The validation of a human enzyme that methylates the ribose of the second transcribed nucleotide encoded by FTSJD1 is reported, henceforth renamed HMTR2 to reflect function.
D-Ribose
Exercise performance and recovery is the main area connected here, and any felt benefit should be read together with the human evidence base.
Representative tier calculated from paper evidence that passed the collection audit.
Main benefit evidence
The representative ingredient tier is calculated from these target-level evidence groups.
Exercise performance and recovery1 studiesTier-CExercise performance and recoverySome positive signal observedFelt benefit focusSupplement contextPotential benefit studied in Exercise performance and recovery.Open metrics>
Blood pressure and vascular health1 studiesTier-CBlood pressure and vascular health markersSignal is still limitedResearch marker focusPatient-group studyThis card is closer to a measured biomarker or lab outcome than a directly felt user benefit.Closer to a research marker than a directly felt benefit.Open metrics>
Recent research
10 new papers were added in this period. No new risk signal was identified.
What's new
Most notable recent finding
Study dosage range (reference only)
Key cautions to review
Standalone side-effect signals and combination cautions are listed separately.
Standalone side effects
Evidence summaries
Paper IDs and full lists are private. Only study types and summaries are shown.
Growth of Bifidobacterium breve UCC2003 on ribose leads to the transcriptional induction of the rbsACBDK gene cluster, which is essential for ribose utilization and its transcription is likely regulated by a LacI‐type regulator encoded by rbsR, located immedia
This study provides the first direct experimental evidence for the essentiality of DprE1 in mycobacteria, and validates DprE1 as a promising target for new anti-mycobacterial drugs.
3 more summariesLimited representative sample by study type.>
In this article, it is reviewed how energy is produced by cellular respiration, the pentose pathway, and the use of supplemental D-ribose, a naturally occurring monosaccharide found in the cells and particularly in the mitochondria.
The results suggest that in vitro glycation of bone using glucose leads to the formation of lower levels of AGEs including PEN, whereas ribosylation appears to support a pathway toward PEN formation.
It is suggested that ZAP-mediated viral mRNA degradation is facilitated by PAR, and provides a biophysical rationale for the reported association of ZAP with RNA stress granules.