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: 114 |
NetGPI | no | yes: 0, no: 114 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 3 |
GO:0016020 | membrane | 2 | 107 |
GO:0110165 | cellular anatomical entity | 1 | 107 |
Related structures:
AlphaFold database: E9AHJ1
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 51 |
GO:0022857 | transmembrane transporter activity | 2 | 51 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 146 | 148 | PF00675 | 0.354 |
CLV_NRD_NRD_1 | 547 | 549 | PF00675 | 0.344 |
CLV_NRD_NRD_1 | 566 | 568 | PF00675 | 0.374 |
CLV_NRD_NRD_1 | 97 | 99 | PF00675 | 0.567 |
CLV_PCSK_FUR_1 | 545 | 549 | PF00082 | 0.433 |
CLV_PCSK_KEX2_1 | 145 | 147 | PF00082 | 0.342 |
CLV_PCSK_KEX2_1 | 246 | 248 | PF00082 | 0.566 |
CLV_PCSK_KEX2_1 | 329 | 331 | PF00082 | 0.340 |
CLV_PCSK_KEX2_1 | 547 | 549 | PF00082 | 0.346 |
CLV_PCSK_KEX2_1 | 566 | 568 | PF00082 | 0.366 |
CLV_PCSK_PC1ET2_1 | 246 | 248 | PF00082 | 0.385 |
CLV_PCSK_PC1ET2_1 | 329 | 331 | PF00082 | 0.380 |
CLV_PCSK_SKI1_1 | 146 | 150 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 246 | 250 | PF00082 | 0.577 |
CLV_PCSK_SKI1_1 | 458 | 462 | PF00082 | 0.282 |
CLV_PCSK_SKI1_1 | 494 | 498 | PF00082 | 0.561 |
CLV_PCSK_SKI1_1 | 548 | 552 | PF00082 | 0.355 |
CLV_PCSK_SKI1_1 | 79 | 83 | PF00082 | 0.374 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.542 |
DOC_CYCLIN_RxL_1 | 455 | 464 | PF00134 | 0.388 |
DOC_MAPK_DCC_7 | 35 | 43 | PF00069 | 0.181 |
DOC_MAPK_gen_1 | 135 | 144 | PF00069 | 0.573 |
DOC_MAPK_gen_1 | 329 | 335 | PF00069 | 0.492 |
DOC_MAPK_MEF2A_6 | 194 | 203 | PF00069 | 0.293 |
DOC_MAPK_MEF2A_6 | 35 | 43 | PF00069 | 0.317 |
DOC_PP2B_LxvP_1 | 426 | 429 | PF13499 | 0.404 |
DOC_PP2B_PxIxI_1 | 404 | 410 | PF00149 | 0.388 |
DOC_USP7_MATH_1 | 187 | 191 | PF00917 | 0.387 |
DOC_USP7_MATH_1 | 351 | 355 | PF00917 | 0.509 |
DOC_USP7_MATH_1 | 412 | 416 | PF00917 | 0.381 |
DOC_USP7_MATH_1 | 429 | 433 | PF00917 | 0.367 |
DOC_USP7_UBL2_3 | 223 | 227 | PF12436 | 0.733 |
DOC_USP7_UBL2_3 | 277 | 281 | PF12436 | 0.599 |
DOC_USP7_UBL2_3 | 365 | 369 | PF12436 | 0.261 |
DOC_USP7_UBL2_3 | 463 | 467 | PF12436 | 0.492 |
DOC_WW_Pin1_4 | 506 | 511 | PF00397 | 0.443 |
LIG_14-3-3_CanoR_1 | 145 | 154 | PF00244 | 0.572 |
LIG_14-3-3_CanoR_1 | 194 | 200 | PF00244 | 0.344 |
LIG_14-3-3_CanoR_1 | 310 | 320 | PF00244 | 0.645 |
LIG_14-3-3_CanoR_1 | 386 | 390 | PF00244 | 0.289 |
LIG_14-3-3_CanoR_1 | 98 | 106 | PF00244 | 0.359 |
LIG_AP2alpha_1 | 440 | 444 | PF02296 | 0.198 |
LIG_deltaCOP1_diTrp_1 | 332 | 338 | PF00928 | 0.504 |
LIG_EH1_1 | 105 | 113 | PF00400 | 0.444 |
LIG_FHA_1 | 115 | 121 | PF00498 | 0.385 |
LIG_FHA_1 | 196 | 202 | PF00498 | 0.352 |
LIG_FHA_1 | 38 | 44 | PF00498 | 0.318 |
LIG_FHA_1 | 401 | 407 | PF00498 | 0.581 |
LIG_FHA_1 | 532 | 538 | PF00498 | 0.397 |
LIG_FHA_1 | 55 | 61 | PF00498 | 0.318 |
LIG_FHA_2 | 250 | 256 | PF00498 | 0.722 |
LIG_GBD_Chelix_1 | 202 | 210 | PF00786 | 0.348 |
LIG_LIR_Apic_2 | 4 | 8 | PF02991 | 0.494 |
LIG_LIR_Gen_1 | 101 | 112 | PF02991 | 0.298 |
LIG_LIR_Gen_1 | 175 | 184 | PF02991 | 0.357 |
LIG_LIR_Gen_1 | 322 | 333 | PF02991 | 0.507 |
LIG_LIR_Gen_1 | 372 | 381 | PF02991 | 0.311 |
LIG_LIR_Gen_1 | 539 | 549 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 101 | 107 | PF02991 | 0.267 |
LIG_LIR_Nem_3 | 161 | 167 | PF02991 | 0.512 |
LIG_LIR_Nem_3 | 175 | 179 | PF02991 | 0.309 |
LIG_LIR_Nem_3 | 322 | 328 | PF02991 | 0.516 |
LIG_LIR_Nem_3 | 372 | 377 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 539 | 544 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 80 | 84 | PF02991 | 0.350 |
LIG_LYPXL_yS_3 | 157 | 160 | PF13949 | 0.440 |
LIG_NRBOX | 421 | 427 | PF00104 | 0.401 |
LIG_Pex14_2 | 163 | 167 | PF04695 | 0.335 |
LIG_Pex14_2 | 440 | 444 | PF04695 | 0.350 |
LIG_PTB_Apo_2 | 360 | 367 | PF02174 | 0.338 |
LIG_PTB_Apo_2 | 90 | 97 | PF02174 | 0.313 |
LIG_PTB_Phospho_1 | 360 | 366 | PF10480 | 0.389 |
LIG_REV1ctd_RIR_1 | 94 | 103 | PF16727 | 0.287 |
LIG_SH2_CRK | 186 | 190 | PF00017 | 0.395 |
LIG_SH2_CRK | 26 | 30 | PF00017 | 0.274 |
LIG_SH2_CRK | 358 | 362 | PF00017 | 0.300 |
LIG_SH2_CRK | 374 | 378 | PF00017 | 0.367 |
LIG_SH2_CRK | 5 | 9 | PF00017 | 0.485 |
LIG_SH2_GRB2like | 186 | 189 | PF00017 | 0.434 |
LIG_SH2_NCK_1 | 186 | 190 | PF00017 | 0.395 |
LIG_SH2_SRC | 186 | 189 | PF00017 | 0.442 |
LIG_SH2_STAP1 | 374 | 378 | PF00017 | 0.362 |
LIG_SH2_STAP1 | 492 | 496 | PF00017 | 0.304 |
LIG_SH2_STAT3 | 153 | 156 | PF00017 | 0.523 |
LIG_SH2_STAT3 | 492 | 495 | PF00017 | 0.357 |
LIG_SH2_STAT5 | 153 | 156 | PF00017 | 0.536 |
LIG_SH2_STAT5 | 164 | 167 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 176 | 179 | PF00017 | 0.313 |
LIG_SH2_STAT5 | 267 | 270 | PF00017 | 0.537 |
LIG_SH2_STAT5 | 473 | 476 | PF00017 | 0.379 |
LIG_SH3_1 | 227 | 233 | PF00018 | 0.701 |
LIG_SH3_3 | 227 | 233 | PF00018 | 0.685 |
LIG_SH3_3 | 245 | 251 | PF00018 | 0.774 |
LIG_SH3_3 | 507 | 513 | PF00018 | 0.360 |
LIG_SUMO_SIM_anti_2 | 117 | 122 | PF11976 | 0.383 |
LIG_SUMO_SIM_anti_2 | 198 | 204 | PF11976 | 0.306 |
LIG_SUMO_SIM_anti_2 | 87 | 93 | PF11976 | 0.438 |
LIG_SUMO_SIM_par_1 | 169 | 175 | PF11976 | 0.297 |
LIG_SUMO_SIM_par_1 | 375 | 382 | PF11976 | 0.333 |
LIG_TRAF2_1 | 252 | 255 | PF00917 | 0.718 |
LIG_TYR_ITIM | 174 | 179 | PF00017 | 0.351 |
LIG_TYR_ITIM | 24 | 29 | PF00017 | 0.287 |
LIG_TYR_ITSM | 370 | 377 | PF00017 | 0.347 |
LIG_UBA3_1 | 425 | 433 | PF00899 | 0.386 |
LIG_WRC_WIRS_1 | 179 | 184 | PF05994 | 0.383 |
LIG_WRC_WIRS_1 | 237 | 242 | PF05994 | 0.462 |
LIG_WRC_WIRS_1 | 441 | 446 | PF05994 | 0.396 |
LIG_WRC_WIRS_1 | 78 | 83 | PF05994 | 0.378 |
MOD_CK1_1 | 283 | 289 | PF00069 | 0.668 |
MOD_CK1_1 | 379 | 385 | PF00069 | 0.344 |
MOD_CK1_1 | 54 | 60 | PF00069 | 0.354 |
MOD_CK2_1 | 249 | 255 | PF00069 | 0.712 |
MOD_CK2_1 | 282 | 288 | PF00069 | 0.697 |
MOD_CMANNOS | 334 | 337 | PF00535 | 0.360 |
MOD_Cter_Amidation | 278 | 281 | PF01082 | 0.510 |
MOD_Cter_Amidation | 516 | 519 | PF01082 | 0.469 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.474 |
MOD_GlcNHglycan | 353 | 356 | PF01048 | 0.374 |
MOD_GlcNHglycan | 374 | 377 | PF01048 | 0.327 |
MOD_GlcNHglycan | 381 | 384 | PF01048 | 0.318 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.380 |
MOD_GSK3_1 | 279 | 286 | PF00069 | 0.708 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.443 |
MOD_GSK3_1 | 372 | 379 | PF00069 | 0.367 |
MOD_GSK3_1 | 446 | 453 | PF00069 | 0.355 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.350 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.326 |
MOD_N-GLC_1 | 531 | 536 | PF02516 | 0.294 |
MOD_N-GLC_1 | 92 | 97 | PF02516 | 0.349 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.271 |
MOD_NEK2_1 | 195 | 200 | PF00069 | 0.283 |
MOD_NEK2_1 | 324 | 329 | PF00069 | 0.390 |
MOD_NEK2_1 | 440 | 445 | PF00069 | 0.355 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.341 |
MOD_NEK2_1 | 84 | 89 | PF00069 | 0.381 |
MOD_PIKK_1 | 152 | 158 | PF00454 | 0.450 |
MOD_PKA_1 | 146 | 152 | PF00069 | 0.535 |
MOD_PKA_1 | 280 | 286 | PF00069 | 0.480 |
MOD_PKA_2 | 146 | 152 | PF00069 | 0.447 |
MOD_PKA_2 | 385 | 391 | PF00069 | 0.312 |
MOD_PKA_2 | 97 | 103 | PF00069 | 0.428 |
MOD_Plk_1 | 133 | 139 | PF00069 | 0.435 |
MOD_Plk_1 | 531 | 537 | PF00069 | 0.311 |
MOD_Plk_1 | 92 | 98 | PF00069 | 0.383 |
MOD_Plk_2-3 | 236 | 242 | PF00069 | 0.674 |
MOD_Plk_4 | 13 | 19 | PF00069 | 0.291 |
MOD_Plk_4 | 172 | 178 | PF00069 | 0.327 |
MOD_Plk_4 | 195 | 201 | PF00069 | 0.368 |
MOD_Plk_4 | 320 | 326 | PF00069 | 0.413 |
MOD_Plk_4 | 369 | 375 | PF00069 | 0.288 |
MOD_Plk_4 | 537 | 543 | PF00069 | 0.277 |
MOD_Plk_4 | 56 | 62 | PF00069 | 0.328 |
MOD_Plk_4 | 84 | 90 | PF00069 | 0.372 |
MOD_Plk_4 | 92 | 98 | PF00069 | 0.379 |
MOD_ProDKin_1 | 506 | 512 | PF00069 | 0.559 |
MOD_SUMO_rev_2 | 239 | 248 | PF00179 | 0.668 |
MOD_SUMO_rev_2 | 304 | 309 | PF00179 | 0.586 |
MOD_SUMO_rev_2 | 362 | 370 | PF00179 | 0.472 |
TRG_DiLeu_BaLyEn_6 | 7 | 12 | PF01217 | 0.402 |
TRG_ENDOCYTIC_2 | 104 | 107 | PF00928 | 0.280 |
TRG_ENDOCYTIC_2 | 128 | 131 | PF00928 | 0.356 |
TRG_ENDOCYTIC_2 | 157 | 160 | PF00928 | 0.464 |
TRG_ENDOCYTIC_2 | 164 | 167 | PF00928 | 0.355 |
TRG_ENDOCYTIC_2 | 176 | 179 | PF00928 | 0.292 |
TRG_ENDOCYTIC_2 | 26 | 29 | PF00928 | 0.397 |
TRG_ENDOCYTIC_2 | 358 | 361 | PF00928 | 0.361 |
TRG_ENDOCYTIC_2 | 374 | 377 | PF00928 | 0.307 |
TRG_ENDOCYTIC_2 | 469 | 472 | PF00928 | 0.322 |
TRG_ENDOCYTIC_2 | 488 | 491 | PF00928 | 0.425 |
TRG_ENDOCYTIC_2 | 546 | 549 | PF00928 | 0.395 |
TRG_ENDOCYTIC_2 | 94 | 97 | PF00928 | 0.342 |
TRG_ER_diArg_1 | 144 | 147 | PF00400 | 0.473 |
TRG_ER_diArg_1 | 546 | 548 | PF00400 | 0.435 |
TRG_ER_diArg_1 | 566 | 568 | PF00400 | 0.445 |
TRG_Pf-PMV_PEXEL_1 | 146 | 150 | PF00026 | 0.507 |
TRG_Pf-PMV_PEXEL_1 | 566 | 570 | PF00026 | 0.488 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6G0 | Leptomonas seymouri | 28% | 92% |
A0A0N1HZC2 | Leptomonas seymouri | 30% | 93% |
A0A0N1IKC5 | Leptomonas seymouri | 31% | 96% |
A0A0N1PAX2 | Leptomonas seymouri | 25% | 100% |
A0A0N1PB63 | Leptomonas seymouri | 26% | 89% |
A0A0N1PD04 | Leptomonas seymouri | 25% | 91% |
A0A0N1PFR4 | Leptomonas seymouri | 33% | 89% |
A0A1X0NKK0 | Trypanosomatidae | 30% | 97% |
A0A1X0NM09 | Trypanosomatidae | 29% | 96% |
A0A1X0NRW5 | Trypanosomatidae | 26% | 84% |
A0A1X0NV13 | Trypanosomatidae | 31% | 90% |
A0A1X0NV19 | Trypanosomatidae | 33% | 98% |
A0A1X0NV27 | Trypanosomatidae | 32% | 98% |
A0A1X0NVF9 | Trypanosomatidae | 23% | 88% |
A0A1X0NVH8 | Trypanosomatidae | 29% | 89% |
A0A1X0NVM7 | Trypanosomatidae | 29% | 91% |
A0A1X0NWQ1 | Trypanosomatidae | 33% | 91% |
A0A1X0NZE6 | Trypanosomatidae | 29% | 98% |
A0A1X0NZU2 | Trypanosomatidae | 32% | 91% |
A0A1X0NZU5 | Trypanosomatidae | 54% | 100% |
A0A1X0NZW1 | Trypanosomatidae | 31% | 97% |
A0A1X0P0M7 | Trypanosomatidae | 28% | 99% |
A0A381MMW5 | Leishmania infantum | 98% | 100% |
A0A3Q8IEC4 | Leishmania donovani | 97% | 90% |
A0A3Q8IF95 | Leishmania donovani | 27% | 93% |
A0A3Q8IIT5 | Leishmania donovani | 31% | 87% |
A0A3Q8ISY9 | Leishmania donovani | 26% | 92% |
A0A3R7JPZ0 | Trypanosoma rangeli | 28% | 100% |
A0A3R7JSQ9 | Trypanosoma rangeli | 29% | 100% |
A0A3R7KKN8 | Trypanosoma rangeli | 32% | 98% |
A0A3R7MAQ7 | Trypanosoma rangeli | 26% | 83% |
A0A3R7N3S6 | Trypanosoma rangeli | 25% | 91% |
A0A3R7N415 | Trypanosoma rangeli | 31% | 98% |
A0A3R7N921 | Trypanosoma rangeli | 27% | 100% |
A0A3R7R443 | Trypanosoma rangeli | 31% | 98% |
A0A3R7R6N6 | Trypanosoma rangeli | 28% | 100% |
A0A3S7WRJ4 | Leishmania donovani | 30% | 91% |
A0A3S7WRJ5 | Leishmania donovani | 32% | 84% |
A0A3S7WRS3 | Leishmania donovani | 25% | 93% |
A0A3S7WSR4 | Leishmania donovani | 30% | 97% |
A0A3S7WWU1 | Leishmania donovani | 26% | 88% |
A0A3S7X2G0 | Leishmania donovani | 97% | 89% |
A0A3S7X2K5 | Leishmania donovani | 100% | 100% |
A0A3S7XB11 | Leishmania donovani | 30% | 97% |
A0A422MSE4 | Trypanosoma rangeli | 32% | 100% |
A0A422MSP6 | Trypanosoma rangeli | 48% | 100% |
A0A422MST9 | Trypanosoma rangeli | 29% | 98% |
A0A422MU68 | Trypanosoma rangeli | 29% | 100% |
A4H6J0 | Leishmania braziliensis | 30% | 100% |
A4H6J1 | Leishmania braziliensis | 32% | 100% |
A4H6Q5 | Leishmania braziliensis | 27% | 100% |
A4HC19 | Leishmania braziliensis | 27% | 100% |
A4HHG2 | Leishmania braziliensis | 30% | 100% |
A4HHG3 | Leishmania braziliensis | 80% | 100% |
A4HHG4 | Leishmania braziliensis | 76% | 100% |
A4HJW3 | Leishmania braziliensis | 27% | 100% |
A4HPE2 | Leishmania braziliensis | 29% | 100% |
A4HUX5 | Leishmania infantum | 30% | 100% |
A4HUX6 | Leishmania infantum | 32% | 100% |
A4HV40 | Leishmania infantum | 25% | 100% |
A4HZF5 | Leishmania infantum | 28% | 100% |
A4HZJ4 | Leishmania infantum | 26% | 100% |
A4I4L2 | Leishmania infantum | 31% | 100% |
A4I7C5 | Leishmania infantum | 27% | 100% |
A4ICI3 | Leishmania infantum | 29% | 100% |
C9ZL97 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 98% |
C9ZL98 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
C9ZL99 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 98% |
C9ZLA0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
C9ZLA1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 98% |
C9ZTR5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 98% |
C9ZTR6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 97% |
C9ZTR7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
C9ZTR8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 98% |
C9ZTR9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
C9ZTS1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 98% |
C9ZUT6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 99% |
D0A7B1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 91% |
D0A7H1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
D0AAQ2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 86% |
E8NHE1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
E9AE01 | Leishmania major | 90% | 100% |
E9AE09 | Leishmania major | 30% | 100% |
E9AE10 | Leishmania major | 30% | 100% |
E9AE11 | Leishmania major | 94% | 100% |
E9AGK5 | Leishmania infantum | 30% | 100% |
E9AHJ0 | Leishmania infantum | 97% | 100% |
E9ALS2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
E9ALS3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9ANL0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9ANL1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
E9ANS1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
E9APJ3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9AT53 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9AVF1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9AVF2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9B2B8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
Q4Q1E4 | Leishmania major | 29% | 100% |
Q4Q5T8 | Leishmania major | 27% | 100% |
Q4QC27 | Leishmania major | 25% | 100% |
Q4QC28 | Leishmania major | 26% | 100% |
Q4QFY5 | Leishmania major | 30% | 100% |
Q4QGU8 | Leishmania major | 26% | 100% |
Q4QH14 | Leishmania major | 31% | 100% |
Q4QH15 | Leishmania major | 30% | 100% |
V5B647 | Trypanosoma cruzi | 31% | 93% |
V5B983 | Trypanosoma cruzi | 46% | 100% |
V5BBB1 | Trypanosoma cruzi | 29% | 99% |
V5BFV8 | Trypanosoma cruzi | 31% | 87% |
V5BQY6 | Trypanosoma cruzi | 29% | 83% |
V5BVP0 | Trypanosoma cruzi | 29% | 99% |
V5BWJ7 | Trypanosoma cruzi | 22% | 100% |
V5DT25 | Trypanosoma cruzi | 30% | 95% |