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: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 15 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 96 |
NetGPI | no | yes: 0, no: 96 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 91 |
GO:0110165 | cellular anatomical entity | 1 | 91 |
Related structures:
AlphaFold database: E9ANL2
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 43 |
GO:0022857 | transmembrane transporter activity | 2 | 43 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 557 | 561 | PF00656 | 0.535 |
CLV_NRD_NRD_1 | 116 | 118 | PF00675 | 0.357 |
CLV_NRD_NRD_1 | 375 | 377 | PF00675 | 0.384 |
CLV_NRD_NRD_1 | 514 | 516 | PF00675 | 0.339 |
CLV_NRD_NRD_1 | 522 | 524 | PF00675 | 0.358 |
CLV_PCSK_KEX2_1 | 116 | 118 | PF00082 | 0.373 |
CLV_PCSK_KEX2_1 | 375 | 377 | PF00082 | 0.368 |
CLV_PCSK_KEX2_1 | 521 | 523 | PF00082 | 0.347 |
CLV_PCSK_PC1ET2_1 | 375 | 377 | PF00082 | 0.392 |
CLV_PCSK_SKI1_1 | 234 | 238 | PF00082 | 0.600 |
CLV_PCSK_SKI1_1 | 408 | 412 | PF00082 | 0.523 |
CLV_PCSK_SKI1_1 | 515 | 519 | PF00082 | 0.350 |
DEG_MDM2_SWIB_1 | 448 | 456 | PF02201 | 0.439 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.358 |
DOC_CKS1_1 | 144 | 149 | PF01111 | 0.190 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 492 | 501 | PF00134 | 0.215 |
DOC_CYCLIN_yCln2_LP_2 | 144 | 150 | PF00134 | 0.190 |
DOC_MAPK_gen_1 | 116 | 123 | PF00069 | 0.531 |
DOC_MAPK_gen_1 | 375 | 384 | PF00069 | 0.566 |
DOC_MAPK_gen_1 | 470 | 480 | PF00069 | 0.402 |
DOC_MAPK_MEF2A_6 | 208 | 217 | PF00069 | 0.489 |
DOC_MAPK_MEF2A_6 | 377 | 386 | PF00069 | 0.559 |
DOC_MAPK_MEF2A_6 | 482 | 491 | PF00069 | 0.312 |
DOC_PP2B_LxvP_1 | 403 | 406 | PF13499 | 0.421 |
DOC_PP4_FxxP_1 | 388 | 391 | PF00568 | 0.418 |
DOC_PP4_FxxP_1 | 41 | 44 | PF00568 | 0.326 |
DOC_SPAK_OSR1_1 | 86 | 90 | PF12202 | 0.320 |
DOC_USP7_MATH_1 | 224 | 228 | PF00917 | 0.345 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.275 |
DOC_USP7_MATH_1 | 406 | 410 | PF00917 | 0.406 |
DOC_USP7_MATH_1 | 415 | 419 | PF00917 | 0.339 |
DOC_USP7_MATH_1 | 530 | 534 | PF00917 | 0.679 |
DOC_USP7_UBL2_3 | 438 | 442 | PF12436 | 0.535 |
DOC_WW_Pin1_4 | 143 | 148 | PF00397 | 0.336 |
DOC_WW_Pin1_4 | 328 | 333 | PF00397 | 0.400 |
DOC_WW_Pin1_4 | 337 | 342 | PF00397 | 0.415 |
LIG_14-3-3_CanoR_1 | 183 | 190 | PF00244 | 0.557 |
LIG_14-3-3_CanoR_1 | 26 | 34 | PF00244 | 0.333 |
LIG_14-3-3_CanoR_1 | 363 | 369 | PF00244 | 0.304 |
LIG_14-3-3_CanoR_1 | 381 | 387 | PF00244 | 0.412 |
LIG_BRCT_BRCA1_1 | 330 | 334 | PF00533 | 0.369 |
LIG_BRCT_BRCA1_1 | 6 | 10 | PF00533 | 0.305 |
LIG_BRCT_BRCA1_1 | 97 | 101 | PF00533 | 0.415 |
LIG_FHA_1 | 130 | 136 | PF00498 | 0.213 |
LIG_FHA_1 | 224 | 230 | PF00498 | 0.340 |
LIG_FHA_1 | 274 | 280 | PF00498 | 0.702 |
LIG_FHA_1 | 296 | 302 | PF00498 | 0.529 |
LIG_FHA_1 | 304 | 310 | PF00498 | 0.498 |
LIG_FHA_1 | 338 | 344 | PF00498 | 0.399 |
LIG_FHA_1 | 390 | 396 | PF00498 | 0.341 |
LIG_FHA_1 | 426 | 432 | PF00498 | 0.310 |
LIG_FHA_1 | 496 | 502 | PF00498 | 0.399 |
LIG_FHA_2 | 285 | 291 | PF00498 | 0.588 |
LIG_FHA_2 | 45 | 51 | PF00498 | 0.469 |
LIG_FHA_2 | 73 | 79 | PF00498 | 0.172 |
LIG_GBD_Chelix_1 | 120 | 128 | PF00786 | 0.430 |
LIG_GBD_Chelix_1 | 215 | 223 | PF00786 | 0.313 |
LIG_GBD_Chelix_1 | 453 | 461 | PF00786 | 0.386 |
LIG_IRF3_LxIS_1 | 504 | 509 | PF10401 | 0.534 |
LIG_LIR_Apic_2 | 288 | 294 | PF02991 | 0.567 |
LIG_LIR_Apic_2 | 385 | 391 | PF02991 | 0.398 |
LIG_LIR_Apic_2 | 50 | 54 | PF02991 | 0.468 |
LIG_LIR_Gen_1 | 253 | 264 | PF02991 | 0.360 |
LIG_LIR_Gen_1 | 308 | 317 | PF02991 | 0.338 |
LIG_LIR_Gen_1 | 323 | 332 | PF02991 | 0.374 |
LIG_LIR_Gen_1 | 47 | 57 | PF02991 | 0.421 |
LIG_LIR_Gen_1 | 502 | 513 | PF02991 | 0.376 |
LIG_LIR_Gen_1 | 7 | 17 | PF02991 | 0.294 |
LIG_LIR_Gen_1 | 75 | 84 | PF02991 | 0.232 |
LIG_LIR_Nem_3 | 308 | 313 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 315 | 320 | PF02991 | 0.321 |
LIG_LIR_Nem_3 | 323 | 327 | PF02991 | 0.333 |
LIG_LIR_Nem_3 | 331 | 337 | PF02991 | 0.303 |
LIG_LIR_Nem_3 | 367 | 372 | PF02991 | 0.577 |
LIG_LIR_Nem_3 | 47 | 52 | PF02991 | 0.374 |
LIG_LIR_Nem_3 | 502 | 508 | PF02991 | 0.324 |
LIG_LIR_Nem_3 | 509 | 513 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 7 | 13 | PF02991 | 0.282 |
LIG_LIR_Nem_3 | 75 | 79 | PF02991 | 0.262 |
LIG_NRBOX | 457 | 463 | PF00104 | 0.306 |
LIG_NRBOX | 496 | 502 | PF00104 | 0.476 |
LIG_NRBOX | 66 | 72 | PF00104 | 0.281 |
LIG_PAM2_1 | 142 | 154 | PF00658 | 0.190 |
LIG_Pex14_2 | 324 | 328 | PF04695 | 0.380 |
LIG_Pex14_2 | 448 | 452 | PF04695 | 0.393 |
LIG_SH2_CRK | 45 | 49 | PF00017 | 0.327 |
LIG_SH2_PTP2 | 291 | 294 | PF00017 | 0.543 |
LIG_SH2_SRC | 179 | 182 | PF00017 | 0.656 |
LIG_SH2_SRC | 505 | 508 | PF00017 | 0.489 |
LIG_SH2_STAP1 | 8 | 12 | PF00017 | 0.298 |
LIG_SH2_STAT3 | 199 | 202 | PF00017 | 0.531 |
LIG_SH2_STAT5 | 150 | 153 | PF00017 | 0.320 |
LIG_SH2_STAT5 | 199 | 202 | PF00017 | 0.551 |
LIG_SH2_STAT5 | 210 | 213 | PF00017 | 0.310 |
LIG_SH2_STAT5 | 222 | 225 | PF00017 | 0.311 |
LIG_SH2_STAT5 | 291 | 294 | PF00017 | 0.548 |
LIG_SH2_STAT5 | 372 | 375 | PF00017 | 0.588 |
LIG_SH2_STAT5 | 40 | 43 | PF00017 | 0.306 |
LIG_SH2_STAT5 | 505 | 508 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 51 | 54 | PF00017 | 0.493 |
LIG_SH2_STAT5 | 550 | 553 | PF00017 | 0.664 |
LIG_SH2_STAT5 | 58 | 61 | PF00017 | 0.332 |
LIG_SH3_2 | 536 | 541 | PF14604 | 0.755 |
LIG_SH3_3 | 218 | 224 | PF00018 | 0.320 |
LIG_SH3_3 | 258 | 264 | PF00018 | 0.370 |
LIG_SH3_3 | 482 | 488 | PF00018 | 0.320 |
LIG_SH3_3 | 533 | 539 | PF00018 | 0.658 |
LIG_SUMO_SIM_anti_2 | 212 | 217 | PF11976 | 0.391 |
LIG_SUMO_SIM_anti_2 | 392 | 398 | PF11976 | 0.326 |
LIG_SUMO_SIM_anti_2 | 426 | 431 | PF11976 | 0.347 |
LIG_SUMO_SIM_par_1 | 156 | 161 | PF11976 | 0.369 |
LIG_SUMO_SIM_par_1 | 392 | 398 | PF11976 | 0.336 |
LIG_SUMO_SIM_par_1 | 428 | 434 | PF11976 | 0.294 |
LIG_SUMO_SIM_par_1 | 92 | 98 | PF11976 | 0.340 |
LIG_TRFH_1 | 40 | 44 | PF08558 | 0.370 |
LIG_TYR_ITIM | 43 | 48 | PF00017 | 0.344 |
LIG_UBA3_1 | 333 | 342 | PF00899 | 0.495 |
MOD_CDK_SPK_2 | 337 | 342 | PF00069 | 0.300 |
MOD_CK1_1 | 137 | 143 | PF00069 | 0.392 |
MOD_CK1_1 | 182 | 188 | PF00069 | 0.542 |
MOD_CK1_1 | 303 | 309 | PF00069 | 0.396 |
MOD_CK1_1 | 335 | 341 | PF00069 | 0.427 |
MOD_CK1_1 | 511 | 517 | PF00069 | 0.466 |
MOD_CK1_1 | 554 | 560 | PF00069 | 0.663 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.370 |
MOD_CK2_1 | 364 | 370 | PF00069 | 0.400 |
MOD_GlcNHglycan | 13 | 16 | PF01048 | 0.326 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.341 |
MOD_GlcNHglycan | 281 | 284 | PF01048 | 0.566 |
MOD_GlcNHglycan | 334 | 337 | PF01048 | 0.375 |
MOD_GlcNHglycan | 358 | 361 | PF01048 | 0.284 |
MOD_GlcNHglycan | 533 | 536 | PF01048 | 0.491 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.347 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.403 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.333 |
MOD_GSK3_1 | 267 | 274 | PF00069 | 0.423 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.436 |
MOD_GSK3_1 | 328 | 335 | PF00069 | 0.424 |
MOD_GSK3_1 | 495 | 502 | PF00069 | 0.393 |
MOD_GSK3_1 | 554 | 561 | PF00069 | 0.593 |
MOD_N-GLC_1 | 328 | 333 | PF02516 | 0.444 |
MOD_N-GLC_1 | 495 | 500 | PF02516 | 0.297 |
MOD_NEK2_1 | 123 | 128 | PF00069 | 0.397 |
MOD_NEK2_1 | 13 | 18 | PF00069 | 0.330 |
MOD_NEK2_1 | 209 | 214 | PF00069 | 0.358 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.384 |
MOD_NEK2_1 | 343 | 348 | PF00069 | 0.406 |
MOD_NEK2_1 | 364 | 369 | PF00069 | 0.400 |
MOD_NEK2_1 | 423 | 428 | PF00069 | 0.345 |
MOD_NEK2_1 | 495 | 500 | PF00069 | 0.342 |
MOD_NEK2_1 | 506 | 511 | PF00069 | 0.339 |
MOD_NEK2_1 | 72 | 77 | PF00069 | 0.304 |
MOD_NEK2_2 | 44 | 49 | PF00069 | 0.245 |
MOD_PIKK_1 | 198 | 204 | PF00454 | 0.492 |
MOD_PIKK_1 | 235 | 241 | PF00454 | 0.463 |
MOD_PIKK_1 | 370 | 376 | PF00454 | 0.454 |
MOD_PIKK_1 | 95 | 101 | PF00454 | 0.431 |
MOD_PKA_2 | 182 | 188 | PF00069 | 0.406 |
MOD_PKA_2 | 267 | 273 | PF00069 | 0.450 |
MOD_PKA_2 | 511 | 517 | PF00069 | 0.372 |
MOD_Plk_1 | 343 | 349 | PF00069 | 0.418 |
MOD_Plk_1 | 495 | 501 | PF00069 | 0.320 |
MOD_Plk_2-3 | 284 | 290 | PF00069 | 0.609 |
MOD_Plk_4 | 102 | 108 | PF00069 | 0.322 |
MOD_Plk_4 | 123 | 129 | PF00069 | 0.368 |
MOD_Plk_4 | 296 | 302 | PF00069 | 0.404 |
MOD_Plk_4 | 305 | 311 | PF00069 | 0.328 |
MOD_Plk_4 | 349 | 355 | PF00069 | 0.307 |
MOD_Plk_4 | 364 | 370 | PF00069 | 0.366 |
MOD_Plk_4 | 390 | 396 | PF00069 | 0.346 |
MOD_Plk_4 | 425 | 431 | PF00069 | 0.328 |
MOD_Plk_4 | 44 | 50 | PF00069 | 0.383 |
MOD_Plk_4 | 554 | 560 | PF00069 | 0.616 |
MOD_Plk_4 | 80 | 86 | PF00069 | 0.332 |
MOD_ProDKin_1 | 143 | 149 | PF00069 | 0.412 |
MOD_ProDKin_1 | 328 | 334 | PF00069 | 0.501 |
MOD_ProDKin_1 | 337 | 343 | PF00069 | 0.518 |
MOD_SUMO_rev_2 | 181 | 191 | PF00179 | 0.458 |
TRG_DiLeu_BaLyEn_6 | 457 | 462 | PF01217 | 0.328 |
TRG_DiLeu_BaLyEn_6 | 485 | 490 | PF01217 | 0.381 |
TRG_ENDOCYTIC_2 | 150 | 153 | PF00928 | 0.287 |
TRG_ENDOCYTIC_2 | 210 | 213 | PF00928 | 0.370 |
TRG_ENDOCYTIC_2 | 222 | 225 | PF00928 | 0.319 |
TRG_ENDOCYTIC_2 | 40 | 43 | PF00928 | 0.315 |
TRG_ENDOCYTIC_2 | 45 | 48 | PF00928 | 0.328 |
TRG_ENDOCYTIC_2 | 49 | 52 | PF00928 | 0.347 |
TRG_ENDOCYTIC_2 | 505 | 508 | PF00928 | 0.388 |
TRG_ENDOCYTIC_2 | 510 | 513 | PF00928 | 0.391 |
TRG_ER_diArg_1 | 521 | 523 | PF00400 | 0.443 |
TRG_Pf-PMV_PEXEL_1 | 460 | 465 | PF00026 | 0.389 |
TRG_Pf-PMV_PEXEL_1 | 516 | 520 | PF00026 | 0.460 |
TRG_Pf-PMV_PEXEL_1 | 522 | 526 | PF00026 | 0.481 |
TRG_Pf-PMV_PEXEL_1 | 569 | 573 | PF00026 | 0.432 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6G0 | Leptomonas seymouri | 39% | 90% |
A0A0N1HT40 | Leptomonas seymouri | 73% | 100% |
A0A0N1HZC2 | Leptomonas seymouri | 27% | 91% |
A0A0N1IKC5 | Leptomonas seymouri | 46% | 94% |
A0A0N1PB63 | Leptomonas seymouri | 25% | 87% |
A0A0S4JR45 | Bodo saltans | 32% | 100% |
A0A1X0NKK0 | Trypanosomatidae | 31% | 94% |
A0A1X0NL32 | Trypanosomatidae | 34% | 92% |
A0A1X0NM09 | Trypanosomatidae | 31% | 94% |
A0A1X0NRW5 | Trypanosomatidae | 40% | 82% |
A0A1X0NV13 | Trypanosomatidae | 48% | 88% |
A0A1X0NV19 | Trypanosomatidae | 48% | 96% |
A0A1X0NV27 | Trypanosomatidae | 48% | 96% |
A0A1X0NVH8 | Trypanosomatidae | 46% | 87% |
A0A1X0NVM7 | Trypanosomatidae | 54% | 89% |
A0A1X0NWQ1 | Trypanosomatidae | 44% | 89% |
A0A1X0NZE6 | Trypanosomatidae | 34% | 96% |
A0A1X0NZU5 | Trypanosomatidae | 33% | 98% |
A0A1X0NZW1 | Trypanosomatidae | 29% | 95% |
A0A1X0P0M7 | Trypanosomatidae | 33% | 97% |
A0A3Q8I7Y9 | Leishmania donovani | 96% | 100% |
A0A3Q8IF95 | Leishmania donovani | 28% | 100% |
A0A3Q8ISY9 | Leishmania donovani | 38% | 90% |
A0A3R7JPZ0 | Trypanosoma rangeli | 26% | 100% |
A0A3R7JSQ9 | Trypanosoma rangeli | 29% | 100% |
A0A3R7KKN8 | Trypanosoma rangeli | 30% | 96% |
A0A3R7MAQ7 | Trypanosoma rangeli | 36% | 81% |
A0A3R7N415 | Trypanosoma rangeli | 30% | 95% |
A0A3R7N921 | Trypanosoma rangeli | 29% | 100% |
A0A3R7R443 | Trypanosoma rangeli | 30% | 96% |
A0A3R7R6N6 | Trypanosoma rangeli | 27% | 100% |
A0A3S7WRJ4 | Leishmania donovani | 46% | 89% |
A0A3S7WRJ5 | Leishmania donovani | 42% | 82% |
A0A3S7WRL4 | Leishmania donovani | 93% | 92% |
A0A3S7WSR4 | Leishmania donovani | 45% | 94% |
A0A3S7WWU1 | Leishmania donovani | 25% | 86% |
A0A3S7XB11 | Leishmania donovani | 29% | 94% |
A0A422MSE4 | Trypanosoma rangeli | 48% | 100% |
A0A422MSP6 | Trypanosoma rangeli | 34% | 100% |
A0A422MST9 | Trypanosoma rangeli | 28% | 95% |
A0A422MU68 | Trypanosoma rangeli | 27% | 100% |
A4H6J0 | Leishmania braziliensis | 46% | 100% |
A4H6J3 | Leishmania braziliensis | 83% | 100% |
A4HC19 | Leishmania braziliensis | 26% | 100% |
A4HJW3 | Leishmania braziliensis | 39% | 100% |
A4HPE2 | Leishmania braziliensis | 28% | 100% |
A4HUX5 | Leishmania infantum | 46% | 89% |
A4HUX6 | Leishmania infantum | 42% | 82% |
A4HUX7 | Leishmania infantum | 93% | 92% |
A4HUX8 | Leishmania infantum | 92% | 98% |
A4HZF5 | Leishmania infantum | 28% | 100% |
A4HZJ4 | Leishmania infantum | 25% | 86% |
A4I7C5 | Leishmania infantum | 39% | 90% |
A4ICI3 | Leishmania infantum | 29% | 94% |
C9ZL97 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 96% |
C9ZL98 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 98% |
C9ZL99 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 96% |
C9ZLA0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 98% |
C9ZLA1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 96% |
C9ZTR5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 96% |
C9ZTR6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 95% |
C9ZTR7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
C9ZTR8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 96% |
C9ZTR9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 98% |
C9ZTS1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 96% |
C9ZUT6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 97% |
D0A7H1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
D0AAQ2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 84% |
E8NHE1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 43% | 100% |
E9AGK5 | Leishmania infantum | 45% | 94% |
E9ANL0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 47% | 100% |
E9ANL1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 43% | 100% |
E9APJ3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 46% | 95% |
E9AT53 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 97% |
E9AVF1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 93% |
E9AVF2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 87% |
E9B2B8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 39% | 90% |
Q4Q1E4 | Leishmania major | 29% | 100% |
Q4Q5T8 | Leishmania major | 38% | 100% |
Q4QC27 | Leishmania major | 26% | 100% |
Q4QC28 | Leishmania major | 30% | 100% |
Q4QFY5 | Leishmania major | 44% | 100% |
Q4QH10 | Leishmania major | 92% | 100% |
Q4QH11 | Leishmania major | 93% | 100% |
Q4QH12 | Leishmania major | 93% | 100% |
Q4QH13 | Leishmania major | 93% | 100% |
Q4QH14 | Leishmania major | 41% | 100% |
Q4QH15 | Leishmania major | 46% | 100% |
V5B647 | Trypanosoma cruzi | 47% | 91% |
V5B983 | Trypanosoma cruzi | 33% | 98% |
V5BBB1 | Trypanosoma cruzi | 45% | 97% |
V5BFV8 | Trypanosoma cruzi | 30% | 86% |
V5BQY6 | Trypanosoma cruzi | 38% | 81% |
V5BVP0 | Trypanosoma cruzi | 46% | 97% |
V5DT25 | Trypanosoma cruzi | 57% | 93% |