Evidence map›Paper›PMID 32121487›Full record

ArticleInternational journal of molecular sciences2020

Structural and Functional Characterization of New SsoPox Variant Points to the Dimer Interface as a Driver for the Increase in Promiscuous Paraoxonase Activity.

Yoko Suzumoto, Orly Dim, Giovanni N Roviello, Franz Worek, Joel L Sussman, Giuseppe Manco

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. 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

6 authors.

Yoko SuzumotoInstitute of Biochemistry and Cell Biology, CNR, 80131 Naples, Italy.
Orly DimThe Weizmann Institute of Science, Rehovot 76100, Israel.
Giovanni N RovielloInstitute of Biostructures and Bioimages, CNR, 80131 Naples, Italy.ORCID 0000-0002-6978-542X
Franz WorekBundeswehr Institute of Pharmacology and Toxicology, Munich, Germany.
Joel L SussmanThe Weizmann Institute of Science, Rehovot 76100, Israel.
Giuseppe MancoInstitute of Biochemistry and Cell Biology, CNR, 80131 Naples, Italy.ORCID 0000-0001-6191-3952

Funding

Campania Region PON FESR 2014-2020 PON03PE_0060_4Ministero dell'Istruzione, dell'Università e della Ricerca PON01_01585
6 · The paper itself

Abstract

Increasing attention is more and more directed toward the thermostable Phosphotriesterase-Like-Lactonase (PLL) family of enzymes, for the efficient and reliable decontamination of toxic nerve agents. In the present study, the DNA Staggered Extension Process (StEP) technique was utilized to obtain new variants of PLL enzymes. Divergent homologous genes encoding PLL enzymes were utilized as templates for gene recombination and yielded a new variant of SsoPox from

Indexed as

Protein MultimerizationAryldialkylphosphataseCarboxylic Ester HydrolasesCatalytic DomainCircular DichroismDirected Molecular EvolutionEnzyme StabilityHydrogen-Ion ConcentrationIonsMetalsModels, MolecularMutant ProteinsNerve AgentsPhosphoric Triester HydrolasesProtein Structure, SecondaryProtein Structure, TertiaryAryldialkylphosphataseCarboxylic Ester HydrolasesgluconolactonaseIonsMetalsMutant ProteinsNerve AgentsPhosphoric Triester Hydrolasesenzymatic detoxification/remediationMolecular evolutionnerve agentsPhosphotriesterase-Like-Lactonases (PLLs), organophosphate (OP) compounds

Identifiers

PMID32121487
PMCPMC7084321

What OpenQuestion holds

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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.