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: 54 |
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: 45, no: 26 |
NetGPI | no | yes: 0, no: 71 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 68 |
GO:0110165 | cellular anatomical entity | 1 | 72 |
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 72 |
GO:0006163 | purine nucleotide metabolic process | 5 | 72 |
GO:0006164 | purine nucleotide biosynthetic process | 6 | 72 |
GO:0006171 | cAMP biosynthetic process | 8 | 72 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 72 |
GO:0006753 | nucleoside phosphate metabolic process | 4 | 72 |
GO:0006793 | phosphorus metabolic process | 3 | 72 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 72 |
GO:0006807 | nitrogen compound metabolic process | 2 | 72 |
GO:0007165 | signal transduction | 2 | 72 |
GO:0008152 | metabolic process | 1 | 72 |
GO:0009058 | biosynthetic process | 2 | 72 |
GO:0009117 | nucleotide metabolic process | 5 | 72 |
GO:0009150 | purine ribonucleotide metabolic process | 6 | 72 |
GO:0009152 | purine ribonucleotide biosynthetic process | 7 | 72 |
GO:0009165 | nucleotide biosynthetic process | 6 | 72 |
GO:0009187 | cyclic nucleotide metabolic process | 6 | 72 |
GO:0009190 | cyclic nucleotide biosynthetic process | 7 | 72 |
GO:0009259 | ribonucleotide metabolic process | 5 | 72 |
GO:0009260 | ribonucleotide biosynthetic process | 6 | 72 |
GO:0009987 | cellular process | 1 | 72 |
GO:0018130 | heterocycle biosynthetic process | 4 | 72 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 72 |
GO:0019637 | organophosphate metabolic process | 3 | 72 |
GO:0019693 | ribose phosphate metabolic process | 4 | 72 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 72 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 72 |
GO:0035556 | intracellular signal transduction | 3 | 72 |
GO:0044237 | cellular metabolic process | 2 | 72 |
GO:0044238 | primary metabolic process | 2 | 72 |
GO:0044249 | cellular biosynthetic process | 3 | 72 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 72 |
GO:0044281 | small molecule metabolic process | 2 | 72 |
GO:0046058 | cAMP metabolic process | 7 | 72 |
GO:0046390 | ribose phosphate biosynthetic process | 5 | 72 |
GO:0046483 | heterocycle metabolic process | 3 | 72 |
GO:0050789 | regulation of biological process | 2 | 72 |
GO:0050794 | regulation of cellular process | 3 | 72 |
GO:0052652 | cyclic purine nucleotide metabolic process | 6 | 72 |
GO:0055086 | nucleobase-containing small molecule metabolic process | 3 | 72 |
GO:0065007 | biological regulation | 1 | 72 |
GO:0071704 | organic substance metabolic process | 2 | 72 |
GO:0072521 | purine-containing compound metabolic process | 4 | 72 |
GO:0072522 | purine-containing compound biosynthetic process | 5 | 72 |
GO:0090407 | organophosphate biosynthetic process | 4 | 72 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 72 |
GO:1901137 | carbohydrate derivative biosynthetic process | 4 | 72 |
GO:1901293 | nucleoside phosphate biosynthetic process | 5 | 72 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 72 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 72 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 72 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 72 |
GO:1901576 | organic substance biosynthetic process | 3 | 72 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 61 |
GO:0016829 | lyase activity | 2 | 61 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 359 | 363 | PF00656 | 0.330 |
CLV_C14_Caspase3-7 | 386 | 390 | PF00656 | 0.470 |
CLV_C14_Caspase3-7 | 636 | 640 | PF00656 | 0.422 |
CLV_C14_Caspase3-7 | 923 | 927 | PF00656 | 0.576 |
CLV_C14_Caspase3-7 | 984 | 988 | PF00656 | 0.504 |
CLV_MEL_PAP_1 | 1057 | 1063 | PF00089 | 0.296 |
CLV_NRD_NRD_1 | 1147 | 1149 | PF00675 | 0.417 |
CLV_NRD_NRD_1 | 1315 | 1317 | PF00675 | 0.499 |
CLV_NRD_NRD_1 | 1354 | 1356 | PF00675 | 0.576 |
CLV_NRD_NRD_1 | 1384 | 1386 | PF00675 | 0.353 |
CLV_NRD_NRD_1 | 207 | 209 | PF00675 | 0.610 |
CLV_NRD_NRD_1 | 432 | 434 | PF00675 | 0.457 |
CLV_NRD_NRD_1 | 691 | 693 | PF00675 | 0.634 |
CLV_NRD_NRD_1 | 9 | 11 | PF00675 | 0.644 |
CLV_PCSK_FUR_1 | 205 | 209 | PF00082 | 0.610 |
CLV_PCSK_KEX2_1 | 1147 | 1149 | PF00082 | 0.417 |
CLV_PCSK_KEX2_1 | 1315 | 1317 | PF00082 | 0.496 |
CLV_PCSK_KEX2_1 | 1354 | 1356 | PF00082 | 0.578 |
CLV_PCSK_KEX2_1 | 1383 | 1385 | PF00082 | 0.345 |
CLV_PCSK_KEX2_1 | 207 | 209 | PF00082 | 0.610 |
CLV_PCSK_KEX2_1 | 690 | 692 | PF00082 | 0.561 |
CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.645 |
CLV_PCSK_SKI1_1 | 128 | 132 | PF00082 | 0.556 |
CLV_PCSK_SKI1_1 | 208 | 212 | PF00082 | 0.598 |
CLV_PCSK_SKI1_1 | 255 | 259 | PF00082 | 0.568 |
CLV_PCSK_SKI1_1 | 434 | 438 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 549 | 553 | PF00082 | 0.462 |
CLV_PCSK_SKI1_1 | 633 | 637 | PF00082 | 0.510 |
CLV_PCSK_SKI1_1 | 747 | 751 | PF00082 | 0.536 |
CLV_Separin_Metazoa | 606 | 610 | PF03568 | 0.307 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.608 |
DEG_SCF_FBW7_2 | 875 | 881 | PF00400 | 0.507 |
DEG_SPOP_SBC_1 | 290 | 294 | PF00917 | 0.440 |
DOC_CDC14_PxL_1 | 131 | 139 | PF14671 | 0.440 |
DOC_CDC14_PxL_1 | 520 | 528 | PF14671 | 0.233 |
DOC_CKS1_1 | 875 | 880 | PF01111 | 0.444 |
DOC_CYCLIN_RxL_1 | 508 | 517 | PF00134 | 0.287 |
DOC_CYCLIN_RxL_1 | 83 | 94 | PF00134 | 0.446 |
DOC_CYCLIN_yCln2_LP_2 | 236 | 242 | PF00134 | 0.474 |
DOC_CYCLIN_yCln2_LP_2 | 336 | 342 | PF00134 | 0.299 |
DOC_CYCLIN_yCln2_LP_2 | 509 | 515 | PF00134 | 0.388 |
DOC_CYCLIN_yCln2_LP_2 | 872 | 878 | PF00134 | 0.449 |
DOC_MAPK_gen_1 | 205 | 214 | PF00069 | 0.309 |
DOC_MAPK_gen_1 | 690 | 699 | PF00069 | 0.238 |
DOC_MAPK_MEF2A_6 | 186 | 193 | PF00069 | 0.411 |
DOC_MAPK_MEF2A_6 | 863 | 871 | PF00069 | 0.318 |
DOC_MAPK_RevD_3 | 1134 | 1148 | PF00069 | 0.559 |
DOC_PP1_RVXF_1 | 509 | 516 | PF00149 | 0.287 |
DOC_PP1_RVXF_1 | 547 | 554 | PF00149 | 0.321 |
DOC_PP1_RVXF_1 | 689 | 696 | PF00149 | 0.243 |
DOC_PP1_RVXF_1 | 745 | 752 | PF00149 | 0.322 |
DOC_PP2B_LxvP_1 | 236 | 239 | PF13499 | 0.333 |
DOC_PP4_FxxP_1 | 165 | 168 | PF00568 | 0.461 |
DOC_USP7_MATH_1 | 1019 | 1023 | PF00917 | 0.621 |
DOC_USP7_MATH_1 | 1260 | 1264 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 1291 | 1295 | PF00917 | 0.724 |
DOC_USP7_MATH_1 | 1303 | 1307 | PF00917 | 0.695 |
DOC_USP7_MATH_1 | 1350 | 1354 | PF00917 | 0.598 |
DOC_USP7_MATH_1 | 1359 | 1363 | PF00917 | 0.558 |
DOC_USP7_MATH_1 | 1365 | 1369 | PF00917 | 0.498 |
DOC_USP7_MATH_1 | 151 | 155 | PF00917 | 0.453 |
DOC_USP7_MATH_1 | 290 | 294 | PF00917 | 0.439 |
DOC_USP7_MATH_1 | 385 | 389 | PF00917 | 0.346 |
DOC_USP7_MATH_1 | 529 | 533 | PF00917 | 0.325 |
DOC_USP7_MATH_1 | 677 | 681 | PF00917 | 0.447 |
DOC_USP7_MATH_1 | 736 | 740 | PF00917 | 0.426 |
DOC_USP7_MATH_1 | 808 | 812 | PF00917 | 0.428 |
DOC_USP7_MATH_1 | 841 | 845 | PF00917 | 0.375 |
DOC_USP7_MATH_1 | 992 | 996 | PF00917 | 0.576 |
DOC_USP7_UBL2_3 | 128 | 132 | PF12436 | 0.368 |
DOC_WW_Pin1_4 | 1082 | 1087 | PF00397 | 0.548 |
DOC_WW_Pin1_4 | 152 | 157 | PF00397 | 0.395 |
DOC_WW_Pin1_4 | 244 | 249 | PF00397 | 0.389 |
DOC_WW_Pin1_4 | 318 | 323 | PF00397 | 0.408 |
DOC_WW_Pin1_4 | 593 | 598 | PF00397 | 0.373 |
DOC_WW_Pin1_4 | 782 | 787 | PF00397 | 0.393 |
DOC_WW_Pin1_4 | 837 | 842 | PF00397 | 0.322 |
DOC_WW_Pin1_4 | 871 | 876 | PF00397 | 0.417 |
DOC_WW_Pin1_4 | 880 | 885 | PF00397 | 0.400 |
DOC_WW_Pin1_4 | 889 | 894 | PF00397 | 0.466 |
LIG_14-3-3_CanoR_1 | 1244 | 1249 | PF00244 | 0.645 |
LIG_14-3-3_CanoR_1 | 1363 | 1368 | PF00244 | 0.553 |
LIG_14-3-3_CanoR_1 | 205 | 214 | PF00244 | 0.344 |
LIG_14-3-3_CanoR_1 | 291 | 298 | PF00244 | 0.402 |
LIG_14-3-3_CanoR_1 | 492 | 498 | PF00244 | 0.292 |
LIG_14-3-3_CanoR_1 | 549 | 554 | PF00244 | 0.309 |
LIG_14-3-3_CanoR_1 | 633 | 642 | PF00244 | 0.412 |
LIG_14-3-3_CanoR_1 | 747 | 752 | PF00244 | 0.448 |
LIG_APCC_ABBA_1 | 141 | 146 | PF00400 | 0.437 |
LIG_APCC_ABBA_1 | 308 | 313 | PF00400 | 0.304 |
LIG_APCC_ABBA_1 | 720 | 725 | PF00400 | 0.311 |
LIG_BIR_III_2 | 928 | 932 | PF00653 | 0.655 |
LIG_BRCT_BRCA1_1 | 1318 | 1322 | PF00533 | 0.685 |
LIG_BRCT_BRCA1_1 | 1334 | 1338 | PF00533 | 0.464 |
LIG_Clathr_ClatBox_1 | 518 | 522 | PF01394 | 0.362 |
LIG_deltaCOP1_diTrp_1 | 217 | 222 | PF00928 | 0.240 |
LIG_EH_1 | 1275 | 1279 | PF12763 | 0.444 |
LIG_eIF4E_1 | 29 | 35 | PF01652 | 0.447 |
LIG_eIF4E_1 | 599 | 605 | PF01652 | 0.255 |
LIG_FHA_1 | 1006 | 1012 | PF00498 | 0.573 |
LIG_FHA_1 | 1015 | 1021 | PF00498 | 0.510 |
LIG_FHA_1 | 1040 | 1046 | PF00498 | 0.515 |
LIG_FHA_1 | 1090 | 1096 | PF00498 | 0.511 |
LIG_FHA_1 | 1244 | 1250 | PF00498 | 0.623 |
LIG_FHA_1 | 305 | 311 | PF00498 | 0.391 |
LIG_FHA_1 | 356 | 362 | PF00498 | 0.448 |
LIG_FHA_1 | 36 | 42 | PF00498 | 0.500 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.503 |
LIG_FHA_1 | 474 | 480 | PF00498 | 0.334 |
LIG_FHA_1 | 639 | 645 | PF00498 | 0.360 |
LIG_FHA_1 | 656 | 662 | PF00498 | 0.348 |
LIG_FHA_1 | 679 | 685 | PF00498 | 0.412 |
LIG_FHA_1 | 818 | 824 | PF00498 | 0.373 |
LIG_FHA_1 | 840 | 846 | PF00498 | 0.469 |
LIG_FHA_1 | 911 | 917 | PF00498 | 0.397 |
LIG_FHA_1 | 958 | 964 | PF00498 | 0.554 |
LIG_FHA_2 | 1032 | 1038 | PF00498 | 0.603 |
LIG_FHA_2 | 1152 | 1158 | PF00498 | 0.727 |
LIG_FHA_2 | 1162 | 1168 | PF00498 | 0.709 |
LIG_FHA_2 | 183 | 189 | PF00498 | 0.447 |
LIG_FHA_2 | 249 | 255 | PF00498 | 0.437 |
LIG_FHA_2 | 319 | 325 | PF00498 | 0.418 |
LIG_FHA_2 | 417 | 423 | PF00498 | 0.410 |
LIG_FHA_2 | 486 | 492 | PF00498 | 0.348 |
LIG_FHA_2 | 634 | 640 | PF00498 | 0.430 |
LIG_FHA_2 | 698 | 704 | PF00498 | 0.333 |
LIG_FHA_2 | 838 | 844 | PF00498 | 0.425 |
LIG_FHA_2 | 941 | 947 | PF00498 | 0.506 |
LIG_FHA_2 | 982 | 988 | PF00498 | 0.508 |
LIG_GBD_Chelix_1 | 1002 | 1010 | PF00786 | 0.414 |
LIG_GBD_Chelix_1 | 1241 | 1249 | PF00786 | 0.260 |
LIG_GBD_Chelix_1 | 279 | 287 | PF00786 | 0.538 |
LIG_GBD_Chelix_1 | 407 | 415 | PF00786 | 0.509 |
LIG_GBD_Chelix_1 | 575 | 583 | PF00786 | 0.441 |
LIG_LIR_Apic_2 | 1036 | 1041 | PF02991 | 0.495 |
LIG_LIR_Apic_2 | 1311 | 1317 | PF02991 | 0.680 |
LIG_LIR_Apic_2 | 452 | 456 | PF02991 | 0.362 |
LIG_LIR_Apic_2 | 591 | 595 | PF02991 | 0.357 |
LIG_LIR_Apic_2 | 596 | 602 | PF02991 | 0.379 |
LIG_LIR_Apic_2 | 667 | 673 | PF02991 | 0.445 |
LIG_LIR_Gen_1 | 1047 | 1057 | PF02991 | 0.559 |
LIG_LIR_Gen_1 | 1069 | 1079 | PF02991 | 0.601 |
LIG_LIR_Gen_1 | 209 | 219 | PF02991 | 0.432 |
LIG_LIR_Gen_1 | 256 | 266 | PF02991 | 0.365 |
LIG_LIR_Gen_1 | 484 | 495 | PF02991 | 0.436 |
LIG_LIR_Gen_1 | 542 | 551 | PF02991 | 0.278 |
LIG_LIR_Gen_1 | 750 | 756 | PF02991 | 0.366 |
LIG_LIR_Gen_1 | 939 | 950 | PF02991 | 0.506 |
LIG_LIR_LC3C_4 | 555 | 558 | PF02991 | 0.234 |
LIG_LIR_Nem_3 | 1021 | 1027 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 1047 | 1053 | PF02991 | 0.507 |
LIG_LIR_Nem_3 | 1069 | 1075 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 1076 | 1082 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 1105 | 1111 | PF02991 | 0.514 |
LIG_LIR_Nem_3 | 1196 | 1201 | PF02991 | 0.633 |
LIG_LIR_Nem_3 | 1319 | 1325 | PF02991 | 0.640 |
LIG_LIR_Nem_3 | 133 | 137 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 1335 | 1341 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 209 | 214 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 217 | 222 | PF02991 | 0.370 |
LIG_LIR_Nem_3 | 307 | 311 | PF02991 | 0.370 |
LIG_LIR_Nem_3 | 430 | 435 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 484 | 490 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 517 | 523 | PF02991 | 0.348 |
LIG_LIR_Nem_3 | 542 | 546 | PF02991 | 0.259 |
LIG_LIR_Nem_3 | 552 | 556 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 750 | 754 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 829 | 833 | PF02991 | 0.261 |
LIG_LIR_Nem_3 | 939 | 945 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 949 | 955 | PF02991 | 0.614 |
LIG_LYPXL_yS_3 | 134 | 137 | PF13949 | 0.308 |
LIG_LYPXL_yS_3 | 523 | 526 | PF13949 | 0.422 |
LIG_LYPXL_yS_3 | 730 | 733 | PF13949 | 0.434 |
LIG_LYPXL_yS_3 | 768 | 771 | PF13949 | 0.258 |
LIG_MYND_3 | 615 | 619 | PF01753 | 0.367 |
LIG_PDZ_Class_3 | 1395 | 1400 | PF00595 | 0.576 |
LIG_Pex14_1 | 218 | 222 | PF04695 | 0.240 |
LIG_Pex14_2 | 165 | 169 | PF04695 | 0.445 |
LIG_PTB_Apo_2 | 390 | 397 | PF02174 | 0.328 |
LIG_PTB_Apo_2 | 607 | 614 | PF02174 | 0.309 |
LIG_PTB_Apo_2 | 69 | 76 | PF02174 | 0.368 |
LIG_PTB_Phospho_1 | 607 | 613 | PF10480 | 0.311 |
LIG_PTB_Phospho_1 | 69 | 75 | PF10480 | 0.376 |
LIG_SH2_CRK | 242 | 246 | PF00017 | 0.379 |
LIG_SH2_CRK | 453 | 457 | PF00017 | 0.362 |
LIG_SH2_CRK | 475 | 479 | PF00017 | 0.360 |
LIG_SH2_CRK | 626 | 630 | PF00017 | 0.430 |
LIG_SH2_CRK | 670 | 674 | PF00017 | 0.474 |
LIG_SH2_GRB2like | 391 | 394 | PF00017 | 0.341 |
LIG_SH2_NCK_1 | 101 | 105 | PF00017 | 0.449 |
LIG_SH2_NCK_1 | 1072 | 1076 | PF00017 | 0.595 |
LIG_SH2_NCK_1 | 242 | 246 | PF00017 | 0.392 |
LIG_SH2_PTP2 | 1038 | 1041 | PF00017 | 0.542 |
LIG_SH2_PTP2 | 611 | 614 | PF00017 | 0.449 |
LIG_SH2_SRC | 1038 | 1041 | PF00017 | 0.554 |
LIG_SH2_SRC | 1072 | 1075 | PF00017 | 0.595 |
LIG_SH2_SRC | 442 | 445 | PF00017 | 0.400 |
LIG_SH2_STAP1 | 1050 | 1054 | PF00017 | 0.560 |
LIG_SH2_STAP1 | 144 | 148 | PF00017 | 0.214 |
LIG_SH2_STAP1 | 312 | 316 | PF00017 | 0.443 |
LIG_SH2_STAP1 | 475 | 479 | PF00017 | 0.228 |
LIG_SH2_STAP1 | 818 | 822 | PF00017 | 0.408 |
LIG_SH2_STAT3 | 469 | 472 | PF00017 | 0.428 |
LIG_SH2_STAT3 | 851 | 854 | PF00017 | 0.336 |
LIG_SH2_STAT5 | 101 | 104 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 1038 | 1041 | PF00017 | 0.484 |
LIG_SH2_STAT5 | 1233 | 1236 | PF00017 | 0.615 |
LIG_SH2_STAT5 | 148 | 151 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 183 | 186 | PF00017 | 0.339 |
LIG_SH2_STAT5 | 213 | 216 | PF00017 | 0.298 |
LIG_SH2_STAT5 | 296 | 299 | PF00017 | 0.320 |
LIG_SH2_STAT5 | 391 | 394 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 435 | 438 | PF00017 | 0.314 |
LIG_SH2_STAT5 | 442 | 445 | PF00017 | 0.299 |
LIG_SH2_STAT5 | 469 | 472 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 475 | 478 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 520 | 523 | PF00017 | 0.349 |
LIG_SH2_STAT5 | 592 | 595 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 611 | 614 | PF00017 | 0.407 |
LIG_SH2_STAT5 | 69 | 72 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 784 | 787 | PF00017 | 0.382 |
LIG_SH2_STAT5 | 919 | 922 | PF00017 | 0.536 |
LIG_SH3_1 | 242 | 248 | PF00018 | 0.261 |
LIG_SH3_2 | 245 | 250 | PF14604 | 0.256 |
LIG_SH3_3 | 1216 | 1222 | PF00018 | 0.594 |
LIG_SH3_3 | 137 | 143 | PF00018 | 0.326 |
LIG_SH3_3 | 1371 | 1377 | PF00018 | 0.518 |
LIG_SH3_3 | 242 | 248 | PF00018 | 0.350 |
LIG_SH3_3 | 518 | 524 | PF00018 | 0.316 |
LIG_SH3_3 | 591 | 597 | PF00018 | 0.375 |
LIG_SH3_3 | 864 | 870 | PF00018 | 0.387 |
LIG_SH3_3 | 872 | 878 | PF00018 | 0.403 |
LIG_SUMO_SIM_anti_2 | 121 | 128 | PF11976 | 0.429 |
LIG_SUMO_SIM_anti_2 | 1370 | 1375 | PF11976 | 0.548 |
LIG_SUMO_SIM_anti_2 | 38 | 43 | PF11976 | 0.422 |
LIG_SUMO_SIM_anti_2 | 713 | 725 | PF11976 | 0.401 |
LIG_SUMO_SIM_anti_2 | 935 | 944 | PF11976 | 0.508 |
LIG_SUMO_SIM_par_1 | 225 | 233 | PF11976 | 0.286 |
LIG_SUMO_SIM_par_1 | 45 | 51 | PF11976 | 0.447 |
LIG_SUMO_SIM_par_1 | 695 | 700 | PF11976 | 0.391 |
LIG_SUMO_SIM_par_1 | 713 | 725 | PF11976 | 0.420 |
LIG_SUMO_SIM_par_1 | 768 | 773 | PF11976 | 0.227 |
LIG_SUMO_SIM_par_1 | 855 | 860 | PF11976 | 0.339 |
LIG_SUMO_SIM_par_1 | 907 | 913 | PF11976 | 0.448 |
LIG_TRAF2_1 | 1046 | 1049 | PF00917 | 0.556 |
LIG_TRAF2_1 | 419 | 422 | PF00917 | 0.458 |
LIG_TYR_ITIM | 1070 | 1075 | PF00017 | 0.482 |
LIG_TYR_ITIM | 521 | 526 | PF00017 | 0.533 |
LIG_TYR_ITIM | 624 | 629 | PF00017 | 0.435 |
LIG_TYR_ITIM | 728 | 733 | PF00017 | 0.379 |
LIG_TYR_ITIM | 917 | 922 | PF00017 | 0.317 |
LIG_UBA3_1 | 193 | 198 | PF00899 | 0.399 |
LIG_UBA3_1 | 622 | 628 | PF00899 | 0.473 |
LIG_UBA3_1 | 798 | 807 | PF00899 | 0.271 |
LIG_WRC_WIRS_1 | 219 | 224 | PF05994 | 0.328 |
LIG_WRC_WIRS_1 | 748 | 753 | PF05994 | 0.576 |
LIG_WRC_WIRS_1 | 771 | 776 | PF05994 | 0.424 |
LIG_WW_3 | 1221 | 1225 | PF00397 | 0.616 |
MOD_CDC14_SPxK_1 | 247 | 250 | PF00782 | 0.279 |
MOD_CDK_SPK_2 | 244 | 249 | PF00069 | 0.290 |
MOD_CDK_SPK_2 | 880 | 885 | PF00069 | 0.358 |
MOD_CDK_SPxK_1 | 244 | 250 | PF00069 | 0.287 |
MOD_CDK_SPxxK_3 | 889 | 896 | PF00069 | 0.454 |
MOD_CK1_1 | 1179 | 1185 | PF00069 | 0.497 |
MOD_CK1_1 | 1294 | 1300 | PF00069 | 0.676 |
MOD_CK1_1 | 329 | 335 | PF00069 | 0.601 |
MOD_CK1_1 | 493 | 499 | PF00069 | 0.433 |
MOD_CK1_1 | 501 | 507 | PF00069 | 0.415 |
MOD_CK1_1 | 637 | 643 | PF00069 | 0.395 |
MOD_CK1_1 | 664 | 670 | PF00069 | 0.388 |
MOD_CK1_1 | 680 | 686 | PF00069 | 0.527 |
MOD_CK1_1 | 758 | 764 | PF00069 | 0.510 |
MOD_CK1_1 | 78 | 84 | PF00069 | 0.429 |
MOD_CK1_1 | 826 | 832 | PF00069 | 0.312 |
MOD_CK1_1 | 874 | 880 | PF00069 | 0.622 |
MOD_CK1_1 | 995 | 1001 | PF00069 | 0.501 |
MOD_CK2_1 | 1043 | 1049 | PF00069 | 0.424 |
MOD_CK2_1 | 1109 | 1115 | PF00069 | 0.365 |
MOD_CK2_1 | 1151 | 1157 | PF00069 | 0.641 |
MOD_CK2_1 | 1161 | 1167 | PF00069 | 0.591 |
MOD_CK2_1 | 1384 | 1390 | PF00069 | 0.424 |
MOD_CK2_1 | 151 | 157 | PF00069 | 0.443 |
MOD_CK2_1 | 182 | 188 | PF00069 | 0.533 |
MOD_CK2_1 | 416 | 422 | PF00069 | 0.431 |
MOD_CK2_1 | 566 | 572 | PF00069 | 0.431 |
MOD_CK2_1 | 60 | 66 | PF00069 | 0.573 |
MOD_CK2_1 | 837 | 843 | PF00069 | 0.440 |
MOD_CK2_1 | 940 | 946 | PF00069 | 0.356 |
MOD_Cter_Amidation | 1145 | 1148 | PF01082 | 0.504 |
MOD_GlcNHglycan | 1021 | 1024 | PF01048 | 0.503 |
MOD_GlcNHglycan | 1144 | 1147 | PF01048 | 0.502 |
MOD_GlcNHglycan | 1170 | 1173 | PF01048 | 0.582 |
MOD_GlcNHglycan | 1262 | 1265 | PF01048 | 0.486 |
MOD_GlcNHglycan | 1271 | 1274 | PF01048 | 0.399 |
MOD_GlcNHglycan | 1293 | 1296 | PF01048 | 0.674 |
MOD_GlcNHglycan | 1301 | 1304 | PF01048 | 0.656 |
MOD_GlcNHglycan | 1305 | 1308 | PF01048 | 0.616 |
MOD_GlcNHglycan | 1318 | 1321 | PF01048 | 0.564 |
MOD_GlcNHglycan | 1363 | 1366 | PF01048 | 0.497 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.532 |
MOD_GlcNHglycan | 172 | 175 | PF01048 | 0.372 |
MOD_GlcNHglycan | 293 | 296 | PF01048 | 0.484 |
MOD_GlcNHglycan | 329 | 332 | PF01048 | 0.611 |
MOD_GlcNHglycan | 411 | 414 | PF01048 | 0.493 |
MOD_GlcNHglycan | 491 | 495 | PF01048 | 0.438 |
MOD_GlcNHglycan | 560 | 564 | PF01048 | 0.363 |
MOD_GlcNHglycan | 579 | 582 | PF01048 | 0.441 |
MOD_GlcNHglycan | 663 | 666 | PF01048 | 0.506 |
MOD_GlcNHglycan | 685 | 688 | PF01048 | 0.452 |
MOD_GlcNHglycan | 762 | 765 | PF01048 | 0.398 |
MOD_GlcNHglycan | 79 | 83 | PF01048 | 0.330 |
MOD_GlcNHglycan | 810 | 813 | PF01048 | 0.580 |
MOD_GlcNHglycan | 825 | 828 | PF01048 | 0.437 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.453 |
MOD_GlcNHglycan | 994 | 997 | PF01048 | 0.448 |
MOD_GSK3_1 | 1039 | 1046 | PF00069 | 0.517 |
MOD_GSK3_1 | 1161 | 1168 | PF00069 | 0.514 |
MOD_GSK3_1 | 1175 | 1182 | PF00069 | 0.425 |
MOD_GSK3_1 | 1222 | 1229 | PF00069 | 0.579 |
MOD_GSK3_1 | 1299 | 1306 | PF00069 | 0.704 |
MOD_GSK3_1 | 1346 | 1353 | PF00069 | 0.539 |
MOD_GSK3_1 | 1359 | 1366 | PF00069 | 0.421 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.483 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.487 |
MOD_GSK3_1 | 326 | 333 | PF00069 | 0.597 |
MOD_GSK3_1 | 334 | 341 | PF00069 | 0.533 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.474 |
MOD_GSK3_1 | 473 | 480 | PF00069 | 0.545 |
MOD_GSK3_1 | 552 | 559 | PF00069 | 0.375 |
MOD_GSK3_1 | 633 | 640 | PF00069 | 0.392 |
MOD_GSK3_1 | 673 | 680 | PF00069 | 0.490 |
MOD_GSK3_1 | 732 | 739 | PF00069 | 0.503 |
MOD_GSK3_1 | 813 | 820 | PF00069 | 0.471 |
MOD_GSK3_1 | 835 | 842 | PF00069 | 0.527 |
MOD_GSK3_1 | 870 | 877 | PF00069 | 0.526 |
MOD_GSK3_1 | 885 | 892 | PF00069 | 0.537 |
MOD_GSK3_1 | 936 | 943 | PF00069 | 0.373 |
MOD_GSK3_1 | 981 | 988 | PF00069 | 0.362 |
MOD_N-GLC_1 | 655 | 660 | PF02516 | 0.454 |
MOD_N-GLC_1 | 782 | 787 | PF02516 | 0.464 |
MOD_N-GLC_1 | 808 | 813 | PF02516 | 0.498 |
MOD_NEK2_1 | 1176 | 1181 | PF00069 | 0.619 |
MOD_NEK2_1 | 1269 | 1274 | PF00069 | 0.466 |
MOD_NEK2_1 | 1308 | 1313 | PF00069 | 0.710 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.455 |
MOD_NEK2_1 | 182 | 187 | PF00069 | 0.446 |
MOD_NEK2_1 | 261 | 266 | PF00069 | 0.383 |
MOD_NEK2_1 | 35 | 40 | PF00069 | 0.428 |
MOD_NEK2_1 | 47 | 52 | PF00069 | 0.350 |
MOD_NEK2_1 | 566 | 571 | PF00069 | 0.575 |
MOD_NEK2_1 | 579 | 584 | PF00069 | 0.356 |
MOD_NEK2_1 | 661 | 666 | PF00069 | 0.368 |
MOD_NEK2_1 | 697 | 702 | PF00069 | 0.457 |
MOD_NEK2_1 | 770 | 775 | PF00069 | 0.569 |
MOD_NEK2_1 | 802 | 807 | PF00069 | 0.442 |
MOD_NEK2_1 | 813 | 818 | PF00069 | 0.419 |
MOD_NEK2_1 | 910 | 915 | PF00069 | 0.335 |
MOD_NEK2_2 | 296 | 301 | PF00069 | 0.561 |
MOD_NEK2_2 | 529 | 534 | PF00069 | 0.396 |
MOD_PIKK_1 | 400 | 406 | PF00454 | 0.466 |
MOD_PK_1 | 1363 | 1369 | PF00069 | 0.406 |
MOD_PK_1 | 740 | 746 | PF00069 | 0.333 |
MOD_PKA_1 | 1354 | 1360 | PF00069 | 0.504 |
MOD_PKA_1 | 1384 | 1390 | PF00069 | 0.420 |
MOD_PKA_2 | 1243 | 1249 | PF00069 | 0.538 |
MOD_PKA_2 | 1291 | 1297 | PF00069 | 0.689 |
MOD_PKA_2 | 1308 | 1314 | PF00069 | 0.596 |
MOD_PKA_2 | 1354 | 1360 | PF00069 | 0.577 |
MOD_PKA_2 | 1384 | 1390 | PF00069 | 0.445 |
MOD_PKA_2 | 206 | 212 | PF00069 | 0.528 |
MOD_PKA_2 | 29 | 35 | PF00069 | 0.506 |
MOD_PKA_2 | 290 | 296 | PF00069 | 0.481 |
MOD_Plk_1 | 361 | 367 | PF00069 | 0.395 |
MOD_Plk_1 | 421 | 427 | PF00069 | 0.426 |
MOD_Plk_1 | 638 | 644 | PF00069 | 0.478 |
MOD_Plk_1 | 655 | 661 | PF00069 | 0.421 |
MOD_Plk_1 | 713 | 719 | PF00069 | 0.490 |
MOD_Plk_1 | 808 | 814 | PF00069 | 0.474 |
MOD_Plk_2-3 | 1394 | 1400 | PF00069 | 0.414 |
MOD_Plk_2-3 | 981 | 987 | PF00069 | 0.352 |
MOD_Plk_4 | 1244 | 1250 | PF00069 | 0.548 |
MOD_Plk_4 | 1280 | 1286 | PF00069 | 0.594 |
MOD_Plk_4 | 1324 | 1330 | PF00069 | 0.559 |
MOD_Plk_4 | 133 | 139 | PF00069 | 0.480 |
MOD_Plk_4 | 1384 | 1390 | PF00069 | 0.420 |
MOD_Plk_4 | 144 | 150 | PF00069 | 0.435 |
MOD_Plk_4 | 35 | 41 | PF00069 | 0.358 |
MOD_Plk_4 | 361 | 367 | PF00069 | 0.497 |
MOD_Plk_4 | 411 | 417 | PF00069 | 0.542 |
MOD_Plk_4 | 421 | 427 | PF00069 | 0.440 |
MOD_Plk_4 | 455 | 461 | PF00069 | 0.201 |
MOD_Plk_4 | 514 | 520 | PF00069 | 0.427 |
MOD_Plk_4 | 552 | 558 | PF00069 | 0.400 |
MOD_Plk_4 | 579 | 585 | PF00069 | 0.316 |
MOD_Plk_4 | 627 | 633 | PF00069 | 0.410 |
MOD_Plk_4 | 714 | 720 | PF00069 | 0.522 |
MOD_Plk_4 | 729 | 735 | PF00069 | 0.425 |
MOD_Plk_4 | 813 | 819 | PF00069 | 0.370 |
MOD_Plk_4 | 912 | 918 | PF00069 | 0.360 |
MOD_Plk_4 | 936 | 942 | PF00069 | 0.354 |
MOD_Plk_4 | 985 | 991 | PF00069 | 0.364 |
MOD_ProDKin_1 | 1082 | 1088 | PF00069 | 0.414 |
MOD_ProDKin_1 | 152 | 158 | PF00069 | 0.476 |
MOD_ProDKin_1 | 244 | 250 | PF00069 | 0.468 |
MOD_ProDKin_1 | 318 | 324 | PF00069 | 0.501 |
MOD_ProDKin_1 | 593 | 599 | PF00069 | 0.448 |
MOD_ProDKin_1 | 782 | 788 | PF00069 | 0.474 |
MOD_ProDKin_1 | 837 | 843 | PF00069 | 0.380 |
MOD_ProDKin_1 | 871 | 877 | PF00069 | 0.509 |
MOD_ProDKin_1 | 880 | 886 | PF00069 | 0.487 |
MOD_ProDKin_1 | 889 | 895 | PF00069 | 0.574 |
MOD_SUMO_rev_2 | 113 | 118 | PF00179 | 0.343 |
MOD_SUMO_rev_2 | 364 | 373 | PF00179 | 0.558 |
TRG_DiLeu_BaEn_1 | 66 | 71 | PF01217 | 0.520 |
TRG_DiLeu_BaEn_1 | 936 | 941 | PF01217 | 0.482 |
TRG_DiLeu_BaEn_2 | 541 | 547 | PF01217 | 0.210 |
TRG_DiLeu_BaEn_2 | 618 | 624 | PF01217 | 0.354 |
TRG_DiLeu_BaEn_3 | 713 | 719 | PF01217 | 0.517 |
TRG_DiLeu_BaEn_4 | 1048 | 1054 | PF01217 | 0.395 |
TRG_DiLeu_BaLyEn_6 | 30 | 35 | PF01217 | 0.457 |
TRG_DiLeu_BaLyEn_6 | 562 | 567 | PF01217 | 0.290 |
TRG_DiLeu_BaLyEn_6 | 766 | 771 | PF01217 | 0.289 |
TRG_DiLeu_LyEn_5 | 1209 | 1214 | PF01217 | 0.534 |
TRG_ENDOCYTIC_2 | 1024 | 1027 | PF00928 | 0.360 |
TRG_ENDOCYTIC_2 | 1050 | 1053 | PF00928 | 0.343 |
TRG_ENDOCYTIC_2 | 1072 | 1075 | PF00928 | 0.476 |
TRG_ENDOCYTIC_2 | 134 | 137 | PF00928 | 0.517 |
TRG_ENDOCYTIC_2 | 311 | 314 | PF00928 | 0.507 |
TRG_ENDOCYTIC_2 | 475 | 478 | PF00928 | 0.327 |
TRG_ENDOCYTIC_2 | 523 | 526 | PF00928 | 0.441 |
TRG_ENDOCYTIC_2 | 543 | 546 | PF00928 | 0.375 |
TRG_ENDOCYTIC_2 | 611 | 614 | PF00928 | 0.552 |
TRG_ENDOCYTIC_2 | 626 | 629 | PF00928 | 0.521 |
TRG_ENDOCYTIC_2 | 730 | 733 | PF00928 | 0.388 |
TRG_ENDOCYTIC_2 | 768 | 771 | PF00928 | 0.557 |
TRG_ENDOCYTIC_2 | 919 | 922 | PF00928 | 0.471 |
TRG_ER_diArg_1 | 1057 | 1060 | PF00400 | 0.354 |
TRG_ER_diArg_1 | 1314 | 1316 | PF00400 | 0.443 |
TRG_ER_diArg_1 | 1354 | 1356 | PF00400 | 0.728 |
TRG_ER_diArg_1 | 1383 | 1385 | PF00400 | 0.400 |
TRG_ER_diArg_1 | 204 | 207 | PF00400 | 0.486 |
TRG_ER_diArg_1 | 689 | 692 | PF00400 | 0.552 |
TRG_ER_diArg_1 | 8 | 10 | PF00400 | 0.558 |
TRG_NES_CRM1_1 | 225 | 237 | PF08389 | 0.408 |
TRG_Pf-PMV_PEXEL_1 | 968 | 972 | PF00026 | 0.428 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4J2K5 | Bodo saltans | 25% | 100% |
A0A1X0P171 | Trypanosomatidae | 31% | 100% |
A0A3Q8IJB0 | Leishmania donovani | 78% | 100% |
A0A3R7R8G4 | Trypanosoma rangeli | 31% | 100% |
A0A3S5H6Z8 | Leishmania donovani | 78% | 100% |
A0A3S7WU91 | Leishmania donovani | 64% | 99% |
A0A3S7WU94 | Leishmania donovani | 53% | 100% |
A0A3S7WU95 | Leishmania donovani | 81% | 100% |
A0A3S7XB85 | Leishmania donovani | 30% | 100% |
A4H8U6 | Leishmania braziliensis | 54% | 100% |
A4H8V5 | Leishmania braziliensis | 59% | 100% |
A4H8V7 | Leishmania braziliensis | 66% | 100% |
A4H8V8 | Leishmania braziliensis | 68% | 100% |
A4HPI4 | Leishmania braziliensis | 27% | 100% |
A4HX84 | Leishmania infantum | 53% | 100% |
A4HX85 | Leishmania infantum | 78% | 100% |
A4HX87 | Leishmania infantum | 64% | 100% |
C9ZM79 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZM80 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZM81 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZM82 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZM83 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZM86 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZN26 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
C9ZN41 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
C9ZN43 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
C9ZN44 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
C9ZN45 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
C9ZN46 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
C9ZNA5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
C9ZNA6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
C9ZNH3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
C9ZNT1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
C9ZPZ6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
C9ZQ51 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
C9ZQ89 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
C9ZQ90 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZQ92 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
C9ZTS4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
C9ZTS5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZTS6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
C9ZUE6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
C9ZWQ5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
C9ZWU1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
C9ZWU2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
C9ZWU3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
C9ZWY7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZZQ4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
D0A0U3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
D0A0W7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
D0A0X5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
D0A1S1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
D0A5D2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
D0A5D5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
D0A5U0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
D0A5U1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
D0A7A0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
D0A9R3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
D0AAV3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
E9AQY0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 66% | 100% |
E9AQY1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 63% | 100% |
E9AQY4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
E9ARD7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 55% | 100% |
Q25263 | Leishmania donovani | 78% | 100% |
Q26721 | Trypanosoma brucei brucei | 33% | 100% |
Q27675 | Leishmania donovani | 53% | 100% |
Q4Q1A1 | Leishmania major | 28% | 100% |
Q4QEH9 | Leishmania major | 78% | 100% |
Q4QEI0 | Leishmania major | 78% | 100% |
Q4QEI1 | Leishmania major | 79% | 100% |
Q4QEI2 | Leishmania major | 61% | 100% |
Q4QEI3 | Leishmania major | 53% | 100% |
Q99279 | Trypanosoma brucei brucei | 29% | 100% |
Q99280 | Trypanosoma brucei brucei | 33% | 100% |
V5AYH7 | Trypanosoma cruzi | 33% | 100% |