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: A4H6J0
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 54 |
GO:0022857 | transmembrane transporter activity | 2 | 54 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 338 | 342 | PF00656 | 0.709 |
CLV_NRD_NRD_1 | 303 | 305 | PF00675 | 0.394 |
CLV_NRD_NRD_1 | 308 | 310 | PF00675 | 0.431 |
CLV_NRD_NRD_1 | 459 | 461 | PF00675 | 0.369 |
CLV_NRD_NRD_1 | 561 | 563 | PF00675 | 0.512 |
CLV_NRD_NRD_1 | 599 | 601 | PF00675 | 0.357 |
CLV_PCSK_KEX2_1 | 303 | 305 | PF00082 | 0.411 |
CLV_PCSK_KEX2_1 | 459 | 461 | PF00082 | 0.353 |
CLV_PCSK_KEX2_1 | 561 | 563 | PF00082 | 0.553 |
CLV_PCSK_KEX2_1 | 599 | 601 | PF00082 | 0.352 |
CLV_PCSK_PC1ET2_1 | 459 | 461 | PF00082 | 0.357 |
CLV_PCSK_PC7_1 | 595 | 601 | PF00082 | 0.402 |
CLV_PCSK_SKI1_1 | 235 | 239 | PF00082 | 0.333 |
CLV_PCSK_SKI1_1 | 245 | 249 | PF00082 | 0.262 |
CLV_PCSK_SKI1_1 | 27 | 31 | PF00082 | 0.243 |
CLV_PCSK_SKI1_1 | 304 | 308 | PF00082 | 0.453 |
CLV_PCSK_SKI1_1 | 348 | 352 | PF00082 | 0.358 |
CLV_PCSK_SKI1_1 | 517 | 521 | PF00082 | 0.292 |
CLV_PCSK_SKI1_1 | 599 | 603 | PF00082 | 0.369 |
DEG_APCC_DBOX_1 | 244 | 252 | PF00400 | 0.497 |
DEG_APCC_DBOX_1 | 26 | 34 | PF00400 | 0.459 |
DOC_CYCLIN_yCln2_LP_2 | 487 | 493 | PF00134 | 0.389 |
DOC_CYCLIN_yCln2_LP_2 | 494 | 500 | PF00134 | 0.246 |
DOC_MAPK_gen_1 | 459 | 468 | PF00069 | 0.533 |
DOC_MAPK_MEF2A_6 | 461 | 470 | PF00069 | 0.533 |
DOC_MAPK_MEF2A_6 | 566 | 575 | PF00069 | 0.317 |
DOC_MAPK_RevD_3 | 294 | 310 | PF00069 | 0.620 |
DOC_PP1_RVXF_1 | 275 | 281 | PF00149 | 0.267 |
DOC_PP2B_LxvP_1 | 487 | 490 | PF13499 | 0.418 |
DOC_PP2B_LxvP_1 | 49 | 52 | PF13499 | 0.365 |
DOC_PP2B_LxvP_1 | 494 | 497 | PF13499 | 0.299 |
DOC_PP4_FxxP_1 | 78 | 81 | PF00568 | 0.312 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.172 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.611 |
DOC_USP7_MATH_1 | 261 | 265 | PF00917 | 0.356 |
DOC_USP7_MATH_1 | 342 | 346 | PF00917 | 0.731 |
DOC_USP7_MATH_1 | 427 | 431 | PF00917 | 0.398 |
DOC_USP7_UBL2_3 | 522 | 526 | PF12436 | 0.529 |
DOC_WW_Pin1_4 | 327 | 332 | PF00397 | 0.566 |
LIG_14-3-3_CanoR_1 | 21 | 28 | PF00244 | 0.576 |
LIG_14-3-3_CanoR_1 | 447 | 453 | PF00244 | 0.298 |
LIG_14-3-3_CanoR_1 | 57 | 65 | PF00244 | 0.342 |
LIG_14-3-3_CanoR_1 | 593 | 598 | PF00244 | 0.580 |
LIG_APCC_ABBAyCdc20_2 | 605 | 611 | PF00400 | 0.587 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.653 |
LIG_deltaCOP1_diTrp_1 | 393 | 399 | PF00928 | 0.363 |
LIG_eIF4E_1 | 597 | 603 | PF01652 | 0.410 |
LIG_FHA_1 | 119 | 125 | PF00498 | 0.293 |
LIG_FHA_1 | 136 | 142 | PF00498 | 0.367 |
LIG_FHA_1 | 199 | 205 | PF00498 | 0.368 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.438 |
LIG_FHA_1 | 261 | 267 | PF00498 | 0.327 |
LIG_FHA_1 | 273 | 279 | PF00498 | 0.286 |
LIG_FHA_1 | 282 | 288 | PF00498 | 0.377 |
LIG_FHA_1 | 389 | 395 | PF00498 | 0.496 |
LIG_FHA_1 | 414 | 420 | PF00498 | 0.316 |
LIG_FHA_1 | 430 | 436 | PF00498 | 0.270 |
LIG_FHA_1 | 46 | 52 | PF00498 | 0.310 |
LIG_FHA_1 | 467 | 473 | PF00498 | 0.463 |
LIG_FHA_1 | 474 | 480 | PF00498 | 0.316 |
LIG_FHA_1 | 584 | 590 | PF00498 | 0.401 |
LIG_FHA_1 | 68 | 74 | PF00498 | 0.331 |
LIG_FHA_2 | 336 | 342 | PF00498 | 0.731 |
LIG_FHA_2 | 350 | 356 | PF00498 | 0.775 |
LIG_FHA_2 | 368 | 374 | PF00498 | 0.596 |
LIG_LIR_Apic_2 | 373 | 379 | PF02991 | 0.551 |
LIG_LIR_Apic_2 | 87 | 91 | PF02991 | 0.471 |
LIG_LIR_Gen_1 | 185 | 195 | PF02991 | 0.285 |
LIG_LIR_Gen_1 | 408 | 417 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 163 | 167 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 174 | 179 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 185 | 190 | PF02991 | 0.257 |
LIG_LIR_Nem_3 | 35 | 39 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 408 | 412 | PF02991 | 0.323 |
LIG_LIR_Nem_3 | 451 | 455 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 549 | 553 | PF02991 | 0.324 |
LIG_LIR_Nem_3 | 87 | 92 | PF02991 | 0.491 |
LIG_NRBOX | 430 | 436 | PF00104 | 0.215 |
LIG_Pex14_2 | 175 | 179 | PF04695 | 0.314 |
LIG_Pex14_2 | 190 | 194 | PF04695 | 0.359 |
LIG_Pex14_2 | 246 | 250 | PF04695 | 0.327 |
LIG_Pex14_2 | 405 | 409 | PF04695 | 0.352 |
LIG_Pex14_2 | 43 | 47 | PF04695 | 0.346 |
LIG_Pex14_2 | 452 | 456 | PF04695 | 0.549 |
LIG_Pex14_2 | 78 | 82 | PF04695 | 0.405 |
LIG_PTB_Apo_2 | 411 | 418 | PF02174 | 0.313 |
LIG_REV1ctd_RIR_1 | 177 | 187 | PF16727 | 0.281 |
LIG_SH2_CRK | 291 | 295 | PF00017 | 0.466 |
LIG_SH2_SRC | 216 | 219 | PF00017 | 0.574 |
LIG_SH2_SRC | 498 | 501 | PF00017 | 0.340 |
LIG_SH2_STAP1 | 45 | 49 | PF00017 | 0.334 |
LIG_SH2_STAP1 | 551 | 555 | PF00017 | 0.277 |
LIG_SH2_STAT3 | 236 | 239 | PF00017 | 0.457 |
LIG_SH2_STAT3 | 551 | 554 | PF00017 | 0.330 |
LIG_SH2_STAT5 | 149 | 152 | PF00017 | 0.477 |
LIG_SH2_STAT5 | 187 | 190 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 236 | 239 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 259 | 262 | PF00017 | 0.293 |
LIG_SH2_STAT5 | 269 | 272 | PF00017 | 0.277 |
LIG_SH2_STAT5 | 376 | 379 | PF00017 | 0.556 |
LIG_SH2_STAT5 | 498 | 501 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 551 | 554 | PF00017 | 0.297 |
LIG_SH2_STAT5 | 597 | 600 | PF00017 | 0.499 |
LIG_SH2_STAT5 | 88 | 91 | PF00017 | 0.476 |
LIG_SH3_3 | 255 | 261 | PF00018 | 0.312 |
LIG_SH3_3 | 293 | 299 | PF00018 | 0.352 |
LIG_SH3_3 | 566 | 572 | PF00018 | 0.317 |
LIG_SH3_4 | 8 | 15 | PF00018 | 0.511 |
LIG_Sin3_3 | 47 | 54 | PF02671 | 0.178 |
LIG_SUMO_SIM_par_1 | 29 | 35 | PF11976 | 0.428 |
LIG_SUMO_SIM_par_1 | 92 | 98 | PF11976 | 0.332 |
LIG_TYR_ITIM | 267 | 272 | PF00017 | 0.283 |
LIG_WRC_WIRS_1 | 172 | 177 | PF05994 | 0.370 |
LIG_WRC_WIRS_1 | 33 | 38 | PF05994 | 0.425 |
LIG_WRC_WIRS_1 | 449 | 454 | PF05994 | 0.246 |
MOD_CDC14_SPxK_1 | 330 | 333 | PF00782 | 0.555 |
MOD_CDK_SPxK_1 | 327 | 333 | PF00069 | 0.562 |
MOD_CK1_1 | 219 | 225 | PF00069 | 0.533 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.305 |
MOD_CK1_1 | 67 | 73 | PF00069 | 0.320 |
MOD_CK1_1 | 98 | 104 | PF00069 | 0.339 |
MOD_CK2_1 | 349 | 355 | PF00069 | 0.757 |
MOD_CK2_1 | 448 | 454 | PF00069 | 0.367 |
MOD_CMANNOS | 395 | 398 | PF00535 | 0.351 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.424 |
MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.324 |
MOD_GlcNHglycan | 263 | 266 | PF01048 | 0.334 |
MOD_GlcNHglycan | 281 | 284 | PF01048 | 0.467 |
MOD_GlcNHglycan | 343 | 347 | PF01048 | 0.409 |
MOD_GlcNHglycan | 424 | 427 | PF01048 | 0.573 |
MOD_GlcNHglycan | 442 | 445 | PF01048 | 0.315 |
MOD_GlcNHglycan | 532 | 535 | PF01048 | 0.287 |
MOD_GlcNHglycan | 581 | 584 | PF01048 | 0.357 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.379 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.498 |
MOD_GSK3_1 | 268 | 275 | PF00069 | 0.300 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.588 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.327 |
MOD_GSK3_1 | 422 | 429 | PF00069 | 0.357 |
MOD_GSK3_1 | 474 | 481 | PF00069 | 0.331 |
MOD_GSK3_1 | 532 | 539 | PF00069 | 0.326 |
MOD_GSK3_1 | 579 | 586 | PF00069 | 0.371 |
MOD_LATS_1 | 591 | 597 | PF00433 | 0.605 |
MOD_N-GLC_1 | 198 | 203 | PF02516 | 0.358 |
MOD_N-GLC_1 | 312 | 317 | PF02516 | 0.532 |
MOD_N-GLC_1 | 413 | 418 | PF02516 | 0.549 |
MOD_N-GLC_1 | 58 | 63 | PF02516 | 0.510 |
MOD_N-GLC_2 | 326 | 328 | PF02516 | 0.377 |
MOD_N-GLC_2 | 388 | 390 | PF02516 | 0.219 |
MOD_NEK2_1 | 13 | 18 | PF00069 | 0.623 |
MOD_NEK2_1 | 160 | 165 | PF00069 | 0.390 |
MOD_NEK2_1 | 197 | 202 | PF00069 | 0.288 |
MOD_NEK2_1 | 229 | 234 | PF00069 | 0.470 |
MOD_NEK2_1 | 270 | 275 | PF00069 | 0.266 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.302 |
MOD_NEK2_1 | 397 | 402 | PF00069 | 0.263 |
MOD_NEK2_1 | 422 | 427 | PF00069 | 0.335 |
MOD_NEK2_1 | 448 | 453 | PF00069 | 0.365 |
MOD_NEK2_1 | 485 | 490 | PF00069 | 0.323 |
MOD_NEK2_1 | 530 | 535 | PF00069 | 0.293 |
MOD_NEK2_1 | 536 | 541 | PF00069 | 0.297 |
MOD_NEK2_1 | 579 | 584 | PF00069 | 0.321 |
MOD_OFUCOSY | 301 | 308 | PF10250 | 0.281 |
MOD_PIKK_1 | 15 | 21 | PF00454 | 0.608 |
MOD_PIKK_1 | 454 | 460 | PF00454 | 0.523 |
MOD_PIKK_1 | 508 | 514 | PF00454 | 0.365 |
MOD_PIKK_1 | 58 | 64 | PF00454 | 0.250 |
MOD_PKA_2 | 20 | 26 | PF00069 | 0.582 |
MOD_PKA_2 | 308 | 314 | PF00069 | 0.596 |
MOD_Plk_1 | 354 | 360 | PF00069 | 0.672 |
MOD_Plk_1 | 413 | 419 | PF00069 | 0.318 |
MOD_Plk_4 | 142 | 148 | PF00069 | 0.277 |
MOD_Plk_4 | 171 | 177 | PF00069 | 0.372 |
MOD_Plk_4 | 381 | 387 | PF00069 | 0.534 |
MOD_Plk_4 | 413 | 419 | PF00069 | 0.302 |
MOD_Plk_4 | 433 | 439 | PF00069 | 0.334 |
MOD_Plk_4 | 448 | 454 | PF00069 | 0.292 |
MOD_Plk_4 | 475 | 481 | PF00069 | 0.317 |
MOD_Plk_4 | 532 | 538 | PF00069 | 0.302 |
MOD_Plk_4 | 95 | 101 | PF00069 | 0.296 |
MOD_ProDKin_1 | 327 | 333 | PF00069 | 0.567 |
MOD_SUMO_rev_2 | 631 | 640 | PF00179 | 0.640 |
TRG_DiLeu_BaLyEn_6 | 225 | 230 | PF01217 | 0.357 |
TRG_DiLeu_BaLyEn_6 | 569 | 574 | PF01217 | 0.314 |
TRG_ENDOCYTIC_2 | 187 | 190 | PF00928 | 0.293 |
TRG_ENDOCYTIC_2 | 269 | 272 | PF00928 | 0.261 |
TRG_ENDOCYTIC_2 | 291 | 294 | PF00928 | 0.305 |
TRG_ENDOCYTIC_2 | 86 | 89 | PF00928 | 0.483 |
TRG_ER_diArg_1 | 302 | 304 | PF00400 | 0.669 |
TRG_ER_diArg_1 | 599 | 601 | PF00400 | 0.566 |
TRG_ER_diArg_1 | 605 | 608 | PF00400 | 0.563 |
TRG_Pf-PMV_PEXEL_1 | 235 | 239 | PF00026 | 0.323 |
TRG_Pf-PMV_PEXEL_1 | 544 | 549 | PF00026 | 0.325 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6G0 | Leptomonas seymouri | 39% | 100% |
A0A0N1HT40 | Leptomonas seymouri | 45% | 100% |
A0A0N1HZC2 | Leptomonas seymouri | 29% | 100% |
A0A0N1IKC5 | Leptomonas seymouri | 54% | 100% |
A0A0N1PB63 | Leptomonas seymouri | 26% | 97% |
A0A0N1PD04 | Leptomonas seymouri | 25% | 100% |
A0A0N1PFR4 | Leptomonas seymouri | 26% | 97% |
A0A0S4JR45 | Bodo saltans | 28% | 100% |
A0A1X0NKK0 | Trypanosomatidae | 31% | 100% |
A0A1X0NM09 | Trypanosomatidae | 30% | 100% |
A0A1X0NRW5 | Trypanosomatidae | 39% | 92% |
A0A1X0NV13 | Trypanosomatidae | 49% | 99% |
A0A1X0NV19 | Trypanosomatidae | 49% | 100% |
A0A1X0NV27 | Trypanosomatidae | 50% | 100% |
A0A1X0NVH8 | Trypanosomatidae | 42% | 97% |
A0A1X0NVM7 | Trypanosomatidae | 48% | 100% |
A0A1X0NWQ1 | Trypanosomatidae | 47% | 100% |
A0A1X0NZE6 | Trypanosomatidae | 31% | 100% |
A0A1X0NZU2 | Trypanosomatidae | 31% | 100% |
A0A1X0NZU5 | Trypanosomatidae | 35% | 100% |
A0A1X0NZW1 | Trypanosomatidae | 27% | 100% |
A0A1X0P0M7 | Trypanosomatidae | 29% | 100% |
A0A381MMW5 | Leishmania infantum | 30% | 98% |
A0A3Q8I7Y9 | Leishmania donovani | 47% | 100% |
A0A3Q8IEC4 | Leishmania donovani | 30% | 99% |
A0A3Q8IF95 | Leishmania donovani | 28% | 100% |
A0A3Q8IIT5 | Leishmania donovani | 25% | 96% |
A0A3Q8ISY9 | Leishmania donovani | 40% | 100% |
A0A3R7JSQ9 | Trypanosoma rangeli | 26% | 100% |
A0A3R7KKN8 | Trypanosoma rangeli | 27% | 100% |
A0A3R7MAQ7 | Trypanosoma rangeli | 34% | 91% |
A0A3R7N3S6 | Trypanosoma rangeli | 24% | 100% |
A0A3R7N415 | Trypanosoma rangeli | 26% | 100% |
A0A3R7N921 | Trypanosoma rangeli | 28% | 100% |
A0A3R7R443 | Trypanosoma rangeli | 28% | 100% |
A0A3S7WRJ4 | Leishmania donovani | 83% | 100% |
A0A3S7WRJ5 | Leishmania donovani | 53% | 92% |
A0A3S7WRL4 | Leishmania donovani | 45% | 100% |
A0A3S7WRS3 | Leishmania donovani | 25% | 100% |
A0A3S7WSR4 | Leishmania donovani | 53% | 100% |
A0A3S7WWU1 | Leishmania donovani | 26% | 97% |
A0A3S7X2G0 | Leishmania donovani | 30% | 98% |
A0A3S7X2K5 | Leishmania donovani | 30% | 100% |
A0A3S7XB11 | Leishmania donovani | 31% | 100% |
A0A422MSE4 | Trypanosoma rangeli | 48% | 100% |
A0A422MSP6 | Trypanosoma rangeli | 33% | 100% |
A0A422MST9 | Trypanosoma rangeli | 27% | 100% |
A0A422MU68 | Trypanosoma rangeli | 28% | 100% |
A4H6J1 | Leishmania braziliensis | 56% | 98% |
A4H6J3 | Leishmania braziliensis | 47% | 100% |
A4H6Q5 | Leishmania braziliensis | 24% | 100% |
A4HC19 | Leishmania braziliensis | 28% | 100% |
A4HHG2 | Leishmania braziliensis | 25% | 95% |
A4HHG3 | Leishmania braziliensis | 32% | 99% |
A4HHG4 | Leishmania braziliensis | 32% | 98% |
A4HJW3 | Leishmania braziliensis | 40% | 100% |
A4HPE2 | Leishmania braziliensis | 29% | 100% |
A4HUX5 | Leishmania infantum | 83% | 100% |
A4HUX6 | Leishmania infantum | 53% | 92% |
A4HUX7 | Leishmania infantum | 45% | 100% |
A4HUX8 | Leishmania infantum | 46% | 100% |
A4HV40 | Leishmania infantum | 25% | 100% |
A4HZF5 | Leishmania infantum | 28% | 100% |
A4HZJ4 | Leishmania infantum | 26% | 97% |
A4I4L2 | Leishmania infantum | 25% | 96% |
A4I7C5 | Leishmania infantum | 40% | 100% |
A4ICI3 | Leishmania infantum | 31% | 100% |
C9ZL97 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZL98 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZL99 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
C9ZLA0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZLA1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
C9ZTR5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 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) | 48% | 100% |
C9ZTR9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 100% |
C9ZTS1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 100% |
C9ZUT6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
D0A7B1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
D0A7H1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
D0AAQ2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 94% |
E8NHE1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 56% | 100% |
E9AE01 | Leishmania major | 29% | 99% |
E9AE09 | Leishmania major | 25% | 99% |
E9AE10 | Leishmania major | 25% | 99% |
E9AE11 | Leishmania major | 31% | 100% |
E9AGK5 | Leishmania infantum | 53% | 100% |
E9AHJ0 | Leishmania infantum | 30% | 99% |
E9AHJ1 | Leishmania infantum | 30% | 100% |
E9ALS2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 99% |
E9ALS3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 96% |
E9ANL0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
E9ANL1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 53% | 98% |
E9ANL2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 46% | 100% |
E9ANS1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
E9APJ3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 53% | 100% |
E9AT53 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9AVF1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9AVF2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 97% |
E9B2B8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 100% |
Q4Q1E4 | Leishmania major | 31% | 100% |
Q4Q5T8 | Leishmania major | 40% | 100% |
Q4QC27 | Leishmania major | 26% | 100% |
Q4QC28 | Leishmania major | 28% | 100% |
Q4QFY5 | Leishmania major | 52% | 99% |
Q4QGU8 | Leishmania major | 25% | 100% |
Q4QH10 | Leishmania major | 46% | 95% |
Q4QH11 | Leishmania major | 46% | 92% |
Q4QH12 | Leishmania major | 46% | 92% |
Q4QH13 | Leishmania major | 46% | 92% |
Q4QH14 | Leishmania major | 53% | 100% |
Q4QH15 | Leishmania major | 82% | 100% |
V5B647 | Trypanosoma cruzi | 46% | 100% |
V5B983 | Trypanosoma cruzi | 32% | 100% |
V5BBB1 | Trypanosoma cruzi | 44% | 100% |
V5BFV8 | Trypanosoma cruzi | 30% | 96% |
V5BQY6 | Trypanosoma cruzi | 35% | 91% |
V5BVP0 | Trypanosoma cruzi | 49% | 100% |
V5DT25 | Trypanosoma cruzi | 48% | 100% |