Evidence map›Paper›PMID 27995966›Full record

ArticleScientific reports2016

Identification of an evolutionary conserved structural loop that is required for the enzymatic and biological function of tryptophan 2,3-dioxygenase.

Helen Michels, Renée I Seinstra, Joost C M Uitdehaag, Mandy Koopman, Martijn van Faassen, Céline N Martineau, Ido P Kema, Rogier Buijsman, Ellen A A Nollen

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.5field-weighted citation impact, top 38% 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

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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

6 citing papers in PubMed, 13 citations in OpenAlex.

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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

9 authors at 3 institutions in 1 country.

Helen MichelsEuropean Research Institute for the Biology of Aging, University of Groningen, University Medical Center Groningen, Laboratory of Molecular Neurobiology of Aging, The Netherlands.
Renée I SeinstraEuropean Research Institute for the Biology of Aging, University of Groningen, University Medical Center Groningen, Laboratory of Molecular Neurobiology of Aging, The Netherlands.
Joost C M UitdehaagNetherlands Translational Research Center B.V., Oss, The Netherlands.
Mandy KoopmanEuropean Research Institute for the Biology of Aging, University of Groningen, University Medical Center Groningen, Laboratory of Molecular Neurobiology of Aging, The Netherlands.
Martijn van FaassenUniversity of Groningen, University Medical Center Groningen, Department of Laboratory Medicine, The Netherlands.
Céline N MartineauEuropean Research Institute for the Biology of Aging, University of Groningen, University Medical Center Groningen, Laboratory of Molecular Neurobiology of Aging, The Netherlands.
Ido P KemaUniversity of Groningen, University Medical Center Groningen, Department of Laboratory Medicine, The Netherlands.
Rogier BuijsmanNetherlands Translational Research Center B.V., Oss, The Netherlands.
Ellen A A NollenEuropean Research Institute for the Biology of Aging, University of Groningen, University Medical Center Groningen, Laboratory of Molecular Neurobiology of Aging, The Netherlands.
University Medical Center Groningen · NLUniversity of Groningen · NLCenter for Translational Molecular Medicine · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The enzyme TDO (tryptophan 2,3-dioxygenase; TDO-2 in Caenorhabditis elegans) is a potential therapeutic target to cancer but is also thought to regulate proteotoxic events seen in the progression of neurodegenerative diseases. To better understand its function and develop specific compounds that target TDO we need to understand the structure of this molecule. In C. elegans we compared multiple different CRISPR/Cas9-induced tdo-2 deletion mutants and identified a motif of three amino acids (PLD) that is required for the enzymatic conversion of tryptophan to N-formylkynurenine. Loss of TDO-2's enzymatic activity in PDL deletion mutants was accompanied by an increase in motility during aging and a prolonged lifespan, which is in line with the previously observed phenotypes induced by a knockdown of the full enzyme. Comparison of sequence structures suggests that blocking this motif might interfere with haem binding, which is essential for the enzyme's activity. The fact that these three residues are situated in an evolutionary conserved structural loop of the enzyme suggests that the findings can be translated to humans. The identification of this specific loop region in TDO-2-essential for its catalytic function-will aid in the design of novel inhibitors to treat diseases in which the TDO enzyme is overexpressed or hyperactive.

Indexed as

Evolution, MolecularAgingAmino Acid MotifsAmino Acid SequenceAnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsCRISPR-Cas SystemsHemeHumansLocomotionLongevityMutagenesisProtein BindingProtein Structure, TertiarySequence AlignmentCaenorhabditis elegans ProteinsHemeTryptophan Oxygenase

Identifiers

PMID27995966
PMCPMC5171515
OpenAlexW2566913350

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Registered trials

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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.