PRISMΔDB

Analyze how specific documents activate the features of the SAE. Select a dataset, a run and a document to begin.

Active Features

1497

0.0
Details List
#1455 Feature 1455
3.1
#2188 Feature 2188
2.9
#163 Feature 163
2.8
#778 Feature 778
2.6
#2710 Feature 2710
2.5
#1071 Feature 1071
2.3
#1541 Feature 1541
2.3
#15 Feature 15
2.2
#251 Feature 251
2.2
#2766 Feature 2766
2.2
#759 Feature 759
2.2
#736 Feature 736
2.2
#2909 Feature 2909
2.1
#1186 Feature 1186
2.1
#2222 Feature 2222
2.1
#357 Feature 357
2.0
#2672 Feature 2672
2.0
#2619 Feature 2619
1.9
#1683 Feature 1683
1.9
#2970 Feature 2970
1.8
#2333 Feature 2333
1.8
#1776 Feature 1776
1.8
#693 Feature 693
1.8
#1550 Feature 1550
1.8
#2658 Feature 2658
1.8
#1693 Feature 1693
1.7
#965 Feature 965
1.7
#681 Feature 681
1.7
#872 Feature 872
1.7
#1420 Feature 1420
1.7
#238 Feature 238
1.7
#2354 Feature 2354
1.7
#31 Feature 31
1.7
#1591 Feature 1591
1.6
#205 Feature 205
1.6
#2408 Feature 2408
1.6
#1572 Feature 1572
1.5
#503 Feature 503
1.5
#1159 Feature 1159
1.5
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1.5
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1.5
#1205 Feature 1205
1.5
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1.5
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1.5
#1958 Feature 1958
1.5
#175 Feature 175
1.5
#1119 Feature 1119
1.5
#1436 Feature 1436
1.5
#1844 Feature 1844
1.5
#505 Feature 505
1.4
#3069 Feature 3069
1.4
#1404 Feature 1404
1.4
#1290 Feature 1290
1.4
#1083 Feature 1083
1.4
#2415 Feature 2415
1.4
#3052 Feature 3052
1.4
#2493 Feature 2493
1.4
#590 Feature 590
1.4
#2081 Feature 2081
1.4
#2337 Feature 2337
1.4
#2962 Feature 2962
1.4
#2118 Feature 2118
1.4
#51 Feature 51
1.4
#1618 Feature 1618
1.4
#402 Feature 402
1.4
#768 Feature 768
1.4
#1763 Feature 1763
1.4
#641 Feature 641
1.3
#669 Feature 669
1.3
#1526 Feature 1526
1.3
#2850 Feature 2850
1.3
#2727 Feature 2727
1.3
#2556 Feature 2556
1.3
#3067 Feature 3067
1.3
#2016 Feature 2016
1.3
#2105 Feature 2105
1.3
#831 Feature 831
1.3
#531 Feature 531
1.3
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1.3
#1551 Feature 1551
1.3
#2309 Feature 2309
1.3
#2961 Feature 2961
1.3
#2663 Feature 2663
1.3
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1.3
#2301 Feature 2301
1.3
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1.3
#247 Feature 247
1.3
#1503 Feature 1503
1.3
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1.3
#673 Feature 673
1.3
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1.3
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1.3
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1.3
#1834 Feature 1834
1.3
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1.3
#550 Feature 550
1.3
#1473 Feature 1473
1.3
#529 Feature 529
1.3
#1180 Feature 1180
1.3
#86 Feature 86
1.3
#2048 Feature 2048
1.3
#2867 Feature 2867
1.2
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1.2
#260 Feature 260
1.2
#1015 Feature 1015
1.2
#1608 Feature 1608
1.2
#3005 Feature 3005
1.2
#285 Feature 285
1.2
#1289 Feature 1289
1.2
#2015 Feature 2015
1.2
#2475 Feature 2475
1.2
#1925 Feature 1925
1.2
#957 Feature 957
1.2
#1209 Feature 1209
1.2
#2985 Feature 2985
1.2
#1794 Feature 1794
1.2
#60 Feature 60
1.2
#2795 Feature 2795
1.2
#2119 Feature 2119
1.2
#2191 Feature 2191
1.2
#538 Feature 538
1.2
#2423 Feature 2423
1.2
#3055 Feature 3055
1.2
#1556 Feature 1556
1.2
#2416 Feature 2416
1.2
#2289 Feature 2289
1.2
#1851 Feature 1851
1.2
#1970 Feature 1970
1.2
#2123 Feature 2123
1.2
#2774 Feature 2774
1.2
#431 Feature 431
1.2
#34 Feature 34
1.2
#1192 Feature 1192
1.2
#2936 Feature 2936
1.2
#316 Feature 316
1.2
#404 Interactions and Mechanisms
1.2
#2357 Feature 2357
1.2
#960 Feature 960
1.2
#1011 Feature 1011
1.2
#1932 Feature 1932
1.2
#672 Feature 672
1.2
#2873 Feature 2873
1.2
#1188 Feature 1188
1.2
#1818 Feature 1818
1.2
#1260 Feature 1260
1.2
#1560 Feature 1560
1.1
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1.1
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1.1
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1.1
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1.1
#2956 Feature 2956
1.1
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1.1
#476 Feature 476
1.1
#704 Feature 704
1.1
#1179 Feature 1179
1.1
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1.1
#800 Feature 800
1.1
#1085 Feature 1085
1.1
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1.1
#248 Feature 248
1.1
#534 Feature 534
1.1
#3026 Feature 3026
1.1
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1.1
#1337 Feature 1337
1.1
#2554 Feature 2554
1.1
#0 Feature 0
1.1
#1367 Feature 1367
1.1
#1695 Feature 1695
1.1
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1.1
#1914 Feature 1914
1.1
#2578 Feature 2578
1.1
#780 Feature 780
1.1
#1316 Feature 1316
1.1
#2160 Feature 2160
1.1
#2144 Feature 2144
1.1
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1.1
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1.1
#1330 Feature 1330
1.1
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1.1
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1.1
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1.1
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1.1
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1.1
#2033 Feature 2033
1.1
#1030 Feature 1030
1.1
#1930 Feature 1930
1.1
#334 Feature 334
1.1
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1.1
#487 Feature 487
1.1
#2837 Feature 2837
1.1
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1.1
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1.1
#1571 Feature 1571
1.1
#491 Feature 491
1.1
#341 Feature 341
1.1
#1210 Feature 1210
1.0
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1.0
#1038 Feature 1038
1.0
#415 Feature 415
1.0
#2661 Feature 2661
1.0
#302 Feature 302
1.0
#1329 Feature 1329
1.0
#1579 Feature 1579
1.0
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1.0
#2866 Feature 2866
1.0
#1816 Feature 1816
1.0
#1801 Feature 1801
1.0
#2825 Feature 2825
1.0
#1409 Feature 1409
1.0
#2791 Feature 2791
1.0
#1620 Feature 1620
1.0
#2678 Feature 2678
1.0
#290 Feature 290
1.0
#2938 Feature 2938
1.0
#2014 Feature 2014
1.0
#2360 Feature 2360
1.0
#808 Feature 808
1.0
#1479 Feature 1479
1.0
#3003 Feature 3003
1.0
#1487 Feature 1487
1.0
#1864 Feature 1864
1.0
#1309 Feature 1309
1.0
#889 Feature 889
1.0
#1212 Feature 1212
1.0
#2438 Feature 2438
1.0
#2805 Feature 2805
1.0
#1619 Feature 1619
1.0
#2005 Feature 2005
1.0
#576 Feature 576
1.0
#869 Feature 869
1.0
#1101 Feature 1101
1.0
#192 Feature 192
1.0
#2122 Feature 2122
1.0
#5 Feature 5
1.0
#420 Feature 420
1.0
#2459 Feature 2459
1.0
#2974 Feature 2974
1.0
#2525 Feature 2525
1.0
#1419 Feature 1419
1.0
#609 Feature 609
1.0
#194 Feature 194
1.0
#1873 Feature 1873
1.0
#1308 Feature 1308
1.0
#224 Feature 224
1.0
#2920 Feature 2920
1.0
#168 Feature 168
1.0
#574 Feature 574
1.0
#1890 Feature 1890
1.0
#1691 Feature 1691
1.0
#551 Feature 551
1.0
#876 Feature 876
1.0
#119 Feature 119
1.0
#2201 Feature 2201
1.0
#979 Feature 979
1.0
#1429 Feature 1429
1.0
#245 Feature 245
1.0
#3002 Feature 3002
1.0
#823 Feature 823
1.0
#847 Feature 847
1.0
#1819 Feature 1819
1.0
#162 Feature 162
1.0
#1410 Feature 1410
0.9
#151 Feature 151
0.9
#1286 Feature 1286
0.9
#2610 Feature 2610
0.9
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0.9
#1421 Feature 1421
0.9
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0.9
#1609 Feature 1609
0.9
#901 Feature 901
0.9
#1896 Feature 1896
0.9
#2352 Feature 2352
0.9
#2863 Feature 2863
0.9
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0.9
#436 Feature 436
0.9
#294 Feature 294
0.9
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0.9
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0.9
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0.9
#1976 Feature 1976
0.9
#1424 Feature 1424
0.9
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0.9
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0.9
#98 Feature 98
0.9
#1837 Feature 1837
0.9
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0.9
#417 Feature 417
0.9
#389 Feature 389
0.9
#2521 Feature 2521
0.9
#1067 Feature 1067
0.9
#515 Feature 515
0.9
#802 Feature 802
0.9
#2240 Feature 2240
0.9
#21 Feature 21
0.9
#78 Feature 78
0.9
#1824 Feature 1824
0.9
#1248 Feature 1248
0.9
#2343 Feature 2343
0.9
#549 Feature 549
0.9
#2622 Feature 2622
0.9
#2732 Feature 2732
0.9
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0.9
#2146 Feature 2146
0.9
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0.9
#1697 Feature 1697
0.9
#116 Feature 116
0.9
#1590 Feature 1590
0.9
#2631 Feature 2631
0.9
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0.9
#1070 Feature 1070
0.9
#2637 Feature 2637
0.9
#772 Feature 772
0.9
#4 Feature 4
0.9
#2481 Feature 2481
0.9
#992 Feature 992
0.9
#575 Feature 575
0.9
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0.9
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0.9
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0.9
#477 Feature 477
0.9
#1859 Feature 1859
0.9
#29 Feature 29
0.9
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0.9
#1391 Feature 1391
0.9
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0.9
#2769 Feature 2769
0.9
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0.9
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0.9
#326 Feature 326
0.9
#1376 Feature 1376
0.9
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0.9
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0.9
#810 Feature 810
0.9
#1430 Feature 1430
0.9
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0.9
#2455 Feature 2455
0.9
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0.9
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0.9
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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Document Content

Generation of histo-blood group B transferase by replacing the N-acetyl-D-galactosamine recognition domain of human A transferase with the galactose-recognition domain of evolutionarily related murine alpha1,3-galactosyltransferase.
The alpha1,3-galactosyl epitope (alpha1-3Gal epitope), a major xenotransplant antigen, is synthesized by alpha1,3-galactosyltransferase (alpha1-3Gal transferase), which is evolutionarily related to the histo-blood group A/B transferases. We constructed structural chimeras between the human type A and murine alpha1-3Gal transferases and examined their activity and specificity. In many instances, a total loss of transferase activity was observed. Certain areas could be exchanged, with a potential diminishing of activity. With a few constructs, changes in acceptor substrate specificity were suspected. Unexpectedly, a functional conversion from A to B transferase activity was observed after replacing the short sequence of human A transferase with the corresponding sequence from murine alpha1-3Gal transferase. Because these two paralogous enzymes differ in 16 positions of the 38 amino acid residues in the replaced region, our finding may suggest that despite separate evolution and diversified acceptors, these glycosyltransferases still share the three-dimensional domain structure that is responsible for their sugar specificity, arguing against the functional requirement of a strong purifying selection playing a role in the evolution of the ABO family of genes.