Transporters, S-adenosylmethionine transporter ADOMET1
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 |
Related structures:
AlphaFold database: A4HUE5
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 | 339 | 343 | PF00656 | 0.572 |
CLV_NRD_NRD_1 | 270 | 272 | PF00675 | 0.364 |
CLV_NRD_NRD_1 | 47 | 49 | PF00675 | 0.433 |
CLV_NRD_NRD_1 | 651 | 653 | PF00675 | 0.306 |
CLV_PCSK_KEX2_1 | 132 | 134 | PF00082 | 0.323 |
CLV_PCSK_KEX2_1 | 299 | 301 | PF00082 | 0.407 |
CLV_PCSK_KEX2_1 | 47 | 49 | PF00082 | 0.467 |
CLV_PCSK_KEX2_1 | 493 | 495 | PF00082 | 0.237 |
CLV_PCSK_KEX2_1 | 519 | 521 | PF00082 | 0.548 |
CLV_PCSK_KEX2_1 | 651 | 653 | PF00082 | 0.316 |
CLV_PCSK_PC1ET2_1 | 132 | 134 | PF00082 | 0.323 |
CLV_PCSK_PC1ET2_1 | 299 | 301 | PF00082 | 0.407 |
CLV_PCSK_PC1ET2_1 | 493 | 495 | PF00082 | 0.237 |
CLV_PCSK_PC1ET2_1 | 519 | 521 | PF00082 | 0.548 |
CLV_PCSK_SKI1_1 | 115 | 119 | PF00082 | 0.380 |
CLV_PCSK_SKI1_1 | 80 | 84 | PF00082 | 0.397 |
DOC_AGCK_PIF_1 | 460 | 465 | PF00069 | 0.218 |
DOC_CYCLIN_yCln2_LP_2 | 626 | 632 | PF00134 | 0.404 |
DOC_MAPK_gen_1 | 132 | 138 | PF00069 | 0.532 |
DOC_MAPK_gen_1 | 256 | 266 | PF00069 | 0.575 |
DOC_MAPK_gen_1 | 493 | 500 | PF00069 | 0.468 |
DOC_MAPK_gen_1 | 519 | 527 | PF00069 | 0.349 |
DOC_MAPK_gen_1 | 636 | 645 | PF00069 | 0.613 |
DOC_MAPK_MEF2A_6 | 226 | 233 | PF00069 | 0.355 |
DOC_MAPK_MEF2A_6 | 519 | 527 | PF00069 | 0.383 |
DOC_MAPK_RevD_3 | 479 | 494 | PF00069 | 0.369 |
DOC_PP1_RVXF_1 | 495 | 501 | PF00149 | 0.545 |
DOC_PP2B_LxvP_1 | 626 | 629 | PF13499 | 0.390 |
DOC_PP2B_LxvP_1 | 632 | 635 | PF13499 | 0.356 |
DOC_PP2B_PxIxI_1 | 226 | 232 | PF00149 | 0.314 |
DOC_PP4_FxxP_1 | 277 | 280 | PF00568 | 0.415 |
DOC_PP4_FxxP_1 | 31 | 34 | PF00568 | 0.588 |
DOC_USP7_MATH_1 | 195 | 199 | PF00917 | 0.506 |
DOC_USP7_MATH_1 | 302 | 306 | PF00917 | 0.586 |
DOC_USP7_MATH_1 | 482 | 486 | PF00917 | 0.403 |
DOC_USP7_MATH_1 | 538 | 542 | PF00917 | 0.341 |
DOC_USP7_MATH_1 | 561 | 565 | PF00917 | 0.512 |
DOC_WW_Pin1_4 | 298 | 303 | PF00397 | 0.615 |
DOC_WW_Pin1_4 | 441 | 446 | PF00397 | 0.357 |
DOC_WW_Pin1_4 | 665 | 670 | PF00397 | 0.676 |
DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.720 |
LIG_14-3-3_CanoR_1 | 103 | 110 | PF00244 | 0.517 |
LIG_14-3-3_CanoR_1 | 256 | 266 | PF00244 | 0.612 |
LIG_14-3-3_CanoR_1 | 304 | 311 | PF00244 | 0.626 |
LIG_14-3-3_CanoR_1 | 497 | 501 | PF00244 | 0.517 |
LIG_14-3-3_CanoR_1 | 580 | 589 | PF00244 | 0.502 |
LIG_Actin_WH2_2 | 49 | 64 | PF00022 | 0.640 |
LIG_APCC_ABBA_1 | 49 | 54 | PF00400 | 0.653 |
LIG_APCC_ABBAyCdc20_2 | 48 | 54 | PF00400 | 0.525 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.800 |
LIG_BRCT_BRCA1_1 | 463 | 467 | PF00533 | 0.343 |
LIG_Clathr_ClatBox_1 | 264 | 268 | PF01394 | 0.473 |
LIG_CtBP_PxDLS_1 | 12 | 16 | PF00389 | 0.625 |
LIG_deltaCOP1_diTrp_1 | 372 | 377 | PF00928 | 0.463 |
LIG_EVH1_1 | 666 | 670 | PF00568 | 0.629 |
LIG_FHA_1 | 116 | 122 | PF00498 | 0.596 |
LIG_FHA_1 | 382 | 388 | PF00498 | 0.382 |
LIG_FHA_1 | 397 | 403 | PF00498 | 0.285 |
LIG_FHA_1 | 446 | 452 | PF00498 | 0.404 |
LIG_FHA_1 | 497 | 503 | PF00498 | 0.518 |
LIG_FHA_1 | 511 | 517 | PF00498 | 0.385 |
LIG_FHA_1 | 629 | 635 | PF00498 | 0.442 |
LIG_FHA_1 | 68 | 74 | PF00498 | 0.584 |
LIG_FHA_2 | 268 | 274 | PF00498 | 0.597 |
LIG_FHA_2 | 598 | 604 | PF00498 | 0.254 |
LIG_HP1_1 | 551 | 555 | PF01393 | 0.425 |
LIG_LIR_Apic_2 | 275 | 280 | PF02991 | 0.415 |
LIG_LIR_Apic_2 | 29 | 34 | PF02991 | 0.633 |
LIG_LIR_Apic_2 | 348 | 354 | PF02991 | 0.556 |
LIG_LIR_Apic_2 | 416 | 422 | PF02991 | 0.444 |
LIG_LIR_Apic_2 | 592 | 596 | PF02991 | 0.328 |
LIG_LIR_Gen_1 | 123 | 130 | PF02991 | 0.546 |
LIG_LIR_Gen_1 | 182 | 193 | PF02991 | 0.555 |
LIG_LIR_Gen_1 | 201 | 209 | PF02991 | 0.530 |
LIG_LIR_Gen_1 | 466 | 475 | PF02991 | 0.356 |
LIG_LIR_Gen_1 | 485 | 491 | PF02991 | 0.420 |
LIG_LIR_Gen_1 | 503 | 512 | PF02991 | 0.316 |
LIG_LIR_Gen_1 | 566 | 576 | PF02991 | 0.542 |
LIG_LIR_Gen_1 | 86 | 94 | PF02991 | 0.565 |
LIG_LIR_Nem_3 | 123 | 128 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 131 | 137 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 182 | 188 | PF02991 | 0.562 |
LIG_LIR_Nem_3 | 201 | 207 | PF02991 | 0.318 |
LIG_LIR_Nem_3 | 241 | 247 | PF02991 | 0.370 |
LIG_LIR_Nem_3 | 371 | 377 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 41 | 46 | PF02991 | 0.620 |
LIG_LIR_Nem_3 | 416 | 421 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 457 | 463 | PF02991 | 0.321 |
LIG_LIR_Nem_3 | 464 | 468 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 485 | 490 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 503 | 508 | PF02991 | 0.353 |
LIG_NRBOX | 611 | 617 | PF00104 | 0.252 |
LIG_PDZ_Class_3 | 686 | 691 | PF00595 | 0.661 |
LIG_Pex14_2 | 168 | 172 | PF04695 | 0.391 |
LIG_Pex14_2 | 463 | 467 | PF04695 | 0.337 |
LIG_Pex14_2 | 487 | 491 | PF04695 | 0.398 |
LIG_PTB_Apo_2 | 459 | 466 | PF02174 | 0.398 |
LIG_PTB_Phospho_1 | 459 | 465 | PF10480 | 0.432 |
LIG_SH2_CRK | 101 | 105 | PF00017 | 0.538 |
LIG_SH2_CRK | 135 | 139 | PF00017 | 0.401 |
LIG_SH2_CRK | 150 | 154 | PF00017 | 0.353 |
LIG_SH2_CRK | 185 | 189 | PF00017 | 0.541 |
LIG_SH2_CRK | 351 | 355 | PF00017 | 0.645 |
LIG_SH2_CRK | 379 | 383 | PF00017 | 0.372 |
LIG_SH2_CRK | 468 | 472 | PF00017 | 0.329 |
LIG_SH2_CRK | 593 | 597 | PF00017 | 0.351 |
LIG_SH2_GRB2like | 439 | 442 | PF00017 | 0.431 |
LIG_SH2_GRB2like | 450 | 453 | PF00017 | 0.383 |
LIG_SH2_NCK_1 | 468 | 472 | PF00017 | 0.327 |
LIG_SH2_PTP2 | 439 | 442 | PF00017 | 0.376 |
LIG_SH2_PTP2 | 524 | 527 | PF00017 | 0.426 |
LIG_SH2_SRC | 439 | 442 | PF00017 | 0.507 |
LIG_SH2_SRC | 450 | 453 | PF00017 | 0.371 |
LIG_SH2_STAP1 | 130 | 134 | PF00017 | 0.527 |
LIG_SH2_STAP1 | 185 | 189 | PF00017 | 0.516 |
LIG_SH2_STAP1 | 379 | 383 | PF00017 | 0.420 |
LIG_SH2_STAP1 | 569 | 573 | PF00017 | 0.365 |
LIG_SH2_STAP1 | 87 | 91 | PF00017 | 0.563 |
LIG_SH2_STAT3 | 433 | 436 | PF00017 | 0.234 |
LIG_SH2_STAT5 | 130 | 133 | PF00017 | 0.528 |
LIG_SH2_STAT5 | 245 | 248 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 433 | 436 | PF00017 | 0.381 |
LIG_SH2_STAT5 | 439 | 442 | PF00017 | 0.373 |
LIG_SH2_STAT5 | 450 | 453 | PF00017 | 0.313 |
LIG_SH2_STAT5 | 524 | 527 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 533 | 536 | PF00017 | 0.320 |
LIG_SH3_1 | 351 | 357 | PF00018 | 0.612 |
LIG_SH3_3 | 321 | 327 | PF00018 | 0.455 |
LIG_SH3_3 | 351 | 357 | PF00018 | 0.622 |
LIG_SH3_3 | 618 | 624 | PF00018 | 0.366 |
LIG_SH3_3 | 664 | 670 | PF00018 | 0.760 |
LIG_SUMO_SIM_anti_2 | 513 | 519 | PF11976 | 0.345 |
LIG_SUMO_SIM_par_1 | 551 | 557 | PF11976 | 0.355 |
LIG_TRAF2_1 | 11 | 14 | PF00917 | 0.767 |
LIG_TRFH_1 | 150 | 154 | PF08558 | 0.388 |
LIG_TYR_ITIM | 148 | 153 | PF00017 | 0.407 |
LIG_UBA3_1 | 148 | 156 | PF00899 | 0.385 |
LIG_UBA3_1 | 264 | 272 | PF00899 | 0.548 |
LIG_Vh1_VBS_1 | 377 | 395 | PF01044 | 0.434 |
LIG_WRC_WIRS_1 | 446 | 451 | PF05994 | 0.361 |
LIG_WRC_WIRS_1 | 502 | 507 | PF05994 | 0.332 |
MOD_CDC14_SPxK_1 | 301 | 304 | PF00782 | 0.259 |
MOD_CDK_SPxK_1 | 298 | 304 | PF00069 | 0.259 |
MOD_CK1_1 | 198 | 204 | PF00069 | 0.373 |
MOD_CK1_1 | 492 | 498 | PF00069 | 0.378 |
MOD_CK1_1 | 668 | 674 | PF00069 | 0.689 |
MOD_CK2_1 | 267 | 273 | PF00069 | 0.458 |
MOD_CK2_1 | 668 | 674 | PF00069 | 0.763 |
MOD_CK2_1 | 8 | 14 | PF00069 | 0.709 |
MOD_Cter_Amidation | 297 | 300 | PF01082 | 0.496 |
MOD_GlcNHglycan | 13 | 18 | PF01048 | 0.653 |
MOD_GlcNHglycan | 157 | 161 | PF01048 | 0.386 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.398 |
MOD_GlcNHglycan | 484 | 487 | PF01048 | 0.372 |
MOD_GlcNHglycan | 582 | 585 | PF01048 | 0.418 |
MOD_GlcNHglycan | 671 | 674 | PF01048 | 0.788 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.433 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.468 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.447 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.401 |
MOD_GSK3_1 | 441 | 448 | PF00069 | 0.266 |
MOD_GSK3_1 | 463 | 470 | PF00069 | 0.405 |
MOD_GSK3_1 | 492 | 499 | PF00069 | 0.390 |
MOD_GSK3_1 | 574 | 581 | PF00069 | 0.402 |
MOD_GSK3_1 | 665 | 672 | PF00069 | 0.734 |
MOD_N-GLC_1 | 461 | 466 | PF02516 | 0.382 |
MOD_N-GLC_2 | 620 | 622 | PF02516 | 0.514 |
MOD_NEK2_1 | 110 | 115 | PF00069 | 0.402 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.309 |
MOD_NEK2_1 | 136 | 141 | PF00069 | 0.364 |
MOD_NEK2_1 | 168 | 173 | PF00069 | 0.371 |
MOD_NEK2_1 | 267 | 272 | PF00069 | 0.436 |
MOD_NEK2_1 | 377 | 382 | PF00069 | 0.398 |
MOD_NEK2_1 | 396 | 401 | PF00069 | 0.324 |
MOD_NEK2_1 | 408 | 413 | PF00069 | 0.344 |
MOD_NEK2_1 | 463 | 468 | PF00069 | 0.389 |
MOD_NEK2_1 | 500 | 505 | PF00069 | 0.393 |
MOD_NEK2_1 | 578 | 583 | PF00069 | 0.381 |
MOD_NEK2_1 | 67 | 72 | PF00069 | 0.478 |
MOD_NEK2_2 | 227 | 232 | PF00069 | 0.495 |
MOD_NEK2_2 | 445 | 450 | PF00069 | 0.363 |
MOD_PKA_2 | 102 | 108 | PF00069 | 0.403 |
MOD_PKA_2 | 496 | 502 | PF00069 | 0.376 |
MOD_PKA_2 | 561 | 567 | PF00069 | 0.361 |
MOD_PKA_2 | 579 | 585 | PF00069 | 0.361 |
MOD_PKA_2 | 676 | 682 | PF00069 | 0.853 |
MOD_Plk_1 | 461 | 467 | PF00069 | 0.399 |
MOD_Plk_4 | 195 | 201 | PF00069 | 0.372 |
MOD_Plk_4 | 212 | 218 | PF00069 | 0.358 |
MOD_Plk_4 | 377 | 383 | PF00069 | 0.382 |
MOD_Plk_4 | 414 | 420 | PF00069 | 0.420 |
MOD_Plk_4 | 445 | 451 | PF00069 | 0.365 |
MOD_Plk_4 | 463 | 469 | PF00069 | 0.490 |
MOD_Plk_4 | 563 | 569 | PF00069 | 0.408 |
MOD_Plk_4 | 628 | 634 | PF00069 | 0.407 |
MOD_ProDKin_1 | 298 | 304 | PF00069 | 0.500 |
MOD_ProDKin_1 | 441 | 447 | PF00069 | 0.357 |
MOD_ProDKin_1 | 665 | 671 | PF00069 | 0.588 |
MOD_ProDKin_1 | 8 | 14 | PF00069 | 0.647 |
MOD_SUMO_for_1 | 26 | 29 | PF00179 | 0.454 |
MOD_SUMO_rev_2 | 641 | 650 | PF00179 | 0.434 |
TRG_DiLeu_BaEn_2 | 260 | 266 | PF01217 | 0.341 |
TRG_ENDOCYTIC_2 | 101 | 104 | PF00928 | 0.351 |
TRG_ENDOCYTIC_2 | 135 | 138 | PF00928 | 0.379 |
TRG_ENDOCYTIC_2 | 150 | 153 | PF00928 | 0.367 |
TRG_ENDOCYTIC_2 | 185 | 188 | PF00928 | 0.371 |
TRG_ENDOCYTIC_2 | 379 | 382 | PF00928 | 0.373 |
TRG_ENDOCYTIC_2 | 439 | 442 | PF00928 | 0.386 |
TRG_ENDOCYTIC_2 | 468 | 471 | PF00928 | 0.382 |
TRG_ENDOCYTIC_2 | 524 | 527 | PF00928 | 0.507 |
TRG_ENDOCYTIC_2 | 549 | 552 | PF00928 | 0.330 |
TRG_ENDOCYTIC_2 | 569 | 572 | PF00928 | 0.366 |
TRG_ENDOCYTIC_2 | 87 | 90 | PF00928 | 0.378 |
TRG_ER_diArg_1 | 46 | 48 | PF00400 | 0.584 |
TRG_ER_diArg_1 | 650 | 652 | PF00400 | 0.326 |
TRG_Pf-PMV_PEXEL_1 | 256 | 261 | PF00026 | 0.515 |
TRG_Pf-PMV_PEXEL_1 | 328 | 332 | PF00026 | 0.495 |
TRG_Pf-PMV_PEXEL_1 | 80 | 85 | PF00026 | 0.231 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2U2 | Leptomonas seymouri | 45% | 98% |
A0A0N1HY49 | Leptomonas seymouri | 46% | 100% |
A0A0N1HZ06 | Leptomonas seymouri | 37% | 100% |
A0A0N1IHL1 | Leptomonas seymouri | 40% | 97% |
A0A0N1PAY4 | Leptomonas seymouri | 45% | 79% |
A0A0N1PB77 | Leptomonas seymouri | 37% | 100% |
A0A0N1PBZ2 | Leptomonas seymouri | 65% | 100% |
A0A0N1PCC1 | Leptomonas seymouri | 42% | 100% |
A0A381MBI0 | Leishmania infantum | 42% | 100% |
A0A3Q8I8X7 | Leishmania donovani | 43% | 100% |
A0A3Q8IAZ0 | Leishmania donovani | 74% | 99% |
A0A3Q8IH50 | Leishmania donovani | 58% | 96% |
A0A3Q8IVN0 | Leishmania donovani | 38% | 100% |
A0A3R7M4J1 | Trypanosoma rangeli | 40% | 100% |
A0A3S5H5P4 | Leishmania donovani | 44% | 100% |
A0A3S5H5V2 | Leishmania donovani | 44% | 100% |
A0A3S5H6F6 | Leishmania donovani | 75% | 99% |
A0A3S5H763 | Leishmania donovani | 53% | 100% |
A0A3S7WR10 | Leishmania donovani | 42% | 93% |
A0A3S7WR14 | Leishmania donovani | 74% | 100% |
A0A3S7WR15 | Leishmania donovani | 99% | 81% |
A0A3S7WR24 | Leishmania donovani | 74% | 98% |
A4H4T8 | Leishmania braziliensis | 41% | 94% |
A4H5Y4 | Leishmania braziliensis | 44% | 100% |
A4H617 | Leishmania braziliensis | 70% | 100% |
A4H618 | Leishmania braziliensis | 68% | 100% |
A4H619 | Leishmania braziliensis | 70% | 100% |
A4H620 | Leishmania braziliensis | 62% | 100% |
A4H6C3 | Leishmania braziliensis | 42% | 98% |
A4HNH7 | Leishmania braziliensis | 35% | 93% |
A4HSS2 | Leishmania infantum | 43% | 100% |
A4HUE4 | Leishmania infantum | 42% | 100% |
A4HUE6 | Leishmania infantum | 74% | 100% |
A4HUE7 | Leishmania infantum | 74% | 99% |
A4HUE8 | Leishmania infantum | 74% | 98% |
A4HUF4 | Leishmania infantum | 75% | 99% |
A4HUF5 | Leishmania infantum | 58% | 100% |
A4HYA9 | Leishmania infantum | 53% | 100% |
A4IC33 | Leishmania infantum | 37% | 100% |
C9ZIK0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
C9ZIK3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
C9ZVE8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
C9ZVE9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
C9ZVF1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
D0A423 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
E8NHQ5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 72% | 100% |
E9AG72 | Leishmania infantum | 43% | 100% |
E9AI40 | Leishmania braziliensis | 77% | 98% |
E9AJY4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 46% | 100% |
E9AKQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 42% | 100% |
E9AL06 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 94% |
E9AN44 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 42% | 100% |
E9AN45 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
E9AN46 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 72% | 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% | 96% |
Q4QDC4 | Leishmania major | 51% | 100% |
Q4QH81 | Leishmania major | 42% | 95% |
Q4QHH7 | Leishmania major | 57% | 98% |
Q4QHH8 | Leishmania major | 71% | 100% |
Q4QHH9 | Leishmania major | 71% | 100% |
Q4QHI0 | Leishmania major | 71% | 100% |
Q4QHI1 | Leishmania major | 72% | 99% |
Q4QHI2 | Leishmania major | 87% | 99% |
Q4QIU9 | Leishmania major | 42% | 100% |
Q4QJ48 | Leishmania major | 41% | 100% |
Q7KIP2 | Leishmania major | 36% | 99% |