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. | yes | 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: 75 |
NetGPI | no | yes: 0, no: 75 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 69 |
GO:0110165 | cellular anatomical entity | 1 | 69 |
GO:0005737 | cytoplasm | 2 | 3 |
Related structures:
AlphaFold database: A4HHG2
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 35 |
GO:0022857 | transmembrane transporter activity | 2 | 35 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 323 | 327 | PF00656 | 0.861 |
CLV_C14_Caspase3-7 | 345 | 349 | PF00656 | 0.792 |
CLV_C14_Caspase3-7 | 412 | 416 | PF00656 | 0.750 |
CLV_NRD_NRD_1 | 212 | 214 | PF00675 | 0.397 |
CLV_NRD_NRD_1 | 239 | 241 | PF00675 | 0.360 |
CLV_NRD_NRD_1 | 364 | 366 | PF00675 | 0.456 |
CLV_NRD_NRD_1 | 403 | 405 | PF00675 | 0.582 |
CLV_NRD_NRD_1 | 507 | 509 | PF00675 | 0.437 |
CLV_NRD_NRD_1 | 646 | 648 | PF00675 | 0.417 |
CLV_PCSK_FUR_1 | 212 | 216 | PF00082 | 0.323 |
CLV_PCSK_FUR_1 | 644 | 648 | PF00082 | 0.492 |
CLV_PCSK_KEX2_1 | 212 | 214 | PF00082 | 0.395 |
CLV_PCSK_KEX2_1 | 239 | 241 | PF00082 | 0.366 |
CLV_PCSK_KEX2_1 | 304 | 306 | PF00082 | 0.473 |
CLV_PCSK_KEX2_1 | 364 | 366 | PF00082 | 0.463 |
CLV_PCSK_KEX2_1 | 507 | 509 | PF00082 | 0.405 |
CLV_PCSK_KEX2_1 | 646 | 648 | PF00082 | 0.402 |
CLV_PCSK_PC1ET2_1 | 214 | 216 | PF00082 | 0.329 |
CLV_PCSK_PC1ET2_1 | 304 | 306 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 214 | 218 | PF00082 | 0.462 |
CLV_PCSK_SKI1_1 | 224 | 228 | PF00082 | 0.453 |
CLV_PCSK_SKI1_1 | 435 | 439 | PF00082 | 0.450 |
CLV_PCSK_SKI1_1 | 479 | 483 | PF00082 | 0.529 |
CLV_PCSK_SKI1_1 | 594 | 598 | PF00082 | 0.360 |
CLV_PCSK_SKI1_1 | 607 | 611 | PF00082 | 0.643 |
CLV_PCSK_SKI1_1 | 75 | 79 | PF00082 | 0.317 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.492 |
DEG_SPOP_SBC_1 | 23 | 27 | PF00917 | 0.468 |
DOC_CYCLIN_RxL_1 | 432 | 441 | PF00134 | 0.630 |
DOC_CYCLIN_yCln2_LP_2 | 544 | 550 | PF00134 | 0.326 |
DOC_MAPK_gen_1 | 103 | 112 | PF00069 | 0.427 |
DOC_MAPK_gen_1 | 268 | 275 | PF00069 | 0.411 |
DOC_MAPK_MEF2A_6 | 268 | 277 | PF00069 | 0.404 |
DOC_MAPK_MEF2A_6 | 435 | 444 | PF00069 | 0.637 |
DOC_MAPK_MEF2A_6 | 479 | 486 | PF00069 | 0.316 |
DOC_MAPK_MEF2A_6 | 621 | 628 | PF00069 | 0.333 |
DOC_MAPK_RevD_3 | 255 | 269 | PF00069 | 0.547 |
DOC_MAPK_RevD_3 | 291 | 305 | PF00069 | 0.357 |
DOC_PP1_RVXF_1 | 73 | 79 | PF00149 | 0.444 |
DOC_PP2B_LxvP_1 | 544 | 547 | PF13499 | 0.338 |
DOC_PP4_FxxP_1 | 121 | 124 | PF00568 | 0.468 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.358 |
DOC_USP7_MATH_1 | 256 | 260 | PF00917 | 0.436 |
DOC_USP7_MATH_1 | 344 | 348 | PF00917 | 0.756 |
DOC_USP7_UBL2_3 | 214 | 218 | PF12436 | 0.515 |
DOC_WW_Pin1_4 | 399 | 404 | PF00397 | 0.802 |
LIG_14-3-3_CanoR_1 | 224 | 229 | PF00244 | 0.621 |
LIG_14-3-3_CanoR_1 | 38 | 44 | PF00244 | 0.420 |
LIG_14-3-3_CanoR_1 | 495 | 503 | PF00244 | 0.368 |
LIG_14-3-3_CanoR_1 | 508 | 517 | PF00244 | 0.631 |
LIG_14-3-3_CanoR_1 | 607 | 612 | PF00244 | 0.341 |
LIG_APCC_ABBA_1 | 30 | 35 | PF00400 | 0.467 |
LIG_BIR_III_2 | 202 | 206 | PF00653 | 0.422 |
LIG_BRCT_BRCA1_1 | 468 | 472 | PF00533 | 0.425 |
LIG_BRCT_BRCA1_1 | 582 | 586 | PF00533 | 0.410 |
LIG_Clathr_ClatBox_1 | 437 | 441 | PF01394 | 0.612 |
LIG_deltaCOP1_diTrp_1 | 441 | 450 | PF00928 | 0.412 |
LIG_eIF4E_1 | 242 | 248 | PF01652 | 0.344 |
LIG_eIF4E_1 | 9 | 15 | PF01652 | 0.596 |
LIG_FHA_1 | 155 | 161 | PF00498 | 0.410 |
LIG_FHA_1 | 225 | 231 | PF00498 | 0.610 |
LIG_FHA_1 | 260 | 266 | PF00498 | 0.477 |
LIG_FHA_1 | 32 | 38 | PF00498 | 0.347 |
LIG_FHA_1 | 437 | 443 | PF00498 | 0.536 |
LIG_FHA_1 | 453 | 459 | PF00498 | 0.423 |
LIG_FHA_1 | 491 | 497 | PF00498 | 0.400 |
LIG_FHA_1 | 511 | 517 | PF00498 | 0.706 |
LIG_FHA_1 | 587 | 593 | PF00498 | 0.354 |
LIG_FHA_1 | 658 | 664 | PF00498 | 0.586 |
LIG_FHA_2 | 321 | 327 | PF00498 | 0.714 |
LIG_FHA_2 | 670 | 676 | PF00498 | 0.744 |
LIG_FXI_DFP_1 | 306 | 310 | PF00024 | 0.401 |
LIG_IRF3_LxIS_1 | 18 | 25 | PF10401 | 0.468 |
LIG_IRF3_LxIS_1 | 252 | 258 | PF10401 | 0.250 |
LIG_IRF3_LxIS_1 | 527 | 532 | PF10401 | 0.230 |
LIG_LIR_Apic_2 | 70 | 74 | PF02991 | 0.517 |
LIG_LIR_Gen_1 | 141 | 152 | PF02991 | 0.549 |
LIG_LIR_Gen_1 | 180 | 190 | PF02991 | 0.352 |
LIG_LIR_Gen_1 | 27 | 37 | PF02991 | 0.431 |
LIG_LIR_Gen_1 | 270 | 280 | PF02991 | 0.352 |
LIG_LIR_Gen_1 | 532 | 541 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 141 | 147 | PF02991 | 0.533 |
LIG_LIR_Nem_3 | 151 | 155 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 177 | 182 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 27 | 33 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 270 | 275 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 308 | 312 | PF02991 | 0.601 |
LIG_LIR_Nem_3 | 432 | 437 | PF02991 | 0.569 |
LIG_LIR_Nem_3 | 469 | 475 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 518 | 524 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 532 | 536 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 83 | 89 | PF02991 | 0.356 |
LIG_LYPXL_yS_3 | 299 | 302 | PF13949 | 0.649 |
LIG_NRBOX | 86 | 92 | PF00104 | 0.415 |
LIG_PALB2_WD40_1 | 163 | 171 | PF16756 | 0.254 |
LIG_Pex14_1 | 446 | 450 | PF04695 | 0.373 |
LIG_Pex14_2 | 164 | 168 | PF04695 | 0.341 |
LIG_Pex14_2 | 445 | 449 | PF04695 | 0.326 |
LIG_Pex14_2 | 597 | 601 | PF04695 | 0.392 |
LIG_Pex14_2 | 92 | 96 | PF04695 | 0.307 |
LIG_PTB_Apo_2 | 162 | 169 | PF02174 | 0.374 |
LIG_PTB_Apo_2 | 619 | 626 | PF02174 | 0.222 |
LIG_SH2_CRK | 144 | 148 | PF00017 | 0.570 |
LIG_SH2_CRK | 71 | 75 | PF00017 | 0.529 |
LIG_SH2_GRB2like | 163 | 166 | PF00017 | 0.412 |
LIG_SH2_PTP2 | 19 | 22 | PF00017 | 0.459 |
LIG_SH2_PTP2 | 272 | 275 | PF00017 | 0.317 |
LIG_SH2_PTP2 | 483 | 486 | PF00017 | 0.301 |
LIG_SH2_STAP1 | 182 | 186 | PF00017 | 0.335 |
LIG_SH2_STAP1 | 314 | 318 | PF00017 | 0.558 |
LIG_SH2_STAP1 | 570 | 574 | PF00017 | 0.559 |
LIG_SH2_STAT3 | 231 | 234 | PF00017 | 0.604 |
LIG_SH2_STAT3 | 467 | 470 | PF00017 | 0.251 |
LIG_SH2_STAT5 | 120 | 123 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 163 | 166 | PF00017 | 0.359 |
LIG_SH2_STAT5 | 184 | 187 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 19 | 22 | PF00017 | 0.421 |
LIG_SH2_STAT5 | 199 | 202 | PF00017 | 0.373 |
LIG_SH2_STAT5 | 242 | 245 | PF00017 | 0.372 |
LIG_SH2_STAT5 | 264 | 267 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 272 | 275 | PF00017 | 0.332 |
LIG_SH2_STAT5 | 483 | 486 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 533 | 536 | PF00017 | 0.351 |
LIG_SH2_STAT5 | 60 | 63 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 89 | 92 | PF00017 | 0.415 |
LIG_SH3_1 | 304 | 310 | PF00018 | 0.714 |
LIG_SH3_2 | 400 | 405 | PF14604 | 0.740 |
LIG_SH3_3 | 133 | 139 | PF00018 | 0.585 |
LIG_SH3_3 | 202 | 208 | PF00018 | 0.515 |
LIG_SH3_3 | 304 | 310 | PF00018 | 0.672 |
LIG_SH3_3 | 397 | 403 | PF00018 | 0.816 |
LIG_SH3_3 | 411 | 417 | PF00018 | 0.708 |
LIG_SH3_3 | 73 | 79 | PF00018 | 0.598 |
LIG_SUMO_SIM_anti_2 | 106 | 111 | PF11976 | 0.290 |
LIG_SUMO_SIM_par_1 | 281 | 287 | PF11976 | 0.439 |
LIG_SUMO_SIM_par_1 | 436 | 441 | PF11976 | 0.595 |
LIG_SUMO_SIM_par_1 | 658 | 664 | PF11976 | 0.729 |
LIG_UBA3_1 | 596 | 603 | PF00899 | 0.494 |
LIG_WRC_WIRS_1 | 430 | 435 | PF05994 | 0.636 |
MOD_CDC14_SPxK_1 | 402 | 405 | PF00782 | 0.810 |
MOD_CDK_SPK_2 | 399 | 404 | PF00069 | 0.679 |
MOD_CDK_SPxK_1 | 399 | 405 | PF00069 | 0.808 |
MOD_CK1_1 | 177 | 183 | PF00069 | 0.383 |
MOD_CK1_1 | 259 | 265 | PF00069 | 0.491 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.324 |
MOD_CK1_1 | 552 | 558 | PF00069 | 0.506 |
MOD_CK1_1 | 634 | 640 | PF00069 | 0.377 |
MOD_CK1_1 | 669 | 675 | PF00069 | 0.743 |
MOD_CK2_1 | 368 | 374 | PF00069 | 0.822 |
MOD_CK2_1 | 391 | 397 | PF00069 | 0.853 |
MOD_CK2_1 | 509 | 515 | PF00069 | 0.663 |
MOD_CMANNOS | 443 | 446 | PF00535 | 0.412 |
MOD_GlcNHglycan | 152 | 155 | PF01048 | 0.421 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.522 |
MOD_GlcNHglycan | 269 | 272 | PF01048 | 0.674 |
MOD_GlcNHglycan | 490 | 493 | PF01048 | 0.391 |
MOD_GlcNHglycan | 497 | 500 | PF01048 | 0.390 |
MOD_GlcNHglycan | 583 | 586 | PF01048 | 0.432 |
MOD_GlcNHglycan | 636 | 639 | PF01048 | 0.423 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.412 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.417 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.386 |
MOD_GSK3_1 | 308 | 315 | PF00069 | 0.671 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.752 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.792 |
MOD_GSK3_1 | 378 | 385 | PF00069 | 0.796 |
MOD_GSK3_1 | 387 | 394 | PF00069 | 0.835 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.342 |
MOD_GSK3_1 | 490 | 497 | PF00069 | 0.441 |
MOD_GSK3_1 | 581 | 588 | PF00069 | 0.401 |
MOD_GSK3_1 | 603 | 610 | PF00069 | 0.414 |
MOD_GSK3_1 | 666 | 673 | PF00069 | 0.702 |
MOD_N-GLC_1 | 174 | 179 | PF02516 | 0.529 |
MOD_N-GLC_1 | 377 | 382 | PF02516 | 0.539 |
MOD_N-GLC_1 | 421 | 426 | PF02516 | 0.394 |
MOD_N-GLC_1 | 666 | 671 | PF02516 | 0.499 |
MOD_N-GLC_2 | 56 | 58 | PF02516 | 0.468 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.404 |
MOD_NEK2_1 | 191 | 196 | PF00069 | 0.381 |
MOD_NEK2_1 | 22 | 27 | PF00069 | 0.383 |
MOD_NEK2_1 | 255 | 260 | PF00069 | 0.413 |
MOD_NEK2_1 | 445 | 450 | PF00069 | 0.396 |
MOD_NEK2_1 | 452 | 457 | PF00069 | 0.340 |
MOD_NEK2_1 | 517 | 522 | PF00069 | 0.391 |
MOD_NEK2_1 | 529 | 534 | PF00069 | 0.350 |
MOD_NEK2_1 | 549 | 554 | PF00069 | 0.500 |
MOD_NEK2_1 | 580 | 585 | PF00069 | 0.408 |
MOD_NEK2_1 | 586 | 591 | PF00069 | 0.396 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.572 |
MOD_NEK2_2 | 226 | 231 | PF00069 | 0.617 |
MOD_NEK2_2 | 28 | 33 | PF00069 | 0.409 |
MOD_NEK2_2 | 562 | 567 | PF00069 | 0.484 |
MOD_OFUCOSY | 614 | 619 | PF10250 | 0.588 |
MOD_PIKK_1 | 466 | 472 | PF00454 | 0.326 |
MOD_PKA_1 | 214 | 220 | PF00069 | 0.671 |
MOD_PKA_2 | 214 | 220 | PF00069 | 0.646 |
MOD_PKA_2 | 494 | 500 | PF00069 | 0.395 |
MOD_Plk_1 | 377 | 383 | PF00069 | 0.749 |
MOD_Plk_1 | 46 | 52 | PF00069 | 0.337 |
MOD_Plk_1 | 475 | 481 | PF00069 | 0.387 |
MOD_Plk_1 | 603 | 609 | PF00069 | 0.314 |
MOD_Plk_1 | 657 | 663 | PF00069 | 0.679 |
MOD_Plk_2-3 | 320 | 326 | PF00069 | 0.803 |
MOD_Plk_4 | 127 | 133 | PF00069 | 0.406 |
MOD_Plk_4 | 155 | 161 | PF00069 | 0.387 |
MOD_Plk_4 | 191 | 197 | PF00069 | 0.347 |
MOD_Plk_4 | 226 | 232 | PF00069 | 0.616 |
MOD_Plk_4 | 256 | 262 | PF00069 | 0.397 |
MOD_Plk_4 | 429 | 435 | PF00069 | 0.592 |
MOD_Plk_4 | 454 | 460 | PF00069 | 0.399 |
MOD_Plk_4 | 517 | 523 | PF00069 | 0.370 |
MOD_Plk_4 | 586 | 592 | PF00069 | 0.431 |
MOD_ProDKin_1 | 399 | 405 | PF00069 | 0.803 |
TRG_ENDOCYTIC_2 | 144 | 147 | PF00928 | 0.526 |
TRG_ENDOCYTIC_2 | 182 | 185 | PF00928 | 0.363 |
TRG_ENDOCYTIC_2 | 19 | 22 | PF00928 | 0.422 |
TRG_ENDOCYTIC_2 | 272 | 275 | PF00928 | 0.318 |
TRG_ENDOCYTIC_2 | 299 | 302 | PF00928 | 0.593 |
TRG_ENDOCYTIC_2 | 430 | 433 | PF00928 | 0.600 |
TRG_ENDOCYTIC_2 | 483 | 486 | PF00928 | 0.370 |
TRG_ENDOCYTIC_2 | 533 | 536 | PF00928 | 0.361 |
TRG_ENDOCYTIC_2 | 578 | 581 | PF00928 | 0.370 |
TRG_ENDOCYTIC_2 | 60 | 63 | PF00928 | 0.345 |
TRG_ENDOCYTIC_2 | 89 | 92 | PF00928 | 0.432 |
TRG_ER_diArg_1 | 211 | 213 | PF00400 | 0.625 |
TRG_ER_diArg_1 | 239 | 241 | PF00400 | 0.563 |
TRG_ER_diArg_1 | 363 | 365 | PF00400 | 0.655 |
TRG_ER_diArg_1 | 506 | 508 | PF00400 | 0.609 |
TRG_ER_diArg_1 | 645 | 647 | PF00400 | 0.642 |
TRG_ER_diArg_1 | 9 | 12 | PF00400 | 0.532 |
TRG_NLS_MonoExtC_3 | 302 | 307 | PF00514 | 0.520 |
TRG_NLS_MonoExtN_4 | 212 | 217 | PF00514 | 0.532 |
TRG_NLS_MonoExtN_4 | 300 | 307 | PF00514 | 0.517 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6G0 | Leptomonas seymouri | 27% | 100% |
A0A0N1HZC2 | Leptomonas seymouri | 28% | 100% |
A0A0N1IKC5 | Leptomonas seymouri | 27% | 100% |
A0A0N1PB63 | Leptomonas seymouri | 26% | 100% |
A0A0N1PD04 | Leptomonas seymouri | 24% | 100% |
A0A0N1PFR4 | Leptomonas seymouri | 65% | 100% |
A0A1X0NKK0 | Trypanosomatidae | 29% | 100% |
A0A1X0NM09 | Trypanosomatidae | 29% | 100% |
A0A1X0NVF9 | Trypanosomatidae | 22% | 100% |
A0A1X0NVM7 | Trypanosomatidae | 28% | 100% |
A0A1X0NWQ1 | Trypanosomatidae | 27% | 100% |
A0A1X0NZE6 | Trypanosomatidae | 25% | 100% |
A0A1X0NZT1 | Trypanosomatidae | 23% | 81% |
A0A1X0NZU2 | Trypanosomatidae | 31% | 100% |
A0A1X0P0M7 | Trypanosomatidae | 25% | 100% |
A0A381MMW5 | Leishmania infantum | 30% | 100% |
A0A3Q8IEC4 | Leishmania donovani | 30% | 100% |
A0A3Q8IF95 | Leishmania donovani | 24% | 100% |
A0A3Q8IIT5 | Leishmania donovani | 83% | 100% |
A0A3Q8ISY9 | Leishmania donovani | 27% | 100% |
A0A3R7KKN8 | Trypanosoma rangeli | 52% | 100% |
A0A3R7N3S6 | Trypanosoma rangeli | 24% | 100% |
A0A3R7N921 | Trypanosoma rangeli | 25% | 100% |
A0A3S7WRJ4 | Leishmania donovani | 25% | 100% |
A0A3S7WRJ5 | Leishmania donovani | 26% | 97% |
A0A3S7WRS3 | Leishmania donovani | 25% | 100% |
A0A3S7WWU1 | Leishmania donovani | 26% | 100% |
A0A3S7X2G0 | Leishmania donovani | 30% | 100% |
A0A3S7X2K5 | Leishmania donovani | 30% | 100% |
A0A3S7XB11 | Leishmania donovani | 27% | 100% |
A0A422MSP6 | Trypanosoma rangeli | 31% | 100% |
A0A422MU68 | Trypanosoma rangeli | 25% | 100% |
A0A422NL17 | Trypanosoma rangeli | 23% | 84% |
A4H6J0 | Leishmania braziliensis | 25% | 98% |
A4H6J1 | Leishmania braziliensis | 27% | 96% |
A4H6Q5 | Leishmania braziliensis | 24% | 97% |
A4HC19 | Leishmania braziliensis | 26% | 99% |
A4HHG3 | Leishmania braziliensis | 30% | 100% |
A4HHG4 | Leishmania braziliensis | 29% | 100% |
A4HJW3 | Leishmania braziliensis | 28% | 100% |
A4HPE2 | Leishmania braziliensis | 28% | 100% |
A4HUX5 | Leishmania infantum | 25% | 100% |
A4HUX6 | Leishmania infantum | 27% | 97% |
A4HV40 | Leishmania infantum | 25% | 100% |
A4HZF5 | Leishmania infantum | 24% | 100% |
A4HZJ4 | Leishmania infantum | 26% | 100% |
A4I4L2 | Leishmania infantum | 82% | 100% |
A4I7C5 | Leishmania infantum | 27% | 100% |
A4ICI3 | Leishmania infantum | 27% | 100% |
D0A7B1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 100% |
E8NHE1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9AE01 | Leishmania major | 30% | 97% |
E9AE09 | Leishmania major | 82% | 100% |
E9AE10 | Leishmania major | 82% | 100% |
E9AE11 | Leishmania major | 31% | 94% |
E9AHJ0 | Leishmania infantum | 30% | 100% |
E9AHJ1 | Leishmania infantum | 30% | 100% |
E9ALS2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9ALS3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |
E9ANL0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
E9ANL1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9ANS1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
E9AT53 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9AVF1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 92% |
E9AVF2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9B2B8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
Q4Q1E4 | Leishmania major | 27% | 92% |
Q4Q5T8 | Leishmania major | 26% | 97% |
Q4QC27 | Leishmania major | 25% | 96% |
Q4QGU8 | Leishmania major | 25% | 100% |
Q4QH14 | Leishmania major | 27% | 98% |
Q4QH15 | Leishmania major | 26% | 98% |
V5BFV8 | Trypanosoma cruzi | 27% | 100% |
V5DT25 | Trypanosoma cruzi | 28% | 100% |