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: 84 |
NetGPI | no | yes: 0, no: 84 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 77 |
GO:0110165 | cellular anatomical entity | 1 | 77 |
GO:0005737 | cytoplasm | 2 | 3 |
Related structures:
AlphaFold database: A4HV40
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 37 |
GO:0022857 | transmembrane transporter activity | 2 | 37 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 355 | 359 | PF00656 | 0.765 |
CLV_NRD_NRD_1 | 305 | 307 | PF00675 | 0.413 |
CLV_NRD_NRD_1 | 489 | 491 | PF00675 | 0.362 |
CLV_NRD_NRD_1 | 88 | 90 | PF00675 | 0.336 |
CLV_PCSK_KEX2_1 | 304 | 306 | PF00082 | 0.449 |
CLV_PCSK_KEX2_1 | 489 | 491 | PF00082 | 0.349 |
CLV_PCSK_PC7_1 | 485 | 491 | PF00082 | 0.383 |
CLV_PCSK_SKI1_1 | 157 | 161 | PF00082 | 0.308 |
CLV_PCSK_SKI1_1 | 360 | 364 | PF00082 | 0.569 |
CLV_PCSK_SKI1_1 | 517 | 521 | PF00082 | 0.530 |
CLV_PCSK_SKI1_1 | 621 | 625 | PF00082 | 0.364 |
DEG_SCF_FBW7_1 | 212 | 218 | PF00400 | 0.374 |
DEG_SCF_FBW7_2 | 294 | 301 | PF00400 | 0.488 |
DEG_SPOP_SBC_1 | 376 | 380 | PF00917 | 0.589 |
DEG_SPOP_SBC_1 | 544 | 548 | PF00917 | 0.431 |
DOC_CDC14_PxL_1 | 497 | 505 | PF14671 | 0.291 |
DOC_CKS1_1 | 212 | 217 | PF01111 | 0.572 |
DOC_CKS1_1 | 295 | 300 | PF01111 | 0.357 |
DOC_CYCLIN_yCln2_LP_2 | 329 | 332 | PF00134 | 0.726 |
DOC_CYCLIN_yCln2_LP_2 | 519 | 525 | PF00134 | 0.282 |
DOC_PP1_RVXF_1 | 515 | 521 | PF00149 | 0.238 |
DOC_PP1_RVXF_1 | 586 | 592 | PF00149 | 0.463 |
DOC_PP2B_LxvP_1 | 210 | 213 | PF13499 | 0.305 |
DOC_PP2B_LxvP_1 | 329 | 332 | PF13499 | 0.685 |
DOC_PP2B_LxvP_1 | 498 | 501 | PF13499 | 0.328 |
DOC_PP2B_LxvP_1 | 519 | 522 | PF13499 | 0.284 |
DOC_PP4_FxxP_1 | 240 | 243 | PF00568 | 0.454 |
DOC_PP4_FxxP_1 | 295 | 298 | PF00568 | 0.429 |
DOC_PP4_FxxP_1 | 79 | 82 | PF00568 | 0.329 |
DOC_USP7_MATH_1 | 215 | 219 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 452 | 456 | PF00917 | 0.428 |
DOC_USP7_MATH_1 | 612 | 616 | PF00917 | 0.383 |
DOC_WW_Pin1_4 | 211 | 216 | PF00397 | 0.577 |
DOC_WW_Pin1_4 | 294 | 299 | PF00397 | 0.352 |
DOC_WW_Pin1_4 | 48 | 53 | PF00397 | 0.259 |
DOC_WW_Pin1_4 | 561 | 566 | PF00397 | 0.310 |
LIG_14-3-3_CanoR_1 | 349 | 357 | PF00244 | 0.589 |
LIG_14-3-3_CanoR_1 | 453 | 459 | PF00244 | 0.407 |
LIG_14-3-3_CanoR_1 | 60 | 66 | PF00244 | 0.382 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.723 |
LIG_BIR_III_2 | 366 | 370 | PF00653 | 0.578 |
LIG_BIR_III_4 | 358 | 362 | PF00653 | 0.746 |
LIG_BRCT_BRCA1_1 | 134 | 138 | PF00533 | 0.325 |
LIG_BRCT_BRCA1_1 | 253 | 257 | PF00533 | 0.356 |
LIG_deltaCOP1_diTrp_1 | 24 | 31 | PF00928 | 0.455 |
LIG_deltaCOP1_diTrp_1 | 422 | 431 | PF00928 | 0.370 |
LIG_EH1_1 | 30 | 38 | PF00400 | 0.274 |
LIG_FHA_1 | 139 | 145 | PF00498 | 0.351 |
LIG_FHA_1 | 202 | 208 | PF00498 | 0.390 |
LIG_FHA_1 | 215 | 221 | PF00498 | 0.537 |
LIG_FHA_1 | 246 | 252 | PF00498 | 0.297 |
LIG_FHA_1 | 259 | 265 | PF00498 | 0.345 |
LIG_FHA_1 | 281 | 287 | PF00498 | 0.387 |
LIG_FHA_1 | 289 | 295 | PF00498 | 0.386 |
LIG_FHA_1 | 378 | 384 | PF00498 | 0.823 |
LIG_FHA_1 | 460 | 466 | PF00498 | 0.322 |
LIG_FHA_1 | 597 | 603 | PF00498 | 0.328 |
LIG_FHA_1 | 69 | 75 | PF00498 | 0.378 |
LIG_FHA_1 | 81 | 87 | PF00498 | 0.354 |
LIG_FHA_1 | 91 | 97 | PF00498 | 0.443 |
LIG_GBD_Chelix_1 | 123 | 131 | PF00786 | 0.383 |
LIG_GBD_Chelix_1 | 255 | 263 | PF00786 | 0.302 |
LIG_GBD_Chelix_1 | 470 | 478 | PF00786 | 0.196 |
LIG_LIR_Apic_2 | 265 | 270 | PF02991 | 0.342 |
LIG_LIR_Apic_2 | 77 | 82 | PF02991 | 0.332 |
LIG_LIR_Gen_1 | 197 | 205 | PF02991 | 0.352 |
LIG_LIR_Gen_1 | 254 | 264 | PF02991 | 0.378 |
LIG_LIR_Gen_1 | 289 | 298 | PF02991 | 0.323 |
LIG_LIR_Gen_1 | 445 | 456 | PF02991 | 0.327 |
LIG_LIR_Gen_1 | 462 | 471 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 150 | 154 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 164 | 168 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 182 | 188 | PF02991 | 0.255 |
LIG_LIR_Nem_3 | 197 | 201 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 254 | 260 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 445 | 451 | PF02991 | 0.320 |
LIG_LIR_Nem_3 | 462 | 467 | PF02991 | 0.337 |
LIG_LIR_Nem_3 | 48 | 53 | PF02991 | 0.311 |
LIG_LIR_Nem_3 | 615 | 620 | PF02991 | 0.352 |
LIG_LYPXL_S_1 | 482 | 486 | PF13949 | 0.226 |
LIG_LYPXL_yS_3 | 483 | 486 | PF13949 | 0.424 |
LIG_MAD2 | 476 | 484 | PF02301 | 0.200 |
LIG_MYND_1 | 388 | 392 | PF01753 | 0.593 |
LIG_Pex14_1 | 107 | 111 | PF04695 | 0.311 |
LIG_Pex14_1 | 27 | 31 | PF04695 | 0.469 |
LIG_Pex14_1 | 424 | 428 | PF04695 | 0.353 |
LIG_Pex14_2 | 181 | 185 | PF04695 | 0.276 |
LIG_Pex14_2 | 240 | 244 | PF04695 | 0.493 |
LIG_Pex14_2 | 253 | 257 | PF04695 | 0.351 |
LIG_Pex14_2 | 520 | 524 | PF04695 | 0.352 |
LIG_REV1ctd_RIR_1 | 178 | 187 | PF16727 | 0.366 |
LIG_RPA_C_Fungi | 485 | 497 | PF08784 | 0.236 |
LIG_SH2_CRK | 448 | 452 | PF00017 | 0.385 |
LIG_SH2_CRK | 554 | 558 | PF00017 | 0.256 |
LIG_SH2_CRK | 620 | 624 | PF00017 | 0.366 |
LIG_SH2_PTP2 | 267 | 270 | PF00017 | 0.373 |
LIG_SH2_SRC | 267 | 270 | PF00017 | 0.441 |
LIG_SH2_STAP1 | 198 | 202 | PF00017 | 0.277 |
LIG_SH2_STAP1 | 554 | 558 | PF00017 | 0.304 |
LIG_SH2_STAT5 | 111 | 114 | PF00017 | 0.350 |
LIG_SH2_STAT5 | 177 | 180 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 209 | 212 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 21 | 24 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 267 | 270 | PF00017 | 0.358 |
LIG_SH2_STAT5 | 558 | 561 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 78 | 81 | PF00017 | 0.327 |
LIG_SH3_3 | 325 | 331 | PF00018 | 0.665 |
LIG_SH3_3 | 382 | 388 | PF00018 | 0.613 |
LIG_SH3_3 | 389 | 395 | PF00018 | 0.599 |
LIG_SUMO_SIM_par_1 | 536 | 543 | PF11976 | 0.260 |
LIG_SUMO_SIM_par_1 | 93 | 100 | PF11976 | 0.361 |
LIG_TYR_ITIM | 207 | 212 | PF00017 | 0.404 |
LIG_UBA3_1 | 144 | 149 | PF00899 | 0.259 |
LIG_WRC_WIRS_1 | 148 | 153 | PF05994 | 0.409 |
MOD_CDK_SPxxK_3 | 48 | 55 | PF00069 | 0.310 |
MOD_CK1_1 | 132 | 138 | PF00069 | 0.328 |
MOD_CK1_1 | 143 | 149 | PF00069 | 0.367 |
MOD_CK1_1 | 377 | 383 | PF00069 | 0.685 |
MOD_CK1_1 | 435 | 441 | PF00069 | 0.321 |
MOD_CK1_1 | 442 | 448 | PF00069 | 0.372 |
MOD_CK1_1 | 48 | 54 | PF00069 | 0.341 |
MOD_CK1_1 | 533 | 539 | PF00069 | 0.317 |
MOD_CK1_1 | 543 | 549 | PF00069 | 0.398 |
MOD_CK1_1 | 77 | 83 | PF00069 | 0.336 |
MOD_CK2_1 | 134 | 140 | PF00069 | 0.333 |
MOD_CK2_1 | 259 | 265 | PF00069 | 0.295 |
MOD_CK2_1 | 59 | 65 | PF00069 | 0.393 |
MOD_CMANNOS | 424 | 427 | PF00535 | 0.377 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.367 |
MOD_GlcNHglycan | 134 | 137 | PF01048 | 0.352 |
MOD_GlcNHglycan | 185 | 188 | PF01048 | 0.300 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.330 |
MOD_GlcNHglycan | 325 | 328 | PF01048 | 0.733 |
MOD_GlcNHglycan | 350 | 353 | PF01048 | 0.715 |
MOD_GlcNHglycan | 434 | 437 | PF01048 | 0.288 |
MOD_GlcNHglycan | 471 | 474 | PF01048 | 0.345 |
MOD_GlcNHglycan | 614 | 617 | PF01048 | 0.378 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.372 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.359 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.339 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.276 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.725 |
MOD_GSK3_1 | 435 | 442 | PF00069 | 0.358 |
MOD_GSK3_1 | 452 | 459 | PF00069 | 0.457 |
MOD_GSK3_1 | 530 | 537 | PF00069 | 0.352 |
MOD_GSK3_1 | 539 | 546 | PF00069 | 0.393 |
MOD_GSK3_1 | 552 | 559 | PF00069 | 0.337 |
MOD_N-GLC_1 | 102 | 107 | PF02516 | 0.424 |
MOD_N-GLC_1 | 442 | 447 | PF02516 | 0.419 |
MOD_NEK2_1 | 118 | 123 | PF00069 | 0.297 |
MOD_NEK2_1 | 134 | 139 | PF00069 | 0.337 |
MOD_NEK2_1 | 168 | 173 | PF00069 | 0.367 |
MOD_NEK2_1 | 181 | 186 | PF00069 | 0.354 |
MOD_NEK2_1 | 194 | 199 | PF00069 | 0.316 |
MOD_NEK2_1 | 201 | 206 | PF00069 | 0.321 |
MOD_NEK2_1 | 251 | 256 | PF00069 | 0.368 |
MOD_NEK2_1 | 259 | 264 | PF00069 | 0.336 |
MOD_NEK2_1 | 286 | 291 | PF00069 | 0.375 |
MOD_NEK2_1 | 293 | 298 | PF00069 | 0.432 |
MOD_NEK2_1 | 323 | 328 | PF00069 | 0.703 |
MOD_NEK2_1 | 45 | 50 | PF00069 | 0.354 |
MOD_NEK2_1 | 456 | 461 | PF00069 | 0.390 |
MOD_NEK2_1 | 539 | 544 | PF00069 | 0.380 |
MOD_NEK2_1 | 545 | 550 | PF00069 | 0.429 |
MOD_NEK2_1 | 556 | 561 | PF00069 | 0.358 |
MOD_NEK2_1 | 59 | 64 | PF00069 | 0.345 |
MOD_NEK2_1 | 97 | 102 | PF00069 | 0.284 |
MOD_PIKK_1 | 129 | 135 | PF00454 | 0.295 |
MOD_PIKK_1 | 399 | 405 | PF00454 | 0.737 |
MOD_PIKK_1 | 59 | 65 | PF00454 | 0.324 |
MOD_PKA_2 | 348 | 354 | PF00069 | 0.717 |
MOD_PKA_2 | 452 | 458 | PF00069 | 0.501 |
MOD_PKA_2 | 59 | 65 | PF00069 | 0.417 |
MOD_Plk_1 | 181 | 187 | PF00069 | 0.350 |
MOD_Plk_1 | 19 | 25 | PF00069 | 0.539 |
MOD_Plk_1 | 442 | 448 | PF00069 | 0.382 |
MOD_Plk_4 | 134 | 140 | PF00069 | 0.336 |
MOD_Plk_4 | 161 | 167 | PF00069 | 0.342 |
MOD_Plk_4 | 168 | 174 | PF00069 | 0.368 |
MOD_Plk_4 | 246 | 252 | PF00069 | 0.347 |
MOD_Plk_4 | 259 | 265 | PF00069 | 0.342 |
MOD_Plk_4 | 435 | 441 | PF00069 | 0.339 |
MOD_Plk_4 | 459 | 465 | PF00069 | 0.318 |
MOD_Plk_4 | 534 | 540 | PF00069 | 0.315 |
MOD_Plk_4 | 552 | 558 | PF00069 | 0.384 |
MOD_Plk_4 | 74 | 80 | PF00069 | 0.372 |
MOD_Plk_4 | 92 | 98 | PF00069 | 0.317 |
MOD_ProDKin_1 | 211 | 217 | PF00069 | 0.462 |
MOD_ProDKin_1 | 294 | 300 | PF00069 | 0.353 |
MOD_ProDKin_1 | 48 | 54 | PF00069 | 0.296 |
MOD_ProDKin_1 | 561 | 567 | PF00069 | 0.310 |
MOD_SUMO_for_1 | 54 | 57 | PF00179 | 0.200 |
TRG_DiLeu_BaLyEn_6 | 498 | 503 | PF01217 | 0.238 |
TRG_DiLeu_BaLyEn_6 | 598 | 603 | PF01217 | 0.382 |
TRG_ENDOCYTIC_2 | 111 | 114 | PF00928 | 0.397 |
TRG_ENDOCYTIC_2 | 177 | 180 | PF00928 | 0.333 |
TRG_ENDOCYTIC_2 | 198 | 201 | PF00928 | 0.338 |
TRG_ENDOCYTIC_2 | 209 | 212 | PF00928 | 0.345 |
TRG_ENDOCYTIC_2 | 448 | 451 | PF00928 | 0.369 |
TRG_ENDOCYTIC_2 | 483 | 486 | PF00928 | 0.355 |
TRG_ENDOCYTIC_2 | 554 | 557 | PF00928 | 0.319 |
TRG_ENDOCYTIC_2 | 61 | 64 | PF00928 | 0.368 |
TRG_ENDOCYTIC_2 | 620 | 623 | PF00928 | 0.380 |
TRG_ENDOCYTIC_2 | 78 | 81 | PF00928 | 0.317 |
TRG_ER_diArg_1 | 304 | 306 | PF00400 | 0.609 |
TRG_ER_diArg_1 | 489 | 491 | PF00400 | 0.401 |
TRG_Pf-PMV_PEXEL_1 | 412 | 416 | PF00026 | 0.297 |
TRG_PTS1 | 624 | 627 | PF00515 | 0.287 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6G0 | Leptomonas seymouri | 23% | 99% |
A0A0N1HZC2 | Leptomonas seymouri | 27% | 100% |
A0A0N1IKC5 | Leptomonas seymouri | 24% | 100% |
A0A0N1PB63 | Leptomonas seymouri | 23% | 95% |
A0A0N1PD04 | Leptomonas seymouri | 63% | 98% |
A0A0N1PFR4 | Leptomonas seymouri | 25% | 95% |
A0A1X0NKK0 | Trypanosomatidae | 24% | 100% |
A0A1X0NM09 | Trypanosomatidae | 25% | 100% |
A0A1X0NRW5 | Trypanosomatidae | 24% | 90% |
A0A1X0NVF9 | Trypanosomatidae | 46% | 94% |
A0A1X0NVM7 | Trypanosomatidae | 24% | 97% |
A0A1X0NZU2 | Trypanosomatidae | 26% | 97% |
A0A1X0NZU5 | Trypanosomatidae | 24% | 100% |
A0A381MMW5 | Leishmania infantum | 24% | 100% |
A0A3Q8IEC4 | Leishmania donovani | 25% | 97% |
A0A3Q8IF95 | Leishmania donovani | 21% | 99% |
A0A3Q8IIT5 | Leishmania donovani | 25% | 93% |
A0A3Q8ISY9 | Leishmania donovani | 23% | 99% |
A0A3R7KKN8 | Trypanosoma rangeli | 25% | 100% |
A0A3R7MAQ7 | Trypanosoma rangeli | 22% | 89% |
A0A3R7N3S6 | Trypanosoma rangeli | 48% | 97% |
A0A3R7N415 | Trypanosoma rangeli | 25% | 100% |
A0A3R7R443 | Trypanosoma rangeli | 24% | 100% |
A0A3S7WRJ4 | Leishmania donovani | 24% | 98% |
A0A3S7WRJ5 | Leishmania donovani | 25% | 90% |
A0A3S7WRS3 | Leishmania donovani | 100% | 100% |
A0A3S7WSR4 | Leishmania donovani | 23% | 100% |
A0A3S7WWU1 | Leishmania donovani | 22% | 94% |
A0A3S7X2G0 | Leishmania donovani | 25% | 96% |
A0A3S7X2K5 | Leishmania donovani | 25% | 100% |
A0A3S7XB11 | Leishmania donovani | 26% | 100% |
A0A422MSP6 | Trypanosoma rangeli | 21% | 100% |
A0A422MU68 | Trypanosoma rangeli | 25% | 100% |
A4H6J0 | Leishmania braziliensis | 25% | 100% |
A4H6J1 | Leishmania braziliensis | 25% | 100% |
A4H6Q5 | Leishmania braziliensis | 71% | 100% |
A4HC19 | Leishmania braziliensis | 22% | 100% |
A4HHG2 | Leishmania braziliensis | 25% | 100% |
A4HHG3 | Leishmania braziliensis | 25% | 100% |
A4HHG4 | Leishmania braziliensis | 26% | 100% |
A4HJW3 | Leishmania braziliensis | 24% | 100% |
A4HPE2 | Leishmania braziliensis | 26% | 100% |
A4HUX5 | Leishmania infantum | 24% | 100% |
A4HUX6 | Leishmania infantum | 24% | 100% |
A4HZF5 | Leishmania infantum | 21% | 99% |
A4HZJ4 | Leishmania infantum | 22% | 94% |
A4I4L2 | Leishmania infantum | 25% | 93% |
A4I7C5 | Leishmania infantum | 23% | 99% |
A4ICI3 | Leishmania infantum | 26% | 100% |
C9ZTS1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
C9ZUT6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 23% | 100% |
D0A7B1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 98% |
E8NHE1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
E9AE01 | Leishmania major | 24% | 100% |
E9AE09 | Leishmania major | 25% | 100% |
E9AE10 | Leishmania major | 25% | 100% |
E9AE11 | Leishmania major | 25% | 100% |
E9AGK5 | Leishmania infantum | 23% | 100% |
E9AHJ0 | Leishmania infantum | 25% | 97% |
E9AHJ1 | Leishmania infantum | 25% | 100% |
E9ALS2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 97% |
E9ALS3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
E9ANL0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
E9ANL1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
E9ANS1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
E9APJ3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9AT53 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 98% |
E9AVF1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 21% | 100% |
E9AVF2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 22% | 100% |
E9B2B8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
Q4Q1E4 | Leishmania major | 26% | 99% |
Q4Q5T8 | Leishmania major | 23% | 100% |
Q4QC27 | Leishmania major | 22% | 100% |
Q4QC28 | Leishmania major | 23% | 100% |
Q4QFY5 | Leishmania major | 24% | 100% |
Q4QGU8 | Leishmania major | 90% | 100% |
Q4QH14 | Leishmania major | 25% | 100% |
Q4QH15 | Leishmania major | 24% | 100% |
V5B647 | Trypanosoma cruzi | 22% | 99% |
V5BFV8 | Trypanosoma cruzi | 23% | 94% |
V5BQY6 | Trypanosoma cruzi | 24% | 89% |
V5BVP0 | Trypanosoma cruzi | 24% | 100% |
V5DT25 | Trypanosoma cruzi | 23% | 100% |