Final Review: Seidler Slides Flashcards

0
Q

What is the agent & target for glycation?

A
Agents = Carbonyls, Aldehydes/Ketones
Targets = Lys, Arg, Cys
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1
Q

What is the agent & target for oxidation?

A
Agent = Hydrogen peroxide, Hydroxyl radical, Super oxide anion radical
Targets = Cys, Met
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2
Q

What is the agent & target for nitration?

A
Agent = NO [-ONOO, NO2]
Target = Tyr
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3
Q

What is the agent & target for nitrosylation?

A
Agents = NO [-ONOO, NO2]
Targets = Cys
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4
Q

What is the agent & target for sulfhydration?

A
Agents = H2S-->HS radical (Hydrogen sulfide)
Target = Cys
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5
Q

What is the agent & target for succination?

A
Agent = Fumarate
Target = Cys
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6
Q

For O-GlcNacylation, which residues must be modified?

A

Thr-229

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7
Q

For S-nitrosylation, what residues must be modified?

A

Cys-152

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8
Q

For N-acetylation, what residues must be modified?

A

Lys-117, 227, 251

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9
Q

Which components of the ATPase are in the F1 unit?

A

All the greek letters (alpha, beta, gamma, delta, epsilon)

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10
Q

What does the F1 unit do?

A

Makes the ATP

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11
Q

Which components of the ATPase are in the F0 unit?

A

All regular letters (A, B, C)

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12
Q

What does the F0 unit do?

A

Translocates proteins

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13
Q

Which enzyme converts ornithine to citrulline?

A

Ornithine Transcarbamoylase with the addition of Cabamoyl phosphate
(Done in mitochondrial matrix)

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14
Q

What enzyme converts citrulline to argininosuccinate?

A

Arginosuccinate Synthetase with addition of Aspartate

cytoplasm

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15
Q

What enzyme converts Argininosuccinate to Arginine?

A

Argininosuccinate Lyase with release of Fumarate

cytoplasm

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16
Q

What enzyme converts Arginine to Ornithine?

A

Argininase with addition of H2O

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17
Q

What final components form the urea from the urea cycle?

A

Arginine + H2O (catalyzed by argininase)

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18
Q

Where does the urea cycle occur?

A

Liver

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19
Q

What helps transfer nitrogens into the urea cycle?

A

Aminotransferases

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20
Q

What is sphingosine derived from?

A

Ser

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21
Q

What is histamine derived from?

22
Q

What is thyroxine derived from?

23
Q

What is epinephrine derived from?

24
What is serotonin derived from?
Trp
25
What is nicotinamide derived from?
Trp
26
In heme synthesis, what is the first (of two talked about) genetic mutation that can occur and what is the enzyme that gets mutated?
Acute intermittent porphyria (hepatic disease) | Porphobilinogen deaminase
27
In heme synthesis, what is the second (of two talked about) genetic mutation that can occur and what is the enzyme that gets mutated?
Congenital erythropoetic prophyria (erythrocite disease) | Uroporphyrinogen III synthase
28
How do you determine if your patient is suffering from one of the heme synthesis diseases?
They will produce an increased amount of the protein before the reaction where the mutation occurs, and will, therefore, produce a decreased amount of heme
29
What do GLP-1 and CCK get released in response to?
Bolus of food
30
Where are GLP-1 and CCK synthesized?
Intestine
31
What do GLP-1 and CCK do?
Cause release of insulin in pancreas and cause brain to feel increased satiety, therefore decreasing food intake and body weight
32
What does leptin do?
Acts on the brain to either suppress or increase appetite
33
Which amino acids are only ketogenic?
Leu, Lys (all others are glucogenic or both glucogenic & ketogenic)
34
What does an increase in leptin expression equal?
Decrease in food intake
35
How does an increase in leptin expression cause a decrease in food intake?
Inhibits NPY and AgRP | Stimulates POMC-->MSH
36
What happens when there is decreased leptin expression?
Stimulates an increase in food intake
37
How does a decrease in leptin expression cause an increase in food intake?
Inhibits POMC--->MSH | Stimulates NPY & AgRP
38
What do NPY and AgRP activation cause?
Increased food intake
39
What do POMC---MSH activation cause?
Decreased food intake
40
What is the name for complex 5 of the ETC?
ATP synthetase
41
How many H+ ions are required to make 1 ATP (1 turn in the ATPase)?
4 H+ ions
42
If the electron donor to the ETC is NADH, which complex does it begin with?
Complex 1 (NADH dehydrogenase)
43
If the electron donor for the ETC is FADH2, which complex does it begin with?
Complex 2
44
What molecule shuttles electrons from complex 1 or 2 to complex 3?
CoQ 10
45
What molecule transfers electrons from complex 3 to complex 4?
Cytochrome C
46
How does NH4 negatively affect the brain?
It causes Glu to be translated to Gln, which requires ATP. This depletes the brains ATP source and is detrimental to brain function
47
After trypsin is activated, how are all other enzymes activated in the duodenum?
Via trypsin
48
How does bilirubin become more water soluble?
Converted to bilirubin diglucuronide
49
How is bilirubin carried to the liver?
In the blood via albumin
50
What converts heme to biliverdin?
RES
51
What is the fate of bilirubin diglucuronide?
Excreted into bile-->gut-->converted to urobolinogen
52
What are the 2 fates for urobolinogen?
1) Reabsorbed in blood, taken to kidney, urinated out | 2) Converted to stercobilin and excreted in feces (contributes to brown color)