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UnknownLife with too much polyprenol: polyprenol reductase deficiency.
Not available
S-EPMC3428379 | biostudies-literature
UnknownIdentification of Abies sibirica L. Polyprenols and Characterisation of Polyprenol-Containing Liposomes.
Not available
S-EPMC7221546 | biostudies-literature
UnknownA UDP-HexNAc:polyprenol-P GalNAc-1-P transferase (WecP) representing a new subgroup of the enzyme family.
Not available
S-EPMC3133024 | biostudies-literature
UnknownSupercritical-CO2 extraction, identification and quantification of polyprenol as a bioactive ingredient from Irish trees species.
Not available
S-EPMC8018978 | biostudies-literature
UnknownInvestigation of the conserved reentrant membrane helix in the monotopic phosphoglycosyl transferase superfamily supports key molecular interactions with polyprenol phosphate substrates.
Not available
S-EPMC6909930 | biostudies-literature
UnknownLipid bilayer nanodisc platform for investigating polyprenol-dependent enzyme interactions and activities.
Not available
S-EPMC3876266 | biostudies-literature
UnknownSynthesis of a Comprehensive Polyprenol Library for Evaluation of Bacterial Enzyme Lipid Substrate Specificity.
Not available
S-EPMC3915775 | biostudies-literature
UnknownStreptomyces coelicolor strains lacking polyprenol phosphate mannose synthase and protein O-mannosyl transferase are hyper-susceptible to multiple antibiotics.
Not available
S-EPMC5882110 | biostudies-literature
TranscriptomicsGene expression in a Streptomyces coelicolor strain defective in sco1423 encoding a polyprenol phosphate mannose synthase (Ppm1) compared to the complemented mutant and the wild type parent
Polyprenol phosphate mannose (PPM) is a lipid linked sugar donor used by extra-cytoplasmic glycosyl tranferases in bacteria. PPM is synthesised by polyprenol phosphate mannose synthase, Ppm1, and in most Actinobacteria is used as the sugar donor for protein O-mannosyl transferase, Pmt, in protein gl...
ORGANISM(S): Streptomyces coelicolor A3(2) 
2018-01-11 | GSE107982 | GEO
UnknownSRD5A3 is required for converting polyprenol to dolichol and is mutated in a congenital glycosylation disorder.
Not available
S-EPMC2940322 | biostudies-literature
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