28. Calculate the overall net charge for the tripeptide leucine-lysine-histidine for pH = 1, 3, 5, 7, 10, and 12 given the following pKa values: amino-terminal amino 9.0; carboxy-terminal carboxyl 2.0; side-chain amino 10.5, and imidazole 6.0. Net charge at pH 1 = Net charge at pH 3 = Net charge at pH 5 = Net charge at pH 7= Net charge at pH 10 = Net charge at pH 12 = 29. What is pl for the tripeptide from previous question? 30. Draw the structure of this tripeptide (leucine-lysine-histidine) with the charges as it would exist at pH S. You do not have to depict the proper stereochemistry in the structure.

Introduction to General, Organic and Biochemistry
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ISBN:9781285869759
Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar Torres
Publisher:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar Torres
Chapter22: Proteins
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28. Calculate the overall net charge for the tripeptide leucine-lysine-histidine for pH = 1, 3, 5, 7, 10, and 12
given the following pKa values:
amino-terminal amino 9.0; carboxy-terminal carboxyl 2,.0; side-chain amino 10.5, and imidazole 6.0.
Net charge at pH 1 =
Net charge at pH 3 =
Net charge at pH 5 =
Net charge at pH 7-
Net charge at pH 10 =
Net charge at pH 12 =
29. What is pl for the tripeptide from previous question?
30. Draw the structure of this tripeptide (leucine-lysine-histidine) with the charges as it would exist at pH S.
You do not have to depict the proper stereochemistry in the structure.
Transcribed Image Text:28. Calculate the overall net charge for the tripeptide leucine-lysine-histidine for pH = 1, 3, 5, 7, 10, and 12 given the following pKa values: amino-terminal amino 9.0; carboxy-terminal carboxyl 2,.0; side-chain amino 10.5, and imidazole 6.0. Net charge at pH 1 = Net charge at pH 3 = Net charge at pH 5 = Net charge at pH 7- Net charge at pH 10 = Net charge at pH 12 = 29. What is pl for the tripeptide from previous question? 30. Draw the structure of this tripeptide (leucine-lysine-histidine) with the charges as it would exist at pH S. You do not have to depict the proper stereochemistry in the structure.
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