Biology · Chemistry
Biomolecules and Enzymes
1,432 Questions
This topic focuses on biomolecules, specifically proteins, enzymes, and amino acids. It includes questions on enzyme structures, protein folding, and catalysis. These concepts are crucial for medical and biology competitive exams.
Enzyme catalysisProtein structuresAmino acid synthesisPolypeptide chainsBiomolecule properties
Biomolecules and Enzymes Questions
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Fibrin
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Prothrombin
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Factor XII
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Plasminogen
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Zymogen
C
Correct answer
Explanation
Factor XII is a protease involved in initiating the intrinsic blood clotting pathway when it binds to abnormal or negatively charged surfaces revealed by damage to endothelial cells of blood vessels.
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Tissue plasminogen activator
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Antithrombin
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Plasmin
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Thrombin
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Prothrombinase
C
Correct answer
Explanation
Plasmin is in fact an active protease, which can break down the fibrin meshwork of the clot by dissolving the clot.
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haemotoxin
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bilirubin
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haematin
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globin
D
Correct answer
Explanation
Haemoglobin consists of two components: heme (iron-containing porphyrin) and globin (protein). When iron is removed from haemoglobin, the remaining protein portion is called globin. This is distinct from bilirubin (a breakdown product) or haematin (an oxidized, iron-containing form).
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All proteins with isoelectric point below pH 7.0 will have negative charge and move towards positive electrode.
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All proteins with isoelectric point above pH 7.0 will have positive charge and move towards negative electrode.
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At isoelectric point, the net charge of protein depends on the nature of aminoacid present in the protein.
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All of the above
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Only 1 and 2
E
Correct answer
Explanation
Options 1 and 2 are true, but 3 is false.
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Blood platelets burst when they come in contact with environment.
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Thromboplastin forms prothrombinase, which activates heparin.
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Thrombin acts as a proteolytic enzyme and converts fibrinogen into fibrin monomers.
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The fibrin monomers polymerise to form long threads.
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The clot seals the wound and the platelets entrapped in the clot release more thromboplastin.
B
Correct answer
Explanation
Thromobplastin forms an enzyme prothrombinase that inactivates heparin andconverts inactive plasma protein; prothrombin into thrombin, which converts fibrinogen into fibrin monomers that polymerise to form long threads to clot the blood.
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Ornithine and Citrulline
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Glycine and Tyrosine
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Valine and Arginine
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Ornithine and Tyrosine
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Arginine and Citrulline
A
Correct answer
Explanation
This option is correct because Ornithine and Citrulline are non-protein amino acids.
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Histidine and tryptophan
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Arginine and lysine
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Tyrosine and tryptophan
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Cystine and tyrosine
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Histidine and tyrosine
B
Correct answer
Explanation
Arginine and lysine are the major amino acids in histone protein of chromosomes.
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Mannose-6-phosphate
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Phosphorylation of tyrosine
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Cleavage of N-terminus of protein
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Cleavage of C-terminus of protein
A
Correct answer
Explanation
Modification of the protein by addition of mannose-6-phosphate is involved in targeting enzymes to the lysosome.
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Proline
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Tryptophan
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Valine
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Histidine
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Alanine
B
Correct answer
Explanation
It is absent in histones.
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P type ATPase
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V type ATPase
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F type ATPase
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ABC transporter
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A type ATPase
D
Correct answer
Explanation
ATP binding cassette transporters are transmembrane proteins that utilize the energy of ATP hydrolysis to carry out translocation of various substrates across membranes. It is also involved in eukaryotic development of resistance to multidrugs.
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Fibrinogen
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Albumin
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Globulin
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Prothrombin
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Haemoglobin
A
Correct answer
Explanation
Fibrinogen is one of the important plasma proteins, which plays an important role in blood coagulation where it is converted by thrombin to fibrin. This is achieved through processes in the coagulation cascade that activates the zymogen prothrombin to the serine protease thrombin, which is responsible for converting fibrinogen into fibrin.
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Threonine to valine
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Glutamic acid to valine
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Glutamic acid to isoleucine
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Alanine to valine
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Glutamic acid to alanine
B
Correct answer
Explanation
The change of glutamic acid to valine in the sixth position of beta globin chain of haemoglobin causes sickle cell anaemia.
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theory of error catastrophe
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somatic mutation theory
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programmed senescence theory
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wear and tear theory
A
Correct answer
Explanation
As per this theory, damage to mechanisms synthesise proteins resulting in faulty proteins, which assemble to a level that causes catastrophic damage to cells, tissues, and organs.
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tryptophan
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histidine
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gLycine
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proline
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arginine
A
Correct answer
Explanation
An essential amino acid or indispensable amino acid is an amino acid that cannot be synthesized natively by the organism being considered, and therefore must be supplied in its diet.
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isoschizomers
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chromomeres
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capsomeres
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capsid
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polymers
C
Correct answer
Explanation
The capsomere is a basic subunit of the capsid, an outer covering of protein that protects the genetic material of a virus.