Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 16 |
NetGPI | no | yes: 0, no: 16 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
Related structures:
AlphaFold database: Q4Q470
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 17 |
GO:0003824 | catalytic activity | 1 | 17 |
GO:0005488 | binding | 1 | 17 |
GO:0005524 | ATP binding | 5 | 17 |
GO:0016462 | pyrophosphatase activity | 5 | 17 |
GO:0016787 | hydrolase activity | 2 | 17 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 17 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 17 |
GO:0016887 | ATP hydrolysis activity | 7 | 17 |
GO:0017076 | purine nucleotide binding | 4 | 17 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 17 |
GO:0030554 | adenyl nucleotide binding | 5 | 17 |
GO:0032553 | ribonucleotide binding | 3 | 17 |
GO:0032555 | purine ribonucleotide binding | 4 | 17 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 17 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 17 |
GO:0036094 | small molecule binding | 2 | 17 |
GO:0043167 | ion binding | 2 | 17 |
GO:0043168 | anion binding | 3 | 17 |
GO:0097159 | organic cyclic compound binding | 2 | 17 |
GO:0097367 | carbohydrate derivative binding | 2 | 17 |
GO:1901265 | nucleoside phosphate binding | 3 | 17 |
GO:1901363 | heterocyclic compound binding | 2 | 17 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 112 | 116 | PF00656 | 0.668 |
CLV_C14_Caspase3-7 | 380 | 384 | PF00656 | 0.746 |
CLV_C14_Caspase3-7 | 409 | 413 | PF00656 | 0.526 |
CLV_C14_Caspase3-7 | 454 | 458 | PF00656 | 0.790 |
CLV_C14_Caspase3-7 | 470 | 474 | PF00656 | 0.641 |
CLV_C14_Caspase3-7 | 58 | 62 | PF00656 | 0.577 |
CLV_C14_Caspase3-7 | 612 | 616 | PF00656 | 0.739 |
CLV_NRD_NRD_1 | 260 | 262 | PF00675 | 0.478 |
CLV_NRD_NRD_1 | 438 | 440 | PF00675 | 0.579 |
CLV_PCSK_FUR_1 | 436 | 440 | PF00082 | 0.623 |
CLV_PCSK_KEX2_1 | 260 | 262 | PF00082 | 0.504 |
CLV_PCSK_KEX2_1 | 350 | 352 | PF00082 | 0.303 |
CLV_PCSK_KEX2_1 | 381 | 383 | PF00082 | 0.404 |
CLV_PCSK_KEX2_1 | 438 | 440 | PF00082 | 0.580 |
CLV_PCSK_KEX2_1 | 506 | 508 | PF00082 | 0.541 |
CLV_PCSK_PC1ET2_1 | 350 | 352 | PF00082 | 0.337 |
CLV_PCSK_PC1ET2_1 | 381 | 383 | PF00082 | 0.402 |
CLV_PCSK_PC1ET2_1 | 506 | 508 | PF00082 | 0.450 |
CLV_PCSK_SKI1_1 | 243 | 247 | PF00082 | 0.424 |
CLV_PCSK_SKI1_1 | 283 | 287 | PF00082 | 0.372 |
CLV_PCSK_SKI1_1 | 325 | 329 | PF00082 | 0.322 |
CLV_PCSK_SKI1_1 | 351 | 355 | PF00082 | 0.308 |
CLV_PCSK_SKI1_1 | 369 | 373 | PF00082 | 0.308 |
CLV_PCSK_SKI1_1 | 484 | 488 | PF00082 | 0.601 |
CLV_PCSK_SKI1_1 | 512 | 516 | PF00082 | 0.372 |
CLV_PCSK_SKI1_1 | 590 | 594 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 83 | 87 | PF00082 | 0.375 |
CLV_PCSK_SKI1_1 | 92 | 96 | PF00082 | 0.399 |
CLV_Separin_Metazoa | 644 | 648 | PF03568 | 0.559 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.427 |
DEG_SPOP_SBC_1 | 60 | 64 | PF00917 | 0.549 |
DOC_CYCLIN_RxL_1 | 191 | 202 | PF00134 | 0.639 |
DOC_CYCLIN_RxL_1 | 258 | 269 | PF00134 | 0.608 |
DOC_CYCLIN_RxL_1 | 280 | 288 | PF00134 | 0.545 |
DOC_CYCLIN_yCln2_LP_2 | 295 | 301 | PF00134 | 0.536 |
DOC_CYCLIN_yCln2_LP_2 | 398 | 404 | PF00134 | 0.529 |
DOC_MAPK_gen_1 | 350 | 358 | PF00069 | 0.491 |
DOC_PP1_RVXF_1 | 259 | 266 | PF00149 | 0.759 |
DOC_PP2B_LxvP_1 | 106 | 109 | PF13499 | 0.663 |
DOC_PP4_FxxP_1 | 67 | 70 | PF00568 | 0.510 |
DOC_SPAK_OSR1_1 | 375 | 379 | PF12202 | 0.576 |
DOC_SPAK_OSR1_1 | 97 | 101 | PF12202 | 0.681 |
DOC_USP7_MATH_1 | 175 | 179 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 199 | 203 | PF00917 | 0.742 |
DOC_USP7_MATH_1 | 226 | 230 | PF00917 | 0.670 |
DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.403 |
DOC_USP7_MATH_1 | 598 | 602 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 613 | 617 | PF00917 | 0.747 |
DOC_USP7_UBL2_3 | 312 | 316 | PF12436 | 0.560 |
DOC_USP7_UBL2_3 | 377 | 381 | PF12436 | 0.596 |
DOC_USP7_UBL2_3 | 502 | 506 | PF12436 | 0.765 |
DOC_WW_Pin1_4 | 129 | 134 | PF00397 | 0.677 |
DOC_WW_Pin1_4 | 622 | 627 | PF00397 | 0.547 |
LIG_14-3-3_CanoR_1 | 140 | 147 | PF00244 | 0.667 |
LIG_14-3-3_CanoR_1 | 148 | 152 | PF00244 | 0.718 |
LIG_14-3-3_CanoR_1 | 186 | 190 | PF00244 | 0.621 |
LIG_14-3-3_CanoR_1 | 272 | 279 | PF00244 | 0.643 |
LIG_14-3-3_CanoR_1 | 360 | 368 | PF00244 | 0.510 |
LIG_14-3-3_CanoR_1 | 52 | 57 | PF00244 | 0.687 |
LIG_14-3-3_CanoR_1 | 573 | 583 | PF00244 | 0.630 |
LIG_14-3-3_CanoR_1 | 83 | 93 | PF00244 | 0.535 |
LIG_Actin_WH2_2 | 134 | 150 | PF00022 | 0.671 |
LIG_Actin_WH2_2 | 3 | 19 | PF00022 | 0.469 |
LIG_Actin_WH2_2 | 537 | 552 | PF00022 | 0.644 |
LIG_BRCT_BRCA1_1 | 293 | 297 | PF00533 | 0.529 |
LIG_BRCT_BRCA1_1 | 372 | 376 | PF00533 | 0.553 |
LIG_BRCT_BRCA1_1 | 63 | 67 | PF00533 | 0.659 |
LIG_CSL_BTD_1 | 44 | 47 | PF09270 | 0.642 |
LIG_eIF4E_1 | 252 | 258 | PF01652 | 0.619 |
LIG_eIF4E_1 | 348 | 354 | PF01652 | 0.539 |
LIG_FHA_1 | 118 | 124 | PF00498 | 0.674 |
LIG_FHA_1 | 140 | 146 | PF00498 | 0.634 |
LIG_FHA_1 | 16 | 22 | PF00498 | 0.374 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.393 |
LIG_FHA_1 | 412 | 418 | PF00498 | 0.630 |
LIG_FHA_1 | 485 | 491 | PF00498 | 0.802 |
LIG_FHA_1 | 511 | 517 | PF00498 | 0.567 |
LIG_FHA_1 | 536 | 542 | PF00498 | 0.495 |
LIG_FHA_1 | 553 | 559 | PF00498 | 0.594 |
LIG_FHA_1 | 577 | 583 | PF00498 | 0.611 |
LIG_FHA_1 | 604 | 610 | PF00498 | 0.635 |
LIG_FHA_1 | 79 | 85 | PF00498 | 0.583 |
LIG_FHA_1 | 89 | 95 | PF00498 | 0.594 |
LIG_FHA_2 | 150 | 156 | PF00498 | 0.734 |
LIG_FHA_2 | 201 | 207 | PF00498 | 0.768 |
LIG_FHA_2 | 257 | 263 | PF00498 | 0.646 |
LIG_FHA_2 | 347 | 353 | PF00498 | 0.544 |
LIG_FHA_2 | 426 | 432 | PF00498 | 0.760 |
LIG_FHA_2 | 452 | 458 | PF00498 | 0.827 |
LIG_FHA_2 | 465 | 471 | PF00498 | 0.750 |
LIG_FHA_2 | 494 | 500 | PF00498 | 0.738 |
LIG_FHA_2 | 636 | 642 | PF00498 | 0.564 |
LIG_GBD_Chelix_1 | 519 | 527 | PF00786 | 0.272 |
LIG_LIR_Apic_2 | 314 | 320 | PF02991 | 0.582 |
LIG_LIR_Apic_2 | 64 | 70 | PF02991 | 0.492 |
LIG_LIR_Gen_1 | 102 | 113 | PF02991 | 0.614 |
LIG_LIR_Gen_1 | 125 | 134 | PF02991 | 0.627 |
LIG_LIR_Gen_1 | 2 | 12 | PF02991 | 0.405 |
LIG_LIR_Gen_1 | 291 | 299 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 102 | 108 | PF02991 | 0.583 |
LIG_LIR_Nem_3 | 125 | 129 | PF02991 | 0.589 |
LIG_LIR_Nem_3 | 188 | 192 | PF02991 | 0.647 |
LIG_LIR_Nem_3 | 2 | 7 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 241 | 245 | PF02991 | 0.671 |
LIG_LIR_Nem_3 | 291 | 295 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 44 | 49 | PF02991 | 0.565 |
LIG_LIR_Nem_3 | 74 | 80 | PF02991 | 0.605 |
LIG_MLH1_MIPbox_1 | 293 | 297 | PF16413 | 0.529 |
LIG_NRBOX | 325 | 331 | PF00104 | 0.463 |
LIG_NRBOX | 588 | 594 | PF00104 | 0.559 |
LIG_Pex14_2 | 292 | 296 | PF04695 | 0.485 |
LIG_Pex14_2 | 372 | 376 | PF04695 | 0.553 |
LIG_PTB_Apo_2 | 6 | 13 | PF02174 | 0.401 |
LIG_SH2_CRK | 126 | 130 | PF00017 | 0.667 |
LIG_SH2_CRK | 254 | 258 | PF00017 | 0.574 |
LIG_SH2_CRK | 317 | 321 | PF00017 | 0.605 |
LIG_SH2_CRK | 331 | 335 | PF00017 | 0.415 |
LIG_SH2_NCK_1 | 317 | 321 | PF00017 | 0.635 |
LIG_SH2_SRC | 317 | 320 | PF00017 | 0.628 |
LIG_SH2_STAP1 | 119 | 123 | PF00017 | 0.660 |
LIG_SH2_STAP1 | 4 | 8 | PF00017 | 0.381 |
LIG_SH2_STAP1 | 80 | 84 | PF00017 | 0.600 |
LIG_SH2_STAT3 | 252 | 255 | PF00017 | 0.527 |
LIG_SH2_STAT5 | 105 | 108 | PF00017 | 0.594 |
LIG_SH2_STAT5 | 119 | 122 | PF00017 | 0.610 |
LIG_SH2_STAT5 | 126 | 129 | PF00017 | 0.648 |
LIG_SH2_STAT5 | 252 | 255 | PF00017 | 0.539 |
LIG_SH2_STAT5 | 284 | 287 | PF00017 | 0.617 |
LIG_SH2_STAT5 | 348 | 351 | PF00017 | 0.423 |
LIG_SH2_STAT5 | 4 | 7 | PF00017 | 0.425 |
LIG_SH2_STAT5 | 40 | 43 | PF00017 | 0.514 |
LIG_SH2_STAT5 | 406 | 409 | PF00017 | 0.519 |
LIG_SH2_STAT5 | 56 | 59 | PF00017 | 0.662 |
LIG_SH2_STAT5 | 575 | 578 | PF00017 | 0.612 |
LIG_SH2_STAT5 | 80 | 83 | PF00017 | 0.550 |
LIG_SH2_STAT5 | 89 | 92 | PF00017 | 0.544 |
LIG_SH3_1 | 317 | 323 | PF00018 | 0.632 |
LIG_SH3_2 | 320 | 325 | PF14604 | 0.568 |
LIG_SH3_3 | 295 | 301 | PF00018 | 0.606 |
LIG_SH3_3 | 317 | 323 | PF00018 | 0.556 |
LIG_SH3_3 | 90 | 96 | PF00018 | 0.637 |
LIG_SUMO_SIM_anti_2 | 640 | 647 | PF11976 | 0.559 |
LIG_SUMO_SIM_par_1 | 511 | 517 | PF11976 | 0.657 |
LIG_TRAF2_1 | 174 | 177 | PF00917 | 0.645 |
LIG_TRAF2_1 | 363 | 366 | PF00917 | 0.470 |
LIG_TRAF2_1 | 460 | 463 | PF00917 | 0.802 |
LIG_TRAF2_1 | 638 | 641 | PF00917 | 0.617 |
LIG_TYR_ITIM | 103 | 108 | PF00017 | 0.644 |
LIG_TYR_ITIM | 240 | 245 | PF00017 | 0.553 |
LIG_UBA3_1 | 192 | 201 | PF00899 | 0.560 |
LIG_UBA3_1 | 303 | 312 | PF00899 | 0.577 |
MOD_CDC14_SPxK_1 | 132 | 135 | PF00782 | 0.577 |
MOD_CDK_SPxK_1 | 129 | 135 | PF00069 | 0.681 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.423 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.639 |
MOD_CK1_1 | 207 | 213 | PF00069 | 0.646 |
MOD_CK1_1 | 288 | 294 | PF00069 | 0.541 |
MOD_CK1_1 | 393 | 399 | PF00069 | 0.609 |
MOD_CK1_1 | 450 | 456 | PF00069 | 0.772 |
MOD_CK1_1 | 55 | 61 | PF00069 | 0.610 |
MOD_CK1_1 | 577 | 583 | PF00069 | 0.637 |
MOD_CK2_1 | 199 | 205 | PF00069 | 0.730 |
MOD_CK2_1 | 226 | 232 | PF00069 | 0.650 |
MOD_CK2_1 | 256 | 262 | PF00069 | 0.527 |
MOD_CK2_1 | 360 | 366 | PF00069 | 0.458 |
MOD_CK2_1 | 425 | 431 | PF00069 | 0.756 |
MOD_CK2_1 | 453 | 459 | PF00069 | 0.799 |
MOD_CK2_1 | 464 | 470 | PF00069 | 0.740 |
MOD_CK2_1 | 493 | 499 | PF00069 | 0.735 |
MOD_CK2_1 | 588 | 594 | PF00069 | 0.653 |
MOD_CK2_1 | 622 | 628 | PF00069 | 0.528 |
MOD_CK2_1 | 635 | 641 | PF00069 | 0.518 |
MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.548 |
MOD_GlcNHglycan | 268 | 271 | PF01048 | 0.437 |
MOD_GlcNHglycan | 287 | 290 | PF01048 | 0.341 |
MOD_GlcNHglycan | 35 | 38 | PF01048 | 0.356 |
MOD_GlcNHglycan | 372 | 375 | PF01048 | 0.309 |
MOD_GlcNHglycan | 443 | 446 | PF01048 | 0.567 |
MOD_GlcNHglycan | 470 | 473 | PF01048 | 0.590 |
MOD_GlcNHglycan | 596 | 599 | PF01048 | 0.459 |
MOD_GlcNHglycan | 615 | 619 | PF01048 | 0.518 |
MOD_GlcNHglycan | 63 | 66 | PF01048 | 0.435 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.443 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.746 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.463 |
MOD_GSK3_1 | 356 | 363 | PF00069 | 0.484 |
MOD_GSK3_1 | 447 | 454 | PF00069 | 0.772 |
MOD_GSK3_1 | 464 | 471 | PF00069 | 0.776 |
MOD_GSK3_1 | 484 | 491 | PF00069 | 0.754 |
MOD_GSK3_1 | 502 | 509 | PF00069 | 0.573 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.689 |
MOD_GSK3_1 | 594 | 601 | PF00069 | 0.621 |
MOD_GSK3_1 | 603 | 610 | PF00069 | 0.756 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.580 |
MOD_N-GLC_1 | 117 | 122 | PF02516 | 0.461 |
MOD_N-GLC_1 | 129 | 134 | PF02516 | 0.505 |
MOD_N-GLC_1 | 468 | 473 | PF02516 | 0.603 |
MOD_N-GLC_1 | 71 | 76 | PF02516 | 0.531 |
MOD_NEK2_1 | 12 | 17 | PF00069 | 0.459 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.642 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.636 |
MOD_NEK2_1 | 285 | 290 | PF00069 | 0.601 |
MOD_NEK2_1 | 33 | 38 | PF00069 | 0.386 |
MOD_NEK2_1 | 354 | 359 | PF00069 | 0.484 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.487 |
MOD_NEK2_1 | 576 | 581 | PF00069 | 0.639 |
MOD_NEK2_2 | 552 | 557 | PF00069 | 0.540 |
MOD_NEK2_2 | 78 | 83 | PF00069 | 0.642 |
MOD_PIKK_1 | 169 | 175 | PF00454 | 0.778 |
MOD_PIKK_1 | 180 | 186 | PF00454 | 0.616 |
MOD_PIKK_1 | 493 | 499 | PF00454 | 0.790 |
MOD_PK_1 | 104 | 110 | PF00069 | 0.607 |
MOD_PKA_1 | 506 | 512 | PF00069 | 0.741 |
MOD_PKA_2 | 139 | 145 | PF00069 | 0.635 |
MOD_PKA_2 | 147 | 153 | PF00069 | 0.632 |
MOD_PKA_2 | 185 | 191 | PF00069 | 0.677 |
MOD_PKA_2 | 506 | 512 | PF00069 | 0.746 |
MOD_Plk_1 | 175 | 181 | PF00069 | 0.634 |
MOD_Plk_1 | 231 | 237 | PF00069 | 0.631 |
MOD_Plk_1 | 510 | 516 | PF00069 | 0.638 |
MOD_Plk_1 | 614 | 620 | PF00069 | 0.628 |
MOD_Plk_2-3 | 457 | 463 | PF00069 | 0.793 |
MOD_Plk_2-3 | 588 | 594 | PF00069 | 0.608 |
MOD_Plk_2-3 | 635 | 641 | PF00069 | 0.632 |
MOD_Plk_4 | 226 | 232 | PF00069 | 0.665 |
MOD_Plk_4 | 291 | 297 | PF00069 | 0.507 |
MOD_Plk_4 | 52 | 58 | PF00069 | 0.625 |
MOD_Plk_4 | 544 | 550 | PF00069 | 0.642 |
MOD_Plk_4 | 577 | 583 | PF00069 | 0.669 |
MOD_Plk_4 | 85 | 91 | PF00069 | 0.610 |
MOD_ProDKin_1 | 129 | 135 | PF00069 | 0.681 |
MOD_ProDKin_1 | 622 | 628 | PF00069 | 0.545 |
MOD_SUMO_for_1 | 419 | 422 | PF00179 | 0.638 |
MOD_SUMO_rev_2 | 236 | 245 | PF00179 | 0.643 |
MOD_SUMO_rev_2 | 308 | 314 | PF00179 | 0.552 |
TRG_DiLeu_BaEn_1 | 588 | 593 | PF01217 | 0.633 |
TRG_DiLeu_BaEn_2 | 175 | 181 | PF01217 | 0.700 |
TRG_DiLeu_BaEn_3 | 176 | 182 | PF01217 | 0.490 |
TRG_DiLeu_BaLyEn_6 | 253 | 258 | PF01217 | 0.619 |
TRG_DiLeu_BaLyEn_6 | 299 | 304 | PF01217 | 0.606 |
TRG_ENDOCYTIC_2 | 105 | 108 | PF00928 | 0.561 |
TRG_ENDOCYTIC_2 | 126 | 129 | PF00928 | 0.638 |
TRG_ENDOCYTIC_2 | 242 | 245 | PF00928 | 0.605 |
TRG_ENDOCYTIC_2 | 254 | 257 | PF00928 | 0.526 |
TRG_ENDOCYTIC_2 | 4 | 7 | PF00928 | 0.408 |
TRG_NES_CRM1_1 | 136 | 149 | PF08389 | 0.599 |
TRG_NES_CRM1_1 | 366 | 380 | PF08389 | 0.553 |
TRG_NES_CRM1_1 | 99 | 112 | PF08389 | 0.558 |
TRG_Pf-PMV_PEXEL_1 | 251 | 255 | PF00026 | 0.323 |
TRG_Pf-PMV_PEXEL_1 | 512 | 517 | PF00026 | 0.372 |
TRG_Pf-PMV_PEXEL_1 | 590 | 594 | PF00026 | 0.435 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4V2 | Leptomonas seymouri | 59% | 97% |
A0A0S4JAD3 | Bodo saltans | 32% | 100% |
A0A1X0NTT2 | Trypanosomatidae | 29% | 97% |
A0A1X0P2Y3 | Trypanosomatidae | 29% | 100% |
A0A1X0P9I4 | Trypanosomatidae | 29% | 81% |
A0A3S7X6K2 | Leishmania donovani | 93% | 100% |
A0A422NUH1 | Trypanosoma rangeli | 30% | 97% |
A0A422P3P3 | Trypanosoma rangeli | 30% | 100% |
A4HLH5 | Leishmania braziliensis | 71% | 100% |
A4I8Y5 | Leishmania infantum | 93% | 100% |
C9ZSJ9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 98% |
D0A1W6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 91% |
E9AU21 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 91% |
E9B3V4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
V5DQN5 | Trypanosoma cruzi | 32% | 100% |