Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000712 | resolution of meiotic recombination intermediates | 4 | 2 |
GO:0000819 | sister chromatid segregation | 4 | 2 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006259 | DNA metabolic process | 4 | 12 |
GO:0006265 | DNA topological change | 5 | 12 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0006996 | organelle organization | 4 | 12 |
GO:0007059 | chromosome segregation | 2 | 2 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016043 | cellular component organization | 3 | 12 |
GO:0022402 | cell cycle process | 2 | 2 |
GO:0022414 | reproductive process | 1 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0051276 | chromosome organization | 5 | 12 |
GO:0061982 | meiosis I cell cycle process | 3 | 2 |
GO:0071103 | DNA conformation change | 6 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0071840 | cellular component organization or biogenesis | 2 | 12 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:0098813 | nuclear chromosome segregation | 3 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
GO:1903046 | meiotic cell cycle process | 2 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003677 | DNA binding | 4 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0003916 | DNA topoisomerase activity | 3 | 12 |
GO:0003918 | DNA topoisomerase type II (double strand cut, ATP-hydrolyzing) activity | 3 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0008094 | ATP-dependent activity, acting on DNA | 2 | 12 |
GO:0016853 | isomerase activity | 2 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0043169 | cation binding | 3 | 12 |
GO:0046872 | metal ion binding | 4 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:0140657 | ATP-dependent activity | 1 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0016491 | oxidoreductase activity | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 1259 | 1263 | PF00656 | 0.678 |
CLV_C14_Caspase3-7 | 1270 | 1274 | PF00656 | 0.444 |
CLV_C14_Caspase3-7 | 1328 | 1332 | PF00656 | 0.776 |
CLV_C14_Caspase3-7 | 1460 | 1464 | PF00656 | 0.662 |
CLV_C14_Caspase3-7 | 1471 | 1475 | PF00656 | 0.696 |
CLV_C14_Caspase3-7 | 1487 | 1491 | PF00656 | 0.420 |
CLV_C14_Caspase3-7 | 430 | 434 | PF00656 | 0.366 |
CLV_C14_Caspase3-7 | 493 | 497 | PF00656 | 0.451 |
CLV_C14_Caspase3-7 | 683 | 687 | PF00656 | 0.303 |
CLV_MEL_PAP_1 | 271 | 277 | PF00089 | 0.251 |
CLV_NRD_NRD_1 | 1003 | 1005 | PF00675 | 0.298 |
CLV_NRD_NRD_1 | 1028 | 1030 | PF00675 | 0.305 |
CLV_NRD_NRD_1 | 1040 | 1042 | PF00675 | 0.300 |
CLV_NRD_NRD_1 | 1099 | 1101 | PF00675 | 0.388 |
CLV_NRD_NRD_1 | 1132 | 1134 | PF00675 | 0.430 |
CLV_NRD_NRD_1 | 1173 | 1175 | PF00675 | 0.489 |
CLV_NRD_NRD_1 | 1184 | 1186 | PF00675 | 0.491 |
CLV_NRD_NRD_1 | 1216 | 1218 | PF00675 | 0.649 |
CLV_NRD_NRD_1 | 1249 | 1251 | PF00675 | 0.636 |
CLV_NRD_NRD_1 | 1317 | 1319 | PF00675 | 0.776 |
CLV_NRD_NRD_1 | 1343 | 1345 | PF00675 | 0.688 |
CLV_NRD_NRD_1 | 1457 | 1459 | PF00675 | 0.625 |
CLV_NRD_NRD_1 | 161 | 163 | PF00675 | 0.369 |
CLV_NRD_NRD_1 | 216 | 218 | PF00675 | 0.347 |
CLV_NRD_NRD_1 | 256 | 258 | PF00675 | 0.451 |
CLV_NRD_NRD_1 | 401 | 403 | PF00675 | 0.471 |
CLV_NRD_NRD_1 | 48 | 50 | PF00675 | 0.405 |
CLV_NRD_NRD_1 | 634 | 636 | PF00675 | 0.272 |
CLV_NRD_NRD_1 | 692 | 694 | PF00675 | 0.299 |
CLV_NRD_NRD_1 | 750 | 752 | PF00675 | 0.424 |
CLV_NRD_NRD_1 | 993 | 995 | PF00675 | 0.306 |
CLV_PCSK_FUR_1 | 1130 | 1134 | PF00082 | 0.417 |
CLV_PCSK_FUR_1 | 1454 | 1458 | PF00082 | 0.672 |
CLV_PCSK_KEX2_1 | 1003 | 1005 | PF00082 | 0.303 |
CLV_PCSK_KEX2_1 | 1028 | 1030 | PF00082 | 0.303 |
CLV_PCSK_KEX2_1 | 1040 | 1042 | PF00082 | 0.303 |
CLV_PCSK_KEX2_1 | 1099 | 1101 | PF00082 | 0.388 |
CLV_PCSK_KEX2_1 | 1132 | 1134 | PF00082 | 0.372 |
CLV_PCSK_KEX2_1 | 1184 | 1186 | PF00082 | 0.480 |
CLV_PCSK_KEX2_1 | 1215 | 1217 | PF00082 | 0.605 |
CLV_PCSK_KEX2_1 | 1248 | 1250 | PF00082 | 0.622 |
CLV_PCSK_KEX2_1 | 1310 | 1312 | PF00082 | 0.742 |
CLV_PCSK_KEX2_1 | 1342 | 1344 | PF00082 | 0.653 |
CLV_PCSK_KEX2_1 | 1435 | 1437 | PF00082 | 0.645 |
CLV_PCSK_KEX2_1 | 1454 | 1456 | PF00082 | 0.458 |
CLV_PCSK_KEX2_1 | 1457 | 1459 | PF00082 | 0.623 |
CLV_PCSK_KEX2_1 | 215 | 217 | PF00082 | 0.349 |
CLV_PCSK_KEX2_1 | 701 | 703 | PF00082 | 0.293 |
CLV_PCSK_KEX2_1 | 993 | 995 | PF00082 | 0.303 |
CLV_PCSK_PC1ET2_1 | 1028 | 1030 | PF00082 | 0.382 |
CLV_PCSK_PC1ET2_1 | 1248 | 1250 | PF00082 | 0.628 |
CLV_PCSK_PC1ET2_1 | 1310 | 1312 | PF00082 | 0.742 |
CLV_PCSK_PC1ET2_1 | 1435 | 1437 | PF00082 | 0.629 |
CLV_PCSK_PC1ET2_1 | 215 | 217 | PF00082 | 0.432 |
CLV_PCSK_PC1ET2_1 | 701 | 703 | PF00082 | 0.303 |
CLV_PCSK_PC1ET2_1 | 993 | 995 | PF00082 | 0.388 |
CLV_PCSK_PC7_1 | 1306 | 1312 | PF00082 | 0.742 |
CLV_PCSK_SKI1_1 | 1003 | 1007 | PF00082 | 0.351 |
CLV_PCSK_SKI1_1 | 1032 | 1036 | PF00082 | 0.340 |
CLV_PCSK_SKI1_1 | 1099 | 1103 | PF00082 | 0.388 |
CLV_PCSK_SKI1_1 | 1175 | 1179 | PF00082 | 0.584 |
CLV_PCSK_SKI1_1 | 1196 | 1200 | PF00082 | 0.493 |
CLV_PCSK_SKI1_1 | 1205 | 1209 | PF00082 | 0.513 |
CLV_PCSK_SKI1_1 | 1250 | 1254 | PF00082 | 0.716 |
CLV_PCSK_SKI1_1 | 1359 | 1363 | PF00082 | 0.537 |
CLV_PCSK_SKI1_1 | 1435 | 1439 | PF00082 | 0.618 |
CLV_PCSK_SKI1_1 | 1443 | 1447 | PF00082 | 0.745 |
CLV_PCSK_SKI1_1 | 227 | 231 | PF00082 | 0.425 |
CLV_PCSK_SKI1_1 | 517 | 521 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 693 | 697 | PF00082 | 0.302 |
CLV_PCSK_SKI1_1 | 770 | 774 | PF00082 | 0.303 |
CLV_PCSK_SKI1_1 | 781 | 785 | PF00082 | 0.303 |
CLV_PCSK_SKI1_1 | 902 | 906 | PF00082 | 0.303 |
DEG_APCC_DBOX_1 | 606 | 614 | PF00400 | 0.475 |
DEG_COP1_1 | 107 | 115 | PF00400 | 0.360 |
DEG_SCF_TRCP1_1 | 1328 | 1333 | PF00400 | 0.539 |
DOC_ANK_TNKS_1 | 1016 | 1023 | PF00023 | 0.424 |
DOC_CDC14_PxL_1 | 405 | 413 | PF14671 | 0.500 |
DOC_CKS1_1 | 541 | 546 | PF01111 | 0.455 |
DOC_CYCLIN_RxL_1 | 1028 | 1037 | PF00134 | 0.338 |
DOC_CYCLIN_RxL_1 | 1193 | 1202 | PF00134 | 0.592 |
DOC_CYCLIN_RxL_1 | 689 | 698 | PF00134 | 0.388 |
DOC_MAPK_gen_1 | 104 | 112 | PF00069 | 0.303 |
DOC_MAPK_gen_1 | 1040 | 1046 | PF00069 | 0.412 |
DOC_MAPK_gen_1 | 1184 | 1190 | PF00069 | 0.498 |
DOC_MAPK_gen_1 | 402 | 408 | PF00069 | 0.479 |
DOC_MAPK_MEF2A_6 | 205 | 214 | PF00069 | 0.447 |
DOC_MAPK_MEF2A_6 | 268 | 275 | PF00069 | 0.451 |
DOC_MAPK_MEF2A_6 | 327 | 334 | PF00069 | 0.451 |
DOC_PP1_RVXF_1 | 556 | 563 | PF00149 | 0.475 |
DOC_PP1_RVXF_1 | 607 | 613 | PF00149 | 0.451 |
DOC_PP1_RVXF_1 | 691 | 698 | PF00149 | 0.303 |
DOC_PP2B_LxvP_1 | 110 | 113 | PF13499 | 0.319 |
DOC_PP2B_LxvP_1 | 1186 | 1189 | PF13499 | 0.464 |
DOC_PP2B_LxvP_1 | 532 | 535 | PF13499 | 0.344 |
DOC_PP4_FxxP_1 | 541 | 544 | PF00568 | 0.451 |
DOC_PP4_FxxP_1 | 563 | 566 | PF00568 | 0.451 |
DOC_PP4_FxxP_1 | 806 | 809 | PF00568 | 0.412 |
DOC_PP4_FxxP_1 | 931 | 934 | PF00568 | 0.319 |
DOC_USP7_MATH_1 | 1070 | 1074 | PF00917 | 0.409 |
DOC_USP7_MATH_1 | 1083 | 1087 | PF00917 | 0.218 |
DOC_USP7_MATH_1 | 1203 | 1207 | PF00917 | 0.598 |
DOC_USP7_MATH_1 | 1252 | 1256 | PF00917 | 0.652 |
DOC_USP7_MATH_1 | 1374 | 1378 | PF00917 | 0.581 |
DOC_USP7_MATH_1 | 1399 | 1403 | PF00917 | 0.725 |
DOC_USP7_MATH_1 | 1475 | 1479 | PF00917 | 0.666 |
DOC_USP7_MATH_1 | 183 | 187 | PF00917 | 0.475 |
DOC_USP7_MATH_1 | 42 | 46 | PF00917 | 0.325 |
DOC_USP7_MATH_2 | 835 | 841 | PF00917 | 0.372 |
DOC_USP7_UBL2_3 | 1028 | 1032 | PF12436 | 0.371 |
DOC_USP7_UBL2_3 | 1175 | 1179 | PF12436 | 0.456 |
DOC_USP7_UBL2_3 | 1201 | 1205 | PF12436 | 0.514 |
DOC_USP7_UBL2_3 | 1243 | 1247 | PF12436 | 0.638 |
DOC_USP7_UBL2_3 | 1316 | 1320 | PF12436 | 0.696 |
DOC_USP7_UBL2_3 | 1446 | 1450 | PF12436 | 0.655 |
DOC_USP7_UBL2_3 | 164 | 168 | PF12436 | 0.473 |
DOC_USP7_UBL2_3 | 314 | 318 | PF12436 | 0.455 |
DOC_USP7_UBL2_3 | 547 | 551 | PF12436 | 0.451 |
DOC_USP7_UBL2_3 | 868 | 872 | PF12436 | 0.321 |
DOC_WW_Pin1_4 | 1139 | 1144 | PF00397 | 0.319 |
DOC_WW_Pin1_4 | 1298 | 1303 | PF00397 | 0.663 |
DOC_WW_Pin1_4 | 51 | 56 | PF00397 | 0.397 |
DOC_WW_Pin1_4 | 540 | 545 | PF00397 | 0.317 |
LIG_14-3-3_CanoR_1 | 1003 | 1012 | PF00244 | 0.424 |
LIG_14-3-3_CanoR_1 | 1436 | 1444 | PF00244 | 0.658 |
LIG_14-3-3_CanoR_1 | 237 | 247 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 257 | 263 | PF00244 | 0.239 |
LIG_14-3-3_CanoR_1 | 398 | 406 | PF00244 | 0.543 |
LIG_14-3-3_CanoR_1 | 424 | 428 | PF00244 | 0.437 |
LIG_14-3-3_CanoR_1 | 489 | 493 | PF00244 | 0.380 |
LIG_14-3-3_CanoR_1 | 49 | 54 | PF00244 | 0.390 |
LIG_14-3-3_CanoR_1 | 657 | 662 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 83 | 93 | PF00244 | 0.424 |
LIG_APCC_ABBA_1 | 36 | 41 | PF00400 | 0.438 |
LIG_BRCT_BRCA1_1 | 148 | 152 | PF00533 | 0.303 |
LIG_Clathr_ClatBox_1 | 200 | 204 | PF01394 | 0.347 |
LIG_Clathr_ClatBox_1 | 985 | 989 | PF01394 | 0.303 |
LIG_CSL_BTD_1 | 110 | 113 | PF09270 | 0.319 |
LIG_CSL_BTD_1 | 52 | 55 | PF09270 | 0.381 |
LIG_CtBP_PxDLS_1 | 1095 | 1099 | PF00389 | 0.217 |
LIG_deltaCOP1_diTrp_1 | 109 | 117 | PF00928 | 0.338 |
LIG_deltaCOP1_diTrp_1 | 1264 | 1269 | PF00928 | 0.635 |
LIG_deltaCOP1_diTrp_1 | 637 | 642 | PF00928 | 0.537 |
LIG_DLG_GKlike_1 | 464 | 471 | PF00625 | 0.498 |
LIG_eIF4E_1 | 195 | 201 | PF01652 | 0.348 |
LIG_eIF4E_1 | 771 | 777 | PF01652 | 0.424 |
LIG_EVH1_1 | 1044 | 1048 | PF00568 | 0.424 |
LIG_FHA_1 | 1004 | 1010 | PF00498 | 0.378 |
LIG_FHA_1 | 1021 | 1027 | PF00498 | 0.182 |
LIG_FHA_1 | 304 | 310 | PF00498 | 0.466 |
LIG_FHA_1 | 31 | 37 | PF00498 | 0.438 |
LIG_FHA_1 | 359 | 365 | PF00498 | 0.384 |
LIG_FHA_1 | 424 | 430 | PF00498 | 0.426 |
LIG_FHA_1 | 438 | 444 | PF00498 | 0.368 |
LIG_FHA_1 | 52 | 58 | PF00498 | 0.319 |
LIG_FHA_1 | 541 | 547 | PF00498 | 0.451 |
LIG_FHA_1 | 817 | 823 | PF00498 | 0.303 |
LIG_FHA_1 | 919 | 925 | PF00498 | 0.424 |
LIG_FHA_1 | 957 | 963 | PF00498 | 0.303 |
LIG_FHA_2 | 1055 | 1061 | PF00498 | 0.340 |
LIG_FHA_2 | 11 | 17 | PF00498 | 0.483 |
LIG_FHA_2 | 1140 | 1146 | PF00498 | 0.334 |
LIG_FHA_2 | 1154 | 1160 | PF00498 | 0.441 |
LIG_FHA_2 | 1358 | 1364 | PF00498 | 0.530 |
LIG_FHA_2 | 18 | 24 | PF00498 | 0.493 |
LIG_FHA_2 | 240 | 246 | PF00498 | 0.378 |
LIG_FHA_2 | 250 | 256 | PF00498 | 0.378 |
LIG_FHA_2 | 428 | 434 | PF00498 | 0.379 |
LIG_FHA_2 | 862 | 868 | PF00498 | 0.314 |
LIG_LIR_Apic_2 | 561 | 566 | PF02991 | 0.451 |
LIG_LIR_Apic_2 | 803 | 809 | PF02991 | 0.303 |
LIG_LIR_Apic_2 | 929 | 934 | PF02991 | 0.319 |
LIG_LIR_Gen_1 | 1102 | 1113 | PF02991 | 0.309 |
LIG_LIR_Gen_1 | 186 | 196 | PF02991 | 0.333 |
LIG_LIR_Gen_1 | 197 | 206 | PF02991 | 0.303 |
LIG_LIR_Gen_1 | 245 | 253 | PF02991 | 0.377 |
LIG_LIR_Gen_1 | 261 | 267 | PF02991 | 0.396 |
LIG_LIR_Gen_1 | 600 | 610 | PF02991 | 0.451 |
LIG_LIR_Gen_1 | 87 | 94 | PF02991 | 0.424 |
LIG_LIR_Gen_1 | 925 | 936 | PF02991 | 0.303 |
LIG_LIR_LC3C_4 | 1021 | 1026 | PF02991 | 0.428 |
LIG_LIR_LC3C_4 | 910 | 915 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 1102 | 1108 | PF02991 | 0.309 |
LIG_LIR_Nem_3 | 114 | 120 | PF02991 | 0.303 |
LIG_LIR_Nem_3 | 186 | 192 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 193 | 198 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 241 | 246 | PF02991 | 0.348 |
LIG_LIR_Nem_3 | 261 | 265 | PF02991 | 0.223 |
LIG_LIR_Nem_3 | 447 | 453 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 600 | 605 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 660 | 664 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 803 | 808 | PF02991 | 0.303 |
LIG_LIR_Nem_3 | 87 | 93 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 898 | 904 | PF02991 | 0.303 |
LIG_LIR_Nem_3 | 925 | 931 | PF02991 | 0.303 |
LIG_LIR_Nem_3 | 982 | 986 | PF02991 | 0.319 |
LIG_LYPXL_S_1 | 194 | 198 | PF13949 | 0.318 |
LIG_LYPXL_S_1 | 249 | 253 | PF13949 | 0.399 |
LIG_LYPXL_yS_3 | 250 | 253 | PF13949 | 0.400 |
LIG_Pex14_1 | 638 | 642 | PF04695 | 0.462 |
LIG_Pex14_1 | 857 | 861 | PF04695 | 0.303 |
LIG_Pex14_1 | 897 | 901 | PF04695 | 0.303 |
LIG_Pex14_2 | 148 | 152 | PF04695 | 0.303 |
LIG_Pex14_2 | 165 | 169 | PF04695 | 0.390 |
LIG_Pex14_2 | 194 | 198 | PF04695 | 0.318 |
LIG_Pex14_2 | 523 | 527 | PF04695 | 0.379 |
LIG_Pex14_2 | 537 | 541 | PF04695 | 0.244 |
LIG_PTB_Apo_2 | 337 | 344 | PF02174 | 0.451 |
LIG_SH2_CRK | 1105 | 1109 | PF00017 | 0.303 |
LIG_SH2_CRK | 189 | 193 | PF00017 | 0.322 |
LIG_SH2_CRK | 262 | 266 | PF00017 | 0.372 |
LIG_SH2_CRK | 587 | 591 | PF00017 | 0.451 |
LIG_SH2_GRB2like | 492 | 495 | PF00017 | 0.511 |
LIG_SH2_NCK_1 | 189 | 193 | PF00017 | 0.322 |
LIG_SH2_NCK_1 | 219 | 223 | PF00017 | 0.337 |
LIG_SH2_NCK_1 | 262 | 266 | PF00017 | 0.396 |
LIG_SH2_NCK_1 | 39 | 43 | PF00017 | 0.440 |
LIG_SH2_NCK_1 | 973 | 977 | PF00017 | 0.412 |
LIG_SH2_PTP2 | 246 | 249 | PF00017 | 0.374 |
LIG_SH2_PTP2 | 807 | 810 | PF00017 | 0.303 |
LIG_SH2_PTP2 | 90 | 93 | PF00017 | 0.424 |
LIG_SH2_SRC | 219 | 222 | PF00017 | 0.292 |
LIG_SH2_SRC | 39 | 42 | PF00017 | 0.443 |
LIG_SH2_SRC | 492 | 495 | PF00017 | 0.395 |
LIG_SH2_SRC | 807 | 810 | PF00017 | 0.303 |
LIG_SH2_SRC | 955 | 958 | PF00017 | 0.317 |
LIG_SH2_STAP1 | 1105 | 1109 | PF00017 | 0.303 |
LIG_SH2_STAT5 | 1043 | 1046 | PF00017 | 0.338 |
LIG_SH2_STAT5 | 1107 | 1110 | PF00017 | 0.303 |
LIG_SH2_STAT5 | 189 | 192 | PF00017 | 0.324 |
LIG_SH2_STAT5 | 246 | 249 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 25 | 28 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 300 | 303 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 371 | 374 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 450 | 453 | PF00017 | 0.368 |
LIG_SH2_STAT5 | 568 | 571 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 601 | 604 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 716 | 719 | PF00017 | 0.303 |
LIG_SH2_STAT5 | 771 | 774 | PF00017 | 0.300 |
LIG_SH2_STAT5 | 807 | 810 | PF00017 | 0.303 |
LIG_SH2_STAT5 | 858 | 861 | PF00017 | 0.303 |
LIG_SH2_STAT5 | 90 | 93 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 955 | 958 | PF00017 | 0.317 |
LIG_SH2_STAT5 | 984 | 987 | PF00017 | 0.342 |
LIG_SH2_STAT5 | 997 | 1000 | PF00017 | 0.303 |
LIG_SH3_2 | 1290 | 1295 | PF14604 | 0.674 |
LIG_SH3_3 | 1042 | 1048 | PF00018 | 0.338 |
LIG_SH3_3 | 1174 | 1180 | PF00018 | 0.567 |
LIG_SH3_3 | 1233 | 1239 | PF00018 | 0.509 |
LIG_SH3_3 | 1287 | 1293 | PF00018 | 0.704 |
LIG_SH3_3 | 1299 | 1305 | PF00018 | 0.550 |
LIG_SH3_3 | 1441 | 1447 | PF00018 | 0.739 |
LIG_SH3_3 | 177 | 183 | PF00018 | 0.387 |
LIG_SH3_3 | 70 | 76 | PF00018 | 0.319 |
LIG_SH3_3 | 806 | 812 | PF00018 | 0.303 |
LIG_SH3_4 | 1316 | 1323 | PF00018 | 0.738 |
LIG_SH3_4 | 1446 | 1453 | PF00018 | 0.697 |
LIG_SUMO_SIM_anti_2 | 1410 | 1417 | PF11976 | 0.562 |
LIG_SUMO_SIM_par_1 | 1021 | 1027 | PF11976 | 0.390 |
LIG_SUMO_SIM_par_1 | 425 | 431 | PF11976 | 0.416 |
LIG_SUMO_SIM_par_1 | 834 | 840 | PF11976 | 0.315 |
LIG_TRAF2_1 | 1058 | 1061 | PF00917 | 0.424 |
LIG_TRAF2_1 | 1263 | 1266 | PF00917 | 0.631 |
LIG_TRAF2_1 | 1479 | 1482 | PF00917 | 0.727 |
LIG_TRAF2_1 | 473 | 476 | PF00917 | 0.452 |
LIG_TRAF2_1 | 864 | 867 | PF00917 | 0.331 |
LIG_TYR_ITIM | 498 | 503 | PF00017 | 0.401 |
LIG_UBA3_1 | 1108 | 1112 | PF00899 | 0.388 |
LIG_UBA3_1 | 1413 | 1420 | PF00899 | 0.587 |
LIG_UBA3_1 | 210 | 215 | PF00899 | 0.419 |
LIG_UBA3_1 | 301 | 308 | PF00899 | 0.556 |
LIG_UBA3_1 | 405 | 410 | PF00899 | 0.500 |
LIG_WRC_WIRS_1 | 1158 | 1163 | PF05994 | 0.555 |
LIG_WRC_WIRS_1 | 191 | 196 | PF05994 | 0.317 |
MOD_CDC14_SPxK_1 | 1301 | 1304 | PF00782 | 0.657 |
MOD_CDK_SPK_2 | 1139 | 1144 | PF00069 | 0.319 |
MOD_CDK_SPK_2 | 1298 | 1303 | PF00069 | 0.663 |
MOD_CDK_SPxK_1 | 1298 | 1304 | PF00069 | 0.661 |
MOD_CDK_SPxxK_3 | 540 | 547 | PF00069 | 0.303 |
MOD_CK1_1 | 1055 | 1061 | PF00069 | 0.303 |
MOD_CK1_1 | 1335 | 1341 | PF00069 | 0.714 |
MOD_CK1_1 | 1379 | 1385 | PF00069 | 0.548 |
MOD_CK1_1 | 1461 | 1467 | PF00069 | 0.671 |
MOD_CK1_1 | 1476 | 1482 | PF00069 | 0.609 |
MOD_CK1_1 | 1483 | 1489 | PF00069 | 0.617 |
MOD_CK1_1 | 1491 | 1497 | PF00069 | 0.475 |
MOD_CK1_1 | 288 | 294 | PF00069 | 0.451 |
MOD_CK1_1 | 434 | 440 | PF00069 | 0.488 |
MOD_CK1_1 | 561 | 567 | PF00069 | 0.443 |
MOD_CK1_1 | 680 | 686 | PF00069 | 0.303 |
MOD_CK1_1 | 718 | 724 | PF00069 | 0.388 |
MOD_CK2_1 | 1004 | 1010 | PF00069 | 0.338 |
MOD_CK2_1 | 1054 | 1060 | PF00069 | 0.391 |
MOD_CK2_1 | 1153 | 1159 | PF00069 | 0.489 |
MOD_CK2_1 | 1260 | 1266 | PF00069 | 0.678 |
MOD_CK2_1 | 1475 | 1481 | PF00069 | 0.724 |
MOD_CK2_1 | 239 | 245 | PF00069 | 0.337 |
MOD_CK2_1 | 249 | 255 | PF00069 | 0.387 |
MOD_CK2_1 | 590 | 596 | PF00069 | 0.528 |
MOD_CK2_1 | 837 | 843 | PF00069 | 0.370 |
MOD_CK2_1 | 861 | 867 | PF00069 | 0.343 |
MOD_CK2_1 | 971 | 977 | PF00069 | 0.372 |
MOD_Cter_Amidation | 1213 | 1216 | PF01082 | 0.634 |
MOD_GlcNHglycan | 1085 | 1088 | PF01048 | 0.459 |
MOD_GlcNHglycan | 1230 | 1233 | PF01048 | 0.615 |
MOD_GlcNHglycan | 1325 | 1331 | PF01048 | 0.757 |
MOD_GlcNHglycan | 1334 | 1337 | PF01048 | 0.694 |
MOD_GlcNHglycan | 1350 | 1353 | PF01048 | 0.631 |
MOD_GlcNHglycan | 1376 | 1379 | PF01048 | 0.609 |
MOD_GlcNHglycan | 1381 | 1384 | PF01048 | 0.629 |
MOD_GlcNHglycan | 1440 | 1443 | PF01048 | 0.613 |
MOD_GlcNHglycan | 1474 | 1478 | PF01048 | 0.717 |
MOD_GlcNHglycan | 1481 | 1486 | PF01048 | 0.630 |
MOD_GlcNHglycan | 185 | 188 | PF01048 | 0.467 |
MOD_GlcNHglycan | 374 | 377 | PF01048 | 0.468 |
MOD_GlcNHglycan | 433 | 436 | PF01048 | 0.363 |
MOD_GlcNHglycan | 592 | 595 | PF01048 | 0.262 |
MOD_GlcNHglycan | 719 | 723 | PF01048 | 0.376 |
MOD_GSK3_1 | 1020 | 1027 | PF00069 | 0.338 |
MOD_GSK3_1 | 1153 | 1160 | PF00069 | 0.528 |
MOD_GSK3_1 | 1326 | 1333 | PF00069 | 0.705 |
MOD_GSK3_1 | 1399 | 1406 | PF00069 | 0.676 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.303 |
MOD_GSK3_1 | 1431 | 1438 | PF00069 | 0.685 |
MOD_GSK3_1 | 1457 | 1464 | PF00069 | 0.669 |
MOD_GSK3_1 | 1469 | 1476 | PF00069 | 0.630 |
MOD_GSK3_1 | 1480 | 1487 | PF00069 | 0.558 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.451 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.451 |
MOD_GSK3_1 | 289 | 296 | PF00069 | 0.451 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.488 |
MOD_GSK3_1 | 392 | 399 | PF00069 | 0.603 |
MOD_GSK3_1 | 419 | 426 | PF00069 | 0.441 |
MOD_GSK3_1 | 427 | 434 | PF00069 | 0.383 |
MOD_GSK3_1 | 488 | 495 | PF00069 | 0.383 |
MOD_GSK3_1 | 637 | 644 | PF00069 | 0.511 |
MOD_GSK3_1 | 726 | 733 | PF00069 | 0.293 |
MOD_GSK3_1 | 817 | 824 | PF00069 | 0.312 |
MOD_GSK3_1 | 918 | 925 | PF00069 | 0.424 |
MOD_GSK3_1 | 971 | 978 | PF00069 | 0.372 |
MOD_N-GLC_1 | 577 | 582 | PF02516 | 0.337 |
MOD_N-GLC_1 | 648 | 653 | PF02516 | 0.275 |
MOD_N-GLC_1 | 816 | 821 | PF02516 | 0.303 |
MOD_NEK2_1 | 1024 | 1029 | PF00069 | 0.303 |
MOD_NEK2_1 | 1054 | 1059 | PF00069 | 0.360 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.304 |
MOD_NEK2_1 | 1387 | 1392 | PF00069 | 0.676 |
MOD_NEK2_1 | 1480 | 1485 | PF00069 | 0.596 |
MOD_NEK2_1 | 167 | 172 | PF00069 | 0.437 |
MOD_NEK2_1 | 285 | 290 | PF00069 | 0.451 |
MOD_NEK2_1 | 384 | 389 | PF00069 | 0.492 |
MOD_NEK2_1 | 590 | 595 | PF00069 | 0.462 |
MOD_NEK2_1 | 704 | 709 | PF00069 | 0.303 |
MOD_NEK2_1 | 730 | 735 | PF00069 | 0.303 |
MOD_NEK2_1 | 741 | 746 | PF00069 | 0.301 |
MOD_NEK2_1 | 826 | 831 | PF00069 | 0.432 |
MOD_NEK2_1 | 859 | 864 | PF00069 | 0.319 |
MOD_NEK2_1 | 86 | 91 | PF00069 | 0.340 |
MOD_NEK2_2 | 1203 | 1208 | PF00069 | 0.417 |
MOD_NEK2_2 | 42 | 47 | PF00069 | 0.442 |
MOD_PIKK_1 | 10 | 16 | PF00454 | 0.436 |
MOD_PIKK_1 | 342 | 348 | PF00454 | 0.451 |
MOD_PIKK_1 | 895 | 901 | PF00454 | 0.303 |
MOD_PKA_1 | 1003 | 1009 | PF00069 | 0.424 |
MOD_PKA_1 | 1052 | 1058 | PF00069 | 0.319 |
MOD_PKA_1 | 1099 | 1105 | PF00069 | 0.424 |
MOD_PKA_1 | 1132 | 1138 | PF00069 | 0.372 |
MOD_PKA_1 | 1435 | 1441 | PF00069 | 0.700 |
MOD_PKA_1 | 1457 | 1463 | PF00069 | 0.584 |
MOD_PKA_1 | 316 | 322 | PF00069 | 0.495 |
MOD_PKA_1 | 49 | 55 | PF00069 | 0.384 |
MOD_PKA_2 | 1003 | 1009 | PF00069 | 0.424 |
MOD_PKA_2 | 1099 | 1105 | PF00069 | 0.424 |
MOD_PKA_2 | 1132 | 1138 | PF00069 | 0.372 |
MOD_PKA_2 | 1321 | 1327 | PF00069 | 0.672 |
MOD_PKA_2 | 1400 | 1406 | PF00069 | 0.718 |
MOD_PKA_2 | 1435 | 1441 | PF00069 | 0.694 |
MOD_PKA_2 | 1457 | 1463 | PF00069 | 0.598 |
MOD_PKA_2 | 273 | 279 | PF00069 | 0.460 |
MOD_PKA_2 | 397 | 403 | PF00069 | 0.539 |
MOD_PKA_2 | 423 | 429 | PF00069 | 0.433 |
MOD_PKA_2 | 488 | 494 | PF00069 | 0.380 |
MOD_PKB_1 | 1130 | 1138 | PF00069 | 0.418 |
MOD_PKB_1 | 1455 | 1463 | PF00069 | 0.635 |
MOD_Plk_1 | 1203 | 1209 | PF00069 | 0.571 |
MOD_Plk_1 | 1221 | 1227 | PF00069 | 0.413 |
MOD_Plk_1 | 1491 | 1497 | PF00069 | 0.615 |
MOD_Plk_1 | 187 | 193 | PF00069 | 0.327 |
MOD_Plk_1 | 225 | 231 | PF00069 | 0.339 |
MOD_Plk_1 | 378 | 384 | PF00069 | 0.495 |
MOD_Plk_1 | 42 | 48 | PF00069 | 0.442 |
MOD_Plk_1 | 464 | 470 | PF00069 | 0.397 |
MOD_Plk_1 | 648 | 654 | PF00069 | 0.458 |
MOD_Plk_1 | 677 | 683 | PF00069 | 0.338 |
MOD_Plk_1 | 718 | 724 | PF00069 | 0.330 |
MOD_Plk_1 | 726 | 732 | PF00069 | 0.271 |
MOD_Plk_1 | 922 | 928 | PF00069 | 0.303 |
MOD_Plk_2-3 | 1258 | 1264 | PF00069 | 0.617 |
MOD_Plk_2-3 | 204 | 210 | PF00069 | 0.379 |
MOD_Plk_2-3 | 30 | 36 | PF00069 | 0.373 |
MOD_Plk_2-3 | 798 | 804 | PF00069 | 0.310 |
MOD_Plk_4 | 1020 | 1026 | PF00069 | 0.338 |
MOD_Plk_4 | 1157 | 1163 | PF00069 | 0.527 |
MOD_Plk_4 | 187 | 193 | PF00069 | 0.327 |
MOD_Plk_4 | 281 | 287 | PF00069 | 0.451 |
MOD_Plk_4 | 364 | 370 | PF00069 | 0.373 |
MOD_Plk_4 | 423 | 429 | PF00069 | 0.433 |
MOD_Plk_4 | 680 | 686 | PF00069 | 0.295 |
MOD_Plk_4 | 726 | 732 | PF00069 | 0.303 |
MOD_Plk_4 | 77 | 83 | PF00069 | 0.388 |
MOD_Plk_4 | 86 | 92 | PF00069 | 0.388 |
MOD_Plk_4 | 975 | 981 | PF00069 | 0.360 |
MOD_ProDKin_1 | 1139 | 1145 | PF00069 | 0.319 |
MOD_ProDKin_1 | 1298 | 1304 | PF00069 | 0.661 |
MOD_ProDKin_1 | 51 | 57 | PF00069 | 0.391 |
MOD_ProDKin_1 | 540 | 546 | PF00069 | 0.317 |
MOD_SUMO_for_1 | 1421 | 1424 | PF00179 | 0.499 |
MOD_SUMO_rev_2 | 1145 | 1154 | PF00179 | 0.392 |
MOD_SUMO_rev_2 | 124 | 134 | PF00179 | 0.303 |
MOD_SUMO_rev_2 | 255 | 260 | PF00179 | 0.418 |
MOD_SUMO_rev_2 | 395 | 405 | PF00179 | 0.532 |
MOD_SUMO_rev_2 | 564 | 574 | PF00179 | 0.475 |
TRG_DiLeu_BaEn_1 | 208 | 213 | PF01217 | 0.363 |
TRG_DiLeu_BaEn_2 | 868 | 874 | PF01217 | 0.303 |
TRG_DiLeu_BaEn_4 | 947 | 953 | PF01217 | 0.319 |
TRG_DiLeu_BaLyEn_6 | 745 | 750 | PF01217 | 0.319 |
TRG_ENDOCYTIC_2 | 1043 | 1046 | PF00928 | 0.303 |
TRG_ENDOCYTIC_2 | 1105 | 1108 | PF00928 | 0.303 |
TRG_ENDOCYTIC_2 | 189 | 192 | PF00928 | 0.324 |
TRG_ENDOCYTIC_2 | 195 | 198 | PF00928 | 0.319 |
TRG_ENDOCYTIC_2 | 246 | 249 | PF00928 | 0.374 |
TRG_ENDOCYTIC_2 | 250 | 253 | PF00928 | 0.384 |
TRG_ENDOCYTIC_2 | 262 | 265 | PF00928 | 0.402 |
TRG_ENDOCYTIC_2 | 450 | 453 | PF00928 | 0.368 |
TRG_ENDOCYTIC_2 | 500 | 503 | PF00928 | 0.417 |
TRG_ENDOCYTIC_2 | 58 | 61 | PF00928 | 0.303 |
TRG_ENDOCYTIC_2 | 587 | 590 | PF00928 | 0.451 |
TRG_ENDOCYTIC_2 | 661 | 664 | PF00928 | 0.451 |
TRG_ENDOCYTIC_2 | 807 | 810 | PF00928 | 0.303 |
TRG_ENDOCYTIC_2 | 833 | 836 | PF00928 | 0.305 |
TRG_ENDOCYTIC_2 | 858 | 861 | PF00928 | 0.303 |
TRG_ENDOCYTIC_2 | 90 | 93 | PF00928 | 0.424 |
TRG_ENDOCYTIC_2 | 901 | 904 | PF00928 | 0.303 |
TRG_ER_diArg_1 | 1002 | 1004 | PF00400 | 0.358 |
TRG_ER_diArg_1 | 1040 | 1042 | PF00400 | 0.422 |
TRG_ER_diArg_1 | 1098 | 1100 | PF00400 | 0.388 |
TRG_ER_diArg_1 | 1130 | 1133 | PF00400 | 0.334 |
TRG_ER_diArg_1 | 1184 | 1187 | PF00400 | 0.458 |
TRG_ER_diArg_1 | 1215 | 1217 | PF00400 | 0.658 |
TRG_ER_diArg_1 | 1295 | 1298 | PF00400 | 0.529 |
TRG_ER_diArg_1 | 1341 | 1344 | PF00400 | 0.728 |
TRG_ER_diArg_1 | 1454 | 1457 | PF00400 | 0.634 |
TRG_ER_diArg_1 | 216 | 218 | PF00400 | 0.350 |
TRG_ER_diArg_1 | 607 | 610 | PF00400 | 0.462 |
TRG_NES_CRM1_1 | 475 | 487 | PF08389 | 0.396 |
TRG_NES_CRM1_1 | 637 | 650 | PF08389 | 0.537 |
TRG_NES_CRM1_1 | 75 | 88 | PF08389 | 0.388 |
TRG_NLS_Bipartite_1 | 1040 | 1055 | PF00514 | 0.372 |
TRG_NLS_Bipartite_1 | 1303 | 1323 | PF00514 | 0.728 |
TRG_NLS_MonoCore_2 | 1027 | 1032 | PF00514 | 0.424 |
TRG_NLS_MonoCore_2 | 1246 | 1251 | PF00514 | 0.666 |
TRG_NLS_MonoCore_2 | 1302 | 1307 | PF00514 | 0.729 |
TRG_NLS_MonoCore_2 | 313 | 318 | PF00514 | 0.537 |
TRG_NLS_MonoExtC_3 | 1027 | 1032 | PF00514 | 0.424 |
TRG_NLS_MonoExtC_3 | 1173 | 1178 | PF00514 | 0.604 |
TRG_NLS_MonoExtC_3 | 1246 | 1251 | PF00514 | 0.625 |
TRG_NLS_MonoExtC_3 | 1317 | 1322 | PF00514 | 0.684 |
TRG_NLS_MonoExtC_3 | 214 | 220 | PF00514 | 0.429 |
TRG_NLS_MonoExtC_3 | 313 | 318 | PF00514 | 0.452 |
TRG_NLS_MonoExtN_4 | 1048 | 1055 | PF00514 | 0.338 |
TRG_NLS_MonoExtN_4 | 1174 | 1179 | PF00514 | 0.603 |
TRG_NLS_MonoExtN_4 | 1247 | 1252 | PF00514 | 0.636 |
TRG_NLS_MonoExtN_4 | 1302 | 1307 | PF00514 | 0.726 |
TRG_NLS_MonoExtN_4 | 1316 | 1323 | PF00514 | 0.610 |
TRG_NLS_MonoExtN_4 | 160 | 166 | PF00514 | 0.370 |
TRG_NLS_MonoExtN_4 | 314 | 319 | PF00514 | 0.475 |
TRG_Pf-PMV_PEXEL_1 | 1032 | 1036 | PF00026 | 0.360 |
TRG_Pf-PMV_PEXEL_1 | 1196 | 1200 | PF00026 | 0.618 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P778 | Leptomonas seymouri | 33% | 100% |
A0A0N1HUJ9 | Leptomonas seymouri | 78% | 100% |
A0A0S4IZ11 | Bodo saltans | 72% | 100% |
A0A0S4JGE3 | Bodo saltans | 36% | 100% |
A0A1X0NUH3 | Trypanosomatidae | 36% | 100% |
A0A3Q8II93 | Leishmania donovani | 96% | 100% |
A0A3R7MTQ1 | Trypanosoma rangeli | 36% | 100% |
A0A3S7WTK8 | Leishmania donovani | 33% | 100% |
A0A422N9B0 | Trypanosoma rangeli | 67% | 100% |
A4H891 | Leishmania braziliensis | 32% | 100% |
A4HGT2 | Leishmania braziliensis | 91% | 100% |
A4HWL4 | Leishmania infantum | 33% | 100% |
A4I3V9 | Leishmania infantum | 98% | 100% |
C9ZXS6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
D0A926 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 64% | 100% |
D0A927 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 65% | 100% |
E9AQC1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
E9B049 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
O16140 | Bombyx mori | 45% | 97% |
O24308 | Pisum sativum | 44% | 100% |
O42130 | Gallus gallus | 44% | 96% |
O42131 | Gallus gallus | 43% | 92% |
O61078 | Leishmania chagasi | 32% | 100% |
O93794 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 44% | 100% |
P06786 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 45% | 100% |
P08096 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 40% | 100% |
P0C9C0 | African swine fever virus (isolate Tick/South Africa/Pretoriuskop Pr4/1996) | 25% | 100% |
P0C9C1 | African swine fever virus (isolate Warthog/Namibia/Wart80/1980) | 25% | 100% |
P0C9C2 | African swine fever virus (isolate Pig/Kenya/KEN-50/1950) | 25% | 100% |
P11388 | Homo sapiens | 45% | 98% |
P12531 | Trypanosoma brucei brucei | 33% | 100% |
P15348 | Drosophila melanogaster | 45% | 100% |
P27570 | Crithidia fasciculata | 33% | 100% |
P30182 | Arabidopsis thaliana | 44% | 100% |
P30190 | Trypanosoma cruzi | 36% | 100% |
P34203 | African swine fever virus (isolate Tick/Malawi/Lil 20-1/1983) | 25% | 100% |
P34534 | Caenorhabditis elegans | 38% | 100% |
P41515 | Cricetulus griseus | 40% | 98% |
P41516 | Rattus norvegicus | 40% | 98% |
P87078 | Candida albicans | 44% | 100% |
P90520 | Dictyostelium discoideum | 41% | 100% |
Q00942 | African swine fever virus (strain Badajoz 1971 Vero-adapted) | 25% | 100% |
Q01320 | Mus musculus | 40% | 98% |
Q01879 | Meyerozyma guilliermondii (strain ATCC 6260 / CBS 566 / DSM 6381 / JCM 1539 / NBRC 10279 / NRRL Y-324) | 43% | 100% |
Q02880 | Homo sapiens | 45% | 92% |
Q196X4 | Invertebrate iridescent virus 3 | 34% | 100% |
Q23670 | Caenorhabditis elegans | 45% | 98% |
Q4QF53 | Leishmania major | 32% | 100% |
Q55BP5 | Dictyostelium discoideum | 42% | 98% |
Q64399 | Cricetulus longicaudatus | 45% | 93% |
Q64511 | Mus musculus | 45% | 93% |
Q9QSK1 | Invertebrate iridescent virus 6 | 31% | 100% |
Q9Y8G8 | Penicillium chrysogenum | 46% | 94% |
V5B5B2 | Trypanosoma cruzi | 71% | 100% |
V5BUD4 | Trypanosoma cruzi | 36% | 100% |