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: 106 |
NetGPI | no | yes: 0, no: 106 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 100 |
GO:0110165 | cellular anatomical entity | 1 | 100 |
GO:0005737 | cytoplasm | 2 | 3 |
Related structures:
AlphaFold database: E9AE11
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 49 |
GO:0022857 | transmembrane transporter activity | 2 | 49 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 642 | 646 | PF00656 | 0.701 |
CLV_NRD_NRD_1 | 216 | 218 | PF00675 | 0.259 |
CLV_NRD_NRD_1 | 437 | 439 | PF00675 | 0.642 |
CLV_NRD_NRD_1 | 617 | 619 | PF00675 | 0.346 |
CLV_PCSK_FUR_1 | 615 | 619 | PF00082 | 0.433 |
CLV_PCSK_KEX2_1 | 215 | 217 | PF00082 | 0.253 |
CLV_PCSK_KEX2_1 | 316 | 318 | PF00082 | 0.403 |
CLV_PCSK_KEX2_1 | 399 | 401 | PF00082 | 0.360 |
CLV_PCSK_KEX2_1 | 617 | 619 | PF00082 | 0.345 |
CLV_PCSK_PC1ET2_1 | 316 | 318 | PF00082 | 0.403 |
CLV_PCSK_PC1ET2_1 | 399 | 401 | PF00082 | 0.424 |
CLV_PCSK_SKI1_1 | 149 | 153 | PF00082 | 0.366 |
CLV_PCSK_SKI1_1 | 216 | 220 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 316 | 320 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 528 | 532 | PF00082 | 0.278 |
CLV_PCSK_SKI1_1 | 564 | 568 | PF00082 | 0.564 |
CLV_PCSK_SKI1_1 | 618 | 622 | PF00082 | 0.352 |
CLV_PCSK_SKI1_1 | 634 | 638 | PF00082 | 0.363 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.668 |
DOC_CYCLIN_RxL_1 | 525 | 534 | PF00134 | 0.375 |
DOC_MAPK_DCC_7 | 105 | 113 | PF00069 | 0.183 |
DOC_MAPK_gen_1 | 205 | 214 | PF00069 | 0.457 |
DOC_MAPK_gen_1 | 399 | 405 | PF00069 | 0.479 |
DOC_MAPK_MEF2A_6 | 105 | 113 | PF00069 | 0.321 |
DOC_MAPK_MEF2A_6 | 264 | 273 | PF00069 | 0.291 |
DOC_PP1_RVXF_1 | 361 | 368 | PF00149 | 0.543 |
DOC_PP2B_LxvP_1 | 496 | 499 | PF13499 | 0.412 |
DOC_PP2B_PxIxI_1 | 474 | 480 | PF00149 | 0.390 |
DOC_SPAK_OSR1_1 | 14 | 18 | PF12202 | 0.524 |
DOC_USP7_MATH_1 | 257 | 261 | PF00917 | 0.312 |
DOC_USP7_MATH_1 | 353 | 357 | PF00917 | 0.772 |
DOC_USP7_MATH_1 | 421 | 425 | PF00917 | 0.536 |
DOC_USP7_MATH_1 | 482 | 486 | PF00917 | 0.365 |
DOC_USP7_MATH_1 | 499 | 503 | PF00917 | 0.374 |
DOC_USP7_UBL2_3 | 293 | 297 | PF12436 | 0.700 |
DOC_USP7_UBL2_3 | 347 | 351 | PF12436 | 0.597 |
DOC_USP7_UBL2_3 | 435 | 439 | PF12436 | 0.274 |
DOC_USP7_UBL2_3 | 533 | 537 | PF12436 | 0.484 |
LIG_14-3-3_CanoR_1 | 168 | 176 | PF00244 | 0.365 |
LIG_14-3-3_CanoR_1 | 215 | 224 | PF00244 | 0.486 |
LIG_14-3-3_CanoR_1 | 264 | 270 | PF00244 | 0.354 |
LIG_14-3-3_CanoR_1 | 380 | 390 | PF00244 | 0.670 |
LIG_14-3-3_CanoR_1 | 438 | 444 | PF00244 | 0.393 |
LIG_14-3-3_CanoR_1 | 456 | 460 | PF00244 | 0.286 |
LIG_14-3-3_CanoR_1 | 8 | 16 | PF00244 | 0.535 |
LIG_AP2alpha_1 | 510 | 514 | PF02296 | 0.199 |
LIG_deltaCOP1_diTrp_1 | 402 | 408 | PF00928 | 0.364 |
LIG_EH1_1 | 175 | 183 | PF00400 | 0.442 |
LIG_FHA_1 | 108 | 114 | PF00498 | 0.335 |
LIG_FHA_1 | 125 | 131 | PF00498 | 0.319 |
LIG_FHA_1 | 185 | 191 | PF00498 | 0.383 |
LIG_FHA_1 | 266 | 272 | PF00498 | 0.345 |
LIG_FHA_1 | 4 | 10 | PF00498 | 0.577 |
LIG_FHA_1 | 471 | 477 | PF00498 | 0.587 |
LIG_FHA_1 | 55 | 61 | PF00498 | 0.341 |
LIG_FHA_1 | 602 | 608 | PF00498 | 0.391 |
LIG_HCF-1_HBM_1 | 4 | 7 | PF13415 | 0.434 |
LIG_LIR_Apic_2 | 74 | 78 | PF02991 | 0.462 |
LIG_LIR_Gen_1 | 13 | 22 | PF02991 | 0.484 |
LIG_LIR_Gen_1 | 171 | 182 | PF02991 | 0.293 |
LIG_LIR_Gen_1 | 392 | 403 | PF02991 | 0.517 |
LIG_LIR_Gen_1 | 442 | 451 | PF02991 | 0.327 |
LIG_LIR_Gen_1 | 594 | 603 | PF02991 | 0.308 |
LIG_LIR_Gen_1 | 609 | 619 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 13 | 18 | PF02991 | 0.503 |
LIG_LIR_Nem_3 | 150 | 154 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 171 | 177 | PF02991 | 0.267 |
LIG_LIR_Nem_3 | 392 | 398 | PF02991 | 0.526 |
LIG_LIR_Nem_3 | 442 | 447 | PF02991 | 0.352 |
LIG_LIR_Nem_3 | 594 | 598 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 609 | 614 | PF02991 | 0.320 |
LIG_LYPXL_yS_3 | 227 | 230 | PF13949 | 0.390 |
LIG_NRBOX | 491 | 497 | PF00104 | 0.395 |
LIG_Pex14_2 | 233 | 237 | PF04695 | 0.335 |
LIG_Pex14_2 | 510 | 514 | PF04695 | 0.351 |
LIG_PTB_Apo_2 | 160 | 167 | PF02174 | 0.304 |
LIG_PTB_Apo_2 | 430 | 437 | PF02174 | 0.346 |
LIG_PTB_Apo_2 | 537 | 544 | PF02174 | 0.542 |
LIG_PTB_Phospho_1 | 430 | 436 | PF10480 | 0.392 |
LIG_PTB_Phospho_1 | 537 | 543 | PF10480 | 0.373 |
LIG_REV1ctd_RIR_1 | 164 | 172 | PF16727 | 0.283 |
LIG_SH2_CRK | 256 | 260 | PF00017 | 0.335 |
LIG_SH2_CRK | 428 | 432 | PF00017 | 0.296 |
LIG_SH2_CRK | 444 | 448 | PF00017 | 0.407 |
LIG_SH2_CRK | 75 | 79 | PF00017 | 0.431 |
LIG_SH2_GRB2like | 256 | 259 | PF00017 | 0.382 |
LIG_SH2_GRB2like | 538 | 541 | PF00017 | 0.303 |
LIG_SH2_NCK_1 | 256 | 260 | PF00017 | 0.320 |
LIG_SH2_SRC | 256 | 259 | PF00017 | 0.366 |
LIG_SH2_STAP1 | 444 | 448 | PF00017 | 0.382 |
LIG_SH2_STAP1 | 562 | 566 | PF00017 | 0.308 |
LIG_SH2_STAT3 | 223 | 226 | PF00017 | 0.450 |
LIG_SH2_STAT3 | 562 | 565 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 223 | 226 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 234 | 237 | PF00017 | 0.323 |
LIG_SH2_STAT5 | 246 | 249 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 337 | 340 | PF00017 | 0.556 |
LIG_SH2_STAT5 | 543 | 546 | PF00017 | 0.371 |
LIG_SH3_1 | 297 | 303 | PF00018 | 0.637 |
LIG_SH3_3 | 297 | 303 | PF00018 | 0.634 |
LIG_SH3_3 | 315 | 321 | PF00018 | 0.790 |
LIG_SH3_3 | 577 | 583 | PF00018 | 0.368 |
LIG_SUMO_SIM_anti_2 | 157 | 163 | PF11976 | 0.423 |
LIG_SUMO_SIM_anti_2 | 187 | 192 | PF11976 | 0.372 |
LIG_SUMO_SIM_anti_2 | 268 | 273 | PF11976 | 0.306 |
LIG_SUMO_SIM_anti_2 | 48 | 57 | PF11976 | 0.337 |
LIG_SUMO_SIM_anti_2 | 594 | 600 | PF11976 | 0.383 |
LIG_SUMO_SIM_par_1 | 445 | 452 | PF11976 | 0.343 |
LIG_TYR_ITIM | 244 | 249 | PF00017 | 0.354 |
LIG_TYR_ITSM | 440 | 447 | PF00017 | 0.347 |
LIG_UBA3_1 | 495 | 503 | PF00899 | 0.398 |
LIG_WRC_WIRS_1 | 148 | 153 | PF05994 | 0.365 |
LIG_WRC_WIRS_1 | 249 | 254 | PF05994 | 0.384 |
LIG_WRC_WIRS_1 | 307 | 312 | PF05994 | 0.480 |
LIG_WRC_WIRS_1 | 511 | 516 | PF05994 | 0.402 |
MOD_CK1_1 | 10 | 16 | PF00069 | 0.426 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.350 |
MOD_CK1_1 | 449 | 455 | PF00069 | 0.352 |
MOD_CK1_1 | 50 | 56 | PF00069 | 0.347 |
MOD_CK2_1 | 352 | 358 | PF00069 | 0.712 |
MOD_CMANNOS | 404 | 407 | PF00535 | 0.355 |
MOD_Cter_Amidation | 348 | 351 | PF01082 | 0.500 |
MOD_Cter_Amidation | 586 | 589 | PF01082 | 0.465 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.251 |
MOD_GlcNHglycan | 423 | 426 | PF01048 | 0.383 |
MOD_GlcNHglycan | 444 | 447 | PF01048 | 0.332 |
MOD_GlcNHglycan | 451 | 454 | PF01048 | 0.301 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.365 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.363 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.337 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.439 |
MOD_GSK3_1 | 390 | 397 | PF00069 | 0.438 |
MOD_GSK3_1 | 442 | 449 | PF00069 | 0.355 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.329 |
MOD_GSK3_1 | 516 | 523 | PF00069 | 0.344 |
MOD_GSK3_1 | 635 | 642 | PF00069 | 0.525 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.394 |
MOD_N-GLC_1 | 162 | 167 | PF02516 | 0.347 |
MOD_N-GLC_1 | 45 | 50 | PF02516 | 0.396 |
MOD_N-GLC_1 | 601 | 606 | PF02516 | 0.288 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.342 |
MOD_NEK2_1 | 154 | 159 | PF00069 | 0.370 |
MOD_NEK2_1 | 22 | 27 | PF00069 | 0.307 |
MOD_NEK2_1 | 265 | 270 | PF00069 | 0.295 |
MOD_NEK2_1 | 394 | 399 | PF00069 | 0.384 |
MOD_NEK2_1 | 45 | 50 | PF00069 | 0.342 |
MOD_NEK2_1 | 510 | 515 | PF00069 | 0.351 |
MOD_NEK2_1 | 87 | 92 | PF00069 | 0.273 |
MOD_NEK2_2 | 27 | 32 | PF00069 | 0.323 |
MOD_PIKK_1 | 222 | 228 | PF00454 | 0.346 |
MOD_PKA_1 | 216 | 222 | PF00069 | 0.410 |
MOD_PKA_2 | 167 | 173 | PF00069 | 0.428 |
MOD_PKA_2 | 216 | 222 | PF00069 | 0.325 |
MOD_PKA_2 | 437 | 443 | PF00069 | 0.535 |
MOD_PKA_2 | 455 | 461 | PF00069 | 0.312 |
MOD_PKA_2 | 7 | 13 | PF00069 | 0.401 |
MOD_Plk_1 | 10 | 16 | PF00069 | 0.528 |
MOD_Plk_1 | 162 | 168 | PF00069 | 0.388 |
MOD_Plk_1 | 203 | 209 | PF00069 | 0.465 |
MOD_Plk_1 | 3 | 9 | PF00069 | 0.565 |
MOD_Plk_1 | 50 | 56 | PF00069 | 0.311 |
MOD_Plk_1 | 601 | 607 | PF00069 | 0.327 |
MOD_Plk_2-3 | 306 | 312 | PF00069 | 0.677 |
MOD_Plk_2-3 | 635 | 641 | PF00069 | 0.505 |
MOD_Plk_4 | 126 | 132 | PF00069 | 0.328 |
MOD_Plk_4 | 154 | 160 | PF00069 | 0.367 |
MOD_Plk_4 | 162 | 168 | PF00069 | 0.372 |
MOD_Plk_4 | 265 | 271 | PF00069 | 0.374 |
MOD_Plk_4 | 27 | 33 | PF00069 | 0.314 |
MOD_Plk_4 | 390 | 396 | PF00069 | 0.410 |
MOD_Plk_4 | 439 | 445 | PF00069 | 0.313 |
MOD_Plk_4 | 50 | 56 | PF00069 | 0.382 |
MOD_Plk_4 | 591 | 597 | PF00069 | 0.316 |
MOD_Plk_4 | 607 | 613 | PF00069 | 0.292 |
MOD_Plk_4 | 83 | 89 | PF00069 | 0.306 |
MOD_SUMO_rev_2 | 309 | 318 | PF00179 | 0.727 |
MOD_SUMO_rev_2 | 374 | 379 | PF00179 | 0.609 |
MOD_SUMO_rev_2 | 432 | 440 | PF00179 | 0.507 |
MOD_SUMO_rev_2 | 633 | 639 | PF00179 | 0.509 |
TRG_DiLeu_BaEn_2 | 10 | 16 | PF01217 | 0.460 |
TRG_ENDOCYTIC_2 | 164 | 167 | PF00928 | 0.351 |
TRG_ENDOCYTIC_2 | 174 | 177 | PF00928 | 0.303 |
TRG_ENDOCYTIC_2 | 198 | 201 | PF00928 | 0.370 |
TRG_ENDOCYTIC_2 | 227 | 230 | PF00928 | 0.389 |
TRG_ENDOCYTIC_2 | 234 | 237 | PF00928 | 0.353 |
TRG_ENDOCYTIC_2 | 246 | 249 | PF00928 | 0.296 |
TRG_ENDOCYTIC_2 | 428 | 431 | PF00928 | 0.363 |
TRG_ENDOCYTIC_2 | 444 | 447 | PF00928 | 0.319 |
TRG_ENDOCYTIC_2 | 538 | 541 | PF00928 | 0.321 |
TRG_ENDOCYTIC_2 | 558 | 561 | PF00928 | 0.447 |
TRG_ENDOCYTIC_2 | 616 | 619 | PF00928 | 0.387 |
TRG_ER_diArg_1 | 214 | 217 | PF00400 | 0.349 |
TRG_ER_diArg_1 | 616 | 618 | PF00400 | 0.443 |
TRG_Pf-PMV_PEXEL_1 | 216 | 220 | PF00026 | 0.380 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6G0 | Leptomonas seymouri | 29% | 100% |
A0A0N1HZC2 | Leptomonas seymouri | 32% | 100% |
A0A0N1IKC5 | Leptomonas seymouri | 32% | 100% |
A0A0N1PB63 | Leptomonas seymouri | 27% | 98% |
A0A0N1PD04 | Leptomonas seymouri | 26% | 100% |
A0A0N1PFR4 | Leptomonas seymouri | 33% | 98% |
A0A0S4JR45 | Bodo saltans | 29% | 100% |
A0A1X0NKK0 | Trypanosomatidae | 31% | 100% |
A0A1X0NM09 | Trypanosomatidae | 29% | 100% |
A0A1X0NV19 | Trypanosomatidae | 33% | 100% |
A0A1X0NV27 | Trypanosomatidae | 32% | 100% |
A0A1X0NVF9 | Trypanosomatidae | 23% | 97% |
A0A1X0NVH8 | Trypanosomatidae | 29% | 98% |
A0A1X0NVM7 | Trypanosomatidae | 30% | 100% |
A0A1X0NWQ1 | Trypanosomatidae | 34% | 100% |
A0A1X0NZE6 | Trypanosomatidae | 30% | 100% |
A0A1X0NZU2 | Trypanosomatidae | 33% | 100% |
A0A1X0NZU5 | Trypanosomatidae | 53% | 100% |
A0A1X0NZW1 | Trypanosomatidae | 32% | 100% |
A0A1X0P0M7 | Trypanosomatidae | 29% | 100% |
A0A381MMW5 | Leishmania infantum | 89% | 99% |
A0A3Q8IEC4 | Leishmania donovani | 88% | 100% |
A0A3Q8IF95 | Leishmania donovani | 27% | 100% |
A0A3Q8IIT5 | Leishmania donovani | 31% | 96% |
A0A3Q8ISY9 | Leishmania donovani | 28% | 100% |
A0A3R7KKN8 | Trypanosoma rangeli | 33% | 100% |
A0A3R7MAQ7 | Trypanosoma rangeli | 27% | 92% |
A0A3R7N3S6 | Trypanosoma rangeli | 26% | 100% |
A0A3R7N415 | Trypanosoma rangeli | 31% | 100% |
A0A3R7N921 | Trypanosoma rangeli | 28% | 100% |
A0A3R7R443 | Trypanosoma rangeli | 31% | 100% |
A0A3S7WRJ4 | Leishmania donovani | 31% | 100% |
A0A3S7WRJ5 | Leishmania donovani | 31% | 93% |
A0A3S7WRS3 | Leishmania donovani | 25% | 100% |
A0A3S7WSR4 | Leishmania donovani | 31% | 100% |
A0A3S7WWU1 | Leishmania donovani | 26% | 98% |
A0A3S7X2G0 | Leishmania donovani | 89% | 99% |
A0A3S7X2K5 | Leishmania donovani | 94% | 100% |
A0A3S7XB11 | Leishmania donovani | 30% | 100% |
A0A422MSE4 | Trypanosoma rangeli | 34% | 100% |
A0A422MSP6 | Trypanosoma rangeli | 48% | 100% |
A0A422MST9 | Trypanosoma rangeli | 31% | 100% |
A0A422MU68 | Trypanosoma rangeli | 31% | 100% |
A4H6J0 | Leishmania braziliensis | 31% | 100% |
A4H6J1 | Leishmania braziliensis | 32% | 99% |
A4H6Q5 | Leishmania braziliensis | 26% | 100% |
A4HC19 | Leishmania braziliensis | 28% | 100% |
A4HHG2 | Leishmania braziliensis | 31% | 96% |
A4HHG3 | Leishmania braziliensis | 76% | 100% |
A4HHG4 | Leishmania braziliensis | 74% | 99% |
A4HJW3 | Leishmania braziliensis | 28% | 100% |
A4HPE2 | Leishmania braziliensis | 31% | 100% |
A4HUX5 | Leishmania infantum | 31% | 100% |
A4HUX6 | Leishmania infantum | 32% | 93% |
A4HV40 | Leishmania infantum | 25% | 100% |
A4HZF5 | Leishmania infantum | 27% | 100% |
A4HZJ4 | Leishmania infantum | 26% | 98% |
A4I4L2 | Leishmania infantum | 30% | 96% |
A4I7C5 | Leishmania infantum | 28% | 100% |
A4ICI3 | Leishmania infantum | 30% | 100% |
C9ZL97 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZL98 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
C9ZL99 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZLA0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZLA1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZTR5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZTR6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
C9ZTR7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
C9ZTR8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZTR9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
C9ZTS1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
C9ZUT6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
D0A7B1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
D0A7H1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
E8NHE1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
E9AE01 | Leishmania major | 94% | 100% |
E9AE09 | Leishmania major | 30% | 100% |
E9AE10 | Leishmania major | 30% | 100% |
E9AGK5 | Leishmania infantum | 31% | 100% |
E9AHJ0 | Leishmania infantum | 88% | 100% |
E9AHJ1 | Leishmania infantum | 94% | 100% |
E9ALS2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
E9ALS3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 96% |
E9ANL0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9ANL1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 99% |
E9ANS1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9APJ3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9AT53 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9AVF1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9AVF2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 98% |
E9B2B8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
Q4Q1E4 | Leishmania major | 30% | 100% |
Q4Q5T8 | Leishmania major | 28% | 100% |
Q4QC27 | Leishmania major | 27% | 100% |
Q4QC28 | Leishmania major | 27% | 100% |
Q4QFY5 | Leishmania major | 31% | 100% |
Q4QGU8 | Leishmania major | 26% | 100% |
Q4QH14 | Leishmania major | 31% | 99% |
Q4QH15 | Leishmania major | 31% | 100% |
V5B647 | Trypanosoma cruzi | 30% | 100% |
V5B983 | Trypanosoma cruzi | 46% | 100% |
V5BFV8 | Trypanosoma cruzi | 31% | 97% |
V5BQY6 | Trypanosoma cruzi | 29% | 92% |
V5BVP0 | Trypanosoma cruzi | 31% | 100% |
V5DT25 | Trypanosoma cruzi | 31% | 100% |