ArticleACS omega2017
On the Role of Catabolic Enzymes in Biosynthetic Models of Glycogen Molecular Weight Distributions.
Article in ACS omega, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
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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.
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.
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Who cites it
0 citing papers in PubMed, 5 citations in OpenAlex.
No citing paper in PubMed yet.
Corrections and comments
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Authors and funding
2 authors at 1 institution in 2 countries.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Glycogen and starch are complex branched polymers of glucose that serve as units of glucose storage in animals and plants, respectively. Changes in the structure of these molecules have been linked to changes in their respective functional properties. Enzymatic models of starch synthesis have provided valuable insights into the biosynthetic origins of starch structure and functional properties but have not successfully been applied to glycogen despite the structural similarities between the two polymers. Modifications to biosynthetic models of starch structure were tested for applicability to glycogen. Mathematical evidence is provided showing the necessity (which has hitherto been in doubt) of considering the effects of catabolic (degradative) enzymes in biosynthesis-based approaches that seek to accurately describe the molecular weight distributions of individual chains of glycogen formed in vivo through glycogenesis. This finding also provides future direction for inferring the dependence of enzyme activities on substrate chain length from in vivo data.
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Registered trials
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