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20 Cards in this Set
- Front
- Back
Hexokinase/glucokinase |
1st enzyme in glycolysis
substrate level feedback |
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Phosphofructokinase-1
(PFK1) |
Glycolysis
+: ADP, AMP, and F-2,6-BP -: ATP and Citrate
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Pyruvate Kinase |
Glycolysis
+: F-1,6-BP -: Acetyl-CoA, ATP, and Phosphorylation (in liver only)
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Pyruvate Dehydrogenase
|
-links glycolysis to the TCA cycle
+: dephophorylation (phosphatase is activated by Insulin, PEP, and AMP and deactivated by ATP, NADH, and acetyl- CoA)
-: phosphorylation by pyruvate dehydrogenase kinase
|
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Isocitrate Dehydrogenase |
TCA enzyme converting Isocitrate to alpha-ketoglutarate
+: ADP -:NADH, ATP, and alpha-ketoglutarate |
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Fatty Acid Transport Shuttle |
Carnitine transfer to fatty acid is inhibited by Malonyl-CoA (a product of fatty acid synthesis)
no futile cycle |
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Acetyl CoA Carboxylase |
Converts Acetyl-CoA to Malonyl-CoA
+: Citrate -:AMP-Kinase, palmitoyl-CoA |
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Hormone Sensitive Lipases |
+: cAMP-dependent PKA, and phosphorylated Perilipin A -: Insulin |
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Fatty Acid Synthetase |
Transcription is controlled by insulin |
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Fructose Diphosphatase
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Gluconeogenic enzyme (removed phosphate from F-1,6-BP)
-: F-2,6-BP and AMP |
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Glycogen Phosphorylase |
+: Calcium (from working muscle) and PO4 by cAMP dependent kinase activated by glucagon signaling
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Glycogen Synthase |
+: G-6-P
-: inactivated by cAMP dependent kinase activate by glucagon signaling
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Phosphoenolpyruvate Carboxykinase (PEPCK) |
transcription increased by Glucagon
Transcription decreased by Insulin |
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Pyruvate Carboxylase |
+: acetyl-CoA |
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Lipoprotein Lipase |
+ in adipocytes after meal due to insulin
+ in muscle cells during fasts due to glucagon |
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Glucose-6-Phosphatase |
Gluconeogenesis
Substrate level regulation |
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Cyanide |
Inhibits ETC by binding cytochrome-c-oxidase more strongly than oxygen |
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Oligomycin |
Inhibits ATP synthase by blocking the flow of protos through the Fo subunit |
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Dinitrophenol |
Uncouples the proton pumping from ATP synthesis because it carries ATP across the membrane itself |
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Rotenone
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Prevents transfer of electrons from complex 1 to ubiquinone by blocking the binding site on ubiquinone |