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: A4HJW3
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 | 258 | 260 | PF00675 | 0.273 |
CLV_NRD_NRD_1 | 491 | 493 | PF00675 | 0.415 |
CLV_PCSK_KEX2_1 | 247 | 249 | PF00082 | 0.244 |
CLV_PCSK_KEX2_1 | 258 | 260 | PF00082 | 0.271 |
CLV_PCSK_KEX2_1 | 40 | 42 | PF00082 | 0.309 |
CLV_PCSK_KEX2_1 | 461 | 463 | PF00082 | 0.366 |
CLV_PCSK_PC1ET2_1 | 247 | 249 | PF00082 | 0.172 |
CLV_PCSK_PC1ET2_1 | 40 | 42 | PF00082 | 0.337 |
CLV_PCSK_PC1ET2_1 | 461 | 463 | PF00082 | 0.368 |
CLV_PCSK_SKI1_1 | 106 | 110 | PF00082 | 0.229 |
CLV_PCSK_SKI1_1 | 243 | 247 | PF00082 | 0.332 |
CLV_PCSK_SKI1_1 | 259 | 263 | PF00082 | 0.262 |
CLV_PCSK_SKI1_1 | 291 | 295 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 40 | 44 | PF00082 | 0.263 |
CLV_PCSK_SKI1_1 | 493 | 497 | PF00082 | 0.510 |
CLV_PCSK_SKI1_1 | 555 | 559 | PF00082 | 0.543 |
DEG_APCC_DBOX_1 | 247 | 255 | PF00400 | 0.420 |
DEG_APCC_DBOX_1 | 491 | 499 | PF00400 | 0.202 |
DOC_CDC14_PxL_1 | 532 | 540 | PF14671 | 0.159 |
DOC_CYCLIN_yCln2_LP_2 | 496 | 502 | PF00134 | 0.246 |
DOC_MAPK_gen_1 | 40 | 47 | PF00069 | 0.450 |
DOC_MAPK_gen_1 | 492 | 500 | PF00069 | 0.240 |
DOC_MAPK_MEF2A_6 | 40 | 49 | PF00069 | 0.482 |
DOC_MAPK_MEF2A_6 | 467 | 476 | PF00069 | 0.478 |
DOC_MAPK_MEF2A_6 | 492 | 500 | PF00069 | 0.336 |
DOC_MAPK_MEF2A_6 | 568 | 575 | PF00069 | 0.291 |
DOC_MAPK_RevD_3 | 477 | 493 | PF00069 | 0.159 |
DOC_PP1_RVXF_1 | 289 | 295 | PF00149 | 0.266 |
DOC_PP2B_LxvP_1 | 114 | 117 | PF13499 | 0.159 |
DOC_PP2B_LxvP_1 | 496 | 499 | PF13499 | 0.289 |
DOC_SPAK_OSR1_1 | 137 | 141 | PF12202 | 0.305 |
DOC_USP7_MATH_1 | 275 | 279 | PF00917 | 0.345 |
DOC_USP7_MATH_1 | 28 | 32 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 343 | 347 | PF00917 | 0.701 |
DOC_USP7_MATH_1 | 422 | 426 | PF00917 | 0.383 |
DOC_USP7_MATH_1 | 576 | 580 | PF00917 | 0.410 |
DOC_USP7_MATH_1 | 605 | 609 | PF00917 | 0.601 |
DOC_USP7_UBL2_3 | 243 | 247 | PF12436 | 0.373 |
DOC_USP7_UBL2_3 | 555 | 559 | PF12436 | 0.394 |
DOC_USP7_UBL2_3 | 67 | 71 | PF12436 | 0.260 |
DOC_WW_Pin1_4 | 253 | 258 | PF00397 | 0.545 |
DOC_WW_Pin1_4 | 424 | 429 | PF00397 | 0.382 |
LIG_14-3-3_CanoR_1 | 12 | 16 | PF00244 | 0.611 |
LIG_14-3-3_CanoR_1 | 19 | 23 | PF00244 | 0.639 |
LIG_14-3-3_CanoR_1 | 344 | 351 | PF00244 | 0.740 |
LIG_14-3-3_CanoR_1 | 354 | 362 | PF00244 | 0.717 |
LIG_14-3-3_CanoR_1 | 614 | 620 | PF00244 | 0.689 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.665 |
LIG_BRCT_BRCA1_1 | 182 | 186 | PF00533 | 0.461 |
LIG_BRCT_BRCA1_1 | 198 | 202 | PF00533 | 0.193 |
LIG_EH1_1 | 151 | 159 | PF00400 | 0.302 |
LIG_eIF4E_1 | 103 | 109 | PF01652 | 0.516 |
LIG_FHA_1 | 207 | 213 | PF00498 | 0.372 |
LIG_FHA_1 | 296 | 302 | PF00498 | 0.377 |
LIG_FHA_1 | 31 | 37 | PF00498 | 0.649 |
LIG_FHA_1 | 383 | 389 | PF00498 | 0.514 |
LIG_FHA_1 | 391 | 397 | PF00498 | 0.496 |
LIG_FHA_1 | 407 | 413 | PF00498 | 0.291 |
LIG_FHA_1 | 428 | 434 | PF00498 | 0.328 |
LIG_FHA_1 | 469 | 475 | PF00498 | 0.461 |
LIG_FHA_1 | 55 | 61 | PF00498 | 0.310 |
LIG_FHA_1 | 587 | 593 | PF00498 | 0.388 |
LIG_FHA_2 | 226 | 232 | PF00498 | 0.434 |
LIG_FHA_2 | 616 | 622 | PF00498 | 0.637 |
LIG_GBD_Chelix_1 | 266 | 274 | PF00786 | 0.301 |
LIG_LIR_Apic_2 | 101 | 105 | PF02991 | 0.470 |
LIG_LIR_Gen_1 | 139 | 147 | PF02991 | 0.332 |
LIG_LIR_Gen_1 | 206 | 215 | PF02991 | 0.321 |
LIG_LIR_Gen_1 | 402 | 412 | PF02991 | 0.317 |
LIG_LIR_Gen_1 | 58 | 68 | PF02991 | 0.340 |
LIG_LIR_Gen_1 | 584 | 594 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 139 | 144 | PF02991 | 0.292 |
LIG_LIR_Nem_3 | 177 | 181 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 183 | 189 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 199 | 205 | PF02991 | 0.256 |
LIG_LIR_Nem_3 | 206 | 211 | PF02991 | 0.297 |
LIG_LIR_Nem_3 | 402 | 407 | PF02991 | 0.312 |
LIG_LIR_Nem_3 | 58 | 64 | PF02991 | 0.348 |
LIG_LIR_Nem_3 | 584 | 590 | PF02991 | 0.337 |
LIG_MLH1_MIPbox_1 | 198 | 202 | PF16413 | 0.193 |
LIG_Pex14_1 | 397 | 401 | PF04695 | 0.333 |
LIG_Pex14_2 | 123 | 127 | PF04695 | 0.235 |
LIG_Pex14_2 | 204 | 208 | PF04695 | 0.351 |
LIG_Pex14_2 | 260 | 264 | PF04695 | 0.327 |
LIG_Pex14_2 | 269 | 273 | PF04695 | 0.312 |
LIG_Pex14_2 | 583 | 587 | PF04695 | 0.358 |
LIG_PTB_Apo_2 | 413 | 420 | PF02174 | 0.306 |
LIG_Rb_pABgroove_1 | 94 | 102 | PF01858 | 0.381 |
LIG_SH2_CRK | 283 | 287 | PF00017 | 0.317 |
LIG_SH2_CRK | 305 | 309 | PF00017 | 0.463 |
LIG_SH2_CRK | 50 | 54 | PF00017 | 0.264 |
LIG_SH2_NCK_1 | 305 | 309 | PF00017 | 0.386 |
LIG_SH2_NCK_1 | 421 | 425 | PF00017 | 0.295 |
LIG_SH2_PTP2 | 591 | 594 | PF00017 | 0.329 |
LIG_SH2_SRC | 8 | 11 | PF00017 | 0.696 |
LIG_SH2_STAP1 | 230 | 234 | PF00017 | 0.551 |
LIG_SH2_STAP1 | 305 | 309 | PF00017 | 0.439 |
LIG_SH2_STAP1 | 522 | 526 | PF00017 | 0.503 |
LIG_SH2_STAP1 | 553 | 557 | PF00017 | 0.272 |
LIG_SH2_STAT3 | 566 | 569 | PF00017 | 0.259 |
LIG_SH2_STAT5 | 203 | 206 | PF00017 | 0.309 |
LIG_SH2_STAT5 | 234 | 237 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 250 | 253 | PF00017 | 0.465 |
LIG_SH2_STAT5 | 553 | 556 | PF00017 | 0.292 |
LIG_SH2_STAT5 | 59 | 62 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 591 | 594 | PF00017 | 0.324 |
LIG_SH3_3 | 217 | 223 | PF00018 | 0.287 |
LIG_SH3_3 | 251 | 257 | PF00018 | 0.482 |
LIG_SH3_3 | 471 | 477 | PF00018 | 0.288 |
LIG_SH3_3 | 617 | 623 | PF00018 | 0.660 |
LIG_SH3_3 | 89 | 95 | PF00018 | 0.386 |
LIG_SUMO_SIM_anti_2 | 298 | 303 | PF11976 | 0.306 |
LIG_SUMO_SIM_anti_2 | 409 | 415 | PF11976 | 0.197 |
LIG_SUMO_SIM_anti_2 | 478 | 483 | PF11976 | 0.294 |
LIG_SUMO_SIM_anti_2 | 485 | 490 | PF11976 | 0.274 |
LIG_SUMO_SIM_anti_2 | 494 | 499 | PF11976 | 0.226 |
LIG_SUMO_SIM_anti_2 | 513 | 520 | PF11976 | 0.306 |
LIG_SUMO_SIM_par_1 | 142 | 150 | PF11976 | 0.317 |
LIG_SUMO_SIM_par_1 | 295 | 300 | PF11976 | 0.354 |
LIG_TRAF2_1 | 14 | 17 | PF00917 | 0.692 |
LIG_TYR_ITIM | 281 | 286 | PF00017 | 0.321 |
LIG_TYR_ITIM | 303 | 308 | PF00017 | 0.331 |
LIG_UBA3_1 | 214 | 221 | PF00899 | 0.322 |
LIG_UBA3_1 | 486 | 493 | PF00899 | 0.375 |
LIG_WRC_WIRS_1 | 175 | 180 | PF05994 | 0.362 |
MOD_CDC14_SPxK_1 | 256 | 259 | PF00782 | 0.419 |
MOD_CDK_SPK_2 | 253 | 258 | PF00069 | 0.429 |
MOD_CDK_SPxK_1 | 253 | 259 | PF00069 | 0.433 |
MOD_CK1_1 | 146 | 152 | PF00069 | 0.371 |
MOD_CK1_1 | 196 | 202 | PF00069 | 0.354 |
MOD_CK1_1 | 206 | 212 | PF00069 | 0.292 |
MOD_CK1_1 | 369 | 375 | PF00069 | 0.523 |
MOD_CK1_1 | 390 | 396 | PF00069 | 0.372 |
MOD_CK1_1 | 402 | 408 | PF00069 | 0.377 |
MOD_CK1_1 | 435 | 441 | PF00069 | 0.353 |
MOD_CK1_1 | 510 | 516 | PF00069 | 0.368 |
MOD_CK1_1 | 534 | 540 | PF00069 | 0.345 |
MOD_CK1_1 | 585 | 591 | PF00069 | 0.356 |
MOD_CK1_1 | 80 | 86 | PF00069 | 0.315 |
MOD_CK2_1 | 11 | 17 | PF00069 | 0.554 |
MOD_CK2_1 | 225 | 231 | PF00069 | 0.279 |
MOD_CK2_1 | 358 | 364 | PF00069 | 0.636 |
MOD_CK2_1 | 369 | 375 | PF00069 | 0.510 |
MOD_CK2_1 | 383 | 389 | PF00069 | 0.384 |
MOD_CK2_1 | 450 | 456 | PF00069 | 0.380 |
MOD_CK2_1 | 615 | 621 | PF00069 | 0.510 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.321 |
MOD_GlcNHglycan | 197 | 201 | PF01048 | 0.295 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.320 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.502 |
MOD_GlcNHglycan | 345 | 348 | PF01048 | 0.537 |
MOD_GlcNHglycan | 368 | 371 | PF01048 | 0.561 |
MOD_GlcNHglycan | 444 | 447 | PF01048 | 0.298 |
MOD_GlcNHglycan | 509 | 512 | PF01048 | 0.289 |
MOD_GlcNHglycan | 578 | 581 | PF01048 | 0.361 |
MOD_GlcNHglycan | 634 | 637 | PF01048 | 0.669 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.297 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.518 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.370 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.334 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.586 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.627 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.561 |
MOD_GSK3_1 | 383 | 390 | PF00069 | 0.444 |
MOD_GSK3_1 | 402 | 409 | PF00069 | 0.369 |
MOD_GSK3_1 | 534 | 541 | PF00069 | 0.316 |
MOD_GSK3_1 | 551 | 558 | PF00069 | 0.388 |
MOD_GSK3_1 | 581 | 588 | PF00069 | 0.364 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.310 |
MOD_N-GLC_1 | 329 | 334 | PF02516 | 0.648 |
MOD_N-GLC_1 | 355 | 360 | PF02516 | 0.712 |
MOD_N-GLC_1 | 614 | 619 | PF02516 | 0.486 |
MOD_N-GLC_1 | 72 | 77 | PF02516 | 0.356 |
MOD_N-GLC_2 | 563 | 565 | PF02516 | 0.428 |
MOD_NEK2_1 | 286 | 291 | PF00069 | 0.279 |
MOD_NEK2_1 | 387 | 392 | PF00069 | 0.394 |
MOD_NEK2_1 | 399 | 404 | PF00069 | 0.297 |
MOD_NEK2_1 | 482 | 487 | PF00069 | 0.287 |
MOD_NEK2_1 | 500 | 505 | PF00069 | 0.340 |
MOD_NEK2_1 | 538 | 543 | PF00069 | 0.289 |
MOD_NEK2_1 | 581 | 586 | PF00069 | 0.311 |
MOD_NEK2_1 | 632 | 637 | PF00069 | 0.684 |
MOD_NEK2_2 | 136 | 141 | PF00069 | 0.334 |
MOD_PIKK_1 | 329 | 335 | PF00454 | 0.564 |
MOD_PIKK_1 | 406 | 412 | PF00454 | 0.349 |
MOD_PIKK_1 | 427 | 433 | PF00454 | 0.385 |
MOD_PIKK_1 | 456 | 462 | PF00454 | 0.400 |
MOD_PIKK_1 | 605 | 611 | PF00454 | 0.438 |
MOD_PIKK_1 | 72 | 78 | PF00454 | 0.278 |
MOD_PKA_2 | 11 | 17 | PF00069 | 0.576 |
MOD_PKA_2 | 136 | 142 | PF00069 | 0.278 |
MOD_PKA_2 | 18 | 24 | PF00069 | 0.458 |
MOD_PKA_2 | 343 | 349 | PF00069 | 0.656 |
MOD_PKA_2 | 358 | 364 | PF00069 | 0.633 |
MOD_Plk_1 | 276 | 282 | PF00069 | 0.368 |
MOD_Plk_1 | 373 | 379 | PF00069 | 0.626 |
MOD_Plk_1 | 605 | 611 | PF00069 | 0.452 |
MOD_Plk_4 | 140 | 146 | PF00069 | 0.334 |
MOD_Plk_4 | 147 | 153 | PF00069 | 0.325 |
MOD_Plk_4 | 156 | 162 | PF00069 | 0.323 |
MOD_Plk_4 | 174 | 180 | PF00069 | 0.376 |
MOD_Plk_4 | 276 | 282 | PF00069 | 0.319 |
MOD_Plk_4 | 303 | 309 | PF00069 | 0.355 |
MOD_Plk_4 | 383 | 389 | PF00069 | 0.405 |
MOD_Plk_4 | 399 | 405 | PF00069 | 0.379 |
MOD_Plk_4 | 432 | 438 | PF00069 | 0.292 |
MOD_Plk_4 | 450 | 456 | PF00069 | 0.359 |
MOD_Plk_4 | 475 | 481 | PF00069 | 0.313 |
MOD_Plk_4 | 482 | 488 | PF00069 | 0.302 |
MOD_Plk_4 | 510 | 516 | PF00069 | 0.327 |
MOD_Plk_4 | 538 | 544 | PF00069 | 0.296 |
MOD_Plk_4 | 55 | 61 | PF00069 | 0.305 |
MOD_Plk_4 | 582 | 588 | PF00069 | 0.275 |
MOD_Plk_4 | 77 | 83 | PF00069 | 0.385 |
MOD_Plk_4 | 84 | 90 | PF00069 | 0.352 |
MOD_ProDKin_1 | 253 | 259 | PF00069 | 0.421 |
MOD_ProDKin_1 | 424 | 430 | PF00069 | 0.477 |
TRG_DiLeu_BaEn_1 | 432 | 437 | PF01217 | 0.302 |
TRG_DiLeu_BaEn_4 | 465 | 471 | PF01217 | 0.262 |
TRG_DiLeu_LyEn_5 | 628 | 633 | PF01217 | 0.711 |
TRG_ENDOCYTIC_2 | 283 | 286 | PF00928 | 0.298 |
TRG_ENDOCYTIC_2 | 305 | 308 | PF00928 | 0.298 |
TRG_ENDOCYTIC_2 | 401 | 404 | PF00928 | 0.334 |
TRG_ENDOCYTIC_2 | 50 | 53 | PF00928 | 0.286 |
TRG_ENDOCYTIC_2 | 530 | 533 | PF00928 | 0.327 |
TRG_ENDOCYTIC_2 | 591 | 594 | PF00928 | 0.382 |
TRG_ENDOCYTIC_2 | 596 | 599 | PF00928 | 0.401 |
TRG_ENDOCYTIC_2 | 61 | 64 | PF00928 | 0.308 |
TRG_ER_diArg_1 | 257 | 259 | PF00400 | 0.310 |
TRG_Pf-PMV_PEXEL_1 | 233 | 237 | PF00026 | 0.350 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6G0 | Leptomonas seymouri | 76% | 100% |
A0A0N1HT40 | Leptomonas seymouri | 41% | 100% |
A0A0N1HZC2 | Leptomonas seymouri | 26% | 100% |
A0A0N1IKC5 | Leptomonas seymouri | 41% | 100% |
A0A0N1PB63 | Leptomonas seymouri | 25% | 97% |
A0A0N1PFR4 | Leptomonas seymouri | 27% | 96% |
A0A0S4JR45 | Bodo saltans | 27% | 100% |
A0A1X0NKK0 | Trypanosomatidae | 27% | 100% |
A0A1X0NL32 | Trypanosomatidae | 30% | 100% |
A0A1X0NM09 | Trypanosomatidae | 26% | 100% |
A0A1X0NRW5 | Trypanosomatidae | 41% | 91% |
A0A1X0NV13 | Trypanosomatidae | 42% | 98% |
A0A1X0NV19 | Trypanosomatidae | 41% | 100% |
A0A1X0NV27 | Trypanosomatidae | 40% | 100% |
A0A1X0NVH8 | Trypanosomatidae | 41% | 96% |
A0A1X0NVM7 | Trypanosomatidae | 42% | 99% |
A0A1X0NWQ1 | Trypanosomatidae | 42% | 99% |
A0A1X0NZE6 | Trypanosomatidae | 30% | 100% |
A0A1X0NZU2 | Trypanosomatidae | 28% | 99% |
A0A1X0NZU5 | Trypanosomatidae | 31% | 100% |
A0A1X0NZW1 | Trypanosomatidae | 27% | 100% |
A0A1X0P0M7 | Trypanosomatidae | 30% | 100% |
A0A381MMW5 | Leishmania infantum | 28% | 97% |
A0A3Q8I7Y9 | Leishmania donovani | 38% | 100% |
A0A3Q8IEC4 | Leishmania donovani | 28% | 98% |
A0A3Q8IF95 | Leishmania donovani | 26% | 100% |
A0A3Q8IIT5 | Leishmania donovani | 27% | 95% |
A0A3Q8ISY9 | Leishmania donovani | 83% | 100% |
A0A3R7JSQ9 | Trypanosoma rangeli | 26% | 100% |
A0A3R7KKN8 | Trypanosoma rangeli | 29% | 100% |
A0A3R7MAQ7 | Trypanosoma rangeli | 39% | 90% |
A0A3R7N415 | Trypanosoma rangeli | 28% | 100% |
A0A3R7N921 | Trypanosoma rangeli | 28% | 100% |
A0A3R7R443 | Trypanosoma rangeli | 27% | 100% |
A0A3S7WRJ4 | Leishmania donovani | 41% | 99% |
A0A3S7WRJ5 | Leishmania donovani | 38% | 91% |
A0A3S7WRL4 | Leishmania donovani | 38% | 100% |
A0A3S7WRS3 | Leishmania donovani | 24% | 100% |
A0A3S7WSR4 | Leishmania donovani | 39% | 100% |
A0A3S7WWU1 | Leishmania donovani | 25% | 96% |
A0A3S7X2G0 | Leishmania donovani | 28% | 97% |
A0A3S7X2K5 | Leishmania donovani | 28% | 100% |
A0A3S7XB11 | Leishmania donovani | 28% | 100% |
A0A422MSE4 | Trypanosoma rangeli | 41% | 100% |
A0A422MSP6 | Trypanosoma rangeli | 30% | 100% |
A0A422MST9 | Trypanosoma rangeli | 27% | 100% |
A0A422MU68 | Trypanosoma rangeli | 25% | 100% |
A4H6J0 | Leishmania braziliensis | 40% | 100% |
A4H6J1 | Leishmania braziliensis | 39% | 100% |
A4H6J3 | Leishmania braziliensis | 38% | 99% |
A4H6Q5 | Leishmania braziliensis | 24% | 100% |
A4HC19 | Leishmania braziliensis | 25% | 100% |
A4HHG2 | Leishmania braziliensis | 28% | 100% |
A4HHG3 | Leishmania braziliensis | 26% | 100% |
A4HHG4 | Leishmania braziliensis | 26% | 100% |
A4HPE2 | Leishmania braziliensis | 27% | 100% |
A4HUX5 | Leishmania infantum | 41% | 99% |
A4HUX6 | Leishmania infantum | 38% | 91% |
A4HUX7 | Leishmania infantum | 38% | 100% |
A4HUX8 | Leishmania infantum | 38% | 100% |
A4HV40 | Leishmania infantum | 24% | 100% |
A4HZF5 | Leishmania infantum | 26% | 100% |
A4HZJ4 | Leishmania infantum | 25% | 96% |
A4I4L2 | Leishmania infantum | 27% | 95% |
A4I7C5 | Leishmania infantum | 84% | 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) | 27% | 100% |
C9ZTR5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
C9ZTR6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
C9ZTR7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
C9ZTR8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
C9ZTR9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
C9ZTS1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
C9ZUT6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
D0A7B1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 23% | 99% |
D0A7H1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
D0AAQ2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 93% |
E8NHE1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 100% |
E9AE01 | Leishmania major | 28% | 100% |
E9AE09 | Leishmania major | 26% | 100% |
E9AE10 | Leishmania major | 26% | 100% |
E9AE11 | Leishmania major | 28% | 100% |
E9AGK5 | Leishmania infantum | 39% | 100% |
E9AHJ0 | Leishmania infantum | 28% | 98% |
E9AHJ1 | Leishmania infantum | 27% | 100% |
E9ALS2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 98% |
E9ALS3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 95% |
E9ANL0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 99% |
E9ANL1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 98% |
E9ANL2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 39% | 100% |
E9ANS1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 100% |
E9APJ3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 100% |
E9AT53 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9AVF1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9AVF2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 96% |
E9B2B8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
Q4Q1E4 | Leishmania major | 28% | 100% |
Q4Q5T8 | Leishmania major | 82% | 100% |
Q4QC27 | Leishmania major | 24% | 100% |
Q4QC28 | Leishmania major | 26% | 96% |
Q4QFY5 | Leishmania major | 40% | 100% |
Q4QGU8 | Leishmania major | 23% | 100% |
Q4QH10 | Leishmania major | 36% | 97% |
Q4QH11 | Leishmania major | 38% | 94% |
Q4QH12 | Leishmania major | 38% | 94% |
Q4QH13 | Leishmania major | 38% | 94% |
Q4QH14 | Leishmania major | 38% | 100% |
Q4QH15 | Leishmania major | 41% | 100% |
V5B647 | Trypanosoma cruzi | 40% | 100% |
V5B983 | Trypanosoma cruzi | 30% | 100% |
V5BBB1 | Trypanosoma cruzi | 39% | 100% |
V5BFV8 | Trypanosoma cruzi | 28% | 95% |
V5BQY6 | Trypanosoma cruzi | 39% | 90% |
V5BVP0 | Trypanosoma cruzi | 41% | 100% |
V5DT25 | Trypanosoma cruzi | 41% | 100% |