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: 101 |
NetGPI | no | yes: 0, no: 101 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 96 |
GO:0110165 | cellular anatomical entity | 1 | 96 |
Related structures:
AlphaFold database: A4H6J3
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 44 |
GO:0022857 | transmembrane transporter activity | 2 | 44 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 560 | 564 | PF00656 | 0.560 |
CLV_C14_Caspase3-7 | 570 | 574 | PF00656 | 0.569 |
CLV_NRD_NRD_1 | 116 | 118 | PF00675 | 0.357 |
CLV_NRD_NRD_1 | 375 | 377 | PF00675 | 0.381 |
CLV_NRD_NRD_1 | 514 | 516 | PF00675 | 0.344 |
CLV_NRD_NRD_1 | 571 | 573 | PF00675 | 0.506 |
CLV_PCSK_KEX2_1 | 116 | 118 | PF00082 | 0.372 |
CLV_PCSK_KEX2_1 | 272 | 274 | PF00082 | 0.408 |
CLV_PCSK_KEX2_1 | 375 | 377 | PF00082 | 0.365 |
CLV_PCSK_KEX2_1 | 571 | 573 | PF00082 | 0.553 |
CLV_PCSK_PC1ET2_1 | 272 | 274 | PF00082 | 0.371 |
CLV_PCSK_PC1ET2_1 | 375 | 377 | PF00082 | 0.384 |
CLV_PCSK_PC7_1 | 268 | 274 | PF00082 | 0.402 |
CLV_PCSK_SKI1_1 | 408 | 412 | PF00082 | 0.517 |
CLV_PCSK_SKI1_1 | 515 | 519 | PF00082 | 0.365 |
DEG_MDM2_SWIB_1 | 448 | 456 | PF02201 | 0.411 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.357 |
DEG_ODPH_VHL_1 | 64 | 76 | PF01847 | 0.328 |
DOC_CYCLIN_RxL_1 | 405 | 415 | PF00134 | 0.189 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 492 | 501 | PF00134 | 0.207 |
DOC_MAPK_DCC_7 | 482 | 491 | PF00069 | 0.212 |
DOC_MAPK_gen_1 | 116 | 123 | PF00069 | 0.524 |
DOC_MAPK_gen_1 | 237 | 245 | PF00069 | 0.371 |
DOC_MAPK_gen_1 | 375 | 384 | PF00069 | 0.560 |
DOC_MAPK_gen_1 | 470 | 480 | PF00069 | 0.404 |
DOC_MAPK_MEF2A_6 | 208 | 217 | PF00069 | 0.483 |
DOC_MAPK_MEF2A_6 | 377 | 386 | PF00069 | 0.561 |
DOC_MAPK_MEF2A_6 | 482 | 491 | PF00069 | 0.270 |
DOC_MAPK_RevD_3 | 258 | 273 | PF00069 | 0.509 |
DOC_PP2B_LxvP_1 | 403 | 406 | PF13499 | 0.419 |
DOC_PP4_FxxP_1 | 388 | 391 | PF00568 | 0.404 |
DOC_PP4_FxxP_1 | 41 | 44 | PF00568 | 0.319 |
DOC_SPAK_OSR1_1 | 86 | 90 | PF12202 | 0.318 |
DOC_USP7_MATH_1 | 224 | 228 | PF00917 | 0.349 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.272 |
DOC_USP7_MATH_1 | 406 | 410 | PF00917 | 0.403 |
DOC_USP7_MATH_1 | 425 | 429 | PF00917 | 0.330 |
DOC_USP7_MATH_1 | 531 | 535 | PF00917 | 0.675 |
DOC_USP7_UBL2_3 | 438 | 442 | PF12436 | 0.546 |
DOC_USP7_UBL2_3 | 473 | 477 | PF12436 | 0.428 |
DOC_WW_Pin1_4 | 143 | 148 | PF00397 | 0.334 |
DOC_WW_Pin1_4 | 328 | 333 | PF00397 | 0.393 |
LIG_14-3-3_CanoR_1 | 26 | 34 | PF00244 | 0.331 |
LIG_14-3-3_CanoR_1 | 363 | 369 | PF00244 | 0.374 |
LIG_14-3-3_CanoR_1 | 381 | 387 | PF00244 | 0.408 |
LIG_14-3-3_CanoR_1 | 515 | 524 | PF00244 | 0.607 |
LIG_BRCT_BRCA1_1 | 147 | 151 | PF00533 | 0.206 |
LIG_BRCT_BRCA1_1 | 330 | 334 | PF00533 | 0.369 |
LIG_BRCT_BRCA1_1 | 6 | 10 | PF00533 | 0.302 |
LIG_BRCT_BRCA1_1 | 97 | 101 | PF00533 | 0.409 |
LIG_FHA_1 | 224 | 230 | PF00498 | 0.334 |
LIG_FHA_1 | 247 | 253 | PF00498 | 0.367 |
LIG_FHA_1 | 296 | 302 | PF00498 | 0.523 |
LIG_FHA_1 | 304 | 310 | PF00498 | 0.453 |
LIG_FHA_1 | 338 | 344 | PF00498 | 0.377 |
LIG_FHA_1 | 390 | 396 | PF00498 | 0.333 |
LIG_FHA_1 | 496 | 502 | PF00498 | 0.400 |
LIG_FHA_2 | 285 | 291 | PF00498 | 0.589 |
LIG_FHA_2 | 45 | 51 | PF00498 | 0.468 |
LIG_FHA_2 | 568 | 574 | PF00498 | 0.668 |
LIG_GBD_Chelix_1 | 120 | 128 | PF00786 | 0.427 |
LIG_GBD_Chelix_1 | 453 | 461 | PF00786 | 0.383 |
LIG_LIR_Apic_2 | 288 | 294 | PF02991 | 0.561 |
LIG_LIR_Apic_2 | 385 | 391 | PF02991 | 0.379 |
LIG_LIR_Apic_2 | 50 | 54 | PF02991 | 0.467 |
LIG_LIR_Gen_1 | 253 | 264 | PF02991 | 0.352 |
LIG_LIR_Gen_1 | 308 | 317 | PF02991 | 0.338 |
LIG_LIR_Gen_1 | 323 | 332 | PF02991 | 0.430 |
LIG_LIR_Gen_1 | 47 | 57 | PF02991 | 0.418 |
LIG_LIR_Gen_1 | 502 | 513 | PF02991 | 0.387 |
LIG_LIR_Gen_1 | 7 | 17 | PF02991 | 0.291 |
LIG_LIR_Nem_3 | 148 | 154 | PF02991 | 0.251 |
LIG_LIR_Nem_3 | 308 | 313 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 315 | 320 | PF02991 | 0.293 |
LIG_LIR_Nem_3 | 323 | 327 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 331 | 337 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 367 | 372 | PF02991 | 0.574 |
LIG_LIR_Nem_3 | 47 | 52 | PF02991 | 0.373 |
LIG_LIR_Nem_3 | 502 | 508 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 7 | 13 | PF02991 | 0.279 |
LIG_LIR_Nem_3 | 75 | 79 | PF02991 | 0.305 |
LIG_LYPXL_SIV_4 | 44 | 52 | PF13949 | 0.269 |
LIG_MLH1_MIPbox_1 | 147 | 151 | PF16413 | 0.209 |
LIG_NRBOX | 346 | 352 | PF00104 | 0.225 |
LIG_NRBOX | 457 | 463 | PF00104 | 0.296 |
LIG_NRBOX | 496 | 502 | PF00104 | 0.475 |
LIG_Pex14_2 | 324 | 328 | PF04695 | 0.411 |
LIG_Pex14_2 | 448 | 452 | PF04695 | 0.355 |
LIG_SH2_CRK | 45 | 49 | PF00017 | 0.325 |
LIG_SH2_PTP2 | 291 | 294 | PF00017 | 0.539 |
LIG_SH2_PTP2 | 505 | 508 | PF00017 | 0.355 |
LIG_SH2_SRC | 505 | 508 | PF00017 | 0.487 |
LIG_SH2_STAP1 | 8 | 12 | PF00017 | 0.294 |
LIG_SH2_STAT3 | 199 | 202 | PF00017 | 0.539 |
LIG_SH2_STAT5 | 150 | 153 | PF00017 | 0.326 |
LIG_SH2_STAT5 | 199 | 202 | PF00017 | 0.558 |
LIG_SH2_STAT5 | 210 | 213 | PF00017 | 0.314 |
LIG_SH2_STAT5 | 222 | 225 | PF00017 | 0.313 |
LIG_SH2_STAT5 | 291 | 294 | PF00017 | 0.542 |
LIG_SH2_STAT5 | 372 | 375 | PF00017 | 0.582 |
LIG_SH2_STAT5 | 40 | 43 | PF00017 | 0.303 |
LIG_SH2_STAT5 | 505 | 508 | PF00017 | 0.338 |
LIG_SH2_STAT5 | 51 | 54 | PF00017 | 0.487 |
LIG_SH2_STAT5 | 58 | 61 | PF00017 | 0.326 |
LIG_SH3_2 | 536 | 541 | PF14604 | 0.753 |
LIG_SH3_3 | 218 | 224 | PF00018 | 0.316 |
LIG_SH3_3 | 258 | 264 | PF00018 | 0.366 |
LIG_SH3_3 | 482 | 488 | PF00018 | 0.287 |
LIG_SH3_3 | 533 | 539 | PF00018 | 0.640 |
LIG_SH3_3 | 60 | 66 | PF00018 | 0.274 |
LIG_SUMO_SIM_anti_2 | 157 | 162 | PF11976 | 0.361 |
LIG_SUMO_SIM_anti_2 | 164 | 170 | PF11976 | 0.377 |
LIG_SUMO_SIM_anti_2 | 212 | 217 | PF11976 | 0.374 |
LIG_SUMO_SIM_anti_2 | 392 | 398 | PF11976 | 0.315 |
LIG_SUMO_SIM_anti_2 | 426 | 431 | PF11976 | 0.336 |
LIG_SUMO_SIM_par_1 | 392 | 398 | PF11976 | 0.309 |
LIG_SUMO_SIM_par_1 | 428 | 434 | PF11976 | 0.290 |
LIG_SUMO_SIM_par_1 | 92 | 98 | PF11976 | 0.336 |
LIG_TRFH_1 | 40 | 44 | PF08558 | 0.367 |
LIG_TYR_ITIM | 43 | 48 | PF00017 | 0.341 |
LIG_UBA3_1 | 333 | 339 | PF00899 | 0.380 |
MOD_CK1_1 | 137 | 143 | PF00069 | 0.380 |
MOD_CK1_1 | 146 | 152 | PF00069 | 0.275 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.266 |
MOD_CK1_1 | 30 | 36 | PF00069 | 0.334 |
MOD_CK1_1 | 303 | 309 | PF00069 | 0.516 |
MOD_CK1_1 | 335 | 341 | PF00069 | 0.344 |
MOD_CK1_1 | 511 | 517 | PF00069 | 0.572 |
MOD_CK1_1 | 554 | 560 | PF00069 | 0.709 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.366 |
MOD_CK2_1 | 364 | 370 | PF00069 | 0.395 |
MOD_GlcNHglycan | 13 | 16 | PF01048 | 0.469 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.321 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.343 |
MOD_GlcNHglycan | 276 | 281 | PF01048 | 0.460 |
MOD_GlcNHglycan | 334 | 337 | PF01048 | 0.520 |
MOD_GlcNHglycan | 347 | 350 | PF01048 | 0.310 |
MOD_GlcNHglycan | 358 | 361 | PF01048 | 0.286 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.346 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.477 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.282 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.376 |
MOD_GSK3_1 | 267 | 274 | PF00069 | 0.537 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.559 |
MOD_GSK3_1 | 328 | 335 | PF00069 | 0.348 |
MOD_GSK3_1 | 339 | 346 | PF00069 | 0.346 |
MOD_GSK3_1 | 495 | 502 | PF00069 | 0.385 |
MOD_GSK3_1 | 567 | 574 | PF00069 | 0.709 |
MOD_N-GLC_1 | 328 | 333 | PF02516 | 0.551 |
MOD_N-GLC_1 | 495 | 500 | PF02516 | 0.320 |
MOD_NEK2_1 | 123 | 128 | PF00069 | 0.397 |
MOD_NEK2_1 | 154 | 159 | PF00069 | 0.294 |
MOD_NEK2_1 | 209 | 214 | PF00069 | 0.348 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.529 |
MOD_NEK2_1 | 337 | 342 | PF00069 | 0.347 |
MOD_NEK2_1 | 343 | 348 | PF00069 | 0.328 |
MOD_NEK2_1 | 364 | 369 | PF00069 | 0.398 |
MOD_NEK2_1 | 423 | 428 | PF00069 | 0.342 |
MOD_NEK2_1 | 495 | 500 | PF00069 | 0.332 |
MOD_NEK2_1 | 551 | 556 | PF00069 | 0.670 |
MOD_NEK2_1 | 72 | 77 | PF00069 | 0.299 |
MOD_NEK2_2 | 44 | 49 | PF00069 | 0.486 |
MOD_PIKK_1 | 198 | 204 | PF00454 | 0.596 |
MOD_PIKK_1 | 370 | 376 | PF00454 | 0.558 |
MOD_PIKK_1 | 95 | 101 | PF00454 | 0.411 |
MOD_PKA_2 | 267 | 273 | PF00069 | 0.551 |
MOD_PKA_2 | 508 | 514 | PF00069 | 0.477 |
MOD_Plk_1 | 19 | 25 | PF00069 | 0.259 |
MOD_Plk_1 | 343 | 349 | PF00069 | 0.332 |
MOD_Plk_1 | 495 | 501 | PF00069 | 0.342 |
MOD_Plk_2-3 | 284 | 290 | PF00069 | 0.677 |
MOD_Plk_4 | 102 | 108 | PF00069 | 0.326 |
MOD_Plk_4 | 123 | 129 | PF00069 | 0.372 |
MOD_Plk_4 | 146 | 152 | PF00069 | 0.294 |
MOD_Plk_4 | 154 | 160 | PF00069 | 0.257 |
MOD_Plk_4 | 238 | 244 | PF00069 | 0.340 |
MOD_Plk_4 | 247 | 253 | PF00069 | 0.365 |
MOD_Plk_4 | 296 | 302 | PF00069 | 0.529 |
MOD_Plk_4 | 305 | 311 | PF00069 | 0.477 |
MOD_Plk_4 | 349 | 355 | PF00069 | 0.314 |
MOD_Plk_4 | 364 | 370 | PF00069 | 0.368 |
MOD_Plk_4 | 390 | 396 | PF00069 | 0.325 |
MOD_Plk_4 | 425 | 431 | PF00069 | 0.323 |
MOD_Plk_4 | 44 | 50 | PF00069 | 0.377 |
MOD_Plk_4 | 59 | 65 | PF00069 | 0.265 |
MOD_Plk_4 | 80 | 86 | PF00069 | 0.275 |
MOD_ProDKin_1 | 143 | 149 | PF00069 | 0.334 |
MOD_ProDKin_1 | 328 | 334 | PF00069 | 0.392 |
MOD_SUMO_for_1 | 524 | 527 | PF00179 | 0.495 |
MOD_SUMO_rev_2 | 185 | 191 | PF00179 | 0.569 |
TRG_DiLeu_BaLyEn_6 | 457 | 462 | PF01217 | 0.318 |
TRG_DiLeu_BaLyEn_6 | 485 | 490 | PF01217 | 0.378 |
TRG_ENDOCYTIC_2 | 150 | 153 | PF00928 | 0.296 |
TRG_ENDOCYTIC_2 | 210 | 213 | PF00928 | 0.367 |
TRG_ENDOCYTIC_2 | 40 | 43 | PF00928 | 0.312 |
TRG_ENDOCYTIC_2 | 45 | 48 | PF00928 | 0.325 |
TRG_ENDOCYTIC_2 | 49 | 52 | PF00928 | 0.485 |
TRG_ENDOCYTIC_2 | 505 | 508 | PF00928 | 0.392 |
TRG_ENDOCYTIC_2 | 510 | 513 | PF00928 | 0.524 |
TRG_Pf-PMV_PEXEL_1 | 182 | 186 | PF00026 | 0.296 |
TRG_Pf-PMV_PEXEL_1 | 460 | 465 | PF00026 | 0.388 |
TRG_Pf-PMV_PEXEL_1 | 516 | 520 | PF00026 | 0.372 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6G0 | Leptomonas seymouri | 39% | 90% |
A0A0N1HT40 | Leptomonas seymouri | 74% | 100% |
A0A0N1HZC2 | Leptomonas seymouri | 30% | 92% |
A0A0N1IKC5 | Leptomonas seymouri | 49% | 95% |
A0A0N1PAX2 | Leptomonas seymouri | 22% | 100% |
A0A0N1PB63 | Leptomonas seymouri | 26% | 87% |
A0A0S4IIJ4 | Bodo saltans | 23% | 100% |
A0A0S4JR45 | Bodo saltans | 31% | 100% |
A0A1X0NKK0 | Trypanosomatidae | 32% | 95% |
A0A1X0NL32 | Trypanosomatidae | 33% | 92% |
A0A1X0NM09 | Trypanosomatidae | 33% | 94% |
A0A1X0NRW5 | Trypanosomatidae | 40% | 82% |
A0A1X0NV13 | Trypanosomatidae | 50% | 88% |
A0A1X0NV19 | Trypanosomatidae | 48% | 96% |
A0A1X0NV27 | Trypanosomatidae | 48% | 96% |
A0A1X0NVH8 | Trypanosomatidae | 45% | 87% |
A0A1X0NVM7 | Trypanosomatidae | 53% | 89% |
A0A1X0NWQ1 | Trypanosomatidae | 45% | 90% |
A0A1X0NZE6 | Trypanosomatidae | 32% | 96% |
A0A1X0NZU2 | Trypanosomatidae | 28% | 89% |
A0A1X0NZU5 | Trypanosomatidae | 33% | 98% |
A0A1X0NZW1 | Trypanosomatidae | 28% | 96% |
A0A1X0P0M7 | Trypanosomatidae | 32% | 97% |
A0A3Q8I7Y9 | Leishmania donovani | 88% | 100% |
A0A3Q8IF95 | Leishmania donovani | 28% | 91% |
A0A3Q8ISY9 | Leishmania donovani | 37% | 91% |
A0A3R7JPZ0 | Trypanosoma rangeli | 27% | 100% |
A0A3R7JSQ9 | Trypanosoma rangeli | 28% | 100% |
A0A3R7KKN8 | Trypanosoma rangeli | 30% | 96% |
A0A3R7MAQ7 | Trypanosoma rangeli | 35% | 81% |
A0A3R7N415 | Trypanosoma rangeli | 29% | 96% |
A0A3R7N921 | Trypanosoma rangeli | 28% | 100% |
A0A3R7R443 | Trypanosoma rangeli | 29% | 96% |
A0A3R7R6N6 | Trypanosoma rangeli | 28% | 100% |
A0A3S7WRJ4 | Leishmania donovani | 48% | 90% |
A0A3S7WRJ5 | Leishmania donovani | 40% | 82% |
A0A3S7WRL4 | Leishmania donovani | 84% | 92% |
A0A3S7WSR4 | Leishmania donovani | 46% | 95% |
A0A3S7WWU1 | Leishmania donovani | 27% | 87% |
A0A3S7XB11 | Leishmania donovani | 30% | 95% |
A0A422MSE4 | Trypanosoma rangeli | 47% | 100% |
A0A422MSP6 | Trypanosoma rangeli | 33% | 100% |
A0A422MST9 | Trypanosoma rangeli | 28% | 96% |
A0A422MU68 | Trypanosoma rangeli | 29% | 100% |
A4H6J0 | Leishmania braziliensis | 47% | 100% |
A4H6J1 | Leishmania braziliensis | 45% | 100% |
A4HC19 | Leishmania braziliensis | 27% | 89% |
A4HHG3 | Leishmania braziliensis | 30% | 89% |
A4HJW3 | Leishmania braziliensis | 38% | 90% |
A4HPE2 | Leishmania braziliensis | 30% | 94% |
A4HUX5 | Leishmania infantum | 48% | 90% |
A4HUX6 | Leishmania infantum | 41% | 82% |
A4HUX7 | Leishmania infantum | 83% | 92% |
A4HUX8 | Leishmania infantum | 83% | 98% |
A4HZF5 | Leishmania infantum | 28% | 91% |
A4HZJ4 | Leishmania infantum | 27% | 87% |
A4I7C5 | Leishmania infantum | 37% | 91% |
A4ICI3 | Leishmania infantum | 30% | 95% |
C9ZL97 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 97% |
C9ZL98 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 99% |
C9ZL99 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 97% |
C9ZLA0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 98% |
C9ZLA1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 97% |
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) | 44% | 100% |
C9ZTR8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 96% |
C9ZTR9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 98% |
C9ZTS1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 96% |
C9ZUT6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 97% |
D0A7H1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
D0AAQ2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 84% |
E8NHE1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 45% | 92% |
E9AGK5 | Leishmania infantum | 46% | 95% |
E9ANL0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 47% | 90% |
E9ANL1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 44% | 88% |
E9ANL2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
E9APJ3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 46% | 95% |
E9AT53 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 97% |
E9AVF1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 94% |
E9AVF2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 87% |
E9B2B8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 91% |
Q4Q1E4 | Leishmania major | 30% | 100% |
Q4Q5T8 | Leishmania major | 37% | 100% |
Q4QC27 | Leishmania major | 28% | 100% |
Q4QC28 | Leishmania major | 29% | 100% |
Q4QFY5 | Leishmania major | 46% | 100% |
Q4QH10 | Leishmania major | 86% | 100% |
Q4QH11 | Leishmania major | 86% | 100% |
Q4QH12 | Leishmania major | 86% | 100% |
Q4QH13 | Leishmania major | 86% | 100% |
Q4QH14 | Leishmania major | 42% | 100% |
Q4QH15 | Leishmania major | 47% | 100% |
V5B647 | Trypanosoma cruzi | 48% | 91% |
V5B983 | Trypanosoma cruzi | 32% | 98% |
V5BBB1 | Trypanosoma cruzi | 47% | 97% |
V5BFV8 | Trypanosoma cruzi | 30% | 86% |
V5BQY6 | Trypanosoma cruzi | 38% | 81% |
V5BVP0 | Trypanosoma cruzi | 47% | 97% |
V5DT25 | Trypanosoma cruzi | 54% | 93% |