Biochem - metabolism :) Flashcards

(45 cards)

1
Q

Rate determining step: glycolysis

A

PFK-1

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2
Q

Rate determining step: Gluconeogenesis

A

fructose-1,6-bisphosphatase

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3
Q

Rate determining step: TCA cycle

A

isocitrate dehydrogenase

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4
Q

Rate determining step: glyogenesis

A

glycogen synthase

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5
Q

Rate determining step: glycogenolysis

A

glycogen phosphorylase

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6
Q

Rate determining step: HMP shunt

A

glucose-6-phosphate dehydrogenase

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7
Q

Rate determining step: de novo pyrimadine synthesis

A

carbamoyl phosphate synthetase II (CPS2)

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8
Q

Rate determining step: de novo purine synthesis

A

glutamine PRPP amidotransferase

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9
Q

Rate determining step: Urea cycle

A

carbamoyl phosphate synthetase I

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10
Q

Rate determining step: fatty acid synthesis

A

acetyl coa carboxylase

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11
Q

Rate determining step: Fatty acid oxidation

A

Carnitine acyltransferase I

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12
Q

Rate determining step: Ketogenesis

A

HMG CoA synthase

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13
Q

Rate determining step: Cholesterol synthesis

A

HMG CoA reductase

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14
Q

Gibbs free energy equation

A

delta G = deltaH - TdeltaS

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15
Q

Drugs that inhibit complex I

A

rotenone
mPP
amytal

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16
Q

Drugs that inhibit complex III

A

antimycin A

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17
Q

Things that inhibit complex IV

A

CO
cyanide
sodium azide (N3-)
H2S

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18
Q

Things that inhibit atp synthase (complex V)

A

oligomycin

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19
Q

4 sites of HMP shunt existence

A

1) rbcs
2) mammary glands
3) liver
4) adrenal cortex

20
Q

fructokinase deficiency causes

A

essential fructosuria (not a big deal)

21
Q

aldolase B deficiency causes

A

fructose intolerance (bad)

22
Q

Rx for fructose intolerance

A

decrease intake of fructose and sucrose

23
Q

galactokinase deficiency

A

relatively mild, only symptom is infantile cataracts, maybe some failure to track objects/lack of social smile.

24
Q

absence of galactose 1 phosphate uridyltransferase

A

classic galactosemia
failure to thrive, jaundice, hepatomegaly, infantile catarcats, disability, E coli sepsis in neonates = severe symptoms soon after starting feeding

25
Rx classic galactosemia
exclude galactose and lactose in diet
26
lack of what enzyme can lead to sorbitol induced osmotic damage
sorbitol dehydrogenase
27
what cells lack sorbitol dehydrogenase
lens, schwann cells, retina, kidneys
28
acidic amino acids
aspartic acid and glutamic acid | negative at body pH
29
basic amino acids
arginine, lysine, histidine | positive at body pH except histidine =no charge
30
essential amino acids
PVT TIM HaLL ``` phenylalanine valine threonine tryptophan isoleucine lysine histidine leucine lysine ```
31
ketogenic amino acids
leucine and lysine
32
fatty acid oxidation (beta oxidation) location
mitochondria
33
glycolysis location
cytosol
34
acetyl-coa production location
mitochondria
35
heme synthesis location
mitochondria and cytosol
36
tca cycle location
mitchondria
37
fatty acid synthesis location
cytosol
38
urea cycle location
both mitochondria and cytosol
39
oxidative phosphorylation location
mitochondria
40
gluconeogenesis location
both mitochondria and cytosol
41
HMP shunt location
cytoplasm
42
protein syntehsis (RER) loctaion
cytoplasm
43
ketogenesis location
mitochondria
44
cholesterol syntehsis
cytoplasm
45
steroid synthesis location
cytoplasm