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. 2013 Jul 23;62(6):597–606. doi: 10.1093/jmicro/dft038

Table 1.

Statistics of the data collection for structural analysis of H+,K+-ATPase in different conformations

Conformation Preparation Cryo-grids used Micrographs
Resolution Phase residual Ref.
Tilt angles
Total
20° 45° 60° 70°
E2AlF Single carbon 121
59 10a 28a 97
328 465 420 1213
E2AlF Carbon sandwich 182 7 48 92 118 54 319 6.5 Å 31.5° [15]
70 120 202 206 119 717
86 205 311 262 217 1081
274 584 660 430 349 2297
E2BeF Carbon sandwich 47 11 20 57 88 8 Å 33.1° [24]
38 24 73 135
47 64 90 201
120 156 286 562
(SCH)E2BeF Carbon sandwich 97 6 43 128 118 295 7 Å 37.1° [16]
14 53 203 210 480
15 59 278 249 601
70 90 542 403 1105
(Rb+)E2AlF Carbon sandwich 78 3 18 68 57 146 8 Å 35.6° [25]
9 29 88 116 242
42 87 208 202 539
80 275 410 402 1167
(K+)E2AlF Carbon sandwich 125 6 34 54 69 163 8 Å 36.9° [25]
38 73 118 126 355
80 100 180 204 564
443 588 430 551 2012

Table shows numbers of ‘micrographs’ used for the structural determination of the indicated conformation of H+,K+-ATPase (see Materials and Methods for details). Numbers of micrographs obtained (fourth rows), selected for scanning (third rows), processed by MRC program (second rows) and finally merged into a 3D structure (first rows) are indicated. Because all of the tilted images were affected by the image-shift due to specimen charging in the case of the single carbon preparation of the E2AlF crystals, micrographs with recognizable diffraction spots in the direction parallel to the tilt axis (as shown in Fig. 4d) were selected (a).