Evidence map›Paper›PMID 28683921›Full record

ArticleAdvances in protein chemistry and structural biology2017

Biology, Mechanism, and Structure of Enzymes in the α-d-Phosphohexomutase Superfamily.

Kyle M Stiers, Andrew G Muenks, Lesa J Beamer

Abstract read
In one paragraph

Article in Advances in protein chemistry and structural biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 1 pooled it
–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

27 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  6. Phosphoglucomutase comes into the spotlight.Journal of experimental botany · 2023
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  14. CT295 IsFrontiers in cellular and infection microbiology · 2022
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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

3 authors.

Kyle M StiersUniversity of Missouri, Columbia, MO, United States.
Andrew G MuenksUniversity of Missouri, Columbia, MO, United States.
Lesa J BeamerUniversity of Missouri, Columbia, MO, United States. Electronic address: beamerl@missouri.edu.

Funding

MOLECULAR BASIS OF GENE EXPRESSION AND SIGNAL PROCESSINGT32GM008396 · NIGMS · UNIVERSITY OF MISSOURI-COLUMBIA · PI HANNINK, MARK · 1991 to 2021
$4.1M
NIGMS NIH HHS T32 GM008396
6 · The paper itself

Abstract

Enzymes in the α-d-phosphohexomutases superfamily catalyze the reversible conversion of phosphosugars, such as glucose 1-phosphate and glucose 6-phosphate. These reactions are fundamental to primary metabolism across the kingdoms of life and are required for a myriad of cellular processes, ranging from exopolysaccharide production to protein glycosylation. The subject of extensive mechanistic characterization during the latter half of the 20th century, these enzymes have recently benefitted from biophysical characterization, including X-ray crystallography, NMR, and hydrogen-deuterium exchange studies. This work has provided new insights into the unique catalytic mechanism of the superfamily, shed light on the molecular determinants of ligand recognition, and revealed the evolutionary conservation of conformational flexibility. Novel associations with inherited metabolic disease and the pathogenesis of bacterial infections have emerged, spurring renewed interest in the long-appreciated functional roles of these enzymes.

Indexed as

Amino Acid SequenceAnimalsBacteriaBacterial InfectionsCatalytic DomainCrystallography, X-RayGlucosephosphatesHumansMetabolic DiseasesMutationNuclear Magnetic Resonance, BiomolecularPhosphoglucomutaseProtein ConformationSequence AlignmentGlucosephosphatesPhosphoglucomutaseConformational changeCrystal structureEnzyme mechanismInherited diseaseMissense variantsOligomersPhosphorylationPhosphosugarProtein flexibility

Identifiers

PMID28683921
PMCPMC5802415

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.