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: 122 |
NetGPI | no | yes: 0, no: 122 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 115 |
GO:0110165 | cellular anatomical entity | 1 | 115 |
GO:0005737 | cytoplasm | 2 | 3 |
Related structures:
AlphaFold database: E9AVF1
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 54 |
GO:0022857 | transmembrane transporter activity | 2 | 54 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 17 | 19 | PF00675 | 0.343 |
CLV_NRD_NRD_1 | 247 | 249 | PF00675 | 0.300 |
CLV_NRD_NRD_1 | 457 | 459 | PF00675 | 0.413 |
CLV_NRD_NRD_1 | 548 | 550 | PF00675 | 0.530 |
CLV_NRD_NRD_1 | 600 | 602 | PF00675 | 0.415 |
CLV_PCSK_KEX2_1 | 17 | 19 | PF00082 | 0.336 |
CLV_PCSK_KEX2_1 | 247 | 249 | PF00082 | 0.301 |
CLV_PCSK_KEX2_1 | 456 | 458 | PF00082 | 0.365 |
CLV_PCSK_KEX2_1 | 600 | 602 | PF00082 | 0.413 |
CLV_PCSK_PC7_1 | 453 | 459 | PF00082 | 0.369 |
CLV_PCSK_PC7_1 | 596 | 602 | PF00082 | 0.453 |
CLV_PCSK_SKI1_1 | 165 | 169 | PF00082 | 0.371 |
CLV_PCSK_SKI1_1 | 437 | 441 | PF00082 | 0.335 |
CLV_PCSK_SKI1_1 | 457 | 461 | PF00082 | 0.395 |
CLV_PCSK_SKI1_1 | 485 | 489 | PF00082 | 0.527 |
CLV_PCSK_SKI1_1 | 537 | 541 | PF00082 | 0.323 |
DEG_SCF_FBW7_1 | 265 | 271 | PF00400 | 0.165 |
DOC_CKS1_1 | 265 | 270 | PF01111 | 0.174 |
DOC_CKS1_1 | 565 | 570 | PF01111 | 0.384 |
DOC_CYCLIN_RxL_1 | 546 | 556 | PF00134 | 0.367 |
DOC_CYCLIN_yClb1_LxF_4 | 535 | 540 | PF00134 | 0.337 |
DOC_MAPK_gen_1 | 155 | 163 | PF00069 | 0.517 |
DOC_MAPK_gen_1 | 222 | 231 | PF00069 | 0.516 |
DOC_MAPK_gen_1 | 453 | 461 | PF00069 | 0.567 |
DOC_MAPK_HePTP_8 | 534 | 546 | PF00069 | 0.208 |
DOC_MAPK_MEF2A_6 | 155 | 163 | PF00069 | 0.471 |
DOC_MAPK_MEF2A_6 | 278 | 286 | PF00069 | 0.296 |
DOC_MAPK_MEF2A_6 | 380 | 388 | PF00069 | 0.530 |
DOC_MAPK_MEF2A_6 | 537 | 546 | PF00069 | 0.453 |
DOC_PP1_RVXF_1 | 435 | 441 | PF00149 | 0.463 |
DOC_PP1_RVXF_1 | 483 | 490 | PF00149 | 0.401 |
DOC_PP1_RVXF_1 | 535 | 541 | PF00149 | 0.337 |
DOC_PP2B_LxvP_1 | 480 | 483 | PF13499 | 0.415 |
DOC_PP4_FxxP_1 | 466 | 469 | PF00568 | 0.391 |
DOC_SPAK_OSR1_1 | 30 | 34 | PF12202 | 0.518 |
DOC_USP7_MATH_1 | 268 | 272 | PF00917 | 0.445 |
DOC_USP7_MATH_1 | 311 | 315 | PF00917 | 0.534 |
DOC_WW_Pin1_4 | 264 | 269 | PF00397 | 0.308 |
DOC_WW_Pin1_4 | 354 | 359 | PF00397 | 0.770 |
DOC_WW_Pin1_4 | 392 | 397 | PF00397 | 0.449 |
DOC_WW_Pin1_4 | 465 | 470 | PF00397 | 0.379 |
DOC_WW_Pin1_4 | 564 | 569 | PF00397 | 0.404 |
LIG_14-3-3_CanoR_1 | 222 | 231 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 458 | 467 | PF00244 | 0.455 |
LIG_APCC_ABBA_1 | 540 | 545 | PF00400 | 0.365 |
LIG_BRCT_BRCA1_1 | 146 | 150 | PF00533 | 0.425 |
LIG_BRCT_BRCA1_1 | 171 | 175 | PF00533 | 0.466 |
LIG_BRCT_BRCA1_1 | 4 | 8 | PF00533 | 0.498 |
LIG_BRCT_BRCA1_1 | 85 | 89 | PF00533 | 0.321 |
LIG_DCNL_PONY_1 | 1 | 4 | PF03556 | 0.526 |
LIG_deltaCOP1_diTrp_1 | 383 | 392 | PF00928 | 0.370 |
LIG_FHA_1 | 107 | 113 | PF00498 | 0.293 |
LIG_FHA_1 | 141 | 147 | PF00498 | 0.315 |
LIG_FHA_1 | 233 | 239 | PF00498 | 0.484 |
LIG_FHA_1 | 256 | 262 | PF00498 | 0.306 |
LIG_FHA_1 | 265 | 271 | PF00498 | 0.337 |
LIG_FHA_1 | 405 | 411 | PF00498 | 0.335 |
LIG_FHA_1 | 419 | 425 | PF00498 | 0.284 |
LIG_FHA_1 | 460 | 466 | PF00498 | 0.314 |
LIG_FHA_1 | 47 | 53 | PF00498 | 0.353 |
LIG_FHA_1 | 524 | 530 | PF00498 | 0.299 |
LIG_FHA_1 | 565 | 571 | PF00498 | 0.314 |
LIG_FHA_1 | 71 | 77 | PF00498 | 0.342 |
LIG_FHA_1 | 94 | 100 | PF00498 | 0.420 |
LIG_FHA_2 | 146 | 152 | PF00498 | 0.374 |
LIG_FHA_2 | 344 | 350 | PF00498 | 0.781 |
LIG_FHA_2 | 372 | 378 | PF00498 | 0.573 |
LIG_FHA_2 | 553 | 559 | PF00498 | 0.250 |
LIG_FHA_2 | 606 | 612 | PF00498 | 0.605 |
LIG_GBD_Chelix_1 | 287 | 295 | PF00786 | 0.343 |
LIG_LIR_Gen_1 | 128 | 137 | PF02991 | 0.342 |
LIG_LIR_Gen_1 | 147 | 154 | PF02991 | 0.490 |
LIG_LIR_Gen_1 | 172 | 183 | PF02991 | 0.414 |
LIG_LIR_Gen_1 | 330 | 341 | PF02991 | 0.708 |
LIG_LIR_Gen_1 | 383 | 392 | PF02991 | 0.329 |
LIG_LIR_Gen_1 | 5 | 16 | PF02991 | 0.630 |
LIG_LIR_Gen_1 | 510 | 521 | PF02991 | 0.555 |
LIG_LIR_Gen_1 | 524 | 533 | PF02991 | 0.356 |
LIG_LIR_Gen_1 | 86 | 95 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 128 | 134 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 147 | 153 | PF02991 | 0.507 |
LIG_LIR_Nem_3 | 172 | 178 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 240 | 246 | PF02991 | 0.581 |
LIG_LIR_Nem_3 | 330 | 336 | PF02991 | 0.694 |
LIG_LIR_Nem_3 | 383 | 388 | PF02991 | 0.311 |
LIG_LIR_Nem_3 | 426 | 431 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 49 | 53 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 5 | 11 | PF02991 | 0.649 |
LIG_LIR_Nem_3 | 510 | 516 | PF02991 | 0.581 |
LIG_LIR_Nem_3 | 86 | 92 | PF02991 | 0.415 |
LIG_PALB2_WD40_1 | 3 | 11 | PF16756 | 0.459 |
LIG_PCNA_yPIPBox_3 | 536 | 550 | PF02747 | 0.423 |
LIG_Pex14_2 | 193 | 197 | PF04695 | 0.356 |
LIG_Pex14_2 | 509 | 513 | PF04695 | 0.558 |
LIG_Pex14_2 | 85 | 89 | PF04695 | 0.422 |
LIG_PTB_Apo_2 | 515 | 522 | PF02174 | 0.580 |
LIG_PTB_Phospho_1 | 515 | 521 | PF10480 | 0.408 |
LIG_SH2_CRK | 131 | 135 | PF00017 | 0.265 |
LIG_SH2_CRK | 253 | 257 | PF00017 | 0.381 |
LIG_SH2_CRK | 333 | 337 | PF00017 | 0.642 |
LIG_SH2_GRB2like | 215 | 218 | PF00017 | 0.408 |
LIG_SH2_NCK_1 | 325 | 329 | PF00017 | 0.477 |
LIG_SH2_NCK_1 | 333 | 337 | PF00017 | 0.505 |
LIG_SH2_SRC | 13 | 16 | PF00017 | 0.409 |
LIG_SH2_STAP1 | 239 | 243 | PF00017 | 0.614 |
LIG_SH2_STAP1 | 253 | 257 | PF00017 | 0.399 |
LIG_SH2_STAP1 | 425 | 429 | PF00017 | 0.387 |
LIG_SH2_STAP1 | 48 | 52 | PF00017 | 0.342 |
LIG_SH2_STAP1 | 53 | 57 | PF00017 | 0.189 |
LIG_SH2_STAP1 | 590 | 594 | PF00017 | 0.551 |
LIG_SH2_STAT3 | 53 | 56 | PF00017 | 0.259 |
LIG_SH2_STAT5 | 13 | 16 | PF00017 | 0.568 |
LIG_SH2_STAT5 | 145 | 148 | PF00017 | 0.386 |
LIG_SH2_STAT5 | 192 | 195 | PF00017 | 0.309 |
LIG_SH2_STAT5 | 272 | 275 | PF00017 | 0.367 |
LIG_SH2_STAT5 | 378 | 381 | PF00017 | 0.535 |
LIG_SH2_STAT5 | 425 | 428 | PF00017 | 0.298 |
LIG_SH2_STAT5 | 446 | 449 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 48 | 51 | PF00017 | 0.337 |
LIG_SH2_STAT5 | 491 | 494 | PF00017 | 0.318 |
LIG_SH2_STAT5 | 495 | 498 | PF00017 | 0.317 |
LIG_SH2_STAT5 | 53 | 56 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 543 | 546 | PF00017 | 0.293 |
LIG_SH3_1 | 365 | 371 | PF00018 | 0.590 |
LIG_SH3_3 | 262 | 268 | PF00018 | 0.309 |
LIG_SH3_3 | 365 | 371 | PF00018 | 0.584 |
LIG_SH3_3 | 41 | 47 | PF00018 | 0.470 |
LIG_SUMO_SIM_anti_2 | 205 | 212 | PF11976 | 0.382 |
LIG_SUMO_SIM_anti_2 | 227 | 233 | PF11976 | 0.587 |
LIG_SUMO_SIM_anti_2 | 526 | 531 | PF11976 | 0.271 |
LIG_TRAF2_1 | 225 | 228 | PF00917 | 0.475 |
LIG_TRAF2_1 | 555 | 558 | PF00917 | 0.348 |
LIG_TYR_ITIM | 251 | 256 | PF00017 | 0.379 |
LIG_UBA3_1 | 478 | 485 | PF00899 | 0.380 |
LIG_WRC_WIRS_1 | 513 | 518 | PF05994 | 0.578 |
MOD_CK1_1 | 271 | 277 | PF00069 | 0.335 |
MOD_CK1_1 | 357 | 363 | PF00069 | 0.760 |
MOD_CK1_1 | 406 | 412 | PF00069 | 0.344 |
MOD_CK1_1 | 418 | 424 | PF00069 | 0.341 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.330 |
MOD_CK2_1 | 145 | 151 | PF00069 | 0.423 |
MOD_CK2_1 | 222 | 228 | PF00069 | 0.503 |
MOD_CK2_1 | 311 | 317 | PF00069 | 0.473 |
MOD_CK2_1 | 552 | 558 | PF00069 | 0.252 |
MOD_CK2_1 | 605 | 611 | PF00069 | 0.599 |
MOD_Cter_Amidation | 454 | 457 | PF01082 | 0.418 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.534 |
MOD_GlcNHglycan | 137 | 140 | PF01048 | 0.354 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.365 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.292 |
MOD_GlcNHglycan | 453 | 456 | PF01048 | 0.445 |
MOD_GlcNHglycan | 62 | 66 | PF01048 | 0.510 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.358 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.345 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.303 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.648 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.361 |
MOD_GSK3_1 | 357 | 364 | PF00069 | 0.753 |
MOD_GSK3_1 | 399 | 406 | PF00069 | 0.427 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.325 |
MOD_GSK3_1 | 512 | 519 | PF00069 | 0.546 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.269 |
MOD_LATS_1 | 449 | 455 | PF00433 | 0.493 |
MOD_N-GLC_1 | 403 | 408 | PF02516 | 0.560 |
MOD_N-GLC_1 | 521 | 526 | PF02516 | 0.440 |
MOD_N-GLC_1 | 559 | 564 | PF02516 | 0.538 |
MOD_NEK2_1 | 112 | 117 | PF00069 | 0.303 |
MOD_NEK2_1 | 140 | 145 | PF00069 | 0.345 |
MOD_NEK2_1 | 170 | 175 | PF00069 | 0.397 |
MOD_NEK2_1 | 178 | 183 | PF00069 | 0.326 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.660 |
MOD_NEK2_1 | 232 | 237 | PF00069 | 0.504 |
MOD_NEK2_1 | 431 | 436 | PF00069 | 0.296 |
MOD_NEK2_1 | 507 | 512 | PF00069 | 0.389 |
MOD_NEK2_1 | 516 | 521 | PF00069 | 0.589 |
MOD_NEK2_1 | 52 | 57 | PF00069 | 0.336 |
MOD_NEK2_1 | 523 | 528 | PF00069 | 0.354 |
MOD_NEK2_1 | 551 | 556 | PF00069 | 0.383 |
MOD_NEK2_1 | 61 | 66 | PF00069 | 0.344 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.243 |
MOD_NEK2_2 | 125 | 130 | PF00069 | 0.298 |
MOD_NEK2_2 | 145 | 150 | PF00069 | 0.444 |
MOD_PIKK_1 | 52 | 58 | PF00454 | 0.295 |
MOD_PIKK_1 | 553 | 559 | PF00454 | 0.386 |
MOD_PIKK_1 | 6 | 12 | PF00454 | 0.613 |
MOD_PKA_2 | 232 | 238 | PF00069 | 0.531 |
MOD_PKB_1 | 220 | 228 | PF00069 | 0.580 |
MOD_Plk_1 | 141 | 147 | PF00069 | 0.323 |
MOD_Plk_1 | 348 | 354 | PF00069 | 0.776 |
MOD_Plk_1 | 521 | 527 | PF00069 | 0.440 |
MOD_Plk_1 | 559 | 565 | PF00069 | 0.304 |
MOD_Plk_1 | 66 | 72 | PF00069 | 0.263 |
MOD_Plk_4 | 141 | 147 | PF00069 | 0.332 |
MOD_Plk_4 | 170 | 176 | PF00069 | 0.370 |
MOD_Plk_4 | 178 | 184 | PF00069 | 0.436 |
MOD_Plk_4 | 255 | 261 | PF00069 | 0.317 |
MOD_Plk_4 | 268 | 274 | PF00069 | 0.447 |
MOD_Plk_4 | 286 | 292 | PF00069 | 0.347 |
MOD_Plk_4 | 371 | 377 | PF00069 | 0.559 |
MOD_Plk_4 | 516 | 522 | PF00069 | 0.539 |
MOD_ProDKin_1 | 264 | 270 | PF00069 | 0.308 |
MOD_ProDKin_1 | 354 | 360 | PF00069 | 0.769 |
MOD_ProDKin_1 | 392 | 398 | PF00069 | 0.449 |
MOD_ProDKin_1 | 465 | 471 | PF00069 | 0.379 |
MOD_ProDKin_1 | 564 | 570 | PF00069 | 0.386 |
TRG_DiLeu_BaEn_1 | 227 | 232 | PF01217 | 0.539 |
TRG_DiLeu_BaEn_4 | 227 | 233 | PF01217 | 0.539 |
TRG_DiLeu_BaLyEn_6 | 245 | 250 | PF01217 | 0.607 |
TRG_DiLeu_BaLyEn_6 | 534 | 539 | PF01217 | 0.301 |
TRG_ENDOCYTIC_2 | 131 | 134 | PF00928 | 0.284 |
TRG_ENDOCYTIC_2 | 253 | 256 | PF00928 | 0.358 |
TRG_ENDOCYTIC_2 | 333 | 336 | PF00928 | 0.501 |
TRG_ENDOCYTIC_2 | 425 | 428 | PF00928 | 0.317 |
TRG_ENDOCYTIC_2 | 543 | 546 | PF00928 | 0.347 |
TRG_ENDOCYTIC_2 | 590 | 593 | PF00928 | 0.526 |
TRG_ER_diArg_1 | 154 | 157 | PF00400 | 0.558 |
TRG_ER_diArg_1 | 219 | 222 | PF00400 | 0.572 |
TRG_ER_diArg_1 | 246 | 248 | PF00400 | 0.509 |
TRG_ER_diArg_1 | 456 | 458 | PF00400 | 0.572 |
TRG_ER_diArg_1 | 600 | 602 | PF00400 | 0.623 |
TRG_Pf-PMV_PEXEL_1 | 236 | 240 | PF00026 | 0.363 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6G0 | Leptomonas seymouri | 26% | 97% |
A0A0N1HT40 | Leptomonas seymouri | 28% | 100% |
A0A0N1HZC2 | Leptomonas seymouri | 42% | 98% |
A0A0N1IKC5 | Leptomonas seymouri | 30% | 100% |
A0A0N1PAX2 | Leptomonas seymouri | 56% | 100% |
A0A0N1PB63 | Leptomonas seymouri | 52% | 93% |
A0A0N1PD04 | Leptomonas seymouri | 22% | 96% |
A0A0N1PFR4 | Leptomonas seymouri | 26% | 93% |
A0A0S4JR45 | Bodo saltans | 25% | 100% |
A0A1X0NKK0 | Trypanosomatidae | 49% | 100% |
A0A1X0NL32 | Trypanosomatidae | 28% | 98% |
A0A1X0NM09 | Trypanosomatidae | 49% | 100% |
A0A1X0NRW5 | Trypanosomatidae | 24% | 88% |
A0A1X0NV13 | Trypanosomatidae | 29% | 94% |
A0A1X0NV19 | Trypanosomatidae | 30% | 100% |
A0A1X0NV27 | Trypanosomatidae | 30% | 100% |
A0A1X0NVH8 | Trypanosomatidae | 26% | 93% |
A0A1X0NVM7 | Trypanosomatidae | 29% | 95% |
A0A1X0NWQ1 | Trypanosomatidae | 25% | 96% |
A0A1X0NZE6 | Trypanosomatidae | 27% | 100% |
A0A1X0NZU2 | Trypanosomatidae | 26% | 95% |
A0A1X0NZU5 | Trypanosomatidae | 27% | 100% |
A0A1X0NZW1 | Trypanosomatidae | 27% | 100% |
A0A1X0P0M7 | Trypanosomatidae | 26% | 100% |
A0A381MMW5 | Leishmania infantum | 27% | 94% |
A0A3Q8I7Y9 | Leishmania donovani | 29% | 100% |
A0A3Q8IEC4 | Leishmania donovani | 27% | 95% |
A0A3Q8IF95 | Leishmania donovani | 88% | 97% |
A0A3Q8IIT5 | Leishmania donovani | 25% | 91% |
A0A3Q8ISY9 | Leishmania donovani | 26% | 97% |
A0A3R7JSQ9 | Trypanosoma rangeli | 27% | 100% |
A0A3R7KKN8 | Trypanosoma rangeli | 26% | 100% |
A0A3R7MAQ7 | Trypanosoma rangeli | 23% | 87% |
A0A3R7N3S6 | Trypanosoma rangeli | 22% | 95% |
A0A3R7N415 | Trypanosoma rangeli | 29% | 100% |
A0A3R7N921 | Trypanosoma rangeli | 30% | 100% |
A0A3R7R443 | Trypanosoma rangeli | 27% | 100% |
A0A3S7WRJ4 | Leishmania donovani | 29% | 96% |
A0A3S7WRJ5 | Leishmania donovani | 29% | 88% |
A0A3S7WRL4 | Leishmania donovani | 29% | 99% |
A0A3S7WRS3 | Leishmania donovani | 21% | 98% |
A0A3S7WSR4 | Leishmania donovani | 29% | 100% |
A0A3S7WWU1 | Leishmania donovani | 51% | 92% |
A0A3S7X2G0 | Leishmania donovani | 27% | 94% |
A0A3S7X2K5 | Leishmania donovani | 25% | 100% |
A0A3S7XB11 | Leishmania donovani | 43% | 100% |
A0A422MSE4 | Trypanosoma rangeli | 30% | 100% |
A0A422MSP6 | Trypanosoma rangeli | 26% | 100% |
A0A422MST9 | Trypanosoma rangeli | 27% | 100% |
A0A422MU68 | Trypanosoma rangeli | 48% | 100% |
A4H6J0 | Leishmania braziliensis | 28% | 100% |
A4H6J1 | Leishmania braziliensis | 30% | 100% |
A4H6J3 | Leishmania braziliensis | 28% | 100% |
A4H6Q5 | Leishmania braziliensis | 21% | 100% |
A4HC19 | Leishmania braziliensis | 50% | 100% |
A4HHG2 | Leishmania braziliensis | 24% | 91% |
A4HHG3 | Leishmania braziliensis | 26% | 100% |
A4HHG4 | Leishmania braziliensis | 26% | 100% |
A4HJW3 | Leishmania braziliensis | 27% | 100% |
A4HPE2 | Leishmania braziliensis | 45% | 100% |
A4HUX5 | Leishmania infantum | 29% | 96% |
A4HUX6 | Leishmania infantum | 28% | 88% |
A4HUX7 | Leishmania infantum | 30% | 99% |
A4HUX8 | Leishmania infantum | 29% | 100% |
A4HV40 | Leishmania infantum | 21% | 98% |
A4HZF5 | Leishmania infantum | 88% | 97% |
A4HZJ4 | Leishmania infantum | 51% | 92% |
A4I4L2 | Leishmania infantum | 25% | 91% |
A4I7C5 | Leishmania infantum | 26% | 97% |
A4ICI3 | Leishmania infantum | 43% | 100% |
C9ZL97 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
C9ZL98 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
C9ZL99 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 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) | 30% | 100% |
C9ZTR6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZTR7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
C9ZTR8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
C9ZTR9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
C9ZTS1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
C9ZUT6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
D0A7H1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
D0AAQ2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 90% |
E8NHE1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9AE01 | Leishmania major | 26% | 100% |
E9AE09 | Leishmania major | 25% | 91% |
E9AE10 | Leishmania major | 25% | 91% |
E9AE11 | Leishmania major | 26% | 100% |
E9AGK5 | Leishmania infantum | 29% | 100% |
E9AHJ0 | Leishmania infantum | 27% | 95% |
E9AHJ1 | Leishmania infantum | 25% | 100% |
E9ALS2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9ALS3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 91% |
E9ANL0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9ANL1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9ANL2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9ANS1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 100% |
E9APJ3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9AT53 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 43% | 99% |
E9AVF2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 49% | 93% |
E9B2B8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 97% |
Q4Q1E4 | Leishmania major | 42% | 100% |
Q4Q5T8 | Leishmania major | 26% | 100% |
Q4QC27 | Leishmania major | 50% | 100% |
Q4QC28 | Leishmania major | 85% | 98% |
Q4QFY5 | Leishmania major | 30% | 100% |
Q4QGU8 | Leishmania major | 20% | 100% |
Q4QH10 | Leishmania major | 29% | 99% |
Q4QH11 | Leishmania major | 29% | 96% |
Q4QH12 | Leishmania major | 29% | 96% |
Q4QH13 | Leishmania major | 29% | 96% |
Q4QH14 | Leishmania major | 28% | 100% |
Q4QH15 | Leishmania major | 29% | 100% |
V5B647 | Trypanosoma cruzi | 28% | 97% |
V5B983 | Trypanosoma cruzi | 28% | 100% |
V5BBB1 | Trypanosoma cruzi | 27% | 100% |
V5BFV8 | Trypanosoma cruzi | 27% | 92% |
V5BQY6 | Trypanosoma cruzi | 25% | 87% |
V5BVP0 | Trypanosoma cruzi | 26% | 100% |
V5DT25 | Trypanosoma cruzi | 27% | 100% |