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: A4HUE6
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_NRD_NRD_1 | 273 | 275 | PF00675 | 0.364 |
CLV_NRD_NRD_1 | 50 | 52 | PF00675 | 0.437 |
CLV_PCSK_KEX2_1 | 135 | 137 | PF00082 | 0.323 |
CLV_PCSK_KEX2_1 | 301 | 303 | PF00082 | 0.407 |
CLV_PCSK_KEX2_1 | 50 | 52 | PF00082 | 0.471 |
CLV_PCSK_KEX2_1 | 521 | 523 | PF00082 | 0.548 |
CLV_PCSK_KEX2_1 | 525 | 527 | PF00082 | 0.548 |
CLV_PCSK_PC1ET2_1 | 135 | 137 | PF00082 | 0.323 |
CLV_PCSK_PC1ET2_1 | 301 | 303 | PF00082 | 0.407 |
CLV_PCSK_PC1ET2_1 | 521 | 523 | PF00082 | 0.548 |
CLV_PCSK_PC1ET2_1 | 525 | 527 | PF00082 | 0.548 |
CLV_PCSK_SKI1_1 | 118 | 122 | PF00082 | 0.380 |
CLV_PCSK_SKI1_1 | 318 | 322 | PF00082 | 0.375 |
DOC_CDC14_PxL_1 | 608 | 616 | PF14671 | 0.357 |
DOC_CKS1_1 | 620 | 625 | PF01111 | 0.458 |
DOC_CYCLIN_yCln2_LP_2 | 625 | 631 | PF00134 | 0.404 |
DOC_MAPK_gen_1 | 135 | 141 | PF00069 | 0.532 |
DOC_MAPK_gen_1 | 259 | 269 | PF00069 | 0.575 |
DOC_MAPK_gen_1 | 521 | 529 | PF00069 | 0.349 |
DOC_MAPK_MEF2A_6 | 229 | 236 | PF00069 | 0.355 |
DOC_PP2B_LxvP_1 | 625 | 628 | PF13499 | 0.390 |
DOC_PP2B_PxIxI_1 | 229 | 235 | PF00149 | 0.314 |
DOC_USP7_MATH_1 | 109 | 113 | PF00917 | 0.618 |
DOC_USP7_MATH_1 | 198 | 202 | PF00917 | 0.506 |
DOC_USP7_MATH_1 | 20 | 24 | PF00917 | 0.698 |
DOC_USP7_MATH_1 | 304 | 308 | PF00917 | 0.586 |
DOC_USP7_MATH_1 | 563 | 567 | PF00917 | 0.512 |
DOC_USP7_MATH_1 | 664 | 668 | PF00917 | 0.599 |
DOC_USP7_MATH_1 | 673 | 677 | PF00917 | 0.776 |
DOC_USP7_UBL2_3 | 521 | 525 | PF12436 | 0.209 |
DOC_WW_Pin1_4 | 105 | 110 | PF00397 | 0.439 |
DOC_WW_Pin1_4 | 300 | 305 | PF00397 | 0.615 |
DOC_WW_Pin1_4 | 443 | 448 | PF00397 | 0.357 |
DOC_WW_Pin1_4 | 619 | 624 | PF00397 | 0.440 |
LIG_14-3-3_CanoR_1 | 259 | 269 | PF00244 | 0.612 |
LIG_14-3-3_CanoR_1 | 306 | 313 | PF00244 | 0.626 |
LIG_14-3-3_CanoR_1 | 443 | 447 | PF00244 | 0.438 |
LIG_14-3-3_CanoR_1 | 96 | 102 | PF00244 | 0.482 |
LIG_APCC_ABBA_1 | 52 | 57 | PF00400 | 0.660 |
LIG_APCC_ABBAyCdc20_2 | 51 | 57 | PF00400 | 0.531 |
LIG_Clathr_ClatBox_1 | 267 | 271 | PF01394 | 0.473 |
LIG_deltaCOP1_diTrp_1 | 594 | 600 | PF00928 | 0.269 |
LIG_EH1_1 | 501 | 509 | PF00400 | 0.367 |
LIG_eIF4E_1 | 608 | 614 | PF01652 | 0.257 |
LIG_FHA_1 | 119 | 125 | PF00498 | 0.596 |
LIG_FHA_1 | 367 | 373 | PF00498 | 0.617 |
LIG_FHA_1 | 384 | 390 | PF00498 | 0.382 |
LIG_FHA_1 | 399 | 405 | PF00498 | 0.285 |
LIG_FHA_1 | 443 | 449 | PF00498 | 0.411 |
LIG_FHA_1 | 499 | 505 | PF00498 | 0.518 |
LIG_FHA_1 | 620 | 626 | PF00498 | 0.444 |
LIG_FHA_1 | 70 | 76 | PF00498 | 0.586 |
LIG_FHA_2 | 271 | 277 | PF00498 | 0.597 |
LIG_GBD_Chelix_1 | 503 | 511 | PF00786 | 0.500 |
LIG_GBD_Chelix_1 | 541 | 549 | PF00786 | 0.530 |
LIG_HP1_1 | 553 | 557 | PF01393 | 0.425 |
LIG_LIR_Apic_2 | 350 | 356 | PF02991 | 0.556 |
LIG_LIR_Apic_2 | 418 | 424 | PF02991 | 0.444 |
LIG_LIR_Apic_2 | 594 | 598 | PF02991 | 0.328 |
LIG_LIR_Apic_2 | 630 | 634 | PF02991 | 0.364 |
LIG_LIR_Gen_1 | 126 | 133 | PF02991 | 0.546 |
LIG_LIR_Gen_1 | 185 | 196 | PF02991 | 0.555 |
LIG_LIR_Gen_1 | 204 | 212 | PF02991 | 0.530 |
LIG_LIR_Gen_1 | 468 | 477 | PF02991 | 0.356 |
LIG_LIR_Gen_1 | 487 | 494 | PF02991 | 0.420 |
LIG_LIR_Gen_1 | 568 | 578 | PF02991 | 0.542 |
LIG_LIR_Gen_1 | 89 | 97 | PF02991 | 0.565 |
LIG_LIR_Nem_3 | 126 | 131 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 134 | 140 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 185 | 191 | PF02991 | 0.562 |
LIG_LIR_Nem_3 | 204 | 210 | PF02991 | 0.318 |
LIG_LIR_Nem_3 | 244 | 250 | PF02991 | 0.370 |
LIG_LIR_Nem_3 | 373 | 379 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 418 | 423 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 44 | 49 | PF02991 | 0.623 |
LIG_LIR_Nem_3 | 446 | 452 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 461 | 465 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 466 | 470 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 487 | 492 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 594 | 600 | PF02991 | 0.318 |
LIG_PCNA_PIPBox_1 | 508 | 517 | PF02747 | 0.228 |
LIG_Pex14_2 | 171 | 175 | PF04695 | 0.391 |
LIG_Pex14_2 | 465 | 469 | PF04695 | 0.337 |
LIG_Pex14_2 | 489 | 493 | PF04695 | 0.398 |
LIG_PTB_Apo_2 | 461 | 468 | PF02174 | 0.398 |
LIG_PTB_Apo_2 | 487 | 494 | PF02174 | 0.466 |
LIG_PTB_Phospho_1 | 461 | 467 | PF10480 | 0.432 |
LIG_Rb_pABgroove_1 | 509 | 517 | PF01858 | 0.360 |
LIG_SH2_CRK | 104 | 108 | PF00017 | 0.538 |
LIG_SH2_CRK | 138 | 142 | PF00017 | 0.401 |
LIG_SH2_CRK | 153 | 157 | PF00017 | 0.353 |
LIG_SH2_CRK | 188 | 192 | PF00017 | 0.541 |
LIG_SH2_CRK | 353 | 357 | PF00017 | 0.645 |
LIG_SH2_CRK | 381 | 385 | PF00017 | 0.372 |
LIG_SH2_CRK | 470 | 474 | PF00017 | 0.329 |
LIG_SH2_CRK | 608 | 612 | PF00017 | 0.384 |
LIG_SH2_GRB2like | 452 | 455 | PF00017 | 0.383 |
LIG_SH2_GRB2like | 608 | 611 | PF00017 | 0.377 |
LIG_SH2_NCK_1 | 336 | 340 | PF00017 | 0.463 |
LIG_SH2_NCK_1 | 470 | 474 | PF00017 | 0.327 |
LIG_SH2_PTP2 | 34 | 37 | PF00017 | 0.625 |
LIG_SH2_SRC | 336 | 339 | PF00017 | 0.466 |
LIG_SH2_SRC | 34 | 37 | PF00017 | 0.631 |
LIG_SH2_SRC | 340 | 343 | PF00017 | 0.453 |
LIG_SH2_SRC | 452 | 455 | PF00017 | 0.371 |
LIG_SH2_STAP1 | 133 | 137 | PF00017 | 0.527 |
LIG_SH2_STAP1 | 188 | 192 | PF00017 | 0.516 |
LIG_SH2_STAP1 | 336 | 340 | PF00017 | 0.458 |
LIG_SH2_STAP1 | 381 | 385 | PF00017 | 0.420 |
LIG_SH2_STAP1 | 449 | 453 | PF00017 | 0.361 |
LIG_SH2_STAP1 | 571 | 575 | PF00017 | 0.365 |
LIG_SH2_STAP1 | 90 | 94 | PF00017 | 0.563 |
LIG_SH2_STAT5 | 133 | 136 | PF00017 | 0.528 |
LIG_SH2_STAT5 | 248 | 251 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 34 | 37 | PF00017 | 0.620 |
LIG_SH2_STAT5 | 435 | 438 | PF00017 | 0.381 |
LIG_SH2_STAT5 | 441 | 444 | PF00017 | 0.373 |
LIG_SH2_STAT5 | 452 | 455 | PF00017 | 0.313 |
LIG_SH2_STAT5 | 467 | 470 | PF00017 | 0.289 |
LIG_SH2_STAT5 | 535 | 538 | PF00017 | 0.320 |
LIG_SH2_STAT5 | 631 | 634 | PF00017 | 0.538 |
LIG_SH2_STAT5 | 74 | 77 | PF00017 | 0.551 |
LIG_SH3_1 | 353 | 359 | PF00018 | 0.612 |
LIG_SH3_3 | 353 | 359 | PF00018 | 0.622 |
LIG_SH3_3 | 617 | 623 | PF00018 | 0.366 |
LIG_SUMO_SIM_anti_2 | 622 | 628 | PF11976 | 0.481 |
LIG_SUMO_SIM_par_1 | 554 | 559 | PF11976 | 0.355 |
LIG_SUMO_SIM_par_1 | 66 | 73 | PF11976 | 0.431 |
LIG_TRFH_1 | 153 | 157 | PF08558 | 0.388 |
LIG_TYR_ITIM | 151 | 156 | PF00017 | 0.407 |
LIG_TYR_ITSM | 466 | 473 | PF00017 | 0.430 |
LIG_UBA3_1 | 151 | 159 | PF00899 | 0.385 |
LIG_UBA3_1 | 267 | 275 | PF00899 | 0.548 |
LIG_UBA3_1 | 488 | 495 | PF00899 | 0.442 |
LIG_UBA3_1 | 514 | 521 | PF00899 | 0.349 |
LIG_Vh1_VBS_1 | 379 | 397 | PF01044 | 0.434 |
LIG_Vh1_VBS_1 | 469 | 487 | PF01044 | 0.413 |
MOD_CDC14_SPxK_1 | 303 | 306 | PF00782 | 0.259 |
MOD_CDK_SPxK_1 | 300 | 306 | PF00069 | 0.259 |
MOD_CK1_1 | 108 | 114 | PF00069 | 0.389 |
MOD_CK1_1 | 201 | 207 | PF00069 | 0.373 |
MOD_CK1_1 | 27 | 33 | PF00069 | 0.528 |
MOD_CK1_1 | 619 | 625 | PF00069 | 0.272 |
MOD_CK2_1 | 270 | 276 | PF00069 | 0.458 |
MOD_CK2_1 | 664 | 670 | PF00069 | 0.614 |
MOD_Cter_Amidation | 299 | 302 | PF01082 | 0.496 |
MOD_DYRK1A_RPxSP_1 | 443 | 447 | PF00069 | 0.442 |
MOD_GlcNHglycan | 160 | 164 | PF01048 | 0.386 |
MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.645 |
MOD_GlcNHglycan | 236 | 239 | PF01048 | 0.398 |
MOD_GlcNHglycan | 670 | 674 | PF01048 | 0.663 |
MOD_GlcNHglycan | 675 | 678 | PF01048 | 0.678 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.433 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.565 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.468 |
MOD_GSK3_1 | 300 | 307 | PF00069 | 0.447 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.507 |
MOD_GSK3_1 | 379 | 386 | PF00069 | 0.401 |
MOD_GSK3_1 | 465 | 472 | PF00069 | 0.405 |
MOD_GSK3_1 | 498 | 505 | PF00069 | 0.391 |
MOD_GSK3_1 | 580 | 587 | PF00069 | 0.400 |
MOD_GSK3_1 | 615 | 622 | PF00069 | 0.411 |
MOD_GSK3_1 | 665 | 672 | PF00069 | 0.623 |
MOD_GSK3_1 | 7 | 14 | PF00069 | 0.622 |
MOD_N-GLC_1 | 463 | 468 | PF02516 | 0.382 |
MOD_N-GLC_2 | 456 | 458 | PF02516 | 0.226 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.701 |
MOD_NEK2_1 | 113 | 118 | PF00069 | 0.402 |
MOD_NEK2_1 | 131 | 136 | PF00069 | 0.309 |
MOD_NEK2_1 | 139 | 144 | PF00069 | 0.364 |
MOD_NEK2_1 | 171 | 176 | PF00069 | 0.371 |
MOD_NEK2_1 | 270 | 275 | PF00069 | 0.436 |
MOD_NEK2_1 | 379 | 384 | PF00069 | 0.398 |
MOD_NEK2_1 | 398 | 403 | PF00069 | 0.324 |
MOD_NEK2_1 | 465 | 470 | PF00069 | 0.389 |
MOD_NEK2_1 | 502 | 507 | PF00069 | 0.393 |
MOD_NEK2_1 | 580 | 585 | PF00069 | 0.381 |
MOD_NEK2_1 | 615 | 620 | PF00069 | 0.480 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.480 |
MOD_NEK2_2 | 230 | 235 | PF00069 | 0.495 |
MOD_PIKK_1 | 1 | 7 | PF00454 | 0.598 |
MOD_PIKK_1 | 24 | 30 | PF00454 | 0.747 |
MOD_PKA_2 | 442 | 448 | PF00069 | 0.486 |
MOD_PKA_2 | 563 | 569 | PF00069 | 0.361 |
MOD_PKB_1 | 277 | 285 | PF00069 | 0.241 |
MOD_Plk_1 | 463 | 469 | PF00069 | 0.399 |
MOD_Plk_1 | 665 | 671 | PF00069 | 0.413 |
MOD_Plk_4 | 198 | 204 | PF00069 | 0.372 |
MOD_Plk_4 | 215 | 221 | PF00069 | 0.358 |
MOD_Plk_4 | 379 | 385 | PF00069 | 0.382 |
MOD_Plk_4 | 416 | 422 | PF00069 | 0.420 |
MOD_Plk_4 | 465 | 471 | PF00069 | 0.490 |
MOD_Plk_4 | 484 | 490 | PF00069 | 0.233 |
MOD_Plk_4 | 498 | 504 | PF00069 | 0.372 |
MOD_Plk_4 | 565 | 571 | PF00069 | 0.408 |
MOD_Plk_4 | 627 | 633 | PF00069 | 0.407 |
MOD_Plk_4 | 70 | 76 | PF00069 | 0.322 |
MOD_ProDKin_1 | 105 | 111 | PF00069 | 0.253 |
MOD_ProDKin_1 | 300 | 306 | PF00069 | 0.500 |
MOD_ProDKin_1 | 443 | 449 | PF00069 | 0.357 |
MOD_ProDKin_1 | 619 | 625 | PF00069 | 0.440 |
MOD_SUMO_rev_2 | 640 | 649 | PF00179 | 0.434 |
TRG_DiLeu_BaEn_2 | 263 | 269 | PF01217 | 0.341 |
TRG_DiLeu_BaLyEn_6 | 609 | 614 | PF01217 | 0.407 |
TRG_DiLeu_BaLyEn_6 | 620 | 625 | PF01217 | 0.347 |
TRG_ENDOCYTIC_2 | 104 | 107 | PF00928 | 0.351 |
TRG_ENDOCYTIC_2 | 138 | 141 | PF00928 | 0.379 |
TRG_ENDOCYTIC_2 | 153 | 156 | PF00928 | 0.367 |
TRG_ENDOCYTIC_2 | 188 | 191 | PF00928 | 0.371 |
TRG_ENDOCYTIC_2 | 381 | 384 | PF00928 | 0.373 |
TRG_ENDOCYTIC_2 | 435 | 438 | PF00928 | 0.385 |
TRG_ENDOCYTIC_2 | 462 | 465 | PF00928 | 0.385 |
TRG_ENDOCYTIC_2 | 470 | 473 | PF00928 | 0.382 |
TRG_ENDOCYTIC_2 | 571 | 574 | PF00928 | 0.366 |
TRG_ENDOCYTIC_2 | 608 | 611 | PF00928 | 0.451 |
TRG_ENDOCYTIC_2 | 90 | 93 | PF00928 | 0.378 |
TRG_ER_diArg_1 | 49 | 51 | PF00400 | 0.591 |
TRG_Pf-PMV_PEXEL_1 | 259 | 264 | PF00026 | 0.515 |
TRG_Pf-PMV_PEXEL_1 | 637 | 641 | PF00026 | 0.307 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2U2 | Leptomonas seymouri | 48% | 97% |
A0A0N1HY49 | Leptomonas seymouri | 46% | 100% |
A0A0N1HZ06 | Leptomonas seymouri | 35% | 100% |
A0A0N1IHL1 | Leptomonas seymouri | 40% | 96% |
A0A0N1PAY4 | Leptomonas seymouri | 46% | 78% |
A0A0N1PB77 | Leptomonas seymouri | 35% | 100% |
A0A0N1PBZ2 | Leptomonas seymouri | 67% | 100% |
A0A0N1PCC1 | Leptomonas seymouri | 43% | 100% |
A0A381MBI0 | Leishmania infantum | 45% | 100% |
A0A3Q8I8X7 | Leishmania donovani | 45% | 100% |
A0A3Q8IAZ0 | Leishmania donovani | 85% | 98% |
A0A3Q8IH50 | Leishmania donovani | 60% | 95% |
A0A3Q8IVN0 | Leishmania donovani | 37% | 100% |
A0A3R7M4J1 | Trypanosoma rangeli | 41% | 100% |
A0A3S5H5P4 | Leishmania donovani | 45% | 100% |
A0A3S5H5V2 | Leishmania donovani | 43% | 100% |
A0A3S5H6F6 | Leishmania donovani | 84% | 98% |
A0A3S5H763 | Leishmania donovani | 55% | 100% |
A0A3S7WR10 | Leishmania donovani | 43% | 92% |
A0A3S7WR14 | Leishmania donovani | 100% | 100% |
A0A3S7WR15 | Leishmania donovani | 72% | 81% |
A0A3S7WR24 | Leishmania donovani | 83% | 97% |
A4H4T8 | Leishmania braziliensis | 41% | 99% |
A4H5Y4 | Leishmania braziliensis | 45% | 100% |
A4H617 | Leishmania braziliensis | 74% | 100% |
A4H618 | Leishmania braziliensis | 72% | 100% |
A4H619 | Leishmania braziliensis | 74% | 100% |
A4H620 | Leishmania braziliensis | 59% | 100% |
A4H6C3 | Leishmania braziliensis | 46% | 100% |
A4HNH7 | Leishmania braziliensis | 36% | 97% |
A4HSS2 | Leishmania infantum | 45% | 100% |
A4HUE4 | Leishmania infantum | 45% | 100% |
A4HUE5 | Leishmania infantum | 74% | 100% |
A4HUE7 | Leishmania infantum | 84% | 98% |
A4HUE8 | Leishmania infantum | 83% | 97% |
A4HUF4 | Leishmania infantum | 82% | 98% |
A4HUF5 | Leishmania infantum | 60% | 100% |
A4HYA9 | Leishmania infantum | 55% | 100% |
A4IC33 | Leishmania infantum | 36% | 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) | 39% | 100% |
C9ZVE9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
C9ZVF1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
D0A423 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
E8NHQ5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 100% |
E9AG72 | Leishmania infantum | 43% | 100% |
E9AI40 | Leishmania braziliensis | 74% | 100% |
E9AJY4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 47% | 100% |
E9AKQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 45% | 100% |
E9AL06 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 43% | 100% |
E9AN44 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 45% | 100% |
E9AN45 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 74% | 100% |
E9AN46 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
E9AN47 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 61% | 100% |
E9ANE5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 47% | 100% |
E9AS42 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 55% | 100% |
E9B741 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 95% |
Q4QDC4 | Leishmania major | 55% | 100% |
Q4QH81 | Leishmania major | 46% | 100% |
Q4QHH7 | Leishmania major | 59% | 100% |
Q4QHH8 | Leishmania major | 79% | 100% |
Q4QHH9 | Leishmania major | 79% | 100% |
Q4QHI0 | Leishmania major | 83% | 100% |
Q4QHI1 | Leishmania major | 93% | 100% |
Q4QHI2 | Leishmania major | 82% | 100% |
Q4QIU9 | Leishmania major | 42% | 100% |
Q4QJ48 | Leishmania major | 44% | 100% |
Q7KIP2 | Leishmania major | 36% | 100% |