TLS Online TPP Program

#Question id: 339


The edges of each base pair are exposed in the major and minor grooves, creating a pattern of hydrogen-bond donors and acceptors and of hydrophobic groups (allowing for Vander Waals interactions) that identifies the base pair. The edge of an C : G base pair displays the following chemical groups in the following order in the major groove:

#SCPH06 I Botany
  1. A hydrogen-bond acceptor (at N7 of guanine), a hydrogen-bond acceptor (the carbonyl on C6 of guanine), a hydrogen-bond donor (the exocyclic amino group on C3 of cytosine), and a small nonpolar hydrogen (the hydrogen at C5 of cytosine)

  2. A hydrogen-bond acceptor (at N7 of guanine), a hydrogen-bond acceptor (the carbonyl on C6 of guanine), a hydrogen-bond donor (the exocyclic amino group on C4 of cytosine), and a small nonpolar hydrogen (the hydrogen at C5 of cytosine)

  3. A small nonpolar hydrogen (the hydrogen at C5 of cytosine), a hydrogen-bond donor (the exocyclic amino group on C4 of cytosine), a hydrogen-bond acceptor (the carbonyl on C6 of guanine) and a hydrogen-bond acceptor (at N7 of guanine)

  4. A small nonpolar hydrogen (the hydrogen at C5 of cytosine), a hydrogen-bond acceptor (the exocyclic amino group on C4 of cytosine), a hydrogen-bond acceptor (the carbonyl on C6 of guanine) and a hydrogen-bond donor (at N7 of guanine)

More Questions
TLS Online TPP Program

#Question id: 12908

#SCPH28 | Zoology

Which statement is incorrect about CRISPR?

TLS Online TPP Program

#Question id: 12909

#SCPH01 Biochemistry

According to the diagram, arrange the steps in correct order: 


1. DNA is then digested by the Cas9 nuclease at specific points on both DNA strands. 
2. Homologous recombination to repair the break and incorporate the new DNA sequence then follows. 
3.The nuclease Cas9 is targeted to DNA by a guide RNA consisting of a specific 20 nucleotide spacer/targeting sequence (crRNA).
 4. That identifies the DNA to be modified, linked to a trans-activating (tracrRNA) sequence necessary for the recruitment and stability of Cas9 nuclease.

TLS Online TPP Program

#Question id: 12909

#SCPH06 I Botany

According to the diagram, arrange the steps in correct order: 


1. DNA is then digested by the Cas9 nuclease at specific points on both DNA strands. 
2. Homologous recombination to repair the break and incorporate the new DNA sequence then follows. 
3.The nuclease Cas9 is targeted to DNA by a guide RNA consisting of a specific 20 nucleotide spacer/targeting sequence (crRNA).
 4. That identifies the DNA to be modified, linked to a trans-activating (tracrRNA) sequence necessary for the recruitment and stability of Cas9 nuclease.

TLS Online TPP Program

#Question id: 12909

#SCPH28 | Zoology

According to the diagram, arrange the steps in correct order: 


1. DNA is then digested by the Cas9 nuclease at specific points on both DNA strands. 
2. Homologous recombination to repair the break and incorporate the new DNA sequence then follows. 
3.The nuclease Cas9 is targeted to DNA by a guide RNA consisting of a specific 20 nucleotide spacer/targeting sequence (crRNA).
 4. That identifies the DNA to be modified, linked to a trans-activating (tracrRNA) sequence necessary for the recruitment and stability of Cas9 nuclease.

TLS Online TPP Program

#Question id: 12910

#SCPH01 Biochemistry

Match the following:
A. RNA analysis               i. Sexing or cell mutation sites               a. Expressed Sequence tag
B. Forensic science           ii. mRNA analysis                                     b.  Analysis of DNA from blood
C. Gene discovery              iii. DNA profiling                                       c. Active latent viral infections
D. Single-cell analysis     iv.  RT–PCR                                             d. Sex determination of unborn

TLS Online TPP Program

#Question id: 12910

#SCPH06 I Botany

Match the following:
A. RNA analysis               i. Sexing or cell mutation sites               a. Expressed Sequence tag
B. Forensic science           ii. mRNA analysis                                     b.  Analysis of DNA from blood
C. Gene discovery              iii. DNA profiling                                       c. Active latent viral infections
D. Single-cell analysis     iv.  RT–PCR                                             d. Sex determination of unborn