To draw: The 5BU-G base pair. Concept introduction: A base analogue is a chemical which that has a similar structure of either a purine or a pyrimidine is called a base analogue. 5-Bromouracil (5BU) is the base analogue that has a similar structure to that of the pyrimidine thymine. Therefore, this structure replaces or substitutes thymine present in a DNA structure and pairs it with adenine. The enol form of 5-Bromouracil causes the tautomeric shift of 5-Bromouracil. This enol form pairs with the guanine base, rather than binding to the adenine.

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Answer 1

Question

Chapter 25, Problem 15E

Summary Introduction

To draw: The 5BU-G base pair.

Concept introduction: A base analogue is a chemical which that has a similar structure of either a purine or a pyrimidine is called a base analogue. 5-Bromouracil (5BU) is the base analogue that has a similar structure to that of the pyrimidine thymine. Therefore, this structure replaces or substitutes thymine present in a DNA structure and pairs it with adenine. The enol form of 5-Bromouracil causes the tautomeric shift of 5-Bromouracil. This enol form pairs with the guanine base, rather than binding to the adenine.

Summary Introduction

To explain: The type of mutation that results in the 5BU-G base pair.

Concept introduction: A base analogue is a chemical that has a similar structure of either a purine or a pyrimidine. 5-Bromouracil (5BU) is the base analogue that has a similar structure to that of the pyrimidine thymine. Therefore, this structure replaces or substitutes thymine present in a DNA structure and pairs with adenine. The enol form of 5-Bromouracil causes the tautomeric shift in 5-Bromouracil. This enol form pairs with the guanine base, rather than binding to the adenine.

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Answer 2

Question

Chapter 25, Problem 15E

Summary Introduction

To draw: The 5BU-G base pair.

Concept introduction: A base analogue is a chemical which that has a similar structure of either a purine or a pyrimidine is called a base analogue. 5-Bromouracil (5BU) is the base analogue that has a similar structure to that of the pyrimidine thymine. Therefore, this structure replaces or substitutes thymine present in a DNA structure and pairs it with adenine. The enol form of 5-Bromouracil causes the tautomeric shift of 5-Bromouracil. This enol form pairs with the guanine base, rather than binding to the adenine.

Summary Introduction

To explain: The type of mutation that results in the 5BU-G base pair.

Concept introduction: A base analogue is a chemical that has a similar structure of either a purine or a pyrimidine. 5-Bromouracil (5BU) is the base analogue that has a similar structure to that of the pyrimidine thymine. Therefore, this structure replaces or substitutes thymine present in a DNA structure and pairs with adenine. The enol form of 5-Bromouracil causes the tautomeric shift in 5-Bromouracil. This enol form pairs with the guanine base, rather than binding to the adenine.

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Answer 3

Question

Chapter 25, Problem 15E

Summary Introduction

To draw: The 5BU-G base pair.

Concept introduction: A base analogue is a chemical which that has a similar structure of either a purine or a pyrimidine is called a base analogue. 5-Bromouracil (5BU) is the base analogue that has a similar structure to that of the pyrimidine thymine. Therefore, this structure replaces or substitutes thymine present in a DNA structure and pairs it with adenine. The enol form of 5-Bromouracil causes the tautomeric shift of 5-Bromouracil. This enol form pairs with the guanine base, rather than binding to the adenine.

Summary Introduction

To explain: The type of mutation that results in the 5BU-G base pair.

Concept introduction: A base analogue is a chemical that has a similar structure of either a purine or a pyrimidine. 5-Bromouracil (5BU) is the base analogue that has a similar structure to that of the pyrimidine thymine. Therefore, this structure replaces or substitutes thymine present in a DNA structure and pairs with adenine. The enol form of 5-Bromouracil causes the tautomeric shift in 5-Bromouracil. This enol form pairs with the guanine base, rather than binding to the adenine.

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Answer 4

Question

Chapter 25, Problem 15E

Summary Introduction

To draw: The 5BU-G base pair.

Concept introduction: A base analogue is a chemical which that has a similar structure of either a purine or a pyrimidine is called a base analogue. 5-Bromouracil (5BU) is the base analogue that has a similar structure to that of the pyrimidine thymine. Therefore, this structure replaces or substitutes thymine present in a DNA structure and pairs it with adenine. The enol form of 5-Bromouracil causes the tautomeric shift of 5-Bromouracil. This enol form pairs with the guanine base, rather than binding to the adenine.

Summary Introduction

To explain: The type of mutation that results in the 5BU-G base pair.

Concept introduction: A base analogue is a chemical that has a similar structure of either a purine or a pyrimidine. 5-Bromouracil (5BU) is the base analogue that has a similar structure to that of the pyrimidine thymine. Therefore, this structure replaces or substitutes thymine present in a DNA structure and pairs with adenine. The enol form of 5-Bromouracil causes the tautomeric shift in 5-Bromouracil. This enol form pairs with the guanine base, rather than binding to the adenine.

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Answer 5

Chapter 25, Problem 15E

Summary Introduction

To draw: The 5BU-G base pair.

Concept introduction: A base analogue is a chemical which that has a similar structure of either a purine or a pyrimidine is called a base analogue. 5-Bromouracil (5BU) is the base analogue that has a similar structure to that of the pyrimidine thymine. Therefore, this structure replaces or substitutes thymine present in a DNA structure and pairs it with adenine. The enol form of 5-Bromouracil causes the tautomeric shift of 5-Bromouracil. This enol form pairs with the guanine base, rather than binding to the adenine.

Summary Introduction

To explain: The type of mutation that results in the 5BU-G base pair.

Concept introduction: A base analogue is a chemical that has a similar structure of either a purine or a pyrimidine. 5-Bromouracil (5BU) is the base analogue that has a similar structure to that of the pyrimidine thymine. Therefore, this structure replaces or substitutes thymine present in a DNA structure and pairs with adenine. The enol form of 5-Bromouracil causes the tautomeric shift in 5-Bromouracil. This enol form pairs with the guanine base, rather than binding to the adenine.

Answer 6

Chapter 25, Problem 15E

Summary Introduction

To draw: The 5BU-G base pair.

Concept introduction: A base analogue is a chemical which that has a similar structure of either a purine or a pyrimidine is called a base analogue. 5-Bromouracil (5BU) is the base analogue that has a similar structure to that of the pyrimidine thymine. Therefore, this structure replaces or substitutes thymine present in a DNA structure and pairs it with adenine. The enol form of 5-Bromouracil causes the tautomeric shift of 5-Bromouracil. This enol form pairs with the guanine base, rather than binding to the adenine.

Answer 7

Chapter 25, Problem 15E

Summary Introduction

To draw: The 5BU-G base pair.

Concept introduction: A base analogue is a chemical which that has a similar structure of either a purine or a pyrimidine is called a base analogue. 5-Bromouracil (5BU) is the base analogue that has a similar structure to that of the pyrimidine thymine. Therefore, this structure replaces or substitutes thymine present in a DNA structure and pairs it with adenine. The enol form of 5-Bromouracil causes the tautomeric shift of 5-Bromouracil. This enol form pairs with the guanine base, rather than binding to the adenine.

Answer 8

Summary Introduction

To explain: The type of mutation that results in the 5BU-G base pair.

Concept introduction: A base analogue is a chemical that has a similar structure of either a purine or a pyrimidine. 5-Bromouracil (5BU) is the base analogue that has a similar structure to that of the pyrimidine thymine. Therefore, this structure replaces or substitutes thymine present in a DNA structure and pairs with adenine. The enol form of 5-Bromouracil causes the tautomeric shift in 5-Bromouracil. This enol form pairs with the guanine base, rather than binding to the adenine.

Answer 9

Summary Introduction

To explain: The type of mutation that results in the 5BU-G base pair.

Concept introduction: A base analogue is a chemical that has a similar structure of either a purine or a pyrimidine. 5-Bromouracil (5BU) is the base analogue that has a similar structure to that of the pyrimidine thymine. Therefore, this structure replaces or substitutes thymine present in a DNA structure and pairs with adenine. The enol form of 5-Bromouracil causes the tautomeric shift in 5-Bromouracil. This enol form pairs with the guanine base, rather than binding to the adenine.

Answer 10

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Answer 11

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Answer 12

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Answer 13

Ch. 25 - Prob. 1E Ch. 25 - Prob. 2E Ch. 25 - 3. You have discovered a drug that inhibits the...Ch. 25 - Prob. 4E Ch. 25 - Prob. 5E Ch. 25 - Prob. 6E Ch. 25 - Prob. 7E Ch. 25 - Prob. 8E Ch. 25 - Prob. 9E Ch. 25 - Prob. 10E

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