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Table 2 Frequency of residues in Ala-X-Ala conformations, their extended state ASA (ESA) values and highest observed ASA (HOA) obtained from the entire data set of proteins (8.9 million residues, overall including residues with different sequence neighbors).

From: Context dependent reference states of solvent accessibility derived from native protein structures and assessed by predictability analysis

Res

Freq

ESA

HOA

CC

Res

Freq

ESA

HOA

CC

C

998

140.4

120

0.9200

L

7428

183.1

173

0.9885

W

889

240.5

217

0.9633

S

3694

117.2

142

0.9885

M

1554

200.1

181

0.9740

T

3049

138.7

149

0.9891

Y

1857

213.7

223

0.9813

Q

2810

178.6

204

0.9893

F

2453

200.7

202

0.9838

N

2910

146.4

176

0.9895

I

4114

185.0

167

0.9843

R

3297

229.0

280

0.9895

H

1849

181.9

200

0.9845

P

2528

141.9

138

0.9901

G

5328

78.7

96

0.9857

K

4192

205.7

219

0.9916

A

8032

110.2

120

0.9873

E

4962

174.7

201

0.9917

V

5704

153.7

148

0.9875

D

4567

144.1

165

0.9934

  1. Correlation coefficient (CC) between relative ASA obtained after normalizing by the Ala-X-Ala extended state (ESA) and tripeptide highest observed ASA (context-dependent ASA) is also provided in the last column. CC values are based on all residues with different sequence neighbor. Residues are arranged in the order of CC values.
  2. Abbreviations: Res: residue ID, Freq: number of residues in Ala-X-Ala conformation, ESA: extended state ASA of Ala-X-Ala conformation, HOA: highest observed ASA in Y-X-Z conformation (any neighbor), CC: correlation coefficient between ESA-normalized and HOA-normalized values in the benchmark data set.