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: 122 |
NetGPI | no | yes: 0, no: 122 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 115 |
GO:0110165 | cellular anatomical entity | 1 | 115 |
GO:0005737 | cytoplasm | 2 | 3 |
Related structures:
AlphaFold database: Q4QC27
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 53 |
GO:0022857 | transmembrane transporter activity | 2 | 53 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 197 | 201 | PF00656 | 0.416 |
CLV_NRD_NRD_1 | 232 | 234 | PF00675 | 0.348 |
CLV_NRD_NRD_1 | 252 | 254 | PF00675 | 0.340 |
CLV_NRD_NRD_1 | 28 | 30 | PF00675 | 0.384 |
CLV_NRD_NRD_1 | 41 | 43 | PF00675 | 0.269 |
CLV_NRD_NRD_1 | 482 | 484 | PF00675 | 0.404 |
CLV_NRD_NRD_1 | 575 | 577 | PF00675 | 0.589 |
CLV_PCSK_KEX2_1 | 232 | 234 | PF00082 | 0.347 |
CLV_PCSK_KEX2_1 | 41 | 43 | PF00082 | 0.321 |
CLV_PCSK_KEX2_1 | 444 | 446 | PF00082 | 0.658 |
CLV_PCSK_KEX2_1 | 575 | 577 | PF00082 | 0.565 |
CLV_PCSK_KEX2_1 | 621 | 623 | PF00082 | 0.372 |
CLV_PCSK_PC1ET2_1 | 444 | 446 | PF00082 | 0.634 |
CLV_PCSK_PC1ET2_1 | 621 | 623 | PF00082 | 0.348 |
CLV_PCSK_SKI1_1 | 17 | 21 | PF00082 | 0.472 |
CLV_PCSK_SKI1_1 | 177 | 181 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 373 | 377 | PF00082 | 0.580 |
CLV_PCSK_SKI1_1 | 465 | 469 | PF00082 | 0.379 |
CLV_PCSK_SKI1_1 | 483 | 487 | PF00082 | 0.406 |
CLV_PCSK_SKI1_1 | 511 | 515 | PF00082 | 0.555 |
DEG_APCC_DBOX_1 | 482 | 490 | PF00400 | 0.548 |
DEG_SPOP_SBC_1 | 189 | 193 | PF00917 | 0.258 |
DOC_CKS1_1 | 591 | 596 | PF01111 | 0.416 |
DOC_MAPK_DCC_7 | 511 | 520 | PF00069 | 0.371 |
DOC_MAPK_gen_1 | 167 | 175 | PF00069 | 0.552 |
DOC_MAPK_gen_1 | 291 | 298 | PF00069 | 0.371 |
DOC_MAPK_gen_1 | 41 | 47 | PF00069 | 0.485 |
DOC_MAPK_gen_1 | 483 | 491 | PF00069 | 0.496 |
DOC_MAPK_MEF2A_6 | 167 | 175 | PF00069 | 0.502 |
DOC_MAPK_MEF2A_6 | 254 | 263 | PF00069 | 0.535 |
DOC_MAPK_MEF2A_6 | 291 | 298 | PF00069 | 0.329 |
DOC_MAPK_MEF2A_6 | 404 | 412 | PF00069 | 0.616 |
DOC_MAPK_MEF2A_6 | 484 | 493 | PF00069 | 0.498 |
DOC_MAPK_MEF2A_6 | 511 | 520 | PF00069 | 0.316 |
DOC_MAPK_MEF2A_6 | 572 | 581 | PF00069 | 0.454 |
DOC_PP1_RVXF_1 | 463 | 469 | PF00149 | 0.497 |
DOC_PP2B_LxvP_1 | 506 | 509 | PF13499 | 0.459 |
DOC_PP2B_LxvP_1 | 577 | 580 | PF13499 | 0.474 |
DOC_PP2B_PxIxI_1 | 515 | 521 | PF00149 | 0.423 |
DOC_PP4_FxxP_1 | 93 | 96 | PF00568 | 0.343 |
DOC_USP7_MATH_1 | 188 | 192 | PF00917 | 0.383 |
DOC_USP7_MATH_1 | 286 | 290 | PF00917 | 0.436 |
DOC_USP7_UBL2_3 | 13 | 17 | PF12436 | 0.732 |
DOC_WW_Pin1_4 | 234 | 239 | PF00397 | 0.685 |
DOC_WW_Pin1_4 | 491 | 496 | PF00397 | 0.406 |
DOC_WW_Pin1_4 | 590 | 595 | PF00397 | 0.450 |
LIG_14-3-3_CanoR_1 | 373 | 378 | PF00244 | 0.745 |
LIG_APCC_ABBA_1 | 518 | 523 | PF00400 | 0.401 |
LIG_BRCT_BRCA1_1 | 190 | 194 | PF00533 | 0.521 |
LIG_Clathr_ClatBox_1 | 348 | 352 | PF01394 | 0.583 |
LIG_Clathr_ClatBox_1 | 407 | 411 | PF01394 | 0.538 |
LIG_Clathr_ClatBox_1 | 519 | 523 | PF01394 | 0.408 |
LIG_deltaCOP1_diTrp_1 | 411 | 419 | PF00928 | 0.393 |
LIG_EH1_1 | 264 | 272 | PF00400 | 0.263 |
LIG_eIF4E_1 | 265 | 271 | PF01652 | 0.333 |
LIG_FHA_1 | 134 | 140 | PF00498 | 0.375 |
LIG_FHA_1 | 21 | 27 | PF00498 | 0.641 |
LIG_FHA_1 | 298 | 304 | PF00498 | 0.406 |
LIG_FHA_1 | 337 | 343 | PF00498 | 0.683 |
LIG_FHA_1 | 4 | 10 | PF00498 | 0.678 |
LIG_FHA_1 | 433 | 439 | PF00498 | 0.357 |
LIG_FHA_1 | 452 | 458 | PF00498 | 0.369 |
LIG_FHA_1 | 591 | 597 | PF00498 | 0.339 |
LIG_FHA_1 | 83 | 89 | PF00498 | 0.361 |
LIG_FHA_2 | 158 | 164 | PF00498 | 0.387 |
LIG_FHA_2 | 191 | 197 | PF00498 | 0.344 |
LIG_FHA_2 | 358 | 364 | PF00498 | 0.815 |
LIG_FHA_2 | 400 | 406 | PF00498 | 0.579 |
LIG_FHA_2 | 74 | 80 | PF00498 | 0.348 |
LIG_GBD_Chelix_1 | 295 | 303 | PF00786 | 0.354 |
LIG_LIR_Gen_1 | 140 | 149 | PF02991 | 0.373 |
LIG_LIR_Gen_1 | 200 | 210 | PF02991 | 0.318 |
LIG_LIR_Gen_1 | 217 | 227 | PF02991 | 0.337 |
LIG_LIR_Gen_1 | 411 | 420 | PF02991 | 0.359 |
LIG_LIR_Gen_1 | 450 | 459 | PF02991 | 0.336 |
LIG_LIR_Gen_1 | 550 | 559 | PF02991 | 0.371 |
LIG_LIR_Gen_1 | 59 | 69 | PF02991 | 0.430 |
LIG_LIR_Gen_1 | 94 | 104 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 140 | 146 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 200 | 205 | PF02991 | 0.289 |
LIG_LIR_Nem_3 | 217 | 222 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 450 | 456 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 524 | 530 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 59 | 65 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 94 | 100 | PF02991 | 0.362 |
LIG_MAD2 | 484 | 492 | PF02301 | 0.588 |
LIG_MLH1_MIPbox_1 | 191 | 195 | PF16413 | 0.383 |
LIG_NRBOX | 413 | 419 | PF00104 | 0.294 |
LIG_PDZ_Class_2 | 624 | 629 | PF00595 | 0.624 |
LIG_Pex14_2 | 107 | 111 | PF04695 | 0.389 |
LIG_Pex14_2 | 205 | 209 | PF04695 | 0.392 |
LIG_Pex14_2 | 46 | 50 | PF04695 | 0.374 |
LIG_Pex14_2 | 535 | 539 | PF04695 | 0.583 |
LIG_Pex14_2 | 65 | 69 | PF04695 | 0.373 |
LIG_PTB_Apo_2 | 545 | 552 | PF02174 | 0.562 |
LIG_SH2_CRK | 143 | 147 | PF00017 | 0.292 |
LIG_SH2_CRK | 265 | 269 | PF00017 | 0.427 |
LIG_SH2_CRK | 97 | 101 | PF00017 | 0.343 |
LIG_SH2_STAP1 | 251 | 255 | PF00017 | 0.651 |
LIG_SH2_STAP1 | 265 | 269 | PF00017 | 0.446 |
LIG_SH2_STAP1 | 453 | 457 | PF00017 | 0.401 |
LIG_SH2_STAP1 | 60 | 64 | PF00017 | 0.368 |
LIG_SH2_STAP1 | 616 | 620 | PF00017 | 0.570 |
LIG_SH2_STAP1 | 97 | 101 | PF00017 | 0.357 |
LIG_SH2_STAT3 | 392 | 395 | PF00017 | 0.703 |
LIG_SH2_STAT5 | 157 | 160 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 204 | 207 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 226 | 229 | PF00017 | 0.524 |
LIG_SH2_STAT5 | 406 | 409 | PF00017 | 0.568 |
LIG_SH2_STAT5 | 453 | 456 | PF00017 | 0.304 |
LIG_SH2_STAT5 | 474 | 477 | PF00017 | 0.559 |
LIG_SH2_STAT5 | 92 | 95 | PF00017 | 0.334 |
LIG_SH2_STAT5 | 97 | 100 | PF00017 | 0.339 |
LIG_SH3_3 | 100 | 106 | PF00018 | 0.556 |
LIG_SH3_3 | 219 | 225 | PF00018 | 0.355 |
LIG_SH3_3 | 253 | 259 | PF00018 | 0.556 |
LIG_SH3_3 | 365 | 371 | PF00018 | 0.757 |
LIG_SH3_3 | 489 | 495 | PF00018 | 0.318 |
LIG_SH3_3 | 510 | 516 | PF00018 | 0.365 |
LIG_SH3_3 | 588 | 594 | PF00018 | 0.356 |
LIG_Sin3_3 | 142 | 149 | PF02671 | 0.382 |
LIG_SUMO_SIM_anti_2 | 217 | 224 | PF11976 | 0.409 |
LIG_SUMO_SIM_anti_2 | 306 | 311 | PF11976 | 0.337 |
LIG_SUMO_SIM_anti_2 | 78 | 85 | PF11976 | 0.368 |
LIG_SUMO_SIM_par_1 | 299 | 304 | PF11976 | 0.379 |
LIG_SUMO_SIM_par_1 | 593 | 599 | PF11976 | 0.375 |
LIG_TYR_ITIM | 141 | 146 | PF00017 | 0.341 |
LIG_TYR_ITIM | 263 | 268 | PF00017 | 0.406 |
LIG_TYR_ITIM | 95 | 100 | PF00017 | 0.349 |
LIG_UBA3_1 | 503 | 511 | PF00899 | 0.420 |
LIG_WRC_WIRS_1 | 558 | 563 | PF05994 | 0.399 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.399 |
MOD_CK1_1 | 289 | 295 | PF00069 | 0.357 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.720 |
MOD_CK1_1 | 382 | 388 | PF00069 | 0.692 |
MOD_CK1_1 | 434 | 440 | PF00069 | 0.355 |
MOD_CK1_1 | 557 | 563 | PF00069 | 0.390 |
MOD_CK1_1 | 78 | 84 | PF00069 | 0.308 |
MOD_CK2_1 | 157 | 163 | PF00069 | 0.432 |
MOD_CK2_1 | 190 | 196 | PF00069 | 0.545 |
MOD_CK2_1 | 357 | 363 | PF00069 | 0.713 |
MOD_CK2_1 | 380 | 386 | PF00069 | 0.675 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.306 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.368 |
MOD_GlcNHglycan | 288 | 291 | PF01048 | 0.618 |
MOD_GlcNHglycan | 363 | 367 | PF01048 | 0.534 |
MOD_GlcNHglycan | 449 | 452 | PF01048 | 0.505 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.479 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.400 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.380 |
MOD_GSK3_1 | 153 | 160 | PF00069 | 0.379 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.376 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.399 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.659 |
MOD_GSK3_1 | 358 | 365 | PF00069 | 0.773 |
MOD_GSK3_1 | 376 | 383 | PF00069 | 0.755 |
MOD_GSK3_1 | 430 | 437 | PF00069 | 0.445 |
MOD_GSK3_1 | 443 | 450 | PF00069 | 0.392 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.360 |
MOD_GSK3_1 | 586 | 593 | PF00069 | 0.401 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.343 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.303 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.343 |
MOD_N-GLC_1 | 286 | 291 | PF02516 | 0.602 |
MOD_N-GLC_1 | 373 | 378 | PF02516 | 0.543 |
MOD_N-GLC_1 | 431 | 436 | PF02516 | 0.585 |
MOD_N-GLC_1 | 547 | 552 | PF02516 | 0.469 |
MOD_NEK2_1 | 110 | 115 | PF00069 | 0.300 |
MOD_NEK2_1 | 182 | 187 | PF00069 | 0.409 |
MOD_NEK2_1 | 190 | 195 | PF00069 | 0.447 |
MOD_NEK2_1 | 244 | 249 | PF00069 | 0.553 |
MOD_NEK2_1 | 303 | 308 | PF00069 | 0.356 |
MOD_NEK2_1 | 430 | 435 | PF00069 | 0.343 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.329 |
MOD_NEK2_1 | 538 | 543 | PF00069 | 0.552 |
MOD_NEK2_1 | 64 | 69 | PF00069 | 0.369 |
MOD_NEK2_1 | 73 | 78 | PF00069 | 0.378 |
MOD_NEK2_2 | 137 | 142 | PF00069 | 0.317 |
MOD_NEK2_2 | 399 | 404 | PF00069 | 0.622 |
MOD_NEK2_2 | 547 | 552 | PF00069 | 0.529 |
MOD_OFUCOSY | 585 | 590 | PF10250 | 0.536 |
MOD_PIKK_1 | 18 | 24 | PF00454 | 0.676 |
MOD_PIKK_1 | 380 | 386 | PF00454 | 0.812 |
MOD_PIKK_1 | 64 | 70 | PF00454 | 0.340 |
MOD_PKA_2 | 358 | 364 | PF00069 | 0.803 |
MOD_Plk_1 | 153 | 159 | PF00069 | 0.351 |
MOD_Plk_1 | 195 | 201 | PF00069 | 0.376 |
MOD_Plk_1 | 373 | 379 | PF00069 | 0.709 |
MOD_Plk_1 | 431 | 437 | PF00069 | 0.353 |
MOD_Plk_1 | 547 | 553 | PF00069 | 0.469 |
MOD_Plk_1 | 78 | 84 | PF00069 | 0.292 |
MOD_Plk_4 | 153 | 159 | PF00069 | 0.358 |
MOD_Plk_4 | 182 | 188 | PF00069 | 0.398 |
MOD_Plk_4 | 190 | 196 | PF00069 | 0.472 |
MOD_Plk_4 | 215 | 221 | PF00069 | 0.283 |
MOD_Plk_4 | 244 | 250 | PF00069 | 0.573 |
MOD_Plk_4 | 303 | 309 | PF00069 | 0.389 |
MOD_Plk_4 | 4 | 10 | PF00069 | 0.698 |
MOD_Plk_4 | 547 | 553 | PF00069 | 0.353 |
MOD_Plk_4 | 554 | 560 | PF00069 | 0.331 |
MOD_Plk_4 | 596 | 602 | PF00069 | 0.356 |
MOD_Plk_4 | 78 | 84 | PF00069 | 0.351 |
MOD_Plk_4 | 95 | 101 | PF00069 | 0.396 |
MOD_ProDKin_1 | 234 | 240 | PF00069 | 0.683 |
MOD_ProDKin_1 | 491 | 497 | PF00069 | 0.406 |
MOD_ProDKin_1 | 590 | 596 | PF00069 | 0.419 |
TRG_DiLeu_BaEn_1 | 344 | 349 | PF01217 | 0.578 |
TRG_DiLeu_BaLyEn_6 | 257 | 262 | PF01217 | 0.637 |
TRG_DiLeu_BaLyEn_6 | 277 | 282 | PF01217 | 0.187 |
TRG_ENDOCYTIC_2 | 143 | 146 | PF00928 | 0.313 |
TRG_ENDOCYTIC_2 | 265 | 268 | PF00928 | 0.393 |
TRG_ENDOCYTIC_2 | 422 | 425 | PF00928 | 0.369 |
TRG_ENDOCYTIC_2 | 453 | 456 | PF00928 | 0.334 |
TRG_ENDOCYTIC_2 | 616 | 619 | PF00928 | 0.545 |
TRG_ENDOCYTIC_2 | 92 | 95 | PF00928 | 0.341 |
TRG_ENDOCYTIC_2 | 97 | 100 | PF00928 | 0.351 |
TRG_ER_diArg_1 | 166 | 169 | PF00400 | 0.593 |
TRG_ER_diArg_1 | 231 | 233 | PF00400 | 0.622 |
TRG_ER_diArg_1 | 291 | 294 | PF00400 | 0.405 |
TRG_ER_diArg_1 | 40 | 42 | PF00400 | 0.490 |
TRG_ER_diArg_1 | 575 | 577 | PF00400 | 0.402 |
TRG_ER_FFAT_1 | 328 | 339 | PF00635 | 0.531 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6G0 | Leptomonas seymouri | 27% | 99% |
A0A0N1HT40 | Leptomonas seymouri | 27% | 100% |
A0A0N1HZC2 | Leptomonas seymouri | 47% | 100% |
A0A0N1IKC5 | Leptomonas seymouri | 27% | 100% |
A0A0N1PB63 | Leptomonas seymouri | 67% | 95% |
A0A0N1PD04 | Leptomonas seymouri | 24% | 98% |
A0A0N1PFR4 | Leptomonas seymouri | 27% | 95% |
A0A0S4JR45 | Bodo saltans | 25% | 100% |
A0A1X0NKK0 | Trypanosomatidae | 50% | 100% |
A0A1X0NM09 | Trypanosomatidae | 50% | 100% |
A0A1X0NRW5 | Trypanosomatidae | 26% | 90% |
A0A1X0NV13 | Trypanosomatidae | 29% | 97% |
A0A1X0NV19 | Trypanosomatidae | 29% | 100% |
A0A1X0NV27 | Trypanosomatidae | 29% | 100% |
A0A1X0NVF9 | Trypanosomatidae | 22% | 94% |
A0A1X0NVH8 | Trypanosomatidae | 25% | 95% |
A0A1X0NVM7 | Trypanosomatidae | 28% | 98% |
A0A1X0NWQ1 | Trypanosomatidae | 26% | 98% |
A0A1X0NZE6 | Trypanosomatidae | 27% | 100% |
A0A1X0NZU2 | Trypanosomatidae | 25% | 97% |
A0A1X0NZU5 | Trypanosomatidae | 27% | 100% |
A0A1X0NZW1 | Trypanosomatidae | 26% | 100% |
A0A1X0P0M7 | Trypanosomatidae | 27% | 100% |
A0A381MMW5 | Leishmania infantum | 26% | 96% |
A0A3Q8I7Y9 | Leishmania donovani | 27% | 100% |
A0A3Q8IEC4 | Leishmania donovani | 26% | 97% |
A0A3Q8IF95 | Leishmania donovani | 50% | 100% |
A0A3Q8IIT5 | Leishmania donovani | 26% | 94% |
A0A3Q8ISY9 | Leishmania donovani | 25% | 99% |
A0A3R7JSQ9 | Trypanosoma rangeli | 23% | 100% |
A0A3R7KKN8 | Trypanosoma rangeli | 26% | 100% |
A0A3R7MAQ7 | Trypanosoma rangeli | 24% | 89% |
A0A3R7N3S6 | Trypanosoma rangeli | 22% | 98% |
A0A3R7N415 | Trypanosoma rangeli | 25% | 100% |
A0A3R7N921 | Trypanosoma rangeli | 29% | 100% |
A0A3R7R443 | Trypanosoma rangeli | 25% | 100% |
A0A3S7WRJ4 | Leishmania donovani | 27% | 98% |
A0A3S7WRJ5 | Leishmania donovani | 26% | 90% |
A0A3S7WRL4 | Leishmania donovani | 28% | 100% |
A0A3S7WRS3 | Leishmania donovani | 22% | 100% |
A0A3S7WSR4 | Leishmania donovani | 26% | 100% |
A0A3S7WWU1 | Leishmania donovani | 95% | 95% |
A0A3S7X2G0 | Leishmania donovani | 26% | 96% |
A0A3S7X2K5 | Leishmania donovani | 25% | 100% |
A0A3S7XB11 | Leishmania donovani | 47% | 100% |
A0A422MSE4 | Trypanosoma rangeli | 30% | 100% |
A0A422MSP6 | Trypanosoma rangeli | 25% | 100% |
A0A422MST9 | Trypanosoma rangeli | 26% | 100% |
A0A422MU68 | Trypanosoma rangeli | 48% | 100% |
A4H6J0 | Leishmania braziliensis | 26% | 98% |
A4H6J1 | Leishmania braziliensis | 27% | 96% |
A4H6J3 | Leishmania braziliensis | 28% | 100% |
A4H6Q5 | Leishmania braziliensis | 23% | 100% |
A4HC19 | Leishmania braziliensis | 76% | 98% |
A4HHG2 | Leishmania braziliensis | 25% | 93% |
A4HHG3 | Leishmania braziliensis | 27% | 97% |
A4HHG4 | Leishmania braziliensis | 28% | 96% |
A4HJW3 | Leishmania braziliensis | 24% | 99% |
A4HPE2 | Leishmania braziliensis | 48% | 100% |
A4HUX5 | Leishmania infantum | 27% | 98% |
A4HUX6 | Leishmania infantum | 26% | 90% |
A4HUX7 | Leishmania infantum | 28% | 100% |
A4HUX8 | Leishmania infantum | 28% | 100% |
A4HV40 | Leishmania infantum | 22% | 100% |
A4HZF5 | Leishmania infantum | 50% | 100% |
A4HZJ4 | Leishmania infantum | 94% | 95% |
A4I4L2 | Leishmania infantum | 25% | 94% |
A4I7C5 | Leishmania infantum | 25% | 99% |
A4ICI3 | Leishmania infantum | 48% | 100% |
C9ZL97 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
C9ZL98 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
C9ZL99 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
C9ZLA0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
C9ZLA1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
C9ZTR5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
C9ZTR6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
C9ZTR7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
C9ZTR8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
C9ZTR9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
C9ZTS1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
C9ZUT6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
D0A7B1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 22% | 98% |
D0A7H1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
D0AAQ2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 92% |
E8NHE1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9AE01 | Leishmania major | 26% | 100% |
E9AE09 | Leishmania major | 25% | 100% |
E9AE10 | Leishmania major | 25% | 100% |
E9AE11 | Leishmania major | 27% | 100% |
E9AGK5 | Leishmania infantum | 26% | 100% |
E9AHJ0 | Leishmania infantum | 26% | 97% |
E9AHJ1 | Leishmania infantum | 25% | 100% |
E9ALS2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 97% |
E9ALS3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 94% |
E9ANL0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 98% |
E9ANL1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 96% |
E9ANL2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9ANS1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 22% | 99% |
E9APJ3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9AT53 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 47% | 100% |
E9AVF1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 50% | 100% |
E9AVF2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 95% |
E9B2B8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 99% |
Q4Q1E4 | Leishmania major | 48% | 99% |
Q4Q5T8 | Leishmania major | 24% | 100% |
Q4QC28 | Leishmania major | 49% | 100% |
Q4QFY5 | Leishmania major | 25% | 100% |
Q4QGU8 | Leishmania major | 23% | 100% |
Q4QH10 | Leishmania major | 26% | 100% |
Q4QH11 | Leishmania major | 27% | 100% |
Q4QH12 | Leishmania major | 27% | 100% |
Q4QH13 | Leishmania major | 27% | 100% |
Q4QH14 | Leishmania major | 27% | 96% |
Q4QH15 | Leishmania major | 26% | 100% |
V5B647 | Trypanosoma cruzi | 29% | 100% |
V5B983 | Trypanosoma cruzi | 28% | 100% |
V5BBB1 | Trypanosoma cruzi | 24% | 100% |
V5BFV8 | Trypanosoma cruzi | 26% | 94% |
V5BQY6 | Trypanosoma cruzi | 26% | 89% |
V5BVP0 | Trypanosoma cruzi | 27% | 100% |
V5DT25 | Trypanosoma cruzi | 27% | 100% |