Transporters, folate/biopterin transporter FT1
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) | yes | 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 |
Related structures:
AlphaFold database: A4HUE8
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 | 0.821 |
CLV_MEL_PAP_1 | 438 | 444 | PF00089 | 0.301 |
CLV_NRD_NRD_1 | 271 | 273 | PF00675 | 0.389 |
CLV_NRD_NRD_1 | 48 | 50 | PF00675 | 0.461 |
CLV_PCSK_KEX2_1 | 133 | 135 | PF00082 | 0.348 |
CLV_PCSK_KEX2_1 | 299 | 301 | PF00082 | 0.432 |
CLV_PCSK_KEX2_1 | 48 | 50 | PF00082 | 0.495 |
CLV_PCSK_KEX2_1 | 519 | 521 | PF00082 | 0.573 |
CLV_PCSK_KEX2_1 | 697 | 699 | PF00082 | 0.481 |
CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.467 |
CLV_PCSK_PC1ET2_1 | 133 | 135 | PF00082 | 0.348 |
CLV_PCSK_PC1ET2_1 | 299 | 301 | PF00082 | 0.432 |
CLV_PCSK_PC1ET2_1 | 519 | 521 | PF00082 | 0.573 |
CLV_PCSK_PC1ET2_1 | 697 | 699 | PF00082 | 0.498 |
CLV_PCSK_PC1ET2_1 | 9 | 11 | PF00082 | 0.467 |
CLV_PCSK_SKI1_1 | 116 | 120 | PF00082 | 0.405 |
CLV_PCSK_SKI1_1 | 316 | 320 | PF00082 | 0.400 |
DEG_APCC_DBOX_1 | 276 | 284 | PF00400 | 0.477 |
DOC_CDC14_PxL_1 | 609 | 617 | PF14671 | 0.382 |
DOC_CKS1_1 | 621 | 626 | PF01111 | 0.483 |
DOC_CYCLIN_yCln2_LP_2 | 626 | 632 | PF00134 | 0.429 |
DOC_MAPK_gen_1 | 133 | 139 | PF00069 | 0.557 |
DOC_MAPK_gen_1 | 257 | 267 | PF00069 | 0.600 |
DOC_MAPK_gen_1 | 272 | 280 | PF00069 | 0.592 |
DOC_MAPK_gen_1 | 519 | 527 | PF00069 | 0.374 |
DOC_MAPK_gen_1 | 637 | 646 | PF00069 | 0.638 |
DOC_MAPK_MEF2A_6 | 227 | 234 | PF00069 | 0.380 |
DOC_MAPK_MEF2A_6 | 519 | 527 | PF00069 | 0.408 |
DOC_PP1_RVXF_1 | 495 | 501 | PF00149 | 0.570 |
DOC_PP2B_LxvP_1 | 626 | 629 | PF13499 | 0.415 |
DOC_PP2B_PxIxI_1 | 227 | 233 | PF00149 | 0.339 |
DOC_USP7_MATH_1 | 199 | 203 | PF00917 | 0.373 |
DOC_USP7_MATH_1 | 302 | 306 | PF00917 | 0.611 |
DOC_USP7_MATH_1 | 561 | 565 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 663 | 667 | PF00917 | 0.687 |
DOC_USP7_MATH_1 | 699 | 703 | PF00917 | 0.795 |
DOC_WW_Pin1_4 | 298 | 303 | PF00397 | 0.640 |
DOC_WW_Pin1_4 | 620 | 625 | PF00397 | 0.465 |
LIG_14-3-3_CanoR_1 | 104 | 111 | PF00244 | 0.542 |
LIG_14-3-3_CanoR_1 | 257 | 267 | PF00244 | 0.637 |
LIG_14-3-3_CanoR_1 | 304 | 311 | PF00244 | 0.651 |
LIG_14-3-3_CanoR_1 | 497 | 501 | PF00244 | 0.542 |
LIG_14-3-3_CanoR_1 | 577 | 586 | PF00244 | 0.550 |
LIG_Actin_WH2_2 | 50 | 65 | PF00022 | 0.668 |
LIG_APCC_ABBA_1 | 50 | 55 | PF00400 | 0.683 |
LIG_APCC_ABBAyCdc20_2 | 49 | 55 | PF00400 | 0.554 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.818 |
LIG_BIR_III_4 | 13 | 17 | PF00653 | 0.772 |
LIG_Clathr_ClatBox_1 | 265 | 269 | PF01394 | 0.498 |
LIG_EH1_1 | 499 | 507 | PF00400 | 0.392 |
LIG_eIF4E_1 | 609 | 615 | PF01652 | 0.282 |
LIG_FHA_1 | 117 | 123 | PF00498 | 0.621 |
LIG_FHA_1 | 365 | 371 | PF00498 | 0.642 |
LIG_FHA_1 | 382 | 388 | PF00498 | 0.407 |
LIG_FHA_1 | 397 | 403 | PF00498 | 0.310 |
LIG_FHA_1 | 481 | 487 | PF00498 | 0.445 |
LIG_FHA_1 | 497 | 503 | PF00498 | 0.543 |
LIG_FHA_1 | 621 | 627 | PF00498 | 0.469 |
LIG_FHA_2 | 269 | 275 | PF00498 | 0.622 |
LIG_FHA_2 | 598 | 604 | PF00498 | 0.279 |
LIG_GBD_Chelix_1 | 478 | 486 | PF00786 | 0.284 |
LIG_GBD_Chelix_1 | 501 | 509 | PF00786 | 0.525 |
LIG_GBD_Chelix_1 | 539 | 547 | PF00786 | 0.555 |
LIG_LIR_Apic_2 | 29 | 35 | PF02991 | 0.655 |
LIG_LIR_Apic_2 | 348 | 354 | PF02991 | 0.581 |
LIG_LIR_Apic_2 | 417 | 422 | PF02991 | 0.467 |
LIG_LIR_Apic_2 | 453 | 457 | PF02991 | 0.383 |
LIG_LIR_Apic_2 | 592 | 596 | PF02991 | 0.353 |
LIG_LIR_Gen_1 | 124 | 131 | PF02991 | 0.571 |
LIG_LIR_Gen_1 | 202 | 210 | PF02991 | 0.555 |
LIG_LIR_Gen_1 | 466 | 475 | PF02991 | 0.381 |
LIG_LIR_Gen_1 | 485 | 492 | PF02991 | 0.445 |
LIG_LIR_Gen_1 | 566 | 576 | PF02991 | 0.567 |
LIG_LIR_Gen_1 | 87 | 95 | PF02991 | 0.590 |
LIG_LIR_Nem_3 | 124 | 129 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 132 | 138 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 202 | 208 | PF02991 | 0.343 |
LIG_LIR_Nem_3 | 242 | 248 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 371 | 377 | PF02991 | 0.550 |
LIG_LIR_Nem_3 | 417 | 421 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 464 | 468 | PF02991 | 0.351 |
LIG_LIR_Nem_3 | 485 | 490 | PF02991 | 0.393 |
LIG_PCNA_PIPBox_1 | 506 | 515 | PF02747 | 0.253 |
LIG_Pex14_2 | 169 | 173 | PF04695 | 0.416 |
LIG_Pex14_2 | 463 | 467 | PF04695 | 0.362 |
LIG_Pex14_2 | 487 | 491 | PF04695 | 0.423 |
LIG_PTB_Apo_2 | 459 | 466 | PF02174 | 0.423 |
LIG_PTB_Apo_2 | 485 | 492 | PF02174 | 0.491 |
LIG_PTB_Phospho_1 | 459 | 465 | PF10480 | 0.457 |
LIG_Rb_pABgroove_1 | 507 | 515 | PF01858 | 0.385 |
LIG_SH2_CRK | 102 | 106 | PF00017 | 0.563 |
LIG_SH2_CRK | 136 | 140 | PF00017 | 0.426 |
LIG_SH2_CRK | 151 | 155 | PF00017 | 0.378 |
LIG_SH2_CRK | 186 | 190 | PF00017 | 0.566 |
LIG_SH2_CRK | 351 | 355 | PF00017 | 0.670 |
LIG_SH2_CRK | 379 | 383 | PF00017 | 0.397 |
LIG_SH2_CRK | 454 | 458 | PF00017 | 0.379 |
LIG_SH2_CRK | 468 | 472 | PF00017 | 0.354 |
LIG_SH2_CRK | 593 | 597 | PF00017 | 0.376 |
LIG_SH2_CRK | 609 | 613 | PF00017 | 0.409 |
LIG_SH2_GRB2like | 450 | 453 | PF00017 | 0.408 |
LIG_SH2_GRB2like | 609 | 612 | PF00017 | 0.402 |
LIG_SH2_NCK_1 | 334 | 338 | PF00017 | 0.488 |
LIG_SH2_NCK_1 | 468 | 472 | PF00017 | 0.352 |
LIG_SH2_PTP2 | 32 | 35 | PF00017 | 0.650 |
LIG_SH2_PTP2 | 524 | 527 | PF00017 | 0.451 |
LIG_SH2_SRC | 32 | 35 | PF00017 | 0.656 |
LIG_SH2_SRC | 334 | 337 | PF00017 | 0.491 |
LIG_SH2_SRC | 338 | 341 | PF00017 | 0.478 |
LIG_SH2_STAP1 | 131 | 135 | PF00017 | 0.552 |
LIG_SH2_STAP1 | 186 | 190 | PF00017 | 0.541 |
LIG_SH2_STAP1 | 334 | 338 | PF00017 | 0.483 |
LIG_SH2_STAP1 | 379 | 383 | PF00017 | 0.445 |
LIG_SH2_STAP1 | 569 | 573 | PF00017 | 0.390 |
LIG_SH2_STAP1 | 88 | 92 | PF00017 | 0.588 |
LIG_SH2_STAT5 | 131 | 134 | PF00017 | 0.553 |
LIG_SH2_STAT5 | 246 | 249 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 32 | 35 | PF00017 | 0.645 |
LIG_SH2_STAT5 | 433 | 436 | PF00017 | 0.406 |
LIG_SH2_STAT5 | 450 | 453 | PF00017 | 0.338 |
LIG_SH2_STAT5 | 465 | 468 | PF00017 | 0.314 |
LIG_SH2_STAT5 | 524 | 527 | PF00017 | 0.353 |
LIG_SH2_STAT5 | 533 | 536 | PF00017 | 0.345 |
LIG_SH3_1 | 351 | 357 | PF00018 | 0.637 |
LIG_SH3_3 | 351 | 357 | PF00018 | 0.647 |
LIG_SH3_3 | 439 | 445 | PF00018 | 0.411 |
LIG_SUMO_SIM_anti_2 | 514 | 519 | PF11976 | 0.371 |
LIG_SUMO_SIM_anti_2 | 631 | 636 | PF11976 | 0.515 |
LIG_SUMO_SIM_par_1 | 480 | 485 | PF11976 | 0.287 |
LIG_SUMO_SIM_par_1 | 552 | 557 | PF11976 | 0.380 |
LIG_TRFH_1 | 151 | 155 | PF08558 | 0.413 |
LIG_TYR_ITIM | 149 | 154 | PF00017 | 0.432 |
LIG_TYR_ITSM | 464 | 471 | PF00017 | 0.455 |
LIG_UBA3_1 | 149 | 157 | PF00899 | 0.410 |
LIG_UBA3_1 | 265 | 273 | PF00899 | 0.573 |
LIG_UBA3_1 | 486 | 493 | PF00899 | 0.467 |
LIG_UBA3_1 | 512 | 519 | PF00899 | 0.374 |
LIG_UBA3_1 | 632 | 637 | PF00899 | 0.287 |
LIG_Vh1_VBS_1 | 377 | 395 | PF01044 | 0.459 |
LIG_Vh1_VBS_1 | 467 | 485 | PF01044 | 0.438 |
MOD_CDC14_SPxK_1 | 301 | 304 | PF00782 | 0.284 |
MOD_CDK_SPxK_1 | 298 | 304 | PF00069 | 0.284 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.414 |
MOD_CK1_1 | 620 | 626 | PF00069 | 0.297 |
MOD_CK1_1 | 666 | 672 | PF00069 | 0.662 |
MOD_CK2_1 | 268 | 274 | PF00069 | 0.483 |
MOD_Cter_Amidation | 297 | 300 | PF01082 | 0.521 |
MOD_Cter_Amidation | 695 | 698 | PF01082 | 0.533 |
MOD_GlcNHglycan | 158 | 162 | PF01048 | 0.411 |
MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.423 |
MOD_GlcNHglycan | 442 | 445 | PF01048 | 0.485 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.458 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.371 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.493 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.472 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.532 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.426 |
MOD_GSK3_1 | 436 | 443 | PF00069 | 0.300 |
MOD_GSK3_1 | 463 | 470 | PF00069 | 0.430 |
MOD_GSK3_1 | 496 | 503 | PF00069 | 0.416 |
MOD_GSK3_1 | 578 | 585 | PF00069 | 0.425 |
MOD_N-GLC_1 | 284 | 289 | PF02516 | 0.247 |
MOD_N-GLC_1 | 461 | 466 | PF02516 | 0.407 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.427 |
MOD_NEK2_1 | 129 | 134 | PF00069 | 0.334 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.389 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.396 |
MOD_NEK2_1 | 209 | 214 | PF00069 | 0.377 |
MOD_NEK2_1 | 268 | 273 | PF00069 | 0.461 |
MOD_NEK2_1 | 377 | 382 | PF00069 | 0.423 |
MOD_NEK2_1 | 396 | 401 | PF00069 | 0.349 |
MOD_NEK2_1 | 463 | 468 | PF00069 | 0.414 |
MOD_NEK2_1 | 500 | 505 | PF00069 | 0.418 |
MOD_NEK2_1 | 578 | 583 | PF00069 | 0.406 |
MOD_NEK2_1 | 617 | 622 | PF00069 | 0.500 |
MOD_NEK2_1 | 68 | 73 | PF00069 | 0.507 |
MOD_NEK2_2 | 228 | 233 | PF00069 | 0.520 |
MOD_PIKK_1 | 179 | 185 | PF00454 | 0.378 |
MOD_PIKK_1 | 597 | 603 | PF00454 | 0.559 |
MOD_PK_1 | 104 | 110 | PF00069 | 0.503 |
MOD_PK_1 | 436 | 442 | PF00069 | 0.439 |
MOD_PKA_2 | 103 | 109 | PF00069 | 0.428 |
MOD_PKA_2 | 440 | 446 | PF00069 | 0.511 |
MOD_PKA_2 | 496 | 502 | PF00069 | 0.401 |
MOD_PKA_2 | 561 | 567 | PF00069 | 0.386 |
MOD_PKA_2 | 579 | 585 | PF00069 | 0.386 |
MOD_Plk_1 | 461 | 467 | PF00069 | 0.424 |
MOD_Plk_4 | 199 | 205 | PF00069 | 0.396 |
MOD_Plk_4 | 209 | 215 | PF00069 | 0.388 |
MOD_Plk_4 | 36 | 42 | PF00069 | 0.544 |
MOD_Plk_4 | 377 | 383 | PF00069 | 0.407 |
MOD_Plk_4 | 414 | 420 | PF00069 | 0.445 |
MOD_Plk_4 | 463 | 469 | PF00069 | 0.515 |
MOD_Plk_4 | 474 | 480 | PF00069 | 0.377 |
MOD_Plk_4 | 482 | 488 | PF00069 | 0.258 |
MOD_Plk_4 | 496 | 502 | PF00069 | 0.397 |
MOD_Plk_4 | 563 | 569 | PF00069 | 0.433 |
MOD_Plk_4 | 628 | 634 | PF00069 | 0.432 |
MOD_ProDKin_1 | 298 | 304 | PF00069 | 0.525 |
MOD_ProDKin_1 | 620 | 626 | PF00069 | 0.465 |
MOD_SUMO_for_1 | 8 | 11 | PF00179 | 0.560 |
MOD_SUMO_rev_2 | 642 | 651 | PF00179 | 0.459 |
TRG_DiLeu_BaEn_2 | 261 | 267 | PF01217 | 0.366 |
TRG_DiLeu_BaLyEn_6 | 610 | 615 | PF01217 | 0.432 |
TRG_DiLeu_BaLyEn_6 | 621 | 626 | PF01217 | 0.372 |
TRG_ENDOCYTIC_2 | 102 | 105 | PF00928 | 0.376 |
TRG_ENDOCYTIC_2 | 136 | 139 | PF00928 | 0.404 |
TRG_ENDOCYTIC_2 | 151 | 154 | PF00928 | 0.392 |
TRG_ENDOCYTIC_2 | 186 | 189 | PF00928 | 0.396 |
TRG_ENDOCYTIC_2 | 379 | 382 | PF00928 | 0.398 |
TRG_ENDOCYTIC_2 | 468 | 471 | PF00928 | 0.407 |
TRG_ENDOCYTIC_2 | 524 | 527 | PF00928 | 0.532 |
TRG_ENDOCYTIC_2 | 569 | 572 | PF00928 | 0.391 |
TRG_ENDOCYTIC_2 | 609 | 612 | PF00928 | 0.476 |
TRG_ENDOCYTIC_2 | 88 | 91 | PF00928 | 0.403 |
TRG_ER_diArg_1 | 47 | 49 | PF00400 | 0.615 |
TRG_Pf-PMV_PEXEL_1 | 257 | 262 | PF00026 | 0.540 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2U2 | Leptomonas seymouri | 47% | 100% |
A0A0N1HY49 | Leptomonas seymouri | 44% | 100% |
A0A0N1HZ06 | Leptomonas seymouri | 37% | 100% |
A0A0N1IHL1 | Leptomonas seymouri | 38% | 99% |
A0A0N1PAY4 | Leptomonas seymouri | 46% | 80% |
A0A0N1PB77 | Leptomonas seymouri | 35% | 100% |
A0A0N1PBZ2 | Leptomonas seymouri | 67% | 100% |
A0A0N1PCC1 | Leptomonas seymouri | 42% | 100% |
A0A381MBI0 | Leishmania infantum | 43% | 100% |
A0A3Q8I8X7 | Leishmania donovani | 42% | 100% |
A0A3Q8IAZ0 | Leishmania donovani | 91% | 100% |
A0A3Q8IH50 | Leishmania donovani | 59% | 98% |
A0A3Q8IVN0 | Leishmania donovani | 38% | 100% |
A0A3R7M4J1 | Trypanosoma rangeli | 40% | 100% |
A0A3S5H5P4 | Leishmania donovani | 43% | 100% |
A0A3S5H5V2 | Leishmania donovani | 42% | 100% |
A0A3S5H6F6 | Leishmania donovani | 95% | 100% |
A0A3S5H763 | Leishmania donovani | 51% | 100% |
A0A3S7WR10 | Leishmania donovani | 43% | 94% |
A0A3S7WR14 | Leishmania donovani | 81% | 100% |
A0A3S7WR15 | Leishmania donovani | 71% | 83% |
A0A3S7WR24 | Leishmania donovani | 99% | 100% |
A4H4T8 | Leishmania braziliensis | 44% | 100% |
A4H5Y4 | Leishmania braziliensis | 44% | 100% |
A4H617 | Leishmania braziliensis | 80% | 100% |
A4H618 | Leishmania braziliensis | 79% | 100% |
A4H619 | Leishmania braziliensis | 81% | 100% |
A4H620 | Leishmania braziliensis | 57% | 100% |
A4H6C3 | Leishmania braziliensis | 43% | 100% |
A4HNH7 | Leishmania braziliensis | 37% | 98% |
A4HSS2 | Leishmania infantum | 44% | 100% |
A4HUE4 | Leishmania infantum | 43% | 100% |
A4HUE5 | Leishmania infantum | 74% | 100% |
A4HUE6 | Leishmania infantum | 83% | 100% |
A4HUE7 | Leishmania infantum | 92% | 100% |
A4HUF4 | Leishmania infantum | 97% | 100% |
A4HUF5 | Leishmania infantum | 58% | 100% |
A4HYA9 | Leishmania infantum | 51% | 100% |
A4IC33 | Leishmania infantum | 37% | 100% |
C9ZIK0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
C9ZIK3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
C9ZVE8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
C9ZVE9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
C9ZVF1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
D0A423 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
E8NHQ5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
E9AG72 | Leishmania infantum | 42% | 100% |
E9AI40 | Leishmania braziliensis | 76% | 100% |
E9AJY4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 45% | 100% |
E9AKQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 42% | 100% |
E9AL06 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 43% | 100% |
E9AN44 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 43% | 100% |
E9AN45 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 74% | 99% |
E9AN46 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
E9AN47 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 59% | 100% |
E9ANE5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 45% | 100% |
E9AS42 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 51% | 100% |
E9B741 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 98% |
Q4QDC4 | Leishmania major | 51% | 100% |
Q4QH81 | Leishmania major | 44% | 100% |
Q4QHH7 | Leishmania major | 57% | 100% |
Q4QHH8 | Leishmania major | 91% | 100% |
Q4QHH9 | Leishmania major | 93% | 100% |
Q4QHI0 | Leishmania major | 88% | 99% |
Q4QHI1 | Leishmania major | 85% | 100% |
Q4QHI2 | Leishmania major | 78% | 100% |
Q4QIU9 | Leishmania major | 44% | 100% |
Q4QJ48 | Leishmania major | 43% | 100% |
Q7KIP2 | Leishmania major | 37% | 100% |