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: 121 |
NetGPI | no | yes: 0, no: 121 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 114 |
GO:0110165 | cellular anatomical entity | 1 | 114 |
GO:0005737 | cytoplasm | 2 | 3 |
Related structures:
AlphaFold database: E8NHE1
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 53 |
GO:0022857 | transmembrane transporter activity | 2 | 53 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 312 | 316 | PF00656 | 0.649 |
CLV_C14_Caspase3-7 | 318 | 322 | PF00656 | 0.667 |
CLV_NRD_NRD_1 | 216 | 218 | PF00675 | 0.327 |
CLV_NRD_NRD_1 | 226 | 228 | PF00675 | 0.327 |
CLV_NRD_NRD_1 | 242 | 244 | PF00675 | 0.283 |
CLV_NRD_NRD_1 | 467 | 469 | PF00675 | 0.359 |
CLV_PCSK_KEX2_1 | 226 | 228 | PF00082 | 0.324 |
CLV_PCSK_KEX2_1 | 24 | 26 | PF00082 | 0.300 |
CLV_PCSK_KEX2_1 | 242 | 244 | PF00082 | 0.296 |
CLV_PCSK_KEX2_1 | 313 | 315 | PF00082 | 0.588 |
CLV_PCSK_KEX2_1 | 365 | 367 | PF00082 | 0.419 |
CLV_PCSK_KEX2_1 | 467 | 469 | PF00082 | 0.343 |
CLV_PCSK_PC1ET2_1 | 24 | 26 | PF00082 | 0.338 |
CLV_PCSK_PC1ET2_1 | 313 | 315 | PF00082 | 0.363 |
CLV_PCSK_PC1ET2_1 | 365 | 367 | PF00082 | 0.454 |
CLV_PCSK_PC1ET2_1 | 467 | 469 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 11 | 15 | PF00082 | 0.372 |
CLV_PCSK_SKI1_1 | 160 | 164 | PF00082 | 0.362 |
CLV_PCSK_SKI1_1 | 184 | 188 | PF00082 | 0.480 |
CLV_PCSK_SKI1_1 | 227 | 231 | PF00082 | 0.381 |
CLV_PCSK_SKI1_1 | 243 | 247 | PF00082 | 0.231 |
CLV_PCSK_SKI1_1 | 275 | 279 | PF00082 | 0.475 |
CLV_PCSK_SKI1_1 | 350 | 354 | PF00082 | 0.365 |
CLV_PCSK_SKI1_1 | 424 | 428 | PF00082 | 0.409 |
CLV_PCSK_SKI1_1 | 525 | 529 | PF00082 | 0.273 |
DEG_APCC_DBOX_1 | 423 | 431 | PF00400 | 0.253 |
DEG_MDM2_SWIB_1 | 41 | 48 | PF02201 | 0.182 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.657 |
DEG_SCF_TRCP1_1 | 321 | 326 | PF00400 | 0.559 |
DOC_CDC14_PxL_1 | 270 | 278 | PF14671 | 0.224 |
DOC_CDC14_PxL_1 | 293 | 301 | PF14671 | 0.471 |
DOC_CYCLIN_yCln2_LP_2 | 495 | 501 | PF00134 | 0.389 |
DOC_CYCLIN_yCln2_LP_2 | 502 | 508 | PF00134 | 0.247 |
DOC_MAPK_DCC_7 | 576 | 585 | PF00069 | 0.205 |
DOC_MAPK_gen_1 | 24 | 31 | PF00069 | 0.453 |
DOC_MAPK_gen_1 | 242 | 250 | PF00069 | 0.454 |
DOC_MAPK_gen_1 | 269 | 278 | PF00069 | 0.389 |
DOC_MAPK_gen_1 | 467 | 476 | PF00069 | 0.524 |
DOC_MAPK_MEF2A_6 | 242 | 250 | PF00069 | 0.473 |
DOC_MAPK_MEF2A_6 | 269 | 278 | PF00069 | 0.381 |
DOC_MAPK_MEF2A_6 | 469 | 478 | PF00069 | 0.525 |
DOC_MAPK_MEF2A_6 | 576 | 585 | PF00069 | 0.268 |
DOC_MAPK_NFAT4_5 | 243 | 251 | PF00069 | 0.446 |
DOC_PP1_RVXF_1 | 273 | 279 | PF00149 | 0.268 |
DOC_PP2B_LxvP_1 | 495 | 498 | PF13499 | 0.417 |
DOC_PP2B_LxvP_1 | 502 | 505 | PF13499 | 0.304 |
DOC_PP4_FxxP_1 | 306 | 309 | PF00568 | 0.694 |
DOC_PP4_FxxP_1 | 86 | 89 | PF00568 | 0.497 |
DOC_SPAK_OSR1_1 | 25 | 29 | PF12202 | 0.514 |
DOC_USP7_MATH_1 | 263 | 267 | PF00917 | 0.440 |
DOC_USP7_MATH_1 | 279 | 283 | PF00917 | 0.434 |
DOC_USP7_MATH_1 | 309 | 313 | PF00917 | 0.666 |
DOC_USP7_MATH_1 | 429 | 433 | PF00917 | 0.391 |
DOC_USP7_MATH_1 | 483 | 487 | PF00917 | 0.375 |
DOC_USP7_UBL2_3 | 530 | 534 | PF12436 | 0.494 |
DOC_WW_Pin1_4 | 338 | 343 | PF00397 | 0.725 |
LIG_14-3-3_CanoR_1 | 121 | 125 | PF00244 | 0.207 |
LIG_14-3-3_CanoR_1 | 152 | 162 | PF00244 | 0.379 |
LIG_14-3-3_CanoR_1 | 455 | 461 | PF00244 | 0.303 |
LIG_14-3-3_CanoR_1 | 603 | 608 | PF00244 | 0.553 |
LIG_BRCT_BRCA1_1 | 546 | 550 | PF00533 | 0.250 |
LIG_deltaCOP1_diTrp_1 | 401 | 410 | PF00928 | 0.505 |
LIG_FHA_1 | 102 | 108 | PF00498 | 0.290 |
LIG_FHA_1 | 154 | 160 | PF00498 | 0.322 |
LIG_FHA_1 | 281 | 287 | PF00498 | 0.382 |
LIG_FHA_1 | 324 | 330 | PF00498 | 0.708 |
LIG_FHA_1 | 397 | 403 | PF00498 | 0.490 |
LIG_FHA_1 | 475 | 481 | PF00498 | 0.464 |
LIG_FHA_1 | 482 | 488 | PF00498 | 0.317 |
LIG_FHA_1 | 522 | 528 | PF00498 | 0.310 |
LIG_FHA_1 | 575 | 581 | PF00498 | 0.319 |
LIG_FHA_1 | 594 | 600 | PF00498 | 0.398 |
LIG_FHA_1 | 66 | 72 | PF00498 | 0.332 |
LIG_FHA_2 | 1 | 7 | PF00498 | 0.641 |
LIG_FHA_2 | 210 | 216 | PF00498 | 0.425 |
LIG_FHA_2 | 378 | 384 | PF00498 | 0.534 |
LIG_GBD_Chelix_1 | 280 | 288 | PF00786 | 0.334 |
LIG_HP1_1 | 582 | 586 | PF01393 | 0.272 |
LIG_LIR_Apic_2 | 381 | 387 | PF02991 | 0.512 |
LIG_LIR_Apic_2 | 85 | 89 | PF02991 | 0.472 |
LIG_LIR_Gen_1 | 123 | 130 | PF02991 | 0.341 |
LIG_LIR_Gen_1 | 266 | 274 | PF02991 | 0.357 |
LIG_LIR_Gen_1 | 408 | 418 | PF02991 | 0.322 |
LIG_LIR_Gen_1 | 42 | 52 | PF02991 | 0.347 |
LIG_LIR_Gen_1 | 547 | 555 | PF02991 | 0.299 |
LIG_LIR_LC3C_4 | 68 | 73 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 161 | 165 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 183 | 189 | PF02991 | 0.258 |
LIG_LIR_Nem_3 | 266 | 270 | PF02991 | 0.333 |
LIG_LIR_Nem_3 | 33 | 37 | PF02991 | 0.351 |
LIG_LIR_Nem_3 | 408 | 413 | PF02991 | 0.303 |
LIG_LIR_Nem_3 | 416 | 420 | PF02991 | 0.324 |
LIG_LIR_Nem_3 | 42 | 48 | PF02991 | 0.337 |
LIG_LIR_Nem_3 | 459 | 463 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 547 | 553 | PF02991 | 0.299 |
LIG_LIR_Nem_3 | 97 | 102 | PF02991 | 0.304 |
LIG_PCNA_PIPBox_1 | 261 | 270 | PF02747 | 0.336 |
LIG_PCNA_yPIPBox_3 | 261 | 275 | PF02747 | 0.317 |
LIG_Pex14_1 | 406 | 410 | PF04695 | 0.332 |
LIG_Pex14_2 | 186 | 190 | PF04695 | 0.364 |
LIG_Pex14_2 | 41 | 45 | PF04695 | 0.348 |
LIG_Pex14_2 | 417 | 421 | PF04695 | 0.368 |
LIG_Pex14_2 | 82 | 86 | PF04695 | 0.423 |
LIG_PTB_Apo_2 | 419 | 426 | PF02174 | 0.319 |
LIG_SH2_CRK | 75 | 79 | PF00017 | 0.314 |
LIG_SH2_CRK | 80 | 84 | PF00017 | 0.311 |
LIG_SH2_PTP2 | 384 | 387 | PF00017 | 0.503 |
LIG_SH2_STAP1 | 43 | 47 | PF00017 | 0.335 |
LIG_SH2_STAP1 | 559 | 563 | PF00017 | 0.282 |
LIG_SH2_STAP1 | 607 | 611 | PF00017 | 0.557 |
LIG_SH2_STAP1 | 80 | 84 | PF00017 | 0.325 |
LIG_SH2_STAT3 | 234 | 237 | PF00017 | 0.496 |
LIG_SH2_STAT3 | 559 | 562 | PF00017 | 0.334 |
LIG_SH2_STAT5 | 177 | 180 | PF00017 | 0.256 |
LIG_SH2_STAT5 | 234 | 237 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 267 | 270 | PF00017 | 0.354 |
LIG_SH2_STAT5 | 289 | 292 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 384 | 387 | PF00017 | 0.513 |
LIG_SH2_STAT5 | 460 | 463 | PF00017 | 0.498 |
LIG_SH2_STAT5 | 506 | 509 | PF00017 | 0.316 |
LIG_SH2_STAT5 | 559 | 562 | PF00017 | 0.300 |
LIG_SH2_STAT5 | 75 | 78 | PF00017 | 0.303 |
LIG_SH2_STAT5 | 99 | 102 | PF00017 | 0.336 |
LIG_SH3_3 | 13 | 19 | PF00018 | 0.592 |
LIG_SH3_3 | 289 | 295 | PF00018 | 0.294 |
LIG_SH3_3 | 576 | 582 | PF00018 | 0.314 |
LIG_SH3_3 | 95 | 101 | PF00018 | 0.289 |
LIG_SUMO_SIM_anti_2 | 140 | 146 | PF11976 | 0.369 |
LIG_SUMO_SIM_anti_2 | 27 | 33 | PF11976 | 0.257 |
LIG_SUMO_SIM_anti_2 | 440 | 447 | PF11976 | 0.262 |
LIG_SUMO_SIM_par_1 | 27 | 33 | PF11976 | 0.428 |
LIG_SUMO_SIM_par_1 | 426 | 432 | PF11976 | 0.260 |
LIG_TRAF2_1 | 3 | 6 | PF00917 | 0.606 |
LIG_TYR_ITIM | 265 | 270 | PF00017 | 0.348 |
LIG_TYR_ITIM | 73 | 78 | PF00017 | 0.300 |
LIG_UBA3_1 | 105 | 114 | PF00899 | 0.269 |
LIG_WRC_WIRS_1 | 159 | 164 | PF05994 | 0.363 |
LIG_WRC_WIRS_1 | 31 | 36 | PF05994 | 0.426 |
LIG_WRC_WIRS_1 | 38 | 43 | PF05994 | 0.430 |
MOD_CK1_1 | 140 | 146 | PF00069 | 0.352 |
MOD_CK1_1 | 322 | 328 | PF00069 | 0.712 |
MOD_CK1_1 | 334 | 340 | PF00069 | 0.767 |
MOD_CK1_1 | 438 | 444 | PF00069 | 0.300 |
MOD_CK2_1 | 177 | 183 | PF00069 | 0.361 |
MOD_CK2_1 | 209 | 215 | PF00069 | 0.438 |
MOD_CK2_1 | 456 | 462 | PF00069 | 0.355 |
MOD_CMANNOS | 403 | 406 | PF00535 | 0.352 |
MOD_GlcNHglycan | 166 | 169 | PF01048 | 0.317 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.324 |
MOD_GlcNHglycan | 321 | 324 | PF01048 | 0.506 |
MOD_GlcNHglycan | 333 | 336 | PF01048 | 0.429 |
MOD_GlcNHglycan | 374 | 377 | PF01048 | 0.439 |
MOD_GlcNHglycan | 431 | 434 | PF01048 | 0.571 |
MOD_GlcNHglycan | 450 | 453 | PF01048 | 0.299 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.461 |
MOD_GlcNHglycan | 591 | 594 | PF01048 | 0.356 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.483 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.344 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.342 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.639 |
MOD_GSK3_1 | 334 | 341 | PF00069 | 0.700 |
MOD_GSK3_1 | 437 | 444 | PF00069 | 0.289 |
MOD_GSK3_1 | 483 | 490 | PF00069 | 0.316 |
MOD_GSK3_1 | 540 | 547 | PF00069 | 0.319 |
MOD_GSK3_1 | 589 | 596 | PF00069 | 0.367 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.271 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.508 |
MOD_LATS_1 | 601 | 607 | PF00433 | 0.591 |
MOD_N-GLC_1 | 299 | 304 | PF02516 | 0.444 |
MOD_NEK2_1 | 158 | 163 | PF00069 | 0.391 |
MOD_NEK2_1 | 188 | 193 | PF00069 | 0.302 |
MOD_NEK2_1 | 257 | 262 | PF00069 | 0.323 |
MOD_NEK2_1 | 298 | 303 | PF00069 | 0.567 |
MOD_NEK2_1 | 331 | 336 | PF00069 | 0.724 |
MOD_NEK2_1 | 405 | 410 | PF00069 | 0.300 |
MOD_NEK2_1 | 456 | 461 | PF00069 | 0.350 |
MOD_NEK2_1 | 493 | 498 | PF00069 | 0.323 |
MOD_NEK2_1 | 538 | 543 | PF00069 | 0.291 |
MOD_NEK2_1 | 544 | 549 | PF00069 | 0.289 |
MOD_NEK2_1 | 589 | 594 | PF00069 | 0.315 |
MOD_NEK2_2 | 120 | 125 | PF00069 | 0.285 |
MOD_OFUCOSY | 573 | 578 | PF10250 | 0.487 |
MOD_PIKK_1 | 209 | 215 | PF00454 | 0.512 |
MOD_PIKK_1 | 257 | 263 | PF00454 | 0.238 |
MOD_PIKK_1 | 462 | 468 | PF00454 | 0.512 |
MOD_PIKK_1 | 56 | 62 | PF00454 | 0.250 |
MOD_PIKK_1 | 605 | 611 | PF00454 | 0.490 |
MOD_PK_1 | 24 | 30 | PF00069 | 0.467 |
MOD_PKA_1 | 217 | 223 | PF00069 | 0.571 |
MOD_PKA_1 | 24 | 30 | PF00069 | 0.468 |
MOD_PKA_2 | 120 | 126 | PF00069 | 0.245 |
MOD_PKA_2 | 24 | 30 | PF00069 | 0.499 |
MOD_PKB_1 | 603 | 611 | PF00069 | 0.403 |
MOD_Plk_1 | 299 | 305 | PF00069 | 0.582 |
MOD_Plk_1 | 435 | 441 | PF00069 | 0.372 |
MOD_Plk_1 | 61 | 67 | PF00069 | 0.261 |
MOD_Plk_2-3 | 377 | 383 | PF00069 | 0.641 |
MOD_Plk_4 | 101 | 107 | PF00069 | 0.286 |
MOD_Plk_4 | 120 | 126 | PF00069 | 0.264 |
MOD_Plk_4 | 263 | 269 | PF00069 | 0.422 |
MOD_Plk_4 | 280 | 286 | PF00069 | 0.355 |
MOD_Plk_4 | 351 | 357 | PF00069 | 0.773 |
MOD_Plk_4 | 389 | 395 | PF00069 | 0.524 |
MOD_Plk_4 | 438 | 444 | PF00069 | 0.254 |
MOD_Plk_4 | 456 | 462 | PF00069 | 0.328 |
MOD_Plk_4 | 483 | 489 | PF00069 | 0.319 |
MOD_Plk_4 | 540 | 546 | PF00069 | 0.298 |
MOD_Plk_4 | 94 | 100 | PF00069 | 0.285 |
MOD_ProDKin_1 | 338 | 344 | PF00069 | 0.726 |
MOD_SUMO_rev_2 | 21 | 26 | PF00179 | 0.533 |
MOD_SUMO_rev_2 | 215 | 220 | PF00179 | 0.555 |
MOD_SUMO_rev_2 | 343 | 352 | PF00179 | 0.741 |
TRG_DiLeu_BaEn_1 | 327 | 332 | PF01217 | 0.564 |
TRG_DiLeu_BaEn_1 | 614 | 619 | PF01217 | 0.507 |
TRG_DiLeu_BaLyEn_6 | 452 | 457 | PF01217 | 0.318 |
TRG_DiLeu_LyEn_5 | 614 | 619 | PF01217 | 0.411 |
TRG_ENDOCYTIC_2 | 267 | 270 | PF00928 | 0.336 |
TRG_ENDOCYTIC_2 | 289 | 292 | PF00928 | 0.301 |
TRG_ENDOCYTIC_2 | 460 | 463 | PF00928 | 0.483 |
TRG_ENDOCYTIC_2 | 75 | 78 | PF00928 | 0.311 |
TRG_ENDOCYTIC_2 | 80 | 83 | PF00928 | 0.321 |
TRG_ENDOCYTIC_2 | 84 | 87 | PF00928 | 0.484 |
TRG_ENDOCYTIC_2 | 99 | 102 | PF00928 | 0.355 |
TRG_ER_diArg_1 | 226 | 228 | PF00400 | 0.550 |
TRG_ER_diArg_1 | 241 | 243 | PF00400 | 0.496 |
TRG_ER_diArg_1 | 615 | 618 | PF00400 | 0.539 |
TRG_NES_CRM1_1 | 62 | 74 | PF08389 | 0.174 |
TRG_Pf-PMV_PEXEL_1 | 217 | 221 | PF00026 | 0.367 |
TRG_Pf-PMV_PEXEL_1 | 552 | 557 | PF00026 | 0.369 |
TRG_Pf-PMV_PEXEL_1 | 610 | 614 | PF00026 | 0.338 |
TRG_Pf-PMV_PEXEL_1 | 617 | 621 | PF00026 | 0.352 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6G0 | Leptomonas seymouri | 39% | 99% |
A0A0N1HT40 | Leptomonas seymouri | 43% | 100% |
A0A0N1HZC2 | Leptomonas seymouri | 31% | 100% |
A0A0N1IKC5 | Leptomonas seymouri | 54% | 100% |
A0A0N1PB63 | Leptomonas seymouri | 28% | 95% |
A0A0N1PD04 | Leptomonas seymouri | 26% | 98% |
A0A0N1PFR4 | Leptomonas seymouri | 27% | 95% |
A0A0S4JR45 | Bodo saltans | 29% | 100% |
A0A1X0NKK0 | Trypanosomatidae | 31% | 100% |
A0A1X0NM09 | Trypanosomatidae | 31% | 100% |
A0A1X0NRW5 | Trypanosomatidae | 39% | 90% |
A0A1X0NV13 | Trypanosomatidae | 50% | 97% |
A0A1X0NV19 | Trypanosomatidae | 54% | 100% |
A0A1X0NV27 | Trypanosomatidae | 54% | 100% |
A0A1X0NVH8 | Trypanosomatidae | 43% | 95% |
A0A1X0NVM7 | Trypanosomatidae | 50% | 97% |
A0A1X0NWQ1 | Trypanosomatidae | 47% | 98% |
A0A1X0NZE6 | Trypanosomatidae | 32% | 100% |
A0A1X0NZU2 | Trypanosomatidae | 31% | 97% |
A0A1X0NZU5 | Trypanosomatidae | 34% | 100% |
A0A1X0NZW1 | Trypanosomatidae | 28% | 100% |
A0A1X0P0M7 | Trypanosomatidae | 31% | 100% |
A0A381MMW5 | Leishmania infantum | 32% | 96% |
A0A3Q8I7Y9 | Leishmania donovani | 44% | 100% |
A0A3Q8IEC4 | Leishmania donovani | 32% | 97% |
A0A3Q8IF95 | Leishmania donovani | 30% | 100% |
A0A3Q8IIT5 | Leishmania donovani | 26% | 93% |
A0A3Q8ISY9 | Leishmania donovani | 37% | 99% |
A0A3R7JSQ9 | Trypanosoma rangeli | 26% | 100% |
A0A3R7KKN8 | Trypanosoma rangeli | 29% | 100% |
A0A3R7MAQ7 | Trypanosoma rangeli | 35% | 89% |
A0A3R7N3S6 | Trypanosoma rangeli | 24% | 97% |
A0A3R7N415 | Trypanosoma rangeli | 28% | 100% |
A0A3R7N921 | Trypanosoma rangeli | 33% | 100% |
A0A3R7R443 | Trypanosoma rangeli | 28% | 100% |
A0A3S7WRJ4 | Leishmania donovani | 57% | 98% |
A0A3S7WRJ5 | Leishmania donovani | 76% | 90% |
A0A3S7WRL4 | Leishmania donovani | 44% | 100% |
A0A3S7WRS3 | Leishmania donovani | 24% | 100% |
A0A3S7WSR4 | Leishmania donovani | 52% | 100% |
A0A3S7WWU1 | Leishmania donovani | 28% | 95% |
A0A3S7X2G0 | Leishmania donovani | 32% | 96% |
A0A3S7X2K5 | Leishmania donovani | 33% | 100% |
A0A3S7XB11 | Leishmania donovani | 31% | 100% |
A0A422MSE4 | Trypanosoma rangeli | 48% | 100% |
A0A422MSP6 | Trypanosoma rangeli | 34% | 100% |
A0A422MST9 | Trypanosoma rangeli | 28% | 100% |
A0A422MU68 | Trypanosoma rangeli | 29% | 100% |
A4H6J0 | Leishmania braziliensis | 56% | 100% |
A4H6J1 | Leishmania braziliensis | 80% | 100% |
A4H6J3 | Leishmania braziliensis | 45% | 97% |
A4H6Q5 | Leishmania braziliensis | 24% | 100% |
A4HC19 | Leishmania braziliensis | 28% | 100% |
A4HHG2 | Leishmania braziliensis | 27% | 100% |
A4HHG3 | Leishmania braziliensis | 33% | 100% |
A4HHG4 | Leishmania braziliensis | 33% | 100% |
A4HJW3 | Leishmania braziliensis | 38% | 100% |
A4HPE2 | Leishmania braziliensis | 31% | 100% |
A4HUX5 | Leishmania infantum | 57% | 98% |
A4HUX6 | Leishmania infantum | 76% | 90% |
A4HUX7 | Leishmania infantum | 44% | 100% |
A4HUX8 | Leishmania infantum | 44% | 100% |
A4HV40 | Leishmania infantum | 24% | 100% |
A4HZF5 | Leishmania infantum | 30% | 100% |
A4HZJ4 | Leishmania infantum | 28% | 95% |
A4I4L2 | Leishmania infantum | 26% | 93% |
A4I7C5 | Leishmania infantum | 37% | 99% |
A4ICI3 | Leishmania infantum | 31% | 100% |
C9ZL97 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
C9ZL98 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZL99 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
C9ZLA0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
C9ZLA1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
C9ZTR5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 100% |
C9ZTR6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 100% |
C9ZTR7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
C9ZTR8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 100% |
C9ZTR9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 100% |
C9ZTS1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 100% |
C9ZUT6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 100% |
D0A7B1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 98% |
D0A7H1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
D0AAQ2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 92% |
E9AE01 | Leishmania major | 32% | 100% |
E9AE09 | Leishmania major | 27% | 100% |
E9AE10 | Leishmania major | 27% | 100% |
E9AE11 | Leishmania major | 32% | 100% |
E9AGK5 | Leishmania infantum | 52% | 100% |
E9AHJ0 | Leishmania infantum | 32% | 97% |
E9AHJ1 | Leishmania infantum | 32% | 100% |
E9ALS2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 97% |
E9ALS3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 93% |
E9ANL0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 59% | 98% |
E9ANL1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 96% |
E9ANL2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 43% | 100% |
E9ANS1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 99% |
E9APJ3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 51% | 100% |
E9AT53 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9AVF1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9AVF2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 95% |
E9B2B8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 99% |
Q4Q1E4 | Leishmania major | 30% | 98% |
Q4Q5T8 | Leishmania major | 37% | 100% |
Q4QC27 | Leishmania major | 29% | 100% |
Q4QC28 | Leishmania major | 29% | 99% |
Q4QFY5 | Leishmania major | 52% | 98% |
Q4QGU8 | Leishmania major | 26% | 100% |
Q4QH10 | Leishmania major | 44% | 95% |
Q4QH11 | Leishmania major | 44% | 92% |
Q4QH12 | Leishmania major | 44% | 92% |
Q4QH13 | Leishmania major | 44% | 92% |
Q4QH14 | Leishmania major | 76% | 100% |
Q4QH15 | Leishmania major | 56% | 100% |
V5B647 | Trypanosoma cruzi | 45% | 100% |
V5B983 | Trypanosoma cruzi | 33% | 100% |
V5BBB1 | Trypanosoma cruzi | 45% | 100% |
V5BFV8 | Trypanosoma cruzi | 32% | 94% |
V5BQY6 | Trypanosoma cruzi | 37% | 89% |
V5BVP0 | Trypanosoma cruzi | 48% | 100% |
V5DT25 | Trypanosoma cruzi | 48% | 100% |