Side 12 of 92 ahted sae MacBook esc 80 F1 F2 F3 14. What is the purpose of the dozens of p53 modifications? Chapter 4: 15. Which groove contains more "information" and why? How do proteins interact specifically with this DiA groove, as when a zinc finger crosses the groove? 16. Which of the following base pairs could proteins distinguish, and why? a. Major groove base pairs (GC/CG, AT/TA, GC/TA, GC/AT) b. Minor groove base pairs (GC/CG, AT/TA, GC/TA, GC/AT) 17. What contributes to DNA stability with regards to Tm? Which type of base pairs takes the most energy to pull apart (i.e. require a higher temperature/Tm to dissociate)? 18. Why would it take longer for more complex DNA to reanneal? 19. Define the following: negative supercoil, positive supercoil, topoisomerase I (note the role of tyrosine) topoisomerase II (note the role of ATP) Chapter 5: 20. Why can RNA form more complex structures than DNA? 21. Explain how riboswitches work. 22. Explain the RNA world hypothesis. How does the ribosome structure support this model? Chapter 7: 23. Describe SDS-PAGE and western blotting, and the knowledge gained from each. 24. How can proteins be used to find their corresponding gene of interest in forward genetics? major difficulty with this approach in humans? 25. How can antibodies be used to identify the sequence and location of human genes? 26. Why was working with DNA more difficult than proteins? 27. What three main tools were available for analyzing and manipulating DNA in the early 19 harre? 2.

Biochemistry
6th Edition
ISBN:9781305577206
Author:Reginald H. Garrett, Charles M. Grisham
Publisher:Reginald H. Garrett, Charles M. Grisham
Chapter28: Dna Metabolism: Replication, Recombination, And Repair
Section: Chapter Questions
Problem 4P: Multiple Replication Forks in E. coli II On the basis of Figure 28.2, draw a simple diagram...
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Question #14

Side 12 of 92 ahted sae
MacBook
esc
80
F1
F2
F3
14. What is the purpose of the dozens of p53 modifications?
Chapter 4:
15. Which groove contains more "information" and why? How do proteins interact specifically with this DiA
groove, as when a zinc finger crosses the groove?
16. Which of the following base pairs could proteins distinguish, and why?
a. Major groove base pairs (GC/CG, AT/TA, GC/TA, GC/AT)
b. Minor groove base pairs (GC/CG, AT/TA, GC/TA, GC/AT)
17. What contributes to DNA stability with regards to Tm? Which type of base pairs takes the most energy to
pull apart (i.e. require a higher temperature/Tm to dissociate)?
18. Why would it take longer for more complex DNA to reanneal?
19. Define the following: negative supercoil, positive supercoil, topoisomerase I (note the role of tyrosine)
topoisomerase II (note the role of ATP)
Chapter 5:
20. Why can RNA form more complex structures than DNA?
21. Explain how riboswitches work.
22. Explain the RNA world hypothesis. How does the ribosome structure support this model?
Chapter 7:
23. Describe SDS-PAGE and western blotting, and the knowledge gained from each.
24. How can proteins be used to find their corresponding gene of interest in forward genetics?
major difficulty with this approach in humans?
25. How can antibodies be used to identify the sequence and location of human genes?
26. Why was working with DNA more difficult than proteins?
27. What three main tools were available for analyzing and manipulating DNA in the early 19
harre?
2.
Transcribed Image Text:Side 12 of 92 ahted sae MacBook esc 80 F1 F2 F3 14. What is the purpose of the dozens of p53 modifications? Chapter 4: 15. Which groove contains more "information" and why? How do proteins interact specifically with this DiA groove, as when a zinc finger crosses the groove? 16. Which of the following base pairs could proteins distinguish, and why? a. Major groove base pairs (GC/CG, AT/TA, GC/TA, GC/AT) b. Minor groove base pairs (GC/CG, AT/TA, GC/TA, GC/AT) 17. What contributes to DNA stability with regards to Tm? Which type of base pairs takes the most energy to pull apart (i.e. require a higher temperature/Tm to dissociate)? 18. Why would it take longer for more complex DNA to reanneal? 19. Define the following: negative supercoil, positive supercoil, topoisomerase I (note the role of tyrosine) topoisomerase II (note the role of ATP) Chapter 5: 20. Why can RNA form more complex structures than DNA? 21. Explain how riboswitches work. 22. Explain the RNA world hypothesis. How does the ribosome structure support this model? Chapter 7: 23. Describe SDS-PAGE and western blotting, and the knowledge gained from each. 24. How can proteins be used to find their corresponding gene of interest in forward genetics? major difficulty with this approach in humans? 25. How can antibodies be used to identify the sequence and location of human genes? 26. Why was working with DNA more difficult than proteins? 27. What three main tools were available for analyzing and manipulating DNA in the early 19 harre? 2.
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