Evidence map›Paper›PMID 34076307›Full record

ArticleProtein science : a publication of the Protein Society2021

Characterization of an aminotransferase from Acanthamoeba polyphaga Mimivirus.

Chase A Seltzner, Justin D Ferek, James B Thoden, Hazel M Holden

Open access · greenAbstract read
In one paragraph

Article in Protein science : a publication of the Protein Society, 2021. 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
0.6field-weighted citation impact, top 32% 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, 3 citations in OpenAlex.

  1. Review
  2. Characterization of an aminotransferase from Acanthamoeba polyphaga Mimivirus.Protein science : a publication of the Protein Society · 2021
    Article
  3. Can Free LivingIranian journal of parasitology
    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

4 authors at 1 institution in 1 country.

Chase A SeltznerDepartment of Biochemistry, University of Wisconsin, Madison, Wisconsin, USA.
Justin D FerekDepartment of Biochemistry, University of Wisconsin, Madison, Wisconsin, USA.
James B ThodenDepartment of Biochemistry, University of Wisconsin, Madison, Wisconsin, USA.
Hazel M HoldenDepartment of Biochemistry, University of Wisconsin, Madison, Wisconsin, USA.ORCID 0000-0001-6214-3638
University of Wisconsin–Madison · US

Funding

Biochemical Investigations of Sugar-Modifying EnzymesR35GM134643 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI HOLDEN, HAZEL M. · 2020 to 2024
$2.0M
NIGMS NIH HHS R35 GM134643
6 · The paper itself

Abstract

Acanthamoeba polyphaga Mimivirus, a complex virus that infects amoeba, was first reported in 2003. It is now known that its DNA genome encodes for nearly 1,000 proteins including enzymes that are required for the biosynthesis of the unusual sugar 4-amino-4,6-dideoxy-d-glucose, also known as d-viosamine. As observed in some bacteria, the pathway for the production of this sugar initiates with a nucleotide-linked sugar, which in the Mimivirus is thought to be UDP-d-glucose. The enzyme required for the installment of the amino group at the C-4' position of the pyranosyl moiety is encoded in the Mimivirus by the L136 gene. Here, we describe a structural and functional analysis of this pyridoxal 5'-phosphate-dependent enzyme, referred to as L136. For this analysis, three high-resolution X-ray structures were determined: the wildtype enzyme/pyridoxamine 5'-phosphate/dTDP complex and the site-directed mutant variant K185A in the presence of either UDP-4-amino-4,6-dideoxy-d-glucose or dTDP-4-amino-4,6-dideoxy-d-glucose. Additionally, the kinetic parameters of the enzyme utilizing either UDP-d-glucose or dTDP-d-glucose were measured and demonstrated that L136 is efficient with both substrates. This is in sharp contrast to the structurally related DesI from Streptomyces venezuelae, whose three-dimensional architecture was previously reported by this laboratory. As determined in this investigation, DesI shows a profound preference in its catalytic efficiency for the dTDP-linked sugar substrate. This difference can be explained in part by a hydrophobic patch in DesI that is missing in L136. Notably, the structure of L136 reported here represents the first three-dimensional model for a virally encoded PLP-dependent enzyme and thus provides new information on sugar aminotransferases in general.

Indexed as

AcanthamoebaAmino Acid SequenceBinding SitesCloning, MolecularCoenzymesCrystallography, X-RayEscherichia coliGene ExpressionGenetic VectorsKineticsMimiviridaeModels, MolecularMutationProtein BindingProtein Conformation, alpha-HelicalProtein Conformation, beta-StrandCoenzymesPyridoxal PhosphatePyridoxaminepyridoxamine phosphateRecombinant ProteinsTransaminasesUridine Diphosphate GlucoseViral Proteins4,6-dideoxy sugar4-aminoquinovoseAcanthamoeba polyphaga Mimivirusaminotransferased-viosaminegiant virusesUDP-4-amino-4,6-dideoxy-d-glucoseviral glycansX-ray structure

Identifiers

PMID34076307
PMCPMC8376416
OpenAlexW3165798799

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.