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Worksheets

CC mod 3

Total questions: 60

Worksheet time: 3600secs

Name
Class
Date
1.

Building blocks of protein

(a)  

2.

Amino acid is synthesized by the body from carbon, nitrogen, hydrogen, oxygen, and sulfur.

a)

Essential amino acids

b)

Non-essential amino acids

3.

All are examples of Uncharged polar amino acids except:

a)

Glutamine

b)

Cysteine

c)

Tyrosine

d)

Tryptophan

4.

Uncharge polar amino acids have a hydrophobic side chain which forms hydrogen bonds with water

a)

True

b)

False

5.

The only proteinogenic amino acid whose side group links to the alpha-amino group

a)

Threonine

b)

Phenylalanine

c)

Proline

d)

Tryptophan

6.

Combines with aspartic acid and methionine to help the liver with the digestion of fats

a)

Threonine

b)

Histidine

c)

Tryptophan

d)

Valine

7.

Branched amino acid that is beneficial for skin, bone, and tissue wound healing

a)

HIS

b)

VAL

c)

ILE

d)

LEU

8.

Source of Lysine

a)

Mushroom

b)

Rice

c)

Beans

d)

Leafy vegetables

9.

Important AA that helps stimulate translation of mRNA by being the first AA incorporated into the N-terminal position of all proteins.

a)

Tryptophan

b)

Histidine

c)

Methionine

d)

Leucine

10.

Arginine is:


I. Used to improve circulation and treat impotence and heart diseases.

II. Helpful in strengthening the immune system, regulate hormones and blood sugar, and promotes male fertility.

III. Beneficial for a healthy nervous system.

IV. Found on fish, seafood, tofu, dried beans, red beans, and black beans

a)

I, II, III, & IV

b)

I, II, & IV

c)

I & II

d)

I, III, &IV

11.

Most abundant amino acid involved in the transport of nitrogen

a)

ASN

b)

GLU

c)

GLY

d)

PRO

12.

Aids in the production of immunoglobulin and antibody

a)

Tyrosine

b)

Glutamic Acid

c)

Alanine

d)

Serine

13.

Glutamine


I. Is important in the metabolism of sugars and fats and aids in transporting potassium into the CSF.

II. Is the most abundant in the body/immune function.

III. Transports ammonia to the liver.

IV. Is metabolized in urea cycle and participate in gluconeogenesis

a)

I, II, III, & IV

b)

I, III, & IV

c)

II & III

d)

I, II, & IV

14.

Tyrosine is a precursor of nitric oxide.

It is a mood elevator, suppresses appetite, and is synthesized from phenylalanine.

a)

1st statement is true, 2nd statement is false.

b)

1st statement is false, 2nd statement is true.

c)

Both are false.

d)

Both are correct

15.

The new amino acid encoded by UAG

(a)  

16.

Are rare inherited disorders of amino acid metabolism and exist in either the activity of a specific enzyme in the metabolic pathway or in the membrane transport system for an amino acids.

(a)  

17.

Phenylketonuria (+) result= bacterial growth <4mg/dL

a)

True

b)

False

18.

An error of metabolism, usually inborn, in which the body cannot effectively breakdown tyrosine

(a)  

19.

Caused by a deficiency of the enzyme tyrosine aminotransferase encoded by the gene TAT.

a)

Type I tyrosinemia

b)

Type II tyrosinemia

c)

Type III tyrosinemia

20.

The last enzyme in a series of five enzymes needed to break down tyrosine

a)

Tyrosine aminotransferase

b)

Fumarylacetoacetate hydrolase

c)

4-hydroxyphenylpyruvate dioxygenase

21.

A rare autosomal recessive metabolic disorder that disrupts or prevents normal metabolism of the branched-chain amino acid leucine.

a)

Alkaptonuria

b)

Isovaleric Acidemia

c)

Cystinuria

d)

Arginosuccinic Aciduria

22.

Maple Syrup Urine Disease:


I. Is characterized by markedly reduced or absence of alpha-keto acid decarboxylase

II. Results to the darkening of urine

III. An inborn error of metabolism causing accumulation of branched-chain amino acid

IV. A type of organic academia

a)

I, II, III, & IV

b)

I, II, & IV

c)

I, III, & IV

d)

III & IV

23.

A defect in the amino acid transport system

a)

Cystinuria

b)

Homocystinuria

c)

Isovaleric acidemia

d)

Arginosuccinic Aciduria

24.

Arginosuccinic Aciduria

a)

Genetic diseases of the urea cycle disorder

b)

Results to elevated levels of homocysteine and methionine in blood and urine

c)

Deficiency in the enzyme arginosuccinic acid lyase

d)

Leads to multisystemic disorder of muscle connective tissue and weakening of the bone

25.

Secondary structure

a)

Winding of polypeptide chain

b)

regular reccuring arrangement of the amino acid chain into a coil or pleated sheet

c)

describes protein as alpha-helix or beta-pleated sheath

d)

Amino acid sequence

26.

3D structure of proteins composed of multiple subunits

a)

Primary

b)

Secondary

c)

Tertiary

d)

Quaternary

27.

Examples of conjugate protein

a)

Protamines

b)

Lipoproteins

c)

Hemoproteins

d)

Nucleoproteins

28.

Examples of Fibrous proteins

a)

Hormones

b)

Myosin

c)

Enzymes

d)

Keratin

29.

Soluble in water and high concentration salt solution

a)

Globulin

b)

Aluminoids

c)

Albumin

30.

Reference value for TP

a)

32-45 g/L

b)

23-35 g/L

c)

60-70 g/L

31.

Protein migration is usually done at a pH of 9.6

a)

True

b)

False

32.

Preferred method for quantification after proteins are separated by electrophoresis

a)

Chromatography

b)

MAss sipectrophotometer

c)

Electrochemistry

d)

Densitometry

33.

4th fastest band in a Normal SPE pattern

a)

Gamma globulin

b)

Beta-globulin

c)

Alpha 1-globulin

d)

Alpha 2-globulin

34.

Examples of Alpha 1-globulin

a)

AAT

b)

AMG

c)

AAG

d)

TBG

35.

Caused by a2-globulin spike in a abnormal SPE pattern

a)

Nephrotic syndrome

b)

Multiple Myeloma

c)

Hepatic cirrhosis

d)

Juvenile cirrhosis

36.

Prealbumin is increased in:

a)

Chronic renal failure

b)

Hepatic damage

c)

Tissue necrosis

d)

Alcoholism

37.

Albumin has a half-life of 14 days.

a)

True

b)

False

38.

The most abundant protein in normal plasma constituting about 2/3 of the TP

(a)  

39.

Globulin

a)

Measured by subtracting albumin from TP

b)

reference range: 35-55 L

c)

reference range: 23-35 g/L

d)

A tetrameric structure

40.

Has the capacity to bind with trypsin and inactivate it

a)

Alpha1-acid glycoprotein

b)

Alpha1-fetoprotein

c)

Alpha1-antichymotrypsin

d)

Alpha1-Antitrypsin

41.

All are measurements used for Alpha-2 macroglobulin except:

a)

Radial immunodiffusion

b)

ultracentrifugation

c)

Electrophoresis

d)

Immunonephelometry

42.

A major beta-globulin protein that transports ferric iron from iron stores to bone marrow.

a)

Fibrinogen

b)

Ceruloplasmin

c)

Siderophilin

d)

Haptoglobin

43.

Fibrinogen is decreased in the following except:

a)

Terminal liver disease,

b)

Septicemia

c)

Fetal death in utero

d)

antepartal hemorrhage

44.

Are complexes of proteins and lipids whose function is to transport cholesterol, TAG, and phospholipid in the blood

a)

Ceruloplasmin

b)

Hemopexin

c)

Beta-lipoprotein

d)

Alpha-1 Fetoprotein

45.

Migrates at the beginning of the beta-globulin region

a)

VLDL

b)

LDL

c)

HDL

d)

Chylomicrons

46.

Measurements used for Alpha-1 Fetoprotein

a)

ELISA

b)

RIA

c)

Gel diffusion

d)

Colorimetry

47.

Hemopexin is a copper-containing serum glycoprotein which functions as circulating oxidase

a)

True

b)

False

48.

A collective term for several proteins that participate in the immune reaction and serve as a link to the inflammatory response

(a)  

49.

In AMI, Myoglobin has a 4-5hrs onset, and 14-16hrs peak

a)

True

b)

False

50.

Specific for heart muscle and useful in monitoring thrombolytic therapy in MI

a)

Troponin I

b)

Troponin T

c)

Troponin C

51.

In heat precipitation test for Bence Jones Protein, heating a sample of urine at 65 deg C will form a precipitate but will redissolve again when heated at 100 deg C.

a)

True

b)

False

52.

In non protein nitrogen, plasma contains 20-35 mg/dl of NPN. It comprises 5% of Uric acid.

a)

First statement is true, second statement is false.

b)

1st statement is false, 2nd statement is true.

c)

Both are true.

d)

Both are false.

53.

A method for BUN where NH3 & CO2 is yielded by the combination of Urea and Urease

a)

Chemical Method

b)

Urease Method

c)

Coupled urease-UV enzymatic method

d)

Isotope Dilution Mass Spectrometry

54.

Creatinine

a)

Elevates first in kidney diseases

b)

Is partially secreted by the proximal tubules

c)

The end product of muscle metabolism derived from creatine

d)

Synthesized in the liver from CO2 and ammonia from deamination of amino acid

55.

Creatinine Method that is popular, inexpensive, rapid and easy to perform.

a)

Folin WU Method

b)

Enzymatic Method

c)

Lloyd's or Fuller's Earth Method

d)

Kinetic Jaffe Method

56.

Azotemia which is usually the result of urinary tract obstruction

a)

Pre renal azotemia

b)

Renal Azotemia

c)

Post renal azotemia

57.

Final breakdown of nucleic acid catabolism in humans

(a)  

58.

All are methods for Uric acid except:

a)

Caraway Method

b)

Uricase Method

c)

Kheldahl Method

d)

Isotope Dilution Mass Spectrometry

59.

A condition where blood uric acid >10 mg/dL can cause the production of urinary tract calculi

a)

Chronic Renal disease

b)

Lesch Nyhan Syndrome

c)

Gout

60.

Specimen for Berthelot Reaction

a)

EDTA

b)

Heparin

c)

Sodium Citrate

d)

Heparin and EDTA