Please help me fill out the boxes in the worksheet GlucoseQ1H₂OGlucose 6-phosphateFructose 6-phosphateH₂OFructose 1,6-bisphosphateDietary FatsGlyceraldehyde3-phosphateDihydroxyacetonephosphateP, NADNADH-1,3-bisphosphoglycerateADPATP3-phosphoglycerate2-phosphoglycerateH₂OPhophoenolpyruvate GDP, CO,ADP PATP, HOOpyruvateGTPOxaloacetateGlyconeogenesisGlycerolLactate

The image represents a simplified overview of several interconnected metabolic pathways, including…

Answered: Please help me fill out the boxes in…

Biochemistry

6th Edition

ISBN:9781305577206

Author:Reginald H. Garrett, Charles M. Grisham

Publisher:Reginald H. Garrett, Charles M. Grisham

Chapter18: Glycolysis

Section: Chapter Questions

Problem 14P: Energetic of Fructose-1 ,6-bis P Hydrolysis (Integrates with Chapter 3.) The standard free energy...

See similar textbooks

Similar questions

Choose the enzyme and cofactors involved in the reaction of fructose-1,6-bisphosphate to fructose-6-phosphate in gluconeogenesis. H H-TOPO Fo HOTH HDH HOH MOTOPOP K E H-TOH H OPO Problem 3 of 17 A B Q D E fructose-1,6-bisphosphatase phosphoglucose isomerase glucose-6-phosphatase phosphoglycerate kinase hexokinase
Energetic of Fructose-1 ,6-bis P Hydrolysis (Integrates with Chapter 3.) The standard free energy change (G) for hydrolysis of fructose-1. 6-bisphosphate (FBP) to fructose-S-phosphate (F-6-P) and P: is -16.7 KJ/mol: FBP + H2O fructose-6-P + Pi The standard free energy change (G) for ATP hydrolysis is -30.5 KJ/mol: ATP + H2O ADP + Pj What is the standard free energy change for the phosphofructokinase reaction: ATP + fructose-6-P ADP + FBP b. What is the equilibrium constant for this reaction? c. Assuming the intracellular concentrations of [ATP] and (ADP] are maintained constant at 4 mM and 1.6 mM, respectively, in a rat liver cell, what will be the ratio of [FBP]/[fructose-6-P] when the phosphofructokinase reaction reaches equilibrium?
Handwritten Identify the molecule names, enzyme name, enzyme classification and change in reaction(for glycolysis pathway)
In class, I mentioned that fructose is metabolized differently in the liver compared to glucose. Refer to the figure shown below to calculate the number ofATPs you would expect from the metabolism of fructose in the liver. Show your work! Fructokinase Fructose Fructose-1-P АТР ADP Aldolase B Dihydroxy- acetone phosphate Glyceraldehyde АТР Triose kinase Triose phosphate isomerase ADP 4 - Glyceraldehyde-3-P Glycolysis Руruvate Acetyl-CoA Fatty acids and triglycerides
Alcohol consumption on an empty stomach results in some interesting biochemical as well as embarrassing behavioral alterations. We will ignore the lat t er. Gluconeogenesis falls; there are increases in intracellular ratios of lactate to pyruvate, of glycerol 3- phosphate to dihydroxyacetone phosphate, of glutamate to α - ketoglutarate , and of D-3- hydroxybutyrate to acetoacetate. Hypoglycemia develops rapidly Blood pH also falls. Alcohol consumption by a well - fed individual does not lead to hypoglycemia or alteration in blood pH . (a) Why does ethanol consumption result in the altered ratios? (b) Why does hypoglycemia and blood acidosis result in the hungry individual? (c) Why does the well-fed person not experience hypoglycemia?
Glutamate is derived from which of the following molecules? oxaloacetate pyruvate O 3-phosphoglycerate chorismate O a-ketoglutarate
C Phosphoglycerate enolase coo O H-C-O-P=O CH₂OH 2-Phosphoglycerate This is a (an) d Tyrosine hydroxylase HO coo NH3 L-Tyrosine This is a (an) 0₂ coo C-O-P-C || CH₂ Phosphoenolpyruvate H₂O + HO HO L-DOPA H₂O coo NH3
Please select appropriate word in each bracket Glycogen provides short term energy storage primarily in liver and muscle. Defects in the enzymes that are required for either glycogen synthesis or breakdown therefore affect levels of [ Select ] ["glucose", "glycogen"] in the bloodstream and the amount of glycogen in the liver. This is exemplified by defects in [ Select ] ["glucose-6-phosphatase", "glycogen synthase"] , which is a deficit in breakdown and delivery, whereas mutations compromising [ Select ] ["glycogen synthase", "glycogen debranching enzyme"] result in a defect in synthesis, but defects in either enzyme produce [ Select ] ["hypoglycemia", "hypothermia"].
Acetyi CoA Oxaloncetate CoA NADH Citrate NAD Isocitrate Malate Funiarate NAD co NADH FADH, FAD a- Ketoghutarate Succinate co, NAD+ ATP Succinyl CuA NADH ADP - P For each molecule of glucose (C6H12O6) oxidized by cellular respiration, how many moles of CO2 are released in the citric acid cycle? (see the figure above) а. 2 b. 4 с. 6 d. 0 е. 3
Which of the following monosaccharide phosphates is NOT produced in the pentose phosphate pathway? O seduheptulose-7-phosphate O mannose-6-phosphate O ribose-5-phosphate O erythrose-4-phosphate
Which of the following glycolytic enzymes catalyzes the conversion of fructose-1,6-bisphosphate into the two product molecules dihydroxyacetone phosphate, and glyceraldehyde-3-phosphate? phosphoglycerate kinase pyruvate kinase malate dehydrogenase aldolase phosphofructokinase
The coenzyme NAD+ is required for which glycolytic reaction shown below? Oglyceraldehyde-3-P→ 1,3-bisphosphoglycerate glucose glucose-6-P fructose-6-P→ fructose-1,6-BP 2-phosphoglycerate → phosphoenolpyruvate

SEE MORE QUESTIONS

Recommended textbooks for you

Biochemistry

ISBN:

9781305577206

Author:

Reginald H. Garrett, Charles M. Grisham

Publisher:

Cengage Learning

Biochemistry

ISBN:

9781305577206

Author:

Reginald H. Garrett, Charles M. Grisham

Publisher:

Cengage Learning

SEE MORE TEXTBOOKS