Some Test1.pdf Final Past Papers Flashcards
(39 cards)
Which enzyme is allosterically modulated by malonyl-CoA? A. Acylcarnitine translocase B. Carnitine palmitoyl-transferase II C. Carnitine palmitoyl-transferase I D. Acyl-CoA synthetase E. ATP Citrate Lyase
C. Carnitine palmitoyl-transferase I
Select the statements valid for the bile acids:
1. In bile acid synthesis, the side chain of cholesterol is oxidized
2. In bile acid synthesis, carbon atoms 7 and 12 are methylated
3. The secondary bile acids are produced from primary bile acids through deconjugation and dehydroxylation at carbon atom 7
4. Glycocholic and taurocholic acid are primary bile acids
5. Lithocholic acid is formed from glycocholic acid by bacteria in the large intestine
A: 1,2,3 B: 1,3,4
C: 1,3,5 D: 2,4,5
E: all of the above
B: 1,3,4 (C7 and 12 are hydroxylated, not methylated, and lithocolic acid is derived from chenodeoxycholyl-CoA)
Which statements are true?
1. Cholesterol is formed from HMG-CoA synthesized in the mitochondria
2. Cholesterol is formed from HMG-COA synthesized in the cytosol
3. Mevalonate is formed from HMG-CoA by decarboxylation
4. NADPH is needed for mevalonate synthesis
5. Production of isopentenyl-pyrophosphate also requires a decarboxylase
A: 2,4,5 B: 1,2,3,4,5
C: 2,3,4 D: 2,3,4,5
E: 1,4,5
A: 2,4,5
(1: HMG-CoA from the mitochondria is for ketone bodies, not for cholesterol, 3: mevalonate is formed by reducing HMG-CoA, requiring NADPH via HMG-CoA Reductase)
Which of the following is NOT true of the fatty acid elongation system of vertebrate cells?
A: it is located in the smooth endoplasmic reticulum
B: it uses malonyl-CoA as a substrate
C: it produces stearoyl-CoA by the extension of palmitoyl-CoA
D: the immediate precursor of the added carbons is acetyl-CoA
E: it involves the same 4 step sequence seen in the fatty acid synthase complex
D: the immediate precursor of the added carbons is acetyl-CoA(correctly, it’s acyl-CoA)
If an aerobic organism (e.g. bacterium E. Coli) were fed each of the following four compounds as a source of energy, the energy yield per mole from these molecules would be, in order:A: glucose > alanine > palmitate (16:0)B: palmitate > alanine > glucoseC: palmitate > glucose > alanineD: glucose > palmitate > alanineE: alanine > glucose > palmitate
C: palmitate > glucose > alanine
(my logic is that alanine can be converted to pyruvate, which will miss out on the ATP formation during glycolysis that otherwise occurs with glucose metabolism)
Transport of fatty acids from the cytoplasm to the mitochondrial matrix requires:
A: ATP, coenzyme A, and hexokinase
B: ATP, carnitine, and coenzyme A
C: carnitine, coenzyme A, and hexokinase
D: ATP, carnitine, and pyruvate dehydrogenase
E: ATP, coenzyme A, and pyruvate dehydrogenase
B: ATP, carnitine, and coenzyme A
Aminophenazone N-demethylation is catalyzed by:A: cytochrome oxidaseB: catalaseC: a cytochrome P450 isoenzymeD: superoxide dismutaseE: S-adenosyl methionine
C: a cytochrome P450 isoenzyme(a CYP monooxygenase)
Activation of protein kinase C1. can be Ca2+ dependent2. can be Ca2+ independent 3 can be induced by diacylglycerol4. can be stimulated by phorbol esthers5. can be phospholipid dependentA: 1,3,4 B: 2,3,4,5C: 1,2,3,4,5 D: 1,5E: 2
C: 1,2,3,4,5
(Pretty sure on this, but other person who did this chose A instead. However, Torocsik said that some PKC types that we don’t need to know don’t even need calcium to be active)
Which factor is NOT involved in the muscle contraction following signal transmission in the neuromuscular junction? A. Ryanodine receptor B. Dihydropyridine receptor C. Nicotinic receptor D. Beta receptor E. L-type Ca2+ channel
D. Beta receptor(assuming they’re talking about the adrenergic one and not something obscure)
Which factor is involved in the efflux of Ca2+ from the mitochondria? A. Ca-uniporter B. IP3 receptor C. Na+-Ca2+ exchange D. T-channel E. Ryanodine receptor
C. Na+-Ca2+ exchange
Which of the following receptors functions as a Ca2+ channel?
A. Nicotinic receptor in the skeletal muscle
B. alpha1 receptor of smooth muscle cells in the blood vessel wall
C. NMDA receptor in the CNS
D. D2 receptor in the striatum
E. muscarinic receptor in the heart
C. NMDA receptor in the CNS
(NMDA is permeable to univalent and divalent cations, AMPA is permeable to univalent. D2 is a Gi GPCR, nicotinic receptors are for univalent cations)
Which Ca2+ channel is rapidly inactivated in the heart?A: L B: N C: P D: T E: cholinergic nicotinic receptor
D: T
not sure why the person who did this before said the L-type was correct…
Which of the following mechanisms are characteristic for the ER? 1. SERCA 2. PMCA 3. IP3 Receptor 4. Ryanodine receptor 5. Na+-Ca2+ exchanger A. 1,2,3 B. 1,3,5 C. 2,3,4 D. 1,3,4 E. 3,4,5
D. 1,3,4
Which statements are true for the IP3 receptor? 1. it is localized both in the plasma membrane and the ER 2. it is a calcium channel 3. it has 4 Ca2+ binding sites 4. it binds ATP 5. it is activated by phospholipase C A: 1,3,5 B: 2,4,5 C: 2,3,4 D: 1,2,3 E: 3,4,5
B: 2,4,5
2 and 5 are definitely true, the ATP binding is new to me but no other options…
Which statement is NOT true concerning the ryanodine receptor?
A. It has a Ca2+ channel
B. It has 4 subunits
C. It is the largest ion channel
D. It is regulated by calmodulin
E. The same isoform is present in the heart and skeletal muscle
E. The same isoform is present in the heart and skeletal muscle
(skeletal muscle = RYR I, heart = RYR 2)
Which statement is true concerning malignant hyperthermia?
1. it is characterized by rigidity of skeletal muscles
2. it is a consequence of abnormal CNS thermoregulation
3. it is the consequence of the mutation of the ryanodine receptor
4. it can be treated with Ca2+ channel blockers
5. it is accompanied by intensive lactate production in the muscle
A: 1,3,5 B: 2,4,5
C: 1,2,4 D: 3,4,5
E: 1,4,5
A: 1,3,5
Which of the following conversions requires more than one step?
1. alanine -> pyruvate
2. Glutamate -> alpha ketoglutarate
3. asparate -> oxaloacetate
4. proline -> glutamate
5. phenylalanine -> succinate
A: 1,2,4 B: 1,3,5C: 2,4,5 D: 1,4,E: 4,5
E: 4,5
alanine -> pyruvate in the same reactions as both Glu -> alphaKG and Asp -> Oxaloacetate. Transaminase rxns
Select the valid statements:
1. S-adenosylmethionine provides methyl-group for the synthesis of epinephrine from norepinephrine
2. S-adenosylmethionine provides methyl-group for the synthesis of phosphatidylcholine from phosphatidylethanolamine
3. S-adenosylmethionine provides methyl-group for the synthesis of dTMP from dUMP
A: 1,2 B: 1,2,3
C: 1 D: 2,3
E: 1,2
A: 1,2
Phenylketonuria is a consequence of: 1. dihydrobiopterin reductase 2. vitamin B6 deficiency 3. phenylalanine hydroxylase 4. defective synthesis of biopterin 5. vitamin C deficiency A: 2,3,4 B: 1,3,4 C: 3,4,5 D: 1,4,5 E: 2,4,5
B: 1,3,4
I believe this is correct but just poorly worded. It should say DEFICIENCY of 1 and 3, while 4 is the only one that is worded correctly.
Which of the following agents and enzymes are required for the synthesis of cystein? 1. methionine 2. adenosylhomocysteinase 3. serine 4. cystathione synthase 5. cystathionase A: all B: 1,2,3,5 C: 1,3,4,5 D: 3,4,5 E: 1,4,5
C: 1,3,4,5
Which enzyme is NOT involved into the heme biosynthesis? A: heme oxygenase B: delta-aminolevulinic acid synthase C: delta-aminolevulinic acid dehydratase D: urophorphyrinogenase III synthase E: urophorphyrinogenase III cosynthase
A: heme oxygenase
(don’t need to know all those other enzymes if you just know that heme oxygenase is part of breaking down heme, not building it)
Glutathione is a(n)
A. product of glutamate and methionine
B. tripeptide of glycine, glutamate, and cysteine
C. enzyme essential in the synthesis of glutamate
D. methyl-group donor in many biosynthetic pathways
B. tripeptide of glycine, glutamate, and cysteine
Which of the listed interrelations are valid for the following two statements:
- The regeneration of S-adenosylmethionine (SAM) does not require energy
- Methyl group is directly transferred from methyl H4folate to S-adenosylhomocysteine
A: Statement 1 and 2 are both valid, and 1 is the consequence of 2
B: Neither statement is valid
C: Statements 1 and 2 are both valid, but there is no causative relation between them
D: Statements 1 is valid, but 2 is not
E: Statement 2 is valid, but 1 is not
B: Neither statement is valid
ATP is required, and methyl from methyl H4folate is transferred to HomoCys, not S-adenosylhomocysteine
What is the consequence of inherited adenosine deaminase deficiency?
A. gout
B. mental retardation with self mutilation
C. immunodeficiency
D. muscle cramps
E. orotic aciduria
C. immunodeficiency