Transporters, folate/biopterin transporter
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: 9 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 52 |
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: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 70 |
NetGPI | no | yes: 0, no: 70 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 71 |
GO:0110165 | cellular anatomical entity | 1 | 71 |
GO:0005737 | cytoplasm | 2 | 6 |
GO:0005886 | plasma membrane | 3 | 1 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pescher et al. (upgregulation) | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Lahav et al. - mRNA
- Protein
|
Related structures:
AlphaFold database: A4HUF4
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 1 |
GO:0015877 | biopterin transport | 5 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0071702 | organic substance transport | 4 | 1 |
GO:0071705 | nitrogen compound transport | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 1 |
GO:0015224 | biopterin transmembrane transporter activity | 3 | 1 |
GO:0022857 | transmembrane transporter activity | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 667 | 671 | PF00656 | 0.737 |
CLV_MEL_PAP_1 | 438 | 444 | PF00089 | 0.219 |
CLV_NRD_NRD_1 | 271 | 273 | PF00675 | 0.309 |
CLV_NRD_NRD_1 | 48 | 50 | PF00675 | 0.384 |
CLV_PCSK_KEX2_1 | 133 | 135 | PF00082 | 0.269 |
CLV_PCSK_KEX2_1 | 299 | 301 | PF00082 | 0.345 |
CLV_PCSK_KEX2_1 | 48 | 50 | PF00082 | 0.417 |
CLV_PCSK_KEX2_1 | 519 | 521 | PF00082 | 0.494 |
CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.383 |
CLV_PCSK_PC1ET2_1 | 133 | 135 | PF00082 | 0.269 |
CLV_PCSK_PC1ET2_1 | 299 | 301 | PF00082 | 0.345 |
CLV_PCSK_PC1ET2_1 | 519 | 521 | PF00082 | 0.494 |
CLV_PCSK_PC1ET2_1 | 9 | 11 | PF00082 | 0.383 |
CLV_PCSK_SKI1_1 | 116 | 120 | PF00082 | 0.326 |
CLV_PCSK_SKI1_1 | 316 | 320 | PF00082 | 0.344 |
DEG_APCC_DBOX_1 | 276 | 284 | PF00400 | 0.394 |
DOC_CDC14_PxL_1 | 609 | 617 | PF14671 | 0.304 |
DOC_CKS1_1 | 621 | 626 | PF01111 | 0.405 |
DOC_CYCLIN_yCln2_LP_2 | 549 | 552 | PF00134 | 0.372 |
DOC_CYCLIN_yCln2_LP_2 | 626 | 632 | PF00134 | 0.352 |
DOC_MAPK_gen_1 | 133 | 139 | PF00069 | 0.479 |
DOC_MAPK_gen_1 | 257 | 267 | PF00069 | 0.521 |
DOC_MAPK_gen_1 | 272 | 280 | PF00069 | 0.511 |
DOC_MAPK_gen_1 | 519 | 527 | PF00069 | 0.295 |
DOC_MAPK_gen_1 | 637 | 646 | PF00069 | 0.558 |
DOC_MAPK_MEF2A_6 | 227 | 234 | PF00069 | 0.301 |
DOC_MAPK_MEF2A_6 | 519 | 527 | PF00069 | 0.329 |
DOC_PP1_RVXF_1 | 495 | 501 | PF00149 | 0.492 |
DOC_PP2B_LxvP_1 | 549 | 552 | PF13499 | 0.313 |
DOC_PP2B_LxvP_1 | 626 | 629 | PF13499 | 0.339 |
DOC_PP2B_PxIxI_1 | 227 | 233 | PF00149 | 0.256 |
DOC_USP7_MATH_1 | 196 | 200 | PF00917 | 0.452 |
DOC_USP7_MATH_1 | 302 | 306 | PF00917 | 0.558 |
DOC_USP7_MATH_1 | 561 | 565 | PF00917 | 0.458 |
DOC_USP7_MATH_1 | 663 | 667 | PF00917 | 0.602 |
DOC_WW_Pin1_4 | 298 | 303 | PF00397 | 0.549 |
DOC_WW_Pin1_4 | 620 | 625 | PF00397 | 0.388 |
LIG_14-3-3_CanoR_1 | 104 | 111 | PF00244 | 0.464 |
LIG_14-3-3_CanoR_1 | 257 | 267 | PF00244 | 0.556 |
LIG_14-3-3_CanoR_1 | 304 | 311 | PF00244 | 0.546 |
LIG_14-3-3_CanoR_1 | 497 | 501 | PF00244 | 0.463 |
LIG_Actin_WH2_2 | 50 | 65 | PF00022 | 0.590 |
LIG_APCC_ABBA_1 | 50 | 55 | PF00400 | 0.604 |
LIG_APCC_ABBAyCdc20_2 | 49 | 55 | PF00400 | 0.473 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.717 |
LIG_BIR_III_4 | 13 | 17 | PF00653 | 0.688 |
LIG_Clathr_ClatBox_1 | 265 | 269 | PF01394 | 0.416 |
LIG_EH1_1 | 499 | 507 | PF00400 | 0.315 |
LIG_eIF4E_1 | 609 | 615 | PF01652 | 0.199 |
LIG_FHA_1 | 117 | 123 | PF00498 | 0.541 |
LIG_FHA_1 | 208 | 214 | PF00498 | 0.312 |
LIG_FHA_1 | 365 | 371 | PF00498 | 0.561 |
LIG_FHA_1 | 382 | 388 | PF00498 | 0.331 |
LIG_FHA_1 | 397 | 403 | PF00498 | 0.231 |
LIG_FHA_1 | 481 | 487 | PF00498 | 0.369 |
LIG_FHA_1 | 497 | 503 | PF00498 | 0.464 |
LIG_FHA_1 | 621 | 627 | PF00498 | 0.391 |
LIG_FHA_2 | 269 | 275 | PF00498 | 0.563 |
LIG_FHA_2 | 598 | 604 | PF00498 | 0.196 |
LIG_GBD_Chelix_1 | 478 | 486 | PF00786 | 0.201 |
LIG_GBD_Chelix_1 | 501 | 509 | PF00786 | 0.446 |
LIG_GBD_Chelix_1 | 539 | 547 | PF00786 | 0.474 |
LIG_HP1_1 | 552 | 556 | PF01393 | 0.374 |
LIG_LIR_Apic_2 | 29 | 35 | PF02991 | 0.577 |
LIG_LIR_Apic_2 | 348 | 354 | PF02991 | 0.502 |
LIG_LIR_Apic_2 | 417 | 422 | PF02991 | 0.389 |
LIG_LIR_Apic_2 | 453 | 457 | PF02991 | 0.304 |
LIG_LIR_Apic_2 | 592 | 596 | PF02991 | 0.275 |
LIG_LIR_Gen_1 | 124 | 131 | PF02991 | 0.493 |
LIG_LIR_Gen_1 | 202 | 209 | PF02991 | 0.474 |
LIG_LIR_Gen_1 | 466 | 475 | PF02991 | 0.303 |
LIG_LIR_Gen_1 | 485 | 492 | PF02991 | 0.368 |
LIG_LIR_Gen_1 | 566 | 576 | PF02991 | 0.489 |
LIG_LIR_Gen_1 | 87 | 95 | PF02991 | 0.511 |
LIG_LIR_Nem_3 | 124 | 129 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 132 | 138 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 202 | 208 | PF02991 | 0.266 |
LIG_LIR_Nem_3 | 242 | 248 | PF02991 | 0.319 |
LIG_LIR_Nem_3 | 371 | 377 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 417 | 421 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 464 | 468 | PF02991 | 0.273 |
LIG_LIR_Nem_3 | 485 | 490 | PF02991 | 0.316 |
LIG_Pex14_2 | 169 | 173 | PF04695 | 0.340 |
LIG_Pex14_2 | 463 | 467 | PF04695 | 0.283 |
LIG_Pex14_2 | 487 | 491 | PF04695 | 0.346 |
LIG_PTB_Apo_2 | 459 | 466 | PF02174 | 0.344 |
LIG_PTB_Apo_2 | 485 | 492 | PF02174 | 0.412 |
LIG_PTB_Phospho_1 | 459 | 465 | PF10480 | 0.375 |
LIG_SH2_CRK | 102 | 106 | PF00017 | 0.485 |
LIG_SH2_CRK | 136 | 140 | PF00017 | 0.349 |
LIG_SH2_CRK | 151 | 155 | PF00017 | 0.301 |
LIG_SH2_CRK | 186 | 190 | PF00017 | 0.487 |
LIG_SH2_CRK | 351 | 355 | PF00017 | 0.588 |
LIG_SH2_CRK | 379 | 383 | PF00017 | 0.320 |
LIG_SH2_CRK | 454 | 458 | PF00017 | 0.300 |
LIG_SH2_CRK | 468 | 472 | PF00017 | 0.276 |
LIG_SH2_CRK | 537 | 541 | PF00017 | 0.334 |
LIG_SH2_CRK | 593 | 597 | PF00017 | 0.298 |
LIG_SH2_CRK | 609 | 613 | PF00017 | 0.329 |
LIG_SH2_GRB2like | 450 | 453 | PF00017 | 0.329 |
LIG_SH2_GRB2like | 609 | 612 | PF00017 | 0.323 |
LIG_SH2_NCK_1 | 334 | 338 | PF00017 | 0.405 |
LIG_SH2_NCK_1 | 468 | 472 | PF00017 | 0.273 |
LIG_SH2_NCK_1 | 537 | 541 | PF00017 | 0.238 |
LIG_SH2_PTP2 | 32 | 35 | PF00017 | 0.574 |
LIG_SH2_PTP2 | 524 | 527 | PF00017 | 0.370 |
LIG_SH2_SRC | 32 | 35 | PF00017 | 0.580 |
LIG_SH2_SRC | 334 | 337 | PF00017 | 0.408 |
LIG_SH2_SRC | 338 | 341 | PF00017 | 0.396 |
LIG_SH2_STAP1 | 131 | 135 | PF00017 | 0.473 |
LIG_SH2_STAP1 | 186 | 190 | PF00017 | 0.463 |
LIG_SH2_STAP1 | 334 | 338 | PF00017 | 0.402 |
LIG_SH2_STAP1 | 379 | 383 | PF00017 | 0.368 |
LIG_SH2_STAP1 | 569 | 573 | PF00017 | 0.314 |
LIG_SH2_STAP1 | 88 | 92 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 131 | 134 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 246 | 249 | PF00017 | 0.412 |
LIG_SH2_STAT5 | 32 | 35 | PF00017 | 0.571 |
LIG_SH2_STAT5 | 433 | 436 | PF00017 | 0.329 |
LIG_SH2_STAT5 | 450 | 453 | PF00017 | 0.260 |
LIG_SH2_STAT5 | 465 | 468 | PF00017 | 0.235 |
LIG_SH2_STAT5 | 524 | 527 | PF00017 | 0.275 |
LIG_SH2_STAT5 | 533 | 536 | PF00017 | 0.266 |
LIG_SH2_STAT5 | 537 | 540 | PF00017 | 0.311 |
LIG_SH3_1 | 351 | 357 | PF00018 | 0.556 |
LIG_SH3_3 | 351 | 357 | PF00018 | 0.567 |
LIG_SH3_3 | 439 | 445 | PF00018 | 0.334 |
LIG_SUMO_SIM_anti_2 | 631 | 636 | PF11976 | 0.437 |
LIG_SUMO_SIM_par_1 | 480 | 485 | PF11976 | 0.205 |
LIG_SUMO_SIM_par_1 | 551 | 557 | PF11976 | 0.303 |
LIG_TRFH_1 | 151 | 155 | PF08558 | 0.336 |
LIG_TYR_ITIM | 149 | 154 | PF00017 | 0.356 |
LIG_TYR_ITSM | 464 | 471 | PF00017 | 0.378 |
LIG_UBA3_1 | 149 | 157 | PF00899 | 0.328 |
LIG_UBA3_1 | 265 | 273 | PF00899 | 0.491 |
LIG_UBA3_1 | 486 | 493 | PF00899 | 0.389 |
LIG_UBA3_1 | 632 | 637 | PF00899 | 0.204 |
LIG_Vh1_VBS_1 | 377 | 395 | PF01044 | 0.382 |
LIG_Vh1_VBS_1 | 467 | 485 | PF01044 | 0.361 |
MOD_CDC14_SPxK_1 | 301 | 304 | PF00782 | 0.202 |
MOD_CDK_SPxK_1 | 298 | 304 | PF00069 | 0.202 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.337 |
MOD_CK1_1 | 199 | 205 | PF00069 | 0.321 |
MOD_CK1_1 | 666 | 672 | PF00069 | 0.581 |
MOD_CK2_1 | 268 | 274 | PF00069 | 0.412 |
MOD_Cter_Amidation | 297 | 300 | PF01082 | 0.442 |
MOD_GlcNHglycan | 158 | 162 | PF01048 | 0.334 |
MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.346 |
MOD_GlcNHglycan | 442 | 445 | PF01048 | 0.407 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.381 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.294 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.415 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.343 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.452 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.349 |
MOD_GSK3_1 | 436 | 443 | PF00069 | 0.218 |
MOD_GSK3_1 | 463 | 470 | PF00069 | 0.354 |
MOD_GSK3_1 | 496 | 503 | PF00069 | 0.339 |
MOD_GSK3_1 | 574 | 581 | PF00069 | 0.350 |
MOD_N-GLC_1 | 284 | 289 | PF02516 | 0.165 |
MOD_N-GLC_1 | 461 | 466 | PF02516 | 0.330 |
MOD_N-GLC_2 | 620 | 622 | PF02516 | 0.458 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.350 |
MOD_NEK2_1 | 129 | 134 | PF00069 | 0.257 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.312 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.319 |
MOD_NEK2_1 | 209 | 214 | PF00069 | 0.300 |
MOD_NEK2_1 | 268 | 273 | PF00069 | 0.408 |
MOD_NEK2_1 | 377 | 382 | PF00069 | 0.347 |
MOD_NEK2_1 | 396 | 401 | PF00069 | 0.272 |
MOD_NEK2_1 | 463 | 468 | PF00069 | 0.337 |
MOD_NEK2_1 | 500 | 505 | PF00069 | 0.341 |
MOD_NEK2_1 | 578 | 583 | PF00069 | 0.330 |
MOD_NEK2_1 | 68 | 73 | PF00069 | 0.426 |
MOD_NEK2_2 | 228 | 233 | PF00069 | 0.440 |
MOD_PIKK_1 | 179 | 185 | PF00454 | 0.301 |
MOD_PIKK_1 | 597 | 603 | PF00454 | 0.478 |
MOD_PK_1 | 104 | 110 | PF00069 | 0.425 |
MOD_PK_1 | 436 | 442 | PF00069 | 0.362 |
MOD_PKA_2 | 103 | 109 | PF00069 | 0.351 |
MOD_PKA_2 | 440 | 446 | PF00069 | 0.432 |
MOD_PKA_2 | 496 | 502 | PF00069 | 0.324 |
MOD_PKA_2 | 561 | 567 | PF00069 | 0.309 |
MOD_Plk_1 | 461 | 467 | PF00069 | 0.347 |
MOD_Plk_4 | 196 | 202 | PF00069 | 0.321 |
MOD_Plk_4 | 209 | 215 | PF00069 | 0.311 |
MOD_Plk_4 | 36 | 42 | PF00069 | 0.469 |
MOD_Plk_4 | 377 | 383 | PF00069 | 0.330 |
MOD_Plk_4 | 414 | 420 | PF00069 | 0.369 |
MOD_Plk_4 | 463 | 469 | PF00069 | 0.436 |
MOD_Plk_4 | 474 | 480 | PF00069 | 0.300 |
MOD_Plk_4 | 482 | 488 | PF00069 | 0.178 |
MOD_Plk_4 | 496 | 502 | PF00069 | 0.320 |
MOD_Plk_4 | 535 | 541 | PF00069 | 0.321 |
MOD_Plk_4 | 563 | 569 | PF00069 | 0.356 |
MOD_Plk_4 | 628 | 634 | PF00069 | 0.356 |
MOD_ProDKin_1 | 298 | 304 | PF00069 | 0.431 |
MOD_ProDKin_1 | 620 | 626 | PF00069 | 0.388 |
MOD_SUMO_for_1 | 8 | 11 | PF00179 | 0.475 |
MOD_SUMO_rev_2 | 642 | 651 | PF00179 | 0.382 |
TRG_DiLeu_BaEn_2 | 261 | 267 | PF01217 | 0.284 |
TRG_DiLeu_BaLyEn_6 | 610 | 615 | PF01217 | 0.355 |
TRG_DiLeu_BaLyEn_6 | 621 | 626 | PF01217 | 0.295 |
TRG_ENDOCYTIC_2 | 102 | 105 | PF00928 | 0.300 |
TRG_ENDOCYTIC_2 | 136 | 139 | PF00928 | 0.327 |
TRG_ENDOCYTIC_2 | 151 | 154 | PF00928 | 0.315 |
TRG_ENDOCYTIC_2 | 186 | 189 | PF00928 | 0.319 |
TRG_ENDOCYTIC_2 | 379 | 382 | PF00928 | 0.321 |
TRG_ENDOCYTIC_2 | 468 | 471 | PF00928 | 0.331 |
TRG_ENDOCYTIC_2 | 524 | 527 | PF00928 | 0.452 |
TRG_ENDOCYTIC_2 | 537 | 540 | PF00928 | 0.353 |
TRG_ENDOCYTIC_2 | 569 | 572 | PF00928 | 0.315 |
TRG_ENDOCYTIC_2 | 609 | 612 | PF00928 | 0.398 |
TRG_ENDOCYTIC_2 | 88 | 91 | PF00928 | 0.327 |
TRG_ER_diArg_1 | 47 | 49 | PF00400 | 0.537 |
TRG_Pf-PMV_PEXEL_1 | 257 | 262 | PF00026 | 0.465 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2U2 | Leptomonas seymouri | 47% | 99% |
A0A0N1HY49 | Leptomonas seymouri | 45% | 100% |
A0A0N1HZ06 | Leptomonas seymouri | 35% | 100% |
A0A0N1IHL1 | Leptomonas seymouri | 37% | 98% |
A0A0N1PAY4 | Leptomonas seymouri | 46% | 79% |
A0A0N1PB77 | Leptomonas seymouri | 34% | 100% |
A0A0N1PBZ2 | Leptomonas seymouri | 67% | 100% |
A0A0N1PCC1 | Leptomonas seymouri | 41% | 100% |
A0A381MBI0 | Leishmania infantum | 42% | 100% |
A0A3Q8I8X7 | Leishmania donovani | 41% | 100% |
A0A3Q8IAZ0 | Leishmania donovani | 92% | 100% |
A0A3Q8IH50 | Leishmania donovani | 59% | 97% |
A0A3Q8IVN0 | Leishmania donovani | 36% | 100% |
A0A3R7M4J1 | Trypanosoma rangeli | 40% | 100% |
A0A3S5H5P4 | Leishmania donovani | 43% | 100% |
A0A3S5H5V2 | Leishmania donovani | 41% | 100% |
A0A3S5H6F6 | Leishmania donovani | 98% | 100% |
A0A3S5H763 | Leishmania donovani | 51% | 100% |
A0A3S7WR10 | Leishmania donovani | 42% | 94% |
A0A3S7WR14 | Leishmania donovani | 80% | 100% |
A0A3S7WR15 | Leishmania donovani | 71% | 82% |
A0A3S7WR24 | Leishmania donovani | 97% | 99% |
A4H4T8 | Leishmania braziliensis | 43% | 100% |
A4H5Y4 | Leishmania braziliensis | 43% | 100% |
A4H617 | Leishmania braziliensis | 80% | 100% |
A4H618 | Leishmania braziliensis | 80% | 100% |
A4H619 | Leishmania braziliensis | 80% | 100% |
A4H620 | Leishmania braziliensis | 57% | 100% |
A4H6C3 | Leishmania braziliensis | 44% | 100% |
A4HNH7 | Leishmania braziliensis | 36% | 98% |
A4HSS2 | Leishmania infantum | 43% | 100% |
A4HUE4 | Leishmania infantum | 42% | 100% |
A4HUE5 | Leishmania infantum | 75% | 100% |
A4HUE6 | Leishmania infantum | 82% | 100% |
A4HUE7 | Leishmania infantum | 92% | 100% |
A4HUE8 | Leishmania infantum | 97% | 100% |
A4HUF5 | Leishmania infantum | 58% | 100% |
A4HYA9 | Leishmania infantum | 51% | 100% |
A4IC33 | Leishmania infantum | 36% | 100% |
C9ZIK0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
C9ZIK3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
C9ZVE8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
C9ZVE9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
C9ZVF1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
D0A423 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
E8NHQ5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
E9AG72 | Leishmania infantum | 41% | 100% |
E9AI40 | Leishmania braziliensis | 76% | 100% |
E9AJY4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 44% | 100% |
E9AKQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 43% | 100% |
E9AL06 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 43% | 100% |
E9AN44 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 42% | 100% |
E9AN45 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 74% | 99% |
E9AN46 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
E9AN47 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 58% | 100% |
E9ANE5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 44% | 100% |
E9AS42 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 51% | 100% |
E9B741 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 98% |
Q4QDC4 | Leishmania major | 51% | 100% |
Q4QH81 | Leishmania major | 43% | 100% |
Q4QHH7 | Leishmania major | 59% | 100% |
Q4QHH8 | Leishmania major | 91% | 100% |
Q4QHH9 | Leishmania major | 91% | 100% |
Q4QHI0 | Leishmania major | 89% | 99% |
Q4QHI1 | Leishmania major | 84% | 100% |
Q4QHI2 | Leishmania major | 79% | 100% |
Q4QIU9 | Leishmania major | 43% | 100% |
Q4QJ48 | Leishmania major | 43% | 100% |
Q7KIP2 | Leishmania major | 36% | 100% |