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. | yes | 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: 75 |
NetGPI | no | yes: 0, no: 75 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 69 |
GO:0110165 | cellular anatomical entity | 1 | 69 |
GO:0005737 | cytoplasm | 2 | 3 |
Related structures:
AlphaFold database: A0A3Q8IIT5
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 34 |
GO:0022857 | transmembrane transporter activity | 2 | 34 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 341 | 345 | PF00656 | 0.819 |
CLV_NRD_NRD_1 | 212 | 214 | PF00675 | 0.450 |
CLV_NRD_NRD_1 | 223 | 225 | PF00675 | 0.456 |
CLV_NRD_NRD_1 | 239 | 241 | PF00675 | 0.413 |
CLV_NRD_NRD_1 | 509 | 511 | PF00675 | 0.492 |
CLV_NRD_NRD_1 | 648 | 650 | PF00675 | 0.486 |
CLV_PCSK_FUR_1 | 646 | 650 | PF00082 | 0.539 |
CLV_PCSK_KEX2_1 | 212 | 214 | PF00082 | 0.448 |
CLV_PCSK_KEX2_1 | 239 | 241 | PF00082 | 0.419 |
CLV_PCSK_KEX2_1 | 304 | 306 | PF00082 | 0.547 |
CLV_PCSK_KEX2_1 | 509 | 511 | PF00082 | 0.466 |
CLV_PCSK_KEX2_1 | 648 | 650 | PF00082 | 0.450 |
CLV_PCSK_PC1ET2_1 | 304 | 306 | PF00082 | 0.521 |
CLV_PCSK_SKI1_1 | 224 | 228 | PF00082 | 0.507 |
CLV_PCSK_SKI1_1 | 326 | 330 | PF00082 | 0.649 |
CLV_PCSK_SKI1_1 | 437 | 441 | PF00082 | 0.510 |
CLV_PCSK_SKI1_1 | 510 | 514 | PF00082 | 0.544 |
CLV_PCSK_SKI1_1 | 596 | 600 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 75 | 79 | PF00082 | 0.361 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.546 |
DEG_SPOP_SBC_1 | 23 | 27 | PF00917 | 0.453 |
DOC_CKS1_1 | 205 | 210 | PF01111 | 0.698 |
DOC_CYCLIN_RxL_1 | 434 | 443 | PF00134 | 0.699 |
DOC_CYCLIN_yCln2_LP_2 | 546 | 552 | PF00134 | 0.375 |
DOC_MAPK_gen_1 | 103 | 112 | PF00069 | 0.474 |
DOC_MAPK_gen_1 | 224 | 230 | PF00069 | 0.623 |
DOC_MAPK_gen_1 | 268 | 275 | PF00069 | 0.483 |
DOC_MAPK_MEF2A_6 | 268 | 277 | PF00069 | 0.458 |
DOC_MAPK_MEF2A_6 | 437 | 446 | PF00069 | 0.689 |
DOC_MAPK_MEF2A_6 | 481 | 488 | PF00069 | 0.349 |
DOC_MAPK_MEF2A_6 | 623 | 630 | PF00069 | 0.379 |
DOC_MAPK_RevD_3 | 255 | 269 | PF00069 | 0.590 |
DOC_MAPK_RevD_3 | 291 | 305 | PF00069 | 0.404 |
DOC_PP1_RVXF_1 | 73 | 79 | PF00149 | 0.641 |
DOC_PP2B_LxvP_1 | 546 | 549 | PF13499 | 0.383 |
DOC_PP4_FxxP_1 | 121 | 124 | PF00568 | 0.510 |
DOC_PP4_FxxP_1 | 71 | 74 | PF00568 | 0.594 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.398 |
DOC_USP7_MATH_1 | 256 | 260 | PF00917 | 0.496 |
DOC_USP7_MATH_1 | 405 | 409 | PF00917 | 0.874 |
DOC_WW_Pin1_4 | 204 | 209 | PF00397 | 0.669 |
DOC_WW_Pin1_4 | 401 | 406 | PF00397 | 0.845 |
LIG_14-3-3_CanoR_1 | 224 | 229 | PF00244 | 0.663 |
LIG_14-3-3_CanoR_1 | 349 | 353 | PF00244 | 0.851 |
LIG_14-3-3_CanoR_1 | 38 | 44 | PF00244 | 0.471 |
LIG_14-3-3_CanoR_1 | 481 | 485 | PF00244 | 0.441 |
LIG_14-3-3_CanoR_1 | 509 | 519 | PF00244 | 0.703 |
LIG_APCC_ABBA_1 | 30 | 35 | PF00400 | 0.474 |
LIG_BRCT_BRCA1_1 | 470 | 474 | PF00533 | 0.477 |
LIG_BRCT_BRCA1_1 | 533 | 537 | PF00533 | 0.316 |
LIG_BRCT_BRCA1_1 | 584 | 588 | PF00533 | 0.435 |
LIG_Clathr_ClatBox_1 | 439 | 443 | PF01394 | 0.638 |
LIG_deltaCOP1_diTrp_1 | 443 | 452 | PF00928 | 0.453 |
LIG_eIF4E_1 | 9 | 15 | PF01652 | 0.641 |
LIG_FHA_1 | 155 | 161 | PF00498 | 0.450 |
LIG_FHA_1 | 225 | 231 | PF00498 | 0.648 |
LIG_FHA_1 | 260 | 266 | PF00498 | 0.531 |
LIG_FHA_1 | 32 | 38 | PF00498 | 0.384 |
LIG_FHA_1 | 439 | 445 | PF00498 | 0.593 |
LIG_FHA_1 | 455 | 461 | PF00498 | 0.410 |
LIG_FHA_1 | 513 | 519 | PF00498 | 0.734 |
LIG_FHA_1 | 589 | 595 | PF00498 | 0.394 |
LIG_FHA_2 | 394 | 400 | PF00498 | 0.926 |
LIG_FXI_DFP_1 | 306 | 310 | PF00024 | 0.440 |
LIG_IRF3_LxIS_1 | 18 | 25 | PF10401 | 0.510 |
LIG_IRF3_LxIS_1 | 252 | 258 | PF10401 | 0.299 |
LIG_LIR_Apic_2 | 70 | 74 | PF02991 | 0.573 |
LIG_LIR_Gen_1 | 141 | 152 | PF02991 | 0.577 |
LIG_LIR_Gen_1 | 180 | 190 | PF02991 | 0.392 |
LIG_LIR_Gen_1 | 27 | 37 | PF02991 | 0.475 |
LIG_LIR_Gen_1 | 270 | 280 | PF02991 | 0.392 |
LIG_LIR_Gen_1 | 327 | 338 | PF02991 | 0.755 |
LIG_LIR_Gen_1 | 483 | 491 | PF02991 | 0.420 |
LIG_LIR_Gen_1 | 534 | 543 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 141 | 147 | PF02991 | 0.576 |
LIG_LIR_Nem_3 | 151 | 155 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 176 | 182 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 27 | 33 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 270 | 275 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 308 | 312 | PF02991 | 0.683 |
LIG_LIR_Nem_3 | 327 | 333 | PF02991 | 0.755 |
LIG_LIR_Nem_3 | 434 | 439 | PF02991 | 0.615 |
LIG_LIR_Nem_3 | 471 | 477 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 483 | 488 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 520 | 526 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 534 | 540 | PF02991 | 0.374 |
LIG_LYPXL_yS_3 | 299 | 302 | PF13949 | 0.694 |
LIG_PALB2_WD40_1 | 163 | 171 | PF16756 | 0.302 |
LIG_Pex14_1 | 448 | 452 | PF04695 | 0.419 |
LIG_Pex14_2 | 164 | 168 | PF04695 | 0.392 |
LIG_Pex14_2 | 447 | 451 | PF04695 | 0.443 |
LIG_Pex14_2 | 584 | 588 | PF04695 | 0.444 |
LIG_Pex14_2 | 599 | 603 | PF04695 | 0.393 |
LIG_Pex14_2 | 92 | 96 | PF04695 | 0.356 |
LIG_PTB_Apo_2 | 162 | 169 | PF02174 | 0.415 |
LIG_SH2_CRK | 144 | 148 | PF00017 | 0.659 |
LIG_SH2_GRB2like | 163 | 166 | PF00017 | 0.417 |
LIG_SH2_GRB2like | 572 | 575 | PF00017 | 0.608 |
LIG_SH2_PTP2 | 19 | 22 | PF00017 | 0.442 |
LIG_SH2_PTP2 | 485 | 488 | PF00017 | 0.338 |
LIG_SH2_STAP1 | 182 | 186 | PF00017 | 0.370 |
LIG_SH2_STAP1 | 314 | 318 | PF00017 | 0.597 |
LIG_SH2_STAP1 | 572 | 576 | PF00017 | 0.594 |
LIG_SH2_STAT3 | 231 | 234 | PF00017 | 0.664 |
LIG_SH2_STAT5 | 120 | 123 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 163 | 166 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 184 | 187 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 19 | 22 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 199 | 202 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 206 | 209 | PF00017 | 0.596 |
LIG_SH2_STAT5 | 242 | 245 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 264 | 267 | PF00017 | 0.487 |
LIG_SH2_STAT5 | 272 | 275 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 485 | 488 | PF00017 | 0.373 |
LIG_SH2_STAT5 | 535 | 538 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 60 | 63 | PF00017 | 0.403 |
LIG_SH3_1 | 304 | 310 | PF00018 | 0.738 |
LIG_SH3_3 | 133 | 139 | PF00018 | 0.639 |
LIG_SH3_3 | 202 | 208 | PF00018 | 0.585 |
LIG_SH3_3 | 304 | 310 | PF00018 | 0.716 |
LIG_SH3_3 | 356 | 362 | PF00018 | 0.809 |
LIG_SH3_3 | 73 | 79 | PF00018 | 0.617 |
LIG_SUMO_SIM_par_1 | 281 | 287 | PF11976 | 0.494 |
LIG_SUMO_SIM_par_1 | 438 | 443 | PF11976 | 0.612 |
LIG_TRAF2_1 | 396 | 399 | PF00917 | 0.861 |
LIG_UBA3_1 | 598 | 605 | PF00899 | 0.534 |
LIG_WRC_WIRS_1 | 432 | 437 | PF05994 | 0.727 |
MOD_CDK_SPK_2 | 401 | 406 | PF00069 | 0.726 |
MOD_CK1_1 | 177 | 183 | PF00069 | 0.449 |
MOD_CK1_1 | 259 | 265 | PF00069 | 0.521 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.370 |
MOD_CK1_1 | 350 | 356 | PF00069 | 0.851 |
MOD_CK1_1 | 39 | 45 | PF00069 | 0.414 |
MOD_CK1_1 | 480 | 486 | PF00069 | 0.423 |
MOD_CK1_1 | 554 | 560 | PF00069 | 0.460 |
MOD_CK2_1 | 393 | 399 | PF00069 | 0.907 |
MOD_CK2_1 | 511 | 517 | PF00069 | 0.748 |
MOD_CMANNOS | 445 | 448 | PF00535 | 0.445 |
MOD_GlcNHglycan | 152 | 155 | PF01048 | 0.466 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.585 |
MOD_GlcNHglycan | 236 | 239 | PF01048 | 0.376 |
MOD_GlcNHglycan | 269 | 272 | PF01048 | 0.707 |
MOD_GlcNHglycan | 372 | 375 | PF01048 | 0.623 |
MOD_GlcNHglycan | 492 | 495 | PF01048 | 0.429 |
MOD_GlcNHglycan | 499 | 502 | PF01048 | 0.440 |
MOD_GlcNHglycan | 585 | 588 | PF01048 | 0.480 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.447 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.451 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.426 |
MOD_GSK3_1 | 308 | 315 | PF00069 | 0.662 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.909 |
MOD_GSK3_1 | 401 | 408 | PF00069 | 0.857 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.406 |
MOD_GSK3_1 | 583 | 590 | PF00069 | 0.427 |
MOD_GSK3_1 | 605 | 612 | PF00069 | 0.476 |
MOD_N-GLC_1 | 177 | 182 | PF02516 | 0.586 |
MOD_N-GLC_2 | 56 | 58 | PF02516 | 0.459 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.447 |
MOD_NEK2_1 | 22 | 27 | PF00069 | 0.412 |
MOD_NEK2_1 | 255 | 260 | PF00069 | 0.436 |
MOD_NEK2_1 | 273 | 278 | PF00069 | 0.442 |
MOD_NEK2_1 | 447 | 452 | PF00069 | 0.424 |
MOD_NEK2_1 | 454 | 459 | PF00069 | 0.385 |
MOD_NEK2_1 | 519 | 524 | PF00069 | 0.435 |
MOD_NEK2_1 | 531 | 536 | PF00069 | 0.397 |
MOD_NEK2_1 | 551 | 556 | PF00069 | 0.471 |
MOD_NEK2_1 | 582 | 587 | PF00069 | 0.433 |
MOD_NEK2_1 | 588 | 593 | PF00069 | 0.432 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.605 |
MOD_NEK2_2 | 28 | 33 | PF00069 | 0.428 |
MOD_NEK2_2 | 564 | 569 | PF00069 | 0.543 |
MOD_OFUCOSY | 616 | 621 | PF10250 | 0.639 |
MOD_PKA_1 | 224 | 230 | PF00069 | 0.708 |
MOD_PKA_1 | 510 | 516 | PF00069 | 0.728 |
MOD_PKA_2 | 214 | 220 | PF00069 | 0.678 |
MOD_PKA_2 | 348 | 354 | PF00069 | 0.893 |
MOD_PKA_2 | 405 | 411 | PF00069 | 0.876 |
MOD_PKA_2 | 480 | 486 | PF00069 | 0.442 |
MOD_Plk_1 | 46 | 52 | PF00069 | 0.386 |
MOD_Plk_1 | 477 | 483 | PF00069 | 0.454 |
MOD_Plk_1 | 605 | 611 | PF00069 | 0.586 |
MOD_Plk_4 | 127 | 133 | PF00069 | 0.461 |
MOD_Plk_4 | 155 | 161 | PF00069 | 0.428 |
MOD_Plk_4 | 256 | 262 | PF00069 | 0.431 |
MOD_Plk_4 | 431 | 437 | PF00069 | 0.648 |
MOD_Plk_4 | 447 | 453 | PF00069 | 0.465 |
MOD_Plk_4 | 456 | 462 | PF00069 | 0.429 |
MOD_Plk_4 | 480 | 486 | PF00069 | 0.376 |
MOD_Plk_4 | 519 | 525 | PF00069 | 0.429 |
MOD_Plk_4 | 531 | 537 | PF00069 | 0.419 |
MOD_ProDKin_1 | 204 | 210 | PF00069 | 0.672 |
MOD_ProDKin_1 | 401 | 407 | PF00069 | 0.845 |
MOD_SUMO_for_1 | 173 | 176 | PF00179 | 0.342 |
MOD_SUMO_rev_2 | 218 | 227 | PF00179 | 0.704 |
MOD_SUMO_rev_2 | 321 | 331 | PF00179 | 0.793 |
TRG_ENDOCYTIC_2 | 144 | 147 | PF00928 | 0.564 |
TRG_ENDOCYTIC_2 | 182 | 185 | PF00928 | 0.448 |
TRG_ENDOCYTIC_2 | 19 | 22 | PF00928 | 0.440 |
TRG_ENDOCYTIC_2 | 272 | 275 | PF00928 | 0.386 |
TRG_ENDOCYTIC_2 | 299 | 302 | PF00928 | 0.635 |
TRG_ENDOCYTIC_2 | 432 | 435 | PF00928 | 0.663 |
TRG_ENDOCYTIC_2 | 485 | 488 | PF00928 | 0.408 |
TRG_ENDOCYTIC_2 | 535 | 538 | PF00928 | 0.385 |
TRG_ENDOCYTIC_2 | 580 | 583 | PF00928 | 0.412 |
TRG_ENDOCYTIC_2 | 60 | 63 | PF00928 | 0.393 |
TRG_ER_diArg_1 | 211 | 213 | PF00400 | 0.685 |
TRG_ER_diArg_1 | 239 | 241 | PF00400 | 0.618 |
TRG_ER_diArg_1 | 508 | 510 | PF00400 | 0.677 |
TRG_ER_diArg_1 | 647 | 649 | PF00400 | 0.701 |
TRG_ER_diArg_1 | 9 | 12 | PF00400 | 0.569 |
TRG_ER_diLys_1 | 668 | 672 | PF00400 | 0.608 |
TRG_NLS_MonoExtC_3 | 302 | 307 | PF00514 | 0.565 |
TRG_NLS_MonoExtN_4 | 300 | 307 | PF00514 | 0.562 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6G0 | Leptomonas seymouri | 28% | 100% |
A0A0N1HZC2 | Leptomonas seymouri | 30% | 100% |
A0A0N1IKC5 | Leptomonas seymouri | 26% | 100% |
A0A0N1PB63 | Leptomonas seymouri | 25% | 100% |
A0A0N1PD04 | Leptomonas seymouri | 23% | 100% |
A0A0N1PFR4 | Leptomonas seymouri | 66% | 100% |
A0A1X0NKK0 | Trypanosomatidae | 28% | 100% |
A0A1X0NM09 | Trypanosomatidae | 27% | 100% |
A0A1X0NVF9 | Trypanosomatidae | 23% | 100% |
A0A1X0NZE6 | Trypanosomatidae | 26% | 100% |
A0A1X0NZT1 | Trypanosomatidae | 24% | 81% |
A0A1X0NZU2 | Trypanosomatidae | 32% | 100% |
A0A1X0NZW1 | Trypanosomatidae | 50% | 100% |
A0A1X0P0M7 | Trypanosomatidae | 25% | 100% |
A0A381MMW5 | Leishmania infantum | 32% | 97% |
A0A3Q8IEC4 | Leishmania donovani | 32% | 96% |
A0A3Q8IF95 | Leishmania donovani | 24% | 96% |
A0A3Q8ISY9 | Leishmania donovani | 28% | 97% |
A0A3R7KKN8 | Trypanosoma rangeli | 52% | 100% |
A0A3R7N3S6 | Trypanosoma rangeli | 22% | 100% |
A0A3R7N921 | Trypanosoma rangeli | 24% | 100% |
A0A3S7WRJ4 | Leishmania donovani | 25% | 100% |
A0A3S7WRJ5 | Leishmania donovani | 27% | 96% |
A0A3S7WRS3 | Leishmania donovani | 25% | 100% |
A0A3S7WWU1 | Leishmania donovani | 27% | 100% |
A0A3S7X2G0 | Leishmania donovani | 31% | 100% |
A0A3S7X2K5 | Leishmania donovani | 31% | 100% |
A0A3S7XB11 | Leishmania donovani | 28% | 100% |
A0A422MU68 | Trypanosoma rangeli | 25% | 100% |
A0A422NL17 | Trypanosoma rangeli | 23% | 83% |
A4H6J0 | Leishmania braziliensis | 25% | 99% |
A4H6J1 | Leishmania braziliensis | 26% | 99% |
A4H6Q5 | Leishmania braziliensis | 24% | 99% |
A4HC19 | Leishmania braziliensis | 24% | 98% |
A4HHG2 | Leishmania braziliensis | 83% | 100% |
A4HHG3 | Leishmania braziliensis | 29% | 97% |
A4HHG4 | Leishmania braziliensis | 29% | 97% |
A4HJW3 | Leishmania braziliensis | 27% | 97% |
A4HPE2 | Leishmania braziliensis | 28% | 94% |
A4HUX5 | Leishmania infantum | 25% | 98% |
A4HUX6 | Leishmania infantum | 26% | 100% |
A4HV40 | Leishmania infantum | 25% | 98% |
A4HZF5 | Leishmania infantum | 24% | 96% |
A4HZJ4 | Leishmania infantum | 27% | 100% |
A4I4L2 | Leishmania infantum | 98% | 100% |
A4I7C5 | Leishmania infantum | 28% | 97% |
A4ICI3 | Leishmania infantum | 28% | 93% |
D0A7B1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
E8NHE1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 94% |
E9AE01 | Leishmania major | 30% | 98% |
E9AE09 | Leishmania major | 93% | 100% |
E9AE10 | Leishmania major | 93% | 100% |
E9AE11 | Leishmania major | 31% | 97% |
E9AHJ0 | Leishmania infantum | 32% | 96% |
E9AHJ1 | Leishmania infantum | 31% | 96% |
E9ALS2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 97% |
E9ALS3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
E9ANL0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 97% |
E9ANL1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 98% |
E9ANS1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 96% |
E9APJ3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 91% |
E9AT53 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 91% |
E9AVF1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 92% |
E9AVF2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9B2B8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 96% |
Q4Q1E4 | Leishmania major | 28% | 93% |
Q4Q5T8 | Leishmania major | 28% | 97% |
Q4QC27 | Leishmania major | 26% | 96% |
Q4QGU8 | Leishmania major | 24% | 99% |
Q4QH14 | Leishmania major | 25% | 98% |
Q4QH15 | Leishmania major | 25% | 98% |
V5BFV8 | Trypanosoma cruzi | 25% | 100% |
V5BWJ7 | Trypanosoma cruzi | 23% | 100% |
V5DT25 | Trypanosoma cruzi | 27% | 100% |