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: 107 |
NetGPI | no | yes: 0, no: 107 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 101 |
GO:0110165 | cellular anatomical entity | 1 | 101 |
GO:0005737 | cytoplasm | 2 | 3 |
Related structures:
AlphaFold database: E9ALS2
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 50 |
GO:0022857 | transmembrane transporter activity | 2 | 50 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 167 | 169 | PF00675 | 0.566 |
CLV_NRD_NRD_1 | 216 | 218 | PF00675 | 0.253 |
CLV_NRD_NRD_1 | 437 | 439 | PF00675 | 0.656 |
CLV_NRD_NRD_1 | 617 | 619 | PF00675 | 0.354 |
CLV_PCSK_FUR_1 | 615 | 619 | PF00082 | 0.436 |
CLV_PCSK_KEX2_1 | 215 | 217 | PF00082 | 0.247 |
CLV_PCSK_KEX2_1 | 316 | 318 | PF00082 | 0.334 |
CLV_PCSK_KEX2_1 | 617 | 619 | PF00082 | 0.350 |
CLV_PCSK_PC1ET2_1 | 316 | 318 | PF00082 | 0.333 |
CLV_PCSK_SKI1_1 | 149 | 153 | PF00082 | 0.365 |
CLV_PCSK_SKI1_1 | 216 | 220 | PF00082 | 0.342 |
CLV_PCSK_SKI1_1 | 316 | 320 | PF00082 | 0.540 |
CLV_PCSK_SKI1_1 | 330 | 334 | PF00082 | 0.423 |
CLV_PCSK_SKI1_1 | 528 | 532 | PF00082 | 0.282 |
CLV_PCSK_SKI1_1 | 564 | 568 | PF00082 | 0.571 |
CLV_PCSK_SKI1_1 | 618 | 622 | PF00082 | 0.358 |
DOC_CYCLIN_RxL_1 | 525 | 534 | PF00134 | 0.383 |
DOC_CYCLIN_yCln2_LP_2 | 65 | 71 | PF00134 | 0.207 |
DOC_MAPK_DCC_7 | 105 | 113 | PF00069 | 0.184 |
DOC_MAPK_gen_1 | 205 | 214 | PF00069 | 0.459 |
DOC_MAPK_MEF2A_6 | 105 | 113 | PF00069 | 0.314 |
DOC_MAPK_MEF2A_6 | 264 | 273 | PF00069 | 0.299 |
DOC_PP2B_LxvP_1 | 496 | 499 | PF13499 | 0.407 |
DOC_PP2B_PxIxI_1 | 474 | 480 | PF00149 | 0.390 |
DOC_SPAK_OSR1_1 | 14 | 18 | PF12202 | 0.526 |
DOC_USP7_MATH_1 | 257 | 261 | PF00917 | 0.334 |
DOC_USP7_MATH_1 | 421 | 425 | PF00917 | 0.519 |
DOC_USP7_MATH_1 | 482 | 486 | PF00917 | 0.373 |
DOC_USP7_MATH_1 | 499 | 503 | PF00917 | 0.379 |
DOC_USP7_UBL2_3 | 293 | 297 | PF12436 | 0.687 |
DOC_USP7_UBL2_3 | 316 | 320 | PF12436 | 0.648 |
DOC_USP7_UBL2_3 | 347 | 351 | PF12436 | 0.588 |
DOC_USP7_UBL2_3 | 435 | 439 | PF12436 | 0.276 |
DOC_USP7_UBL2_3 | 533 | 537 | PF12436 | 0.491 |
DOC_WW_Pin1_4 | 576 | 581 | PF00397 | 0.440 |
LIG_14-3-3_CanoR_1 | 168 | 176 | PF00244 | 0.357 |
LIG_14-3-3_CanoR_1 | 215 | 224 | PF00244 | 0.486 |
LIG_14-3-3_CanoR_1 | 264 | 270 | PF00244 | 0.341 |
LIG_14-3-3_CanoR_1 | 380 | 390 | PF00244 | 0.676 |
LIG_14-3-3_CanoR_1 | 438 | 444 | PF00244 | 0.395 |
LIG_14-3-3_CanoR_1 | 456 | 460 | PF00244 | 0.288 |
LIG_AP2alpha_1 | 510 | 514 | PF02296 | 0.200 |
LIG_deltaCOP1_diTrp_1 | 402 | 408 | PF00928 | 0.367 |
LIG_EH1_1 | 175 | 183 | PF00400 | 0.440 |
LIG_FHA_1 | 108 | 114 | PF00498 | 0.322 |
LIG_FHA_1 | 125 | 131 | PF00498 | 0.315 |
LIG_FHA_1 | 185 | 191 | PF00498 | 0.381 |
LIG_FHA_1 | 266 | 272 | PF00498 | 0.380 |
LIG_FHA_1 | 471 | 477 | PF00498 | 0.585 |
LIG_FHA_1 | 55 | 61 | PF00498 | 0.345 |
LIG_FHA_1 | 602 | 608 | PF00498 | 0.394 |
LIG_FHA_1 | 64 | 70 | PF00498 | 0.290 |
LIG_FHA_2 | 320 | 326 | PF00498 | 0.693 |
LIG_FHA_2 | 46 | 52 | PF00498 | 0.265 |
LIG_GBD_Chelix_1 | 272 | 280 | PF00786 | 0.346 |
LIG_LIR_Gen_1 | 112 | 120 | PF02991 | 0.358 |
LIG_LIR_Gen_1 | 13 | 22 | PF02991 | 0.496 |
LIG_LIR_Gen_1 | 171 | 182 | PF02991 | 0.299 |
LIG_LIR_Gen_1 | 392 | 403 | PF02991 | 0.516 |
LIG_LIR_Gen_1 | 442 | 451 | PF02991 | 0.332 |
LIG_LIR_Gen_1 | 609 | 619 | PF02991 | 0.351 |
LIG_LIR_Nem_3 | 112 | 117 | PF02991 | 0.314 |
LIG_LIR_Nem_3 | 13 | 18 | PF02991 | 0.509 |
LIG_LIR_Nem_3 | 150 | 154 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 171 | 177 | PF02991 | 0.269 |
LIG_LIR_Nem_3 | 231 | 237 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 29 | 34 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 392 | 398 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 442 | 447 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 609 | 614 | PF02991 | 0.328 |
LIG_LYPXL_yS_3 | 227 | 230 | PF13949 | 0.390 |
LIG_NRBOX | 491 | 497 | PF00104 | 0.393 |
LIG_NRBOX | 90 | 96 | PF00104 | 0.293 |
LIG_Pex14_2 | 233 | 237 | PF04695 | 0.334 |
LIG_Pex14_2 | 510 | 514 | PF04695 | 0.347 |
LIG_PTB_Apo_2 | 160 | 167 | PF02174 | 0.308 |
LIG_PTB_Apo_2 | 430 | 437 | PF02174 | 0.348 |
LIG_PTB_Phospho_1 | 430 | 436 | PF10480 | 0.395 |
LIG_REV1ctd_RIR_1 | 164 | 173 | PF16727 | 0.286 |
LIG_SH2_CRK | 428 | 432 | PF00017 | 0.303 |
LIG_SH2_CRK | 444 | 448 | PF00017 | 0.410 |
LIG_SH2_NCK_1 | 256 | 260 | PF00017 | 0.322 |
LIG_SH2_NCK_1 | 96 | 100 | PF00017 | 0.447 |
LIG_SH2_SRC | 256 | 259 | PF00017 | 0.370 |
LIG_SH2_STAP1 | 444 | 448 | PF00017 | 0.385 |
LIG_SH2_STAP1 | 562 | 566 | PF00017 | 0.315 |
LIG_SH2_STAP1 | 96 | 100 | PF00017 | 0.422 |
LIG_SH2_STAT3 | 223 | 226 | PF00017 | 0.450 |
LIG_SH2_STAT3 | 562 | 565 | PF00017 | 0.371 |
LIG_SH2_STAT5 | 223 | 226 | PF00017 | 0.465 |
LIG_SH2_STAT5 | 234 | 237 | PF00017 | 0.324 |
LIG_SH2_STAT5 | 246 | 249 | PF00017 | 0.303 |
LIG_SH2_STAT5 | 337 | 340 | PF00017 | 0.524 |
LIG_SH2_STAT5 | 543 | 546 | PF00017 | 0.375 |
LIG_SH3_1 | 297 | 303 | PF00018 | 0.631 |
LIG_SH3_3 | 297 | 303 | PF00018 | 0.601 |
LIG_SH3_3 | 395 | 401 | PF00018 | 0.571 |
LIG_SH3_3 | 577 | 583 | PF00018 | 0.380 |
LIG_SUMO_SIM_anti_2 | 157 | 163 | PF11976 | 0.425 |
LIG_SUMO_SIM_anti_2 | 187 | 192 | PF11976 | 0.374 |
LIG_SUMO_SIM_anti_2 | 268 | 274 | PF11976 | 0.310 |
LIG_SUMO_SIM_par_1 | 366 | 376 | PF11976 | 0.664 |
LIG_SUMO_SIM_par_1 | 445 | 452 | PF11976 | 0.335 |
LIG_TRAF2_1 | 322 | 325 | PF00917 | 0.688 |
LIG_TYR_ITIM | 244 | 249 | PF00017 | 0.377 |
LIG_TYR_ITSM | 440 | 447 | PF00017 | 0.351 |
LIG_UBA3_1 | 495 | 503 | PF00899 | 0.407 |
LIG_WRC_WIRS_1 | 148 | 153 | PF05994 | 0.381 |
LIG_WRC_WIRS_1 | 249 | 254 | PF05994 | 0.455 |
LIG_WRC_WIRS_1 | 28 | 33 | PF05994 | 0.447 |
LIG_WRC_WIRS_1 | 307 | 312 | PF05994 | 0.392 |
LIG_WRC_WIRS_1 | 511 | 516 | PF05994 | 0.388 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.341 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.354 |
MOD_CK1_1 | 449 | 455 | PF00069 | 0.343 |
MOD_CK2_1 | 319 | 325 | PF00069 | 0.634 |
MOD_CMANNOS | 404 | 407 | PF00535 | 0.358 |
MOD_Cter_Amidation | 348 | 351 | PF01082 | 0.496 |
MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.327 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.407 |
MOD_GlcNHglycan | 423 | 426 | PF01048 | 0.399 |
MOD_GlcNHglycan | 444 | 447 | PF01048 | 0.330 |
MOD_GlcNHglycan | 451 | 454 | PF01048 | 0.317 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.350 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.318 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.341 |
MOD_GSK3_1 | 390 | 397 | PF00069 | 0.453 |
MOD_GSK3_1 | 442 | 449 | PF00069 | 0.353 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.313 |
MOD_GSK3_1 | 516 | 523 | PF00069 | 0.347 |
MOD_N-GLC_1 | 162 | 167 | PF02516 | 0.338 |
MOD_N-GLC_1 | 45 | 50 | PF02516 | 0.383 |
MOD_N-GLC_1 | 601 | 606 | PF02516 | 0.291 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.339 |
MOD_NEK2_1 | 154 | 159 | PF00069 | 0.375 |
MOD_NEK2_1 | 176 | 181 | PF00069 | 0.305 |
MOD_NEK2_1 | 265 | 270 | PF00069 | 0.312 |
MOD_NEK2_1 | 394 | 399 | PF00069 | 0.386 |
MOD_NEK2_1 | 45 | 50 | PF00069 | 0.357 |
MOD_NEK2_1 | 510 | 515 | PF00069 | 0.339 |
MOD_NEK2_2 | 109 | 114 | PF00069 | 0.356 |
MOD_NEK2_2 | 27 | 32 | PF00069 | 0.333 |
MOD_PIKK_1 | 222 | 228 | PF00454 | 0.346 |
MOD_PIKK_1 | 633 | 639 | PF00454 | 0.510 |
MOD_PKA_1 | 216 | 222 | PF00069 | 0.423 |
MOD_PKA_2 | 167 | 173 | PF00069 | 0.415 |
MOD_PKA_2 | 216 | 222 | PF00069 | 0.327 |
MOD_PKA_2 | 437 | 443 | PF00069 | 0.550 |
MOD_PKA_2 | 455 | 461 | PF00069 | 0.316 |
MOD_Plk_1 | 10 | 16 | PF00069 | 0.528 |
MOD_Plk_1 | 162 | 168 | PF00069 | 0.365 |
MOD_Plk_1 | 50 | 56 | PF00069 | 0.313 |
MOD_Plk_1 | 601 | 607 | PF00069 | 0.310 |
MOD_Plk_2-3 | 306 | 312 | PF00069 | 0.625 |
MOD_Plk_4 | 109 | 115 | PF00069 | 0.303 |
MOD_Plk_4 | 126 | 132 | PF00069 | 0.325 |
MOD_Plk_4 | 154 | 160 | PF00069 | 0.366 |
MOD_Plk_4 | 162 | 168 | PF00069 | 0.372 |
MOD_Plk_4 | 265 | 271 | PF00069 | 0.351 |
MOD_Plk_4 | 27 | 33 | PF00069 | 0.325 |
MOD_Plk_4 | 390 | 396 | PF00069 | 0.425 |
MOD_Plk_4 | 439 | 445 | PF00069 | 0.316 |
MOD_Plk_4 | 607 | 613 | PF00069 | 0.281 |
MOD_ProDKin_1 | 576 | 582 | PF00069 | 0.556 |
MOD_SUMO_rev_2 | 309 | 318 | PF00179 | 0.601 |
MOD_SUMO_rev_2 | 324 | 332 | PF00179 | 0.505 |
MOD_SUMO_rev_2 | 374 | 379 | PF00179 | 0.590 |
MOD_SUMO_rev_2 | 432 | 440 | PF00179 | 0.308 |
TRG_DiLeu_BaEn_2 | 10 | 16 | PF01217 | 0.462 |
TRG_ENDOCYTIC_2 | 164 | 167 | PF00928 | 0.342 |
TRG_ENDOCYTIC_2 | 174 | 177 | PF00928 | 0.280 |
TRG_ENDOCYTIC_2 | 198 | 201 | PF00928 | 0.370 |
TRG_ENDOCYTIC_2 | 227 | 230 | PF00928 | 0.391 |
TRG_ENDOCYTIC_2 | 234 | 237 | PF00928 | 0.354 |
TRG_ENDOCYTIC_2 | 246 | 249 | PF00928 | 0.303 |
TRG_ENDOCYTIC_2 | 428 | 431 | PF00928 | 0.371 |
TRG_ENDOCYTIC_2 | 444 | 447 | PF00928 | 0.322 |
TRG_ENDOCYTIC_2 | 539 | 542 | PF00928 | 0.321 |
TRG_ENDOCYTIC_2 | 616 | 619 | PF00928 | 0.400 |
TRG_ER_diArg_1 | 214 | 217 | PF00400 | 0.360 |
TRG_ER_diArg_1 | 616 | 618 | PF00400 | 0.443 |
TRG_Pf-PMV_PEXEL_1 | 216 | 220 | PF00026 | 0.382 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6G0 | Leptomonas seymouri | 29% | 100% |
A0A0N1HZC2 | Leptomonas seymouri | 29% | 100% |
A0A0N1IKC5 | Leptomonas seymouri | 31% | 100% |
A0A0N1PB63 | Leptomonas seymouri | 26% | 98% |
A0A0N1PD04 | Leptomonas seymouri | 25% | 100% |
A0A0N1PFR4 | Leptomonas seymouri | 32% | 98% |
A0A0S4JR45 | Bodo saltans | 31% | 100% |
A0A1X0NKK0 | Trypanosomatidae | 30% | 100% |
A0A1X0NM09 | Trypanosomatidae | 29% | 100% |
A0A1X0NV27 | Trypanosomatidae | 33% | 100% |
A0A1X0NVF9 | Trypanosomatidae | 23% | 97% |
A0A1X0NVH8 | Trypanosomatidae | 28% | 98% |
A0A1X0NVM7 | Trypanosomatidae | 30% | 100% |
A0A1X0NWQ1 | Trypanosomatidae | 33% | 100% |
A0A1X0NZE6 | Trypanosomatidae | 29% | 100% |
A0A1X0NZU2 | Trypanosomatidae | 33% | 100% |
A0A1X0NZU5 | Trypanosomatidae | 54% | 100% |
A0A1X0NZW1 | Trypanosomatidae | 31% | 100% |
A0A1X0P0M7 | Trypanosomatidae | 28% | 100% |
A0A381MMW5 | Leishmania infantum | 93% | 99% |
A0A3Q8IEC4 | Leishmania donovani | 93% | 100% |
A0A3Q8IF95 | Leishmania donovani | 28% | 100% |
A0A3Q8IIT5 | Leishmania donovani | 31% | 96% |
A0A3Q8ISY9 | Leishmania donovani | 29% | 100% |
A0A3R7KKN8 | Trypanosoma rangeli | 32% | 100% |
A0A3R7MAQ7 | Trypanosoma rangeli | 27% | 92% |
A0A3R7N3S6 | Trypanosoma rangeli | 25% | 100% |
A0A3R7N415 | Trypanosoma rangeli | 31% | 100% |
A0A3R7N921 | Trypanosoma rangeli | 30% | 100% |
A0A3R7R443 | Trypanosoma rangeli | 30% | 100% |
A0A3S7WRJ4 | Leishmania donovani | 29% | 100% |
A0A3S7WRJ5 | Leishmania donovani | 33% | 93% |
A0A3S7WRS3 | Leishmania donovani | 25% | 100% |
A0A3S7WSR4 | Leishmania donovani | 31% | 100% |
A0A3S7WWU1 | Leishmania donovani | 26% | 98% |
A0A3S7X2G0 | Leishmania donovani | 93% | 99% |
A0A3S7X2K5 | Leishmania donovani | 90% | 100% |
A0A3S7XB11 | Leishmania donovani | 30% | 100% |
A0A422MSE4 | Trypanosoma rangeli | 35% | 100% |
A0A422MSP6 | Trypanosoma rangeli | 48% | 100% |
A0A422MST9 | Trypanosoma rangeli | 30% | 100% |
A0A422MU68 | Trypanosoma rangeli | 30% | 100% |
A4H6J0 | Leishmania braziliensis | 30% | 100% |
A4H6J1 | Leishmania braziliensis | 32% | 100% |
A4H6Q5 | Leishmania braziliensis | 26% | 100% |
A4HC19 | Leishmania braziliensis | 27% | 100% |
A4HHG2 | Leishmania braziliensis | 30% | 100% |
A4HHG3 | Leishmania braziliensis | 82% | 100% |
A4HHG4 | Leishmania braziliensis | 72% | 100% |
A4HJW3 | Leishmania braziliensis | 29% | 100% |
A4HPE2 | Leishmania braziliensis | 30% | 99% |
A4HUX5 | Leishmania infantum | 30% | 100% |
A4HUX6 | Leishmania infantum | 33% | 93% |
A4HV40 | Leishmania infantum | 24% | 100% |
A4HZF5 | Leishmania infantum | 28% | 100% |
A4HZJ4 | Leishmania infantum | 26% | 98% |
A4I4L2 | Leishmania infantum | 31% | 96% |
A4I7C5 | Leishmania infantum | 28% | 100% |
A4ICI3 | Leishmania infantum | 30% | 100% |
C9ZL97 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZL98 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZL99 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
C9ZLA0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
C9ZLA1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
C9ZTR5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
C9ZTR6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
C9ZTR7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
C9ZTR8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZTR9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZTS1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZUT6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
D0A7B1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
D0A7H1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
D0AAQ2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 95% |
E8NHE1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
E9AE01 | Leishmania major | 92% | 100% |
E9AE09 | Leishmania major | 30% | 100% |
E9AE10 | Leishmania major | 30% | 100% |
E9AE11 | Leishmania major | 85% | 100% |
E9AGK5 | Leishmania infantum | 31% | 100% |
E9AHJ0 | Leishmania infantum | 94% | 100% |
E9AHJ1 | Leishmania infantum | 90% | 100% |
E9ALS3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 96% |
E9ANL0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9ANL1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 99% |
E9ANS1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
E9APJ3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9AT53 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9AVF1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9AVF2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 98% |
E9B2B8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
Q4Q1E4 | Leishmania major | 29% | 98% |
Q4Q5T8 | Leishmania major | 28% | 100% |
Q4QC27 | Leishmania major | 26% | 100% |
Q4QC28 | Leishmania major | 27% | 96% |
Q4QFY5 | Leishmania major | 31% | 99% |
Q4QGU8 | Leishmania major | 25% | 100% |
Q4QH14 | Leishmania major | 30% | 100% |
Q4QH15 | Leishmania major | 30% | 100% |
V5B647 | Trypanosoma cruzi | 31% | 100% |
V5B983 | Trypanosoma cruzi | 47% | 100% |
V5BBB1 | Trypanosoma cruzi | 31% | 100% |
V5BFV8 | Trypanosoma cruzi | 32% | 97% |
V5BQY6 | Trypanosoma cruzi | 30% | 92% |
V5BVP0 | Trypanosoma cruzi | 30% | 100% |
V5DT25 | Trypanosoma cruzi | 30% | 100% |