glycosidic bond and composition of:
which of the enzymes is incorrectly paired with its location of function?
isocitrate dehydrogenase and glyoxosome
what does glucagon upregulate?
glycogen phosphorylase A
which steps of glycolosis generate ATP? (2)
1,3 bisphosphate –> 3 phosphoglycerate
phosphoenolpyruvate –> pyruvate
glycogen synthase:
requires glucose-1-P to be activated by UDP
what is correct about the citric acid cycle?
directly generates 2 water molecules/acyl-CoA
the structure shown below is:
fructose-2,6-bisphosphate
triglyceride levels of the 4 lipoproteins
chylomicrons: 85
VLDL: 50
LDL: 10
HDL: 4
which enzyme is mismatched with is function?
lipoamine - deamination
which of the following is true about ketogenesis?
ketogenesis is absent in people with systemic carnitine deficiency
omega oxidation of fatty acids:
involves sequentially alcohol, aldehyde and acid intermediates
identify the ketone bodies (structure)
CH3 - C(=O) - CH2 - C (=O,O-) and
CH3 - C(H,OH) - CH2 - C (=O, O-)
what is thiolase involved in? (4)
what phospho/sphingolipids are found primarily in the outer leaflet of the plasma membrane?
phosphotidylcholine and sphingomyelin
peroxisomal B-oxidation of fatty acids involves:
lioprotein lipase action involves:
activation of the enzyme by alipoprotein CII
pyruvate kinase remains active in muscle during glycogenolysis because:
PFK-1 is downregulated by:
ATP and citrate
which of the following enzymes/pathways is correctly listed with its regualtor?
all of the above
Fehlings solution?
steps of mitochondrial B-oxidation of fatty acids to acetyl CoA:
occur while fatty acids are attached to coenzyme A
pyruvate dehydrogenase:
human G6PD deficiency results in:
which of the following statements about the synthesis of DHA from an essential acid in mamals is (are) correct?
all of the above