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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
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
Enzyme
In enzymology, a β-phosphoglucomutase (EC 5.4.2.6) is an enzyme that catalyzes the chemical reaction β-D-glucose 1-phosphate ⇌ {\displaystyle \rightleftharpoons
Beta-phosphoglucomutase
Protein-coding gene in the species Homo sapiens
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
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
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
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
Exercise phenomenon
seen in some medical conditions, such as McArdle disease (GSD-V) and Phosphoglucomutase deficiency (PGM1-CDG/CDG1T/GSD-XIV). Unlike non-affected individuals
Second_wind
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
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
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
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
Polymerisation of glucose molecules into glycogen
Glucose-6-phosphate is converted into glucose-1-phosphate by the action of phosphoglucomutase, passing through the obligatory intermediate glucose-1,6-bisphosphate
Glycogenesis
Topics referred to by the same term
Look up PGM in Wiktionary, the free dictionary. PGM may refer to: Phosphoglucomutase, an enzyme that interconverts G6P and G1P Phosphoglycerate mutase
PGM
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
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
deficiency Phosphoglucomutase deficiency type 1 Phosphoglucomutase deficiency type 2 Phosphoglucomutase deficiency type 3 Phosphoglucomutase deficiency
List_of_diseases_(P)
Medical condition
G-6-P is converted into glucose-1-phosphate (G-1-P) by the action of phosphoglucomutase (PGM), passing through the obligatory intermediate glucose-1,6-bisphosphate
Inborn errors of carbohydrate metabolism
Inborn_errors_of_carbohydrate_metabolism
Plant growth in reaction to gravity and bending of leaves and roots
accumulation, such as those affecting the PGM1 (which encodes the enzyme phosphoglucomutase) gene in Arabidopsis, causing plastids – the presumptive statoliths
Gravitropism
In enzymology, a phosphoglucomutase (glucose-cofactor) (EC 5.4.2.5) is an enzyme that catalyzes the chemical reaction alpha-D-glucose 1-phosphate ⇌ D-glucose
Phosphoglucomutase (glucose-cofactor)
Phosphoglucomutase_(glucose-cofactor)
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
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
British biochemist (1918–2013)
Sanger, F. (1961), "An amino acid sequence in the active centre of phosphoglucomutase", Biochemical Journal, 79 (3): 456–469, doi:10.1042/bj0790456, PMC 1205670
Frederick_Sanger
Type of enzyme
activation of the glycolytic pathway. 3. It acts as a coenzyme for phosphoglucomutase in glycolysis and gluconeogenesis. 4. It acts as a cofactor for phosphopentomutase
Glucose-1,6-bisphosphate synthase
Glucose-1,6-bisphosphate_synthase
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
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
Genus of bacteria
subunit alpha, translation initiation factor IF-3, phosphomannomutase-phosphoglucomutase, LPS export ABC transporter ATP-binding protein, and NADH-quinone
Coxiella_(bacterium)
Conserved RNA structure
of 'algC' genes, which are known to encode phosphomannomutases or phosphoglucomutases. However, in rare examples, it is associated with other genes whose
AlgC_RNA_motif
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
Index of enzymes associated with the same name
Glucose phosphomutase may refer to: Phosphoglucomutase (glucose-cofactor), an enzyme Phosphoglucomutase, an enzyme This set index page lists enzyme articles
Glucose_phosphomutase
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
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
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
bisphosphoglycerate mutase EC 5.4.2.5: phosphoglucomutase (glucose-cofactor) EC 5.4.2.6: β-phosphoglucomutase EC 5.4.2.7: phosphopentomutase EC 5.4.2
List_of_EC_numbers_(EC_5)
Canadian geneticist
in 1970 with a thesis entitled Studies on the genetic variation of phosphoglucomutase in man. McAlpine was mentored and supervised by women in her field
Phyllis_McAlpine
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
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
Chemical compound
Glucose 6-phosphate (6). Galactokinase (GK), Galactose-1-phosphate uridylyltransferase (GALT), UDP-glucose 4-epimerase (UGE), phosphoglucomutase (PGM)
Uridine_diphosphate_galactose
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
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
Muscular diseases caused by defects in metabolic processes
determine "second wind" which is also seen in McArdle disease (GSD-V) and phosphoglucomutase deficiency (PGM1-CDG/CDG1T/GSD-XIV). A cardiopulmonary exercise test
Metabolic_myopathy
Protein
2-phosphoglycerate by moving a single phosphate group within a single molecule. Phosphoglucomutase Methylmalonyl-CoA mutase Phosphoglycerate mutase Nelson, David; Cox
Mutase
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
5.3.4 Protein disulfide isomerase (EC 5.3.4.1) Category:EC 5.4.2 Phosphoglucomutase (EC 5.4.2.2) Category:EC 5.99.1 Topoisomerase (type I: EC 5.99.1.2
List_of_enzymes
Biological process
glycogen phosphorylase. G-1-P is then converted into G-6-P by enzyme phosphoglucomutase. A water molecule hydrolyses G-6-P to glucose, the enzyme is glucose-6-phosphatase
Glucose_cycle
GlmU, which produce UDP-GlcNAc in bacteria, are also present with phosphoglucomutase (PGM). Half of the species also have MurT and GatD, known to perform
Pseudopeptidoglycan
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
Human protein and coding gene
(September 1996). "Identification of an S100A1/S100B target protein: phosphoglucomutase". Cell Calcium. 20 (3): 279–85. doi:10.1016/S0143-4160(96)90033-0
S100B
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
Medical condition
(DDOST-CDG) 614507 DDOST 1p36.12 It (PGM1-CDG) (formerly GSD-XIV) Phosphoglucomutase deficiency 614921 PGM1 1p31.3 DPM2-CDG n/a DPM2 9q34.13 TUSC3-CDG
Congenital disorder of glycosylation
Congenital_disorder_of_glycosylation
Class of enzymes
of the Leloir pathway may be isomerized to glucose-6-phosphate by phosphoglucomutase. Glucose-6-phosphate readily enters glycolysis, leading to the production
UDP-glucose_4-epimerase
Protein-coding gene in the species Homo sapiens
(September 1996). "Identification of an S100A1/S100B target protein: phosphoglucomutase". Cell Calcium. 20 (3): 279–285. doi:10.1016/S0143-4160(96)90033-0
S100A1
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
Proteins II: "Comparative Aspects of the Structure and Function of Phosphoglucomutase" David Durant University of Miami (none) James D. Dutcher Squibb Institute
List of participants in the Evolving Genes and Proteins symposium
List_of_participants_in_the_Evolving_Genes_and_Proteins_symposium
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
Mammalian protein found in Homo sapiens
C-terminal binding protein 1-S158, Raf1-S338, Arpc1b-T21, DLC1-S88, phosphoglucomutase 1-T466, SMART/HDAC1-associated repressor protein-S3486-T3568, Tubulin
PAK1
Microbial gene found in Klebsiella aerogenes KCTC 2190
HMW1 adhesin is glycosylated in a process that requires HMW1C and phosphoglucomutase, an enzyme involved in lipooligosaccharide biosynthesis". Molecular
N-glycosyltransferase
Species of bacterium
the glycolysis and gluconeogenesis pathways, including glucokinase, phosphoglucomutase, phosphofructokinase, and enolase. D. marmoris is able to utilize
Deinococcus_marmoris
and 2Q4R. Small DM, Matheson NK (1979). "Phosphomannomutase and phosphoglucomutase in developing Cassia corymbosa seeds". Phytochemistry. 18 (7): 1147–1150
Phosphomannomutase
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)
PHOSPHOGLUCOMUTASE
PHOSPHOGLUCOMUTASE
PHOSPHOGLUCOMUTASE
PHOSPHOGLUCOMUTASE
Boy/Male
Irish Latin
noble.
Girl/Female
Arabic, Muslim
Pleiades
Male
Russian
(ЯроÑлав) Russian form of Polish JarosÅ‚aw, YAROSLAV means "spring glory."
Surname or Lastname
English
English : occupational name from an agent derivative of Middle English tingle (see Tingle).German : occupational or status name for a medieval judge or court official, from Old High German ding ‘legal proceeding’.German : variant of Tengler.
Girl/Female
Tamil
Foolwati | பூலவதீ, பூலவதீ
Delicate as a flower
Boy/Male
Hindu, Indian
Green
Boy/Male
Hindu, Indian, Sanskrit, Telugu
Character; Nature
Surname or Lastname
English
English : from Middle English, Old French sur(ri)gien (from a derivative of Late Latin chirurgia ‘handiwork’), hence an occupational name for a person who performed operations, mostly amputations. Before the advent of anaesthetics, only crude surgery was possible, and the calling was often combined with that of the barber or bath house attendant.French : topographic name for someone who lived close to a gushing spring.
Boy/Male
Basque Spanish
Blond.
Boy/Male
Indian
Scratching, Scraping
PHOSPHOGLUCOMUTASE
PHOSPHOGLUCOMUTASE
PHOSPHOGLUCOMUTASE
PHOSPHOGLUCOMUTASE
PHOSPHOGLUCOMUTASE