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Protein-coding gene in the species Homo sapiens
Koda Y, Soejima M, Kimura H (March 2002). "Identification of human phosphoglucomutase 3 (PGM3) as N-acetylglucosamine-phosphate mutase (AGM1)". Annals of
Phosphoglucomutase_3
Metabolic enzyme
Phosphoglucomutase (EC 5.4.2.2) is an enzyme that transfers a phosphate group on an α-D-glucose monomer from the 1 to the 6 position in the forward direction
Phosphoglucomutase
Genetic disorder
genetic disorder of the immune system associated with diminished phosphoglucomutase 3 function. PGM3 is an enzyme which in humans is encoded by gene PGM3
PGM3_deficiency
Protein-coding gene in the species Homo sapiens
Phosphoglucomutase-like protein 5 is an enzyme that in humans is encoded by the PGM5 gene. GRCm38: Ensembl release 89: ENSMUSG00000041731 – Ensembl, May
PGM5
Protein-coding gene in humans
Phosphoglucomutase-1 is an enzyme that in humans is encoded by the PGM1 gene. The protein encoded by this gene is an isozyme of phosphoglucomutase (PGM)
PGM1
Breakdown of glycogen
glucose-6-phosphate (which often ends up in glycolysis) by the enzyme phosphoglucomutase. Glucose residues are phosphorolysed from branches of glycogen until
Glycogenolysis
Medical condition
proteins (genes SLC37A4, SLC17A3) yet are still considered GSDs. Phosphoglucomutase deficiency (gene PGM1) was declassed as a GSD due to it also affecting
Glycogen_storage_disease
Protein
glycolysis, it changes 3-phosphoglycerate to 2-phosphoglycerate by moving a single phosphate group within a single molecule. Phosphoglucomutase Methylmalonyl-CoA
Mutase
Metabolic pathway for the catabolism of D-galactose
UDP-galactose to UDP-glucose for the transferase reaction. Additionally, phosphoglucomutase converts the D-glucose 1-phosphate to D-glucose 6-phosphate. Anomer
Leloir_pathway
deficiency Phosphoglucomutase deficiency type 1 Phosphoglucomutase deficiency type 2 Phosphoglucomutase deficiency type 3 Phosphoglucomutase deficiency
List_of_diseases_(P)
Chemical compound
converted to G6P, the molecule can be turned into glucose 1-phosphate by phosphoglucomutase. Glucose 1-phosphate can then be combined with uridine triphosphate
Glucose_6-phosphate
Chemical compound
catabolism it must first be converted to glucose 6-phosphate by the enzyme phosphoglucomutase in a free equilibrium. One reason that cells form glucose 1-phosphate
Glucose_1-phosphate
Phosphoglucomutase-2 is an enzyme that in humans is encoded by the PGM2 gene. PGM2 is a major isozyme in red blood cells. GRCh38: Ensembl release 89: ENSG00000169299
PGM2
Metabolic pathways to build molecules
glycogen-storing pathway. It is changed to glucose-1-phosphate by phosphoglucomutase and then to UDP-glucose by UTP--glucose-1-phosphate uridylyltransferase
Anabolism
Physiological molecule and therapeutic drug
hasE (phosphoglucoisomerase), or glucose-1-phosphate using pgm (α-phosphoglucomutase), where those both undergo different sets of reactions. UDP-glucuronic
Hyaluronic_acid
Series of interconnected biochemical reactions
form of glucose 1-phosphate (G1P). The G1P is converted to G6P by phosphoglucomutase. G6P is readily fed into glycolysis, (or can go into the pentose phosphate
Cori_cycle
Exercise phenomenon
glycogen breakdown and synthesis in phosphoglucomutase 1 deficiency". Molecular Genetics and Metabolism. 122 (3): 117–121. doi:10.1016/j.ymgme.2017.08
Second_wind
Type of plastid, double-enveloped organelles in plant cells
well as growth of roots along the gravity vector. A plant lacking in phosphoglucomutase, for example, is a starchless mutant plant, thus preventing the settling
Amyloplast
Type of enzyme
involved in activation of the glycolytic pathway. 3. It acts as a coenzyme for phosphoglucomutase in glycolysis and gluconeogenesis. 4. It acts as a
Glucose-1,6-bisphosphate synthase
Glucose-1,6-bisphosphate_synthase
Indications of a specific illness, including psychiatric
metabolic myopathy of McArdle's disease (GSD-V) and some individuals with phosphoglucomutase deficiency (CDG1T/GSD-XIV), initially experience exercise intolerance
Signs_and_symptoms
Argentine biochemist (1927–2002)
Malcolm Dixon on the mechanism of metal activation of the enzyme phosphoglucomutase. During this work, he collaborated with Frederick Sanger, whose group
César_Milstein
Medical condition
glycogen breakdown and synthesis in phosphoglucomutase 1 deficiency". Molecular Genetics and Metabolism. 122 (3): 117–121. doi:10.1016/j.ymgme.2017.08
Inborn errors of carbohydrate metabolism
Inborn_errors_of_carbohydrate_metabolism
Human protein and coding gene
1996). "Identification of an S100A1/S100B target protein: phosphoglucomutase". Cell Calcium. 20 (3): 279–85. doi:10.1016/S0143-4160(96)90033-0. PMID 8894274
S100B
Category:EC 5.3.3 Enoyl CoA isomerase (EC 5.3.3.8) Category:EC 5.3.4 Protein disulfide isomerase (EC 5.3.4.1) Category:EC 5.4.2 Phosphoglucomutase (EC 5.4.2
List_of_enzymes
British biochemist (1918–2013)
(1961), "An amino acid sequence in the active centre of phosphoglucomutase", Biochemical Journal, 79 (3): 456–469, doi:10.1042/bj0790456, PMC 1205670, PMID 13771000
Frederick_Sanger
Class of enzymes
glucose-1-phosphate generated in step 3 of the Leloir pathway may be isomerized to glucose-6-phosphate by phosphoglucomutase. Glucose-6-phosphate readily enters
UDP-glucose_4-epimerase
Medical condition
Module in Biomedical Sciences. doi:10.1016/B978-0-12-801238-3.04632-8. ISBN 978-0-12-801238-3. Züchner S, Dallman J, Wen R, Beecham G, Naj A, Farooq A,
Congenital disorder of glycosylation
Congenital_disorder_of_glycosylation
Glucose polymer used as energy store in animals
Glucose-1-phosphate is then converted to glucose 6 phosphate (G6P) by phosphoglucomutase. A special debranching enzyme is needed to remove the α(1→6) branches
Glycogen
Species of cephalopods known as the Hawaiian bobtail squid
1251214 DeLoney, C.R., T.M. Bartley & K.L. Visick 2002. "Role for phosphoglucomutase in Aliivibrio fischeri-Euprymna scolopes symbiosis" (PDF). Archived
Euprymna_scolopes
Retention of sperm by female after mating
that ovipositing is nonrandom and females lay eggs with varying PGM (phosphoglucomutase) genotypes in different environments in order to optimize offspring
Female_sperm_storage
Class of enzymes which convert a molecule between isomeric forms
technique elucidated the kinetics and mechanism underlying the action of phosphoglucomutase, favoring the model of indirect transfer of phosphate with one intermediate
Isomerase
Muscular diseases caused by defects in metabolic processes
glycogen breakdown and synthesis in phosphoglucomutase 1 deficiency". Molecular Genetics and Metabolism. 122 (3): 117–121. doi:10.1016/j.ymgme.2017.08
Metabolic_myopathy
Type of disposable battery
synthetic pathway, where 13 enzymes, such as glucose 6-phosphate and phosphoglucomutase, act as catalysts (the substance that is both reactant and product)
Sugar_battery
Superfamily of enzymes
Four well studied subgroups in the superfamily are: Phosphoglucomutase (PGM) Phosphoglucomutase/Phosphomannomutase (PGM/PMM) Phosphoglucosamine mutase
Alpha-D-phosphohexomutase superfamily
Alpha-D-phosphohexomutase_superfamily
Class of enzymes
enzymes in the glycogenic pathway including glycogen synthase and phosphoglucomutase. UTP—glucose-1-phosphate uridylyltransferase has been found to be
UTP—glucose-1-phosphate uridylyltransferase
UTP—glucose-1-phosphate_uridylyltransferase
Effort to determine the DNA sequence of the chimpanzee genome
if these inserted genes confer a selective advantage. PGM5P4. The phosphoglucomutase pseudogene of human chromosome 2. This gene is incomplete and doesn't
Chimpanzee_genome_project
Protein metabolic pathway
Hyperammonemia is also seen post-exercise in McArdle disease (GSD-V) and phosphoglucomutase deficiency (PGM1-CDG, formerly GSD-XIV), due to the purine nucleotide
Purine_nucleotide_cycle
Class of enzymes
metabolism, it must be converted to glucose-6-phosphate by the enzyme phosphoglucomutase. Although the reaction is reversible in vitro, within the cell the
Glycogen_phosphorylase
Genus of bacteria
reductase subunit alpha, translation initiation factor IF-3, phosphomannomutase-phosphoglucomutase, LPS export ABC transporter ATP-binding protein, and NADH-quinone
Coxiella_(bacterium)
Protein family
that include phosphatases, phosphonatases, P-type ATPases, beta-phosphoglucomutases, phosphomannomutases, and dehalogenases, and are involved in a variety
Haloacid dehydrogenase superfamily
Haloacid_dehydrogenase_superfamily
Medical condition
High galactose-1-phosphate levels have been shown to interfere with phosphoglucomutase, glycogen phosphorylase, UDP-glycopyrophosphorylase, activity in bacterial
Galactose epimerase deficiency
Galactose_epimerase_deficiency
3-diphosphoglycerate-independent) EC 5.4.2.2: phosphoglucomutase (α-D-glucose-1,6-bisphosphate-dependent) EC 5.4.2.3: phosphoacetylglucosamine mutase EC 5.4
List_of_EC_numbers_(EC_5)
Mammalian protein found in humans
C-terminal binding protein 1-S158, Raf1-S338, Arpc1b-T21, DLC1-S88, phosphoglucomutase 1-T466, SMART/HDAC1-associated repressor protein-S3486-T3568, Tubulin
PAK1
Class of enzymes
α-D-glucose-1-phosphate is converted to glucose 6-phosphate by the action of phosphoglucomutase. Glucose-6-phosphate is an extremely important intermediate for several
Sucrose_phosphorylase
Metabolic process
glucose-1-phosphate will be converted to glucose-6-phosphate by the enzyme phosphoglucomutase. Disruptions in the Leloir pathway can lead to a rare inherited genetic
Galactolysis
Microbial gene found in Klebsiella aerogenes KCTC 2190
that requires HMW1C and phosphoglucomutase, an enzyme involved in lipooligosaccharide biosynthesis". Molecular Microbiology. 48 (3): 737–751. doi:10.1046/j
N-glycosyltransferase
Protein-coding gene in humans
1996). "Identification of an S100A1/S100B target protein: phosphoglucomutase". Cell Calcium. 20 (3): 279–285. doi:10.1016/S0143-4160(96)90033-0. PMID 8894274
S100A1
Chemical compound
diphosphate-Galactose/Glucose-4-epimerase (UGE) in plants". Plant Growth Regulation. 93 (3): 267–278. Bibcode:2021PGroR..93..267H. doi:10.1007/s10725-020-00686-1.{{cite
Uridine_diphosphate_galactose
750.250 – bisphosphoglycerate mutase MeSH D08.811.399.520.750.625 – phosphoglucomutase MeSH D08.811.399.520.750.700 – phosphoglycerate mutase MeSH D08.811
List_of_MeSH_codes_(D08)
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PHOSPHOGLUCOMUTASE 3
PHOSPHOGLUCOMUTASE 3
PHOSPHOGLUCOMUTASE 3
PHOSPHOGLUCOMUTASE 3
PHOSPHOGLUCOMUTASE 3
PHOSPHOGLUCOMUTASE 3
PHOSPHOGLUCOMUTASE 3
PHOSPHOGLUCOMUTASE 3
PHOSPHOGLUCOMUTASE 3
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