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: 120 |
NetGPI | no | yes: 0, no: 120 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 113 |
GO:0110165 | cellular anatomical entity | 1 | 113 |
GO:0005737 | cytoplasm | 2 | 3 |
Related structures:
AlphaFold database: E9AVF2
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 53 |
GO:0022857 | transmembrane transporter activity | 2 | 53 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 232 | 234 | PF00675 | 0.313 |
CLV_NRD_NRD_1 | 252 | 254 | PF00675 | 0.307 |
CLV_NRD_NRD_1 | 28 | 30 | PF00675 | 0.356 |
CLV_NRD_NRD_1 | 41 | 43 | PF00675 | 0.244 |
CLV_NRD_NRD_1 | 479 | 481 | PF00675 | 0.364 |
CLV_NRD_NRD_1 | 572 | 574 | PF00675 | 0.561 |
CLV_PCSK_KEX2_1 | 232 | 234 | PF00082 | 0.316 |
CLV_PCSK_KEX2_1 | 41 | 43 | PF00082 | 0.297 |
CLV_PCSK_KEX2_1 | 441 | 443 | PF00082 | 0.605 |
CLV_PCSK_KEX2_1 | 572 | 574 | PF00082 | 0.538 |
CLV_PCSK_KEX2_1 | 618 | 620 | PF00082 | 0.351 |
CLV_PCSK_PC1ET2_1 | 441 | 443 | PF00082 | 0.605 |
CLV_PCSK_PC1ET2_1 | 618 | 620 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 177 | 181 | PF00082 | 0.364 |
CLV_PCSK_SKI1_1 | 462 | 466 | PF00082 | 0.351 |
CLV_PCSK_SKI1_1 | 480 | 484 | PF00082 | 0.301 |
CLV_PCSK_SKI1_1 | 508 | 512 | PF00082 | 0.526 |
CLV_PCSK_SKI1_1 | 642 | 646 | PF00082 | 0.511 |
DEG_APCC_DBOX_1 | 479 | 487 | PF00400 | 0.563 |
DEG_SPOP_SBC_1 | 189 | 193 | PF00917 | 0.227 |
DOC_CKS1_1 | 588 | 593 | PF01111 | 0.384 |
DOC_MAPK_DCC_7 | 508 | 517 | PF00069 | 0.340 |
DOC_MAPK_gen_1 | 167 | 175 | PF00069 | 0.521 |
DOC_MAPK_gen_1 | 290 | 298 | PF00069 | 0.338 |
DOC_MAPK_gen_1 | 41 | 47 | PF00069 | 0.454 |
DOC_MAPK_gen_1 | 480 | 488 | PF00069 | 0.466 |
DOC_MAPK_gen_1 | 569 | 578 | PF00069 | 0.430 |
DOC_MAPK_MEF2A_6 | 167 | 175 | PF00069 | 0.476 |
DOC_MAPK_MEF2A_6 | 290 | 298 | PF00069 | 0.301 |
DOC_MAPK_MEF2A_6 | 401 | 409 | PF00069 | 0.586 |
DOC_MAPK_MEF2A_6 | 481 | 490 | PF00069 | 0.480 |
DOC_MAPK_MEF2A_6 | 508 | 517 | PF00069 | 0.292 |
DOC_MAPK_MEF2A_6 | 569 | 578 | PF00069 | 0.429 |
DOC_PP1_RVXF_1 | 460 | 466 | PF00149 | 0.462 |
DOC_PP2B_LxvP_1 | 503 | 506 | PF13499 | 0.429 |
DOC_PP2B_LxvP_1 | 574 | 577 | PF13499 | 0.448 |
DOC_PP2B_PxIxI_1 | 512 | 518 | PF00149 | 0.393 |
DOC_PP4_FxxP_1 | 93 | 96 | PF00568 | 0.316 |
DOC_USP7_MATH_1 | 188 | 192 | PF00917 | 0.363 |
DOC_USP7_MATH_1 | 286 | 290 | PF00917 | 0.408 |
DOC_USP7_MATH_1 | 629 | 633 | PF00917 | 0.725 |
DOC_WW_Pin1_4 | 234 | 239 | PF00397 | 0.658 |
DOC_WW_Pin1_4 | 488 | 493 | PF00397 | 0.376 |
DOC_WW_Pin1_4 | 587 | 592 | PF00397 | 0.418 |
LIG_APCC_ABBA_1 | 515 | 520 | PF00400 | 0.370 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.536 |
LIG_BRCT_BRCA1_1 | 16 | 20 | PF00533 | 0.493 |
LIG_BRCT_BRCA1_1 | 183 | 187 | PF00533 | 0.458 |
LIG_BRCT_BRCA1_1 | 190 | 194 | PF00533 | 0.490 |
LIG_Clathr_ClatBox_1 | 348 | 352 | PF01394 | 0.570 |
LIG_Clathr_ClatBox_1 | 404 | 408 | PF01394 | 0.508 |
LIG_Clathr_ClatBox_1 | 516 | 520 | PF01394 | 0.377 |
LIG_deltaCOP1_diTrp_1 | 408 | 416 | PF00928 | 0.367 |
LIG_FHA_1 | 134 | 140 | PF00498 | 0.350 |
LIG_FHA_1 | 205 | 211 | PF00498 | 0.358 |
LIG_FHA_1 | 21 | 27 | PF00498 | 0.604 |
LIG_FHA_1 | 298 | 304 | PF00498 | 0.378 |
LIG_FHA_1 | 337 | 343 | PF00498 | 0.699 |
LIG_FHA_1 | 430 | 436 | PF00498 | 0.331 |
LIG_FHA_1 | 441 | 447 | PF00498 | 0.368 |
LIG_FHA_1 | 449 | 455 | PF00498 | 0.335 |
LIG_FHA_1 | 588 | 594 | PF00498 | 0.313 |
LIG_FHA_1 | 83 | 89 | PF00498 | 0.334 |
LIG_FHA_2 | 158 | 164 | PF00498 | 0.368 |
LIG_FHA_2 | 191 | 197 | PF00498 | 0.314 |
LIG_FHA_2 | 247 | 253 | PF00498 | 0.520 |
LIG_FHA_2 | 358 | 364 | PF00498 | 0.788 |
LIG_FHA_2 | 397 | 403 | PF00498 | 0.552 |
LIG_FHA_2 | 74 | 80 | PF00498 | 0.320 |
LIG_IRF3_LxIS_1 | 484 | 491 | PF10401 | 0.444 |
LIG_LIR_Gen_1 | 140 | 149 | PF02991 | 0.343 |
LIG_LIR_Gen_1 | 184 | 195 | PF02991 | 0.388 |
LIG_LIR_Gen_1 | 200 | 210 | PF02991 | 0.290 |
LIG_LIR_Gen_1 | 218 | 227 | PF02991 | 0.303 |
LIG_LIR_Gen_1 | 306 | 316 | PF02991 | 0.342 |
LIG_LIR_Gen_1 | 408 | 418 | PF02991 | 0.330 |
LIG_LIR_Gen_1 | 447 | 456 | PF02991 | 0.310 |
LIG_LIR_Gen_1 | 547 | 556 | PF02991 | 0.316 |
LIG_LIR_Gen_1 | 59 | 69 | PF02991 | 0.409 |
LIG_LIR_Gen_1 | 94 | 104 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 140 | 146 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 200 | 205 | PF02991 | 0.261 |
LIG_LIR_Nem_3 | 207 | 212 | PF02991 | 0.303 |
LIG_LIR_Nem_3 | 218 | 222 | PF02991 | 0.258 |
LIG_LIR_Nem_3 | 306 | 311 | PF02991 | 0.280 |
LIG_LIR_Nem_3 | 447 | 453 | PF02991 | 0.343 |
LIG_LIR_Nem_3 | 521 | 527 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 59 | 65 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 94 | 100 | PF02991 | 0.340 |
LIG_MAD2 | 481 | 489 | PF02301 | 0.514 |
LIG_MLH1_MIPbox_1 | 191 | 195 | PF16413 | 0.354 |
LIG_NRBOX | 410 | 416 | PF00104 | 0.264 |
LIG_Pex14_2 | 107 | 111 | PF04695 | 0.502 |
LIG_Pex14_2 | 205 | 209 | PF04695 | 0.362 |
LIG_Pex14_2 | 46 | 50 | PF04695 | 0.349 |
LIG_Pex14_2 | 532 | 536 | PF04695 | 0.548 |
LIG_Pex14_2 | 65 | 69 | PF04695 | 0.348 |
LIG_PTB_Apo_2 | 542 | 549 | PF02174 | 0.531 |
LIG_SH2_CRK | 143 | 147 | PF00017 | 0.266 |
LIG_SH2_CRK | 265 | 269 | PF00017 | 0.390 |
LIG_SH2_CRK | 97 | 101 | PF00017 | 0.313 |
LIG_SH2_SRC | 284 | 287 | PF00017 | 0.464 |
LIG_SH2_STAP1 | 251 | 255 | PF00017 | 0.623 |
LIG_SH2_STAP1 | 265 | 269 | PF00017 | 0.415 |
LIG_SH2_STAP1 | 450 | 454 | PF00017 | 0.376 |
LIG_SH2_STAP1 | 60 | 64 | PF00017 | 0.338 |
LIG_SH2_STAP1 | 613 | 617 | PF00017 | 0.549 |
LIG_SH2_STAP1 | 97 | 101 | PF00017 | 0.327 |
LIG_SH2_STAT3 | 389 | 392 | PF00017 | 0.673 |
LIG_SH2_STAT5 | 157 | 160 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 204 | 207 | PF00017 | 0.316 |
LIG_SH2_STAT5 | 226 | 229 | PF00017 | 0.495 |
LIG_SH2_STAT5 | 284 | 287 | PF00017 | 0.384 |
LIG_SH2_STAT5 | 403 | 406 | PF00017 | 0.533 |
LIG_SH2_STAT5 | 450 | 453 | PF00017 | 0.277 |
LIG_SH2_STAT5 | 471 | 474 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 92 | 95 | PF00017 | 0.306 |
LIG_SH2_STAT5 | 97 | 100 | PF00017 | 0.312 |
LIG_SH3_3 | 100 | 106 | PF00018 | 0.395 |
LIG_SH3_3 | 219 | 225 | PF00018 | 0.327 |
LIG_SH3_3 | 253 | 259 | PF00018 | 0.530 |
LIG_SH3_3 | 365 | 371 | PF00018 | 0.743 |
LIG_SH3_3 | 486 | 492 | PF00018 | 0.287 |
LIG_SH3_3 | 507 | 513 | PF00018 | 0.330 |
LIG_SH3_3 | 585 | 591 | PF00018 | 0.326 |
LIG_SUMO_SIM_anti_2 | 207 | 214 | PF11976 | 0.358 |
LIG_SUMO_SIM_anti_2 | 218 | 224 | PF11976 | 0.378 |
LIG_SUMO_SIM_anti_2 | 76 | 85 | PF11976 | 0.377 |
LIG_SUMO_SIM_par_1 | 135 | 140 | PF11976 | 0.357 |
LIG_SUMO_SIM_par_1 | 299 | 304 | PF11976 | 0.351 |
LIG_SUMO_SIM_par_1 | 590 | 596 | PF11976 | 0.345 |
LIG_TYR_ITIM | 141 | 146 | PF00017 | 0.311 |
LIG_TYR_ITIM | 95 | 100 | PF00017 | 0.322 |
LIG_UBA3_1 | 500 | 508 | PF00899 | 0.388 |
LIG_WRC_WIRS_1 | 206 | 211 | PF05994 | 0.203 |
LIG_WRC_WIRS_1 | 555 | 560 | PF05994 | 0.365 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.373 |
MOD_CK1_1 | 246 | 252 | PF00069 | 0.560 |
MOD_CK1_1 | 289 | 295 | PF00069 | 0.336 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.700 |
MOD_CK1_1 | 330 | 336 | PF00069 | 0.638 |
MOD_CK1_1 | 379 | 385 | PF00069 | 0.674 |
MOD_CK1_1 | 431 | 437 | PF00069 | 0.332 |
MOD_CK1_1 | 554 | 560 | PF00069 | 0.352 |
MOD_CK1_1 | 632 | 638 | PF00069 | 0.691 |
MOD_CK1_1 | 78 | 84 | PF00069 | 0.278 |
MOD_CK2_1 | 157 | 163 | PF00069 | 0.411 |
MOD_CK2_1 | 190 | 196 | PF00069 | 0.515 |
MOD_CK2_1 | 246 | 252 | PF00069 | 0.515 |
MOD_CK2_1 | 322 | 328 | PF00069 | 0.559 |
MOD_CK2_1 | 357 | 363 | PF00069 | 0.767 |
MOD_CK2_1 | 377 | 383 | PF00069 | 0.693 |
MOD_CK2_1 | 624 | 630 | PF00069 | 0.546 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.344 |
MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.432 |
MOD_GlcNHglycan | 328 | 332 | PF01048 | 0.464 |
MOD_GlcNHglycan | 363 | 367 | PF01048 | 0.519 |
MOD_GlcNHglycan | 446 | 449 | PF01048 | 0.470 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.383 |
MOD_GlcNHglycan | 626 | 629 | PF01048 | 0.324 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.353 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.648 |
MOD_GSK3_1 | 153 | 160 | PF00069 | 0.352 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.351 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.487 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.386 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.369 |
MOD_GSK3_1 | 358 | 365 | PF00069 | 0.717 |
MOD_GSK3_1 | 373 | 380 | PF00069 | 0.711 |
MOD_GSK3_1 | 427 | 434 | PF00069 | 0.420 |
MOD_GSK3_1 | 440 | 447 | PF00069 | 0.366 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.333 |
MOD_GSK3_1 | 583 | 590 | PF00069 | 0.373 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.320 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.334 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.313 |
MOD_N-GLC_1 | 373 | 378 | PF02516 | 0.562 |
MOD_N-GLC_1 | 428 | 433 | PF02516 | 0.557 |
MOD_N-GLC_1 | 544 | 549 | PF02516 | 0.438 |
MOD_NEK2_1 | 145 | 150 | PF00069 | 0.338 |
MOD_NEK2_1 | 182 | 187 | PF00069 | 0.383 |
MOD_NEK2_1 | 190 | 195 | PF00069 | 0.421 |
MOD_NEK2_1 | 205 | 210 | PF00069 | 0.297 |
MOD_NEK2_1 | 244 | 249 | PF00069 | 0.534 |
MOD_NEK2_1 | 303 | 308 | PF00069 | 0.326 |
MOD_NEK2_1 | 427 | 432 | PF00069 | 0.313 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.304 |
MOD_NEK2_1 | 535 | 540 | PF00069 | 0.524 |
MOD_NEK2_1 | 624 | 629 | PF00069 | 0.557 |
MOD_NEK2_1 | 73 | 78 | PF00069 | 0.351 |
MOD_NEK2_2 | 396 | 401 | PF00069 | 0.593 |
MOD_NEK2_2 | 544 | 549 | PF00069 | 0.497 |
MOD_OFUCOSY | 582 | 587 | PF10250 | 0.508 |
MOD_PIKK_1 | 18 | 24 | PF00454 | 0.635 |
MOD_PIKK_1 | 377 | 383 | PF00454 | 0.773 |
MOD_PIKK_1 | 68 | 74 | PF00454 | 0.326 |
MOD_PKA_2 | 289 | 295 | PF00069 | 0.324 |
MOD_PKA_2 | 3 | 9 | PF00069 | 0.496 |
MOD_PKA_2 | 358 | 364 | PF00069 | 0.788 |
MOD_PKA_2 | 624 | 630 | PF00069 | 0.583 |
MOD_Plk_1 | 153 | 159 | PF00069 | 0.321 |
MOD_Plk_1 | 428 | 434 | PF00069 | 0.326 |
MOD_Plk_1 | 544 | 550 | PF00069 | 0.438 |
MOD_Plk_1 | 78 | 84 | PF00069 | 0.264 |
MOD_Plk_4 | 153 | 159 | PF00069 | 0.332 |
MOD_Plk_4 | 182 | 188 | PF00069 | 0.371 |
MOD_Plk_4 | 190 | 196 | PF00069 | 0.444 |
MOD_Plk_4 | 205 | 211 | PF00069 | 0.253 |
MOD_Plk_4 | 215 | 221 | PF00069 | 0.256 |
MOD_Plk_4 | 246 | 252 | PF00069 | 0.548 |
MOD_Plk_4 | 297 | 303 | PF00069 | 0.341 |
MOD_Plk_4 | 544 | 550 | PF00069 | 0.323 |
MOD_Plk_4 | 551 | 557 | PF00069 | 0.300 |
MOD_Plk_4 | 593 | 599 | PF00069 | 0.296 |
MOD_Plk_4 | 78 | 84 | PF00069 | 0.324 |
MOD_Plk_4 | 95 | 101 | PF00069 | 0.375 |
MOD_ProDKin_1 | 234 | 240 | PF00069 | 0.657 |
MOD_ProDKin_1 | 488 | 494 | PF00069 | 0.376 |
MOD_ProDKin_1 | 587 | 593 | PF00069 | 0.386 |
MOD_SUMO_rev_2 | 246 | 256 | PF00179 | 0.548 |
TRG_DiLeu_BaEn_1 | 344 | 349 | PF01217 | 0.565 |
TRG_ENDOCYTIC_2 | 143 | 146 | PF00928 | 0.286 |
TRG_ENDOCYTIC_2 | 265 | 268 | PF00928 | 0.359 |
TRG_ENDOCYTIC_2 | 419 | 422 | PF00928 | 0.327 |
TRG_ENDOCYTIC_2 | 450 | 453 | PF00928 | 0.308 |
TRG_ENDOCYTIC_2 | 613 | 616 | PF00928 | 0.518 |
TRG_ENDOCYTIC_2 | 92 | 95 | PF00928 | 0.313 |
TRG_ENDOCYTIC_2 | 97 | 100 | PF00928 | 0.323 |
TRG_ER_diArg_1 | 166 | 169 | PF00400 | 0.564 |
TRG_ER_diArg_1 | 231 | 233 | PF00400 | 0.586 |
TRG_ER_diArg_1 | 40 | 42 | PF00400 | 0.466 |
TRG_ER_diArg_1 | 572 | 574 | PF00400 | 0.374 |
TRG_PTS2 | 1 | 19 | PF00400 | 0.494 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6G0 | Leptomonas seymouri | 25% | 100% |
A0A0N1HT40 | Leptomonas seymouri | 27% | 100% |
A0A0N1HZC2 | Leptomonas seymouri | 45% | 100% |
A0A0N1IKC5 | Leptomonas seymouri | 26% | 100% |
A0A0N1PB63 | Leptomonas seymouri | 66% | 100% |
A0A0N1PD04 | Leptomonas seymouri | 23% | 100% |
A0A0N1PFR4 | Leptomonas seymouri | 27% | 100% |
A0A0S4JR45 | Bodo saltans | 25% | 100% |
A0A1X0NKK0 | Trypanosomatidae | 49% | 100% |
A0A1X0NM09 | Trypanosomatidae | 48% | 100% |
A0A1X0NRW5 | Trypanosomatidae | 24% | 95% |
A0A1X0NV13 | Trypanosomatidae | 27% | 100% |
A0A1X0NV19 | Trypanosomatidae | 28% | 100% |
A0A1X0NV27 | Trypanosomatidae | 28% | 100% |
A0A1X0NVH8 | Trypanosomatidae | 25% | 100% |
A0A1X0NVM7 | Trypanosomatidae | 27% | 100% |
A0A1X0NWQ1 | Trypanosomatidae | 25% | 100% |
A0A1X0NZE6 | Trypanosomatidae | 27% | 100% |
A0A1X0NZU2 | Trypanosomatidae | 24% | 100% |
A0A1X0NZU5 | Trypanosomatidae | 27% | 100% |
A0A1X0NZW1 | Trypanosomatidae | 28% | 100% |
A0A1X0P0M7 | Trypanosomatidae | 26% | 100% |
A0A381MMW5 | Leishmania infantum | 26% | 100% |
A0A3Q8I7Y9 | Leishmania donovani | 26% | 100% |
A0A3Q8IEC4 | Leishmania donovani | 25% | 100% |
A0A3Q8IF95 | Leishmania donovani | 50% | 100% |
A0A3Q8IIT5 | Leishmania donovani | 26% | 98% |
A0A3Q8ISY9 | Leishmania donovani | 26% | 100% |
A0A3R7KKN8 | Trypanosoma rangeli | 26% | 100% |
A0A3R7MAQ7 | Trypanosoma rangeli | 24% | 94% |
A0A3R7N3S6 | Trypanosoma rangeli | 22% | 100% |
A0A3R7N415 | Trypanosoma rangeli | 26% | 100% |
A0A3R7N921 | Trypanosoma rangeli | 28% | 100% |
A0A3R7R443 | Trypanosoma rangeli | 24% | 100% |
A0A3S7WRJ4 | Leishmania donovani | 27% | 100% |
A0A3S7WRJ5 | Leishmania donovani | 26% | 95% |
A0A3S7WRL4 | Leishmania donovani | 27% | 100% |
A0A3S7WRS3 | Leishmania donovani | 22% | 100% |
A0A3S7WSR4 | Leishmania donovani | 26% | 100% |
A0A3S7WWU1 | Leishmania donovani | 88% | 100% |
A0A3S7X2G0 | Leishmania donovani | 25% | 100% |
A0A3S7X2K5 | Leishmania donovani | 25% | 100% |
A0A3S7XB11 | Leishmania donovani | 49% | 100% |
A0A422MSE4 | Trypanosoma rangeli | 29% | 100% |
A0A422MSP6 | Trypanosoma rangeli | 26% | 100% |
A0A422MST9 | Trypanosoma rangeli | 25% | 100% |
A0A422MU68 | Trypanosoma rangeli | 46% | 100% |
A4H6J0 | Leishmania braziliensis | 27% | 100% |
A4H6J1 | Leishmania braziliensis | 28% | 100% |
A4H6J3 | Leishmania braziliensis | 26% | 95% |
A4H6Q5 | Leishmania braziliensis | 22% | 98% |
A4HC19 | Leishmania braziliensis | 74% | 100% |
A4HHG2 | Leishmania braziliensis | 25% | 100% |
A4HHG3 | Leishmania braziliensis | 27% | 100% |
A4HHG4 | Leishmania braziliensis | 27% | 100% |
A4HJW3 | Leishmania braziliensis | 24% | 100% |
A4HPE2 | Leishmania braziliensis | 47% | 100% |
A4HUX5 | Leishmania infantum | 26% | 100% |
A4HUX6 | Leishmania infantum | 26% | 95% |
A4HUX7 | Leishmania infantum | 27% | 100% |
A4HUX8 | Leishmania infantum | 27% | 100% |
A4HV40 | Leishmania infantum | 22% | 100% |
A4HZF5 | Leishmania infantum | 50% | 100% |
A4HZJ4 | Leishmania infantum | 88% | 100% |
A4I4L2 | Leishmania infantum | 25% | 98% |
A4I7C5 | Leishmania infantum | 26% | 100% |
A4ICI3 | Leishmania infantum | 49% | 100% |
C9ZL97 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
C9ZL98 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
C9ZL99 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
C9ZLA0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
C9ZLA1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
C9ZTR5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
C9ZTR6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
C9ZTR7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
C9ZTR8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
C9ZTR9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
C9ZTS1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
C9ZUT6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
D0A7B1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 22% | 100% |
D0A7H1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
D0AAQ2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 97% |
E8NHE1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9AE01 | Leishmania major | 25% | 100% |
E9AE09 | Leishmania major | 24% | 100% |
E9AE10 | Leishmania major | 24% | 100% |
E9AE11 | Leishmania major | 26% | 100% |
E9AGK5 | Leishmania infantum | 26% | 100% |
E9AHJ0 | Leishmania infantum | 26% | 100% |
E9AHJ1 | Leishmania infantum | 25% | 100% |
E9ALS2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9ALS3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
E9ANL0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9ANL1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9ANL2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 97% |
E9ANS1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 22% | 100% |
E9APJ3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 99% |
E9AT53 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 47% | 96% |
E9AVF1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 49% | 99% |
E9B2B8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
Q4Q1E4 | Leishmania major | 48% | 99% |
Q4Q5T8 | Leishmania major | 25% | 100% |
Q4QC27 | Leishmania major | 88% | 100% |
Q4QC28 | Leishmania major | 48% | 97% |
Q4QFY5 | Leishmania major | 26% | 97% |
Q4QGU8 | Leishmania major | 21% | 100% |
Q4QH10 | Leishmania major | 25% | 95% |
Q4QH11 | Leishmania major | 26% | 91% |
Q4QH12 | Leishmania major | 26% | 91% |
Q4QH13 | Leishmania major | 26% | 91% |
Q4QH14 | Leishmania major | 25% | 100% |
Q4QH15 | Leishmania major | 26% | 100% |
V5B647 | Trypanosoma cruzi | 28% | 100% |
V5B983 | Trypanosoma cruzi | 27% | 100% |
V5BBB1 | Trypanosoma cruzi | 25% | 100% |
V5BFV8 | Trypanosoma cruzi | 25% | 99% |
V5BQY6 | Trypanosoma cruzi | 23% | 94% |
V5BVP0 | Trypanosoma cruzi | 26% | 100% |
V5DT25 | Trypanosoma cruzi | 28% | 100% |