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: 120 |
NetGPI | no | yes: 0, no: 120 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 113 |
GO:0110165 | cellular anatomical entity | 1 | 113 |
GO:0005737 | cytoplasm | 2 | 3 |
Related structures:
AlphaFold database: Q4Q5T8
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 55 |
GO:0022857 | transmembrane transporter activity | 2 | 55 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 124 | 128 | PF00656 | 0.165 |
CLV_NRD_NRD_1 | 12 | 14 | PF00675 | 0.515 |
CLV_NRD_NRD_1 | 256 | 258 | PF00675 | 0.261 |
CLV_NRD_NRD_1 | 341 | 343 | PF00675 | 0.558 |
CLV_NRD_NRD_1 | 459 | 461 | PF00675 | 0.393 |
CLV_PCSK_KEX2_1 | 12 | 14 | PF00082 | 0.501 |
CLV_PCSK_KEX2_1 | 256 | 258 | PF00082 | 0.273 |
CLV_PCSK_KEX2_1 | 341 | 343 | PF00082 | 0.552 |
CLV_PCSK_KEX2_1 | 38 | 40 | PF00082 | 0.306 |
CLV_PCSK_KEX2_1 | 459 | 461 | PF00082 | 0.376 |
CLV_PCSK_PC1ET2_1 | 38 | 40 | PF00082 | 0.343 |
CLV_PCSK_PC1ET2_1 | 459 | 461 | PF00082 | 0.380 |
CLV_PCSK_SKI1_1 | 104 | 108 | PF00082 | 0.231 |
CLV_PCSK_SKI1_1 | 231 | 235 | PF00082 | 0.303 |
CLV_PCSK_SKI1_1 | 256 | 260 | PF00082 | 0.240 |
CLV_PCSK_SKI1_1 | 30 | 34 | PF00082 | 0.404 |
CLV_PCSK_SKI1_1 | 341 | 345 | PF00082 | 0.496 |
CLV_PCSK_SKI1_1 | 38 | 42 | PF00082 | 0.267 |
DOC_CKS1_1 | 613 | 618 | PF01111 | 0.765 |
DOC_MAPK_gen_1 | 256 | 265 | PF00069 | 0.454 |
DOC_MAPK_gen_1 | 38 | 45 | PF00069 | 0.459 |
DOC_MAPK_gen_1 | 459 | 468 | PF00069 | 0.555 |
DOC_MAPK_MEF2A_6 | 259 | 267 | PF00069 | 0.331 |
DOC_MAPK_MEF2A_6 | 38 | 47 | PF00069 | 0.484 |
DOC_MAPK_MEF2A_6 | 461 | 470 | PF00069 | 0.552 |
DOC_MAPK_MEF2A_6 | 491 | 498 | PF00069 | 0.347 |
DOC_MAPK_MEF2A_6 | 566 | 573 | PF00069 | 0.294 |
DOC_PP1_RVXF_1 | 287 | 293 | PF00149 | 0.268 |
DOC_PP2B_LxvP_1 | 472 | 475 | PF13499 | 0.306 |
DOC_SPAK_OSR1_1 | 135 | 139 | PF12202 | 0.307 |
DOC_USP7_MATH_1 | 273 | 277 | PF00917 | 0.354 |
DOC_USP7_MATH_1 | 336 | 340 | PF00917 | 0.804 |
DOC_USP7_MATH_1 | 420 | 424 | PF00917 | 0.385 |
DOC_USP7_MATH_1 | 574 | 578 | PF00917 | 0.416 |
DOC_USP7_MATH_1 | 611 | 615 | PF00917 | 0.687 |
DOC_USP7_UBL2_3 | 241 | 245 | PF12436 | 0.374 |
DOC_USP7_UBL2_3 | 553 | 557 | PF12436 | 0.399 |
DOC_WW_Pin1_4 | 251 | 256 | PF00397 | 0.512 |
DOC_WW_Pin1_4 | 327 | 332 | PF00397 | 0.689 |
DOC_WW_Pin1_4 | 425 | 430 | PF00397 | 0.389 |
DOC_WW_Pin1_4 | 612 | 617 | PF00397 | 0.695 |
LIG_14-3-3_CanoR_1 | 19 | 26 | PF00244 | 0.656 |
LIG_14-3-3_CanoR_1 | 341 | 349 | PF00244 | 0.757 |
LIG_14-3-3_CanoR_1 | 352 | 360 | PF00244 | 0.692 |
LIG_14-3-3_CanoR_1 | 612 | 616 | PF00244 | 0.683 |
LIG_Actin_WH2_2 | 594 | 611 | PF00022 | 0.634 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.647 |
LIG_BRCT_BRCA1_1 | 180 | 184 | PF00533 | 0.457 |
LIG_deltaCOP1_diTrp_1 | 492 | 498 | PF00928 | 0.205 |
LIG_EH1_1 | 106 | 114 | PF00400 | 0.368 |
LIG_EH1_1 | 149 | 157 | PF00400 | 0.306 |
LIG_eIF4E_1 | 101 | 107 | PF01652 | 0.519 |
LIG_FHA_1 | 289 | 295 | PF00498 | 0.345 |
LIG_FHA_1 | 29 | 35 | PF00498 | 0.656 |
LIG_FHA_1 | 389 | 395 | PF00498 | 0.501 |
LIG_FHA_1 | 405 | 411 | PF00498 | 0.295 |
LIG_FHA_1 | 426 | 432 | PF00498 | 0.346 |
LIG_FHA_1 | 467 | 473 | PF00498 | 0.464 |
LIG_FHA_2 | 232 | 238 | PF00498 | 0.419 |
LIG_FHA_2 | 31 | 37 | PF00498 | 0.628 |
LIG_FHA_2 | 425 | 431 | PF00498 | 0.308 |
LIG_FHA_2 | 71 | 77 | PF00498 | 0.261 |
LIG_GBD_Chelix_1 | 264 | 272 | PF00786 | 0.300 |
LIG_LIR_Apic_2 | 99 | 103 | PF02991 | 0.471 |
LIG_LIR_Gen_1 | 137 | 145 | PF02991 | 0.336 |
LIG_LIR_Gen_1 | 204 | 213 | PF02991 | 0.331 |
LIG_LIR_Gen_1 | 291 | 300 | PF02991 | 0.355 |
LIG_LIR_Gen_1 | 383 | 394 | PF02991 | 0.513 |
LIG_LIR_Gen_1 | 492 | 500 | PF02991 | 0.294 |
LIG_LIR_Gen_1 | 56 | 66 | PF02991 | 0.349 |
LIG_LIR_Gen_1 | 582 | 592 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 137 | 142 | PF02991 | 0.299 |
LIG_LIR_Nem_3 | 175 | 179 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 181 | 187 | PF02991 | 0.321 |
LIG_LIR_Nem_3 | 197 | 203 | PF02991 | 0.258 |
LIG_LIR_Nem_3 | 204 | 209 | PF02991 | 0.298 |
LIG_LIR_Nem_3 | 291 | 295 | PF02991 | 0.308 |
LIG_LIR_Nem_3 | 383 | 389 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 492 | 496 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 56 | 62 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 582 | 588 | PF02991 | 0.341 |
LIG_PCNA_yPIPBox_3 | 275 | 289 | PF02747 | 0.238 |
LIG_Pex14_1 | 395 | 399 | PF04695 | 0.338 |
LIG_Pex14_2 | 121 | 125 | PF04695 | 0.237 |
LIG_Pex14_2 | 202 | 206 | PF04695 | 0.355 |
LIG_Pex14_2 | 258 | 262 | PF04695 | 0.331 |
LIG_Pex14_2 | 581 | 585 | PF04695 | 0.361 |
LIG_PTB_Apo_2 | 411 | 418 | PF02174 | 0.310 |
LIG_Rb_pABgroove_1 | 92 | 100 | PF01858 | 0.384 |
LIG_RPA_C_Fungi | 337 | 349 | PF08784 | 0.674 |
LIG_SH2_CRK | 260 | 264 | PF00017 | 0.385 |
LIG_SH2_CRK | 281 | 285 | PF00017 | 0.388 |
LIG_SH2_CRK | 303 | 307 | PF00017 | 0.465 |
LIG_SH2_CRK | 48 | 52 | PF00017 | 0.285 |
LIG_SH2_NCK_1 | 303 | 307 | PF00017 | 0.389 |
LIG_SH2_NCK_1 | 419 | 423 | PF00017 | 0.364 |
LIG_SH2_PTP2 | 589 | 592 | PF00017 | 0.329 |
LIG_SH2_SRC | 8 | 11 | PF00017 | 0.660 |
LIG_SH2_STAP1 | 228 | 232 | PF00017 | 0.432 |
LIG_SH2_STAP1 | 303 | 307 | PF00017 | 0.441 |
LIG_SH2_STAP1 | 399 | 403 | PF00017 | 0.163 |
LIG_SH2_STAP1 | 520 | 524 | PF00017 | 0.369 |
LIG_SH2_STAP1 | 551 | 555 | PF00017 | 0.327 |
LIG_SH2_STAT5 | 201 | 204 | PF00017 | 0.310 |
LIG_SH2_STAT5 | 232 | 235 | PF00017 | 0.316 |
LIG_SH2_STAT5 | 248 | 251 | PF00017 | 0.317 |
LIG_SH2_STAT5 | 551 | 554 | PF00017 | 0.356 |
LIG_SH2_STAT5 | 57 | 60 | PF00017 | 0.324 |
LIG_SH2_STAT5 | 589 | 592 | PF00017 | 0.325 |
LIG_SH3_3 | 215 | 221 | PF00018 | 0.295 |
LIG_SH3_3 | 249 | 255 | PF00018 | 0.323 |
LIG_SH3_3 | 267 | 273 | PF00018 | 0.303 |
LIG_SH3_3 | 610 | 616 | PF00018 | 0.523 |
LIG_SH3_3 | 87 | 93 | PF00018 | 0.390 |
LIG_SUMO_SIM_anti_2 | 476 | 483 | PF11976 | 0.297 |
LIG_SUMO_SIM_anti_2 | 511 | 518 | PF11976 | 0.310 |
LIG_SUMO_SIM_par_1 | 29 | 36 | PF11976 | 0.524 |
LIG_SUMO_SIM_par_1 | 476 | 483 | PF11976 | 0.305 |
LIG_TRAF2_1 | 14 | 17 | PF00917 | 0.665 |
LIG_TYR_ITIM | 279 | 284 | PF00017 | 0.339 |
LIG_UBA3_1 | 484 | 491 | PF00899 | 0.383 |
LIG_WRC_WIRS_1 | 173 | 178 | PF05994 | 0.363 |
LIG_WRC_WIRS_1 | 495 | 500 | PF05994 | 0.396 |
MOD_CDC14_SPxK_1 | 254 | 257 | PF00782 | 0.386 |
MOD_CDK_SPK_2 | 251 | 256 | PF00069 | 0.432 |
MOD_CDK_SPxK_1 | 251 | 257 | PF00069 | 0.386 |
MOD_CK1_1 | 388 | 394 | PF00069 | 0.376 |
MOD_CK1_1 | 433 | 439 | PF00069 | 0.356 |
MOD_CK1_1 | 508 | 514 | PF00069 | 0.372 |
MOD_CK1_1 | 532 | 538 | PF00069 | 0.346 |
MOD_CK1_1 | 583 | 589 | PF00069 | 0.360 |
MOD_CK1_1 | 78 | 84 | PF00069 | 0.328 |
MOD_CK2_1 | 11 | 17 | PF00069 | 0.570 |
MOD_CK2_1 | 223 | 229 | PF00069 | 0.272 |
MOD_CK2_1 | 231 | 237 | PF00069 | 0.265 |
MOD_CK2_1 | 30 | 36 | PF00069 | 0.481 |
MOD_CK2_1 | 356 | 362 | PF00069 | 0.532 |
MOD_CK2_1 | 367 | 373 | PF00069 | 0.497 |
MOD_CK2_1 | 381 | 387 | PF00069 | 0.384 |
MOD_CK2_1 | 424 | 430 | PF00069 | 0.285 |
MOD_CK2_1 | 448 | 454 | PF00069 | 0.392 |
MOD_CK2_1 | 70 | 76 | PF00069 | 0.326 |
MOD_Cter_Amidation | 10 | 13 | PF01082 | 0.654 |
MOD_DYRK1A_RPxSP_1 | 612 | 616 | PF00069 | 0.415 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.365 |
MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.317 |
MOD_GlcNHglycan | 203 | 206 | PF01048 | 0.320 |
MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.276 |
MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.332 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.478 |
MOD_GlcNHglycan | 372 | 376 | PF01048 | 0.496 |
MOD_GlcNHglycan | 442 | 445 | PF01048 | 0.301 |
MOD_GlcNHglycan | 507 | 510 | PF01048 | 0.293 |
MOD_GlcNHglycan | 576 | 579 | PF01048 | 0.365 |
MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.302 |
MOD_GlcNHglycan | 76 | 80 | PF01048 | 0.305 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.614 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.337 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.592 |
MOD_GSK3_1 | 352 | 359 | PF00069 | 0.627 |
MOD_GSK3_1 | 367 | 374 | PF00069 | 0.577 |
MOD_GSK3_1 | 381 | 388 | PF00069 | 0.449 |
MOD_GSK3_1 | 420 | 427 | PF00069 | 0.424 |
MOD_GSK3_1 | 494 | 501 | PF00069 | 0.376 |
MOD_GSK3_1 | 531 | 538 | PF00069 | 0.319 |
MOD_GSK3_1 | 549 | 556 | PF00069 | 0.397 |
MOD_GSK3_1 | 579 | 586 | PF00069 | 0.367 |
MOD_GSK3_1 | 611 | 618 | PF00069 | 0.559 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.316 |
MOD_N-GLC_1 | 194 | 199 | PF02516 | 0.303 |
MOD_N-GLC_1 | 327 | 332 | PF02516 | 0.661 |
MOD_N-GLC_1 | 353 | 358 | PF02516 | 0.706 |
MOD_N-GLC_1 | 70 | 75 | PF02516 | 0.379 |
MOD_N-GLC_2 | 561 | 563 | PF02516 | 0.430 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.291 |
MOD_NEK2_1 | 385 | 390 | PF00069 | 0.402 |
MOD_NEK2_1 | 397 | 402 | PF00069 | 0.304 |
MOD_NEK2_1 | 480 | 485 | PF00069 | 0.291 |
MOD_NEK2_1 | 494 | 499 | PF00069 | 0.297 |
MOD_NEK2_1 | 531 | 536 | PF00069 | 0.288 |
MOD_NEK2_1 | 579 | 584 | PF00069 | 0.312 |
MOD_NEK2_1 | 630 | 635 | PF00069 | 0.688 |
MOD_NEK2_2 | 381 | 386 | PF00069 | 0.480 |
MOD_PIKK_1 | 18 | 24 | PF00454 | 0.677 |
MOD_PIKK_1 | 404 | 410 | PF00454 | 0.353 |
MOD_PIKK_1 | 454 | 460 | PF00454 | 0.421 |
MOD_PIKK_1 | 70 | 76 | PF00454 | 0.291 |
MOD_PKA_1 | 240 | 246 | PF00069 | 0.397 |
MOD_PKA_1 | 341 | 347 | PF00069 | 0.417 |
MOD_PKA_2 | 11 | 17 | PF00069 | 0.618 |
MOD_PKA_2 | 134 | 140 | PF00069 | 0.281 |
MOD_PKA_2 | 18 | 24 | PF00069 | 0.460 |
MOD_PKA_2 | 341 | 347 | PF00069 | 0.684 |
MOD_PKA_2 | 356 | 362 | PF00069 | 0.556 |
MOD_PKA_2 | 611 | 617 | PF00069 | 0.572 |
MOD_Plk_1 | 75 | 81 | PF00069 | 0.305 |
MOD_Plk_4 | 129 | 135 | PF00069 | 0.273 |
MOD_Plk_4 | 145 | 151 | PF00069 | 0.328 |
MOD_Plk_4 | 154 | 160 | PF00069 | 0.327 |
MOD_Plk_4 | 172 | 178 | PF00069 | 0.379 |
MOD_Plk_4 | 301 | 307 | PF00069 | 0.359 |
MOD_Plk_4 | 381 | 387 | PF00069 | 0.413 |
MOD_Plk_4 | 397 | 403 | PF00069 | 0.356 |
MOD_Plk_4 | 430 | 436 | PF00069 | 0.295 |
MOD_Plk_4 | 448 | 454 | PF00069 | 0.372 |
MOD_Plk_4 | 473 | 479 | PF00069 | 0.314 |
MOD_Plk_4 | 480 | 486 | PF00069 | 0.304 |
MOD_Plk_4 | 508 | 514 | PF00069 | 0.331 |
MOD_Plk_4 | 536 | 542 | PF00069 | 0.298 |
MOD_Plk_4 | 580 | 586 | PF00069 | 0.282 |
MOD_ProDKin_1 | 251 | 257 | PF00069 | 0.375 |
MOD_ProDKin_1 | 327 | 333 | PF00069 | 0.625 |
MOD_ProDKin_1 | 425 | 431 | PF00069 | 0.478 |
MOD_ProDKin_1 | 612 | 618 | PF00069 | 0.636 |
MOD_SUMO_rev_2 | 226 | 233 | PF00179 | 0.330 |
TRG_DiLeu_BaEn_1 | 430 | 435 | PF01217 | 0.306 |
TRG_DiLeu_BaEn_4 | 463 | 469 | PF01217 | 0.267 |
TRG_DiLeu_LyEn_5 | 626 | 631 | PF01217 | 0.719 |
TRG_ENDOCYTIC_2 | 260 | 263 | PF00928 | 0.363 |
TRG_ENDOCYTIC_2 | 281 | 284 | PF00928 | 0.302 |
TRG_ENDOCYTIC_2 | 303 | 306 | PF00928 | 0.302 |
TRG_ENDOCYTIC_2 | 399 | 402 | PF00928 | 0.352 |
TRG_ENDOCYTIC_2 | 48 | 51 | PF00928 | 0.289 |
TRG_ENDOCYTIC_2 | 528 | 531 | PF00928 | 0.331 |
TRG_ENDOCYTIC_2 | 589 | 592 | PF00928 | 0.383 |
TRG_ENDOCYTIC_2 | 59 | 62 | PF00928 | 0.286 |
TRG_ENDOCYTIC_2 | 594 | 597 | PF00928 | 0.405 |
TRG_ER_diArg_1 | 255 | 257 | PF00400 | 0.304 |
TRG_ER_diArg_1 | 341 | 343 | PF00400 | 0.663 |
TRG_Pf-PMV_PEXEL_1 | 13 | 17 | PF00026 | 0.720 |
TRG_Pf-PMV_PEXEL_1 | 231 | 235 | PF00026 | 0.340 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6G0 | Leptomonas seymouri | 74% | 100% |
A0A0N1HT40 | Leptomonas seymouri | 40% | 100% |
A0A0N1HZC2 | Leptomonas seymouri | 26% | 100% |
A0A0N1IKC5 | Leptomonas seymouri | 40% | 100% |
A0A0N1PB63 | Leptomonas seymouri | 25% | 96% |
A0A0N1PD04 | Leptomonas seymouri | 22% | 99% |
A0A0N1PFR4 | Leptomonas seymouri | 27% | 96% |
A0A0S4JR45 | Bodo saltans | 27% | 100% |
A0A1X0NKK0 | Trypanosomatidae | 27% | 100% |
A0A1X0NL32 | Trypanosomatidae | 30% | 100% |
A0A1X0NM09 | Trypanosomatidae | 25% | 100% |
A0A1X0NRW5 | Trypanosomatidae | 42% | 91% |
A0A1X0NV13 | Trypanosomatidae | 42% | 98% |
A0A1X0NV19 | Trypanosomatidae | 39% | 100% |
A0A1X0NV27 | Trypanosomatidae | 38% | 100% |
A0A1X0NVH8 | Trypanosomatidae | 40% | 96% |
A0A1X0NVM7 | Trypanosomatidae | 40% | 98% |
A0A1X0NWQ1 | Trypanosomatidae | 43% | 99% |
A0A1X0NZE6 | Trypanosomatidae | 31% | 100% |
A0A1X0NZU2 | Trypanosomatidae | 29% | 98% |
A0A1X0NZU5 | Trypanosomatidae | 32% | 100% |
A0A1X0NZW1 | Trypanosomatidae | 27% | 100% |
A0A1X0P0M7 | Trypanosomatidae | 29% | 100% |
A0A381MMW5 | Leishmania infantum | 27% | 97% |
A0A3Q8I7Y9 | Leishmania donovani | 37% | 100% |
A0A3Q8IEC4 | Leishmania donovani | 27% | 98% |
A0A3Q8IF95 | Leishmania donovani | 26% | 100% |
A0A3Q8IIT5 | Leishmania donovani | 28% | 94% |
A0A3Q8ISY9 | Leishmania donovani | 94% | 100% |
A0A3R7JSQ9 | Trypanosoma rangeli | 26% | 100% |
A0A3R7KKN8 | Trypanosoma rangeli | 30% | 100% |
A0A3R7MAQ7 | Trypanosoma rangeli | 39% | 90% |
A0A3R7N415 | Trypanosoma rangeli | 28% | 100% |
A0A3R7N921 | Trypanosoma rangeli | 28% | 100% |
A0A3R7R443 | Trypanosoma rangeli | 28% | 100% |
A0A3S7WRJ4 | Leishmania donovani | 40% | 99% |
A0A3S7WRJ5 | Leishmania donovani | 37% | 91% |
A0A3S7WRL4 | Leishmania donovani | 37% | 100% |
A0A3S7WRS3 | Leishmania donovani | 23% | 100% |
A0A3S7WSR4 | Leishmania donovani | 41% | 100% |
A0A3S7WWU1 | Leishmania donovani | 25% | 96% |
A0A3S7X2G0 | Leishmania donovani | 27% | 97% |
A0A3S7X2K5 | Leishmania donovani | 27% | 100% |
A0A3S7XB11 | Leishmania donovani | 28% | 100% |
A0A422MSE4 | Trypanosoma rangeli | 40% | 100% |
A0A422MSP6 | Trypanosoma rangeli | 31% | 100% |
A0A422MST9 | Trypanosoma rangeli | 27% | 100% |
A0A422MU68 | Trypanosoma rangeli | 24% | 100% |
A4H6J0 | Leishmania braziliensis | 40% | 99% |
A4H6J1 | Leishmania braziliensis | 38% | 97% |
A4H6J3 | Leishmania braziliensis | 37% | 100% |
A4H6Q5 | Leishmania braziliensis | 23% | 100% |
A4HC19 | Leishmania braziliensis | 25% | 98% |
A4HHG2 | Leishmania braziliensis | 26% | 94% |
A4HHG3 | Leishmania braziliensis | 27% | 98% |
A4HHG4 | Leishmania braziliensis | 27% | 97% |
A4HJW3 | Leishmania braziliensis | 82% | 100% |
A4HPE2 | Leishmania braziliensis | 28% | 100% |
A4HUX5 | Leishmania infantum | 40% | 99% |
A4HUX6 | Leishmania infantum | 37% | 91% |
A4HUX7 | Leishmania infantum | 37% | 100% |
A4HUX8 | Leishmania infantum | 38% | 100% |
A4HV40 | Leishmania infantum | 23% | 100% |
A4HZF5 | Leishmania infantum | 26% | 100% |
A4HZJ4 | Leishmania infantum | 25% | 96% |
A4I4L2 | Leishmania infantum | 27% | 94% |
A4I7C5 | Leishmania infantum | 94% | 100% |
A4ICI3 | Leishmania infantum | 28% | 100% |
C9ZL97 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
C9ZL98 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
C9ZL99 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
C9ZLA0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
C9ZLA1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
C9ZTR5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
C9ZTR6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
C9ZTR7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
C9ZTR8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
C9ZTR9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
C9ZTS1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
C9ZUT6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
D0A7H1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
D0AAQ2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 93% |
E8NHE1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 100% |
E9AE01 | Leishmania major | 28% | 100% |
E9AE09 | Leishmania major | 27% | 100% |
E9AE10 | Leishmania major | 27% | 100% |
E9AE11 | Leishmania major | 28% | 100% |
E9AGK5 | Leishmania infantum | 41% | 100% |
E9AHJ0 | Leishmania infantum | 27% | 98% |
E9AHJ1 | Leishmania infantum | 27% | 100% |
E9ALS2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 98% |
E9ALS3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 94% |
E9ANL0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 39% | 99% |
E9ANL1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 97% |
E9ANL2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 100% |
E9ANS1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 100% |
E9APJ3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 41% | 100% |
E9AT53 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9AVF1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9AVF2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 96% |
E9B2B8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
Q4Q1E4 | Leishmania major | 27% | 100% |
Q4QC27 | Leishmania major | 24% | 100% |
Q4QC28 | Leishmania major | 25% | 100% |
Q4QFY5 | Leishmania major | 41% | 100% |
Q4QGU8 | Leishmania major | 23% | 100% |
Q4QH10 | Leishmania major | 36% | 100% |
Q4QH11 | Leishmania major | 37% | 100% |
Q4QH12 | Leishmania major | 37% | 100% |
Q4QH13 | Leishmania major | 37% | 100% |
Q4QH14 | Leishmania major | 37% | 97% |
Q4QH15 | Leishmania major | 40% | 100% |
V5B647 | Trypanosoma cruzi | 42% | 100% |
V5B983 | Trypanosoma cruzi | 31% | 100% |
V5BBB1 | Trypanosoma cruzi | 42% | 100% |
V5BFV8 | Trypanosoma cruzi | 29% | 95% |
V5BQY6 | Trypanosoma cruzi | 39% | 90% |
V5BVP0 | Trypanosoma cruzi | 41% | 100% |
V5DT25 | Trypanosoma cruzi | 41% | 100% |