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. | yes | yes: 42 |
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 | yes | yes: 41, no: 22 |
NetGPI | no | yes: 0, no: 63 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 61 |
GO:0110165 | cellular anatomical entity | 1 | 64 |
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 64 |
GO:0006163 | purine nucleotide metabolic process | 5 | 64 |
GO:0006164 | purine nucleotide biosynthetic process | 6 | 64 |
GO:0006171 | cAMP biosynthetic process | 8 | 64 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 64 |
GO:0006753 | nucleoside phosphate metabolic process | 4 | 64 |
GO:0006793 | phosphorus metabolic process | 3 | 64 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 64 |
GO:0006807 | nitrogen compound metabolic process | 2 | 64 |
GO:0007165 | signal transduction | 2 | 64 |
GO:0008152 | metabolic process | 1 | 64 |
GO:0009058 | biosynthetic process | 2 | 64 |
GO:0009117 | nucleotide metabolic process | 5 | 64 |
GO:0009150 | purine ribonucleotide metabolic process | 6 | 64 |
GO:0009152 | purine ribonucleotide biosynthetic process | 7 | 64 |
GO:0009165 | nucleotide biosynthetic process | 6 | 64 |
GO:0009187 | cyclic nucleotide metabolic process | 6 | 64 |
GO:0009190 | cyclic nucleotide biosynthetic process | 7 | 64 |
GO:0009259 | ribonucleotide metabolic process | 5 | 64 |
GO:0009260 | ribonucleotide biosynthetic process | 6 | 64 |
GO:0009987 | cellular process | 1 | 64 |
GO:0018130 | heterocycle biosynthetic process | 4 | 64 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 64 |
GO:0019637 | organophosphate metabolic process | 3 | 64 |
GO:0019693 | ribose phosphate metabolic process | 4 | 64 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 64 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 64 |
GO:0035556 | intracellular signal transduction | 3 | 64 |
GO:0044237 | cellular metabolic process | 2 | 64 |
GO:0044238 | primary metabolic process | 2 | 64 |
GO:0044249 | cellular biosynthetic process | 3 | 64 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 64 |
GO:0044281 | small molecule metabolic process | 2 | 64 |
GO:0046058 | cAMP metabolic process | 7 | 64 |
GO:0046390 | ribose phosphate biosynthetic process | 5 | 64 |
GO:0046483 | heterocycle metabolic process | 3 | 64 |
GO:0050789 | regulation of biological process | 2 | 64 |
GO:0050794 | regulation of cellular process | 3 | 64 |
GO:0052652 | cyclic purine nucleotide metabolic process | 6 | 64 |
GO:0055086 | nucleobase-containing small molecule metabolic process | 3 | 64 |
GO:0065007 | biological regulation | 1 | 64 |
GO:0071704 | organic substance metabolic process | 2 | 64 |
GO:0072521 | purine-containing compound metabolic process | 4 | 64 |
GO:0072522 | purine-containing compound biosynthetic process | 5 | 64 |
GO:0090407 | organophosphate biosynthetic process | 4 | 64 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 64 |
GO:1901137 | carbohydrate derivative biosynthetic process | 4 | 64 |
GO:1901293 | nucleoside phosphate biosynthetic process | 5 | 64 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 64 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 64 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 64 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 64 |
GO:1901576 | organic substance biosynthetic process | 3 | 64 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 55 |
GO:0016829 | lyase activity | 2 | 55 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 1221 | 1225 | PF00656 | 0.673 |
CLV_C14_Caspase3-7 | 321 | 325 | PF00656 | 0.383 |
CLV_C14_Caspase3-7 | 455 | 459 | PF00656 | 0.385 |
CLV_C14_Caspase3-7 | 850 | 854 | PF00656 | 0.607 |
CLV_C14_Caspase3-7 | 911 | 915 | PF00656 | 0.485 |
CLV_NRD_NRD_1 | 1150 | 1152 | PF00675 | 0.310 |
CLV_NRD_NRD_1 | 1179 | 1181 | PF00675 | 0.377 |
CLV_NRD_NRD_1 | 1213 | 1215 | PF00675 | 0.434 |
CLV_NRD_NRD_1 | 1234 | 1236 | PF00675 | 0.525 |
CLV_NRD_NRD_1 | 137 | 139 | PF00675 | 0.533 |
CLV_NRD_NRD_1 | 194 | 196 | PF00675 | 0.517 |
CLV_NRD_NRD_1 | 79 | 81 | PF00675 | 0.614 |
CLV_PCSK_KEX2_1 | 1150 | 1152 | PF00082 | 0.364 |
CLV_PCSK_KEX2_1 | 1213 | 1215 | PF00082 | 0.434 |
CLV_PCSK_KEX2_1 | 1232 | 1234 | PF00082 | 0.499 |
CLV_PCSK_KEX2_1 | 1322 | 1324 | PF00082 | 0.396 |
CLV_PCSK_KEX2_1 | 137 | 139 | PF00082 | 0.569 |
CLV_PCSK_KEX2_1 | 194 | 196 | PF00082 | 0.599 |
CLV_PCSK_KEX2_1 | 662 | 664 | PF00082 | 0.455 |
CLV_PCSK_KEX2_1 | 747 | 749 | PF00082 | 0.467 |
CLV_PCSK_PC1ET2_1 | 1232 | 1234 | PF00082 | 0.535 |
CLV_PCSK_PC1ET2_1 | 1322 | 1324 | PF00082 | 0.396 |
CLV_PCSK_PC1ET2_1 | 662 | 664 | PF00082 | 0.455 |
CLV_PCSK_PC1ET2_1 | 747 | 749 | PF00082 | 0.467 |
CLV_PCSK_SKI1_1 | 1026 | 1030 | PF00082 | 0.185 |
CLV_PCSK_SKI1_1 | 1150 | 1154 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 1284 | 1288 | PF00082 | 0.316 |
CLV_PCSK_SKI1_1 | 1323 | 1327 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 255 | 259 | PF00082 | 0.533 |
CLV_PCSK_SKI1_1 | 267 | 271 | PF00082 | 0.522 |
CLV_PCSK_SKI1_1 | 387 | 391 | PF00082 | 0.564 |
CLV_PCSK_SKI1_1 | 487 | 491 | PF00082 | 0.570 |
CLV_PCSK_SKI1_1 | 579 | 583 | PF00082 | 0.564 |
CLV_PCSK_SKI1_1 | 635 | 639 | PF00082 | 0.611 |
CLV_PCSK_SKI1_1 | 648 | 652 | PF00082 | 0.508 |
CLV_PCSK_SKI1_1 | 663 | 667 | PF00082 | 0.577 |
CLV_PCSK_SKI1_1 | 703 | 707 | PF00082 | 0.595 |
CLV_PCSK_SKI1_1 | 739 | 743 | PF00082 | 0.572 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.370 |
DEG_SCF_FBW7_2 | 1302 | 1307 | PF00400 | 0.385 |
DEG_SPOP_SBC_1 | 116 | 120 | PF00917 | 0.270 |
DEG_SPOP_SBC_1 | 814 | 818 | PF00917 | 0.323 |
DOC_CKS1_1 | 672 | 677 | PF01111 | 0.280 |
DOC_CYCLIN_yCln2_LP_2 | 32 | 38 | PF00134 | 0.416 |
DOC_CYCLIN_yCln2_LP_2 | 515 | 521 | PF00134 | 0.450 |
DOC_MAPK_DCC_7 | 18 | 26 | PF00069 | 0.394 |
DOC_MAPK_DCC_7 | 513 | 521 | PF00069 | 0.353 |
DOC_MAPK_FxFP_2 | 234 | 237 | PF00069 | 0.237 |
DOC_MAPK_gen_1 | 1213 | 1220 | PF00069 | 0.669 |
DOC_MAPK_gen_1 | 1232 | 1239 | PF00069 | 0.657 |
DOC_MAPK_gen_1 | 137 | 145 | PF00069 | 0.310 |
DOC_MAPK_gen_1 | 224 | 232 | PF00069 | 0.296 |
DOC_MAPK_MEF2A_6 | 18 | 27 | PF00069 | 0.389 |
DOC_MAPK_MEF2A_6 | 225 | 234 | PF00069 | 0.200 |
DOC_MAPK_MEF2A_6 | 252 | 261 | PF00069 | 0.443 |
DOC_PP1_RVXF_1 | 1130 | 1136 | PF00149 | 0.417 |
DOC_PP1_RVXF_1 | 139 | 146 | PF00149 | 0.387 |
DOC_PP1_RVXF_1 | 167 | 173 | PF00149 | 0.282 |
DOC_PP1_RVXF_1 | 353 | 359 | PF00149 | 0.432 |
DOC_PP1_RVXF_1 | 660 | 667 | PF00149 | 0.353 |
DOC_PP2B_LxvP_1 | 1370 | 1373 | PF13499 | 0.597 |
DOC_PP2B_LxvP_1 | 32 | 35 | PF13499 | 0.388 |
DOC_PP2B_PxIxI_1 | 493 | 499 | PF00149 | 0.253 |
DOC_PP4_FxxP_1 | 1143 | 1146 | PF00568 | 0.620 |
DOC_PP4_FxxP_1 | 234 | 237 | PF00568 | 0.286 |
DOC_PP4_FxxP_1 | 520 | 523 | PF00568 | 0.304 |
DOC_USP7_MATH_1 | 1077 | 1081 | PF00917 | 0.678 |
DOC_USP7_MATH_1 | 116 | 120 | PF00917 | 0.419 |
DOC_USP7_MATH_1 | 1190 | 1194 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 1228 | 1232 | PF00917 | 0.654 |
DOC_USP7_MATH_1 | 1242 | 1246 | PF00917 | 0.739 |
DOC_USP7_MATH_1 | 1272 | 1276 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 1394 | 1398 | PF00917 | 0.496 |
DOC_USP7_MATH_1 | 282 | 286 | PF00917 | 0.344 |
DOC_USP7_MATH_1 | 319 | 323 | PF00917 | 0.327 |
DOC_USP7_MATH_1 | 377 | 381 | PF00917 | 0.421 |
DOC_USP7_MATH_1 | 396 | 400 | PF00917 | 0.217 |
DOC_USP7_MATH_1 | 464 | 468 | PF00917 | 0.372 |
DOC_USP7_MATH_1 | 477 | 481 | PF00917 | 0.304 |
DOC_USP7_MATH_1 | 572 | 576 | PF00917 | 0.458 |
DOC_USP7_MATH_1 | 656 | 660 | PF00917 | 0.416 |
DOC_USP7_MATH_1 | 719 | 723 | PF00917 | 0.399 |
DOC_USP7_MATH_1 | 79 | 83 | PF00917 | 0.386 |
DOC_USP7_MATH_1 | 814 | 818 | PF00917 | 0.509 |
DOC_USP7_MATH_1 | 885 | 889 | PF00917 | 0.569 |
DOC_USP7_MATH_2 | 963 | 969 | PF00917 | 0.385 |
DOC_USP7_UBL2_3 | 1134 | 1138 | PF12436 | 0.640 |
DOC_USP7_UBL2_3 | 298 | 302 | PF12436 | 0.503 |
DOC_USP7_UBL2_3 | 599 | 603 | PF12436 | 0.259 |
DOC_WW_Pin1_4 | 1144 | 1149 | PF00397 | 0.596 |
DOC_WW_Pin1_4 | 1222 | 1227 | PF00397 | 0.638 |
DOC_WW_Pin1_4 | 1300 | 1305 | PF00397 | 0.428 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.487 |
DOC_WW_Pin1_4 | 348 | 353 | PF00397 | 0.241 |
DOC_WW_Pin1_4 | 490 | 495 | PF00397 | 0.416 |
DOC_WW_Pin1_4 | 506 | 511 | PF00397 | 0.359 |
DOC_WW_Pin1_4 | 654 | 659 | PF00397 | 0.388 |
DOC_WW_Pin1_4 | 671 | 676 | PF00397 | 0.474 |
DOC_WW_Pin1_4 | 695 | 700 | PF00397 | 0.350 |
DOC_WW_Pin1_4 | 82 | 87 | PF00397 | 0.367 |
LIG_14-3-3_CanoR_1 | 1170 | 1177 | PF00244 | 0.624 |
LIG_14-3-3_CanoR_1 | 1213 | 1219 | PF00244 | 0.634 |
LIG_14-3-3_CanoR_1 | 1233 | 1238 | PF00244 | 0.670 |
LIG_14-3-3_CanoR_1 | 1241 | 1247 | PF00244 | 0.730 |
LIG_14-3-3_CanoR_1 | 1343 | 1351 | PF00244 | 0.610 |
LIG_14-3-3_CanoR_1 | 267 | 275 | PF00244 | 0.419 |
LIG_14-3-3_CanoR_1 | 336 | 340 | PF00244 | 0.341 |
LIG_14-3-3_CanoR_1 | 44 | 48 | PF00244 | 0.363 |
LIG_14-3-3_CanoR_1 | 579 | 588 | PF00244 | 0.417 |
LIG_14-3-3_CanoR_1 | 682 | 688 | PF00244 | 0.463 |
LIG_14-3-3_CanoR_1 | 709 | 714 | PF00244 | 0.343 |
LIG_14-3-3_CanoR_1 | 80 | 86 | PF00244 | 0.356 |
LIG_Actin_WH2_2 | 1032 | 1049 | PF00022 | 0.437 |
LIG_APCC_ABBA_1 | 637 | 642 | PF00400 | 0.317 |
LIG_BIR_III_2 | 1088 | 1092 | PF00653 | 0.531 |
LIG_BRCT_BRCA1_1 | 1215 | 1219 | PF00533 | 0.654 |
LIG_BRCT_BRCA1_1 | 215 | 219 | PF00533 | 0.400 |
LIG_BRCT_BRCA1_1 | 222 | 226 | PF00533 | 0.374 |
LIG_BRCT_BRCA1_1 | 230 | 234 | PF00533 | 0.355 |
LIG_BRCT_BRCA1_1 | 466 | 470 | PF00533 | 0.338 |
LIG_BRCT_BRCA1_1 | 683 | 687 | PF00533 | 0.291 |
LIG_CSL_BTD_1 | 672 | 675 | PF09270 | 0.286 |
LIG_EVH1_1 | 1145 | 1149 | PF00568 | 0.472 |
LIG_FHA_1 | 1007 | 1013 | PF00498 | 0.489 |
LIG_FHA_1 | 1019 | 1025 | PF00498 | 0.489 |
LIG_FHA_1 | 1169 | 1175 | PF00498 | 0.599 |
LIG_FHA_1 | 1253 | 1259 | PF00498 | 0.664 |
LIG_FHA_1 | 1275 | 1281 | PF00498 | 0.705 |
LIG_FHA_1 | 1342 | 1348 | PF00498 | 0.586 |
LIG_FHA_1 | 1375 | 1381 | PF00498 | 0.596 |
LIG_FHA_1 | 150 | 156 | PF00498 | 0.318 |
LIG_FHA_1 | 20 | 26 | PF00498 | 0.418 |
LIG_FHA_1 | 200 | 206 | PF00498 | 0.348 |
LIG_FHA_1 | 351 | 357 | PF00498 | 0.347 |
LIG_FHA_1 | 427 | 433 | PF00498 | 0.326 |
LIG_FHA_1 | 493 | 499 | PF00498 | 0.366 |
LIG_FHA_1 | 59 | 65 | PF00498 | 0.375 |
LIG_FHA_1 | 591 | 597 | PF00498 | 0.345 |
LIG_FHA_1 | 721 | 727 | PF00498 | 0.402 |
LIG_FHA_1 | 730 | 736 | PF00498 | 0.384 |
LIG_FHA_1 | 761 | 767 | PF00498 | 0.464 |
LIG_FHA_1 | 96 | 102 | PF00498 | 0.405 |
LIG_FHA_2 | 1027 | 1033 | PF00498 | 0.596 |
LIG_FHA_2 | 1099 | 1105 | PF00498 | 0.623 |
LIG_FHA_2 | 1109 | 1115 | PF00498 | 0.495 |
LIG_FHA_2 | 1356 | 1362 | PF00498 | 0.435 |
LIG_FHA_2 | 144 | 150 | PF00498 | 0.464 |
LIG_FHA_2 | 173 | 179 | PF00498 | 0.420 |
LIG_FHA_2 | 453 | 459 | PF00498 | 0.440 |
LIG_FHA_2 | 467 | 473 | PF00498 | 0.221 |
LIG_FHA_2 | 868 | 874 | PF00498 | 0.485 |
LIG_FHA_2 | 909 | 915 | PF00498 | 0.490 |
LIG_FHA_2 | 943 | 949 | PF00498 | 0.492 |
LIG_GBD_Chelix_1 | 838 | 846 | PF00786 | 0.240 |
LIG_GBD_Chelix_1 | 929 | 937 | PF00786 | 0.394 |
LIG_IRF3_LxIS_1 | 426 | 433 | PF10401 | 0.408 |
LIG_LIR_Apic_2 | 231 | 237 | PF02991 | 0.432 |
LIG_LIR_Apic_2 | 517 | 523 | PF02991 | 0.366 |
LIG_LIR_Apic_2 | 695 | 699 | PF02991 | 0.417 |
LIG_LIR_Gen_1 | 1103 | 1113 | PF02991 | 0.675 |
LIG_LIR_Gen_1 | 1389 | 1396 | PF02991 | 0.410 |
LIG_LIR_Gen_1 | 159 | 168 | PF02991 | 0.425 |
LIG_LIR_Gen_1 | 216 | 226 | PF02991 | 0.331 |
LIG_LIR_Gen_1 | 245 | 251 | PF02991 | 0.433 |
LIG_LIR_Gen_1 | 341 | 352 | PF02991 | 0.371 |
LIG_LIR_Gen_1 | 777 | 782 | PF02991 | 0.417 |
LIG_LIR_Gen_1 | 866 | 877 | PF02991 | 0.487 |
LIG_LIR_Gen_1 | 948 | 957 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 986 | 996 | PF02991 | 0.579 |
LIG_LIR_Nem_3 | 1103 | 1109 | PF02991 | 0.689 |
LIG_LIR_Nem_3 | 1121 | 1127 | PF02991 | 0.635 |
LIG_LIR_Nem_3 | 1217 | 1223 | PF02991 | 0.662 |
LIG_LIR_Nem_3 | 1321 | 1327 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 159 | 163 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 216 | 222 | PF02991 | 0.267 |
LIG_LIR_Nem_3 | 245 | 250 | PF02991 | 0.427 |
LIG_LIR_Nem_3 | 341 | 347 | PF02991 | 0.374 |
LIG_LIR_Nem_3 | 402 | 408 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 644 | 650 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 866 | 872 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 948 | 954 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 968 | 974 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 986 | 992 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 993 | 999 | PF02991 | 0.463 |
LIG_MLH1_MIPbox_1 | 1216 | 1220 | PF16413 | 0.495 |
LIG_NRBOX | 24 | 30 | PF00104 | 0.354 |
LIG_OCRL_FandH_1 | 357 | 369 | PF00620 | 0.213 |
LIG_Pex14_2 | 222 | 226 | PF04695 | 0.258 |
LIG_PTB_Apo_2 | 616 | 623 | PF02174 | 0.423 |
LIG_PTB_Phospho_1 | 616 | 622 | PF10480 | 0.214 |
LIG_Rb_pABgroove_1 | 634 | 642 | PF01858 | 0.332 |
LIG_RPA_C_Fungi | 1201 | 1213 | PF08784 | 0.317 |
LIG_SH2_CRK | 443 | 447 | PF00017 | 0.468 |
LIG_SH2_CRK | 647 | 651 | PF00017 | 0.554 |
LIG_SH2_CRK | 696 | 700 | PF00017 | 0.547 |
LIG_SH2_CRK | 999 | 1003 | PF00017 | 0.466 |
LIG_SH2_GRB2like | 1127 | 1130 | PF00017 | 0.511 |
LIG_SH2_GRB2like | 1159 | 1162 | PF00017 | 0.333 |
LIG_SH2_GRB2like | 1290 | 1293 | PF00017 | 0.405 |
LIG_SH2_GRB2like | 526 | 529 | PF00017 | 0.303 |
LIG_SH2_NCK_1 | 208 | 212 | PF00017 | 0.370 |
LIG_SH2_NCK_1 | 214 | 218 | PF00017 | 0.295 |
LIG_SH2_NCK_1 | 716 | 720 | PF00017 | 0.553 |
LIG_SH2_NCK_1 | 951 | 955 | PF00017 | 0.397 |
LIG_SH2_PTP2 | 160 | 163 | PF00017 | 0.518 |
LIG_SH2_SRC | 1159 | 1162 | PF00017 | 0.560 |
LIG_SH2_SRC | 1290 | 1293 | PF00017 | 0.405 |
LIG_SH2_SRC | 526 | 529 | PF00017 | 0.549 |
LIG_SH2_SRC | 800 | 803 | PF00017 | 0.356 |
LIG_SH2_STAP1 | 1388 | 1392 | PF00017 | 0.259 |
LIG_SH2_STAP1 | 392 | 396 | PF00017 | 0.284 |
LIG_SH2_STAP1 | 731 | 735 | PF00017 | 0.493 |
LIG_SH2_STAT3 | 622 | 625 | PF00017 | 0.289 |
LIG_SH2_STAT3 | 731 | 734 | PF00017 | 0.524 |
LIG_SH2_STAT5 | 1123 | 1126 | PF00017 | 0.502 |
LIG_SH2_STAT5 | 1127 | 1130 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 1159 | 1162 | PF00017 | 0.502 |
LIG_SH2_STAT5 | 1338 | 1341 | PF00017 | 0.264 |
LIG_SH2_STAT5 | 1388 | 1391 | PF00017 | 0.240 |
LIG_SH2_STAT5 | 1392 | 1395 | PF00017 | 0.225 |
LIG_SH2_STAT5 | 144 | 147 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 160 | 163 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 174 | 177 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 201 | 204 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 273 | 276 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 357 | 360 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 367 | 370 | PF00017 | 0.342 |
LIG_SH2_STAT5 | 440 | 443 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 534 | 537 | PF00017 | 0.492 |
LIG_SH2_STAT5 | 622 | 625 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 731 | 734 | PF00017 | 0.379 |
LIG_SH2_STAT5 | 774 | 777 | PF00017 | 0.549 |
LIG_SH2_STAT5 | 793 | 796 | PF00017 | 0.283 |
LIG_SH2_STAT5 | 800 | 803 | PF00017 | 0.377 |
LIG_SH3_2 | 1146 | 1151 | PF14604 | 0.560 |
LIG_SH3_2 | 672 | 677 | PF14604 | 0.337 |
LIG_SH3_3 | 1046 | 1052 | PF00018 | 0.232 |
LIG_SH3_3 | 1143 | 1149 | PF00018 | 0.412 |
LIG_SH3_3 | 1220 | 1226 | PF00018 | 0.600 |
LIG_SH3_3 | 256 | 262 | PF00018 | 0.376 |
LIG_SH3_3 | 276 | 282 | PF00018 | 0.511 |
LIG_SH3_3 | 669 | 675 | PF00018 | 0.345 |
LIG_SUMO_SIM_anti_2 | 152 | 159 | PF11976 | 0.298 |
LIG_SUMO_SIM_anti_2 | 22 | 28 | PF11976 | 0.421 |
LIG_SUMO_SIM_anti_2 | 227 | 234 | PF11976 | 0.507 |
LIG_SUMO_SIM_anti_2 | 608 | 614 | PF11976 | 0.469 |
LIG_SUMO_SIM_anti_2 | 863 | 871 | PF11976 | 0.336 |
LIG_SUMO_SIM_par_1 | 1162 | 1169 | PF11976 | 0.335 |
LIG_SUMO_SIM_par_1 | 1252 | 1261 | PF11976 | 0.367 |
LIG_SUMO_SIM_par_1 | 1264 | 1271 | PF11976 | 0.580 |
LIG_SUMO_SIM_par_1 | 152 | 159 | PF11976 | 0.318 |
LIG_SUMO_SIM_par_1 | 387 | 393 | PF11976 | 0.531 |
LIG_SUMO_SIM_par_1 | 427 | 433 | PF11976 | 0.294 |
LIG_SUMO_SIM_par_1 | 608 | 614 | PF11976 | 0.520 |
LIG_SUMO_SIM_par_1 | 635 | 642 | PF11976 | 0.507 |
LIG_TRAF2_1 | 1029 | 1032 | PF00917 | 0.391 |
LIG_TYR_ITIM | 158 | 163 | PF00017 | 0.329 |
LIG_TYR_ITIM | 342 | 347 | PF00017 | 0.564 |
LIG_TYR_ITIM | 441 | 446 | PF00017 | 0.549 |
LIG_TYR_ITIM | 980 | 985 | PF00017 | 0.460 |
LIG_UBA3_1 | 1312 | 1319 | PF00899 | 0.264 |
LIG_UBA3_1 | 246 | 252 | PF00899 | 0.511 |
LIG_UBA3_1 | 896 | 905 | PF00899 | 0.340 |
LIG_Vh1_VBS_1 | 827 | 845 | PF01044 | 0.348 |
LIG_WW_3 | 1147 | 1151 | PF00397 | 0.560 |
LIG_WW_3 | 3 | 7 | PF00397 | 0.318 |
MOD_CDC14_SPxK_1 | 1147 | 1150 | PF00782 | 0.555 |
MOD_CDK_SPK_2 | 671 | 676 | PF00069 | 0.327 |
MOD_CDK_SPxK_1 | 1144 | 1150 | PF00069 | 0.549 |
MOD_CDK_SPxK_1 | 671 | 677 | PF00069 | 0.327 |
MOD_CDK_SPxxK_3 | 1144 | 1151 | PF00069 | 0.582 |
MOD_CDK_SPxxK_3 | 348 | 355 | PF00069 | 0.274 |
MOD_CDK_SPxxK_3 | 506 | 513 | PF00069 | 0.537 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.447 |
MOD_CK1_1 | 1068 | 1074 | PF00069 | 0.567 |
MOD_CK1_1 | 1125 | 1131 | PF00069 | 0.376 |
MOD_CK1_1 | 118 | 124 | PF00069 | 0.331 |
MOD_CK1_1 | 1252 | 1258 | PF00069 | 0.611 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.446 |
MOD_CK1_1 | 399 | 405 | PF00069 | 0.445 |
MOD_CK1_1 | 566 | 572 | PF00069 | 0.468 |
MOD_CK1_1 | 590 | 596 | PF00069 | 0.503 |
MOD_CK1_1 | 657 | 663 | PF00069 | 0.365 |
MOD_CK1_1 | 681 | 687 | PF00069 | 0.496 |
MOD_CK1_1 | 698 | 704 | PF00069 | 0.402 |
MOD_CK1_1 | 712 | 718 | PF00069 | 0.408 |
MOD_CK1_1 | 754 | 760 | PF00069 | 0.449 |
MOD_CK1_1 | 808 | 814 | PF00069 | 0.622 |
MOD_CK1_1 | 816 | 822 | PF00069 | 0.532 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.402 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.539 |
MOD_CK1_1 | 958 | 964 | PF00069 | 0.396 |
MOD_CK2_1 | 1026 | 1032 | PF00069 | 0.341 |
MOD_CK2_1 | 1102 | 1108 | PF00069 | 0.421 |
MOD_CK2_1 | 125 | 131 | PF00069 | 0.546 |
MOD_CK2_1 | 1272 | 1278 | PF00069 | 0.641 |
MOD_CK2_1 | 1295 | 1301 | PF00069 | 0.320 |
MOD_CK2_1 | 1355 | 1361 | PF00069 | 0.248 |
MOD_CK2_1 | 1395 | 1401 | PF00069 | 0.560 |
MOD_CK2_1 | 174 | 180 | PF00069 | 0.516 |
MOD_CK2_1 | 250 | 256 | PF00069 | 0.465 |
MOD_CK2_1 | 395 | 401 | PF00069 | 0.475 |
MOD_CK2_1 | 466 | 472 | PF00069 | 0.355 |
MOD_CK2_1 | 506 | 512 | PF00069 | 0.425 |
MOD_CK2_1 | 776 | 782 | PF00069 | 0.266 |
MOD_CK2_1 | 867 | 873 | PF00069 | 0.336 |
MOD_Cter_Amidation | 660 | 663 | PF01082 | 0.265 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.536 |
MOD_GlcNHglycan | 1072 | 1076 | PF01048 | 0.531 |
MOD_GlcNHglycan | 1124 | 1127 | PF01048 | 0.362 |
MOD_GlcNHglycan | 1171 | 1174 | PF01048 | 0.462 |
MOD_GlcNHglycan | 1220 | 1223 | PF01048 | 0.581 |
MOD_GlcNHglycan | 1270 | 1273 | PF01048 | 0.396 |
MOD_GlcNHglycan | 1297 | 1300 | PF01048 | 0.489 |
MOD_GlcNHglycan | 1344 | 1347 | PF01048 | 0.240 |
MOD_GlcNHglycan | 1397 | 1400 | PF01048 | 0.617 |
MOD_GlcNHglycan | 179 | 185 | PF01048 | 0.553 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.417 |
MOD_GlcNHglycan | 227 | 230 | PF01048 | 0.314 |
MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.545 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.437 |
MOD_GlcNHglycan | 398 | 401 | PF01048 | 0.467 |
MOD_GlcNHglycan | 466 | 469 | PF01048 | 0.465 |
MOD_GlcNHglycan | 552 | 555 | PF01048 | 0.456 |
MOD_GlcNHglycan | 565 | 568 | PF01048 | 0.423 |
MOD_GlcNHglycan | 607 | 610 | PF01048 | 0.454 |
MOD_GlcNHglycan | 659 | 662 | PF01048 | 0.400 |
MOD_GlcNHglycan | 683 | 686 | PF01048 | 0.545 |
MOD_GlcNHglycan | 723 | 726 | PF01048 | 0.540 |
MOD_GlcNHglycan | 810 | 813 | PF01048 | 0.670 |
MOD_GlcNHglycan | 887 | 890 | PF01048 | 0.494 |
MOD_GlcNHglycan | 93 | 97 | PF01048 | 0.556 |
MOD_GlcNHglycan | 957 | 960 | PF01048 | 0.438 |
MOD_GlcNHglycan | 971 | 974 | PF01048 | 0.364 |
MOD_GSK3_1 | 1002 | 1009 | PF00069 | 0.383 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.377 |
MOD_GSK3_1 | 1098 | 1105 | PF00069 | 0.462 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.403 |
MOD_GSK3_1 | 1159 | 1166 | PF00069 | 0.532 |
MOD_GSK3_1 | 1214 | 1221 | PF00069 | 0.588 |
MOD_GSK3_1 | 1264 | 1271 | PF00069 | 0.587 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.568 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.386 |
MOD_GSK3_1 | 1337 | 1344 | PF00069 | 0.485 |
MOD_GSK3_1 | 282 | 289 | PF00069 | 0.595 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.482 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.330 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.271 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.437 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.483 |
MOD_GSK3_1 | 426 | 433 | PF00069 | 0.404 |
MOD_GSK3_1 | 447 | 454 | PF00069 | 0.469 |
MOD_GSK3_1 | 464 | 471 | PF00069 | 0.427 |
MOD_GSK3_1 | 477 | 484 | PF00069 | 0.402 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.344 |
MOD_GSK3_1 | 568 | 575 | PF00069 | 0.482 |
MOD_GSK3_1 | 814 | 821 | PF00069 | 0.580 |
MOD_GSK3_1 | 863 | 870 | PF00069 | 0.353 |
MOD_GSK3_1 | 908 | 915 | PF00069 | 0.342 |
MOD_GSK3_1 | 965 | 972 | PF00069 | 0.470 |
MOD_N-GLC_1 | 1183 | 1188 | PF02516 | 0.479 |
MOD_N-GLC_1 | 1327 | 1332 | PF02516 | 0.466 |
MOD_N-GLC_1 | 527 | 532 | PF02516 | 0.531 |
MOD_N-GLC_1 | 990 | 995 | PF02516 | 0.484 |
MOD_N-GLC_2 | 10 | 12 | PF02516 | 0.659 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.496 |
MOD_NEK2_1 | 1136 | 1141 | PF00069 | 0.423 |
MOD_NEK2_1 | 1163 | 1168 | PF00069 | 0.558 |
MOD_NEK2_1 | 125 | 130 | PF00069 | 0.502 |
MOD_NEK2_1 | 1268 | 1273 | PF00069 | 0.603 |
MOD_NEK2_1 | 172 | 177 | PF00069 | 0.542 |
MOD_NEK2_1 | 199 | 204 | PF00069 | 0.487 |
MOD_NEK2_1 | 250 | 255 | PF00069 | 0.448 |
MOD_NEK2_1 | 265 | 270 | PF00069 | 0.291 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.373 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.578 |
MOD_NEK2_1 | 318 | 323 | PF00069 | 0.507 |
MOD_NEK2_1 | 390 | 395 | PF00069 | 0.489 |
MOD_NEK2_1 | 430 | 435 | PF00069 | 0.356 |
MOD_NEK2_1 | 481 | 486 | PF00069 | 0.465 |
MOD_NEK2_1 | 563 | 568 | PF00069 | 0.524 |
MOD_NEK2_1 | 573 | 578 | PF00069 | 0.444 |
MOD_NEK2_1 | 67 | 72 | PF00069 | 0.321 |
MOD_NEK2_1 | 687 | 692 | PF00069 | 0.545 |
MOD_NEK2_1 | 746 | 751 | PF00069 | 0.464 |
MOD_NEK2_1 | 878 | 883 | PF00069 | 0.414 |
MOD_OFUCOSY | 1269 | 1276 | PF10250 | 0.621 |
MOD_PIKK_1 | 1098 | 1104 | PF00454 | 0.602 |
MOD_PIKK_1 | 1190 | 1196 | PF00454 | 0.558 |
MOD_PIKK_1 | 1355 | 1361 | PF00454 | 0.264 |
MOD_PIKK_1 | 350 | 356 | PF00454 | 0.478 |
MOD_PIKK_1 | 452 | 458 | PF00454 | 0.572 |
MOD_PIKK_1 | 641 | 647 | PF00454 | 0.482 |
MOD_PIKK_1 | 729 | 735 | PF00454 | 0.400 |
MOD_PK_1 | 1008 | 1014 | PF00069 | 0.253 |
MOD_PK_1 | 1214 | 1220 | PF00069 | 0.368 |
MOD_PK_1 | 1233 | 1239 | PF00069 | 0.345 |
MOD_PKA_1 | 1213 | 1219 | PF00069 | 0.579 |
MOD_PKA_1 | 1233 | 1239 | PF00069 | 0.610 |
MOD_PKA_1 | 137 | 143 | PF00069 | 0.298 |
MOD_PKA_2 | 1169 | 1175 | PF00069 | 0.498 |
MOD_PKA_2 | 1213 | 1219 | PF00069 | 0.588 |
MOD_PKA_2 | 1233 | 1239 | PF00069 | 0.340 |
MOD_PKA_2 | 1342 | 1348 | PF00069 | 0.264 |
MOD_PKA_2 | 137 | 143 | PF00069 | 0.299 |
MOD_PKA_2 | 17 | 23 | PF00069 | 0.482 |
MOD_PKA_2 | 335 | 341 | PF00069 | 0.475 |
MOD_PKA_2 | 43 | 49 | PF00069 | 0.523 |
MOD_PKA_2 | 681 | 687 | PF00069 | 0.558 |
MOD_PKA_2 | 79 | 85 | PF00069 | 0.469 |
MOD_PKA_2 | 848 | 854 | PF00069 | 0.439 |
MOD_Plk_1 | 1102 | 1108 | PF00069 | 0.494 |
MOD_Plk_1 | 1183 | 1189 | PF00069 | 0.429 |
MOD_Plk_1 | 1252 | 1258 | PF00069 | 0.518 |
MOD_Plk_1 | 1327 | 1333 | PF00069 | 0.462 |
MOD_Plk_1 | 1361 | 1367 | PF00069 | 0.194 |
MOD_Plk_1 | 300 | 306 | PF00069 | 0.556 |
MOD_Plk_1 | 426 | 432 | PF00069 | 0.417 |
MOD_Plk_1 | 471 | 477 | PF00069 | 0.446 |
MOD_Plk_1 | 482 | 488 | PF00069 | 0.477 |
MOD_Plk_1 | 57 | 63 | PF00069 | 0.356 |
MOD_Plk_1 | 641 | 647 | PF00069 | 0.429 |
MOD_Plk_1 | 678 | 684 | PF00069 | 0.544 |
MOD_Plk_1 | 739 | 745 | PF00069 | 0.459 |
MOD_Plk_2-3 | 908 | 914 | PF00069 | 0.334 |
MOD_Plk_4 | 1020 | 1026 | PF00069 | 0.309 |
MOD_Plk_4 | 106 | 112 | PF00069 | 0.441 |
MOD_Plk_4 | 1159 | 1165 | PF00069 | 0.511 |
MOD_Plk_4 | 121 | 127 | PF00069 | 0.422 |
MOD_Plk_4 | 1214 | 1220 | PF00069 | 0.587 |
MOD_Plk_4 | 1252 | 1258 | PF00069 | 0.629 |
MOD_Plk_4 | 156 | 162 | PF00069 | 0.461 |
MOD_Plk_4 | 201 | 207 | PF00069 | 0.501 |
MOD_Plk_4 | 228 | 234 | PF00069 | 0.462 |
MOD_Plk_4 | 260 | 266 | PF00069 | 0.426 |
MOD_Plk_4 | 282 | 288 | PF00069 | 0.533 |
MOD_Plk_4 | 343 | 349 | PF00069 | 0.448 |
MOD_Plk_4 | 521 | 527 | PF00069 | 0.407 |
MOD_Plk_4 | 545 | 551 | PF00069 | 0.472 |
MOD_Plk_4 | 709 | 715 | PF00069 | 0.360 |
MOD_Plk_4 | 819 | 825 | PF00069 | 0.374 |
MOD_Plk_4 | 863 | 869 | PF00069 | 0.334 |
MOD_Plk_4 | 912 | 918 | PF00069 | 0.347 |
MOD_ProDKin_1 | 1144 | 1150 | PF00069 | 0.490 |
MOD_ProDKin_1 | 1222 | 1228 | PF00069 | 0.546 |
MOD_ProDKin_1 | 1300 | 1306 | PF00069 | 0.253 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.484 |
MOD_ProDKin_1 | 348 | 354 | PF00069 | 0.273 |
MOD_ProDKin_1 | 490 | 496 | PF00069 | 0.516 |
MOD_ProDKin_1 | 506 | 512 | PF00069 | 0.439 |
MOD_ProDKin_1 | 654 | 660 | PF00069 | 0.476 |
MOD_ProDKin_1 | 671 | 677 | PF00069 | 0.598 |
MOD_ProDKin_1 | 695 | 701 | PF00069 | 0.423 |
MOD_ProDKin_1 | 82 | 88 | PF00069 | 0.452 |
MOD_SUMO_for_1 | 858 | 861 | PF00179 | 0.205 |
MOD_SUMO_rev_2 | 253 | 260 | PF00179 | 0.472 |
MOD_SUMO_rev_2 | 290 | 300 | PF00179 | 0.587 |
TRG_DiLeu_BaEn_1 | 153 | 158 | PF01217 | 0.307 |
TRG_DiLeu_BaEn_1 | 256 | 261 | PF01217 | 0.275 |
TRG_DiLeu_BaEn_1 | 863 | 868 | PF01217 | 0.459 |
TRG_DiLeu_BaEn_3 | 1030 | 1036 | PF01217 | 0.194 |
TRG_DiLeu_BaEn_3 | 1094 | 1100 | PF01217 | 0.465 |
TRG_ENDOCYTIC_2 | 1338 | 1341 | PF00928 | 0.264 |
TRG_ENDOCYTIC_2 | 1392 | 1395 | PF00928 | 0.252 |
TRG_ENDOCYTIC_2 | 160 | 163 | PF00928 | 0.372 |
TRG_ENDOCYTIC_2 | 189 | 192 | PF00928 | 0.539 |
TRG_ENDOCYTIC_2 | 344 | 347 | PF00928 | 0.396 |
TRG_ENDOCYTIC_2 | 357 | 360 | PF00928 | 0.235 |
TRG_ENDOCYTIC_2 | 405 | 408 | PF00928 | 0.432 |
TRG_ENDOCYTIC_2 | 443 | 446 | PF00928 | 0.450 |
TRG_ENDOCYTIC_2 | 647 | 650 | PF00928 | 0.388 |
TRG_ENDOCYTIC_2 | 778 | 781 | PF00928 | 0.563 |
TRG_ENDOCYTIC_2 | 951 | 954 | PF00928 | 0.342 |
TRG_ENDOCYTIC_2 | 982 | 985 | PF00928 | 0.354 |
TRG_ENDOCYTIC_2 | 999 | 1002 | PF00928 | 0.452 |
TRG_ER_diArg_1 | 1149 | 1151 | PF00400 | 0.532 |
TRG_ER_diArg_1 | 1177 | 1180 | PF00400 | 0.546 |
TRG_ER_diArg_1 | 1212 | 1214 | PF00400 | 0.333 |
TRG_ER_diArg_1 | 1233 | 1235 | PF00400 | 0.556 |
TRG_ER_diArg_1 | 137 | 139 | PF00400 | 0.480 |
TRG_ER_diArg_1 | 193 | 195 | PF00400 | 0.499 |
TRG_ER_diArg_1 | 974 | 977 | PF00400 | 0.334 |
TRG_NLS_MonoCore_2 | 1231 | 1236 | PF00514 | 0.400 |
TRG_Pf-PMV_PEXEL_1 | 1026 | 1030 | PF00026 | 0.194 |
TRG_Pf-PMV_PEXEL_1 | 1180 | 1185 | PF00026 | 0.669 |
TRG_Pf-PMV_PEXEL_1 | 513 | 517 | PF00026 | 0.304 |
TRG_Pf-PMV_PEXEL_1 | 648 | 652 | PF00026 | 0.553 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P457 | Leptomonas seymouri | 40% | 100% |
A0A1X0P171 | Trypanosomatidae | 29% | 100% |
A0A3Q8IJB0 | Leishmania donovani | 27% | 100% |
A0A3S5H6Z8 | Leishmania donovani | 27% | 100% |
A0A3S7WU91 | Leishmania donovani | 28% | 99% |
A0A3S7WU95 | Leishmania donovani | 27% | 100% |
A0A3S7XB85 | Leishmania donovani | 86% | 99% |
A4H8U6 | Leishmania braziliensis | 29% | 100% |
A4H8V5 | Leishmania braziliensis | 29% | 100% |
A4H8V7 | Leishmania braziliensis | 31% | 100% |
A4H8V8 | Leishmania braziliensis | 28% | 100% |
A4HPI4 | Leishmania braziliensis | 69% | 100% |
A4HX85 | Leishmania infantum | 26% | 100% |
A4HX87 | Leishmania infantum | 28% | 100% |
A4IDA6 | Leishmania infantum | 87% | 100% |
C9ZM79 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
C9ZM80 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZM81 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZM82 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
C9ZM83 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 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) | 29% | 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) | 29% | 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% |
C9ZNT1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
C9ZPZ6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
C9ZQ51 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZQ89 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZQ90 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
C9ZQ92 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZTS4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZTS5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZTS6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
C9ZUE6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZWQ5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZWU1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZWU2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
C9ZWU3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZWY7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZZQ4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
D0A0U3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
D0A0W7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
D0A0X5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
D0A1S1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
D0A5D2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 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) | 27% | 100% |
D0A9R3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
D0AAV3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
E9AQY2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9AQY4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9AT96 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 99% |
Q25263 | Leishmania donovani | 27% | 100% |
Q26721 | Trypanosoma brucei brucei | 29% | 100% |
Q27675 | Leishmania donovani | 30% | 100% |
Q4QEH9 | Leishmania major | 27% | 100% |
Q4QEI0 | Leishmania major | 28% | 100% |
Q4QEI1 | Leishmania major | 28% | 100% |
Q99279 | Trypanosoma brucei brucei | 28% | 100% |
Q99280 | Trypanosoma brucei brucei | 29% | 100% |