Protein family
Protein sequence
Protein function
Catalytic activity
EC number
EC number description
2.7.1.11
Transferases;
Transferring phosphorus-containing groups;
Phosphotransferases with an alcohol group as acceptor;
6-phosphofructokinase
PDB | Resolution (Å) | PDB name |
---|---|---|
4OMT | 6.0 | Crystal structure of human muscle phosphofructokinase (dissociated homodimer) |
GO ontology | GO term | GO description |
---|---|---|
Biological Process | GO:0061621 | canonical glycolysis |
Biological Process | GO:0030388 | fructose 1,6-bisphosphate metabolic process |
Biological Process | GO:0006002 | fructose 6-phosphate metabolic process |
Biological Process | GO:0042593 | glucose homeostasis |
Biological Process | GO:0005980 | glycogen catabolic process |
Biological Process | GO:0093001 | glycolysis from storage polysaccharide through glucose-1-phosphate |
Biological Process | GO:0006096 | glycolytic process |
Biological Process | GO:0061615 | glycolytic process through fructose-6-phosphate |
Biological Process | GO:0046716 | muscle cell cellular homeostasis |
Biological Process | GO:0032024 | positive regulation of insulin secretion |
Biological Process | GO:0045944 | positive regulation of transcription by RNA polymerase II |
Molecular Function | GO:0003872 | 6-phosphofructokinase activity |
Molecular Function | GO:0016208 | AMP binding |
Molecular Function | GO:0005524 | ATP binding |
Molecular Function | GO:0070061 | fructose binding |
Molecular Function | GO:0070095 | fructose-6-phosphate binding |
Molecular Function | GO:0042802 | identical protein binding |
Molecular Function | GO:0019900 | kinase binding |
Molecular Function | GO:0046872 | metal ion binding |
Molecular Function | GO:0048029 | monosaccharide binding |
Cellular Component | GO:0005945 | 6-phosphofructokinase complex |
Cellular Component | GO:0016324 | apical plasma membrane |
Cellular Component | GO:0005829 | cytosol |
Cellular Component | GO:0016020 | membrane |
Cellular Component | GO:0005634 | nucleus |
Cellular Component | GO:0097228 | sperm principal piece |
InterPro | InterPro name |
---|---|
IPR000023 | Phosphofructokinase domain |
IPR009161 | ATP-dependent 6-phosphofructokinase, eukaryotic-type |
IPR015912 | Phosphofructokinase, conserved site |
IPR022953 | ATP-dependent 6-phosphofructokinase |
IPR035966 | Phosphofructokinase superfamily |
IPR041914 | ATP-dependent 6-phosphofructokinase, vertebrate-type |
Pfam | Pfam name |
---|---|
PF00365 | Phosphofructokinase |
Reactome | Reactome Name | Node type | Reactome Root | Reactome Root Name |
---|---|---|---|---|
R-HSA-70171 | Glycolysis | Internal node | R-HSA-1430728 | Metabolism |
Location | ECO term | Pubmed |
---|---|---|
Cytoplasm | ECO:0000255 |
HPO ID | HPO name |
---|---|
HP:0000007 | Autosomal recessive inheritance |
HP:0000790 | Hematuria |
HP:0000952 | Jaundice |
HP:0001081 | Cholelithiasis |
HP:0001324 | Muscle weakness |
HP:0001878 | Hemolytic anemia |
HP:0001903 | Anemia |
HP:0001923 | Reticulocytosis |
HP:0001997 | Gout |
HP:0002149 | Hyperuricemia |
HP:0002486 | Myotonia |
HP:0003202 | Skeletal muscle atrophy |
HP:0003236 | Elevated circulating creatine kinase concentration |
HP:0003326 | Myalgia |
HP:0003388 | Easy fatigability |
HP:0003546 | Exercise intolerance |
HP:0003557 | Increased variability in muscle fiber diameter |
HP:0003573 | Increased total bilirubin |
HP:0003621 | Juvenile onset |
HP:0003710 | Exercise-induced muscle cramps |
HP:0003738 | Exercise-induced myalgia |
HP:0008305 | Exercise-induced myoglobinuria |
HP:0008967 | Exercise-induced muscle stiffness |
HP:0009020 | Exercise-induced muscle fatigue |
HP:0009051 | Increased muscle glycogen content |
HP:0011463 | Childhood onset |
HP:0012544 | Elevated circulating aldolase concentration |
HP:0025435 | Increased circulating lactate dehydrogenase concentration |
HP:0030271 | Reduced erythrocyte 2,3-diphosphoglycerate concentration |
Disease name | MONDO ID | ICD10 | ICD10 chapter | OMIM | Orphanet |
---|---|---|---|---|---|
glycogen storage disease vii | MONDO:0009295 | E74 | chapter4, Endocrine, nutritional and metabolic diseases | OMIM:232800 | Orphanet:371 |