Nutrient transporter belonging to the Major Facilitator Superfamily (MFS). Probable nutrient transporter. Heavily expanded in all parazitic species.. 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: 0 | 
| Forrest at al. (procyclic) | no | yes: 0 | 
| Silverman et al. | no | yes: 0 | 
| Pissara et al. | no | yes: 15 | 
| Source | Evidence on protein | Close homologs | 
|---|---|---|
| Pires et al. | no | yes: 0 | 
| Source | Evidence on protein | Close homologs | 
|---|---|---|
| Silverman et al. | no | yes: 0 | 
| Source | Evidence on protein | Close homologs | 
|---|---|---|
| Jamdhade et al. | no | yes: 0 | 
| Source | Evidence on protein | Close homologs | 
|---|---|---|
| DeepLoc | ||
| SignalP6 | no | yes: 0, no: 97 | 
| NetGPI | no | yes: 0, no: 97 | 
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0016020 | membrane | 2 | 92 | 
| GO:0110165 | cellular anatomical entity | 1 | 92 | 
Related structures:
AlphaFold database: A0A3S7WRL4
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0005215 | transporter activity | 1 | 43 | 
| GO:0022857 | transmembrane transporter activity | 2 | 43 | 
| Leishmania | From | To | Domain/Motif | Score | 
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 607 | 611 | PF00656 | 0.570 | 
| CLV_NRD_NRD_1 | 166 | 168 | PF00675 | 0.359 | 
| CLV_NRD_NRD_1 | 39 | 41 | PF00675 | 0.267 | 
| CLV_NRD_NRD_1 | 425 | 427 | PF00675 | 0.368 | 
| CLV_NRD_NRD_1 | 565 | 567 | PF00675 | 0.336 | 
| CLV_NRD_NRD_1 | 572 | 574 | PF00675 | 0.362 | 
| CLV_NRD_NRD_1 | 617 | 619 | PF00675 | 0.586 | 
| CLV_PCSK_KEX2_1 | 166 | 168 | PF00082 | 0.374 | 
| CLV_PCSK_KEX2_1 | 39 | 41 | PF00082 | 0.324 | 
| CLV_PCSK_KEX2_1 | 425 | 427 | PF00082 | 0.350 | 
| CLV_PCSK_KEX2_1 | 565 | 567 | PF00082 | 0.333 | 
| CLV_PCSK_KEX2_1 | 571 | 573 | PF00082 | 0.341 | 
| CLV_PCSK_PC1ET2_1 | 425 | 427 | PF00082 | 0.371 | 
| CLV_PCSK_SKI1_1 | 284 | 288 | PF00082 | 0.600 | 
| CLV_PCSK_SKI1_1 | 458 | 462 | PF00082 | 0.526 | 
| CLV_PCSK_SKI1_1 | 565 | 569 | PF00082 | 0.344 | 
| DEG_APCC_DBOX_1 | 39 | 47 | PF00400 | 0.477 | 
| DEG_Kelch_Keap1_1 | 329 | 334 | PF01344 | 0.729 | 
| DEG_MDM2_SWIB_1 | 498 | 506 | PF02201 | 0.415 | 
| DOC_CKS1_1 | 194 | 199 | PF01111 | 0.190 | 
| DOC_CYCLIN_yClb5_NLxxxL_5 | 542 | 551 | PF00134 | 0.215 | 
| DOC_CYCLIN_yCln2_LP_2 | 194 | 200 | PF00134 | 0.384 | 
| DOC_MAPK_gen_1 | 166 | 173 | PF00069 | 0.527 | 
| DOC_MAPK_gen_1 | 39 | 46 | PF00069 | 0.472 | 
| DOC_MAPK_gen_1 | 425 | 434 | PF00069 | 0.548 | 
| DOC_MAPK_gen_1 | 520 | 530 | PF00069 | 0.417 | 
| DOC_MAPK_MEF2A_6 | 258 | 267 | PF00069 | 0.487 | 
| DOC_MAPK_MEF2A_6 | 427 | 436 | PF00069 | 0.546 | 
| DOC_MAPK_MEF2A_6 | 532 | 541 | PF00069 | 0.313 | 
| DOC_PP2B_LxvP_1 | 453 | 456 | PF13499 | 0.420 | 
| DOC_PP4_FxxP_1 | 438 | 441 | PF00568 | 0.421 | 
| DOC_PP4_FxxP_1 | 91 | 94 | PF00568 | 0.324 | 
| DOC_SPAK_OSR1_1 | 136 | 140 | PF12202 | 0.321 | 
| DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.353 | 
| DOC_USP7_MATH_1 | 456 | 460 | PF00917 | 0.408 | 
| DOC_USP7_MATH_1 | 465 | 469 | PF00917 | 0.330 | 
| DOC_USP7_MATH_1 | 54 | 58 | PF00917 | 0.329 | 
| DOC_USP7_MATH_1 | 580 | 584 | PF00917 | 0.690 | 
| DOC_USP7_MATH_1 | 601 | 605 | PF00917 | 0.666 | 
| DOC_USP7_UBL2_3 | 488 | 492 | PF12436 | 0.477 | 
| DOC_WW_Pin1_4 | 193 | 198 | PF00397 | 0.337 | 
| DOC_WW_Pin1_4 | 378 | 383 | PF00397 | 0.419 | 
| DOC_WW_Pin1_4 | 387 | 392 | PF00397 | 0.393 | 
| LIG_14-3-3_CanoR_1 | 233 | 241 | PF00244 | 0.546 | 
| LIG_14-3-3_CanoR_1 | 318 | 324 | PF00244 | 0.586 | 
| LIG_14-3-3_CanoR_1 | 33 | 41 | PF00244 | 0.550 | 
| LIG_14-3-3_CanoR_1 | 413 | 419 | PF00244 | 0.306 | 
| LIG_14-3-3_CanoR_1 | 431 | 437 | PF00244 | 0.417 | 
| LIG_14-3-3_CanoR_1 | 76 | 84 | PF00244 | 0.334 | 
| LIG_Actin_WH2_2 | 560 | 577 | PF00022 | 0.623 | 
| LIG_BRCT_BRCA1_1 | 147 | 151 | PF00533 | 0.413 | 
| LIG_BRCT_BRCA1_1 | 380 | 384 | PF00533 | 0.385 | 
| LIG_BRCT_BRCA1_1 | 56 | 60 | PF00533 | 0.370 | 
| LIG_FHA_1 | 274 | 280 | PF00498 | 0.339 | 
| LIG_FHA_1 | 346 | 352 | PF00498 | 0.509 | 
| LIG_FHA_1 | 354 | 360 | PF00498 | 0.493 | 
| LIG_FHA_1 | 388 | 394 | PF00498 | 0.383 | 
| LIG_FHA_1 | 440 | 446 | PF00498 | 0.344 | 
| LIG_FHA_1 | 448 | 454 | PF00498 | 0.334 | 
| LIG_FHA_1 | 476 | 482 | PF00498 | 0.306 | 
| LIG_FHA_1 | 546 | 552 | PF00498 | 0.392 | 
| LIG_FHA_2 | 335 | 341 | PF00498 | 0.517 | 
| LIG_FHA_2 | 95 | 101 | PF00498 | 0.470 | 
| LIG_GBD_Chelix_1 | 170 | 178 | PF00786 | 0.430 | 
| LIG_GBD_Chelix_1 | 265 | 273 | PF00786 | 0.315 | 
| LIG_GBD_Chelix_1 | 503 | 511 | PF00786 | 0.387 | 
| LIG_IRF3_LxIS_1 | 554 | 559 | PF10401 | 0.520 | 
| LIG_LIR_Apic_2 | 100 | 104 | PF02991 | 0.470 | 
| LIG_LIR_Apic_2 | 338 | 344 | PF02991 | 0.510 | 
| LIG_LIR_Apic_2 | 435 | 441 | PF02991 | 0.384 | 
| LIG_LIR_Gen_1 | 303 | 314 | PF02991 | 0.360 | 
| LIG_LIR_Gen_1 | 358 | 367 | PF02991 | 0.345 | 
| LIG_LIR_Gen_1 | 373 | 382 | PF02991 | 0.373 | 
| LIG_LIR_Gen_1 | 450 | 460 | PF02991 | 0.338 | 
| LIG_LIR_Gen_1 | 48 | 54 | PF02991 | 0.327 | 
| LIG_LIR_Gen_1 | 552 | 563 | PF02991 | 0.363 | 
| LIG_LIR_Gen_1 | 57 | 67 | PF02991 | 0.353 | 
| LIG_LIR_Gen_1 | 97 | 107 | PF02991 | 0.422 | 
| LIG_LIR_Nem_3 | 125 | 129 | PF02991 | 0.263 | 
| LIG_LIR_Nem_3 | 358 | 363 | PF02991 | 0.311 | 
| LIG_LIR_Nem_3 | 365 | 370 | PF02991 | 0.310 | 
| LIG_LIR_Nem_3 | 373 | 377 | PF02991 | 0.337 | 
| LIG_LIR_Nem_3 | 381 | 387 | PF02991 | 0.340 | 
| LIG_LIR_Nem_3 | 417 | 422 | PF02991 | 0.552 | 
| LIG_LIR_Nem_3 | 450 | 455 | PF02991 | 0.260 | 
| LIG_LIR_Nem_3 | 48 | 52 | PF02991 | 0.351 | 
| LIG_LIR_Nem_3 | 552 | 558 | PF02991 | 0.325 | 
| LIG_LIR_Nem_3 | 559 | 563 | PF02991 | 0.481 | 
| LIG_LIR_Nem_3 | 57 | 63 | PF02991 | 0.336 | 
| LIG_LIR_Nem_3 | 97 | 102 | PF02991 | 0.372 | 
| LIG_NRBOX | 116 | 122 | PF00104 | 0.285 | 
| LIG_NRBOX | 507 | 513 | PF00104 | 0.304 | 
| LIG_NRBOX | 546 | 552 | PF00104 | 0.476 | 
| LIG_PAM2_1 | 192 | 204 | PF00658 | 0.190 | 
| LIG_Pex14_2 | 374 | 378 | PF04695 | 0.373 | 
| LIG_Pex14_2 | 498 | 502 | PF04695 | 0.398 | 
| LIG_SH2_CRK | 41 | 45 | PF00017 | 0.328 | 
| LIG_SH2_CRK | 95 | 99 | PF00017 | 0.329 | 
| LIG_SH2_PTP2 | 341 | 344 | PF00017 | 0.503 | 
| LIG_SH2_SRC | 555 | 558 | PF00017 | 0.476 | 
| LIG_SH2_SRC | 600 | 603 | PF00017 | 0.775 | 
| LIG_SH2_STAP1 | 58 | 62 | PF00017 | 0.358 | 
| LIG_SH2_STAT3 | 249 | 252 | PF00017 | 0.478 | 
| LIG_SH2_STAT5 | 101 | 104 | PF00017 | 0.491 | 
| LIG_SH2_STAT5 | 108 | 111 | PF00017 | 0.331 | 
| LIG_SH2_STAT5 | 200 | 203 | PF00017 | 0.331 | 
| LIG_SH2_STAT5 | 249 | 252 | PF00017 | 0.499 | 
| LIG_SH2_STAT5 | 260 | 263 | PF00017 | 0.316 | 
| LIG_SH2_STAT5 | 272 | 275 | PF00017 | 0.315 | 
| LIG_SH2_STAT5 | 341 | 344 | PF00017 | 0.509 | 
| LIG_SH2_STAT5 | 422 | 425 | PF00017 | 0.555 | 
| LIG_SH2_STAT5 | 555 | 558 | PF00017 | 0.332 | 
| LIG_SH2_STAT5 | 90 | 93 | PF00017 | 0.308 | 
| LIG_SH3_2 | 586 | 591 | PF14604 | 0.770 | 
| LIG_SH3_3 | 268 | 274 | PF00018 | 0.329 | 
| LIG_SH3_3 | 308 | 314 | PF00018 | 0.372 | 
| LIG_SH3_3 | 532 | 538 | PF00018 | 0.327 | 
| LIG_SH3_3 | 583 | 589 | PF00018 | 0.678 | 
| LIG_SUMO_SIM_anti_2 | 262 | 267 | PF11976 | 0.378 | 
| LIG_SUMO_SIM_anti_2 | 442 | 448 | PF11976 | 0.320 | 
| LIG_SUMO_SIM_anti_2 | 476 | 481 | PF11976 | 0.341 | 
| LIG_SUMO_SIM_par_1 | 142 | 148 | PF11976 | 0.341 | 
| LIG_SUMO_SIM_par_1 | 206 | 211 | PF11976 | 0.370 | 
| LIG_SUMO_SIM_par_1 | 42 | 48 | PF11976 | 0.436 | 
| LIG_SUMO_SIM_par_1 | 442 | 448 | PF11976 | 0.323 | 
| LIG_SUMO_SIM_par_1 | 478 | 484 | PF11976 | 0.294 | 
| LIG_TRFH_1 | 90 | 94 | PF08558 | 0.372 | 
| LIG_TYR_ITIM | 93 | 98 | PF00017 | 0.346 | 
| LIG_UBA3_1 | 383 | 392 | PF00899 | 0.401 | 
| LIG_WRC_WIRS_1 | 46 | 51 | PF05994 | 0.420 | 
| MOD_CDK_SPK_2 | 387 | 392 | PF00069 | 0.261 | 
| MOD_CK1_1 | 145 | 151 | PF00069 | 0.361 | 
| MOD_CK1_1 | 187 | 193 | PF00069 | 0.385 | 
| MOD_CK1_1 | 232 | 238 | PF00069 | 0.618 | 
| MOD_CK1_1 | 329 | 335 | PF00069 | 0.650 | 
| MOD_CK1_1 | 353 | 359 | PF00069 | 0.511 | 
| MOD_CK1_1 | 385 | 391 | PF00069 | 0.371 | 
| MOD_CK1_1 | 561 | 567 | PF00069 | 0.564 | 
| MOD_CK1_1 | 604 | 610 | PF00069 | 0.761 | 
| MOD_CK2_1 | 15 | 21 | PF00069 | 0.637 | 
| MOD_CK2_1 | 414 | 420 | PF00069 | 0.377 | 
| MOD_CK2_1 | 5 | 11 | PF00069 | 0.624 | 
| MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.326 | 
| MOD_GlcNHglycan | 276 | 279 | PF01048 | 0.343 | 
| MOD_GlcNHglycan | 326 | 331 | PF01048 | 0.479 | 
| MOD_GlcNHglycan | 384 | 387 | PF01048 | 0.526 | 
| MOD_GlcNHglycan | 397 | 400 | PF01048 | 0.331 | 
| MOD_GlcNHglycan | 408 | 411 | PF01048 | 0.283 | 
| MOD_GlcNHglycan | 603 | 606 | PF01048 | 0.504 | 
| MOD_GlcNHglycan | 63 | 66 | PF01048 | 0.473 | 
| MOD_GSK3_1 | 158 | 165 | PF00069 | 0.346 | 
| MOD_GSK3_1 | 220 | 227 | PF00069 | 0.511 | 
| MOD_GSK3_1 | 346 | 353 | PF00069 | 0.536 | 
| MOD_GSK3_1 | 378 | 385 | PF00069 | 0.377 | 
| MOD_GSK3_1 | 395 | 402 | PF00069 | 0.295 | 
| MOD_GSK3_1 | 545 | 552 | PF00069 | 0.388 | 
| MOD_GSK3_1 | 604 | 611 | PF00069 | 0.725 | 
| MOD_GSK3_1 | 72 | 79 | PF00069 | 0.279 | 
| MOD_N-GLC_1 | 378 | 383 | PF02516 | 0.584 | 
| MOD_N-GLC_1 | 545 | 550 | PF02516 | 0.292 | 
| MOD_NEK2_1 | 122 | 127 | PF00069 | 0.302 | 
| MOD_NEK2_1 | 173 | 178 | PF00069 | 0.395 | 
| MOD_NEK2_1 | 259 | 264 | PF00069 | 0.355 | 
| MOD_NEK2_1 | 27 | 32 | PF00069 | 0.579 | 
| MOD_NEK2_1 | 350 | 355 | PF00069 | 0.508 | 
| MOD_NEK2_1 | 393 | 398 | PF00069 | 0.358 | 
| MOD_NEK2_1 | 414 | 419 | PF00069 | 0.383 | 
| MOD_NEK2_1 | 447 | 452 | PF00069 | 0.301 | 
| MOD_NEK2_1 | 473 | 478 | PF00069 | 0.338 | 
| MOD_NEK2_1 | 545 | 550 | PF00069 | 0.339 | 
| MOD_NEK2_1 | 556 | 561 | PF00069 | 0.331 | 
| MOD_NEK2_1 | 63 | 68 | PF00069 | 0.276 | 
| MOD_NEK2_2 | 94 | 99 | PF00069 | 0.487 | 
| MOD_PIKK_1 | 145 | 151 | PF00454 | 0.415 | 
| MOD_PIKK_1 | 248 | 254 | PF00454 | 0.541 | 
| MOD_PIKK_1 | 285 | 291 | PF00454 | 0.359 | 
| MOD_PIKK_1 | 420 | 426 | PF00454 | 0.532 | 
| MOD_PKA_2 | 232 | 238 | PF00069 | 0.521 | 
| MOD_PKA_2 | 317 | 323 | PF00069 | 0.563 | 
| MOD_PKA_2 | 561 | 567 | PF00069 | 0.499 | 
| MOD_Plk_1 | 393 | 399 | PF00069 | 0.346 | 
| MOD_Plk_1 | 545 | 551 | PF00069 | 0.311 | 
| MOD_Plk_2-3 | 334 | 340 | PF00069 | 0.608 | 
| MOD_Plk_2-3 | 5 | 11 | PF00069 | 0.492 | 
| MOD_Plk_4 | 130 | 136 | PF00069 | 0.277 | 
| MOD_Plk_4 | 152 | 158 | PF00069 | 0.320 | 
| MOD_Plk_4 | 173 | 179 | PF00069 | 0.365 | 
| MOD_Plk_4 | 346 | 352 | PF00069 | 0.513 | 
| MOD_Plk_4 | 355 | 361 | PF00069 | 0.478 | 
| MOD_Plk_4 | 399 | 405 | PF00069 | 0.316 | 
| MOD_Plk_4 | 414 | 420 | PF00069 | 0.337 | 
| MOD_Plk_4 | 440 | 446 | PF00069 | 0.330 | 
| MOD_Plk_4 | 447 | 453 | PF00069 | 0.321 | 
| MOD_Plk_4 | 94 | 100 | PF00069 | 0.381 | 
| MOD_ProDKin_1 | 193 | 199 | PF00069 | 0.337 | 
| MOD_ProDKin_1 | 378 | 384 | PF00069 | 0.415 | 
| MOD_ProDKin_1 | 387 | 393 | PF00069 | 0.390 | 
| MOD_SUMO_rev_2 | 232 | 241 | PF00179 | 0.555 | 
| TRG_DiLeu_BaLyEn_6 | 507 | 512 | PF01217 | 0.329 | 
| TRG_DiLeu_BaLyEn_6 | 535 | 540 | PF01217 | 0.319 | 
| TRG_ENDOCYTIC_2 | 200 | 203 | PF00928 | 0.302 | 
| TRG_ENDOCYTIC_2 | 260 | 263 | PF00928 | 0.376 | 
| TRG_ENDOCYTIC_2 | 41 | 44 | PF00928 | 0.296 | 
| TRG_ENDOCYTIC_2 | 555 | 558 | PF00928 | 0.378 | 
| TRG_ENDOCYTIC_2 | 560 | 563 | PF00928 | 0.513 | 
| TRG_ENDOCYTIC_2 | 90 | 93 | PF00928 | 0.317 | 
| TRG_ENDOCYTIC_2 | 95 | 98 | PF00928 | 0.330 | 
| TRG_ENDOCYTIC_2 | 99 | 102 | PF00928 | 0.489 | 
| TRG_ER_diArg_1 | 39 | 41 | PF00400 | 0.441 | 
| TRG_ER_diArg_1 | 565 | 567 | PF00400 | 0.548 | 
| TRG_ER_diArg_1 | 571 | 573 | PF00400 | 0.556 | 
| TRG_NLS_MonoCore_2 | 617 | 622 | PF00514 | 0.581 | 
| TRG_Pf-PMV_PEXEL_1 | 33 | 37 | PF00026 | 0.412 | 
| TRG_Pf-PMV_PEXEL_1 | 510 | 515 | PF00026 | 0.414 | 
| TRG_Pf-PMV_PEXEL_1 | 566 | 570 | PF00026 | 0.357 | 
| TRG_Pf-PMV_PEXEL_1 | 572 | 576 | PF00026 | 0.385 | 
| Protein | Taxonomy | Sequence identity | Coverage | 
|---|---|---|---|
| A0A0N0P6G0 | Leptomonas seymouri | 38% | 98% | 
| A0A0N1HT40 | Leptomonas seymouri | 74% | 100% | 
| A0A0N1HZC2 | Leptomonas seymouri | 28% | 99% | 
| A0A0N1IKC5 | Leptomonas seymouri | 47% | 100% | 
| A0A0N1PB63 | Leptomonas seymouri | 27% | 94% | 
| A0A0S4IIJ4 | Bodo saltans | 22% | 100% | 
| A0A0S4JR45 | Bodo saltans | 33% | 100% | 
| A0A1X0NKK0 | Trypanosomatidae | 33% | 100% | 
| A0A1X0NL32 | Trypanosomatidae | 34% | 99% | 
| A0A1X0NM09 | Trypanosomatidae | 31% | 100% | 
| A0A1X0NRW5 | Trypanosomatidae | 40% | 89% | 
| A0A1X0NV13 | Trypanosomatidae | 49% | 96% | 
| A0A1X0NV19 | Trypanosomatidae | 48% | 100% | 
| A0A1X0NV27 | Trypanosomatidae | 49% | 100% | 
| A0A1X0NVH8 | Trypanosomatidae | 45% | 94% | 
| A0A1X0NVM7 | Trypanosomatidae | 53% | 96% | 
| A0A1X0NWQ1 | Trypanosomatidae | 44% | 97% | 
| A0A1X0NZE6 | Trypanosomatidae | 33% | 100% | 
| A0A1X0NZU2 | Trypanosomatidae | 28% | 96% | 
| A0A1X0NZU5 | Trypanosomatidae | 34% | 100% | 
| A0A1X0NZW1 | Trypanosomatidae | 29% | 100% | 
| A0A1X0P0M7 | Trypanosomatidae | 32% | 100% | 
| A0A3Q8I7Y9 | Leishmania donovani | 100% | 100% | 
| A0A3Q8IF95 | Leishmania donovani | 29% | 100% | 
| A0A3Q8ISY9 | Leishmania donovani | 38% | 100% | 
| A0A3R7JSQ9 | Trypanosoma rangeli | 29% | 100% | 
| A0A3R7KKN8 | Trypanosoma rangeli | 30% | 100% | 
| A0A3R7MAQ7 | Trypanosoma rangeli | 35% | 88% | 
| A0A3R7N415 | Trypanosoma rangeli | 30% | 100% | 
| A0A3R7N921 | Trypanosoma rangeli | 28% | 100% | 
| A0A3R7R443 | Trypanosoma rangeli | 29% | 100% | 
| A0A3S7WRJ4 | Leishmania donovani | 46% | 98% | 
| A0A3S7WRJ5 | Leishmania donovani | 40% | 100% | 
| A0A3S7WSR4 | Leishmania donovani | 45% | 100% | 
| A0A3S7WWU1 | Leishmania donovani | 28% | 94% | 
| A0A3S7XB11 | Leishmania donovani | 29% | 100% | 
| A0A422MSE4 | Trypanosoma rangeli | 48% | 100% | 
| A0A422MSP6 | Trypanosoma rangeli | 34% | 100% | 
| A0A422MST9 | Trypanosoma rangeli | 29% | 100% | 
| A0A422MU68 | Trypanosoma rangeli | 27% | 100% | 
| A4H6J0 | Leishmania braziliensis | 45% | 100% | 
| A4H6J1 | Leishmania braziliensis | 45% | 100% | 
| A4H6J3 | Leishmania braziliensis | 84% | 100% | 
| A4HC19 | Leishmania braziliensis | 27% | 100% | 
| A4HJW3 | Leishmania braziliensis | 38% | 100% | 
| A4HPE2 | Leishmania braziliensis | 29% | 100% | 
| A4HUX5 | Leishmania infantum | 46% | 98% | 
| A4HUX6 | Leishmania infantum | 41% | 100% | 
| A4HUX7 | Leishmania infantum | 99% | 100% | 
| A4HUX8 | Leishmania infantum | 97% | 100% | 
| A4HZF5 | Leishmania infantum | 29% | 100% | 
| A4HZJ4 | Leishmania infantum | 27% | 100% | 
| A4I7C5 | Leishmania infantum | 38% | 100% | 
| A4ICI3 | Leishmania infantum | 29% | 100% | 
| C9ZL97 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% | 
| C9ZL98 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% | 
| C9ZL99 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% | 
| C9ZLA0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% | 
| C9ZLA1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% | 
| C9ZTR5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 100% | 
| C9ZTR6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 100% | 
| C9ZTR7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% | 
| C9ZTR8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 100% | 
| C9ZTR9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 100% | 
| C9ZTS1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 100% | 
| C9ZUT6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% | 
| D0A7H1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% | 
| D0AAQ2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 91% | 
| E8NHE1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 44% | 100% | 
| E9AGK5 | Leishmania infantum | 45% | 100% | 
| E9ANL0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 46% | 100% | 
| E9ANL1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 44% | 100% | 
| E9ANL2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% | 
| E9APJ3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 45% | 100% | 
| E9AT53 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% | 
| E9AVF1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% | 
| E9AVF2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% | 
| E9B2B8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 100% | 
| Q4Q1E4 | Leishmania major | 29% | 100% | 
| Q4Q5T8 | Leishmania major | 37% | 100% | 
| Q4QC27 | Leishmania major | 28% | 100% | 
| Q4QC28 | Leishmania major | 31% | 100% | 
| Q4QFY5 | Leishmania major | 45% | 100% | 
| Q4QH10 | Leishmania major | 96% | 100% | 
| Q4QH11 | Leishmania major | 97% | 100% | 
| Q4QH12 | Leishmania major | 97% | 100% | 
| Q4QH13 | Leishmania major | 97% | 100% | 
| Q4QH14 | Leishmania major | 41% | 100% | 
| Q4QH15 | Leishmania major | 47% | 100% | 
| V5B647 | Trypanosoma cruzi | 46% | 99% | 
| V5B983 | Trypanosoma cruzi | 33% | 100% | 
| V5BBB1 | Trypanosoma cruzi | 45% | 100% | 
| V5BFV8 | Trypanosoma cruzi | 30% | 93% | 
| V5BQY6 | Trypanosoma cruzi | 38% | 88% | 
| V5BVP0 | Trypanosoma cruzi | 47% | 100% | 
| V5DT25 | Trypanosoma cruzi | 57% | 100% |