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: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 15 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 97 |
NetGPI | no | yes: 0, no: 97 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 92 |
GO:0110165 | cellular anatomical entity | 1 | 92 |
Related structures:
AlphaFold database: A0A3S7WRL4
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 43 |
GO:0022857 | transmembrane transporter activity | 2 | 43 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 607 | 611 | PF00656 | 0.570 |
CLV_NRD_NRD_1 | 166 | 168 | PF00675 | 0.359 |
CLV_NRD_NRD_1 | 39 | 41 | PF00675 | 0.267 |
CLV_NRD_NRD_1 | 425 | 427 | PF00675 | 0.368 |
CLV_NRD_NRD_1 | 565 | 567 | PF00675 | 0.336 |
CLV_NRD_NRD_1 | 572 | 574 | PF00675 | 0.362 |
CLV_NRD_NRD_1 | 617 | 619 | PF00675 | 0.586 |
CLV_PCSK_KEX2_1 | 166 | 168 | PF00082 | 0.374 |
CLV_PCSK_KEX2_1 | 39 | 41 | PF00082 | 0.324 |
CLV_PCSK_KEX2_1 | 425 | 427 | PF00082 | 0.350 |
CLV_PCSK_KEX2_1 | 565 | 567 | PF00082 | 0.333 |
CLV_PCSK_KEX2_1 | 571 | 573 | PF00082 | 0.341 |
CLV_PCSK_PC1ET2_1 | 425 | 427 | PF00082 | 0.371 |
CLV_PCSK_SKI1_1 | 284 | 288 | PF00082 | 0.600 |
CLV_PCSK_SKI1_1 | 458 | 462 | PF00082 | 0.526 |
CLV_PCSK_SKI1_1 | 565 | 569 | PF00082 | 0.344 |
DEG_APCC_DBOX_1 | 39 | 47 | PF00400 | 0.477 |
DEG_Kelch_Keap1_1 | 329 | 334 | PF01344 | 0.729 |
DEG_MDM2_SWIB_1 | 498 | 506 | PF02201 | 0.415 |
DOC_CKS1_1 | 194 | 199 | PF01111 | 0.190 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 542 | 551 | PF00134 | 0.215 |
DOC_CYCLIN_yCln2_LP_2 | 194 | 200 | PF00134 | 0.384 |
DOC_MAPK_gen_1 | 166 | 173 | PF00069 | 0.527 |
DOC_MAPK_gen_1 | 39 | 46 | PF00069 | 0.472 |
DOC_MAPK_gen_1 | 425 | 434 | PF00069 | 0.548 |
DOC_MAPK_gen_1 | 520 | 530 | PF00069 | 0.417 |
DOC_MAPK_MEF2A_6 | 258 | 267 | PF00069 | 0.487 |
DOC_MAPK_MEF2A_6 | 427 | 436 | PF00069 | 0.546 |
DOC_MAPK_MEF2A_6 | 532 | 541 | PF00069 | 0.313 |
DOC_PP2B_LxvP_1 | 453 | 456 | PF13499 | 0.420 |
DOC_PP4_FxxP_1 | 438 | 441 | PF00568 | 0.421 |
DOC_PP4_FxxP_1 | 91 | 94 | PF00568 | 0.324 |
DOC_SPAK_OSR1_1 | 136 | 140 | PF12202 | 0.321 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.353 |
DOC_USP7_MATH_1 | 456 | 460 | PF00917 | 0.408 |
DOC_USP7_MATH_1 | 465 | 469 | PF00917 | 0.330 |
DOC_USP7_MATH_1 | 54 | 58 | PF00917 | 0.329 |
DOC_USP7_MATH_1 | 580 | 584 | PF00917 | 0.690 |
DOC_USP7_MATH_1 | 601 | 605 | PF00917 | 0.666 |
DOC_USP7_UBL2_3 | 488 | 492 | PF12436 | 0.477 |
DOC_WW_Pin1_4 | 193 | 198 | PF00397 | 0.337 |
DOC_WW_Pin1_4 | 378 | 383 | PF00397 | 0.419 |
DOC_WW_Pin1_4 | 387 | 392 | PF00397 | 0.393 |
LIG_14-3-3_CanoR_1 | 233 | 241 | PF00244 | 0.546 |
LIG_14-3-3_CanoR_1 | 318 | 324 | PF00244 | 0.586 |
LIG_14-3-3_CanoR_1 | 33 | 41 | PF00244 | 0.550 |
LIG_14-3-3_CanoR_1 | 413 | 419 | PF00244 | 0.306 |
LIG_14-3-3_CanoR_1 | 431 | 437 | PF00244 | 0.417 |
LIG_14-3-3_CanoR_1 | 76 | 84 | PF00244 | 0.334 |
LIG_Actin_WH2_2 | 560 | 577 | PF00022 | 0.623 |
LIG_BRCT_BRCA1_1 | 147 | 151 | PF00533 | 0.413 |
LIG_BRCT_BRCA1_1 | 380 | 384 | PF00533 | 0.385 |
LIG_BRCT_BRCA1_1 | 56 | 60 | PF00533 | 0.370 |
LIG_FHA_1 | 274 | 280 | PF00498 | 0.339 |
LIG_FHA_1 | 346 | 352 | PF00498 | 0.509 |
LIG_FHA_1 | 354 | 360 | PF00498 | 0.493 |
LIG_FHA_1 | 388 | 394 | PF00498 | 0.383 |
LIG_FHA_1 | 440 | 446 | PF00498 | 0.344 |
LIG_FHA_1 | 448 | 454 | PF00498 | 0.334 |
LIG_FHA_1 | 476 | 482 | PF00498 | 0.306 |
LIG_FHA_1 | 546 | 552 | PF00498 | 0.392 |
LIG_FHA_2 | 335 | 341 | PF00498 | 0.517 |
LIG_FHA_2 | 95 | 101 | PF00498 | 0.470 |
LIG_GBD_Chelix_1 | 170 | 178 | PF00786 | 0.430 |
LIG_GBD_Chelix_1 | 265 | 273 | PF00786 | 0.315 |
LIG_GBD_Chelix_1 | 503 | 511 | PF00786 | 0.387 |
LIG_IRF3_LxIS_1 | 554 | 559 | PF10401 | 0.520 |
LIG_LIR_Apic_2 | 100 | 104 | PF02991 | 0.470 |
LIG_LIR_Apic_2 | 338 | 344 | PF02991 | 0.510 |
LIG_LIR_Apic_2 | 435 | 441 | PF02991 | 0.384 |
LIG_LIR_Gen_1 | 303 | 314 | PF02991 | 0.360 |
LIG_LIR_Gen_1 | 358 | 367 | PF02991 | 0.345 |
LIG_LIR_Gen_1 | 373 | 382 | PF02991 | 0.373 |
LIG_LIR_Gen_1 | 450 | 460 | PF02991 | 0.338 |
LIG_LIR_Gen_1 | 48 | 54 | PF02991 | 0.327 |
LIG_LIR_Gen_1 | 552 | 563 | PF02991 | 0.363 |
LIG_LIR_Gen_1 | 57 | 67 | PF02991 | 0.353 |
LIG_LIR_Gen_1 | 97 | 107 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 125 | 129 | PF02991 | 0.263 |
LIG_LIR_Nem_3 | 358 | 363 | PF02991 | 0.311 |
LIG_LIR_Nem_3 | 365 | 370 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 373 | 377 | PF02991 | 0.337 |
LIG_LIR_Nem_3 | 381 | 387 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 417 | 422 | PF02991 | 0.552 |
LIG_LIR_Nem_3 | 450 | 455 | PF02991 | 0.260 |
LIG_LIR_Nem_3 | 48 | 52 | PF02991 | 0.351 |
LIG_LIR_Nem_3 | 552 | 558 | PF02991 | 0.325 |
LIG_LIR_Nem_3 | 559 | 563 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 57 | 63 | PF02991 | 0.336 |
LIG_LIR_Nem_3 | 97 | 102 | PF02991 | 0.372 |
LIG_NRBOX | 116 | 122 | PF00104 | 0.285 |
LIG_NRBOX | 507 | 513 | PF00104 | 0.304 |
LIG_NRBOX | 546 | 552 | PF00104 | 0.476 |
LIG_PAM2_1 | 192 | 204 | PF00658 | 0.190 |
LIG_Pex14_2 | 374 | 378 | PF04695 | 0.373 |
LIG_Pex14_2 | 498 | 502 | PF04695 | 0.398 |
LIG_SH2_CRK | 41 | 45 | PF00017 | 0.328 |
LIG_SH2_CRK | 95 | 99 | PF00017 | 0.329 |
LIG_SH2_PTP2 | 341 | 344 | PF00017 | 0.503 |
LIG_SH2_SRC | 555 | 558 | PF00017 | 0.476 |
LIG_SH2_SRC | 600 | 603 | PF00017 | 0.775 |
LIG_SH2_STAP1 | 58 | 62 | PF00017 | 0.358 |
LIG_SH2_STAT3 | 249 | 252 | PF00017 | 0.478 |
LIG_SH2_STAT5 | 101 | 104 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 108 | 111 | PF00017 | 0.331 |
LIG_SH2_STAT5 | 200 | 203 | PF00017 | 0.331 |
LIG_SH2_STAT5 | 249 | 252 | PF00017 | 0.499 |
LIG_SH2_STAT5 | 260 | 263 | PF00017 | 0.316 |
LIG_SH2_STAT5 | 272 | 275 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 341 | 344 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 422 | 425 | PF00017 | 0.555 |
LIG_SH2_STAT5 | 555 | 558 | PF00017 | 0.332 |
LIG_SH2_STAT5 | 90 | 93 | PF00017 | 0.308 |
LIG_SH3_2 | 586 | 591 | PF14604 | 0.770 |
LIG_SH3_3 | 268 | 274 | PF00018 | 0.329 |
LIG_SH3_3 | 308 | 314 | PF00018 | 0.372 |
LIG_SH3_3 | 532 | 538 | PF00018 | 0.327 |
LIG_SH3_3 | 583 | 589 | PF00018 | 0.678 |
LIG_SUMO_SIM_anti_2 | 262 | 267 | PF11976 | 0.378 |
LIG_SUMO_SIM_anti_2 | 442 | 448 | PF11976 | 0.320 |
LIG_SUMO_SIM_anti_2 | 476 | 481 | PF11976 | 0.341 |
LIG_SUMO_SIM_par_1 | 142 | 148 | PF11976 | 0.341 |
LIG_SUMO_SIM_par_1 | 206 | 211 | PF11976 | 0.370 |
LIG_SUMO_SIM_par_1 | 42 | 48 | PF11976 | 0.436 |
LIG_SUMO_SIM_par_1 | 442 | 448 | PF11976 | 0.323 |
LIG_SUMO_SIM_par_1 | 478 | 484 | PF11976 | 0.294 |
LIG_TRFH_1 | 90 | 94 | PF08558 | 0.372 |
LIG_TYR_ITIM | 93 | 98 | PF00017 | 0.346 |
LIG_UBA3_1 | 383 | 392 | PF00899 | 0.401 |
LIG_WRC_WIRS_1 | 46 | 51 | PF05994 | 0.420 |
MOD_CDK_SPK_2 | 387 | 392 | PF00069 | 0.261 |
MOD_CK1_1 | 145 | 151 | PF00069 | 0.361 |
MOD_CK1_1 | 187 | 193 | PF00069 | 0.385 |
MOD_CK1_1 | 232 | 238 | PF00069 | 0.618 |
MOD_CK1_1 | 329 | 335 | PF00069 | 0.650 |
MOD_CK1_1 | 353 | 359 | PF00069 | 0.511 |
MOD_CK1_1 | 385 | 391 | PF00069 | 0.371 |
MOD_CK1_1 | 561 | 567 | PF00069 | 0.564 |
MOD_CK1_1 | 604 | 610 | PF00069 | 0.761 |
MOD_CK2_1 | 15 | 21 | PF00069 | 0.637 |
MOD_CK2_1 | 414 | 420 | PF00069 | 0.377 |
MOD_CK2_1 | 5 | 11 | PF00069 | 0.624 |
MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.326 |
MOD_GlcNHglycan | 276 | 279 | PF01048 | 0.343 |
MOD_GlcNHglycan | 326 | 331 | PF01048 | 0.479 |
MOD_GlcNHglycan | 384 | 387 | PF01048 | 0.526 |
MOD_GlcNHglycan | 397 | 400 | PF01048 | 0.331 |
MOD_GlcNHglycan | 408 | 411 | PF01048 | 0.283 |
MOD_GlcNHglycan | 603 | 606 | PF01048 | 0.504 |
MOD_GlcNHglycan | 63 | 66 | PF01048 | 0.473 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.346 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.511 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.536 |
MOD_GSK3_1 | 378 | 385 | PF00069 | 0.377 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.295 |
MOD_GSK3_1 | 545 | 552 | PF00069 | 0.388 |
MOD_GSK3_1 | 604 | 611 | PF00069 | 0.725 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.279 |
MOD_N-GLC_1 | 378 | 383 | PF02516 | 0.584 |
MOD_N-GLC_1 | 545 | 550 | PF02516 | 0.292 |
MOD_NEK2_1 | 122 | 127 | PF00069 | 0.302 |
MOD_NEK2_1 | 173 | 178 | PF00069 | 0.395 |
MOD_NEK2_1 | 259 | 264 | PF00069 | 0.355 |
MOD_NEK2_1 | 27 | 32 | PF00069 | 0.579 |
MOD_NEK2_1 | 350 | 355 | PF00069 | 0.508 |
MOD_NEK2_1 | 393 | 398 | PF00069 | 0.358 |
MOD_NEK2_1 | 414 | 419 | PF00069 | 0.383 |
MOD_NEK2_1 | 447 | 452 | PF00069 | 0.301 |
MOD_NEK2_1 | 473 | 478 | PF00069 | 0.338 |
MOD_NEK2_1 | 545 | 550 | PF00069 | 0.339 |
MOD_NEK2_1 | 556 | 561 | PF00069 | 0.331 |
MOD_NEK2_1 | 63 | 68 | PF00069 | 0.276 |
MOD_NEK2_2 | 94 | 99 | PF00069 | 0.487 |
MOD_PIKK_1 | 145 | 151 | PF00454 | 0.415 |
MOD_PIKK_1 | 248 | 254 | PF00454 | 0.541 |
MOD_PIKK_1 | 285 | 291 | PF00454 | 0.359 |
MOD_PIKK_1 | 420 | 426 | PF00454 | 0.532 |
MOD_PKA_2 | 232 | 238 | PF00069 | 0.521 |
MOD_PKA_2 | 317 | 323 | PF00069 | 0.563 |
MOD_PKA_2 | 561 | 567 | PF00069 | 0.499 |
MOD_Plk_1 | 393 | 399 | PF00069 | 0.346 |
MOD_Plk_1 | 545 | 551 | PF00069 | 0.311 |
MOD_Plk_2-3 | 334 | 340 | PF00069 | 0.608 |
MOD_Plk_2-3 | 5 | 11 | PF00069 | 0.492 |
MOD_Plk_4 | 130 | 136 | PF00069 | 0.277 |
MOD_Plk_4 | 152 | 158 | PF00069 | 0.320 |
MOD_Plk_4 | 173 | 179 | PF00069 | 0.365 |
MOD_Plk_4 | 346 | 352 | PF00069 | 0.513 |
MOD_Plk_4 | 355 | 361 | PF00069 | 0.478 |
MOD_Plk_4 | 399 | 405 | PF00069 | 0.316 |
MOD_Plk_4 | 414 | 420 | PF00069 | 0.337 |
MOD_Plk_4 | 440 | 446 | PF00069 | 0.330 |
MOD_Plk_4 | 447 | 453 | PF00069 | 0.321 |
MOD_Plk_4 | 94 | 100 | PF00069 | 0.381 |
MOD_ProDKin_1 | 193 | 199 | PF00069 | 0.337 |
MOD_ProDKin_1 | 378 | 384 | PF00069 | 0.415 |
MOD_ProDKin_1 | 387 | 393 | PF00069 | 0.390 |
MOD_SUMO_rev_2 | 232 | 241 | PF00179 | 0.555 |
TRG_DiLeu_BaLyEn_6 | 507 | 512 | PF01217 | 0.329 |
TRG_DiLeu_BaLyEn_6 | 535 | 540 | PF01217 | 0.319 |
TRG_ENDOCYTIC_2 | 200 | 203 | PF00928 | 0.302 |
TRG_ENDOCYTIC_2 | 260 | 263 | PF00928 | 0.376 |
TRG_ENDOCYTIC_2 | 41 | 44 | PF00928 | 0.296 |
TRG_ENDOCYTIC_2 | 555 | 558 | PF00928 | 0.378 |
TRG_ENDOCYTIC_2 | 560 | 563 | PF00928 | 0.513 |
TRG_ENDOCYTIC_2 | 90 | 93 | PF00928 | 0.317 |
TRG_ENDOCYTIC_2 | 95 | 98 | PF00928 | 0.330 |
TRG_ENDOCYTIC_2 | 99 | 102 | PF00928 | 0.489 |
TRG_ER_diArg_1 | 39 | 41 | PF00400 | 0.441 |
TRG_ER_diArg_1 | 565 | 567 | PF00400 | 0.548 |
TRG_ER_diArg_1 | 571 | 573 | PF00400 | 0.556 |
TRG_NLS_MonoCore_2 | 617 | 622 | PF00514 | 0.581 |
TRG_Pf-PMV_PEXEL_1 | 33 | 37 | PF00026 | 0.412 |
TRG_Pf-PMV_PEXEL_1 | 510 | 515 | PF00026 | 0.414 |
TRG_Pf-PMV_PEXEL_1 | 566 | 570 | PF00026 | 0.357 |
TRG_Pf-PMV_PEXEL_1 | 572 | 576 | PF00026 | 0.385 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6G0 | Leptomonas seymouri | 38% | 98% |
A0A0N1HT40 | Leptomonas seymouri | 74% | 100% |
A0A0N1HZC2 | Leptomonas seymouri | 28% | 99% |
A0A0N1IKC5 | Leptomonas seymouri | 47% | 100% |
A0A0N1PB63 | Leptomonas seymouri | 27% | 94% |
A0A0S4IIJ4 | Bodo saltans | 22% | 100% |
A0A0S4JR45 | Bodo saltans | 33% | 100% |
A0A1X0NKK0 | Trypanosomatidae | 33% | 100% |
A0A1X0NL32 | Trypanosomatidae | 34% | 99% |
A0A1X0NM09 | Trypanosomatidae | 31% | 100% |
A0A1X0NRW5 | Trypanosomatidae | 40% | 89% |
A0A1X0NV13 | Trypanosomatidae | 49% | 96% |
A0A1X0NV19 | Trypanosomatidae | 48% | 100% |
A0A1X0NV27 | Trypanosomatidae | 49% | 100% |
A0A1X0NVH8 | Trypanosomatidae | 45% | 94% |
A0A1X0NVM7 | Trypanosomatidae | 53% | 96% |
A0A1X0NWQ1 | Trypanosomatidae | 44% | 97% |
A0A1X0NZE6 | Trypanosomatidae | 33% | 100% |
A0A1X0NZU2 | Trypanosomatidae | 28% | 96% |
A0A1X0NZU5 | Trypanosomatidae | 34% | 100% |
A0A1X0NZW1 | Trypanosomatidae | 29% | 100% |
A0A1X0P0M7 | Trypanosomatidae | 32% | 100% |
A0A3Q8I7Y9 | Leishmania donovani | 100% | 100% |
A0A3Q8IF95 | Leishmania donovani | 29% | 100% |
A0A3Q8ISY9 | Leishmania donovani | 38% | 100% |
A0A3R7JSQ9 | Trypanosoma rangeli | 29% | 100% |
A0A3R7KKN8 | Trypanosoma rangeli | 30% | 100% |
A0A3R7MAQ7 | Trypanosoma rangeli | 35% | 88% |
A0A3R7N415 | Trypanosoma rangeli | 30% | 100% |
A0A3R7N921 | Trypanosoma rangeli | 28% | 100% |
A0A3R7R443 | Trypanosoma rangeli | 29% | 100% |
A0A3S7WRJ4 | Leishmania donovani | 46% | 98% |
A0A3S7WRJ5 | Leishmania donovani | 40% | 100% |
A0A3S7WSR4 | Leishmania donovani | 45% | 100% |
A0A3S7WWU1 | Leishmania donovani | 28% | 94% |
A0A3S7XB11 | Leishmania donovani | 29% | 100% |
A0A422MSE4 | Trypanosoma rangeli | 48% | 100% |
A0A422MSP6 | Trypanosoma rangeli | 34% | 100% |
A0A422MST9 | Trypanosoma rangeli | 29% | 100% |
A0A422MU68 | Trypanosoma rangeli | 27% | 100% |
A4H6J0 | Leishmania braziliensis | 45% | 100% |
A4H6J1 | Leishmania braziliensis | 45% | 100% |
A4H6J3 | Leishmania braziliensis | 84% | 100% |
A4HC19 | Leishmania braziliensis | 27% | 100% |
A4HJW3 | Leishmania braziliensis | 38% | 100% |
A4HPE2 | Leishmania braziliensis | 29% | 100% |
A4HUX5 | Leishmania infantum | 46% | 98% |
A4HUX6 | Leishmania infantum | 41% | 100% |
A4HUX7 | Leishmania infantum | 99% | 100% |
A4HUX8 | Leishmania infantum | 97% | 100% |
A4HZF5 | Leishmania infantum | 29% | 100% |
A4HZJ4 | Leishmania infantum | 27% | 100% |
A4I7C5 | Leishmania infantum | 38% | 100% |
A4ICI3 | Leishmania infantum | 29% | 100% |
C9ZL97 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
C9ZL98 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
C9ZL99 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
C9ZLA0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZLA1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
C9ZTR5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 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) | 46% | 100% |
C9ZTR9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 100% |
C9ZTS1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 100% |
C9ZUT6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
D0A7H1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
D0AAQ2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 91% |
E8NHE1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 44% | 100% |
E9AGK5 | Leishmania infantum | 45% | 100% |
E9ANL0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 46% | 100% |
E9ANL1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 44% | 100% |
E9ANL2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
E9APJ3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 45% | 100% |
E9AT53 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9AVF1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9AVF2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9B2B8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 100% |
Q4Q1E4 | Leishmania major | 29% | 100% |
Q4Q5T8 | Leishmania major | 37% | 100% |
Q4QC27 | Leishmania major | 28% | 100% |
Q4QC28 | Leishmania major | 31% | 100% |
Q4QFY5 | Leishmania major | 45% | 100% |
Q4QH10 | Leishmania major | 96% | 100% |
Q4QH11 | Leishmania major | 97% | 100% |
Q4QH12 | Leishmania major | 97% | 100% |
Q4QH13 | Leishmania major | 97% | 100% |
Q4QH14 | Leishmania major | 41% | 100% |
Q4QH15 | Leishmania major | 47% | 100% |
V5B647 | Trypanosoma cruzi | 46% | 99% |
V5B983 | Trypanosoma cruzi | 33% | 100% |
V5BBB1 | Trypanosoma cruzi | 45% | 100% |
V5BFV8 | Trypanosoma cruzi | 30% | 93% |
V5BQY6 | Trypanosoma cruzi | 38% | 88% |
V5BVP0 | Trypanosoma cruzi | 47% | 100% |
V5DT25 | Trypanosoma cruzi | 57% | 100% |