Carries an ATP pyrophosphate-lyase domain on its cytoplasmic segment. Likely acts as a receptor for some unknown extracellular stimulus. Extremely expanded kinetoplastid protein family.. Expressed in the insect stage (promastigote) but not in the mammalian host stage of the parasite life cycle.. Localization: Cell surface (by feature)
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 2 |
Forrest at al. (procyclic) | no | yes: 2 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 51 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 5 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | yes | yes: 44, no: 26 |
NetGPI | no | yes: 0, no: 70 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 66 |
GO:0110165 | cellular anatomical entity | 1 | 71 |
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 71 |
GO:0006163 | purine nucleotide metabolic process | 5 | 71 |
GO:0006164 | purine nucleotide biosynthetic process | 6 | 71 |
GO:0006171 | cAMP biosynthetic process | 8 | 71 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 71 |
GO:0006753 | nucleoside phosphate metabolic process | 4 | 71 |
GO:0006793 | phosphorus metabolic process | 3 | 71 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 71 |
GO:0006807 | nitrogen compound metabolic process | 2 | 71 |
GO:0007165 | signal transduction | 2 | 71 |
GO:0008152 | metabolic process | 1 | 71 |
GO:0009058 | biosynthetic process | 2 | 71 |
GO:0009117 | nucleotide metabolic process | 5 | 71 |
GO:0009150 | purine ribonucleotide metabolic process | 6 | 71 |
GO:0009152 | purine ribonucleotide biosynthetic process | 7 | 71 |
GO:0009165 | nucleotide biosynthetic process | 6 | 71 |
GO:0009187 | cyclic nucleotide metabolic process | 6 | 71 |
GO:0009190 | cyclic nucleotide biosynthetic process | 7 | 71 |
GO:0009259 | ribonucleotide metabolic process | 5 | 71 |
GO:0009260 | ribonucleotide biosynthetic process | 6 | 71 |
GO:0009987 | cellular process | 1 | 71 |
GO:0018130 | heterocycle biosynthetic process | 4 | 71 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 71 |
GO:0019637 | organophosphate metabolic process | 3 | 71 |
GO:0019693 | ribose phosphate metabolic process | 4 | 71 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 71 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 71 |
GO:0035556 | intracellular signal transduction | 3 | 71 |
GO:0044237 | cellular metabolic process | 2 | 71 |
GO:0044238 | primary metabolic process | 2 | 71 |
GO:0044249 | cellular biosynthetic process | 3 | 71 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 71 |
GO:0044281 | small molecule metabolic process | 2 | 71 |
GO:0046058 | cAMP metabolic process | 7 | 71 |
GO:0046390 | ribose phosphate biosynthetic process | 5 | 71 |
GO:0046483 | heterocycle metabolic process | 3 | 71 |
GO:0050789 | regulation of biological process | 2 | 71 |
GO:0050794 | regulation of cellular process | 3 | 71 |
GO:0052652 | cyclic purine nucleotide metabolic process | 6 | 71 |
GO:0055086 | nucleobase-containing small molecule metabolic process | 3 | 71 |
GO:0065007 | biological regulation | 1 | 71 |
GO:0071704 | organic substance metabolic process | 2 | 71 |
GO:0072521 | purine-containing compound metabolic process | 4 | 71 |
GO:0072522 | purine-containing compound biosynthetic process | 5 | 71 |
GO:0090407 | organophosphate biosynthetic process | 4 | 71 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 71 |
GO:1901137 | carbohydrate derivative biosynthetic process | 4 | 71 |
GO:1901293 | nucleoside phosphate biosynthetic process | 5 | 71 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 71 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 71 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 71 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 71 |
GO:1901576 | organic substance biosynthetic process | 3 | 71 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 60 |
GO:0016829 | lyase activity | 2 | 60 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 1229 | 1233 | PF00656 | 0.639 |
CLV_C14_Caspase3-7 | 241 | 245 | PF00656 | 0.172 |
CLV_C14_Caspase3-7 | 321 | 325 | PF00656 | 0.331 |
CLV_C14_Caspase3-7 | 42 | 46 | PF00656 | 0.378 |
CLV_C14_Caspase3-7 | 455 | 459 | PF00656 | 0.343 |
CLV_C14_Caspase3-7 | 810 | 814 | PF00656 | 0.434 |
CLV_C14_Caspase3-7 | 858 | 862 | PF00656 | 0.586 |
CLV_C14_Caspase3-7 | 919 | 923 | PF00656 | 0.456 |
CLV_NRD_NRD_1 | 1158 | 1160 | PF00675 | 0.270 |
CLV_NRD_NRD_1 | 1187 | 1189 | PF00675 | 0.331 |
CLV_NRD_NRD_1 | 1221 | 1223 | PF00675 | 0.375 |
CLV_NRD_NRD_1 | 1242 | 1244 | PF00675 | 0.464 |
CLV_NRD_NRD_1 | 194 | 196 | PF00675 | 0.475 |
CLV_NRD_NRD_1 | 823 | 825 | PF00675 | 0.567 |
CLV_PCSK_KEX2_1 | 1158 | 1160 | PF00082 | 0.322 |
CLV_PCSK_KEX2_1 | 1221 | 1223 | PF00082 | 0.375 |
CLV_PCSK_KEX2_1 | 1242 | 1244 | PF00082 | 0.461 |
CLV_PCSK_KEX2_1 | 1330 | 1332 | PF00082 | 0.367 |
CLV_PCSK_KEX2_1 | 194 | 196 | PF00082 | 0.557 |
CLV_PCSK_KEX2_1 | 677 | 679 | PF00082 | 0.597 |
CLV_PCSK_KEX2_1 | 747 | 749 | PF00082 | 0.452 |
CLV_PCSK_KEX2_1 | 823 | 825 | PF00082 | 0.491 |
CLV_PCSK_KEX2_1 | 964 | 966 | PF00082 | 0.208 |
CLV_PCSK_PC1ET2_1 | 1330 | 1332 | PF00082 | 0.364 |
CLV_PCSK_PC1ET2_1 | 677 | 679 | PF00082 | 0.639 |
CLV_PCSK_PC1ET2_1 | 747 | 749 | PF00082 | 0.452 |
CLV_PCSK_PC1ET2_1 | 964 | 966 | PF00082 | 0.246 |
CLV_PCSK_SKI1_1 | 1158 | 1162 | PF00082 | 0.341 |
CLV_PCSK_SKI1_1 | 1331 | 1335 | PF00082 | 0.364 |
CLV_PCSK_SKI1_1 | 267 | 271 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 315 | 319 | PF00082 | 0.573 |
CLV_PCSK_SKI1_1 | 387 | 391 | PF00082 | 0.531 |
CLV_PCSK_SKI1_1 | 487 | 491 | PF00082 | 0.518 |
CLV_PCSK_SKI1_1 | 589 | 593 | PF00082 | 0.545 |
CLV_PCSK_SKI1_1 | 635 | 639 | PF00082 | 0.590 |
CLV_PCSK_SKI1_1 | 663 | 667 | PF00082 | 0.541 |
CLV_PCSK_SKI1_1 | 703 | 707 | PF00082 | 0.559 |
CLV_PCSK_SKI1_1 | 80 | 84 | PF00082 | 0.612 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.460 |
DEG_SPOP_SBC_1 | 239 | 243 | PF00917 | 0.194 |
DEG_SPOP_SBC_1 | 377 | 381 | PF00917 | 0.182 |
DEG_SPOP_SBC_1 | 814 | 818 | PF00917 | 0.357 |
DOC_CKS1_1 | 672 | 677 | PF01111 | 0.243 |
DOC_CYCLIN_yCln2_LP_2 | 32 | 38 | PF00134 | 0.376 |
DOC_CYCLIN_yCln2_LP_2 | 515 | 521 | PF00134 | 0.420 |
DOC_MAPK_DCC_7 | 513 | 521 | PF00069 | 0.316 |
DOC_MAPK_gen_1 | 1221 | 1228 | PF00069 | 0.627 |
DOC_MAPK_gen_1 | 1240 | 1249 | PF00069 | 0.677 |
DOC_MAPK_MEF2A_6 | 1240 | 1249 | PF00069 | 0.651 |
DOC_MAPK_MEF2A_6 | 252 | 261 | PF00069 | 0.408 |
DOC_PP1_RVXF_1 | 139 | 146 | PF00149 | 0.335 |
DOC_PP1_RVXF_1 | 167 | 173 | PF00149 | 0.248 |
DOC_PP1_RVXF_1 | 353 | 359 | PF00149 | 0.411 |
DOC_PP1_RVXF_1 | 661 | 667 | PF00149 | 0.318 |
DOC_PP2B_LxvP_1 | 1378 | 1381 | PF13499 | 0.566 |
DOC_PP2B_LxvP_1 | 32 | 35 | PF13499 | 0.351 |
DOC_PP2B_PxIxI_1 | 493 | 499 | PF00149 | 0.217 |
DOC_PP4_FxxP_1 | 1151 | 1154 | PF00568 | 0.583 |
DOC_PP4_FxxP_1 | 235 | 238 | PF00568 | 0.225 |
DOC_PP4_FxxP_1 | 520 | 523 | PF00568 | 0.266 |
DOC_USP7_MATH_1 | 1085 | 1089 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 116 | 120 | PF00917 | 0.365 |
DOC_USP7_MATH_1 | 1207 | 1211 | PF00917 | 0.689 |
DOC_USP7_MATH_1 | 1236 | 1240 | PF00917 | 0.610 |
DOC_USP7_MATH_1 | 1250 | 1254 | PF00917 | 0.617 |
DOC_USP7_MATH_1 | 1280 | 1284 | PF00917 | 0.482 |
DOC_USP7_MATH_1 | 1303 | 1307 | PF00917 | 0.564 |
DOC_USP7_MATH_1 | 1402 | 1406 | PF00917 | 0.460 |
DOC_USP7_MATH_1 | 156 | 160 | PF00917 | 0.362 |
DOC_USP7_MATH_1 | 238 | 242 | PF00917 | 0.362 |
DOC_USP7_MATH_1 | 317 | 321 | PF00917 | 0.316 |
DOC_USP7_MATH_1 | 377 | 381 | PF00917 | 0.396 |
DOC_USP7_MATH_1 | 412 | 416 | PF00917 | 0.329 |
DOC_USP7_MATH_1 | 464 | 468 | PF00917 | 0.340 |
DOC_USP7_MATH_1 | 572 | 576 | PF00917 | 0.453 |
DOC_USP7_MATH_1 | 656 | 660 | PF00917 | 0.383 |
DOC_USP7_MATH_1 | 719 | 723 | PF00917 | 0.356 |
DOC_USP7_MATH_1 | 814 | 818 | PF00917 | 0.550 |
DOC_USP7_MATH_1 | 822 | 826 | PF00917 | 0.485 |
DOC_USP7_MATH_1 | 893 | 897 | PF00917 | 0.534 |
DOC_USP7_UBL2_3 | 1142 | 1146 | PF12436 | 0.610 |
DOC_WW_Pin1_4 | 1 | 6 | PF00397 | 0.439 |
DOC_WW_Pin1_4 | 1152 | 1157 | PF00397 | 0.559 |
DOC_WW_Pin1_4 | 1230 | 1235 | PF00397 | 0.580 |
DOC_WW_Pin1_4 | 1308 | 1313 | PF00397 | 0.571 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.405 |
DOC_WW_Pin1_4 | 275 | 280 | PF00397 | 0.400 |
DOC_WW_Pin1_4 | 348 | 353 | PF00397 | 0.231 |
DOC_WW_Pin1_4 | 490 | 495 | PF00397 | 0.378 |
DOC_WW_Pin1_4 | 506 | 511 | PF00397 | 0.328 |
DOC_WW_Pin1_4 | 671 | 676 | PF00397 | 0.445 |
DOC_WW_Pin1_4 | 695 | 700 | PF00397 | 0.317 |
DOC_WW_Pin1_4 | 751 | 756 | PF00397 | 0.306 |
DOC_WW_Pin1_4 | 82 | 87 | PF00397 | 0.307 |
LIG_14-3-3_CanoR_1 | 1178 | 1185 | PF00244 | 0.578 |
LIG_14-3-3_CanoR_1 | 1221 | 1227 | PF00244 | 0.549 |
LIG_14-3-3_CanoR_1 | 1242 | 1246 | PF00244 | 0.629 |
LIG_14-3-3_CanoR_1 | 1256 | 1266 | PF00244 | 0.642 |
LIG_14-3-3_CanoR_1 | 1351 | 1359 | PF00244 | 0.579 |
LIG_14-3-3_CanoR_1 | 267 | 274 | PF00244 | 0.396 |
LIG_14-3-3_CanoR_1 | 336 | 340 | PF00244 | 0.322 |
LIG_14-3-3_CanoR_1 | 579 | 586 | PF00244 | 0.386 |
LIG_14-3-3_CanoR_1 | 682 | 688 | PF00244 | 0.420 |
LIG_14-3-3_CanoR_1 | 709 | 714 | PF00244 | 0.297 |
LIG_14-3-3_CanoR_1 | 823 | 832 | PF00244 | 0.225 |
LIG_Actin_WH2_2 | 1040 | 1057 | PF00022 | 0.541 |
LIG_APCC_ABBA_1 | 637 | 642 | PF00400 | 0.293 |
LIG_BIR_III_4 | 1094 | 1098 | PF00653 | 0.495 |
LIG_BRCT_BRCA1_1 | 1223 | 1227 | PF00533 | 0.576 |
LIG_BRCT_BRCA1_1 | 1310 | 1314 | PF00533 | 0.557 |
LIG_BRCT_BRCA1_1 | 215 | 219 | PF00533 | 0.364 |
LIG_BRCT_BRCA1_1 | 222 | 226 | PF00533 | 0.334 |
LIG_BRCT_BRCA1_1 | 230 | 234 | PF00533 | 0.309 |
LIG_BRCT_BRCA1_1 | 466 | 470 | PF00533 | 0.294 |
LIG_BRCT_BRCA1_1 | 683 | 687 | PF00533 | 0.248 |
LIG_BRCT_BRCA1_2 | 466 | 472 | PF00533 | 0.187 |
LIG_CSL_BTD_1 | 672 | 675 | PF09270 | 0.248 |
LIG_EVH1_1 | 1153 | 1157 | PF00568 | 0.433 |
LIG_FHA_1 | 1015 | 1021 | PF00498 | 0.460 |
LIG_FHA_1 | 1027 | 1033 | PF00498 | 0.461 |
LIG_FHA_1 | 1177 | 1183 | PF00498 | 0.555 |
LIG_FHA_1 | 1261 | 1267 | PF00498 | 0.671 |
LIG_FHA_1 | 1337 | 1343 | PF00498 | 0.552 |
LIG_FHA_1 | 1350 | 1356 | PF00498 | 0.574 |
LIG_FHA_1 | 1383 | 1389 | PF00498 | 0.564 |
LIG_FHA_1 | 150 | 156 | PF00498 | 0.279 |
LIG_FHA_1 | 20 | 26 | PF00498 | 0.374 |
LIG_FHA_1 | 200 | 206 | PF00498 | 0.311 |
LIG_FHA_1 | 351 | 357 | PF00498 | 0.351 |
LIG_FHA_1 | 493 | 499 | PF00498 | 0.326 |
LIG_FHA_1 | 59 | 65 | PF00498 | 0.326 |
LIG_FHA_1 | 632 | 638 | PF00498 | 0.414 |
LIG_FHA_1 | 730 | 736 | PF00498 | 0.350 |
LIG_FHA_1 | 96 | 102 | PF00498 | 0.359 |
LIG_FHA_2 | 103 | 109 | PF00498 | 0.291 |
LIG_FHA_2 | 1035 | 1041 | PF00498 | 0.546 |
LIG_FHA_2 | 1364 | 1370 | PF00498 | 0.393 |
LIG_FHA_2 | 144 | 150 | PF00498 | 0.422 |
LIG_FHA_2 | 453 | 459 | PF00498 | 0.403 |
LIG_FHA_2 | 876 | 882 | PF00498 | 0.456 |
LIG_FHA_2 | 917 | 923 | PF00498 | 0.460 |
LIG_FHA_2 | 951 | 957 | PF00498 | 0.459 |
LIG_GBD_Chelix_1 | 937 | 945 | PF00786 | 0.364 |
LIG_IRF3_LxIS_1 | 426 | 433 | PF10401 | 0.376 |
LIG_LIR_Apic_2 | 517 | 523 | PF02991 | 0.329 |
LIG_LIR_Gen_1 | 1043 | 1054 | PF02991 | 0.544 |
LIG_LIR_Gen_1 | 1111 | 1121 | PF02991 | 0.620 |
LIG_LIR_Gen_1 | 1397 | 1404 | PF02991 | 0.373 |
LIG_LIR_Gen_1 | 159 | 168 | PF02991 | 0.393 |
LIG_LIR_Gen_1 | 216 | 226 | PF02991 | 0.299 |
LIG_LIR_Gen_1 | 244 | 251 | PF02991 | 0.376 |
LIG_LIR_Gen_1 | 558 | 568 | PF02991 | 0.213 |
LIG_LIR_Gen_1 | 777 | 784 | PF02991 | 0.373 |
LIG_LIR_Gen_1 | 874 | 885 | PF02991 | 0.457 |
LIG_LIR_Gen_1 | 931 | 938 | PF02991 | 0.414 |
LIG_LIR_Gen_1 | 994 | 1004 | PF02991 | 0.552 |
LIG_LIR_Nem_3 | 1001 | 1007 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 1043 | 1049 | PF02991 | 0.557 |
LIG_LIR_Nem_3 | 1111 | 1117 | PF02991 | 0.635 |
LIG_LIR_Nem_3 | 1129 | 1135 | PF02991 | 0.599 |
LIG_LIR_Nem_3 | 1147 | 1153 | PF02991 | 0.579 |
LIG_LIR_Nem_3 | 1225 | 1231 | PF02991 | 0.599 |
LIG_LIR_Nem_3 | 1329 | 1335 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 159 | 163 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 216 | 222 | PF02991 | 0.240 |
LIG_LIR_Nem_3 | 231 | 237 | PF02991 | 0.208 |
LIG_LIR_Nem_3 | 244 | 250 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 403 | 408 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 558 | 563 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 644 | 650 | PF02991 | 0.292 |
LIG_LIR_Nem_3 | 874 | 880 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 910 | 915 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 931 | 935 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 956 | 962 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 994 | 1000 | PF02991 | 0.472 |
LIG_MLH1_MIPbox_1 | 1224 | 1228 | PF16413 | 0.456 |
LIG_NRBOX | 24 | 30 | PF00104 | 0.291 |
LIG_PCNA_yPIPBox_3 | 1169 | 1178 | PF02747 | 0.381 |
LIG_Pex14_2 | 222 | 226 | PF04695 | 0.216 |
LIG_Rb_pABgroove_1 | 634 | 642 | PF01858 | 0.305 |
LIG_SH2_CRK | 1007 | 1011 | PF00017 | 0.546 |
LIG_SH2_CRK | 443 | 447 | PF00017 | 0.338 |
LIG_SH2_CRK | 560 | 564 | PF00017 | 0.431 |
LIG_SH2_CRK | 696 | 700 | PF00017 | 0.403 |
LIG_SH2_GRB2like | 1135 | 1138 | PF00017 | 0.577 |
LIG_SH2_GRB2like | 1167 | 1170 | PF00017 | 0.434 |
LIG_SH2_GRB2like | 526 | 529 | PF00017 | 0.223 |
LIG_SH2_NCK_1 | 716 | 720 | PF00017 | 0.398 |
LIG_SH2_NCK_1 | 959 | 963 | PF00017 | 0.494 |
LIG_SH2_PTP2 | 160 | 163 | PF00017 | 0.383 |
LIG_SH2_SRC | 1167 | 1170 | PF00017 | 0.602 |
LIG_SH2_SRC | 526 | 529 | PF00017 | 0.410 |
LIG_SH2_SRC | 800 | 803 | PF00017 | 0.244 |
LIG_SH2_STAP1 | 1396 | 1400 | PF00017 | 0.390 |
LIG_SH2_STAP1 | 174 | 178 | PF00017 | 0.341 |
LIG_SH2_STAP1 | 392 | 396 | PF00017 | 0.221 |
LIG_SH2_STAP1 | 731 | 735 | PF00017 | 0.364 |
LIG_SH2_STAT3 | 731 | 734 | PF00017 | 0.397 |
LIG_SH2_STAT5 | 1131 | 1134 | PF00017 | 0.555 |
LIG_SH2_STAT5 | 1135 | 1138 | PF00017 | 0.514 |
LIG_SH2_STAT5 | 1150 | 1153 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 1167 | 1170 | PF00017 | 0.569 |
LIG_SH2_STAT5 | 1346 | 1349 | PF00017 | 0.393 |
LIG_SH2_STAT5 | 1396 | 1399 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 1400 | 1403 | PF00017 | 0.371 |
LIG_SH2_STAT5 | 144 | 147 | PF00017 | 0.329 |
LIG_SH2_STAT5 | 160 | 163 | PF00017 | 0.266 |
LIG_SH2_STAT5 | 174 | 177 | PF00017 | 0.306 |
LIG_SH2_STAT5 | 201 | 204 | PF00017 | 0.403 |
LIG_SH2_STAT5 | 273 | 276 | PF00017 | 0.356 |
LIG_SH2_STAT5 | 357 | 360 | PF00017 | 0.313 |
LIG_SH2_STAT5 | 367 | 370 | PF00017 | 0.262 |
LIG_SH2_STAT5 | 440 | 443 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 534 | 537 | PF00017 | 0.370 |
LIG_SH2_STAT5 | 731 | 734 | PF00017 | 0.309 |
LIG_SH2_STAT5 | 774 | 777 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 793 | 796 | PF00017 | 0.209 |
LIG_SH2_STAT5 | 800 | 803 | PF00017 | 0.262 |
LIG_SH3_2 | 1154 | 1159 | PF14604 | 0.613 |
LIG_SH3_2 | 279 | 284 | PF14604 | 0.362 |
LIG_SH3_2 | 672 | 677 | PF14604 | 0.250 |
LIG_SH3_3 | 1054 | 1060 | PF00018 | 0.381 |
LIG_SH3_3 | 1151 | 1157 | PF00018 | 0.513 |
LIG_SH3_3 | 1228 | 1234 | PF00018 | 0.634 |
LIG_SH3_3 | 256 | 262 | PF00018 | 0.275 |
LIG_SH3_3 | 276 | 282 | PF00018 | 0.353 |
LIG_SH3_3 | 669 | 675 | PF00018 | 0.257 |
LIG_SUMO_SIM_anti_2 | 152 | 159 | PF11976 | 0.217 |
LIG_SUMO_SIM_anti_2 | 22 | 28 | PF11976 | 0.373 |
LIG_SUMO_SIM_anti_2 | 227 | 234 | PF11976 | 0.182 |
LIG_SUMO_SIM_anti_2 | 608 | 614 | PF11976 | 0.344 |
LIG_SUMO_SIM_anti_2 | 632 | 642 | PF11976 | 0.339 |
LIG_SUMO_SIM_anti_2 | 871 | 879 | PF11976 | 0.459 |
LIG_SUMO_SIM_par_1 | 1170 | 1177 | PF11976 | 0.434 |
LIG_SUMO_SIM_par_1 | 1272 | 1279 | PF11976 | 0.648 |
LIG_SUMO_SIM_par_1 | 1285 | 1293 | PF11976 | 0.610 |
LIG_SUMO_SIM_par_1 | 152 | 159 | PF11976 | 0.230 |
LIG_SUMO_SIM_par_1 | 387 | 393 | PF11976 | 0.401 |
LIG_SUMO_SIM_par_1 | 608 | 614 | PF11976 | 0.392 |
LIG_SUMO_SIM_par_1 | 632 | 642 | PF11976 | 0.358 |
LIG_TRAF2_1 | 1037 | 1040 | PF00917 | 0.488 |
LIG_TYR_ITIM | 441 | 446 | PF00017 | 0.409 |
LIG_UBA3_1 | 1320 | 1327 | PF00899 | 0.393 |
LIG_UBA3_1 | 246 | 252 | PF00899 | 0.359 |
LIG_UBA3_1 | 904 | 913 | PF00899 | 0.444 |
LIG_WW_3 | 1155 | 1159 | PF00397 | 0.617 |
MOD_CDC14_SPxK_1 | 1155 | 1158 | PF00782 | 0.609 |
MOD_CDK_SPK_2 | 275 | 280 | PF00069 | 0.220 |
MOD_CDK_SPK_2 | 671 | 676 | PF00069 | 0.244 |
MOD_CDK_SPK_2 | 751 | 756 | PF00069 | 0.231 |
MOD_CDK_SPxK_1 | 1152 | 1158 | PF00069 | 0.606 |
MOD_CDK_SPxK_1 | 671 | 677 | PF00069 | 0.244 |
MOD_CDK_SPxxK_3 | 1152 | 1159 | PF00069 | 0.632 |
MOD_CDK_SPxxK_3 | 348 | 355 | PF00069 | 0.230 |
MOD_CDK_SPxxK_3 | 506 | 513 | PF00069 | 0.404 |
MOD_CDK_SPxxK_3 | 671 | 678 | PF00069 | 0.426 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.324 |
MOD_CK1_1 | 1076 | 1082 | PF00069 | 0.612 |
MOD_CK1_1 | 1133 | 1139 | PF00069 | 0.476 |
MOD_CK1_1 | 118 | 124 | PF00069 | 0.223 |
MOD_CK1_1 | 1260 | 1266 | PF00069 | 0.642 |
MOD_CK1_1 | 1292 | 1298 | PF00069 | 0.671 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.322 |
MOD_CK1_1 | 242 | 248 | PF00069 | 0.376 |
MOD_CK1_1 | 566 | 572 | PF00069 | 0.353 |
MOD_CK1_1 | 590 | 596 | PF00069 | 0.384 |
MOD_CK1_1 | 681 | 687 | PF00069 | 0.361 |
MOD_CK1_1 | 698 | 704 | PF00069 | 0.290 |
MOD_CK1_1 | 712 | 718 | PF00069 | 0.317 |
MOD_CK1_1 | 754 | 760 | PF00069 | 0.340 |
MOD_CK1_1 | 808 | 814 | PF00069 | 0.451 |
MOD_CK1_1 | 816 | 822 | PF00069 | 0.498 |
MOD_CK1_1 | 826 | 832 | PF00069 | 0.355 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.392 |
MOD_CK1_1 | 966 | 972 | PF00069 | 0.491 |
MOD_CK2_1 | 1028 | 1034 | PF00069 | 0.481 |
MOD_CK2_1 | 1194 | 1200 | PF00069 | 0.583 |
MOD_CK2_1 | 125 | 131 | PF00069 | 0.373 |
MOD_CK2_1 | 1280 | 1286 | PF00069 | 0.684 |
MOD_CK2_1 | 1303 | 1309 | PF00069 | 0.393 |
MOD_CK2_1 | 1363 | 1369 | PF00069 | 0.406 |
MOD_CK2_1 | 250 | 256 | PF00069 | 0.330 |
MOD_CK2_1 | 442 | 448 | PF00069 | 0.356 |
MOD_CK2_1 | 506 | 512 | PF00069 | 0.319 |
MOD_CK2_1 | 656 | 662 | PF00069 | 0.406 |
MOD_CK2_1 | 814 | 820 | PF00069 | 0.504 |
MOD_CK2_1 | 875 | 881 | PF00069 | 0.457 |
MOD_Cter_Amidation | 962 | 965 | PF01082 | 0.156 |
MOD_GlcNHglycan | 1179 | 1182 | PF01048 | 0.325 |
MOD_GlcNHglycan | 1196 | 1199 | PF01048 | 0.422 |
MOD_GlcNHglycan | 1228 | 1231 | PF01048 | 0.384 |
MOD_GlcNHglycan | 1278 | 1281 | PF01048 | 0.285 |
MOD_GlcNHglycan | 1305 | 1308 | PF01048 | 0.367 |
MOD_GlcNHglycan | 1352 | 1355 | PF01048 | 0.180 |
MOD_GlcNHglycan | 1404 | 1407 | PF01048 | 0.459 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.530 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.540 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.509 |
MOD_GlcNHglycan | 227 | 230 | PF01048 | 0.430 |
MOD_GlcNHglycan | 253 | 256 | PF01048 | 0.553 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.525 |
MOD_GlcNHglycan | 401 | 405 | PF01048 | 0.575 |
MOD_GlcNHglycan | 466 | 469 | PF01048 | 0.526 |
MOD_GlcNHglycan | 502 | 505 | PF01048 | 0.552 |
MOD_GlcNHglycan | 552 | 555 | PF01048 | 0.532 |
MOD_GlcNHglycan | 565 | 568 | PF01048 | 0.537 |
MOD_GlcNHglycan | 607 | 610 | PF01048 | 0.539 |
MOD_GlcNHglycan | 659 | 662 | PF01048 | 0.496 |
MOD_GlcNHglycan | 683 | 686 | PF01048 | 0.605 |
MOD_GlcNHglycan | 723 | 726 | PF01048 | 0.588 |
MOD_GlcNHglycan | 810 | 813 | PF01048 | 0.685 |
MOD_GlcNHglycan | 895 | 898 | PF01048 | 0.368 |
MOD_GlcNHglycan | 93 | 97 | PF01048 | 0.602 |
MOD_GlcNHglycan | 965 | 968 | PF01048 | 0.332 |
MOD_GlcNHglycan | 979 | 982 | PF01048 | 0.269 |
MOD_GSK3_1 | 1010 | 1017 | PF00069 | 0.487 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.295 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.291 |
MOD_GSK3_1 | 1167 | 1174 | PF00069 | 0.587 |
MOD_GSK3_1 | 1222 | 1229 | PF00069 | 0.612 |
MOD_GSK3_1 | 1272 | 1279 | PF00069 | 0.649 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.410 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.316 |
MOD_GSK3_1 | 1345 | 1352 | PF00069 | 0.565 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.343 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.326 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.277 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.263 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.296 |
MOD_GSK3_1 | 464 | 471 | PF00069 | 0.290 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.284 |
MOD_GSK3_1 | 568 | 575 | PF00069 | 0.361 |
MOD_GSK3_1 | 616 | 623 | PF00069 | 0.358 |
MOD_GSK3_1 | 627 | 634 | PF00069 | 0.383 |
MOD_GSK3_1 | 822 | 829 | PF00069 | 0.422 |
MOD_GSK3_1 | 871 | 878 | PF00069 | 0.470 |
MOD_GSK3_1 | 916 | 923 | PF00069 | 0.463 |
MOD_LATS_1 | 1187 | 1193 | PF00433 | 0.465 |
MOD_N-GLC_1 | 1335 | 1340 | PF02516 | 0.364 |
MOD_N-GLC_1 | 430 | 435 | PF02516 | 0.565 |
MOD_N-GLC_1 | 527 | 532 | PF02516 | 0.610 |
MOD_N-GLC_2 | 10 | 12 | PF02516 | 0.452 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.360 |
MOD_NEK2_1 | 1144 | 1149 | PF00069 | 0.513 |
MOD_NEK2_1 | 1171 | 1176 | PF00069 | 0.603 |
MOD_NEK2_1 | 1241 | 1246 | PF00069 | 0.651 |
MOD_NEK2_1 | 125 | 130 | PF00069 | 0.350 |
MOD_NEK2_1 | 1276 | 1281 | PF00069 | 0.675 |
MOD_NEK2_1 | 172 | 177 | PF00069 | 0.385 |
MOD_NEK2_1 | 199 | 204 | PF00069 | 0.341 |
MOD_NEK2_1 | 250 | 255 | PF00069 | 0.327 |
MOD_NEK2_1 | 265 | 270 | PF00069 | 0.235 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.286 |
MOD_NEK2_1 | 318 | 323 | PF00069 | 0.373 |
MOD_NEK2_1 | 390 | 395 | PF00069 | 0.379 |
MOD_NEK2_1 | 430 | 435 | PF00069 | 0.257 |
MOD_NEK2_1 | 481 | 486 | PF00069 | 0.336 |
MOD_NEK2_1 | 563 | 568 | PF00069 | 0.387 |
MOD_NEK2_1 | 573 | 578 | PF00069 | 0.348 |
MOD_NEK2_1 | 665 | 670 | PF00069 | 0.291 |
MOD_NEK2_1 | 688 | 693 | PF00069 | 0.393 |
MOD_NEK2_1 | 746 | 751 | PF00069 | 0.362 |
MOD_NEK2_1 | 805 | 810 | PF00069 | 0.344 |
MOD_NEK2_1 | 886 | 891 | PF00069 | 0.504 |
MOD_NEK2_2 | 584 | 589 | PF00069 | 0.448 |
MOD_OFUCOSY | 1277 | 1284 | PF10250 | 0.470 |
MOD_PIKK_1 | 1363 | 1369 | PF00454 | 0.393 |
MOD_PIKK_1 | 208 | 214 | PF00454 | 0.263 |
MOD_PIKK_1 | 268 | 274 | PF00454 | 0.350 |
MOD_PIKK_1 | 350 | 356 | PF00454 | 0.371 |
MOD_PIKK_1 | 452 | 458 | PF00454 | 0.424 |
MOD_PIKK_1 | 641 | 647 | PF00454 | 0.360 |
MOD_PIKK_1 | 729 | 735 | PF00454 | 0.299 |
MOD_PK_1 | 1016 | 1022 | PF00069 | 0.390 |
MOD_PK_1 | 1222 | 1228 | PF00069 | 0.619 |
MOD_PK_1 | 442 | 448 | PF00069 | 0.205 |
MOD_PKA_1 | 1221 | 1227 | PF00069 | 0.592 |
MOD_PKA_1 | 823 | 829 | PF00069 | 0.233 |
MOD_PKA_2 | 1177 | 1183 | PF00069 | 0.562 |
MOD_PKA_2 | 1221 | 1227 | PF00069 | 0.615 |
MOD_PKA_2 | 1241 | 1247 | PF00069 | 0.666 |
MOD_PKA_2 | 1350 | 1356 | PF00069 | 0.402 |
MOD_PKA_2 | 335 | 341 | PF00069 | 0.367 |
MOD_PKA_2 | 43 | 49 | PF00069 | 0.355 |
MOD_PKA_2 | 563 | 569 | PF00069 | 0.338 |
MOD_PKA_2 | 578 | 584 | PF00069 | 0.375 |
MOD_PKA_2 | 656 | 662 | PF00069 | 0.429 |
MOD_PKA_2 | 681 | 687 | PF00069 | 0.400 |
MOD_PKA_2 | 814 | 820 | PF00069 | 0.486 |
MOD_PKA_2 | 822 | 828 | PF00069 | 0.468 |
MOD_PKA_2 | 856 | 862 | PF00069 | 0.527 |
MOD_Plk_1 | 482 | 488 | PF00069 | 0.372 |
MOD_Plk_1 | 641 | 647 | PF00069 | 0.336 |
MOD_Plk_1 | 678 | 684 | PF00069 | 0.400 |
MOD_Plk_1 | 739 | 745 | PF00069 | 0.356 |
MOD_Plk_2-3 | 1034 | 1040 | PF00069 | 0.374 |
MOD_Plk_2-3 | 916 | 922 | PF00069 | 0.456 |
MOD_Plk_4 | 1028 | 1034 | PF00069 | 0.436 |
MOD_Plk_4 | 106 | 112 | PF00069 | 0.317 |
MOD_Plk_4 | 1167 | 1173 | PF00069 | 0.567 |
MOD_Plk_4 | 121 | 127 | PF00069 | 0.284 |
MOD_Plk_4 | 1222 | 1228 | PF00069 | 0.500 |
MOD_Plk_4 | 1260 | 1266 | PF00069 | 0.685 |
MOD_Plk_4 | 156 | 162 | PF00069 | 0.342 |
MOD_Plk_4 | 201 | 207 | PF00069 | 0.364 |
MOD_Plk_4 | 242 | 248 | PF00069 | 0.355 |
MOD_Plk_4 | 260 | 266 | PF00069 | 0.320 |
MOD_Plk_4 | 343 | 349 | PF00069 | 0.361 |
MOD_Plk_4 | 412 | 418 | PF00069 | 0.281 |
MOD_Plk_4 | 521 | 527 | PF00069 | 0.306 |
MOD_Plk_4 | 545 | 551 | PF00069 | 0.343 |
MOD_Plk_4 | 709 | 715 | PF00069 | 0.267 |
MOD_Plk_4 | 827 | 833 | PF00069 | 0.289 |
MOD_Plk_4 | 871 | 877 | PF00069 | 0.456 |
MOD_Plk_4 | 920 | 926 | PF00069 | 0.467 |
MOD_ProDKin_1 | 1 | 7 | PF00069 | 0.440 |
MOD_ProDKin_1 | 1152 | 1158 | PF00069 | 0.560 |
MOD_ProDKin_1 | 1230 | 1236 | PF00069 | 0.579 |
MOD_ProDKin_1 | 1308 | 1314 | PF00069 | 0.571 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.404 |
MOD_ProDKin_1 | 275 | 281 | PF00069 | 0.399 |
MOD_ProDKin_1 | 348 | 354 | PF00069 | 0.230 |
MOD_ProDKin_1 | 490 | 496 | PF00069 | 0.378 |
MOD_ProDKin_1 | 506 | 512 | PF00069 | 0.330 |
MOD_ProDKin_1 | 671 | 677 | PF00069 | 0.445 |
MOD_ProDKin_1 | 695 | 701 | PF00069 | 0.317 |
MOD_ProDKin_1 | 751 | 757 | PF00069 | 0.305 |
MOD_ProDKin_1 | 82 | 88 | PF00069 | 0.309 |
MOD_SUMO_for_1 | 781 | 784 | PF00179 | 0.427 |
MOD_SUMO_rev_2 | 1232 | 1241 | PF00179 | 0.435 |
TRG_DiLeu_BaEn_1 | 153 | 158 | PF01217 | 0.226 |
TRG_DiLeu_BaEn_1 | 256 | 261 | PF01217 | 0.204 |
TRG_DiLeu_BaEn_1 | 871 | 876 | PF01217 | 0.548 |
TRG_DiLeu_BaEn_2 | 661 | 667 | PF01217 | 0.250 |
TRG_DiLeu_BaEn_3 | 1102 | 1108 | PF01217 | 0.541 |
TRG_DiLeu_BaLyEn_6 | 357 | 362 | PF01217 | 0.200 |
TRG_DiLeu_BaLyEn_6 | 660 | 665 | PF01217 | 0.260 |
TRG_ENDOCYTIC_2 | 1007 | 1010 | PF00928 | 0.541 |
TRG_ENDOCYTIC_2 | 1131 | 1134 | PF00928 | 0.388 |
TRG_ENDOCYTIC_2 | 1150 | 1153 | PF00928 | 0.549 |
TRG_ENDOCYTIC_2 | 1346 | 1349 | PF00928 | 0.393 |
TRG_ENDOCYTIC_2 | 1400 | 1403 | PF00928 | 0.386 |
TRG_ENDOCYTIC_2 | 160 | 163 | PF00928 | 0.273 |
TRG_ENDOCYTIC_2 | 189 | 192 | PF00928 | 0.384 |
TRG_ENDOCYTIC_2 | 405 | 408 | PF00928 | 0.340 |
TRG_ENDOCYTIC_2 | 443 | 446 | PF00928 | 0.342 |
TRG_ENDOCYTIC_2 | 560 | 563 | PF00928 | 0.439 |
TRG_ENDOCYTIC_2 | 647 | 650 | PF00928 | 0.294 |
TRG_ENDOCYTIC_2 | 778 | 781 | PF00928 | 0.403 |
TRG_ENDOCYTIC_2 | 959 | 962 | PF00928 | 0.462 |
TRG_ER_diArg_1 | 1157 | 1159 | PF00400 | 0.597 |
TRG_ER_diArg_1 | 1185 | 1188 | PF00400 | 0.598 |
TRG_ER_diArg_1 | 1220 | 1222 | PF00400 | 0.637 |
TRG_ER_diArg_1 | 1241 | 1243 | PF00400 | 0.680 |
TRG_ER_diArg_1 | 193 | 195 | PF00400 | 0.360 |
TRG_ER_diArg_1 | 982 | 985 | PF00400 | 0.456 |
TRG_Pf-PMV_PEXEL_1 | 1188 | 1193 | PF00026 | 0.487 |
TRG_Pf-PMV_PEXEL_1 | 360 | 364 | PF00026 | 0.487 |
TRG_Pf-PMV_PEXEL_1 | 513 | 517 | PF00026 | 0.431 |
TRG_Pf-PMV_PEXEL_1 | 990 | 994 | PF00026 | 0.156 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P457 | Leptomonas seymouri | 41% | 100% |
A0A1X0P171 | Trypanosomatidae | 29% | 100% |
A0A3Q8IJB0 | Leishmania donovani | 27% | 100% |
A0A3S5H6Z8 | Leishmania donovani | 27% | 100% |
A0A3S7WU91 | Leishmania donovani | 28% | 100% |
A0A3S7WU94 | Leishmania donovani | 30% | 100% |
A0A3S7WU95 | Leishmania donovani | 27% | 100% |
A4H8U6 | Leishmania braziliensis | 30% | 100% |
A4H8V5 | Leishmania braziliensis | 30% | 100% |
A4H8V7 | Leishmania braziliensis | 31% | 100% |
A4H8V8 | Leishmania braziliensis | 28% | 100% |
A4HPI4 | Leishmania braziliensis | 70% | 100% |
A4HX84 | Leishmania infantum | 30% | 100% |
A4HX85 | Leishmania infantum | 27% | 100% |
A4HX87 | Leishmania infantum | 28% | 100% |
A4IDA6 | Leishmania infantum | 98% | 99% |
C9ZM79 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZM80 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZM81 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
C9ZM82 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
C9ZM83 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
C9ZM86 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
C9ZN26 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZN41 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
C9ZN43 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZN44 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
C9ZN45 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
C9ZN46 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
C9ZNA5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZNA6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
C9ZNH3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
C9ZNT1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
C9ZPZ6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
C9ZQ51 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
C9ZQ89 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZQ90 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZQ92 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZTS4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
C9ZTS5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZTS6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
C9ZUE6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZWQ5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
C9ZWU1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
C9ZWU2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
C9ZWU3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZWY7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
C9ZZQ4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
D0A0U3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
D0A0W7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
D0A0X5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
D0A1S1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
D0A5D2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
D0A5D5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
D0A5U0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
D0A5U1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
D0A7A0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
D0A9R3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
D0AAV3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
E9AQY1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9AQY2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9AQY4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9AT96 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |
Q25263 | Leishmania donovani | 28% | 100% |
Q26721 | Trypanosoma brucei brucei | 28% | 100% |
Q4Q1A1 | Leishmania major | 86% | 99% |
Q4QEH9 | Leishmania major | 27% | 100% |
Q4QEI0 | Leishmania major | 28% | 100% |
Q4QEI1 | Leishmania major | 27% | 100% |
Q4QEI2 | Leishmania major | 28% | 100% |
Q4QEI3 | Leishmania major | 29% | 100% |
Q99279 | Trypanosoma brucei brucei | 28% | 100% |
Q99280 | Trypanosoma brucei brucei | 29% | 100% |
V5AYH7 | Trypanosoma cruzi | 31% | 100% |