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: 3 |
| Silverman et al. | no | yes: 0 |
| Pissara et al. | no | yes: 36 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| Pires et al. | no | yes: 0 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| Silverman et al. | no | yes: 6 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| Jamdhade et al. | no | yes: 0 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| DeepLoc | ||
| SignalP6 | no | yes: 0, no: 121 |
| NetGPI | no | yes: 0, no: 121 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0016020 | membrane | 2 | 114 |
| GO:0110165 | cellular anatomical entity | 1 | 114 |
| GO:0005737 | cytoplasm | 2 | 3 |
Related structures:
AlphaFold database: A0A3Q8ISY9
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005215 | transporter activity | 1 | 55 |
| GO:0022857 | transmembrane transporter activity | 2 | 55 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_NRD_NRD_1 | 12 | 14 | PF00675 | 0.511 |
| CLV_NRD_NRD_1 | 256 | 258 | PF00675 | 0.261 |
| CLV_NRD_NRD_1 | 341 | 343 | PF00675 | 0.543 |
| CLV_NRD_NRD_1 | 459 | 461 | PF00675 | 0.387 |
| CLV_PCSK_KEX2_1 | 12 | 14 | PF00082 | 0.501 |
| CLV_PCSK_KEX2_1 | 256 | 258 | PF00082 | 0.276 |
| CLV_PCSK_KEX2_1 | 341 | 343 | PF00082 | 0.532 |
| CLV_PCSK_KEX2_1 | 459 | 461 | PF00082 | 0.372 |
| CLV_PCSK_PC1ET2_1 | 459 | 461 | PF00082 | 0.372 |
| CLV_PCSK_SKI1_1 | 104 | 108 | PF00082 | 0.236 |
| CLV_PCSK_SKI1_1 | 231 | 235 | PF00082 | 0.304 |
| CLV_PCSK_SKI1_1 | 256 | 260 | PF00082 | 0.241 |
| CLV_PCSK_SKI1_1 | 289 | 293 | PF00082 | 0.479 |
| CLV_PCSK_SKI1_1 | 30 | 34 | PF00082 | 0.409 |
| CLV_PCSK_SKI1_1 | 341 | 345 | PF00082 | 0.347 |
| CLV_PCSK_SKI1_1 | 363 | 367 | PF00082 | 0.446 |
| DOC_CYCLIN_yCln2_LP_2 | 284 | 290 | PF00134 | 0.282 |
| DOC_MAPK_gen_1 | 256 | 265 | PF00069 | 0.451 |
| DOC_MAPK_gen_1 | 459 | 468 | PF00069 | 0.553 |
| DOC_MAPK_MEF2A_6 | 259 | 267 | PF00069 | 0.327 |
| DOC_MAPK_MEF2A_6 | 39 | 47 | PF00069 | 0.488 |
| DOC_MAPK_MEF2A_6 | 461 | 470 | PF00069 | 0.550 |
| DOC_MAPK_MEF2A_6 | 491 | 498 | PF00069 | 0.383 |
| DOC_MAPK_MEF2A_6 | 566 | 573 | PF00069 | 0.295 |
| DOC_PP1_RVXF_1 | 287 | 293 | PF00149 | 0.269 |
| DOC_PP2B_LxvP_1 | 472 | 475 | PF13499 | 0.281 |
| DOC_SPAK_OSR1_1 | 135 | 139 | PF12202 | 0.308 |
| DOC_USP7_MATH_1 | 273 | 277 | PF00917 | 0.355 |
| DOC_USP7_MATH_1 | 336 | 340 | PF00917 | 0.706 |
| DOC_USP7_MATH_1 | 420 | 424 | PF00917 | 0.407 |
| DOC_USP7_MATH_1 | 574 | 578 | PF00917 | 0.414 |
| DOC_USP7_MATH_1 | 611 | 615 | PF00917 | 0.683 |
| DOC_USP7_UBL2_3 | 241 | 245 | PF12436 | 0.374 |
| DOC_USP7_UBL2_3 | 553 | 557 | PF12436 | 0.399 |
| DOC_WW_Pin1_4 | 251 | 256 | PF00397 | 0.512 |
| DOC_WW_Pin1_4 | 425 | 430 | PF00397 | 0.391 |
| DOC_WW_Pin1_4 | 612 | 617 | PF00397 | 0.698 |
| LIG_14-3-3_CanoR_1 | 19 | 26 | PF00244 | 0.653 |
| LIG_14-3-3_CanoR_1 | 341 | 349 | PF00244 | 0.765 |
| LIG_14-3-3_CanoR_1 | 352 | 360 | PF00244 | 0.695 |
| LIG_14-3-3_CanoR_1 | 612 | 616 | PF00244 | 0.668 |
| LIG_Actin_WH2_2 | 594 | 611 | PF00022 | 0.635 |
| LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.639 |
| LIG_BIR_III_4 | 127 | 131 | PF00653 | 0.160 |
| LIG_BRCT_BRCA1_1 | 180 | 184 | PF00533 | 0.469 |
| LIG_deltaCOP1_diTrp_1 | 492 | 498 | PF00928 | 0.206 |
| LIG_EH1_1 | 106 | 114 | PF00400 | 0.369 |
| LIG_EH1_1 | 149 | 157 | PF00400 | 0.307 |
| LIG_eIF4E_1 | 101 | 107 | PF01652 | 0.519 |
| LIG_FHA_1 | 29 | 35 | PF00498 | 0.643 |
| LIG_FHA_1 | 294 | 300 | PF00498 | 0.374 |
| LIG_FHA_1 | 389 | 395 | PF00498 | 0.501 |
| LIG_FHA_1 | 405 | 411 | PF00498 | 0.319 |
| LIG_FHA_1 | 426 | 432 | PF00498 | 0.334 |
| LIG_FHA_1 | 467 | 473 | PF00498 | 0.479 |
| LIG_FHA_2 | 224 | 230 | PF00498 | 0.426 |
| LIG_FHA_2 | 232 | 238 | PF00498 | 0.420 |
| LIG_FHA_2 | 31 | 37 | PF00498 | 0.644 |
| LIG_GBD_Chelix_1 | 264 | 272 | PF00786 | 0.306 |
| LIG_IRF3_LxIS_1 | 466 | 471 | PF10401 | 0.374 |
| LIG_LIR_Apic_2 | 99 | 103 | PF02991 | 0.472 |
| LIG_LIR_Gen_1 | 137 | 145 | PF02991 | 0.333 |
| LIG_LIR_Gen_1 | 204 | 213 | PF02991 | 0.342 |
| LIG_LIR_Gen_1 | 383 | 394 | PF02991 | 0.511 |
| LIG_LIR_Gen_1 | 492 | 500 | PF02991 | 0.168 |
| LIG_LIR_Gen_1 | 56 | 66 | PF02991 | 0.342 |
| LIG_LIR_Gen_1 | 582 | 592 | PF02991 | 0.333 |
| LIG_LIR_Nem_3 | 137 | 142 | PF02991 | 0.295 |
| LIG_LIR_Nem_3 | 175 | 179 | PF02991 | 0.334 |
| LIG_LIR_Nem_3 | 181 | 187 | PF02991 | 0.343 |
| LIG_LIR_Nem_3 | 197 | 203 | PF02991 | 0.261 |
| LIG_LIR_Nem_3 | 204 | 209 | PF02991 | 0.306 |
| LIG_LIR_Nem_3 | 383 | 389 | PF02991 | 0.522 |
| LIG_LIR_Nem_3 | 492 | 496 | PF02991 | 0.392 |
| LIG_LIR_Nem_3 | 56 | 62 | PF02991 | 0.347 |
| LIG_LIR_Nem_3 | 582 | 588 | PF02991 | 0.342 |
| LIG_PCNA_yPIPBox_3 | 275 | 289 | PF02747 | 0.239 |
| LIG_Pex14_1 | 395 | 399 | PF04695 | 0.339 |
| LIG_Pex14_2 | 121 | 125 | PF04695 | 0.238 |
| LIG_Pex14_2 | 202 | 206 | PF04695 | 0.370 |
| LIG_Pex14_2 | 258 | 262 | PF04695 | 0.332 |
| LIG_Pex14_2 | 581 | 585 | PF04695 | 0.350 |
| LIG_PTB_Apo_2 | 411 | 418 | PF02174 | 0.296 |
| LIG_Rb_pABgroove_1 | 92 | 100 | PF01858 | 0.385 |
| LIG_RPA_C_Fungi | 337 | 349 | PF08784 | 0.663 |
| LIG_SH2_CRK | 260 | 264 | PF00017 | 0.381 |
| LIG_SH2_CRK | 281 | 285 | PF00017 | 0.384 |
| LIG_SH2_CRK | 303 | 307 | PF00017 | 0.465 |
| LIG_SH2_CRK | 48 | 52 | PF00017 | 0.283 |
| LIG_SH2_NCK_1 | 419 | 423 | PF00017 | 0.392 |
| LIG_SH2_PTP2 | 589 | 592 | PF00017 | 0.333 |
| LIG_SH2_SRC | 8 | 11 | PF00017 | 0.627 |
| LIG_SH2_STAP1 | 228 | 232 | PF00017 | 0.433 |
| LIG_SH2_STAP1 | 520 | 524 | PF00017 | 0.369 |
| LIG_SH2_STAP1 | 551 | 555 | PF00017 | 0.328 |
| LIG_SH2_STAT5 | 201 | 204 | PF00017 | 0.305 |
| LIG_SH2_STAT5 | 232 | 235 | PF00017 | 0.319 |
| LIG_SH2_STAT5 | 248 | 251 | PF00017 | 0.319 |
| LIG_SH2_STAT5 | 303 | 306 | PF00017 | 0.314 |
| LIG_SH2_STAT5 | 551 | 554 | PF00017 | 0.357 |
| LIG_SH2_STAT5 | 57 | 60 | PF00017 | 0.331 |
| LIG_SH2_STAT5 | 589 | 592 | PF00017 | 0.328 |
| LIG_SH3_3 | 215 | 221 | PF00018 | 0.292 |
| LIG_SH3_3 | 249 | 255 | PF00018 | 0.325 |
| LIG_SH3_3 | 267 | 273 | PF00018 | 0.304 |
| LIG_SH3_3 | 87 | 93 | PF00018 | 0.381 |
| LIG_SUMO_SIM_anti_2 | 476 | 481 | PF11976 | 0.300 |
| LIG_SUMO_SIM_anti_2 | 483 | 488 | PF11976 | 0.282 |
| LIG_SUMO_SIM_anti_2 | 511 | 518 | PF11976 | 0.317 |
| LIG_SUMO_SIM_par_1 | 29 | 36 | PF11976 | 0.516 |
| LIG_SUMO_SIM_par_1 | 466 | 471 | PF11976 | 0.238 |
| LIG_TRAF2_1 | 14 | 17 | PF00917 | 0.672 |
| LIG_TYR_ITIM | 279 | 284 | PF00017 | 0.338 |
| LIG_UBA3_1 | 484 | 491 | PF00899 | 0.366 |
| LIG_WRC_WIRS_1 | 173 | 178 | PF05994 | 0.363 |
| LIG_WRC_WIRS_1 | 495 | 500 | PF05994 | 0.174 |
| MOD_CDC14_SPxK_1 | 254 | 257 | PF00782 | 0.387 |
| MOD_CDK_SPK_2 | 251 | 256 | PF00069 | 0.433 |
| MOD_CDK_SPxK_1 | 251 | 257 | PF00069 | 0.387 |
| MOD_CK1_1 | 388 | 394 | PF00069 | 0.364 |
| MOD_CK1_1 | 400 | 406 | PF00069 | 0.382 |
| MOD_CK1_1 | 433 | 439 | PF00069 | 0.346 |
| MOD_CK1_1 | 508 | 514 | PF00069 | 0.373 |
| MOD_CK1_1 | 532 | 538 | PF00069 | 0.350 |
| MOD_CK1_1 | 583 | 589 | PF00069 | 0.361 |
| MOD_CK1_1 | 78 | 84 | PF00069 | 0.327 |
| MOD_CK2_1 | 11 | 17 | PF00069 | 0.574 |
| MOD_CK2_1 | 223 | 229 | PF00069 | 0.272 |
| MOD_CK2_1 | 231 | 237 | PF00069 | 0.264 |
| MOD_CK2_1 | 30 | 36 | PF00069 | 0.489 |
| MOD_CK2_1 | 356 | 362 | PF00069 | 0.581 |
| MOD_CK2_1 | 367 | 373 | PF00069 | 0.514 |
| MOD_CK2_1 | 381 | 387 | PF00069 | 0.377 |
| MOD_CK2_1 | 448 | 454 | PF00069 | 0.394 |
| MOD_Cter_Amidation | 10 | 13 | PF01082 | 0.646 |
| MOD_DYRK1A_RPxSP_1 | 612 | 616 | PF00069 | 0.410 |
| MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.364 |
| MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.322 |
| MOD_GlcNHglycan | 203 | 206 | PF01048 | 0.290 |
| MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.333 |
| MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.517 |
| MOD_GlcNHglycan | 372 | 376 | PF01048 | 0.530 |
| MOD_GlcNHglycan | 442 | 445 | PF01048 | 0.314 |
| MOD_GlcNHglycan | 507 | 510 | PF01048 | 0.297 |
| MOD_GlcNHglycan | 576 | 579 | PF01048 | 0.363 |
| MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.302 |
| MOD_GSK3_1 | 11 | 18 | PF00069 | 0.613 |
| MOD_GSK3_1 | 157 | 164 | PF00069 | 0.335 |
| MOD_GSK3_1 | 26 | 33 | PF00069 | 0.615 |
| MOD_GSK3_1 | 352 | 359 | PF00069 | 0.669 |
| MOD_GSK3_1 | 367 | 374 | PF00069 | 0.560 |
| MOD_GSK3_1 | 381 | 388 | PF00069 | 0.446 |
| MOD_GSK3_1 | 400 | 407 | PF00069 | 0.316 |
| MOD_GSK3_1 | 494 | 501 | PF00069 | 0.174 |
| MOD_GSK3_1 | 531 | 538 | PF00069 | 0.316 |
| MOD_GSK3_1 | 579 | 586 | PF00069 | 0.366 |
| MOD_GSK3_1 | 611 | 618 | PF00069 | 0.555 |
| MOD_GSK3_1 | 75 | 82 | PF00069 | 0.314 |
| MOD_N-GLC_1 | 194 | 199 | PF02516 | 0.307 |
| MOD_N-GLC_1 | 327 | 332 | PF02516 | 0.734 |
| MOD_N-GLC_1 | 353 | 358 | PF02516 | 0.590 |
| MOD_N-GLC_1 | 70 | 75 | PF02516 | 0.362 |
| MOD_N-GLC_2 | 561 | 563 | PF02516 | 0.440 |
| MOD_NEK2_1 | 371 | 376 | PF00069 | 0.435 |
| MOD_NEK2_1 | 385 | 390 | PF00069 | 0.412 |
| MOD_NEK2_1 | 397 | 402 | PF00069 | 0.281 |
| MOD_NEK2_1 | 468 | 473 | PF00069 | 0.265 |
| MOD_NEK2_1 | 480 | 485 | PF00069 | 0.317 |
| MOD_NEK2_1 | 494 | 499 | PF00069 | 0.174 |
| MOD_NEK2_1 | 531 | 536 | PF00069 | 0.288 |
| MOD_NEK2_1 | 579 | 584 | PF00069 | 0.315 |
| MOD_NEK2_1 | 630 | 635 | PF00069 | 0.684 |
| MOD_NEK2_2 | 134 | 139 | PF00069 | 0.339 |
| MOD_NEK2_2 | 381 | 386 | PF00069 | 0.481 |
| MOD_PIKK_1 | 18 | 24 | PF00454 | 0.659 |
| MOD_PIKK_1 | 404 | 410 | PF00454 | 0.385 |
| MOD_PIKK_1 | 454 | 460 | PF00454 | 0.421 |
| MOD_PIKK_1 | 70 | 76 | PF00454 | 0.283 |
| MOD_PK_1 | 75 | 81 | PF00069 | 0.380 |
| MOD_PKA_1 | 240 | 246 | PF00069 | 0.398 |
| MOD_PKA_1 | 341 | 347 | PF00069 | 0.410 |
| MOD_PKA_2 | 11 | 17 | PF00069 | 0.646 |
| MOD_PKA_2 | 134 | 140 | PF00069 | 0.282 |
| MOD_PKA_2 | 18 | 24 | PF00069 | 0.539 |
| MOD_PKA_2 | 341 | 347 | PF00069 | 0.657 |
| MOD_PKA_2 | 356 | 362 | PF00069 | 0.602 |
| MOD_PKA_2 | 611 | 617 | PF00069 | 0.569 |
| MOD_Plk_4 | 154 | 160 | PF00069 | 0.323 |
| MOD_Plk_4 | 172 | 178 | PF00069 | 0.379 |
| MOD_Plk_4 | 381 | 387 | PF00069 | 0.414 |
| MOD_Plk_4 | 397 | 403 | PF00069 | 0.395 |
| MOD_Plk_4 | 430 | 436 | PF00069 | 0.319 |
| MOD_Plk_4 | 448 | 454 | PF00069 | 0.373 |
| MOD_Plk_4 | 473 | 479 | PF00069 | 0.320 |
| MOD_Plk_4 | 480 | 486 | PF00069 | 0.292 |
| MOD_Plk_4 | 508 | 514 | PF00069 | 0.328 |
| MOD_Plk_4 | 536 | 542 | PF00069 | 0.300 |
| MOD_Plk_4 | 580 | 586 | PF00069 | 0.278 |
| MOD_Plk_4 | 75 | 81 | PF00069 | 0.385 |
| MOD_ProDKin_1 | 251 | 257 | PF00069 | 0.375 |
| MOD_ProDKin_1 | 425 | 431 | PF00069 | 0.482 |
| MOD_ProDKin_1 | 612 | 618 | PF00069 | 0.641 |
| TRG_DiLeu_BaEn_1 | 430 | 435 | PF01217 | 0.307 |
| TRG_DiLeu_BaEn_2 | 625 | 631 | PF01217 | 0.447 |
| TRG_DiLeu_BaEn_4 | 463 | 469 | PF01217 | 0.270 |
| TRG_ENDOCYTIC_2 | 260 | 263 | PF00928 | 0.363 |
| TRG_ENDOCYTIC_2 | 281 | 284 | PF00928 | 0.302 |
| TRG_ENDOCYTIC_2 | 303 | 306 | PF00928 | 0.303 |
| TRG_ENDOCYTIC_2 | 399 | 402 | PF00928 | 0.378 |
| TRG_ENDOCYTIC_2 | 48 | 51 | PF00928 | 0.292 |
| TRG_ENDOCYTIC_2 | 528 | 531 | PF00928 | 0.332 |
| TRG_ENDOCYTIC_2 | 589 | 592 | PF00928 | 0.387 |
| TRG_ENDOCYTIC_2 | 59 | 62 | PF00928 | 0.401 |
| TRG_ENDOCYTIC_2 | 594 | 597 | PF00928 | 0.406 |
| TRG_ER_diArg_1 | 255 | 257 | PF00400 | 0.305 |
| TRG_ER_diArg_1 | 341 | 343 | PF00400 | 0.676 |
| TRG_Pf-PMV_PEXEL_1 | 13 | 17 | PF00026 | 0.708 |
| TRG_Pf-PMV_PEXEL_1 | 231 | 235 | PF00026 | 0.342 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P6G0 | Leptomonas seymouri | 75% | 100% |
| A0A0N1HT40 | Leptomonas seymouri | 40% | 100% |
| A0A0N1HZC2 | Leptomonas seymouri | 26% | 100% |
| A0A0N1IKC5 | Leptomonas seymouri | 40% | 100% |
| A0A0N1PB63 | Leptomonas seymouri | 25% | 96% |
| A0A0N1PFR4 | Leptomonas seymouri | 28% | 96% |
| A0A0S4IIJ4 | Bodo saltans | 22% | 100% |
| A0A0S4JR45 | Bodo saltans | 27% | 100% |
| A0A1X0NKK0 | Trypanosomatidae | 26% | 100% |
| A0A1X0NL32 | Trypanosomatidae | 30% | 100% |
| A0A1X0NM09 | Trypanosomatidae | 24% | 100% |
| A0A1X0NRW5 | Trypanosomatidae | 41% | 91% |
| A0A1X0NV13 | Trypanosomatidae | 43% | 98% |
| A0A1X0NV19 | Trypanosomatidae | 40% | 100% |
| A0A1X0NV27 | Trypanosomatidae | 39% | 100% |
| A0A1X0NVH8 | Trypanosomatidae | 39% | 96% |
| A0A1X0NVM7 | Trypanosomatidae | 41% | 98% |
| A0A1X0NWQ1 | Trypanosomatidae | 42% | 99% |
| A0A1X0NZE6 | Trypanosomatidae | 31% | 100% |
| A0A1X0NZU2 | Trypanosomatidae | 29% | 98% |
| A0A1X0NZU5 | Trypanosomatidae | 31% | 100% |
| A0A1X0NZW1 | Trypanosomatidae | 28% | 100% |
| A0A1X0P0M7 | Trypanosomatidae | 29% | 100% |
| A0A381MMW5 | Leishmania infantum | 27% | 100% |
| A0A3Q8I7Y9 | Leishmania donovani | 38% | 93% |
| A0A3Q8IEC4 | Leishmania donovani | 27% | 100% |
| A0A3Q8IF95 | Leishmania donovani | 26% | 100% |
| A0A3Q8IIT5 | Leishmania donovani | 28% | 94% |
| A0A3R7JSQ9 | Trypanosoma rangeli | 26% | 100% |
| A0A3R7KKN8 | Trypanosoma rangeli | 29% | 100% |
| A0A3R7MAQ7 | Trypanosoma rangeli | 39% | 90% |
| A0A3R7N415 | Trypanosoma rangeli | 28% | 100% |
| A0A3R7N921 | Trypanosoma rangeli | 29% | 100% |
| A0A3R7R443 | Trypanosoma rangeli | 27% | 100% |
| A0A3S7WRJ4 | Leishmania donovani | 40% | 99% |
| A0A3S7WRJ5 | Leishmania donovani | 37% | 91% |
| A0A3S7WRL4 | Leishmania donovani | 38% | 100% |
| A0A3S7WRS3 | Leishmania donovani | 23% | 100% |
| A0A3S7WSR4 | Leishmania donovani | 41% | 100% |
| A0A3S7WWU1 | Leishmania donovani | 25% | 96% |
| A0A3S7X2G0 | Leishmania donovani | 28% | 97% |
| A0A3S7X2K5 | Leishmania donovani | 28% | 100% |
| A0A3S7XB11 | Leishmania donovani | 27% | 100% |
| A0A422MSE4 | Trypanosoma rangeli | 41% | 100% |
| A0A422MSP6 | Trypanosoma rangeli | 30% | 100% |
| A0A422MST9 | Trypanosoma rangeli | 27% | 100% |
| A0A422MU68 | Trypanosoma rangeli | 24% | 100% |
| A4H6J0 | Leishmania braziliensis | 40% | 100% |
| A4H6J1 | Leishmania braziliensis | 38% | 100% |
| A4H6J3 | Leishmania braziliensis | 37% | 100% |
| A4H6Q5 | Leishmania braziliensis | 23% | 100% |
| A4HC19 | Leishmania braziliensis | 26% | 100% |
| A4HHG2 | Leishmania braziliensis | 27% | 100% |
| A4HHG3 | Leishmania braziliensis | 27% | 99% |
| A4HHG4 | Leishmania braziliensis | 26% | 99% |
| A4HJW3 | Leishmania braziliensis | 83% | 100% |
| A4HPE2 | Leishmania braziliensis | 27% | 100% |
| A4HUX5 | Leishmania infantum | 40% | 100% |
| A4HUX6 | Leishmania infantum | 38% | 100% |
| A4HUX7 | Leishmania infantum | 38% | 100% |
| A4HUX8 | Leishmania infantum | 38% | 100% |
| A4HV40 | Leishmania infantum | 23% | 100% |
| A4HZF5 | Leishmania infantum | 26% | 100% |
| A4HZJ4 | Leishmania infantum | 25% | 100% |
| A4I4L2 | Leishmania infantum | 27% | 94% |
| A4I7C5 | Leishmania infantum | 100% | 100% |
| A4ICI3 | Leishmania infantum | 27% | 100% |
| C9ZL97 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
| C9ZL98 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
| C9ZL99 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
| C9ZLA0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
| C9ZLA1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
| C9ZTR5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
| C9ZTR6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
| C9ZTR7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
| C9ZTR8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
| C9ZTR9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
| C9ZTS1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
| C9ZUT6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
| D0A7B1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 23% | 99% |
| D0A7H1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
| D0AAQ2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 93% |
| E8NHE1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 100% |
| E9AE01 | Leishmania major | 27% | 100% |
| E9AE09 | Leishmania major | 27% | 94% |
| E9AE10 | Leishmania major | 27% | 94% |
| E9AE11 | Leishmania major | 28% | 100% |
| E9AGK5 | Leishmania infantum | 40% | 100% |
| E9AHJ0 | Leishmania infantum | 27% | 100% |
| E9AHJ1 | Leishmania infantum | 26% | 100% |
| E9ALS2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
| E9ALS3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 94% |
| E9ANL0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 100% |
| E9ANL1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 100% |
| E9ANL2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 97% |
| E9ANS1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
| E9APJ3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 99% |
| E9AT53 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
| E9AVF1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
| E9AVF2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
| E9B2B8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
| Q4Q1E4 | Leishmania major | 27% | 100% |
| Q4Q5T8 | Leishmania major | 94% | 100% |
| Q4QC27 | Leishmania major | 25% | 100% |
| Q4QC28 | Leishmania major | 25% | 100% |
| Q4QFY5 | Leishmania major | 40% | 100% |
| Q4QGU8 | Leishmania major | 23% | 100% |
| Q4QH10 | Leishmania major | 36% | 98% |
| Q4QH11 | Leishmania major | 37% | 95% |
| Q4QH12 | Leishmania major | 37% | 95% |
| Q4QH13 | Leishmania major | 38% | 95% |
| Q4QH14 | Leishmania major | 36% | 100% |
| Q4QH15 | Leishmania major | 41% | 100% |
| V5B647 | Trypanosoma cruzi | 42% | 100% |
| V5B983 | Trypanosoma cruzi | 31% | 100% |
| V5BBB1 | Trypanosoma cruzi | 42% | 100% |
| V5BFV8 | Trypanosoma cruzi | 30% | 95% |
| V5BQY6 | Trypanosoma cruzi | 40% | 90% |
| V5BVP0 | Trypanosoma cruzi | 42% | 100% |
| V5DT25 | Trypanosoma cruzi | 41% | 100% |