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GLUT 2
low affinity transporter in hepatocytes and pancreatic cells
captures excess glucose primarly for storage
GLUT 4
in adipose tissues and muscle and responds to glucose concentration in peripheral blood
Glycolysis
cytoplasmic pathway converst glucose into two pyruvate molecules, releasing energy captured in two substrate level phsophorylation and oxidation reaction
hexokiases
widely distributed in tissues and is inhibited by its product G6P
glucokinase
found in liver cells and pancreatic B islet cells
where is heoxkinases present
in most tissues
where is glucokinase present
in hepatocytes and pancreatic B ilets
PFK 1
rate limiting enzyme and main control point in glycolysis. phosphorylate F6P to F16BP activated by AMP, F26BP inhibited by ATP and citrate
3 phosphoglycerale kinase
transfer high energy phosphate from 13 PPG to ADP forming ATP and 3Phosphoglycerate
Pyruvate Kinase
activated by F16BP
feed forward activation
product of earlier reaction prepare, later reaciton in glycolysis
PFK2
produce F26BP actiavtes PFK 1, activated insulin and inhibited by glucagon
Glyveraldehyde 3 Phosphate Dehydrogenase
produce NADH, feed into electron transport chain
3 Phosphoglycerate kinase and pyruvate kinase
each perform substrate level phsophorylation, placing P1 onto ADP to form ATP
galactose
comes from lactose in milk, it is trapped in cell by galactokinase and converted to glucose 1 phosphate via galactose 1 phosphate.
Fructose
comes from honey, fruit and sucrose. It is trapped in cell by fructokinase and then cleaved by aldolase B to form glyceraldehyde and DHAP
Pyruvate Dehydrognease
refer to complex enzymes convert pyruvate to acetyl CoA
Glycogen
branced polymer of glucose
Glycogenesis
syntehsis fo glycogen granules
Glycogen synthesis
creates alpha 1,4 glycosidic links between glucose molecules. It is activated by insulin in liver and muscle
Branching enzyme
moves a block of oligoglucose form one chain and adds it to the growign glycogen as a new branc using an alpha 1,6 glycosidic
Glycogenolysis
process fo breaking down glycogen
glycogen phosphorylase
removes single glucose one phosphate molecules by breaking alpha 1,4 glycosidic links.
Debranching enzyme
moves a block of oligoglucose form one branch and connects it to the chain using an alpha 1,4 glycosidic link.
Isoforms
slightly different versions of the same protein
glycogen storage disease
disease characterized by accumulation or lack of glycogen in one or more tissues
Glucogenic amino acids
converted into intermediates that feed into glucogensis
Ketogenic amino acid
used as alternative fuel
Important substrate for gluconeogenesis
Glycerol 3 phosphate, lactate and glucogenic amino acid
Pyruvate carboxylase
converst pyruvate into oxaloacetate, which is converted by phosphoenolase pyruvate by phosphoenolpyruvate.
Fructose 1,6 biphosphatase
converts fructose 1,6 biphosphate to fructose 6 phosphate, by passing phosphofructokinase 1. This is the rate limiting step of gluconeogensis
Glucose 6 phosphotase
converst glucose 6 phosphate to free glucose, bypassing glucokinase.
Pentose Phosphate Pathway
generating NADPH and sugar for biosynthesis
Functions of NADPH
biosyntehsis fatty acid and cholesterol
Assiting cellular bleach production in certain WBC, contribute to baterial activity
Maintence of supply of reduced glutathione to protect against reactive oxygen species
Glutathione
reducing agent hlep reverse radical formation before damage is done to cell