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: 119 | 
| NetGPI | no | yes: 0, no: 119 | 
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0016020 | membrane | 2 | 112 | 
| GO:0110165 | cellular anatomical entity | 1 | 112 | 
| GO:0005737 | cytoplasm | 2 | 3 | 
Related structures:
AlphaFold database: A0A3S7WRJ5
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0005215 | transporter activity | 1 | 53 | 
| GO:0022857 | transmembrane transporter activity | 2 | 53 | 
| Leishmania | From | To | Domain/Motif | Score | 
|---|---|---|---|---|
| CLV_NRD_NRD_1 | 216 | 218 | PF00675 | 0.327 | 
| CLV_NRD_NRD_1 | 226 | 228 | PF00675 | 0.328 | 
| CLV_NRD_NRD_1 | 242 | 244 | PF00675 | 0.290 | 
| CLV_NRD_NRD_1 | 329 | 331 | PF00675 | 0.476 | 
| CLV_NRD_NRD_1 | 467 | 469 | PF00675 | 0.367 | 
| CLV_NRD_NRD_1 | 667 | 669 | PF00675 | 0.589 | 
| CLV_PCSK_KEX2_1 | 226 | 228 | PF00082 | 0.324 | 
| CLV_PCSK_KEX2_1 | 24 | 26 | PF00082 | 0.299 | 
| CLV_PCSK_KEX2_1 | 242 | 244 | PF00082 | 0.304 | 
| CLV_PCSK_KEX2_1 | 329 | 331 | PF00082 | 0.529 | 
| CLV_PCSK_KEX2_1 | 467 | 469 | PF00082 | 0.350 | 
| CLV_PCSK_PC1ET2_1 | 24 | 26 | PF00082 | 0.336 | 
| CLV_PCSK_PC1ET2_1 | 467 | 469 | PF00082 | 0.352 | 
| CLV_PCSK_SKI1_1 | 11 | 15 | PF00082 | 0.367 | 
| CLV_PCSK_SKI1_1 | 160 | 164 | PF00082 | 0.363 | 
| CLV_PCSK_SKI1_1 | 184 | 188 | PF00082 | 0.485 | 
| CLV_PCSK_SKI1_1 | 227 | 231 | PF00082 | 0.386 | 
| CLV_PCSK_SKI1_1 | 243 | 247 | PF00082 | 0.239 | 
| CLV_PCSK_SKI1_1 | 275 | 279 | PF00082 | 0.479 | 
| CLV_PCSK_SKI1_1 | 352 | 356 | PF00082 | 0.380 | 
| CLV_PCSK_SKI1_1 | 395 | 399 | PF00082 | 0.360 | 
| CLV_PCSK_SKI1_1 | 440 | 444 | PF00082 | 0.316 | 
| CLV_PCSK_SKI1_1 | 525 | 529 | PF00082 | 0.277 | 
| CLV_PCSK_SKI1_1 | 577 | 581 | PF00082 | 0.512 | 
| DEG_APCC_DBOX_1 | 242 | 250 | PF00400 | 0.489 | 
| DEG_APCC_DBOX_1 | 439 | 447 | PF00400 | 0.386 | 
| DEG_MDM2_SWIB_1 | 41 | 48 | PF02201 | 0.184 | 
| DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.655 | 
| DOC_CDC14_PxL_1 | 270 | 278 | PF14671 | 0.222 | 
| DOC_CDC14_PxL_1 | 293 | 301 | PF14671 | 0.516 | 
| DOC_CYCLIN_yCln2_LP_2 | 495 | 501 | PF00134 | 0.388 | 
| DOC_MAPK_DCC_7 | 576 | 585 | PF00069 | 0.240 | 
| DOC_MAPK_gen_1 | 24 | 31 | PF00069 | 0.453 | 
| DOC_MAPK_gen_1 | 242 | 250 | PF00069 | 0.459 | 
| DOC_MAPK_gen_1 | 269 | 278 | PF00069 | 0.392 | 
| DOC_MAPK_gen_1 | 467 | 476 | PF00069 | 0.532 | 
| DOC_MAPK_gen_1 | 576 | 583 | PF00069 | 0.336 | 
| DOC_MAPK_MEF2A_6 | 242 | 250 | PF00069 | 0.474 | 
| DOC_MAPK_MEF2A_6 | 269 | 278 | PF00069 | 0.371 | 
| DOC_MAPK_MEF2A_6 | 469 | 478 | PF00069 | 0.529 | 
| DOC_MAPK_MEF2A_6 | 576 | 585 | PF00069 | 0.305 | 
| DOC_MAPK_NFAT4_5 | 243 | 251 | PF00069 | 0.447 | 
| DOC_PP1_RVXF_1 | 273 | 279 | PF00149 | 0.268 | 
| DOC_PP1_RVXF_1 | 642 | 649 | PF00149 | 0.518 | 
| DOC_PP2B_LxvP_1 | 495 | 498 | PF13499 | 0.420 | 
| DOC_PP2B_LxvP_1 | 502 | 505 | PF13499 | 0.299 | 
| DOC_PP2B_LxvP_1 | 540 | 543 | PF13499 | 0.464 | 
| DOC_PP4_FxxP_1 | 686 | 689 | PF00568 | 0.577 | 
| DOC_PP4_FxxP_1 | 86 | 89 | PF00568 | 0.500 | 
| DOC_SPAK_OSR1_1 | 25 | 29 | PF12202 | 0.515 | 
| DOC_USP7_MATH_1 | 263 | 267 | PF00917 | 0.440 | 
| DOC_USP7_MATH_1 | 279 | 283 | PF00917 | 0.378 | 
| DOC_USP7_MATH_1 | 309 | 313 | PF00917 | 0.618 | 
| DOC_USP7_MATH_1 | 364 | 368 | PF00917 | 0.762 | 
| DOC_USP7_MATH_1 | 429 | 433 | PF00917 | 0.391 | 
| DOC_USP7_MATH_1 | 510 | 514 | PF00917 | 0.313 | 
| DOC_USP7_UBL2_3 | 530 | 534 | PF12436 | 0.496 | 
| DOC_WW_Pin1_4 | 357 | 362 | PF00397 | 0.786 | 
| LIG_14-3-3_CanoR_1 | 121 | 125 | PF00244 | 0.208 | 
| LIG_14-3-3_CanoR_1 | 152 | 162 | PF00244 | 0.381 | 
| LIG_14-3-3_CanoR_1 | 395 | 401 | PF00244 | 0.473 | 
| LIG_14-3-3_CanoR_1 | 440 | 446 | PF00244 | 0.379 | 
| LIG_14-3-3_CanoR_1 | 455 | 461 | PF00244 | 0.303 | 
| LIG_14-3-3_CanoR_1 | 473 | 479 | PF00244 | 0.446 | 
| LIG_14-3-3_CanoR_1 | 603 | 608 | PF00244 | 0.559 | 
| LIG_BRCT_BRCA1_1 | 423 | 427 | PF00533 | 0.363 | 
| LIG_deltaCOP1_diTrp_1 | 401 | 410 | PF00928 | 0.505 | 
| LIG_FHA_1 | 102 | 108 | PF00498 | 0.293 | 
| LIG_FHA_1 | 154 | 160 | PF00498 | 0.480 | 
| LIG_FHA_1 | 281 | 287 | PF00498 | 0.386 | 
| LIG_FHA_1 | 334 | 340 | PF00498 | 0.715 | 
| LIG_FHA_1 | 397 | 403 | PF00498 | 0.491 | 
| LIG_FHA_1 | 410 | 416 | PF00498 | 0.303 | 
| LIG_FHA_1 | 475 | 481 | PF00498 | 0.465 | 
| LIG_FHA_1 | 487 | 493 | PF00498 | 0.318 | 
| LIG_FHA_1 | 522 | 528 | PF00498 | 0.315 | 
| LIG_FHA_1 | 594 | 600 | PF00498 | 0.400 | 
| LIG_FHA_1 | 66 | 72 | PF00498 | 0.333 | 
| LIG_FHA_1 | 672 | 678 | PF00498 | 0.579 | 
| LIG_FHA_2 | 1 | 7 | PF00498 | 0.633 | 
| LIG_FHA_2 | 396 | 402 | PF00498 | 0.540 | 
| LIG_FHA_2 | 688 | 694 | PF00498 | 0.781 | 
| LIG_LIR_Apic_2 | 381 | 387 | PF02991 | 0.510 | 
| LIG_LIR_Apic_2 | 667 | 673 | PF02991 | 0.577 | 
| LIG_LIR_Apic_2 | 85 | 89 | PF02991 | 0.477 | 
| LIG_LIR_Gen_1 | 123 | 130 | PF02991 | 0.342 | 
| LIG_LIR_Gen_1 | 266 | 274 | PF02991 | 0.361 | 
| LIG_LIR_Gen_1 | 42 | 52 | PF02991 | 0.356 | 
| LIG_LIR_Gen_1 | 423 | 433 | PF02991 | 0.332 | 
| LIG_LIR_LC3C_4 | 68 | 73 | PF02991 | 0.440 | 
| LIG_LIR_Nem_3 | 161 | 165 | PF02991 | 0.339 | 
| LIG_LIR_Nem_3 | 183 | 189 | PF02991 | 0.260 | 
| LIG_LIR_Nem_3 | 266 | 270 | PF02991 | 0.338 | 
| LIG_LIR_Nem_3 | 301 | 306 | PF02991 | 0.632 | 
| LIG_LIR_Nem_3 | 33 | 37 | PF02991 | 0.357 | 
| LIG_LIR_Nem_3 | 42 | 48 | PF02991 | 0.344 | 
| LIG_LIR_Nem_3 | 423 | 428 | PF02991 | 0.312 | 
| LIG_LIR_Nem_3 | 459 | 463 | PF02991 | 0.531 | 
| LIG_LIR_Nem_3 | 513 | 519 | PF02991 | 0.416 | 
| LIG_LIR_Nem_3 | 97 | 102 | PF02991 | 0.305 | 
| LIG_MYND_1 | 305 | 309 | PF01753 | 0.497 | 
| LIG_PCNA_PIPBox_1 | 261 | 270 | PF02747 | 0.334 | 
| LIG_PCNA_yPIPBox_3 | 261 | 275 | PF02747 | 0.315 | 
| LIG_Pex14_1 | 406 | 410 | PF04695 | 0.335 | 
| LIG_Pex14_2 | 186 | 190 | PF04695 | 0.365 | 
| LIG_Pex14_2 | 41 | 45 | PF04695 | 0.349 | 
| LIG_Pex14_2 | 417 | 421 | PF04695 | 0.369 | 
| LIG_Pex14_2 | 460 | 464 | PF04695 | 0.541 | 
| LIG_Pex14_2 | 82 | 86 | PF04695 | 0.424 | 
| LIG_PTB_Apo_2 | 297 | 304 | PF02174 | 0.448 | 
| LIG_PTB_Apo_2 | 598 | 605 | PF02174 | 0.466 | 
| LIG_PTB_Phospho_1 | 297 | 303 | PF10480 | 0.448 | 
| LIG_PTB_Phospho_1 | 598 | 604 | PF10480 | 0.460 | 
| LIG_SH2_CRK | 289 | 293 | PF00017 | 0.474 | 
| LIG_SH2_CRK | 516 | 520 | PF00017 | 0.175 | 
| LIG_SH2_CRK | 670 | 674 | PF00017 | 0.578 | 
| LIG_SH2_CRK | 80 | 84 | PF00017 | 0.312 | 
| LIG_SH2_NCK_1 | 670 | 674 | PF00017 | 0.578 | 
| LIG_SH2_PTP2 | 303 | 306 | PF00017 | 0.479 | 
| LIG_SH2_PTP2 | 384 | 387 | PF00017 | 0.505 | 
| LIG_SH2_SRC | 303 | 306 | PF00017 | 0.654 | 
| LIG_SH2_SRC | 670 | 673 | PF00017 | 0.578 | 
| LIG_SH2_STAP1 | 289 | 293 | PF00017 | 0.435 | 
| LIG_SH2_STAP1 | 43 | 47 | PF00017 | 0.337 | 
| LIG_SH2_STAP1 | 559 | 563 | PF00017 | 0.284 | 
| LIG_SH2_STAP1 | 80 | 84 | PF00017 | 0.326 | 
| LIG_SH2_STAT3 | 234 | 237 | PF00017 | 0.499 | 
| LIG_SH2_STAT3 | 559 | 562 | PF00017 | 0.333 | 
| LIG_SH2_STAT5 | 177 | 180 | PF00017 | 0.259 | 
| LIG_SH2_STAT5 | 234 | 237 | PF00017 | 0.510 | 
| LIG_SH2_STAT5 | 267 | 270 | PF00017 | 0.354 | 
| LIG_SH2_STAT5 | 289 | 292 | PF00017 | 0.328 | 
| LIG_SH2_STAT5 | 303 | 306 | PF00017 | 0.537 | 
| LIG_SH2_STAT5 | 384 | 387 | PF00017 | 0.514 | 
| LIG_SH2_STAT5 | 559 | 562 | PF00017 | 0.300 | 
| LIG_SH2_STAT5 | 607 | 610 | PF00017 | 0.493 | 
| LIG_SH2_STAT5 | 99 | 102 | PF00017 | 0.343 | 
| LIG_SH3_3 | 13 | 19 | PF00018 | 0.589 | 
| LIG_SH3_3 | 289 | 295 | PF00018 | 0.302 | 
| LIG_SH3_3 | 303 | 309 | PF00018 | 0.635 | 
| LIG_SH3_3 | 576 | 582 | PF00018 | 0.315 | 
| LIG_SH3_3 | 95 | 101 | PF00018 | 0.291 | 
| LIG_SUMO_SIM_anti_2 | 282 | 288 | PF11976 | 0.307 | 
| LIG_SUMO_SIM_anti_2 | 441 | 447 | PF11976 | 0.262 | 
| LIG_SUMO_SIM_par_1 | 27 | 33 | PF11976 | 0.429 | 
| LIG_SxIP_EBH_1 | 297 | 311 | PF03271 | 0.478 | 
| LIG_TRAF2_1 | 3 | 6 | PF00917 | 0.596 | 
| LIG_TRAF2_1 | 324 | 327 | PF00917 | 0.660 | 
| LIG_TYR_ITIM | 265 | 270 | PF00017 | 0.425 | 
| LIG_TYR_ITIM | 287 | 292 | PF00017 | 0.335 | 
| LIG_TYR_ITIM | 78 | 83 | PF00017 | 0.321 | 
| LIG_UBA3_1 | 105 | 114 | PF00899 | 0.270 | 
| LIG_WRC_WIRS_1 | 159 | 164 | PF05994 | 0.370 | 
| LIG_WRC_WIRS_1 | 288 | 293 | PF05994 | 0.200 | 
| LIG_WRC_WIRS_1 | 31 | 36 | PF05994 | 0.427 | 
| LIG_WRC_WIRS_1 | 38 | 43 | PF05994 | 0.431 | 
| LIG_WRC_WIRS_1 | 457 | 462 | PF05994 | 0.238 | 
| MOD_CK1_1 | 367 | 373 | PF00069 | 0.641 | 
| MOD_CK1_1 | 409 | 415 | PF00069 | 0.357 | 
| MOD_CK1_1 | 438 | 444 | PF00069 | 0.362 | 
| MOD_CK1_1 | 634 | 640 | PF00069 | 0.526 | 
| MOD_CK2_1 | 177 | 183 | PF00069 | 0.444 | 
| MOD_CK2_1 | 334 | 340 | PF00069 | 0.687 | 
| MOD_CK2_1 | 395 | 401 | PF00069 | 0.404 | 
| MOD_CK2_1 | 456 | 462 | PF00069 | 0.354 | 
| MOD_CK2_1 | 687 | 693 | PF00069 | 0.722 | 
| MOD_CMANNOS | 403 | 406 | PF00535 | 0.357 | 
| MOD_Cter_Amidation | 327 | 330 | PF01082 | 0.405 | 
| MOD_Cter_Amidation | 574 | 577 | PF01082 | 0.470 | 
| MOD_GlcNHglycan | 166 | 169 | PF01048 | 0.321 | 
| MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.338 | 
| MOD_GlcNHglycan | 431 | 434 | PF01048 | 0.456 | 
| MOD_GlcNHglycan | 450 | 453 | PF01048 | 0.302 | 
| MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.305 | 
| MOD_GlcNHglycan | 512 | 515 | PF01048 | 0.292 | 
| MOD_GlcNHglycan | 540 | 543 | PF01048 | 0.294 | 
| MOD_GlcNHglycan | 545 | 548 | PF01048 | 0.272 | 
| MOD_GlcNHglycan | 591 | 594 | PF01048 | 0.357 | 
| MOD_GlcNHglycan | 633 | 636 | PF01048 | 0.552 | 
| MOD_GlcNHglycan | 656 | 659 | PF01048 | 0.662 | 
| MOD_GlcNHglycan | 678 | 682 | PF01048 | 0.645 | 
| MOD_GSK3_1 | 143 | 150 | PF00069 | 0.337 | 
| MOD_GSK3_1 | 160 | 167 | PF00069 | 0.354 | 
| MOD_GSK3_1 | 259 | 266 | PF00069 | 0.357 | 
| MOD_GSK3_1 | 331 | 338 | PF00069 | 0.556 | 
| MOD_GSK3_1 | 405 | 412 | PF00069 | 0.323 | 
| MOD_GSK3_1 | 429 | 436 | PF00069 | 0.430 | 
| MOD_GSK3_1 | 482 | 489 | PF00069 | 0.319 | 
| MOD_GSK3_1 | 589 | 596 | PF00069 | 0.374 | 
| MOD_GSK3_1 | 61 | 68 | PF00069 | 0.323 | 
| MOD_GSK3_1 | 90 | 97 | PF00069 | 0.373 | 
| MOD_LATS_1 | 662 | 668 | PF00433 | 0.451 | 
| MOD_N-GLC_1 | 299 | 304 | PF02516 | 0.547 | 
| MOD_N-GLC_1 | 395 | 400 | PF02516 | 0.489 | 
| MOD_N-GLC_1 | 421 | 426 | PF02516 | 0.422 | 
| MOD_NEK2_1 | 158 | 163 | PF00069 | 0.395 | 
| MOD_NEK2_1 | 188 | 193 | PF00069 | 0.296 | 
| MOD_NEK2_1 | 257 | 262 | PF00069 | 0.330 | 
| MOD_NEK2_1 | 287 | 292 | PF00069 | 0.329 | 
| MOD_NEK2_1 | 298 | 303 | PF00069 | 0.441 | 
| MOD_NEK2_1 | 405 | 410 | PF00069 | 0.304 | 
| MOD_NEK2_1 | 421 | 426 | PF00069 | 0.302 | 
| MOD_NEK2_1 | 456 | 461 | PF00069 | 0.349 | 
| MOD_NEK2_1 | 481 | 486 | PF00069 | 0.333 | 
| MOD_NEK2_1 | 538 | 543 | PF00069 | 0.292 | 
| MOD_NEK2_1 | 677 | 682 | PF00069 | 0.454 | 
| MOD_PIKK_1 | 209 | 215 | PF00454 | 0.444 | 
| MOD_PIKK_1 | 257 | 263 | PF00454 | 0.244 | 
| MOD_PIKK_1 | 462 | 468 | PF00454 | 0.379 | 
| MOD_PIKK_1 | 56 | 62 | PF00454 | 0.292 | 
| MOD_PKA_1 | 217 | 223 | PF00069 | 0.468 | 
| MOD_PKA_2 | 120 | 126 | PF00069 | 0.282 | 
| MOD_Plk_1 | 299 | 305 | PF00069 | 0.462 | 
| MOD_Plk_1 | 331 | 337 | PF00069 | 0.644 | 
| MOD_Plk_1 | 395 | 401 | PF00069 | 0.500 | 
| MOD_Plk_1 | 421 | 427 | PF00069 | 0.378 | 
| MOD_Plk_1 | 61 | 67 | PF00069 | 0.309 | 
| MOD_Plk_4 | 101 | 107 | PF00069 | 0.291 | 
| MOD_Plk_4 | 115 | 121 | PF00069 | 0.274 | 
| MOD_Plk_4 | 263 | 269 | PF00069 | 0.421 | 
| MOD_Plk_4 | 280 | 286 | PF00069 | 0.357 | 
| MOD_Plk_4 | 287 | 293 | PF00069 | 0.361 | 
| MOD_Plk_4 | 299 | 305 | PF00069 | 0.480 | 
| MOD_Plk_4 | 389 | 395 | PF00069 | 0.391 | 
| MOD_Plk_4 | 413 | 419 | PF00069 | 0.345 | 
| MOD_Plk_4 | 421 | 427 | PF00069 | 0.355 | 
| MOD_Plk_4 | 441 | 447 | PF00069 | 0.319 | 
| MOD_Plk_4 | 456 | 462 | PF00069 | 0.328 | 
| MOD_Plk_4 | 487 | 493 | PF00069 | 0.310 | 
| MOD_Plk_4 | 62 | 68 | PF00069 | 0.387 | 
| MOD_Plk_4 | 94 | 100 | PF00069 | 0.293 | 
| MOD_ProDKin_1 | 357 | 363 | PF00069 | 0.759 | 
| MOD_SUMO_rev_2 | 21 | 26 | PF00179 | 0.399 | 
| MOD_SUMO_rev_2 | 643 | 653 | PF00179 | 0.561 | 
| TRG_DiLeu_BaEn_1 | 620 | 625 | PF01217 | 0.448 | 
| TRG_DiLeu_BaLyEn_6 | 452 | 457 | PF01217 | 0.319 | 
| TRG_DiLeu_BaLyEn_6 | 579 | 584 | PF01217 | 0.417 | 
| TRG_ENDOCYTIC_2 | 267 | 270 | PF00928 | 0.409 | 
| TRG_ENDOCYTIC_2 | 289 | 292 | PF00928 | 0.308 | 
| TRG_ENDOCYTIC_2 | 303 | 306 | PF00928 | 0.444 | 
| TRG_ENDOCYTIC_2 | 516 | 519 | PF00928 | 0.405 | 
| TRG_ENDOCYTIC_2 | 80 | 83 | PF00928 | 0.322 | 
| TRG_ENDOCYTIC_2 | 84 | 87 | PF00928 | 0.337 | 
| TRG_ENDOCYTIC_2 | 99 | 102 | PF00928 | 0.356 | 
| TRG_ER_diArg_1 | 226 | 228 | PF00400 | 0.429 | 
| TRG_ER_diArg_1 | 241 | 243 | PF00400 | 0.361 | 
| TRG_ER_diArg_1 | 310 | 313 | PF00400 | 0.620 | 
| TRG_ER_diArg_1 | 615 | 618 | PF00400 | 0.436 | 
| TRG_NES_CRM1_1 | 62 | 74 | PF08389 | 0.184 | 
| TRG_Pf-PMV_PEXEL_1 | 217 | 221 | PF00026 | 0.444 | 
| TRG_Pf-PMV_PEXEL_1 | 552 | 557 | PF00026 | 0.374 | 
| TRG_Pf-PMV_PEXEL_1 | 610 | 614 | PF00026 | 0.430 | 
| Protein | Taxonomy | Sequence identity | Coverage | 
|---|---|---|---|
| A0A0N0P6G0 | Leptomonas seymouri | 37% | 100% | 
| A0A0N1HT40 | Leptomonas seymouri | 41% | 100% | 
| A0A0N1HZC2 | Leptomonas seymouri | 28% | 100% | 
| A0A0N1IKC5 | Leptomonas seymouri | 52% | 100% | 
| A0A0N1PB63 | Leptomonas seymouri | 28% | 100% | 
| A0A0N1PD04 | Leptomonas seymouri | 26% | 100% | 
| A0A0N1PFR4 | Leptomonas seymouri | 27% | 100% | 
| A0A1X0NKK0 | Trypanosomatidae | 30% | 100% | 
| A0A1X0NM09 | Trypanosomatidae | 29% | 100% | 
| A0A1X0NRW5 | Trypanosomatidae | 37% | 100% | 
| A0A1X0NV13 | Trypanosomatidae | 47% | 100% | 
| A0A1X0NV19 | Trypanosomatidae | 50% | 100% | 
| A0A1X0NV27 | Trypanosomatidae | 50% | 100% | 
| A0A1X0NVH8 | Trypanosomatidae | 41% | 100% | 
| A0A1X0NVM7 | Trypanosomatidae | 48% | 100% | 
| A0A1X0NWQ1 | Trypanosomatidae | 44% | 100% | 
| A0A1X0NZE6 | Trypanosomatidae | 33% | 100% | 
| A0A1X0NZU2 | Trypanosomatidae | 30% | 100% | 
| A0A1X0NZU5 | Trypanosomatidae | 34% | 100% | 
| A0A1X0NZW1 | Trypanosomatidae | 27% | 100% | 
| A0A1X0P0M7 | Trypanosomatidae | 30% | 100% | 
| A0A381MMW5 | Leishmania infantum | 32% | 100% | 
| A0A3Q8I7Y9 | Leishmania donovani | 41% | 89% | 
| A0A3Q8IEC4 | Leishmania donovani | 32% | 100% | 
| A0A3Q8IF95 | Leishmania donovani | 30% | 100% | 
| A0A3Q8IIT5 | Leishmania donovani | 27% | 100% | 
| A0A3Q8ISY9 | Leishmania donovani | 37% | 100% | 
| A0A3R7KKN8 | Trypanosoma rangeli | 28% | 100% | 
| A0A3R7MAQ7 | Trypanosoma rangeli | 34% | 99% | 
| A0A3R7N3S6 | Trypanosoma rangeli | 25% | 100% | 
| A0A3R7N415 | Trypanosoma rangeli | 26% | 100% | 
| A0A3R7N921 | Trypanosoma rangeli | 33% | 100% | 
| A0A3R7R443 | Trypanosoma rangeli | 27% | 100% | 
| A0A3S7WRJ4 | Leishmania donovani | 51% | 98% | 
| A0A3S7WRL4 | Leishmania donovani | 40% | 100% | 
| A0A3S7WRS3 | Leishmania donovani | 25% | 100% | 
| A0A3S7WSR4 | Leishmania donovani | 49% | 100% | 
| A0A3S7WWU1 | Leishmania donovani | 26% | 100% | 
| A0A3S7X2G0 | Leishmania donovani | 32% | 100% | 
| A0A3S7X2K5 | Leishmania donovani | 32% | 100% | 
| A0A3S7XB11 | Leishmania donovani | 31% | 100% | 
| A0A422MSE4 | Trypanosoma rangeli | 46% | 100% | 
| A0A422MSP6 | Trypanosoma rangeli | 34% | 100% | 
| A0A422MST9 | Trypanosoma rangeli | 26% | 100% | 
| A0A422MU68 | Trypanosoma rangeli | 26% | 100% | 
| A4H6J0 | Leishmania braziliensis | 53% | 100% | 
| A4H6J1 | Leishmania braziliensis | 70% | 100% | 
| A4H6J3 | Leishmania braziliensis | 40% | 89% | 
| A4H6Q5 | Leishmania braziliensis | 24% | 100% | 
| A4HC19 | Leishmania braziliensis | 27% | 100% | 
| A4HHG2 | Leishmania braziliensis | 26% | 100% | 
| A4HHG3 | Leishmania braziliensis | 33% | 100% | 
| A4HHG4 | Leishmania braziliensis | 33% | 100% | 
| A4HJW3 | Leishmania braziliensis | 38% | 100% | 
| A4HPE2 | Leishmania braziliensis | 29% | 100% | 
| A4HUX5 | Leishmania infantum | 52% | 99% | 
| A4HUX6 | Leishmania infantum | 99% | 100% | 
| A4HUX7 | Leishmania infantum | 40% | 94% | 
| A4HUX8 | Leishmania infantum | 40% | 90% | 
| A4HV40 | Leishmania infantum | 25% | 100% | 
| A4HZF5 | Leishmania infantum | 30% | 100% | 
| A4HZJ4 | Leishmania infantum | 26% | 100% | 
| A4I4L2 | Leishmania infantum | 26% | 100% | 
| A4I7C5 | Leishmania infantum | 37% | 100% | 
| A4ICI3 | Leishmania infantum | 31% | 100% | 
| C9ZL97 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% | 
| C9ZL98 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% | 
| C9ZL99 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 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) | 49% | 100% | 
| C9ZTR6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% | 
| C9ZTR7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% | 
| C9ZTR8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% | 
| C9ZTR9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% | 
| C9ZTS1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 100% | 
| C9ZUT6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% | 
| D0A7B1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 100% | 
| D0A7H1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% | 
| D0AAQ2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% | 
| E8NHE1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 100% | 
| E9AE01 | Leishmania major | 31% | 100% | 
| E9AE09 | Leishmania major | 26% | 100% | 
| E9AE10 | Leishmania major | 26% | 100% | 
| E9AE11 | Leishmania major | 31% | 100% | 
| E9AGK5 | Leishmania infantum | 49% | 98% | 
| E9AHJ0 | Leishmania infantum | 32% | 100% | 
| E9AHJ1 | Leishmania infantum | 32% | 100% | 
| E9ALS2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% | 
| E9ALS3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% | 
| E9ANL0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 52% | 100% | 
| E9ANL1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 99% | 
| E9ANL2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 42% | 97% | 
| E9ANS1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% | 
| E9APJ3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 49% | 97% | 
| E9AT53 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 96% | 
| E9AVF1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% | 
| E9AVF2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% | 
| E9B2B8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 100% | 
| Q4Q1E4 | Leishmania major | 29% | 99% | 
| Q4Q5T8 | Leishmania major | 37% | 100% | 
| Q4QC27 | Leishmania major | 26% | 100% | 
| Q4QC28 | Leishmania major | 29% | 98% | 
| Q4QFY5 | Leishmania major | 50% | 97% | 
| Q4QGU8 | Leishmania major | 24% | 100% | 
| Q4QH10 | Leishmania major | 42% | 96% | 
| Q4QH11 | Leishmania major | 42% | 93% | 
| Q4QH12 | Leishmania major | 42% | 93% | 
| Q4QH13 | Leishmania major | 42% | 93% | 
| Q4QH14 | Leishmania major | 91% | 100% | 
| Q4QH15 | Leishmania major | 52% | 99% | 
| V5B647 | Trypanosoma cruzi | 44% | 100% | 
| V5B983 | Trypanosoma cruzi | 32% | 100% | 
| V5BBB1 | Trypanosoma cruzi | 44% | 100% | 
| V5BFV8 | Trypanosoma cruzi | 31% | 100% | 
| V5BQY6 | Trypanosoma cruzi | 37% | 99% | 
| V5BVP0 | Trypanosoma cruzi | 45% | 100% | 
| V5DT25 | Trypanosoma cruzi | 46% | 100% |