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: 122 |
NetGPI | no | yes: 0, no: 122 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 115 |
GO:0110165 | cellular anatomical entity | 1 | 115 |
GO:0005737 | cytoplasm | 2 | 3 |
Related structures:
AlphaFold database: A0A3S7WRJ4
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 | 228 | 230 | PF00675 | 0.251 |
CLV_NRD_NRD_1 | 308 | 310 | PF00675 | 0.425 |
CLV_NRD_NRD_1 | 323 | 325 | PF00675 | 0.569 |
CLV_NRD_NRD_1 | 328 | 330 | PF00675 | 0.585 |
CLV_NRD_NRD_1 | 457 | 459 | PF00675 | 0.363 |
CLV_NRD_NRD_1 | 597 | 599 | PF00675 | 0.346 |
CLV_PCSK_KEX2_1 | 228 | 230 | PF00082 | 0.246 |
CLV_PCSK_KEX2_1 | 308 | 310 | PF00082 | 0.453 |
CLV_PCSK_KEX2_1 | 323 | 325 | PF00082 | 0.582 |
CLV_PCSK_KEX2_1 | 328 | 330 | PF00082 | 0.594 |
CLV_PCSK_KEX2_1 | 457 | 459 | PF00082 | 0.347 |
CLV_PCSK_KEX2_1 | 559 | 561 | PF00082 | 0.578 |
CLV_PCSK_KEX2_1 | 597 | 599 | PF00082 | 0.343 |
CLV_PCSK_PC1ET2_1 | 457 | 459 | PF00082 | 0.350 |
CLV_PCSK_PC1ET2_1 | 559 | 561 | PF00082 | 0.591 |
CLV_PCSK_PC7_1 | 304 | 310 | PF00082 | 0.432 |
CLV_PCSK_PC7_1 | 324 | 330 | PF00082 | 0.373 |
CLV_PCSK_PC7_1 | 593 | 599 | PF00082 | 0.397 |
CLV_PCSK_SKI1_1 | 229 | 233 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 245 | 249 | PF00082 | 0.235 |
CLV_PCSK_SKI1_1 | 27 | 31 | PF00082 | 0.257 |
CLV_PCSK_SKI1_1 | 515 | 519 | PF00082 | 0.275 |
CLV_PCSK_SKI1_1 | 597 | 601 | PF00082 | 0.364 |
DEG_APCC_DBOX_1 | 26 | 34 | PF00400 | 0.464 |
DOC_CYCLIN_yClb1_LxF_4 | 275 | 280 | PF00134 | 0.318 |
DOC_CYCLIN_yCln2_LP_2 | 485 | 491 | PF00134 | 0.392 |
DOC_CYCLIN_yCln2_LP_2 | 492 | 498 | PF00134 | 0.249 |
DOC_MAPK_gen_1 | 457 | 466 | PF00069 | 0.527 |
DOC_MAPK_JIP1_4 | 274 | 280 | PF00069 | 0.162 |
DOC_MAPK_MEF2A_6 | 459 | 468 | PF00069 | 0.529 |
DOC_MAPK_MEF2A_6 | 564 | 573 | PF00069 | 0.305 |
DOC_PP1_RVXF_1 | 275 | 281 | PF00149 | 0.272 |
DOC_PP2B_LxvP_1 | 485 | 488 | PF13499 | 0.421 |
DOC_PP2B_LxvP_1 | 49 | 52 | PF13499 | 0.367 |
DOC_PP2B_LxvP_1 | 492 | 495 | PF13499 | 0.302 |
DOC_PP4_FxxP_1 | 78 | 81 | PF00568 | 0.317 |
DOC_USP7_MATH_1 | 261 | 265 | PF00917 | 0.359 |
DOC_USP7_MATH_1 | 297 | 301 | PF00917 | 0.444 |
DOC_USP7_MATH_1 | 344 | 348 | PF00917 | 0.720 |
DOC_USP7_MATH_1 | 355 | 359 | PF00917 | 0.723 |
DOC_USP7_MATH_1 | 425 | 429 | PF00917 | 0.375 |
DOC_USP7_UBL2_3 | 520 | 524 | PF12436 | 0.497 |
DOC_USP7_UBL2_3 | 555 | 559 | PF12436 | 0.421 |
LIG_14-3-3_CanoR_1 | 20 | 28 | PF00244 | 0.551 |
LIG_14-3-3_CanoR_1 | 328 | 336 | PF00244 | 0.793 |
LIG_14-3-3_CanoR_1 | 445 | 451 | PF00244 | 0.309 |
LIG_14-3-3_CanoR_1 | 57 | 65 | PF00244 | 0.340 |
LIG_14-3-3_CanoR_1 | 591 | 596 | PF00244 | 0.568 |
LIG_deltaCOP1_diTrp_1 | 391 | 397 | PF00928 | 0.506 |
LIG_FHA_1 | 119 | 125 | PF00498 | 0.308 |
LIG_FHA_1 | 136 | 142 | PF00498 | 0.314 |
LIG_FHA_1 | 199 | 205 | PF00498 | 0.371 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.442 |
LIG_FHA_1 | 261 | 267 | PF00498 | 0.331 |
LIG_FHA_1 | 282 | 288 | PF00498 | 0.373 |
LIG_FHA_1 | 387 | 393 | PF00498 | 0.495 |
LIG_FHA_1 | 412 | 418 | PF00498 | 0.328 |
LIG_FHA_1 | 428 | 434 | PF00498 | 0.274 |
LIG_FHA_1 | 46 | 52 | PF00498 | 0.318 |
LIG_FHA_1 | 465 | 471 | PF00498 | 0.468 |
LIG_FHA_1 | 472 | 478 | PF00498 | 0.323 |
LIG_FHA_1 | 582 | 588 | PF00498 | 0.396 |
LIG_FHA_1 | 619 | 625 | PF00498 | 0.638 |
LIG_FHA_1 | 68 | 74 | PF00498 | 0.338 |
LIG_FHA_2 | 368 | 374 | PF00498 | 0.528 |
LIG_FHA_2 | 82 | 88 | PF00498 | 0.469 |
LIG_Integrin_isoDGR_2 | 326 | 328 | PF01839 | 0.374 |
LIG_LIR_Apic_2 | 371 | 377 | PF02991 | 0.509 |
LIG_LIR_Apic_2 | 87 | 91 | PF02991 | 0.475 |
LIG_LIR_Gen_1 | 129 | 137 | PF02991 | 0.346 |
LIG_LIR_Gen_1 | 185 | 195 | PF02991 | 0.288 |
LIG_LIR_Gen_1 | 288 | 299 | PF02991 | 0.352 |
LIG_LIR_Gen_1 | 406 | 415 | PF02991 | 0.374 |
LIG_LIR_Gen_1 | 84 | 94 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 129 | 133 | PF02991 | 0.309 |
LIG_LIR_Nem_3 | 163 | 167 | PF02991 | 0.336 |
LIG_LIR_Nem_3 | 174 | 179 | PF02991 | 0.319 |
LIG_LIR_Nem_3 | 185 | 190 | PF02991 | 0.261 |
LIG_LIR_Nem_3 | 288 | 294 | PF02991 | 0.295 |
LIG_LIR_Nem_3 | 35 | 39 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 406 | 410 | PF02991 | 0.329 |
LIG_LIR_Nem_3 | 449 | 453 | PF02991 | 0.534 |
LIG_LIR_Nem_3 | 84 | 89 | PF02991 | 0.355 |
LIG_NRBOX | 428 | 434 | PF00104 | 0.219 |
LIG_Pex14_1 | 244 | 248 | PF04695 | 0.454 |
LIG_Pex14_2 | 175 | 179 | PF04695 | 0.307 |
LIG_Pex14_2 | 190 | 194 | PF04695 | 0.360 |
LIG_Pex14_2 | 246 | 250 | PF04695 | 0.330 |
LIG_Pex14_2 | 403 | 407 | PF04695 | 0.354 |
LIG_Pex14_2 | 43 | 47 | PF04695 | 0.351 |
LIG_Pex14_2 | 450 | 454 | PF04695 | 0.544 |
LIG_Pex14_2 | 78 | 82 | PF04695 | 0.411 |
LIG_PTB_Apo_2 | 409 | 416 | PF02174 | 0.337 |
LIG_SH2_CRK | 291 | 295 | PF00017 | 0.466 |
LIG_SH2_CRK | 86 | 90 | PF00017 | 0.463 |
LIG_SH2_GRB2like | 269 | 272 | PF00017 | 0.352 |
LIG_SH2_PTP2 | 374 | 377 | PF00017 | 0.504 |
LIG_SH2_SRC | 216 | 219 | PF00017 | 0.576 |
LIG_SH2_SRC | 496 | 499 | PF00017 | 0.347 |
LIG_SH2_STAP1 | 45 | 49 | PF00017 | 0.342 |
LIG_SH2_STAP1 | 549 | 553 | PF00017 | 0.292 |
LIG_SH2_STAT3 | 236 | 239 | PF00017 | 0.462 |
LIG_SH2_STAT3 | 549 | 552 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 149 | 152 | PF00017 | 0.496 |
LIG_SH2_STAT5 | 187 | 190 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 236 | 239 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 259 | 262 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 269 | 272 | PF00017 | 0.281 |
LIG_SH2_STAT5 | 374 | 377 | PF00017 | 0.512 |
LIG_SH2_STAT5 | 496 | 499 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 549 | 552 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 88 | 91 | PF00017 | 0.485 |
LIG_SH3_3 | 293 | 299 | PF00018 | 0.360 |
LIG_SH3_3 | 564 | 570 | PF00018 | 0.320 |
LIG_SH3_3 | 607 | 613 | PF00018 | 0.608 |
LIG_Sin3_3 | 47 | 54 | PF02671 | 0.179 |
LIG_SUMO_SIM_anti_2 | 284 | 291 | PF11976 | 0.300 |
LIG_SUMO_SIM_anti_2 | 626 | 634 | PF11976 | 0.739 |
LIG_SUMO_SIM_par_1 | 29 | 35 | PF11976 | 0.431 |
LIG_SUMO_SIM_par_1 | 571 | 576 | PF11976 | 0.337 |
LIG_SUMO_SIM_par_1 | 92 | 98 | PF11976 | 0.332 |
LIG_TRAF2_1 | 222 | 225 | PF00917 | 0.407 |
LIG_TYR_ITIM | 289 | 294 | PF00017 | 0.340 |
LIG_WRC_WIRS_1 | 127 | 132 | PF05994 | 0.366 |
LIG_WRC_WIRS_1 | 172 | 177 | PF05994 | 0.365 |
LIG_WRC_WIRS_1 | 33 | 38 | PF05994 | 0.430 |
LIG_WRC_WIRS_1 | 447 | 452 | PF05994 | 0.502 |
LIG_WRC_WIRS_1 | 592 | 597 | PF05994 | 0.550 |
MOD_CK1_1 | 129 | 135 | PF00069 | 0.371 |
MOD_CK1_1 | 219 | 225 | PF00069 | 0.534 |
MOD_CK1_1 | 300 | 306 | PF00069 | 0.569 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.312 |
MOD_CK1_1 | 67 | 73 | PF00069 | 0.322 |
MOD_CK1_1 | 98 | 104 | PF00069 | 0.334 |
MOD_CK2_1 | 219 | 225 | PF00069 | 0.437 |
MOD_CK2_1 | 328 | 334 | PF00069 | 0.769 |
MOD_CK2_1 | 446 | 452 | PF00069 | 0.360 |
MOD_CMANNOS | 393 | 396 | PF00535 | 0.358 |
MOD_Cter_Amidation | 326 | 329 | PF01082 | 0.384 |
MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.323 |
MOD_GlcNHglycan | 263 | 266 | PF01048 | 0.338 |
MOD_GlcNHglycan | 440 | 443 | PF01048 | 0.303 |
MOD_GlcNHglycan | 530 | 533 | PF01048 | 0.294 |
MOD_GlcNHglycan | 579 | 582 | PF01048 | 0.362 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.358 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.487 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.371 |
MOD_GSK3_1 | 308 | 315 | PF00069 | 0.619 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.334 |
MOD_GSK3_1 | 427 | 434 | PF00069 | 0.290 |
MOD_GSK3_1 | 472 | 479 | PF00069 | 0.324 |
MOD_GSK3_1 | 530 | 537 | PF00069 | 0.325 |
MOD_GSK3_1 | 573 | 580 | PF00069 | 0.373 |
MOD_LATS_1 | 589 | 595 | PF00433 | 0.603 |
MOD_N-GLC_1 | 198 | 203 | PF02516 | 0.365 |
MOD_N-GLC_1 | 312 | 317 | PF02516 | 0.526 |
MOD_N-GLC_1 | 411 | 416 | PF02516 | 0.567 |
MOD_N-GLC_1 | 58 | 63 | PF02516 | 0.508 |
MOD_N-GLC_2 | 386 | 388 | PF02516 | 0.215 |
MOD_NEK2_1 | 160 | 165 | PF00069 | 0.392 |
MOD_NEK2_1 | 197 | 202 | PF00069 | 0.293 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.309 |
MOD_NEK2_1 | 395 | 400 | PF00069 | 0.304 |
MOD_NEK2_1 | 420 | 425 | PF00069 | 0.327 |
MOD_NEK2_1 | 446 | 451 | PF00069 | 0.355 |
MOD_NEK2_1 | 528 | 533 | PF00069 | 0.297 |
MOD_NEK2_1 | 534 | 539 | PF00069 | 0.295 |
MOD_NEK2_1 | 577 | 582 | PF00069 | 0.318 |
MOD_NEK2_2 | 81 | 86 | PF00069 | 0.483 |
MOD_PIKK_1 | 182 | 188 | PF00454 | 0.348 |
MOD_PIKK_1 | 231 | 237 | PF00454 | 0.518 |
MOD_PIKK_1 | 452 | 458 | PF00454 | 0.513 |
MOD_PIKK_1 | 506 | 512 | PF00454 | 0.371 |
MOD_PIKK_1 | 58 | 64 | PF00454 | 0.253 |
MOD_PKA_1 | 308 | 314 | PF00069 | 0.599 |
MOD_PKA_1 | 328 | 334 | PF00069 | 0.582 |
MOD_PKA_2 | 308 | 314 | PF00069 | 0.598 |
MOD_PKA_2 | 322 | 328 | PF00069 | 0.781 |
MOD_PKA_2 | 631 | 637 | PF00069 | 0.779 |
MOD_PKB_1 | 591 | 599 | PF00069 | 0.415 |
MOD_Plk_1 | 317 | 323 | PF00069 | 0.656 |
MOD_Plk_1 | 344 | 350 | PF00069 | 0.709 |
MOD_Plk_1 | 411 | 417 | PF00069 | 0.334 |
MOD_Plk_2-3 | 317 | 323 | PF00069 | 0.730 |
MOD_Plk_4 | 142 | 148 | PF00069 | 0.330 |
MOD_Plk_4 | 171 | 177 | PF00069 | 0.372 |
MOD_Plk_4 | 282 | 288 | PF00069 | 0.342 |
MOD_Plk_4 | 379 | 385 | PF00069 | 0.527 |
MOD_Plk_4 | 411 | 417 | PF00069 | 0.317 |
MOD_Plk_4 | 431 | 437 | PF00069 | 0.320 |
MOD_Plk_4 | 446 | 452 | PF00069 | 0.335 |
MOD_Plk_4 | 473 | 479 | PF00069 | 0.321 |
MOD_Plk_4 | 534 | 540 | PF00069 | 0.302 |
MOD_Plk_4 | 81 | 87 | PF00069 | 0.371 |
MOD_Plk_4 | 95 | 101 | PF00069 | 0.294 |
TRG_DiLeu_BaLyEn_6 | 442 | 447 | PF01217 | 0.324 |
TRG_DiLeu_BaLyEn_6 | 567 | 572 | PF01217 | 0.318 |
TRG_ENDOCYTIC_2 | 187 | 190 | PF00928 | 0.301 |
TRG_ENDOCYTIC_2 | 269 | 272 | PF00928 | 0.263 |
TRG_ENDOCYTIC_2 | 291 | 294 | PF00928 | 0.308 |
TRG_ENDOCYTIC_2 | 592 | 595 | PF00928 | 0.527 |
TRG_ENDOCYTIC_2 | 86 | 89 | PF00928 | 0.486 |
TRG_ER_diArg_1 | 228 | 230 | PF00400 | 0.474 |
TRG_ER_diArg_1 | 597 | 599 | PF00400 | 0.557 |
TRG_ER_diArg_1 | 603 | 606 | PF00400 | 0.558 |
TRG_Pf-PMV_PEXEL_1 | 20 | 24 | PF00026 | 0.405 |
TRG_Pf-PMV_PEXEL_1 | 542 | 547 | PF00026 | 0.389 |
TRG_Pf-PMV_PEXEL_1 | 598 | 602 | PF00026 | 0.354 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6G0 | Leptomonas seymouri | 40% | 100% |
A0A0N1HT40 | Leptomonas seymouri | 46% | 100% |
A0A0N1HZC2 | Leptomonas seymouri | 30% | 100% |
A0A0N1IKC5 | Leptomonas seymouri | 56% | 100% |
A0A0N1PB63 | Leptomonas seymouri | 29% | 97% |
A0A0N1PD04 | Leptomonas seymouri | 23% | 100% |
A0A0N1PFR4 | Leptomonas seymouri | 27% | 97% |
A0A0S4JR45 | Bodo saltans | 29% | 100% |
A0A1X0NKK0 | Trypanosomatidae | 32% | 100% |
A0A1X0NL32 | Trypanosomatidae | 33% | 100% |
A0A1X0NM09 | Trypanosomatidae | 30% | 100% |
A0A1X0NRW5 | Trypanosomatidae | 39% | 92% |
A0A1X0NV13 | Trypanosomatidae | 51% | 99% |
A0A1X0NV19 | Trypanosomatidae | 51% | 100% |
A0A1X0NV27 | Trypanosomatidae | 52% | 100% |
A0A1X0NVH8 | Trypanosomatidae | 43% | 97% |
A0A1X0NVM7 | Trypanosomatidae | 49% | 99% |
A0A1X0NWQ1 | Trypanosomatidae | 48% | 100% |
A0A1X0NZE6 | Trypanosomatidae | 33% | 100% |
A0A1X0NZU2 | Trypanosomatidae | 30% | 99% |
A0A1X0NZU5 | Trypanosomatidae | 34% | 100% |
A0A1X0NZW1 | Trypanosomatidae | 29% | 100% |
A0A1X0P0M7 | Trypanosomatidae | 31% | 100% |
A0A381MMW5 | Leishmania infantum | 30% | 100% |
A0A3Q8I7Y9 | Leishmania donovani | 48% | 92% |
A0A3Q8IEC4 | Leishmania donovani | 30% | 100% |
A0A3Q8IF95 | Leishmania donovani | 30% | 100% |
A0A3Q8IIT5 | Leishmania donovani | 25% | 100% |
A0A3Q8ISY9 | Leishmania donovani | 40% | 100% |
A0A3R7JSQ9 | Trypanosoma rangeli | 27% | 100% |
A0A3R7KKN8 | Trypanosoma rangeli | 29% | 100% |
A0A3R7MAQ7 | Trypanosoma rangeli | 36% | 91% |
A0A3R7N3S6 | Trypanosoma rangeli | 22% | 99% |
A0A3R7N415 | Trypanosoma rangeli | 27% | 100% |
A0A3R7N921 | Trypanosoma rangeli | 29% | 100% |
A0A3R7R443 | Trypanosoma rangeli | 29% | 100% |
A0A3S7WRJ5 | Leishmania donovani | 51% | 92% |
A0A3S7WRL4 | Leishmania donovani | 46% | 100% |
A0A3S7WRS3 | Leishmania donovani | 24% | 100% |
A0A3S7WSR4 | Leishmania donovani | 55% | 100% |
A0A3S7WWU1 | Leishmania donovani | 27% | 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% |
A4H6J0 | Leishmania braziliensis | 83% | 100% |
A4H6J1 | Leishmania braziliensis | 55% | 100% |
A4H6J3 | Leishmania braziliensis | 48% | 98% |
A4H6Q5 | Leishmania braziliensis | 25% | 100% |
A4HC19 | Leishmania braziliensis | 28% | 100% |
A4HHG2 | Leishmania braziliensis | 25% | 100% |
A4HHG3 | Leishmania braziliensis | 31% | 100% |
A4HHG4 | Leishmania braziliensis | 32% | 100% |
A4HJW3 | Leishmania braziliensis | 41% | 100% |
A4HPE2 | Leishmania braziliensis | 31% | 100% |
A4HUX5 | Leishmania infantum | 100% | 100% |
A4HUX6 | Leishmania infantum | 51% | 100% |
A4HUX7 | Leishmania infantum | 47% | 99% |
A4HUX8 | Leishmania infantum | 47% | 99% |
A4HV40 | Leishmania infantum | 24% | 100% |
A4HZF5 | Leishmania infantum | 30% | 100% |
A4HZJ4 | Leishmania infantum | 27% | 100% |
A4I4L2 | Leishmania infantum | 25% | 100% |
A4I7C5 | Leishmania infantum | 40% | 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) | 29% | 100% |
C9ZL99 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
C9ZLA0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
C9ZLA1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
C9ZTR5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 100% |
C9ZTR6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 100% |
C9ZTR7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% |
C9ZTR8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 100% |
C9ZTR9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 100% |
C9ZTS1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 100% |
C9ZUT6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% |
D0A7B1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
D0A7H1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
D0AAQ2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 94% |
E8NHE1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 57% | 100% |
E9AE01 | Leishmania major | 31% | 100% |
E9AE09 | Leishmania major | 26% | 100% |
E9AE10 | Leishmania major | 26% | 100% |
E9AE11 | Leishmania major | 31% | 100% |
E9AGK5 | Leishmania infantum | 55% | 99% |
E9AHJ0 | Leishmania infantum | 30% | 100% |
E9AHJ1 | Leishmania infantum | 30% | 100% |
E9ALS2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9ALS3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9ANL0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
E9ANL1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 54% | 100% |
E9ANL2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 46% | 94% |
E9ANS1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
E9APJ3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 54% | 99% |
E9AT53 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9AVF1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 99% |
E9AVF2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9B2B8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 39% | 100% |
Q4Q1E4 | Leishmania major | 31% | 100% |
Q4Q5T8 | Leishmania major | 40% | 100% |
Q4QC27 | Leishmania major | 27% | 100% |
Q4QC28 | Leishmania major | 29% | 95% |
Q4QFY5 | Leishmania major | 54% | 98% |
Q4QGU8 | Leishmania major | 23% | 100% |
Q4QH10 | Leishmania major | 48% | 96% |
Q4QH11 | Leishmania major | 47% | 93% |
Q4QH12 | Leishmania major | 47% | 93% |
Q4QH13 | Leishmania major | 47% | 93% |
Q4QH14 | Leishmania major | 53% | 100% |
Q4QH15 | Leishmania major | 95% | 100% |
V5B647 | Trypanosoma cruzi | 46% | 100% |
V5B983 | Trypanosoma cruzi | 33% | 100% |
V5BBB1 | Trypanosoma cruzi | 45% | 100% |
V5BFV8 | Trypanosoma cruzi | 30% | 96% |
V5BQY6 | Trypanosoma cruzi | 37% | 91% |
V5BVP0 | Trypanosoma cruzi | 50% | 100% |
V5DT25 | Trypanosoma cruzi | 50% | 100% |