Carbs V Flashcards

1
Q

What do proteoglycans do that contribute to the extracellular matrix?

A

acidic and hydrophilic character of proteoglycans

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2
Q

What contributes to the gel-like property of the ECM?

A

proteoglycans

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3
Q

What forms the core protein of proteoglycans?

A

hyaluronic acid

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4
Q

What are the carbohydrate sidechains of the proteoglycans?

A

glycosaminoglycans

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5
Q

the carbohydrate side chains consist of proteoglycans consist what kind of acid?

A

glucoronic or iduronic acid

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6
Q

What charge do glycosaminoglycans possess?

A

negative

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7
Q

What does this negative charge of GAGs do?

A

attracts and entraps water

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8
Q

Sugar residues are attached to proteoglycans at what amino acid residues?

A

serine and asparagine

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9
Q

What do the carbohydrate side chain of GAGs consist of?

A

alternating amino-sugar and acid side chain

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10
Q

What transfers sulfate groups? When does this transfer occur?

A

sulfotransferases

AFTER the polysaccharide chains have been synthesized

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11
Q

When are the proteoglycans attached to hyaluronic acid?

A

after the proteoglycan has been secreted

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12
Q

Where are proteoglycans degraded?

A

lysosome

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13
Q

Where are proteoglycans sulfated?

A

Golgi

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14
Q

What are mucopolysaccharidoses?

A

genetic defect in any one of the lysosomal hydrolase protein that degrade proteoglycans

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15
Q

Hunter Syndrome?

A

dermatan sulfate and heparan sulfate

iduronate sulfatase

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16
Q

Hurler-Scheie syndrome?

A

Dermatan sulfate and heparan sulfate

alpha-iduronase

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17
Q

Sanfilippo’s Syndrome

A

Heparan sulfate

18
Q

What three sugars does the body need for protein glycosylation?

A

mannose

fucose

galactose

19
Q

How is UDP-glucose converted to UDP-galactose?

A

UDPG 4 Epimerase

20
Q

Where do glycosylation reactions occur?

21
Q

What are xenobiotics generally attached to to contribute to their hydrophobicity?

A

UDP-glucoronate

22
Q

What enzyme performs these xenobiotic glycosylation reactions?

A

UDP-glucoronate glucoroosyltransferase (UGT)

23
Q

What pathway does acetominophen get shuttled to if the orignal is overwhelmed?

24
Q

What sugar is transferred to bilirubin to aid in its’ excretion?

A

glucoronic acid

25
What activates PFK II?
F6P and AMP
26
WHat inactivates PFK II?
PKA
27
What are the two pathways that RBCs can metabolize carbohydrates?
glycolysis and PPP
28
What can muscle and hearts cells not metabolically perform?
Fatty acid synthesis
29
During proteoglycan synthesis, what amino acid residues are sugar residues attached?
serine and asparagine
30
Where are proteoglycans degraded?
lysosomes
31
What component of the proteoglycan requires specific hydrolases for its degradation in the lysosome?
glycosaminoglycan
32
Deficiency in what enzyme causes Hurler-Scheie disease?
alpha-iduronase
33
Deficiency in what enzyme causes Hunter?
Iduronate Sulfatase
34
What enzyme converts Glc-6-P to F-6-P?
phosphoglucose isomerase
35
What enzyme converts F6P to M6P?
phosphomannose isomerase
36
Where do glycosylation reactions occur?
Liver
37
What serves as an activated sugar substrate for glycosylation reactions?
UDP-glucoronate
38
What enzyme is responsible for detoxifying substrates in the liver?
UDP-glucoronate glucoronosyltransferase
39
What molecules does UDP-glucoronate offer for detoxification of substrates?
glucoronic acid
40
What system will be activated by acetominophen if UGT pathway is overwhelmed?
p450
41
What does p450 oxidize acetominophen to? What does the molecule do?
NAQBI. NAQBI causes liver damage due to the production of free radicals
42
What molecule is transferred to bilirubin for its excretion?
glucoronic acid