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: 32 |
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: 124 |
NetGPI | no | yes: 0, no: 124 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 117 |
GO:0110165 | cellular anatomical entity | 1 | 117 |
GO:0005737 | cytoplasm | 2 | 3 |
Related structures:
AlphaFold database: E9APJ3
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 | 274 | 276 | PF00675 | 0.465 |
CLV_NRD_NRD_1 | 306 | 308 | PF00675 | 0.444 |
CLV_NRD_NRD_1 | 544 | 546 | PF00675 | 0.518 |
CLV_NRD_NRD_1 | 574 | 576 | PF00675 | 0.345 |
CLV_NRD_NRD_1 | 585 | 587 | PF00675 | 0.369 |
CLV_PCSK_KEX2_1 | 20 | 22 | PF00082 | 0.358 |
CLV_PCSK_KEX2_1 | 306 | 308 | PF00082 | 0.471 |
CLV_PCSK_KEX2_1 | 437 | 439 | PF00082 | 0.346 |
CLV_PCSK_KEX2_1 | 442 | 444 | PF00082 | 0.321 |
CLV_PCSK_KEX2_1 | 574 | 576 | PF00082 | 0.347 |
CLV_PCSK_KEX2_1 | 585 | 587 | PF00082 | 0.366 |
CLV_PCSK_PC1ET2_1 | 20 | 22 | PF00082 | 0.389 |
CLV_PCSK_PC1ET2_1 | 437 | 439 | PF00082 | 0.352 |
CLV_PCSK_PC1ET2_1 | 442 | 444 | PF00082 | 0.327 |
CLV_PCSK_PC7_1 | 438 | 444 | PF00082 | 0.323 |
CLV_PCSK_SKI1_1 | 365 | 369 | PF00082 | 0.343 |
CLV_PCSK_SKI1_1 | 410 | 414 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 469 | 473 | PF00082 | 0.518 |
DEG_APCC_DBOX_1 | 26 | 34 | PF00400 | 0.465 |
DEG_APCC_DBOX_1 | 409 | 417 | PF00400 | 0.393 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.714 |
DOC_AGCK_PIF_1 | 43 | 48 | PF00069 | 0.424 |
DOC_CYCLIN_RxL_1 | 362 | 369 | PF00134 | 0.548 |
DOC_CYCLIN_yCln2_LP_2 | 207 | 213 | PF00134 | 0.424 |
DOC_CYCLIN_yCln2_LP_2 | 472 | 478 | PF00134 | 0.250 |
DOC_MAPK_FxFP_2 | 101 | 104 | PF00069 | 0.419 |
DOC_MAPK_gen_1 | 275 | 281 | PF00069 | 0.328 |
DOC_MAPK_gen_1 | 442 | 450 | PF00069 | 0.465 |
DOC_MAPK_gen_1 | 5 | 13 | PF00069 | 0.586 |
DOC_MAPK_gen_1 | 545 | 552 | PF00069 | 0.342 |
DOC_MAPK_MEF2A_6 | 27 | 35 | PF00069 | 0.493 |
DOC_MAPK_MEF2A_6 | 442 | 450 | PF00069 | 0.478 |
DOC_MAPK_MEF2A_6 | 5 | 13 | PF00069 | 0.660 |
DOC_MAPK_MEF2A_6 | 545 | 554 | PF00069 | 0.307 |
DOC_PP1_RVXF_1 | 276 | 282 | PF00149 | 0.273 |
DOC_PP2B_LxvP_1 | 207 | 210 | PF13499 | 0.303 |
DOC_PP2B_LxvP_1 | 450 | 453 | PF13499 | 0.307 |
DOC_PP2B_LxvP_1 | 465 | 468 | PF13499 | 0.418 |
DOC_PP2B_LxvP_1 | 472 | 475 | PF13499 | 0.304 |
DOC_PP4_FxxP_1 | 101 | 104 | PF00568 | 0.415 |
DOC_PP4_FxxP_1 | 338 | 341 | PF00568 | 0.759 |
DOC_USP7_MATH_1 | 453 | 457 | PF00917 | 0.383 |
DOC_USP7_MATH_1 | 514 | 518 | PF00917 | 0.294 |
DOC_USP7_MATH_1 | 562 | 566 | PF00917 | 0.394 |
DOC_USP7_UBL2_3 | 16 | 20 | PF12436 | 0.568 |
DOC_WW_Pin1_4 | 306 | 311 | PF00397 | 0.626 |
DOC_WW_Pin1_4 | 337 | 342 | PF00397 | 0.745 |
DOC_WW_Pin1_4 | 589 | 594 | PF00397 | 0.666 |
LIG_14-3-3_CanoR_1 | 21 | 28 | PF00244 | 0.549 |
LIG_14-3-3_CanoR_1 | 410 | 416 | PF00244 | 0.369 |
LIG_14-3-3_CanoR_1 | 425 | 431 | PF00244 | 0.311 |
LIG_14-3-3_CanoR_1 | 574 | 581 | PF00244 | 0.582 |
LIG_14-3-3_CanoR_1 | 58 | 66 | PF00244 | 0.340 |
LIG_BRCT_BRCA1_1 | 393 | 397 | PF00533 | 0.383 |
LIG_BRCT_BRCA1_1 | 44 | 48 | PF00533 | 0.356 |
LIG_BRCT_BRCA1_1 | 99 | 103 | PF00533 | 0.328 |
LIG_eIF4E_1 | 187 | 193 | PF01652 | 0.269 |
LIG_eIF4E_1 | 248 | 254 | PF01652 | 0.287 |
LIG_EVH1_2 | 298 | 302 | PF00568 | 0.294 |
LIG_FHA_1 | 262 | 268 | PF00498 | 0.334 |
LIG_FHA_1 | 359 | 365 | PF00498 | 0.505 |
LIG_FHA_1 | 407 | 413 | PF00498 | 0.272 |
LIG_FHA_1 | 421 | 427 | PF00498 | 0.352 |
LIG_FHA_1 | 445 | 451 | PF00498 | 0.466 |
LIG_FHA_1 | 45 | 51 | PF00498 | 0.317 |
LIG_FHA_1 | 452 | 458 | PF00498 | 0.322 |
LIG_FHA_1 | 487 | 493 | PF00498 | 0.287 |
LIG_FHA_1 | 559 | 565 | PF00498 | 0.406 |
LIG_FHA_1 | 593 | 599 | PF00498 | 0.685 |
LIG_FHA_2 | 213 | 219 | PF00498 | 0.430 |
LIG_FHA_2 | 223 | 229 | PF00498 | 0.426 |
LIG_FHA_2 | 328 | 334 | PF00498 | 0.763 |
LIG_FHA_2 | 348 | 354 | PF00498 | 0.537 |
LIG_FHA_2 | 60 | 66 | PF00498 | 0.266 |
LIG_IRF3_LxIS_1 | 444 | 449 | PF10401 | 0.372 |
LIG_LIR_Apic_2 | 351 | 357 | PF02991 | 0.515 |
LIG_LIR_Apic_2 | 88 | 92 | PF02991 | 0.476 |
LIG_LIR_Apic_2 | 99 | 104 | PF02991 | 0.327 |
LIG_LIR_Gen_1 | 269 | 277 | PF02991 | 0.291 |
LIG_LIR_Gen_1 | 280 | 289 | PF02991 | 0.351 |
LIG_LIR_Gen_1 | 378 | 388 | PF02991 | 0.325 |
LIG_LIR_Gen_1 | 45 | 55 | PF02991 | 0.356 |
LIG_LIR_Gen_1 | 84 | 95 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 136 | 141 | PF02991 | 0.320 |
LIG_LIR_Nem_3 | 164 | 168 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 175 | 180 | PF02991 | 0.322 |
LIG_LIR_Nem_3 | 25 | 31 | PF02991 | 0.501 |
LIG_LIR_Nem_3 | 269 | 273 | PF02991 | 0.263 |
LIG_LIR_Nem_3 | 280 | 284 | PF02991 | 0.309 |
LIG_LIR_Nem_3 | 290 | 295 | PF02991 | 0.291 |
LIG_LIR_Nem_3 | 378 | 383 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 394 | 400 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 42 | 46 | PF02991 | 0.348 |
LIG_LIR_Nem_3 | 47 | 51 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 527 | 531 | PF02991 | 0.325 |
LIG_LIR_Nem_3 | 572 | 576 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 84 | 90 | PF02991 | 0.354 |
LIG_Pex14_1 | 245 | 249 | PF04695 | 0.456 |
LIG_Pex14_1 | 376 | 380 | PF04695 | 0.336 |
LIG_Pex14_2 | 177 | 181 | PF04695 | 0.306 |
LIG_Pex14_2 | 191 | 195 | PF04695 | 0.363 |
LIG_Pex14_2 | 247 | 251 | PF04695 | 0.333 |
LIG_Pex14_2 | 288 | 292 | PF04695 | 0.311 |
LIG_PTB_Apo_2 | 389 | 396 | PF02174 | 0.344 |
LIG_PTB_Phospho_1 | 389 | 395 | PF10480 | 0.432 |
LIG_SH2_CRK | 249 | 253 | PF00017 | 0.379 |
LIG_SH2_CRK | 83 | 87 | PF00017 | 0.317 |
LIG_SH2_GRB2like | 326 | 329 | PF00017 | 0.555 |
LIG_SH2_PTP2 | 354 | 357 | PF00017 | 0.508 |
LIG_SH2_PTP2 | 89 | 92 | PF00017 | 0.426 |
LIG_SH2_SRC | 217 | 220 | PF00017 | 0.575 |
LIG_SH2_SRC | 476 | 479 | PF00017 | 0.325 |
LIG_SH2_SRC | 87 | 90 | PF00017 | 0.533 |
LIG_SH2_STAP1 | 46 | 50 | PF00017 | 0.345 |
LIG_SH2_STAP1 | 576 | 580 | PF00017 | 0.563 |
LIG_SH2_STAP1 | 83 | 87 | PF00017 | 0.335 |
LIG_SH2_STAT3 | 529 | 532 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 150 | 153 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 187 | 190 | PF00017 | 0.288 |
LIG_SH2_STAT5 | 270 | 273 | PF00017 | 0.282 |
LIG_SH2_STAT5 | 354 | 357 | PF00017 | 0.515 |
LIG_SH2_STAT5 | 395 | 398 | PF00017 | 0.294 |
LIG_SH2_STAT5 | 430 | 433 | PF00017 | 0.505 |
LIG_SH2_STAT5 | 46 | 49 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 476 | 479 | PF00017 | 0.313 |
LIG_SH2_STAT5 | 529 | 532 | PF00017 | 0.300 |
LIG_SH2_STAT5 | 89 | 92 | PF00017 | 0.486 |
LIG_SH3_3 | 256 | 262 | PF00018 | 0.303 |
LIG_SH3_3 | 545 | 551 | PF00018 | 0.318 |
LIG_SH3_3 | 76 | 82 | PF00018 | 0.387 |
LIG_SUMO_SIM_anti_2 | 142 | 149 | PF11976 | 0.366 |
LIG_SUMO_SIM_anti_2 | 411 | 417 | PF11976 | 0.269 |
LIG_SUMO_SIM_par_1 | 444 | 449 | PF11976 | 0.417 |
LIG_SUMO_SIM_par_1 | 489 | 494 | PF11976 | 0.294 |
LIG_SUMO_SIM_par_1 | 93 | 100 | PF11976 | 0.483 |
LIG_TRAF2_1 | 54 | 57 | PF00917 | 0.268 |
LIG_TYR_ITIM | 268 | 273 | PF00017 | 0.290 |
LIG_TYR_ITIM | 81 | 86 | PF00017 | 0.326 |
LIG_UBA3_1 | 396 | 404 | PF00899 | 0.396 |
LIG_UBA3_1 | 463 | 469 | PF00899 | 0.379 |
LIG_WRC_WIRS_1 | 162 | 167 | PF05994 | 0.371 |
LIG_WRC_WIRS_1 | 98 | 103 | PF05994 | 0.326 |
MOD_CK1_1 | 143 | 149 | PF00069 | 0.356 |
MOD_CK1_1 | 220 | 226 | PF00069 | 0.535 |
MOD_CK1_1 | 327 | 333 | PF00069 | 0.710 |
MOD_CK1_1 | 406 | 412 | PF00069 | 0.303 |
MOD_CK1_1 | 42 | 48 | PF00069 | 0.286 |
MOD_CK1_1 | 592 | 598 | PF00069 | 0.668 |
MOD_CK1_1 | 67 | 73 | PF00069 | 0.331 |
MOD_CK2_1 | 212 | 218 | PF00069 | 0.442 |
MOD_CK2_1 | 220 | 226 | PF00069 | 0.436 |
MOD_CK2_1 | 426 | 432 | PF00069 | 0.369 |
MOD_CK2_1 | 51 | 57 | PF00069 | 0.305 |
MOD_CK2_1 | 594 | 600 | PF00069 | 0.624 |
MOD_CMANNOS | 373 | 376 | PF00535 | 0.360 |
MOD_Cter_Amidation | 273 | 276 | PF01082 | 0.546 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.326 |
MOD_GlcNHglycan | 420 | 423 | PF01048 | 0.303 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.466 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.358 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.467 |
MOD_GSK3_1 | 283 | 290 | PF00069 | 0.371 |
MOD_GSK3_1 | 402 | 409 | PF00069 | 0.370 |
MOD_GSK3_1 | 453 | 460 | PF00069 | 0.325 |
MOD_GSK3_1 | 487 | 494 | PF00069 | 0.345 |
MOD_GSK3_1 | 536 | 543 | PF00069 | 0.413 |
MOD_GSK3_1 | 558 | 565 | PF00069 | 0.376 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.275 |
MOD_N-GLC_1 | 327 | 332 | PF02516 | 0.425 |
MOD_N-GLC_1 | 390 | 395 | PF02516 | 0.448 |
MOD_NEK2_1 | 139 | 144 | PF00069 | 0.344 |
MOD_NEK2_1 | 161 | 166 | PF00069 | 0.394 |
MOD_NEK2_1 | 375 | 380 | PF00069 | 0.306 |
MOD_NEK2_1 | 426 | 431 | PF00069 | 0.362 |
MOD_NEK2_1 | 446 | 451 | PF00069 | 0.345 |
MOD_NEK2_1 | 463 | 468 | PF00069 | 0.321 |
MOD_NEK2_1 | 486 | 491 | PF00069 | 0.361 |
MOD_NEK2_1 | 536 | 541 | PF00069 | 0.408 |
MOD_NEK2_1 | 556 | 561 | PF00069 | 0.317 |
MOD_NEK2_1 | 581 | 586 | PF00069 | 0.535 |
MOD_PIKK_1 | 432 | 438 | PF00454 | 0.517 |
MOD_PIKK_1 | 59 | 65 | PF00454 | 0.254 |
MOD_PKA_1 | 20 | 26 | PF00069 | 0.549 |
MOD_PKA_1 | 574 | 580 | PF00069 | 0.539 |
MOD_PKA_2 | 20 | 26 | PF00069 | 0.547 |
MOD_PKA_2 | 57 | 63 | PF00069 | 0.299 |
MOD_PKA_2 | 574 | 580 | PF00069 | 0.488 |
MOD_Plk_1 | 217 | 223 | PF00069 | 0.536 |
MOD_Plk_1 | 390 | 396 | PF00069 | 0.406 |
MOD_Plk_1 | 64 | 70 | PF00069 | 0.264 |
MOD_Plk_2-3 | 347 | 353 | PF00069 | 0.638 |
MOD_Plk_4 | 127 | 133 | PF00069 | 0.342 |
MOD_Plk_4 | 134 | 140 | PF00069 | 0.332 |
MOD_Plk_4 | 146 | 152 | PF00069 | 0.477 |
MOD_Plk_4 | 161 | 167 | PF00069 | 0.377 |
MOD_Plk_4 | 172 | 178 | PF00069 | 0.375 |
MOD_Plk_4 | 283 | 289 | PF00069 | 0.343 |
MOD_Plk_4 | 359 | 365 | PF00069 | 0.518 |
MOD_Plk_4 | 391 | 397 | PF00069 | 0.320 |
MOD_Plk_4 | 411 | 417 | PF00069 | 0.323 |
MOD_Plk_4 | 426 | 432 | PF00069 | 0.344 |
MOD_Plk_4 | 453 | 459 | PF00069 | 0.325 |
MOD_Plk_4 | 487 | 493 | PF00069 | 0.324 |
MOD_Plk_4 | 536 | 542 | PF00069 | 0.384 |
MOD_Plk_4 | 71 | 77 | PF00069 | 0.361 |
MOD_Plk_4 | 81 | 87 | PF00069 | 0.373 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.291 |
MOD_ProDKin_1 | 306 | 312 | PF00069 | 0.628 |
MOD_ProDKin_1 | 337 | 343 | PF00069 | 0.744 |
MOD_ProDKin_1 | 589 | 595 | PF00069 | 0.675 |
MOD_SUMO_rev_2 | 3 | 9 | PF00179 | 0.638 |
TRG_DiLeu_BaLyEn_6 | 422 | 427 | PF01217 | 0.327 |
TRG_DiLeu_BaLyEn_6 | 548 | 553 | PF01217 | 0.315 |
TRG_ENDOCYTIC_2 | 129 | 132 | PF00928 | 0.287 |
TRG_ENDOCYTIC_2 | 190 | 193 | PF00928 | 0.318 |
TRG_ENDOCYTIC_2 | 248 | 251 | PF00928 | 0.362 |
TRG_ENDOCYTIC_2 | 270 | 273 | PF00928 | 0.264 |
TRG_ENDOCYTIC_2 | 83 | 86 | PF00928 | 0.327 |
TRG_ENDOCYTIC_2 | 87 | 90 | PF00928 | 0.487 |
TRG_ER_diArg_1 | 573 | 575 | PF00400 | 0.559 |
TRG_ER_diArg_1 | 585 | 588 | PF00400 | 0.576 |
TRG_Pf-PMV_PEXEL_1 | 522 | 527 | PF00026 | 0.335 |
TRG_Pf-PMV_PEXEL_1 | 579 | 583 | PF00026 | 0.363 |
TRG_Pf-PMV_PEXEL_1 | 585 | 589 | PF00026 | 0.391 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6G0 | Leptomonas seymouri | 38% | 95% |
A0A0N1HT40 | Leptomonas seymouri | 46% | 100% |
A0A0N1HZC2 | Leptomonas seymouri | 32% | 96% |
A0A0N1IKC5 | Leptomonas seymouri | 71% | 99% |
A0A0N1PAX2 | Leptomonas seymouri | 23% | 100% |
A0A0N1PB63 | Leptomonas seymouri | 27% | 91% |
A0A0N1PD04 | Leptomonas seymouri | 24% | 94% |
A0A0N1PFR4 | Leptomonas seymouri | 24% | 91% |
A0A0S4JR45 | Bodo saltans | 32% | 100% |
A0A1X0NKK0 | Trypanosomatidae | 31% | 99% |
A0A1X0NL32 | Trypanosomatidae | 35% | 96% |
A0A1X0NM09 | Trypanosomatidae | 32% | 99% |
A0A1X0NRW5 | Trypanosomatidae | 40% | 87% |
A0A1X0NV13 | Trypanosomatidae | 50% | 93% |
A0A1X0NV19 | Trypanosomatidae | 51% | 100% |
A0A1X0NV27 | Trypanosomatidae | 52% | 100% |
A0A1X0NVH8 | Trypanosomatidae | 45% | 91% |
A0A1X0NVM7 | Trypanosomatidae | 47% | 93% |
A0A1X0NWQ1 | Trypanosomatidae | 48% | 94% |
A0A1X0NZE6 | Trypanosomatidae | 33% | 100% |
A0A1X0NZU2 | Trypanosomatidae | 30% | 93% |
A0A1X0NZU5 | Trypanosomatidae | 33% | 100% |
A0A1X0NZW1 | Trypanosomatidae | 28% | 100% |
A0A1X0P0M7 | Trypanosomatidae | 33% | 100% |
A0A381MMW5 | Leishmania infantum | 32% | 92% |
A0A3Q8I7Y9 | Leishmania donovani | 45% | 100% |
A0A3Q8IEC4 | Leishmania donovani | 32% | 93% |
A0A3Q8IF95 | Leishmania donovani | 29% | 96% |
A0A3Q8IIT5 | Leishmania donovani | 24% | 90% |
A0A3Q8ISY9 | Leishmania donovani | 40% | 95% |
A0A3R7JPZ0 | Trypanosoma rangeli | 27% | 100% |
A0A3R7JSQ9 | Trypanosoma rangeli | 26% | 100% |
A0A3R7KKN8 | Trypanosoma rangeli | 29% | 100% |
A0A3R7MAQ7 | Trypanosoma rangeli | 37% | 85% |
A0A3R7N3S6 | Trypanosoma rangeli | 23% | 93% |
A0A3R7N415 | Trypanosoma rangeli | 27% | 100% |
A0A3R7N921 | Trypanosoma rangeli | 30% | 100% |
A0A3R7R443 | Trypanosoma rangeli | 28% | 100% |
A0A3R7R6N6 | Trypanosoma rangeli | 27% | 100% |
A0A3S7WRJ4 | Leishmania donovani | 54% | 94% |
A0A3S7WRJ5 | Leishmania donovani | 49% | 86% |
A0A3S7WRL4 | Leishmania donovani | 45% | 97% |
A0A3S7WRS3 | Leishmania donovani | 25% | 96% |
A0A3S7WSR4 | Leishmania donovani | 91% | 99% |
A0A3S7WWU1 | Leishmania donovani | 26% | 91% |
A0A3S7X2G0 | Leishmania donovani | 32% | 92% |
A0A3S7X2K5 | Leishmania donovani | 30% | 100% |
A0A3S7XB11 | Leishmania donovani | 32% | 99% |
A0A422MSE4 | Trypanosoma rangeli | 48% | 100% |
A0A422MSP6 | Trypanosoma rangeli | 31% | 100% |
A0A422MST9 | Trypanosoma rangeli | 26% | 100% |
A0A422MU68 | Trypanosoma rangeli | 28% | 100% |
A4H6J0 | Leishmania braziliensis | 53% | 100% |
A4H6J1 | Leishmania braziliensis | 51% | 100% |
A4H6J3 | Leishmania braziliensis | 46% | 100% |
A4H6Q5 | Leishmania braziliensis | 25% | 100% |
A4HC19 | Leishmania braziliensis | 27% | 100% |
A4HHG3 | Leishmania braziliensis | 31% | 100% |
A4HHG4 | Leishmania braziliensis | 31% | 100% |
A4HJW3 | Leishmania braziliensis | 40% | 100% |
A4HPE2 | Leishmania braziliensis | 33% | 100% |
A4HUX5 | Leishmania infantum | 54% | 94% |
A4HUX6 | Leishmania infantum | 49% | 86% |
A4HUX7 | Leishmania infantum | 45% | 97% |
A4HUX8 | Leishmania infantum | 45% | 100% |
A4HV40 | Leishmania infantum | 25% | 96% |
A4HZF5 | Leishmania infantum | 29% | 96% |
A4HZJ4 | Leishmania infantum | 26% | 91% |
A4I4L2 | Leishmania infantum | 24% | 90% |
A4I7C5 | Leishmania infantum | 40% | 95% |
A4ICI3 | Leishmania infantum | 32% | 99% |
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) | 30% | 100% |
C9ZTR5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 52% | 100% |
C9ZTR6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 52% | 100% |
C9ZTR7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 100% |
C9ZTR8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 100% |
C9ZTR9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 54% | 100% |
C9ZTS1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 52% | 100% |
C9ZUT6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% |
D0A7B1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 94% |
D0A7H1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
D0AAQ2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 88% |
E8NHE1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 51% | 100% |
E9AE01 | Leishmania major | 32% | 100% |
E9AE09 | Leishmania major | 25% | 100% |
E9AE10 | Leishmania major | 25% | 100% |
E9AE11 | Leishmania major | 31% | 100% |
E9AGK5 | Leishmania infantum | 91% | 99% |
E9AHJ0 | Leishmania infantum | 32% | 93% |
E9AHJ1 | Leishmania infantum | 30% | 100% |
E9ALS2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9ALS3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
E9ANL0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 54% | 100% |
E9ANL1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 50% | 100% |
E9ANL2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 46% | 100% |
E9ANS1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9AT53 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
E9AVF1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 98% |
E9AVF2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 91% |
E9B2B8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 39% | 95% |
Q4Q1E4 | Leishmania major | 32% | 100% |
Q4Q5T8 | Leishmania major | 41% | 100% |
Q4QC27 | Leishmania major | 27% | 100% |
Q4QC28 | Leishmania major | 28% | 100% |
Q4QFY5 | Leishmania major | 90% | 100% |
Q4QGU8 | Leishmania major | 24% | 100% |
Q4QH10 | Leishmania major | 45% | 100% |
Q4QH11 | Leishmania major | 46% | 98% |
Q4QH12 | Leishmania major | 46% | 98% |
Q4QH13 | Leishmania major | 46% | 98% |
Q4QH14 | Leishmania major | 48% | 100% |
Q4QH15 | Leishmania major | 54% | 100% |
V5B647 | Trypanosoma cruzi | 48% | 96% |
V5B983 | Trypanosoma cruzi | 33% | 100% |
V5BBB1 | Trypanosoma cruzi | 47% | 100% |
V5BFV8 | Trypanosoma cruzi | 32% | 90% |
V5BQY6 | Trypanosoma cruzi | 37% | 85% |
V5BVP0 | Trypanosoma cruzi | 49% | 100% |
V5DT25 | Trypanosoma cruzi | 47% | 98% |