After oxaloacetate has been formed from pyruvate (gluconeogenesis), it may exit the mitochondria and enter the cytosol via the _____ shuttle
Where in the cell does conversion of oxaloacetate -> PEP take place?_____
One component of bile is _____, which is the major bile pigment
Atrophy via decrease in cell size may occur via _____ degradation of cytoskeleton
What is the charge of the amino acid histidine at body pH?_____
Free radicals may be eliminated via _____ (e.g. reduced glutathione and vitamins A, C, and E)
Conjugated (direct) bilirubin is excreted in bile and metabolized by bacterial flora, producing _____
Albinism is usually due to decreased _____ activity or defective tyrosine transport
What vitamin is derived from the amino acid tryptophan?_____
Reduced tetrahydrofolate (methyl-THF) is the _____ form of THF
TCA cycle reactions and regulation
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Electron transport chain and oxidative phosphorylation
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Pentose phosphate pathway
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Gluconeogenesis
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Glycogen metabolism
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Amino acid metabolism
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Integration of metabolic pathways
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Fed state vs. fasting state metabolism
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Exercise metabolism
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Alcohol metabolism
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Metabolic adaptations in starvation
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Metabolic disorders overview
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