Table 1 Mapping and comparison of lysine solvent accessibilities to Cryo-EM structures

From: In vivo conformational space and defects of misfolded CFTR variants by covalent protein painting

Position

Sequence

Mean surface accessibility (%)

Wt Cryo-EM structure

Wt Cryo-EM structure, ATP bound, phosphorylated

wt

∆F508

K52

QIPSVDSADNLSEKL

nd

92.6

accessible (93.75 Å2)

accessible (13.39 Å2)

K95

LGEVTKAVQPL

96.1

77.0

partially accessible (3.51 Å2)

accessible (35.78 Å2)

K273

VITSEMIENIQSVKAY

61.8

95.0

inaccessible (0.48 Å2)

partially accessible (6.92 Å2)

K283

CWEEAMEKMIENLRQTEL

98.7

98.9

accessible (53.98 Å2)

accessible (39.15 Å2)

K370

DSLGAINKIQDF

99.8

99.0

accessible (41.45 Å2)

accessible (29.92 Å2)

K370/K377

DSGAINKIQDFLQKQEY

99.8

98.9

accessible (41.45 Å2, 39.11 Å2)

accessible (29.92 Å2, 36.11 Å2)

K411

not present in CryoEM

 

K420

not present in CryoEM

 

K442

SLLGTPVLKDINF

99.2

95.7

accessible (39.53 Å2)

accessible (47.84 Å2)

K464

AVAGSTGAGKTSLL

99.7

93.0

accessible (9.59 Å2)

partially accessible (4.36 Å2)

K536

AEKDNIVLGEGGITL

98.8

94.7

accessible (51.94 Å2)

accessible (26.99 Å2)

K584

GYLDVLTEKEIF

nd

91.9

accessible (8.91 Å2)

accessible (18.03 Å2)

K1060

ESEGRSPIFTHLVTSLKGLW

99.0

98.5

accessible (49.05 Å2)

partially accessible (3.15 Å2)

K1080

FETLFHKAL

99.9

99.7

accessible (59.33 Å2)

accessible (35.59 Å2)

K1165

KFIDMPTEGKPT

99.5

96.6

accessible (19.66 Å2)

accessible (54.57 Å2)

K1218

TAKYTEGGNAILENISF

nd

89.3

accessible (41.39 Å2)

accessible (30.56 Å2)

K1292

GVIPQKVF

nd

94.4

accessible (48.20 Å2)

partially accessible (3.01 Å2)

K1302

RKNLDPYEQWSDQEIW

98.4

97.9

accessible (26.64 Å2)

accessible (13.86 Å2)

K1317

KVADEVGLRSVIEQFPGKLDF

99.7

99.5

accessible (37.29 Å2)

accessible (53.09 Å2)

K1334

RSVIEQFPGKLDF

99.9

nd

accessible (56.92 Å2)

accessible (49.60 Å2)

K1420

LVIEENKVRQY

99.3

94.8

accessible (51.71 Å2)

accessible (51.65 Å2)

K1429

DSIQKLL

99.9

99.5

accessible (57.27 Å2)

accessible (33.64 Å2)

  1. Quantified lysines and respective peptide sequences were mapped onto the available Cryo-EM structures 5UAK and 6MSM and solvent accessible isosurfaces probed with a rolling probe.