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Table 4 Prediction of the clustered human proteome.

From: pkaPS: prediction of protein kinase A phosphorylation sites with the simplified kinase-substrate binding model

Cluster number

Total entries

Predicted S/T (%)

Predicted S/T

Predicted entries (%)

Predicted entries

Common domains/superfamily

171

21

39.7

52

100

21

High mobility group

88

32

36.2

141

100

32

Histone H2A

43

48

30.8

518

91.7

44

Splicing factor, predicted RNA-binding

84

34

29

249

100

34

TAFII28-like

109

27

27.3

81

100

27

Unknown

72

36

26.4

101

94.4

34

GAGE protein

131

24

24.7

80

87.5

21

Ribosomal protein L21e

123

25

22.8

146

100

25

Ribosomal protein L22

172

21

22.5

108

100

21

Histone H2B

33

59

21.6

390

98.3

58

Cyclophilin-like

94

30

21.1

111

93.3

28

Histones H3/H4

105

27

20.9

88

96.3

26

KRAB domain

7

136

20

1300

96.3

131

GTPase-activating protein

10

123

19.7

412

84.6

104

Unknown

115

26

19.6

126

100

26

60S ribosomal protein L6

154

22

18.7

94

100

22

HIV-1 Vpr-binding, High mobility group

79

35

17.5

206

91.4

32

Ras GTPase-activating protein

38

52

17.4

287

92.3

48

Septins

153

22

16.3

105

77.3

17

RNA-binding protein TIA-1/TIAR (RRM superfamily)

160

22

16.1

465

100

22

Uncharacterized conserved protein (KOG4791)

  1. The table shows the 20 clusters with the best ratio between predicted and total S/T-sites. The column to the right displays a summary of the cluster with respect to the most common domains found using the CDD [85] and PFAM [86] databases (e-value cutoff of 0.01). Lower cluster numbers indicate clusters with more sequences included.