Biochem Flashcards

0
Q

On tRNA where is the anticodon found?

A

Top loop

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
1
Q

On t RNA where is the AA found?

A

3’ end

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

B1 is cofactor for what rxns?

A
Decarboxilation. 
A- alpha ketoglutarate dehydrogenase (TCA)
T- transketolase (HMP shunt)
P- pyruvate dehydrogenase (glycolysis)
Branched chain AA dehydrogenase
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

B2 cofactor in what rxns?

A

Oxidation and reduction. FAD and FMN

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

B3 cofactor for what rxns?

A

Redox. NAD, NADP

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Biotin is important for what reactions?

A

Carboxylation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

B6 is important for the synthesis of what molecules?

A

Cystathionine,heme, niacin, Gaba and histamine

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Deficiency caused by raw eggs

A

Biotin

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Decreased adult hair, loss of taste, anosmia

A

Zinc deficiency

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Tryptophan derivatives

A

Niacin

Serotonin –>melatonin

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Glycine Derivatives

A

Porphyrin –> heme

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Arginine Derivatives

A

Creatine, urea, nitric oxide

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Glutamate derivatives

A

GABA, glutathione

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Dandy walker (embryology qt)

A

Large posterior fossa, absent cerebellar vermis, cystic enlargement of fourth ventricle

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Phenylalanine derivatives

A

Tyrosine -> dopa-> dopamine-> NE-> epi

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Rate limiting step for glycolysis

A

Phosphofructokinase 1

irreversible

16
Q

Rate limiting step for gluconeogenesis

A

Fructose 1,6 bisphosphatase

17
Q

Rate limiting step for TCA cycle

A

Isocitrate dehydrogenase

18
Q

Rate limiting step for glycogen synthesis

A

Glycogen synthase

19
Q

Rate limiting step for glycogenolysis

A

Glycogen phosphorylase

20
Q

Rate limiting step for HMP shunt

A

G6PDEHYDROGENASE

21
Q

Vitamin K catalyzes what reaction

A

Gamma carboxylation of glutamic acids

22
Q

What reactions take place in the mitochondria

A

Beta oxidation, acetyl CoA production, TCA cycle, oxidative phosphorylation

23
Q

What reactions take place in the cytoplasm

A

Glycolysis, fatty acid synthesis, HMP Shunt, protein synthesis, steroid synthesis

24
Q

What reactions take place both in the mitochondria and cytoplasm

A

HUGs take 2:
Heme synthesis
Urea cycle
Gluconeogenesis

25
Q

What is the rate limiting step in de novo pyrimidine synthesis

A

Carbamoyl phosphate synthetase II

26
Q

What is the rate limiting step of de novo purine synthesis

A

Glutamine PR PP aminotransferase

27
Q

What is the rate limiting step of the urea cycle

A

Carbamoyl phosphate synthetase I

28
Q

What is the rate limiting step of fatty acid synthesis

And what is the product?

A

Acetyl CoA carboxylase

Malonyl CoA

29
Q

What is the rate limiting step of fatty acid oxidation

A

Carnitine acyltransferase I

30
Q

What is the rate limiting step of ketogenesis

what is the rate limiting step of cholesterol synthesis

A

HMG CoA synthase

HMG CoA reductase

31
Q

Severe fasting hypoglycemia, increased glycogen in liver, increase blood lactate, hepatomegaly. Disease?

What enzyme is deficient?

A

VonGierkes

G6P

32
Q

Cardiomegaly systemic findings leading to Early death. Disease?

Enzyme deficiency?

A

Pompes

Lysosomal alpha 1,4 glucosidase

33
Q

Milder form of type I with normal blood lactate levels. Disease?

Enzyme deficiency?

A

Cori disease

Debranching enzyme alpha 1,6 glucosidedase

34
Q

Increased glycogen in muscle but cannot break it down. painful muscle cramps, myoglobinuria with strenuous exercise. Disease?

deficient enzyme?

A

Mc Ardle’s disease

Skeletal muscle glycogen phosphorylase