Evidence map›Paper›PMID 25961325›Full record

ArticleActa crystallographica. Section F, Structural biology communications2015

Iron superoxide dismutases in eukaryotic pathogens: new insights from Apicomplexa and Trypanosoma structures.

Isabelle Q H Phan, Douglas R Davies, Nilmar Silvio Moretti, Dhanasekaran Shanmugam, Igor Cestari, Atashi Anupama, James W Fairman, Thomas E Edwards, Kenneth Stuart, Sergio Schenkman and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Acta crystallographica. Section F, Structural biology communications, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

10 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Crystal structure of an iron superoxide dismutase from the pathogenic amoeba Acanthamoeba castellanii.Acta crystallographica. Section F, Structural biology communications · 2019
    Article
  9. Redox Balance Keepers and Possible Cell Functions Managed by Redox Homeostasis inFrontiers in cellular and infection microbiology · 2019
    Review
  10. Review
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

11 authors at 4 institutions in 3 countries.

Isabelle Q H PhanSeattle Structural Genomics Center for Infectious Disease (SSGCID), USA.
Douglas R DaviesSeattle Structural Genomics Center for Infectious Disease (SSGCID), USA.
Nilmar Silvio MorettiSeattle Biomedical Research Institute, 307 Westlake Avenue North, Suite 500, Seattle, WA 98109, USA.
Dhanasekaran ShanmugamCSIR-National Chemical Laboratory, Pune 411 008, India.
Igor CestariSeattle Biomedical Research Institute, 307 Westlake Avenue North, Suite 500, Seattle, WA 98109, USA.
Atashi AnupamaSeattle Biomedical Research Institute, 307 Westlake Avenue North, Suite 500, Seattle, WA 98109, USA.
James W FairmanSeattle Structural Genomics Center for Infectious Disease (SSGCID), USA.
Thomas E EdwardsSeattle Structural Genomics Center for Infectious Disease (SSGCID), USA.
Kenneth StuartSeattle Structural Genomics Center for Infectious Disease (SSGCID), USA.
Sergio SchenkmanDepartmento de Microbiologia, Imunologia e Parasitologia, Universidade Federal de São Paulo (UNIFESP), São Paulo, Brazil.
Peter J MylerSeattle Structural Genomics Center for Infectious Disease (SSGCID), USA.
Joint Center for Structural Genomics · USCenter for Infectious Disease Research · USNational Chemical Laboratory · INUniversidade Federal de São Paulo · BR

Funding

Genome wide assessment of essential genes in Trypanosoma bruceiR01AI078962 · NIAID · SEATTLE BIOMEDICAL RESEARCH INSTITUTE · PI STUART, KENNETH D · 2010 to 2012
$2.5M
NIAID NIH HHS HHSN272201200025CNIAID NIH HHS R01 AI078962PHS HHS HHSN272201200025C
6 · The paper itself

Abstract

Prior studies have highlighted the potential of superoxide dismutases as drug targets in eukaryotic pathogens. This report presents the structures of three iron-dependent superoxide dismutases (FeSODs) from Trypanosoma cruzi, Leishmania major and Babesia bovis. Comparison with existing structures from Plasmodium and other trypanosome isoforms shows a very conserved overall fold with subtle differences. In particular, structural data suggest that B. bovis FeSOD may display similar resistance to peroxynitrite-mediated inactivation via an intramolecular electron-transfer pathway as previously described in T. cruzi FeSOD isoform B, thus providing valuable information for structure-based drug design. Furthermore, lysine-acetylation results in T. cruzi indicate that acetylation occurs at a position close to that responsible for the regulation of acetylation-mediated activity in the human enzyme.

Indexed as

Amino Acid SequenceApicomplexaBabesia bovisCrystallizationCrystallography, X-RayEukaryotaHumansLeishmania majorMolecular Sequence DataProtein Structure, SecondaryProtein Structure, TertiarySuperoxide DismutaseTrypanosoma cruziSuperoxide DismutaseApicomplexairon superoxide dismutaseTrypanosoma

Identifiers

PMID25961325
PMCPMC4427173
OpenAlexW1860789078

What OpenQuestion holds

Textmetadata
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.