TABLE 5.1 Properties of the common amino acids found in proteins pK, of a-COOH Group pk, of a-NH Group pK, of lonizing Side Chain Abbreviations: 1- Residue Mass Occurrence in Name and 3-letter codes (daltons) Proteins (mol %) Alanine A, Ala 2.3 9.7 71.08 8.7 Arginine R, Arg 2.2 9.0 12.5 156.20 5.0 Asparagine N, Asn 2.0 8.8 114.11 4.2 D, Asp C, Cys Q, Gin E, Glu G, Gly Н, His I, lle Aspartic acid 2.1 9.8 3.9 115.09 5.9 Cysteine 1.8 10.8 8.3 103.14 1.3 Glutamine 2.2 9.1 128.14 3.7 Glutamic acid 2.2 9.7 4.2 129.12 6.6 Glycine 2.3 9.6 57.06 7.9 Histidine 1.8 9.2 6.0 137.15 2.4 Isoleucine 2.4 9.7 113.17 5.5 Leucine L, Leu 2.4 9.6 113.17 8.9 K, Lys М, Met F, Phe Lysine 2.2 9.0 10.0 128.18 5.5 Methionine 2.3 9.2 131.21 2.0 Phenylalanine 1.8 9.1 147.18 4.0 Proline P, Pro 2.0 10.6 97.12 4.7 Serine S, Ser 2.2 9.2 87.08 5.8 Threonine T, Thr 2.6 10.4 101.11 5.6 Tryptophan W, Trp 2.4 9.4 186.21 1.5 Tyrosine Y, Tyr 2.2 9.1 10.1 163.18 3.5 Valine V, Val 2.3 9.6 99.14 7.2

Biochemistry
9th Edition
ISBN:9781319114671
Author:Lubert Stryer, Jeremy M. Berg, John L. Tymoczko, Gregory J. Gatto Jr.
Publisher:Lubert Stryer, Jeremy M. Berg, John L. Tymoczko, Gregory J. Gatto Jr.
Chapter1: Biochemistry: An Evolving Science
Section: Chapter Questions
Problem 1P
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Draw the structure of the peptide DTLH, showing the backbone and sidechain
atoms in the ionization states favored at pH = 7.0.
(a) Draw a water molecule making a hydrogen bond to a side-chain H-bond
donor.
(b) Draw a water molecule making a hydrogen bond to a main-chain H-bond acceptor.                                                                                                           (c) Using the values of pKas given in as shown, calculate the pI for DTLH.

TABLE 5.1 Properties of the common amino acids found in proteins
pK, of a-COOH
Group
pk, of a-NH
Group
pK, of lonizing
Side Chain
Abbreviations: 1-
Residue Mass
Occurrence in
Name
and 3-letter codes
(daltons)
Proteins (mol %)
Alanine
A, Ala
2.3
9.7
71.08
8.7
Arginine
R, Arg
2.2
9.0
12.5
156.20
5.0
Asparagine
N, Asn
2.0
8.8
114.11
4.2
D, Asp
C, Cys
Q, Gin
E, Glu
G, Gly
Н, His
I, lle
Aspartic acid
2.1
9.8
3.9
115.09
5.9
Cysteine
1.8
10.8
8.3
103.14
1.3
Glutamine
2.2
9.1
128.14
3.7
Glutamic acid
2.2
9.7
4.2
129.12
6.6
Glycine
2.3
9.6
57.06
7.9
Histidine
1.8
9.2
6.0
137.15
2.4
Isoleucine
2.4
9.7
113.17
5.5
Leucine
L, Leu
2.4
9.6
113.17
8.9
K, Lys
М, Met
F, Phe
Lysine
2.2
9.0
10.0
128.18
5.5
Methionine
2.3
9.2
131.21
2.0
Phenylalanine
1.8
9.1
147.18
4.0
Proline
P, Pro
2.0
10.6
97.12
4.7
Serine
S, Ser
2.2
9.2
87.08
5.8
Threonine
T, Thr
2.6
10.4
101.11
5.6
Tryptophan
W, Trp
2.4
9.4
186.21
1.5
Tyrosine
Y, Tyr
2.2
9.1
10.1
163.18
3.5
Valine
V, Val
2.3
9.6
99.14
7.2
Transcribed Image Text:TABLE 5.1 Properties of the common amino acids found in proteins pK, of a-COOH Group pk, of a-NH Group pK, of lonizing Side Chain Abbreviations: 1- Residue Mass Occurrence in Name and 3-letter codes (daltons) Proteins (mol %) Alanine A, Ala 2.3 9.7 71.08 8.7 Arginine R, Arg 2.2 9.0 12.5 156.20 5.0 Asparagine N, Asn 2.0 8.8 114.11 4.2 D, Asp C, Cys Q, Gin E, Glu G, Gly Н, His I, lle Aspartic acid 2.1 9.8 3.9 115.09 5.9 Cysteine 1.8 10.8 8.3 103.14 1.3 Glutamine 2.2 9.1 128.14 3.7 Glutamic acid 2.2 9.7 4.2 129.12 6.6 Glycine 2.3 9.6 57.06 7.9 Histidine 1.8 9.2 6.0 137.15 2.4 Isoleucine 2.4 9.7 113.17 5.5 Leucine L, Leu 2.4 9.6 113.17 8.9 K, Lys М, Met F, Phe Lysine 2.2 9.0 10.0 128.18 5.5 Methionine 2.3 9.2 131.21 2.0 Phenylalanine 1.8 9.1 147.18 4.0 Proline P, Pro 2.0 10.6 97.12 4.7 Serine S, Ser 2.2 9.2 87.08 5.8 Threonine T, Thr 2.6 10.4 101.11 5.6 Tryptophan W, Trp 2.4 9.4 186.21 1.5 Tyrosine Y, Tyr 2.2 9.1 10.1 163.18 3.5 Valine V, Val 2.3 9.6 99.14 7.2
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