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EC Tree
IUBMB Comments D-Glucose, D-mannose, D-fructose, sorbitol and D-glucosamine can act as acceptors; ITP and dATP can act as donors. The liver isoenzyme has sometimes been called glucokinase.
The taxonomic range for the selected organisms is: Solanum tuberosum The expected taxonomic range for this enzyme is: Eukaryota, Bacteria, Archaea
Synonyms
hexokinase, hexokinase ii, hexokinase 2, hexokinase i, hk ii, hxk, liver glucokinase, hexokinase 1, hexokinase-2, hkdc1,
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ATP-D-hexose 6-phosphotransferase
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ATP-dependent hexokinase
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brain form hexokinase
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glucose ATP phosphotransferase
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hexokinase (phosphorylating)
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hexokinase type IV
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hexokinase type IV glucokinase
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hexokinase, tumor isozyme
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kinase, hexo- (phosphorylating)
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muscle form hexokinase
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phospho group transfer
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-, -, -, -, -, -, -, -, -, -, -, -, -, -, -, -
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ATP:D-hexose 6-phosphotransferase
D-Glucose, D-mannose, D-fructose, sorbitol and D-glucosamine can act as acceptors; ITP and dATP can act as donors. The liver isoenzyme has sometimes been called glucokinase.
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ATP + D-glucose
ADP + D-glucose 6-phosphate
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?
D-fructose + ATP
ADP + D-fructose 6-phosphate
D-glucose + ATP
ADP + D-glucose 6-phosphate
D-glucose + ATP
D-glucose 6-phosphate + ADP
D-mannose + ATP
ADP + D-mannose 6-phosphate
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HK1: 53% of the activity with glucose, HK2: 22% of the activity with glucose, HK3: 45% of the activity with glucose
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?
GTP + D-glucose
GDP + D-glucose 6-phosphate
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UTP + D-glucose
UDP + D-glucose 6-phosphate
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D-fructose + ATP
ADP + D-fructose 6-phosphate
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HK3: 16% of the activity with glucose
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D-fructose + ATP
ADP + D-fructose 6-phosphate
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HK1: 4% of the activity with glucose, HK2: 3% of the activity with glucose
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?
D-fructose + ATP
ADP + D-fructose 6-phosphate
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HK3: 5% of the activity with glucose
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D-glucose + ATP
ADP + D-glucose 6-phosphate
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D-glucose + ATP
ADP + D-glucose 6-phosphate
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D-glucose + ATP
D-glucose 6-phosphate + ADP
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glucose metabolism
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D-glucose + ATP
D-glucose 6-phosphate + ADP
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organ- and development-specific changes in the abundance of the various enzyme forms contribute to the regulation of hexose metabolism
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D-glucose + ATP
D-glucose 6-phosphate + ADP
D-glucose + ATP
D-glucose 6-phosphate + ADP
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glucose metabolism
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D-glucose + ATP
D-glucose 6-phosphate + ADP
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organ- and development-specific changes in the abundance of the various enzyme forms contribute to the regulation of hexose metabolism
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?
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ADP
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ADP
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isoenzymes HK1 and HK2, competitive to ATP, 0.5 mM: 4-5fold inhibition
D-glucose 6-phosphate
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isoenzyme HK1, not HK2, noncompetitive to glucose
D-glucose 6-phosphate
hexokinase 1
additional information
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no inhibition of hexokinase 2: D-glucose 6-phosphate
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additional information
no inhibition of hexokinase 2: D-glucose 6-phosphate
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additional information
no inhibition of hexokinase 2: D-glucose 6-phosphate
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additional information
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D-glucose 6-phosphate has no effect
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additional information
D-glucose 6-phosphate has no effect
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additional information
D-glucose 6-phosphate has no effect
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0.09
ATP
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HK1
8.7
D-fructose
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HK3
0.035
D-glucose
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HK3
0.038
D-mannose
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HK3
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4 - 4.1
D-glucose 6-phosphate
0.04
ADP
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HK1
4
D-glucose 6-phosphate
pH 7, hexokinase 1
4.1
D-glucose 6-phosphate
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HK1, at pH 7
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6.7 - 9
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pH 6.7: about 40% of activity maximum, pH 9: about 70% of activity maximum, isoenzyme HK1
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SwissProt
brenda
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brenda
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brenda
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brenda
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developing
brenda
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organ- and development-specific changes in the abundance of the 3 isoenzymes
brenda
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malfunction
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transgenic Solanum tuberosum roots are altered in their hexokinase activity by transformation with an hexokinase cDNA in sense or antisense orientation. Altering root hexokinase activity levels impacts on growth rate and hexokinase has a high flux control coefficient over glucose phosphorylation but does not control glycolytic flux or respiration rate. It is concluded that futile cycling of hexose-phosphate can be partially responsible for the differences in energetic status in roots with high and low hexokinase activity and possibly cause the observed alterations in growth in transgenic roots
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HXK1_SOLTU
498
1
54130
Swiss-Prot
Secretory Pathway (Reliability: 2 )
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66000
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HK1 and HK2, gel filtration
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-180°C, 2 months, stable
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3 isoenzymes: HK1: 140fold, HK2: 40fold, HK3: 25fold
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using hydrophobic-interaction chromatography on a butyl-sepharose 4 Fast Flow column. Main hexokinase isoform is purified to homogeneity using further chromatographic separations on red dye, DEAE Fractogel, hydroxyapatite, cibacron blue, and MonoQ matrices
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Renz, A.; Merlo, L.; Stitt, M.
Partial purification from potato tubers of three fructokinases and three hexokinases which show differing organ and developmental specificity
Planta
190
156-165
1993
Solanum tuberosum
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brenda
Renz, A.; Stitt, M.
Substrate specificity and product inhibition of different forms of fructokinases and hexokinases in developing potato tubers
Planta
190
166-175
1993
Solanum tuberosum
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brenda
Claeyssen, E.; Rivoal, J.
Isozymes of plant hexokinase: occurrence, properties and functions
Phytochemistry
68
709-731
2007
Saccharomyces cerevisiae, Solanum lycopersicum, Pisum sativum, Solanum tuberosum, Solanum tuberosum (O64390), Solanum tuberosum (Q9SQ76), Triticum aestivum, Zea mays, Solanum chacoense, Capsicum chacoense, Arabidopsis thaliana (Q9FZG4), Arabidopsis thaliana
brenda
Moisan, M.; Rivoal, J.
Purification to homogeneity and characterization of nonproteolyzed potato (Solanum tuberosum) tuber hexokinase 1
Botany
89
289-299
2011
Solanum tuberosum
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brenda
Claeyssen, E.; Dorion, S.; Clendenning, A.; He, J.Z.; Wally, O.; Chen, J.; Auslender, E.L.; Moisan, M.C.; Jolicoeur, M.; Rivoal, J.
The futile cycling of hexose phosphates could account for the fact that hexokinase exerts a high control on glucose phosphorylation but not on glycolytic rate in transgenic potato (Solanum tuberosum) roots
PLoS ONE
8
e53898
2013
Solanum tuberosum
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