Table 8

Comparison to other protein disorder predictors over a blind-test set. The non-redundant blind-test set contained 1,304 recent PDB chains that were unrelated to any VSL2 training sequence. The three VSL2 predictors were re-trained with all 1,327 training sequences. The prediction accuracies were calculated at default thresholds, e.g. 0.5 for VL-XT, VL3-E, VSL1, VSL2B, VSL2P and VSL2.

SN

SP

ACC

SNS

SNL

AUC


VL-XT

56.0

77.9

67.0

55.8

53.0

74.4

VL3-E

28.4

91.4

59.9

26.8

59.7

69.2

DisEMBL

25.9

97.9

61.9

25.7

26.5

83.9

RONN

34.7

88.8

61.8

33.6

56.4

67.2

DISOPRED2

53.8

94.7

74.2

53.5

48.6

84.6

VSL1

75.6

85.8

80.7

76.1

63.6

88.5

VSL2B

73.7

80.8

77.3

74.2

63.1

84.1

VSL2P

78.4

80.4

79.4

78.5

71.6

86.7

VSL2

79.4

81.4

80.4

79.6

73.7

87.5


(a) per-chain


SN

SP

ACC

SNS

SNL

AUC


VL-XT

54.2

79.2

66.7

54.7

52.3

74.0

VL3-E

36.5

93.9

65.2

30.5

59.2

75.9

DisEMBL

25.3

98.3

61.8

25.4

24.7

80.1

RONN

41.6

89.1

65.4

39.1

51.2

71.3

DISOPRED2

47.8

95.6

71.7

48.7

44.6

83.4

VSL1

68.3

87.4

77.9

70.9

58.3

86.2

VSL2B

67.1

82.6

74.8

68.9

60.3

82.0

VSL2P

72.7

82.5

77.6

74.2

67.1

85.3

VSL2

74.7

82.8

78.7

76.1

69.4

86.3


(b) per-residue


Peng et al. BMC Bioinformatics 2006 7:208   doi:10.1186/1471-2105-7-208

Open Data