Test 19 - Biochem Flashcards

(37 cards)

0
Q

Tetrahydrobiopterin is a cofactor in the synthesis of what?

1500

A

1) Tyrosine
2) DOPA
3) Serotonin
4) N.O.

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1
Q

In the Urea cycle, which cofactor is required to activate Carbamoyl Phosphate Synthase I

A

N-acetylglutamate

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2
Q

Which enzyme converts procollagen to tropocollagen by removing the globular portions in the extracellular space?

1245

A

Procollagen peptidase

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3
Q

Which enzyme is affected in Riboflavin (B2) deficiency?

1807

A

Succinate Dehydrogenase

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4
Q

Proprionic acid is the intermediate in the catabolism of what?

1340

A

Branched chain amino acids

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5
Q

Which enzyme is responsible for the conversion of proionyl CoA to Methylmalonyl CoA and congenital deficiency can lead to proprionic acidemia?

1340

A

Proprionyl CoA Carboxylase

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6
Q

What is the function of the 16s rRNA sequence in prokaryotes? (2)

1972

A

1) 16s is found in the 30s subunit.
2) 16s rRNA contains a sequence complementary to the Shine-Delgarno sequence on mRNA. Binding of these 2 is needed for initiation of protein translation.

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7
Q

Which G protein is involved with IP3 second messenger system?

1122

A

Gq

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8
Q

Activation of Phospholipase C forms what?

1122

A

DAG and IP3

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9
Q

What bond type stabilizes the secondary structure of proteins?

2026

A

Hydrogen bonds

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10
Q

What are the very strong covalent bonds between 2 cysteine residues within the same polypeptide chain that enhance a proteins ability to withstand degradation?

2026

A

Disulfide Bonds

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11
Q

What is an immediate source of nitrogen for urea in the urea cycle?

1481

A

Aspartate

NH3

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12
Q

Deficiency of which enzyme can cause increased lactate levels in the blood?

A

Pyruvate dehydrogenase

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13
Q

Which enzyme catalyzes the first step in the B-oxidation pathway and is the most commonly deficient enzyme?

1888

A

Acyl-CoA Dehydrogenase

(pt. unable to break down fatty acids during prolonged fasting.

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14
Q

Fetal hemoglobin binds oxygen with a higher affinity due to its inability to interact with what?

1387

A

2-3, DPG.

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15
Q

Which RNA polymerase activity is restricted to the Nucleolus?

2039

A

RNA Polymerase I

16
Q

DNA synthesis only occurs in which direction?

1418

17
Q

Which substrates accumulate in lead poisoning?

1157

A

1) Protoporphyrin

2) Delta-ALA

18
Q

Delta-aminolevulinic acid synthase requires which cofactor?

A

B6 (Pyridoxal phosphate)

19
Q

Supplementation of what can moderately increase dTMP levels, thereby reducing erythroid precursor cell apoptosis due to deficiency of folate?

1847

20
Q

Thiamine deficiency can be diagnosed how?

A

Measure erythrocyte transketolase activity

21
Q

Thiamine (B1) is a cofactor for which enzyme reactions?

FA: 92

A

1) Pyruvate dehydrogenase
2) Alpha-ketoglutarate dehydrogenase
3) Transketolase
4) Branched-chain ketoacid dehydrogenase

22
Q

Which functions does DNA Polymerase I have? (3)

1434

A

1) 5’-3’ exonuclease
2) 3’-5’ exonuclease
3) 5’-3’ polymerase

23
Q

What is meant by bacterial mRNA can be polycistronic? Example?

1485

A
  • 1 mRNA can code for several proteins

- bacterial lac operon

24
In patients with methemoglobinemia, what is normal in the blood? 1416
Partial pressure of oxygen because the amount of oxygen dissolved in the plasma is the same.
25
What is the most abundant amino acid found in collagen? 1248
Glycine
26
What is a transcription factor (capable of DNA binding) that is associated with Neurofibromatosis? 2031 FA: 232
N-myc
27
Beta thalassemia is caused by mutations which result in what? 1940
Defective transcription, processing, and translation of Beta-globin mRNA.
28
Which vitamin supplementation should be considered in a patient with Measles? 1045
Vitamin A
29
What is the function of ApoE 3 & 4? 2064
VLDL and Chylomicron remnant uptake by liver cells
30
What is the function of ApoA-I 2064
LCAT activation
31
What is function of ApoB-48? 2064
Chylomicron assembly and secretion by the intestines
32
What is the function of ApoB-100? | 2064
LDL particle uptake by hepatic cells
33
What is the function of ApoC II? 2064
Lipoprotein Lipase activation
34
What are the symptoms of an infant with classic galactosemia?
Vomiting, lethargy, and failure to thrive soon after breastfeeding is begun.
35
What enzyme is deficient in classic galactosemia? What reaction does it facilitate? 1071
Deficiency: Galactose 1-phosphate uridyl transferase Reaction: Galactose 1-Phosphate -> UDP- Galactose
36
Which disorder can result from constitutive action of Tyrosine Kinase which results in increased STAT. 8540
Myeloproliferative disorders