Evidence map›Paper›PMID 39216472›Full record

ArticleStructure (London, England : 1993)2024

Structural insights into the convergent evolution of sulfoxide synthase EgtB-IV, an ergothioneine-biosynthetic homolog of ovothiol synthase OvoA.

Kendra A Ireland, Chase M Kayrouz, Marissa L Abbott, Mohammad R Seyedsayamdost, Katherine M Davis

Abstract read
In one paragraph

Article in Structure (London, England : 1993), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Kendra A IrelandDepartment of Chemistry, Emory University, Atlanta, GA 30322, USA.
Chase M KayrouzDepartment of Chemistry, Princeton University, Princeton, NJ 08544, USA.
Marissa L AbbottDepartment of Chemistry, Princeton University, Princeton, NJ 08544, USA.
Mohammad R SeyedsayamdostDepartment of Chemistry, Princeton University, Princeton, NJ 08544, USA; Department of Molecular Biology, Princeton University, Princeton, NJ 08544, USA.
Katherine M DavisDepartment of Chemistry, Emory University, Atlanta, GA 30322, USA. Electronic address: katherine.davis@emory.edu.

Funding

Training and OutreachP30GM124166 · NIGMS · CORNELL UNIVERSITY · PI RICHARD A. CERIONE · 2019 to 2026
$28.3M
Unraveling the dynamics that enable unusual heme enzyme reactivityR35GM147557 · NIGMS · EMORY UNIVERSITY · PI Katherine Marie Davis · 2022 to 2026
$1.9M
Toward a Chemo-Enzymatic Synthesis of Vancomycin and Its AnalogsR01GM129496 · NIGMS · PRINCETON UNIVERSITY · PI SEYEDSAYAMDOST, MOHAMMAD R · 2019 to 2022
$1.2M
NIGMS NIH HHS P30 GM124166NIGMS NIH HHS R01 GM129496NIGMS NIH HHS R35 GM147557
6 · The paper itself

Abstract

Non-heme iron-dependent sulfoxide/selenoxide synthases (NHISS) constitute a unique metalloenzyme class capable of installing a C-S/Se bond onto histidine to generate thio/selenoimidazole antioxidants, such as ergothioneine and ovothiol. These natural products are increasingly recognized for their health benefits. Among associated ergothioneine-biosynthetic enzymes, type IV EgtBs stand out, as they exhibit low sequence similarity with other EgtB subfamilies due to their recent divergence from the ovothiol-biosynthetic enzyme OvoA. Herein, we present crystal structures of two representative EgtB-IV enzymes, offering insights into the basis for this evolutionary convergence and enhancing our understanding of NHISS active site organization more broadly. The ability to interpret how key residues modulate substrate specificity and regioselectivity has implications for downstream identification of divergent reactivity within the NHISS family. To this end, we identify a previously unclassified clade of OvoA-like enzymes with a seemingly hybrid set of characteristics, suggesting they may represent an evolutionary intermediate between OvoA and EgtB-IV.

Indexed as

Catalytic DomainErgothioneineEvolution, MolecularModels, MolecularAmino Acid SequenceCrystallography, X-RayProtein BindingSubstrate SpecificityErgothioneineantioxidantconvergent evolutionEgtBergothioneinenatural productnon-heme ironOvoAovothiolsulfoxide synthaseX-ray crystallography

Identifiers

PMID39216472
PMCPMC11560578

What OpenQuestion holds

Textmetadata
LicenceTDM
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.