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1. Which of these statements best describes the function of the cell membrane?
1/1
Benar
It controls w hich
2. The component molecules of the cell membrane have two main parts, the head and the tail.
These parts are either hydrophobic (repelled by water) or hydrophilic (attracted to water). Which is
which?
1/1
Benar
Both Hydrophobic
Both Hydrophilic
Hydrophilic Head
1/1
Option 1
Benar
Option 2
Option 3
Option 4
Yang lain:
Option 1
4. According to the answer in no. 3; What is the role of the following structure in cell membranes?
1/1
Benar
The structure is p
5. How fast do the large polar substances diffuse accross the membrane?
1/1
Very fast
Fast
Very slow
Benar
Sloe
Yang lain:
Very slow
1/1
L-seryl-L-valyl-L-tyrosine.
Benar
L-seryl-L-valyl-L-phenylalanine.
L-phenylalanyl-L-valyl-L-serine.
L-tyrosyl-L-valyl-L-serine.
L-seryl-L-valyl-L-
7. Which of the following statements is not true regarding protein primary structure?
0/1
The amino acids in the primary structure are held together by covalent bonds.
Salah
The peptide bonds in protein are made during the transcription process in protein synthesis.
The peptide bonds in protein are made during the transcription process in protein synthesis.
8. Which of the following descriptions best describes the quaternary structure of proteins?
1/1
Benar
The arrangement
Salah
10. Protein is one of the drug targets. Which the protein can not do as drug target?
0/1
Enzyme
Receptor
Protein transport
Salah
Protein transport
11. Drugs interact with their targets by binding to binding sites. In these binding site, there are some
term was used to describe the interaction between drug and their targets as mention below, except:
1/1
Binding interaction
Spesific region
Binding region
Benar
Functional group
Binding region
12. Drug interact with their targets by establishing non covalent or covalent bond. What are the
relative strengths of different types of non covalent bonds?
1/1
Benar
13. Which of the following atoms in the structure below is likely to be the strongest hydrogen bond
acceptor?
1/1
The aniline nitrogen.
Benar
The carboxylate o
1/1
They increase the rate of reaction by lowering the transition state energy
Benar
They raise activation energy to shift the equilibrium to favor the products
1/1
Benar
Substrates fit into active sites and bind to functional groups within the active site.
An active site contains amino acids which are important to the binding process and the catalytic
mechanism.
An active site is n
16. As the substrate enters the active site, its functional groups come close to the functional groups
of a number of amino acids. What happens as a result?
1/1
Benar
The substrate enters the active site of the protein, and nothing changes
17. Which of the following descriptions best describes a competitive enzyme inhibitor?
1/1
A drug that binds to an active site and inhibits the enzyme, but which is displaced by increasing the
concentration of substrate.
Benar
A drug that binds to an active site and inhibits the enzyme, but which is not displaced by increasing
the concentration of substrate.
A drug that binds to a different binding site from the active site and affects the activity of the
enzyme.
18. Which statement best describes the relevance of an allosteric binding site to medicinal
chemistry?
1/1
It is more hydrophobic than normal binding sites and accepts hydrophobic drugs in preference to
hydrophilic drugs.
A larger variety of drug structures will bind to the allosteric site than to the active site.
Drugs can be designed based on the structure of the endogenous chemicals which bind to allosteric
sites and control enzyme activity.
Benar
Drugs can be designed based on the transition state of the enzyme-catalysed reaction.
19. Identify the kind of bonding forces which are typically involved in binding a drug to an enzyme's
active site.
1/1
Benar
A combination of
20. Consider the following enzyme-catalysed reaction carried out on glycogen. What is the
substrate?
0/1
Glucose-1-phosphate.
Adrenaline.
Glycogen
AMP
Salah
AMP
Glucose-1-phosphate.
1/1
Glucose-1-phosphate.
Benar
Phosphorylase a.
Glycogen
AMP
Glucose-1-phosp
22. Lactate dehydrogenase (LDH or LD) is an enzyme found in nearly all living cells (animals, plants,
and prokaryotes). LDH catalyzes the conversion of lactate to pyruvate and back, as it converts NAD+
to NADH and back according to the reaction below, identify the type of the reaction which is
catalysed by LDH!
0/1
Oxidation
Reduction
Hydrolation
Salah
Substitution
Hydrolation
Oxidation
23. According to reaction the reaction below, at high concentrations of lactate, lactate can inhibit
these reaction, and the rate of conversion of pyruvate to lactate is decreased. These process
corespond to …….
0/1
Feedback inhibition
Allosteric inhibition
Un competitive inhibition
Salah
Non competitive in
Feedback inhibition
Benar
Receptors contain a hollow or cleft on their surface which is known as a binding site.
Most receptors a
25. A chemical messenger is any compound that serves to transmit a message and activates the
receptor. Which of the following compond is not a chemical messenger?
1/1
Hormone
Pheromone
Prostaglandine
ATP
Benar
ATP
1/1
Neurotransmitters only have small distances to cover to reach their target cells.
Benar
Neurotransmitters
27. There is a fine balance required for the binding interactions of a neurotransmitter with its
receptor. Which of the following statements best expands on this statement?
1/1
It is important that the binding interactions involve a mixture of van der Waals interactions,
hydrogen bonds and ionic bonds since neurotransmitters have different functional groups.
The binding interactions must be of the correct nature to match the functional groups of the
neurotransmitter and the functional groups in the binding site.
The binding interactions must be sufficiently strong that the neurotransmitter binds long enough to
have an effect, but not too strong in case the neurotransmitter remains permanently bound.
Benar
There must be the correct balance of hydrophilic and hydrophobic interactions to ensure that the
chemical messenger can enter a hydrophobic binding site.
28. When a membrane-bound receptor binds its chemical messenger, an induced fit takes place
which leads to secondary effects, allowing a chemical message to be received within the cell. Which
of the following mechanisms is not involved in this process?
0/1
Salah
29. Which of the following statements is not true regarding the binding site of a receptor?
1/1
Benar
Chemical messengers fit into binding sites and bind to functional groups within the binding site.
The binding site contains amino acids which are important to the binding process.
30. Which of the following statements is not true about a ligand-gated ion channel receptor?
1/1
Neurotransmitters can act as the chemical messengers for ligand-gated ion channels.
Benar
Some ion channel receptors are controlled by differences in membrane potential rather than by
ligands.
Ligand-gated ion
31. Which of the following statements is not true about ligand-gated ion channels?
0/1
The process by which an ion channel opens as a result of receptor-ligand binding is known as gating.
Salah
The opening of cationic ion channels generally leads to polarisation of the cell.
The process by w
The opening of cationic ion channels generally leads to polarisation of the cell.
32. The nicotinic receptor controls an ion channel. Which of the following statements is true about
the -subunit of this ion channel?
0/1
Salah
The binding site for the neurotransmitter resides solely on the N-terminal chain.
The binding site for the neurotransmitter resides solely on the N-terminal chain.
33. Which of the following statements is true about a G-protein coupled receptor?
0/1
Salah
The binding region for the G-protein involves one of the intracellular loops and the C-terminal chain.
The binding region for the G-protein involves one of the intracellular loops and the C-terminal chain.
1/1
Small G-proteins bind GDP in the resting state and GTP in the active state.
Benar
Small G-proteins
35. Which of the following statements is true about a tyrosine kinase linked receptor?
0/1
Salah
It has one hydrophobic transmembrane region.
0/1
Salah
The phosphorylat
0/1
They contain a binding region for DNA near the middle of the protein.
They are activated by hydrophobic molecules which are synthesised within the cell.
Salah
They contain a binding region for DNA near the middle of the protein.
0/1
Salah
39. Which of the following statements is generally true regarding the chemical messengers for
intracellular receptors?
0/1
Salah
1/1
A compound that has the same effect on a receptor as the endogenous chemical messenger.
Benar
A compound that binds to a receptor, and activates it, but to a lesser extent than the endogenous
chemical messenger.
A compound that binds to a receptor fails to activate it and prevents the endogenous chemical
messenger from binding.
A compound that binds to a receptor fails to activate it and leads to a drop in inherent biological
activity. 4
A compound that
41. Which of the following is not a necessary requirement when designing an agonist?
0/1
Salah
0/1
An agonist.
Salah
An allosteric antagonist.
An inverse agonist.
An agonist.
1/1
ATP.
Benar
CTP.
GTP
UTP
ATP.
1/1
Dimerisation.
Receptor binding.
Base pairing.
Benar
Polymerisation.
Base pairing.
45. What non-covalent bonding interactions do the nucleic acid bases form in DNA secondary
structure?
1/1
Benar
Hydrogen bonds
1/1
It catalyses crossing over of DNA strands to relieve the tension created in DNA when the DNA double
helix is unravelled.
Benar
It catalyses cross
47. Which of the following is not true when RNA is compared with DNA?
1/1
Benar
1/1
Alkylating agent
Chain destroyer
Benar
Intercalating agent
Chain destroyer
49. Which of the following statement is not true about an intercalating agent?
1/1
Intercalating drugs are compounds that contain planar or heteroaromatic features that slip between
the base pair layers of the DNA double helix.
They are inserted between the nucleic acid base pairs only via the major groove.
Benar
50. Which of the following statement is not true about an alkylating agent?
0/1
Salah
Alkylation of nucl
51. The following agent is used for the treatment of Hodgkin's lymphoma as part of a multi-drug
regime.
1/1
A topoisomerase inhibitor.
An alkylating agent.
Benar
An antimetabolite.
A receptor antagonist.
An alkylating age
52. Which of the following statement is not true about an chain terminator agents on DNA?
1/1
They must have to mimic natural nucleosides.
They act as 'false substrates' and are incorporated into the growing DNA chain during replication.
Benar
1/1
Option 1
Option 2
Option 3
Benar
Option 4
Option 3
54. Which of the following terms best describes the study of how drugs reach their target in the
body and how the levels of a drug in the blood are affected by absorption, distribution, metabolism,
and excretion?
1/1
Pharmacokinetics.
Benar
Pharmacodynamics.
Structure-activity relationships.
Pharmacokinetics
55. Which of the following is one of the rules in Lipinski's rule of five?
1/1
56. Some orally active drugs do not obey the rule of five. For example, some polar drugs with a
molecular weight between 200 and 500 are found to be orally active. Which of the following
mechanisms is the most likely reason for this?
0/1
Pinocytosis.
Ion channels.
Salah
Ion channels.
57. What role does drug metabolism play in making the excretion of drugs more efficient?
1/1
Benar
It makes drugs less reactive.
It makes drugs mo
58. Why may a drug bearing an ester group that is important to target binding have a limited
duration of action?
1/1
Benar
59. Some drugs are excreted more efficiently than others. Which of the following statements is the
best general explanation for this?
1/1
Benar
Hydrophilic drugs
60. The following agent is cocaine. Which of the following side in the structure below is likely to be
hydrolised?
1/1
A dan C
Benar
B dan D
B dan C
A dan D
A dan C
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B. Match the following statement to their correct answer By Type The "Alphabetic Answer which is
Gived on The Optional Answer Below" (Sectin 4).
Skor bagian1/10
61. The process which is described as being the net movement of water molecules from an area of
low concentration of solute to an area with a higher concentration of solute……………
0/1
B,osmosis
A
62. The physiochemical factor which affect the permeability coefficient of the molecules crossing the
membrane …………..
0/1
E, solubility in lipid
63. The amino acid that does not show hydrophobic characters ……………
0/1
I, tyrosine
64. The strongest form of intermolecular bonding that could be formed involving the residue of the
amino acid threonine ……………………..
0/1
65. Which the amino acid can interact with drug by ionic interaction!
0/1
j, glutamine
A, active site
67. The side chain amino acid in protein can participate in intermolecular interaction with a drug.
The type of interaction of the drug wich have an aromatic group ………………..
0/1
68. Some enzymes have a binding site which is not recognised by the normal substrate, and affects
the activity of the enzyme if it is occupied by a ligand. What term is used for such a binding site?
0/1
0/1
70. Which of the following terms refers to the process by which a substrate binds to an active site
and alters the shape of that active site?
1/1
D
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(A) Active Site, (B) Osmosis, (C) Tryptophan, (D) Induce fit, (E) Solubility in lipid, (F) Binding side, (G)
Allosteric binding site, (H) Hydrogen bonding interaction, (I) Tyrosine, (J) Glutamine, (K) Van der
Waals interactions, (L) Hydrophobicity
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