Page last updated: 2024-11-13

mannosylglycerate

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

Description

2-(alpha-D-mannosyl)-D-glycerate : Conjugate base of 2-(alpha-D-mannosyl)-D-glyceric acid [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Cross-References

ID SourceID
PubMed CID46878394
CHEBI ID57541
MeSH IDM0355373

Synonyms (11)

Synonym
2-o-(alpha-d-mannosyl)-d-glycerate
2-o-(alpha-d-mannopyranosyl)-d-glycerate
mannosylglycerate
CHEBI:57541
2-(alpha-d-mannosyl)-d-glycerate anion
2-(alpha-d-mannosyl)-d-glycerate
(2r)-2-o-(alpha-d-mannosyl)-glycerate
(2r)-3-hydroxy-2-(alpha-d-mannopyranosyloxy)propanoate
Q27124767
2(alpha-d-mannosyl)-d-glycerate
DTXSID001344043

Research Excerpts

Overview

Mannosylglycerate is an intracellular organic solute found in some red algae, and several thermophilic bacteria and hyperthermophilic archaea. It has a remarkable ability to protect proteins from thermal denaturation.

ExcerptReferenceRelevance
"Mannosylglycerate (MG) is an intracellular organic solute found in some red algae, and several thermophilic bacteria and hyperthermophilic archaea. "( To be or not to be a compatible solute: bioversatility of mannosylglycerate and glucosylglycerate.
da Costa, MS; Empadinhas, N, 2008
)
2.03
"Mannosylglycerate is a compatible solute typical of thermophilic marine microorganisms that has a remarkable ability to protect proteins from thermal denaturation. "( Mannosylglycerate stabilizes staphylococcal nuclease with restriction of slow β-sheet motions.
Lamosa, P; Matzapetakis, M; Pais, TM; Santos, H; Turner, DL, 2012
)
3.26

Effects

ExcerptReferenceRelevance
"Mannosylglycerate (MG) has been detected in several members of (hyper)thermophilic bacteria and archaea, in which it responds primarily to osmotic stress."( Mannosylglycerate: structural analysis of biosynthesis and evolutionary history.
Borges, N; Gonçalves, LG; Gonçalves, S; Jorge, CD; Matias, PM; Santos, H, 2014
)
2.57
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
carbohydrate acid anion
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Research

Studies (36)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's1 (2.78)18.2507
2000's18 (50.00)29.6817
2010's16 (44.44)24.3611
2020's1 (2.78)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 22.83

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be moderate demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index22.83 (24.57)
Research Supply Index3.61 (2.92)
Research Growth Index5.86 (4.65)
Search Engine Demand Index21.17 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (22.83)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews6 (16.67%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other30 (83.33%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]