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: 123 |
NetGPI | no | yes: 0, no: 123 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 116 |
GO:0110165 | cellular anatomical entity | 1 | 116 |
GO:0005737 | cytoplasm | 2 | 3 |
Related structures:
AlphaFold database: A4HPE2
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 55 |
GO:0022857 | transmembrane transporter activity | 2 | 55 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 248 | 250 | PF00675 | 0.258 |
CLV_NRD_NRD_1 | 331 | 333 | PF00675 | 0.551 |
CLV_NRD_NRD_1 | 464 | 466 | PF00675 | 0.369 |
CLV_PCSK_KEX2_1 | 248 | 250 | PF00082 | 0.270 |
CLV_PCSK_KEX2_1 | 30 | 32 | PF00082 | 0.286 |
CLV_PCSK_PC1ET2_1 | 30 | 32 | PF00082 | 0.323 |
CLV_PCSK_SKI1_1 | 166 | 170 | PF00082 | 0.358 |
CLV_PCSK_SKI1_1 | 181 | 185 | PF00082 | 0.465 |
CLV_PCSK_SKI1_1 | 465 | 469 | PF00082 | 0.302 |
CLV_PCSK_SKI1_1 | 545 | 549 | PF00082 | 0.317 |
CLV_PCSK_SKI1_1 | 600 | 604 | PF00082 | 0.360 |
DEG_APCC_DBOX_1 | 464 | 472 | PF00400 | 0.565 |
DEG_APCC_DBOX_1 | 605 | 613 | PF00400 | 0.451 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.706 |
DOC_ANK_TNKS_1 | 157 | 164 | PF00023 | 0.549 |
DOC_CKS1_1 | 573 | 578 | PF01111 | 0.382 |
DOC_CKS1_1 | 605 | 610 | PF01111 | 0.439 |
DOC_CYCLIN_yCln2_LP_2 | 495 | 501 | PF00134 | 0.245 |
DOC_MAPK_gen_1 | 156 | 164 | PF00069 | 0.513 |
DOC_MAPK_gen_1 | 465 | 473 | PF00069 | 0.463 |
DOC_MAPK_MEF2A_6 | 156 | 164 | PF00069 | 0.469 |
DOC_MAPK_MEF2A_6 | 391 | 398 | PF00069 | 0.530 |
DOC_MAPK_MEF2A_6 | 465 | 473 | PF00069 | 0.470 |
DOC_MAPK_RevD_3 | 234 | 249 | PF00069 | 0.462 |
DOC_PP1_RVXF_1 | 511 | 518 | PF00149 | 0.394 |
DOC_PP2B_LxvP_1 | 488 | 491 | PF13499 | 0.403 |
DOC_PP2B_PxIxI_1 | 497 | 503 | PF00149 | 0.377 |
DOC_PP2B_PxIxI_1 | 575 | 581 | PF00149 | 0.384 |
DOC_PP4_FxxP_1 | 82 | 85 | PF00568 | 0.311 |
DOC_USP7_MATH_1 | 232 | 236 | PF00917 | 0.487 |
DOC_USP7_MATH_2 | 311 | 317 | PF00917 | 0.735 |
DOC_USP7_UBL2_3 | 554 | 558 | PF12436 | 0.402 |
DOC_WW_Pin1_4 | 350 | 355 | PF00397 | 0.756 |
DOC_WW_Pin1_4 | 458 | 463 | PF00397 | 0.516 |
DOC_WW_Pin1_4 | 572 | 577 | PF00397 | 0.405 |
DOC_WW_Pin1_4 | 604 | 609 | PF00397 | 0.614 |
LIG_14-3-3_CanoR_1 | 425 | 434 | PF00244 | 0.378 |
LIG_14-3-3_CanoR_1 | 447 | 451 | PF00244 | 0.301 |
LIG_14-3-3_CanoR_1 | 600 | 609 | PF00244 | 0.587 |
LIG_14-3-3_CanoR_1 | 61 | 69 | PF00244 | 0.337 |
LIG_AP2alpha_1 | 54 | 58 | PF02296 | 0.265 |
LIG_APCC_ABBA_1 | 500 | 505 | PF00400 | 0.369 |
LIG_APCC_ABBA_1 | 51 | 56 | PF00400 | 0.359 |
LIG_BIR_III_4 | 321 | 325 | PF00653 | 0.715 |
LIG_BRCT_BRCA1_1 | 138 | 142 | PF00533 | 0.387 |
LIG_BRCT_BRCA1_1 | 315 | 319 | PF00533 | 0.701 |
LIG_BRCT_BRCA1_1 | 45 | 49 | PF00533 | 0.338 |
LIG_BRCT_BRCA1_1 | 54 | 58 | PF00533 | 0.266 |
LIG_Clathr_ClatBox_1 | 366 | 370 | PF01394 | 0.793 |
LIG_Clathr_ClatBox_1 | 501 | 505 | PF01394 | 0.376 |
LIG_deltaCOP1_diTrp_1 | 393 | 401 | PF00928 | 0.361 |
LIG_FHA_1 | 10 | 16 | PF00498 | 0.567 |
LIG_FHA_1 | 103 | 109 | PF00498 | 0.280 |
LIG_FHA_1 | 123 | 129 | PF00498 | 0.304 |
LIG_FHA_1 | 197 | 203 | PF00498 | 0.359 |
LIG_FHA_1 | 265 | 271 | PF00498 | 0.326 |
LIG_FHA_1 | 286 | 292 | PF00498 | 0.368 |
LIG_FHA_1 | 415 | 421 | PF00498 | 0.329 |
LIG_FHA_1 | 426 | 432 | PF00498 | 0.342 |
LIG_FHA_1 | 434 | 440 | PF00498 | 0.323 |
LIG_FHA_1 | 468 | 474 | PF00498 | 0.464 |
LIG_FHA_1 | 533 | 539 | PF00498 | 0.292 |
LIG_FHA_1 | 573 | 579 | PF00498 | 0.308 |
LIG_FHA_1 | 581 | 587 | PF00498 | 0.391 |
LIG_FHA_1 | 72 | 78 | PF00498 | 0.332 |
LIG_FHA_2 | 147 | 153 | PF00498 | 0.339 |
LIG_FHA_2 | 316 | 322 | PF00498 | 0.615 |
LIG_FHA_2 | 336 | 342 | PF00498 | 0.767 |
LIG_FHA_2 | 343 | 349 | PF00498 | 0.759 |
LIG_FHA_2 | 382 | 388 | PF00498 | 0.577 |
LIG_GBD_Chelix_1 | 204 | 212 | PF00786 | 0.431 |
LIG_GBD_Chelix_1 | 482 | 490 | PF00786 | 0.226 |
LIG_LIR_Apic_2 | 603 | 608 | PF02991 | 0.427 |
LIG_LIR_Gen_1 | 189 | 198 | PF02991 | 0.284 |
LIG_LIR_Gen_1 | 38 | 48 | PF02991 | 0.332 |
LIG_LIR_Gen_1 | 384 | 394 | PF02991 | 0.512 |
LIG_LIR_Gen_1 | 433 | 441 | PF02991 | 0.298 |
LIG_LIR_Nem_3 | 129 | 134 | PF02991 | 0.296 |
LIG_LIR_Nem_3 | 189 | 194 | PF02991 | 0.257 |
LIG_LIR_Nem_3 | 38 | 43 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 384 | 389 | PF02991 | 0.526 |
LIG_LIR_Nem_3 | 393 | 398 | PF02991 | 0.306 |
LIG_LIR_Nem_3 | 433 | 438 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 506 | 512 | PF02991 | 0.398 |
LIG_MAD2 | 466 | 474 | PF02301 | 0.555 |
LIG_Pex14_2 | 216 | 220 | PF04695 | 0.408 |
LIG_Pex14_2 | 5 | 9 | PF04695 | 0.631 |
LIG_Pex14_2 | 517 | 521 | PF04695 | 0.554 |
LIG_Pex14_2 | 54 | 58 | PF04695 | 0.301 |
LIG_PTB_Apo_2 | 527 | 534 | PF02174 | 0.529 |
LIG_SH2_CRK | 252 | 256 | PF00017 | 0.371 |
LIG_SH2_CRK | 273 | 277 | PF00017 | 0.317 |
LIG_SH2_CRK | 605 | 609 | PF00017 | 0.510 |
LIG_SH2_CRK | 86 | 90 | PF00017 | 0.309 |
LIG_SH2_NCK_1 | 273 | 277 | PF00017 | 0.318 |
LIG_SH2_NCK_1 | 90 | 94 | PF00017 | 0.371 |
LIG_SH2_PTP2 | 254 | 257 | PF00017 | 0.330 |
LIG_SH2_PTP2 | 499 | 502 | PF00017 | 0.356 |
LIG_SH2_SRC | 90 | 93 | PF00017 | 0.528 |
LIG_SH2_STAP1 | 240 | 244 | PF00017 | 0.560 |
LIG_SH2_STAP1 | 435 | 439 | PF00017 | 0.366 |
LIG_SH2_STAP1 | 598 | 602 | PF00017 | 0.544 |
LIG_SH2_STAT5 | 14 | 17 | PF00017 | 0.566 |
LIG_SH2_STAT5 | 193 | 196 | PF00017 | 0.310 |
LIG_SH2_STAT5 | 215 | 218 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 254 | 257 | PF00017 | 0.329 |
LIG_SH2_STAT5 | 273 | 276 | PF00017 | 0.277 |
LIG_SH2_STAT5 | 419 | 422 | PF00017 | 0.298 |
LIG_SH2_STAT5 | 435 | 438 | PF00017 | 0.266 |
LIG_SH2_STAT5 | 456 | 459 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 499 | 502 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 503 | 506 | PF00017 | 0.311 |
LIG_SH2_STAT5 | 7 | 10 | PF00017 | 0.600 |
LIG_SH2_STAT5 | 81 | 84 | PF00017 | 0.304 |
LIG_SH3_3 | 305 | 311 | PF00018 | 0.581 |
LIG_SH3_3 | 373 | 379 | PF00018 | 0.600 |
LIG_SH3_3 | 471 | 477 | PF00018 | 0.286 |
LIG_SH3_3 | 570 | 576 | PF00018 | 0.313 |
LIG_SUMO_SIM_anti_2 | 146 | 152 | PF11976 | 0.355 |
LIG_SUMO_SIM_anti_2 | 575 | 581 | PF11976 | 0.367 |
LIG_SUMO_SIM_par_1 | 146 | 152 | PF11976 | 0.238 |
LIG_SUMO_SIM_par_1 | 198 | 203 | PF11976 | 0.338 |
LIG_SUMO_SIM_par_1 | 325 | 330 | PF11976 | 0.563 |
LIG_SUMO_SIM_par_1 | 365 | 370 | PF11976 | 0.576 |
LIG_SUMO_SIM_par_1 | 575 | 581 | PF11976 | 0.334 |
LIG_TYR_ITIM | 250 | 255 | PF00017 | 0.371 |
LIG_TYR_ITIM | 271 | 276 | PF00017 | 0.284 |
LIG_TYR_ITIM | 79 | 84 | PF00017 | 0.298 |
LIG_TYR_ITIM | 88 | 93 | PF00017 | 0.317 |
LIG_UBA3_1 | 547 | 554 | PF00899 | 0.449 |
LIG_WRC_WIRS_1 | 2 | 7 | PF05994 | 0.485 |
MOD_CDK_SPxK_1 | 604 | 610 | PF00069 | 0.437 |
MOD_CDK_SPxxK_3 | 458 | 465 | PF00069 | 0.592 |
MOD_CDK_SPxxK_3 | 604 | 611 | PF00069 | 0.443 |
MOD_CK1_1 | 146 | 152 | PF00069 | 0.347 |
MOD_CK1_1 | 174 | 180 | PF00069 | 0.359 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.500 |
MOD_CK1_1 | 353 | 359 | PF00069 | 0.753 |
MOD_CK1_1 | 433 | 439 | PF00069 | 0.356 |
MOD_CK1_1 | 532 | 538 | PF00069 | 0.344 |
MOD_CK1_1 | 70 | 76 | PF00069 | 0.322 |
MOD_CK2_1 | 146 | 152 | PF00069 | 0.388 |
MOD_CK2_1 | 335 | 341 | PF00069 | 0.741 |
MOD_CK2_1 | 342 | 348 | PF00069 | 0.751 |
MOD_CK2_1 | 381 | 387 | PF00069 | 0.546 |
MOD_Cter_Amidation | 330 | 333 | PF01082 | 0.377 |
MOD_GlcNHglycan | 138 | 141 | PF01048 | 0.342 |
MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.453 |
MOD_GlcNHglycan | 442 | 445 | PF01048 | 0.297 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.651 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.304 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.339 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.228 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.279 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.333 |
MOD_GSK3_1 | 381 | 388 | PF00069 | 0.588 |
MOD_GSK3_1 | 409 | 416 | PF00069 | 0.408 |
MOD_GSK3_1 | 585 | 592 | PF00069 | 0.367 |
MOD_GSK3_1 | 600 | 607 | PF00069 | 0.547 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.269 |
MOD_N-GLC_1 | 186 | 191 | PF02516 | 0.460 |
MOD_N-GLC_1 | 223 | 228 | PF02516 | 0.168 |
MOD_N-GLC_1 | 413 | 418 | PF02516 | 0.550 |
MOD_N-GLC_1 | 529 | 534 | PF02516 | 0.437 |
MOD_N-GLC_1 | 62 | 67 | PF02516 | 0.504 |
MOD_N-GLC_2 | 136 | 138 | PF02516 | 0.357 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.662 |
MOD_NEK2_1 | 134 | 139 | PF00069 | 0.337 |
MOD_NEK2_1 | 171 | 176 | PF00069 | 0.379 |
MOD_NEK2_1 | 196 | 201 | PF00069 | 0.287 |
MOD_NEK2_1 | 263 | 268 | PF00069 | 0.322 |
MOD_NEK2_1 | 271 | 276 | PF00069 | 0.259 |
MOD_NEK2_1 | 291 | 296 | PF00069 | 0.318 |
MOD_NEK2_1 | 35 | 40 | PF00069 | 0.299 |
MOD_NEK2_1 | 9 | 14 | PF00069 | 0.563 |
MOD_NEK2_2 | 126 | 131 | PF00069 | 0.285 |
MOD_NEK2_2 | 232 | 237 | PF00069 | 0.502 |
MOD_PIKK_1 | 600 | 606 | PF00454 | 0.514 |
MOD_PIKK_1 | 7 | 13 | PF00454 | 0.593 |
MOD_PKA_2 | 446 | 452 | PF00069 | 0.330 |
MOD_PKB_1 | 221 | 229 | PF00069 | 0.512 |
MOD_Plk_1 | 362 | 368 | PF00069 | 0.685 |
MOD_Plk_1 | 529 | 535 | PF00069 | 0.437 |
MOD_Plk_1 | 67 | 73 | PF00069 | 0.259 |
MOD_Plk_4 | 143 | 149 | PF00069 | 0.326 |
MOD_Plk_4 | 171 | 177 | PF00069 | 0.365 |
MOD_Plk_4 | 196 | 202 | PF00069 | 0.252 |
MOD_Plk_4 | 235 | 241 | PF00069 | 0.490 |
MOD_Plk_4 | 291 | 297 | PF00069 | 0.357 |
MOD_Plk_4 | 35 | 41 | PF00069 | 0.302 |
MOD_Plk_4 | 362 | 368 | PF00069 | 0.773 |
MOD_Plk_4 | 381 | 387 | PF00069 | 0.558 |
MOD_Plk_4 | 406 | 412 | PF00069 | 0.341 |
MOD_Plk_4 | 414 | 420 | PF00069 | 0.306 |
MOD_Plk_4 | 43 | 49 | PF00069 | 0.311 |
MOD_Plk_4 | 430 | 436 | PF00069 | 0.252 |
MOD_Plk_4 | 585 | 591 | PF00069 | 0.276 |
MOD_ProDKin_1 | 350 | 356 | PF00069 | 0.755 |
MOD_ProDKin_1 | 458 | 464 | PF00069 | 0.519 |
MOD_ProDKin_1 | 572 | 578 | PF00069 | 0.384 |
MOD_ProDKin_1 | 604 | 610 | PF00069 | 0.618 |
MOD_SUMO_rev_2 | 27 | 32 | PF00179 | 0.510 |
TRG_ENDOCYTIC_2 | 132 | 135 | PF00928 | 0.278 |
TRG_ENDOCYTIC_2 | 193 | 196 | PF00928 | 0.311 |
TRG_ENDOCYTIC_2 | 252 | 255 | PF00928 | 0.357 |
TRG_ENDOCYTIC_2 | 273 | 276 | PF00928 | 0.259 |
TRG_ENDOCYTIC_2 | 435 | 438 | PF00928 | 0.299 |
TRG_ENDOCYTIC_2 | 499 | 502 | PF00928 | 0.355 |
TRG_ENDOCYTIC_2 | 598 | 601 | PF00928 | 0.520 |
TRG_ENDOCYTIC_2 | 81 | 84 | PF00928 | 0.309 |
TRG_ENDOCYTIC_2 | 86 | 89 | PF00928 | 0.318 |
TRG_ENDOCYTIC_2 | 90 | 93 | PF00928 | 0.482 |
TRG_ER_diArg_1 | 155 | 158 | PF00400 | 0.526 |
TRG_ER_diArg_1 | 220 | 223 | PF00400 | 0.509 |
TRG_ER_diArg_1 | 247 | 249 | PF00400 | 0.458 |
TRG_ER_diLys_1 | 610 | 614 | PF00400 | 0.491 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6G0 | Leptomonas seymouri | 28% | 97% |
A0A0N1HT40 | Leptomonas seymouri | 30% | 100% |
A0A0N1HZC2 | Leptomonas seymouri | 72% | 98% |
A0A0N1IKC5 | Leptomonas seymouri | 32% | 100% |
A0A0N1PAX2 | Leptomonas seymouri | 39% | 100% |
A0A0N1PB63 | Leptomonas seymouri | 47% | 93% |
A0A0N1PD04 | Leptomonas seymouri | 24% | 96% |
A0A0N1PFR4 | Leptomonas seymouri | 29% | 93% |
A0A0S4JR45 | Bodo saltans | 25% | 100% |
A0A1X0NKK0 | Trypanosomatidae | 54% | 100% |
A0A1X0NL32 | Trypanosomatidae | 30% | 98% |
A0A1X0NM09 | Trypanosomatidae | 54% | 100% |
A0A1X0NRW5 | Trypanosomatidae | 26% | 88% |
A0A1X0NV13 | Trypanosomatidae | 31% | 94% |
A0A1X0NV19 | Trypanosomatidae | 32% | 100% |
A0A1X0NV27 | Trypanosomatidae | 30% | 100% |
A0A1X0NVH8 | Trypanosomatidae | 30% | 93% |
A0A1X0NVM7 | Trypanosomatidae | 30% | 95% |
A0A1X0NWQ1 | Trypanosomatidae | 29% | 96% |
A0A1X0NZE6 | Trypanosomatidae | 32% | 100% |
A0A1X0NZU2 | Trypanosomatidae | 28% | 95% |
A0A1X0NZU5 | Trypanosomatidae | 30% | 100% |
A0A1X0NZW1 | Trypanosomatidae | 29% | 100% |
A0A1X0P0M7 | Trypanosomatidae | 31% | 100% |
A0A381MMW5 | Leishmania infantum | 29% | 94% |
A0A3Q8I7Y9 | Leishmania donovani | 29% | 100% |
A0A3Q8IEC4 | Leishmania donovani | 29% | 95% |
A0A3Q8IF95 | Leishmania donovani | 45% | 97% |
A0A3Q8IIT5 | Leishmania donovani | 28% | 91% |
A0A3Q8ISY9 | Leishmania donovani | 27% | 97% |
A0A3R7JSQ9 | Trypanosoma rangeli | 27% | 100% |
A0A3R7KKN8 | Trypanosoma rangeli | 30% | 100% |
A0A3R7MAQ7 | Trypanosoma rangeli | 26% | 87% |
A0A3R7N3S6 | Trypanosoma rangeli | 24% | 95% |
A0A3R7N415 | Trypanosoma rangeli | 31% | 100% |
A0A3R7N921 | Trypanosoma rangeli | 29% | 100% |
A0A3R7R443 | Trypanosoma rangeli | 29% | 100% |
A0A3S7WRJ4 | Leishmania donovani | 31% | 96% |
A0A3S7WRJ5 | Leishmania donovani | 29% | 88% |
A0A3S7WRL4 | Leishmania donovani | 29% | 99% |
A0A3S7WRS3 | Leishmania donovani | 26% | 98% |
A0A3S7WSR4 | Leishmania donovani | 32% | 100% |
A0A3S7WWU1 | Leishmania donovani | 48% | 92% |
A0A3S7X2G0 | Leishmania donovani | 29% | 94% |
A0A3S7X2K5 | Leishmania donovani | 29% | 100% |
A0A3S7XB11 | Leishmania donovani | 87% | 100% |
A0A422MSE4 | Trypanosoma rangeli | 32% | 100% |
A0A422MSP6 | Trypanosoma rangeli | 28% | 100% |
A0A422MST9 | Trypanosoma rangeli | 30% | 100% |
A0A422MU68 | Trypanosoma rangeli | 50% | 100% |
A4H6J0 | Leishmania braziliensis | 29% | 100% |
A4H6J1 | Leishmania braziliensis | 32% | 100% |
A4H6J3 | Leishmania braziliensis | 30% | 100% |
A4H6Q5 | Leishmania braziliensis | 25% | 100% |
A4HC19 | Leishmania braziliensis | 48% | 100% |
A4HHG2 | Leishmania braziliensis | 28% | 100% |
A4HHG3 | Leishmania braziliensis | 29% | 100% |
A4HHG4 | Leishmania braziliensis | 30% | 100% |
A4HJW3 | Leishmania braziliensis | 27% | 100% |
A4HUX5 | Leishmania infantum | 31% | 96% |
A4HUX6 | Leishmania infantum | 29% | 88% |
A4HUX7 | Leishmania infantum | 29% | 99% |
A4HUX8 | Leishmania infantum | 28% | 100% |
A4HV40 | Leishmania infantum | 26% | 98% |
A4HZF5 | Leishmania infantum | 45% | 97% |
A4HZJ4 | Leishmania infantum | 47% | 92% |
A4I4L2 | Leishmania infantum | 27% | 91% |
A4I7C5 | Leishmania infantum | 27% | 97% |
A4ICI3 | Leishmania infantum | 87% | 100% |
C9ZL97 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZL98 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
C9ZL99 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZLA0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZLA1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
C9ZTR5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
C9ZTR6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
C9ZTR7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZTR8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
C9ZTR9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
C9ZTS1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZUT6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
D0A7B1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 95% |
D0A7H1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
D0AAQ2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 90% |
E8NHE1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 98% |
E9AE01 | Leishmania major | 30% | 100% |
E9AE09 | Leishmania major | 27% | 100% |
E9AE10 | Leishmania major | 27% | 100% |
E9AE11 | Leishmania major | 31% | 100% |
E9AGK5 | Leishmania infantum | 32% | 100% |
E9AHJ0 | Leishmania infantum | 29% | 95% |
E9AHJ1 | Leishmania infantum | 29% | 100% |
E9ALS2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 95% |
E9ALS3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 91% |
E9ANL0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 96% |
E9ANL1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 94% |
E9ANL2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9ANS1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 97% |
E9APJ3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
E9AT53 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
E9AVF1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 45% | 100% |
E9AVF2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 47% | 93% |
E9B2B8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 97% |
Q4Q1E4 | Leishmania major | 87% | 99% |
Q4Q5T8 | Leishmania major | 28% | 100% |
Q4QC27 | Leishmania major | 48% | 100% |
Q4QC28 | Leishmania major | 44% | 99% |
Q4QFY5 | Leishmania major | 31% | 100% |
Q4QGU8 | Leishmania major | 26% | 100% |
Q4QH10 | Leishmania major | 28% | 97% |
Q4QH11 | Leishmania major | 28% | 95% |
Q4QH12 | Leishmania major | 28% | 95% |
Q4QH13 | Leishmania major | 29% | 95% |
Q4QH14 | Leishmania major | 29% | 100% |
Q4QH15 | Leishmania major | 31% | 100% |
V5B647 | Trypanosoma cruzi | 31% | 97% |
V5B983 | Trypanosoma cruzi | 30% | 100% |
V5BBB1 | Trypanosoma cruzi | 29% | 100% |
V5BFV8 | Trypanosoma cruzi | 29% | 92% |
V5BQY6 | Trypanosoma cruzi | 26% | 87% |
V5BVP0 | Trypanosoma cruzi | 29% | 100% |
V5DT25 | Trypanosoma cruzi | 29% | 100% |