Metabolism Reactions Flashcards
Glucose –> Phosphoenolpyruvate (What process is this?)
Initial steps of Glycolysis
Phosphoenolpyruvate –> Pyruvate (Enzyme)
Pyruvate Kinase
Pyruvate –> Oxaloacetate (Enzyme)
Pyruvate Carboxylase
Pyruvate –> Lactic acid (Enzyme)
Lactate Dehydrogenase
Pyruvate –> Acetyl CoA, which enters TCA cycle (Enzyme)
Pyruvate Dehydrogenase
Galactose –> Galactose 1-Phosphate
Galactokinase (defiency = mild galactosemia)
Galactose -1-Phosphate –> Glucose 1-phosphate
Galactose 1-phosphate uridyltransferase (defiency severe galactosemia)
Glucose –> Glucose 6-Phosphate (Liver, Beta cells of pancreas)
Glucokinase
Glucose-6-phosphate –> Glucose
Glucose-6-phosphatase (Von Gierke’s)
Glucose-6-phosphate –> 6-phosphogluconate/6phosphogluconolactone
Glucose 6-phosphate dehydrogenaase (G6PD) (Deficiency = no HMP shunt)
Fructose -6phosphate –> Fructose 1,6, bisphosphate
Phosphofructokinase -1 (Defiency= no glycolysis)
Fructose 1,6, bisphosphate –> Fructose 6-phosphate
Fructose 1,6, bisphosphatase
Fructose –> Fructose 1-phosphate
Fructokinase (deficiency = essential fructosuria)
Fructose 1-phosphate –> Glyceraldehyde/DHAP
Aldolase B
HMG CoA –> Mevalonate –> Cholesterol
HMG CoA reductase
Oxaloacetate –> Phosphoenolpyruvate (PEP)
PEP Carboxykinase
Isocitrate –> alpha-ketoglutarate (Within TCA cycle)
Isocitrate Dehydrogenase
Oxaloacetate –> Citrate (TCA Cycle)
Citrate Synthase
Alpha-ketoglutarate –> Succinyl Co-A
Alpha ketoglutrate Dehydrogenase
Ornithine –> Citrulline (Urea Cycle)
Ornithine Transcarbamylase
Glucose –> Glucose 6-Phosphate (Tissues, NOT liver/beta cells of pancreas)
Hexokinase
What are the enzymes and end product when the body is in a FASTING state
Increased glucagon, CAMP, Protein Kinase A, FBPase-2 –> More Gluconeogenesis
What are the enzymes and end product when the body is in a FED state
Increased insulin, Decreased CAMP, PKA, FBPase-2 –> More Glycolysis
Pyruvate –> Alanine
ALT
O2 –> O2* (reactive species, superoxide)
NADPH
O2* –> H2O2
Superoxide dismutase
H2O2 –> HOCL
Myeloperoxidase
Glucose –> Sorbitol
Aldose Reductase
Sorbitol –> Fructose
Sorbitol Dehydrogenase
Ornithine + Carbamoyl Phosphate –> Citrulline
Ornithine Transcarbamylase
CO2 + NH3 –> Carbamoyl Phosphate
Carbamoyl Phosphate Synthetase I (rate-limiting of urea cycle)
Homocysteine + B6 –> Cystathionine –> Cysteine
Cystathionine Synthase
Homocysteine + B12 –> Methionine
Homocysteine Methyltransferase
Blocked degradation of branched amino acids (Isoleucine, Leucine, Valine)
Maple Syrup Urine Disease, increased alpha-ketoacids in blood. Sxn: CNS defects, intellectual disability, death, urine smells like maple syrup/burnt sugar. Tx: Restrict isoleucine, leucine, valine, supplement with thiamine
Glycogen –> Glucose
Glycogen Phosphorylase (upregulated by Glucagon, Calcium, Calcium-calmodulin in muscle during contraction)
Glucose –> Glycogen
Glycogen Synthase (Upregulated by Insulin)
Fed State (Insulin release)
Glycolysis and aerobic respiration
Fasting State (Glucagon release) or Adrenaline
Hepatic glycogenolysis (major), Hepatic Gluconeogenesis, Adipose release of free fatty acids