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IN SILICO METHODS

Total questions: 20

Worksheet time: 20mins

Name
Class
Date
1.

1. Which one is used for molecular docking?

a.

a)

HEX

b)

b. Maestro

c)

c. KEGG

d)

d. UniProt

2.

2. __________ is the small molecule database


a)

a. KEGG

b)

b. Zinc

c)

c. UniProt

d)

d. NCBI

3.

3. ADME stands for

a)

a. Absorption, Distribution, Metabolism and Excretion

b)

b. Administration, Distribution, Metabolism and Excretion

c)

c. Absorption, disintegration, Metabolism and Efficacy

d)

d. Administration, disintegration, Metabolism and Efficacy

4.

4. _________ could be a drug molecule

a)

a. Small molecule

b)

b. Ion

c)

c. Peptide

d)

d. All the above

5.

5. What kind of interaction typically involved in the binding of drug to the active site of the target protein

a)

a. van der Waals interaction

b)

b. ionic bond

c)

c. H-bond

d)

d. All the above

6.

6. ________ the most common drug target?

a)

a. DNA

b)

b. RNA

c)

c. G-protein coupled receptor

d)

d. None of the above

7.

7. HTVS

a)

a. High Throughput Virtual search

b)

b. High throughput Virtual screening

c)

c. Hit-Identification Through Virtual Screening

d)

d. Hit-identification Through Virtual search

8.

8. __________ is the protein structure database

a)

a. UniProt

b)

b. SwissProt

c)

c. Swiss Model

d)

d. PDB

9.

9. Lipinski’s Rule of Five includes

a)

a. Molecular weight

b)

b. HBD

c)

c. HBA

d)

d. All the above

10.

10. Appraise the compound Doxorubicin for compliance with the Rule of Five parameter

Molecular weight = 543 g mol-1

LogP = -1.33

HBD = 7

HBA = 12

a)

a. Number of violation 3

b)

b. Number of violation 2

c)

c. Number of violation 1

d)

d. No violation

11.

Which of the following is not include to computer-aided drug discovery for lead discovery....

a)

a. Library design

b)

b. Docking scoring

c)

c. Target Flexibility

d)

d. Target druggability

12.

These followings are the part of SARS-Cov 2, except.

a)

a. spike glycoprotein

b)

b. protein membrane

c)

c. envelope membrane protein

d)

d. genomic DNA

13.

Drugs candidate can be attached to protein target via mechanism below, except?

a)

a. phi phi stacking

b)

b. hidrophobic

c)

c. metal binding

d)

d. hidrogen binding

14.

Which of the following is not an application of computational methods in drug discovery?

a)

a. QSAR

b)

b. Molecular Docking

c)

c. Cell line testing

d)

d. Virtual Screening

15.

Which format will support to Autodock Vina

a)

PDF

b)

PDB

c)

SDF

d)

MOL

16.

Which one of the following software used for protein file conversion

a)

Pyrx

b)

OpenBabel

c)

Autodock

d)

iGemdock

17.

What is AutoDock used for?

a)

A software tool for protein-ligand docking, predicting how small molecules bind to a receptor.

b)

A database for storing protein sequences.

c)

A simulation software for protein folding.

d)

A tool for visualizing molecular structures.

18.

What is Prokka used for?

a)

A software tool for annotating genes in prokaryotic genomes.

b)

A database for storing genomic sequences.

c)

A tool for visualizing protein structures.

d)

A platform for conducting phylogenetic analysis.

19.

What does BLAST stand for?

a)

Basic Local Alignment Search Tool

b)

Biological Local Alignment Search Tool

c)

Basic Local Alignment Sequence Tool

d)

Biological Local Alignment Sequence Tool

20.

TYpe name Roll nO and university name or college name

4 lines