin ring of heme, which is further bound to hemoglobin. Pathogenic bacteria utilize secreted hemophores to acquire heme from heme sources such as hemoglobin. Bacillus anthracis, the causative agent of anthrax disease, secretes two hemophores, IsdX1 and IsdX2, to acquire heme from host hemoglobin and enhance bacterial replication in iron-starved environments. Both proteins contain NEAr-iron Transporter (NEAT) domains, a conserved protein module that functions in heme acquisition in Gram-positive pathogens. Here, we report the structure of IsdX1, the first of a Gram-positive hemophore, with and without bound heme. Overall, IsdX1 forms an immunoglobin-like fold that contains, similar to other NEAT proteins, a 3(10)-helix near the heme-binding site. Because the mechanistic function of this helix in NEAT proteins is not yet defined, we focused on the contribution of this region to hemophore and NEAT protein activity, both biochemically and biologically in cultured cells. Site-directed mutagenesis of amino acids in and adjacent to the helix identified residues important for heme and hemoglobin association, with some mutations affecting both properties and other mutations affecting only heme stabilization. IsdX1 with mutations that reduced the ability to associate with hemoglobin and bind heme failed to restore the growth of a hemophore-deficient strain of B. anthracis on hemoglobin as the sole iron source. These data indicate that not only is the 3(10)-helix important for NEAT protein biology, but also that the processes of hemoglobin and heme binding can be both separate as well as coupled, the latter function being necessary for maximal heme-scavenging activity. These studies enhance our understanding of NEAT domain and hemophore function and set the stage for structure-based inhibitor design to block NEAT domain interaction with upstream ligands.

Indexed as

Amino Acid SequenceAnthraxBacillus anthracisBacterial Outer Membrane ProteinsHemeHemoglobinsIronIron-Binding ProteinsMolecular Sequence DataProtein BindingProtein Structure, TertiarySequence AlignmentBacterial Outer Membrane ProteinsHemeHemoglobinsIronIron-Binding Proteins

Identifiers

PMID22412371
PMCPMC3297588
OpenAlexW1982638010

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.