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: 71 |
NetGPI | no | yes: 0, no: 71 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 72 |
GO:0110165 | cellular anatomical entity | 1 | 72 |
GO:0005737 | cytoplasm | 2 | 6 |
GO:0005886 | plasma membrane | 3 | 1 |
Related structures:
AlphaFold database: E9AN45
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 | 299 | 303 | PF00656 | 0.645 |
CLV_NRD_NRD_1 | 232 | 234 | PF00675 | 0.391 |
CLV_NRD_NRD_1 | 240 | 242 | PF00675 | 0.369 |
CLV_NRD_NRD_1 | 614 | 616 | PF00675 | 0.327 |
CLV_NRD_NRD_1 | 9 | 11 | PF00675 | 0.495 |
CLV_PCSK_FUR_1 | 238 | 242 | PF00082 | 0.284 |
CLV_PCSK_KEX2_1 | 240 | 242 | PF00082 | 0.330 |
CLV_PCSK_KEX2_1 | 457 | 459 | PF00082 | 0.262 |
CLV_PCSK_KEX2_1 | 483 | 485 | PF00082 | 0.575 |
CLV_PCSK_KEX2_1 | 651 | 653 | PF00082 | 0.511 |
CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.528 |
CLV_PCSK_KEX2_1 | 94 | 96 | PF00082 | 0.346 |
CLV_PCSK_PC1ET2_1 | 457 | 459 | PF00082 | 0.262 |
CLV_PCSK_PC1ET2_1 | 483 | 485 | PF00082 | 0.575 |
CLV_PCSK_PC1ET2_1 | 651 | 653 | PF00082 | 0.535 |
CLV_PCSK_PC1ET2_1 | 94 | 96 | PF00082 | 0.346 |
CLV_PCSK_PC7_1 | 236 | 242 | PF00082 | 0.230 |
CLV_PCSK_SKI1_1 | 42 | 46 | PF00082 | 0.419 |
CLV_PCSK_SKI1_1 | 77 | 81 | PF00082 | 0.407 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.542 |
DOC_AGCK_PIF_1 | 424 | 429 | PF00069 | 0.242 |
DOC_CDC14_PxL_1 | 8 | 16 | PF14671 | 0.594 |
DOC_CYCLIN_yCln2_LP_2 | 590 | 596 | PF00134 | 0.425 |
DOC_MAPK_gen_1 | 218 | 228 | PF00069 | 0.602 |
DOC_MAPK_gen_1 | 457 | 464 | PF00069 | 0.495 |
DOC_MAPK_gen_1 | 483 | 491 | PF00069 | 0.377 |
DOC_MAPK_gen_1 | 600 | 609 | PF00069 | 0.639 |
DOC_MAPK_gen_1 | 94 | 100 | PF00069 | 0.554 |
DOC_MAPK_MEF2A_6 | 188 | 195 | PF00069 | 0.382 |
DOC_MAPK_MEF2A_6 | 483 | 491 | PF00069 | 0.410 |
DOC_MAPK_RevD_3 | 443 | 458 | PF00069 | 0.398 |
DOC_PP1_RVXF_1 | 459 | 465 | PF00149 | 0.559 |
DOC_PP2B_LxvP_1 | 590 | 593 | PF13499 | 0.411 |
DOC_PP2B_LxvP_1 | 596 | 599 | PF13499 | 0.380 |
DOC_PP2B_PxIxI_1 | 188 | 194 | PF00149 | 0.338 |
DOC_PP4_FxxP_1 | 239 | 242 | PF00568 | 0.439 |
DOC_USP7_MATH_1 | 160 | 164 | PF00917 | 0.378 |
DOC_USP7_MATH_1 | 264 | 268 | PF00917 | 0.613 |
DOC_USP7_MATH_1 | 446 | 450 | PF00917 | 0.432 |
DOC_USP7_MATH_1 | 502 | 506 | PF00917 | 0.370 |
DOC_USP7_MATH_1 | 525 | 529 | PF00917 | 0.539 |
DOC_USP7_MATH_1 | 629 | 633 | PF00917 | 0.863 |
DOC_USP7_UBL2_3 | 612 | 616 | PF12436 | 0.496 |
DOC_WW_Pin1_4 | 260 | 265 | PF00397 | 0.641 |
DOC_WW_Pin1_4 | 405 | 410 | PF00397 | 0.387 |
DOC_WW_Pin1_4 | 584 | 589 | PF00397 | 0.469 |
DOC_WW_Pin1_4 | 630 | 635 | PF00397 | 0.694 |
LIG_14-3-3_CanoR_1 | 218 | 228 | PF00244 | 0.637 |
LIG_14-3-3_CanoR_1 | 266 | 273 | PF00244 | 0.651 |
LIG_14-3-3_CanoR_1 | 461 | 465 | PF00244 | 0.545 |
LIG_14-3-3_CanoR_1 | 544 | 553 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 65 | 72 | PF00244 | 0.545 |
LIG_BRCT_BRCA1_1 | 427 | 431 | PF00533 | 0.371 |
LIG_Clathr_ClatBox_1 | 226 | 230 | PF01394 | 0.497 |
LIG_deltaCOP1_diTrp_1 | 336 | 341 | PF00928 | 0.490 |
LIG_FHA_1 | 30 | 36 | PF00498 | 0.612 |
LIG_FHA_1 | 329 | 335 | PF00498 | 0.642 |
LIG_FHA_1 | 346 | 352 | PF00498 | 0.405 |
LIG_FHA_1 | 361 | 367 | PF00498 | 0.308 |
LIG_FHA_1 | 410 | 416 | PF00498 | 0.433 |
LIG_FHA_1 | 461 | 467 | PF00498 | 0.540 |
LIG_FHA_1 | 475 | 481 | PF00498 | 0.404 |
LIG_FHA_1 | 593 | 599 | PF00498 | 0.471 |
LIG_FHA_1 | 78 | 84 | PF00498 | 0.622 |
LIG_FHA_2 | 230 | 236 | PF00498 | 0.609 |
LIG_FHA_2 | 633 | 639 | PF00498 | 0.757 |
LIG_HP1_1 | 515 | 519 | PF01393 | 0.454 |
LIG_LIR_Apic_2 | 237 | 242 | PF02991 | 0.439 |
LIG_LIR_Apic_2 | 380 | 386 | PF02991 | 0.456 |
LIG_LIR_Apic_2 | 556 | 560 | PF02991 | 0.356 |
LIG_LIR_Gen_1 | 144 | 155 | PF02991 | 0.572 |
LIG_LIR_Gen_1 | 163 | 171 | PF02991 | 0.551 |
LIG_LIR_Gen_1 | 430 | 439 | PF02991 | 0.377 |
LIG_LIR_Gen_1 | 449 | 455 | PF02991 | 0.436 |
LIG_LIR_Gen_1 | 467 | 476 | PF02991 | 0.345 |
LIG_LIR_Gen_1 | 48 | 56 | PF02991 | 0.592 |
LIG_LIR_Gen_1 | 530 | 539 | PF02991 | 0.565 |
LIG_LIR_Gen_1 | 85 | 92 | PF02991 | 0.574 |
LIG_LIR_Nem_3 | 144 | 150 | PF02991 | 0.578 |
LIG_LIR_Nem_3 | 163 | 169 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 203 | 209 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 336 | 341 | PF02991 | 0.548 |
LIG_LIR_Nem_3 | 380 | 385 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 421 | 427 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 428 | 432 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 449 | 454 | PF02991 | 0.397 |
LIG_LIR_Nem_3 | 467 | 472 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 85 | 90 | PF02991 | 0.548 |
LIG_LIR_Nem_3 | 93 | 99 | PF02991 | 0.548 |
LIG_NRBOX | 575 | 581 | PF00104 | 0.276 |
LIG_PDZ_Class_3 | 650 | 655 | PF00595 | 0.657 |
LIG_Pex14_2 | 130 | 134 | PF04695 | 0.421 |
LIG_Pex14_2 | 427 | 431 | PF04695 | 0.360 |
LIG_Pex14_2 | 451 | 455 | PF04695 | 0.420 |
LIG_PTB_Apo_2 | 423 | 430 | PF02174 | 0.425 |
LIG_PTB_Phospho_1 | 423 | 429 | PF10480 | 0.457 |
LIG_SH2_CRK | 112 | 116 | PF00017 | 0.377 |
LIG_SH2_CRK | 147 | 151 | PF00017 | 0.568 |
LIG_SH2_CRK | 315 | 319 | PF00017 | 0.669 |
LIG_SH2_CRK | 343 | 347 | PF00017 | 0.401 |
LIG_SH2_CRK | 432 | 436 | PF00017 | 0.352 |
LIG_SH2_CRK | 557 | 561 | PF00017 | 0.379 |
LIG_SH2_CRK | 63 | 67 | PF00017 | 0.566 |
LIG_SH2_CRK | 97 | 101 | PF00017 | 0.423 |
LIG_SH2_GRB2like | 403 | 406 | PF00017 | 0.460 |
LIG_SH2_GRB2like | 414 | 417 | PF00017 | 0.410 |
LIG_SH2_NCK_1 | 432 | 436 | PF00017 | 0.354 |
LIG_SH2_PTP2 | 403 | 406 | PF00017 | 0.405 |
LIG_SH2_PTP2 | 488 | 491 | PF00017 | 0.451 |
LIG_SH2_SRC | 297 | 300 | PF00017 | 0.490 |
LIG_SH2_SRC | 403 | 406 | PF00017 | 0.534 |
LIG_SH2_SRC | 414 | 417 | PF00017 | 0.398 |
LIG_SH2_STAP1 | 147 | 151 | PF00017 | 0.540 |
LIG_SH2_STAP1 | 343 | 347 | PF00017 | 0.449 |
LIG_SH2_STAP1 | 49 | 53 | PF00017 | 0.590 |
LIG_SH2_STAP1 | 533 | 537 | PF00017 | 0.395 |
LIG_SH2_STAP1 | 92 | 96 | PF00017 | 0.555 |
LIG_SH2_STAT3 | 397 | 400 | PF00017 | 0.258 |
LIG_SH2_STAT5 | 207 | 210 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 397 | 400 | PF00017 | 0.406 |
LIG_SH2_STAT5 | 403 | 406 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 414 | 417 | PF00017 | 0.333 |
LIG_SH2_STAT5 | 453 | 456 | PF00017 | 0.504 |
LIG_SH2_STAT5 | 488 | 491 | PF00017 | 0.356 |
LIG_SH2_STAT5 | 497 | 500 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 92 | 95 | PF00017 | 0.552 |
LIG_SH3_1 | 315 | 321 | PF00018 | 0.637 |
LIG_SH3_3 | 283 | 289 | PF00018 | 0.472 |
LIG_SH3_3 | 290 | 296 | PF00018 | 0.472 |
LIG_SH3_3 | 315 | 321 | PF00018 | 0.648 |
LIG_SH3_3 | 582 | 588 | PF00018 | 0.395 |
LIG_SH3_3 | 628 | 634 | PF00018 | 0.786 |
LIG_SUMO_SIM_anti_2 | 477 | 483 | PF11976 | 0.369 |
LIG_SUMO_SIM_par_1 | 515 | 521 | PF11976 | 0.384 |
LIG_TRFH_1 | 112 | 116 | PF08558 | 0.417 |
LIG_TYR_ITIM | 110 | 115 | PF00017 | 0.433 |
LIG_UBA3_1 | 110 | 118 | PF00899 | 0.409 |
LIG_UBA3_1 | 226 | 234 | PF00899 | 0.572 |
LIG_Vh1_VBS_1 | 341 | 359 | PF01044 | 0.463 |
LIG_WRC_WIRS_1 | 410 | 415 | PF05994 | 0.391 |
LIG_WRC_WIRS_1 | 466 | 471 | PF05994 | 0.361 |
MOD_CDC14_SPxK_1 | 263 | 266 | PF00782 | 0.283 |
MOD_CDK_SPxK_1 | 260 | 266 | PF00069 | 0.283 |
MOD_CK1_1 | 456 | 462 | PF00069 | 0.407 |
MOD_CK1_1 | 632 | 638 | PF00069 | 0.692 |
MOD_CK1_1 | 67 | 73 | PF00069 | 0.408 |
MOD_CK2_1 | 229 | 235 | PF00069 | 0.468 |
MOD_CK2_1 | 632 | 638 | PF00069 | 0.774 |
MOD_Cter_Amidation | 259 | 262 | PF01082 | 0.523 |
MOD_GlcNHglycan | 119 | 123 | PF01048 | 0.407 |
MOD_GlcNHglycan | 195 | 198 | PF01048 | 0.427 |
MOD_GlcNHglycan | 448 | 451 | PF01048 | 0.384 |
MOD_GlcNHglycan | 546 | 549 | PF01048 | 0.447 |
MOD_GlcNHglycan | 635 | 638 | PF01048 | 0.758 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.496 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.476 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.415 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.290 |
MOD_GSK3_1 | 427 | 434 | PF00069 | 0.425 |
MOD_GSK3_1 | 456 | 463 | PF00069 | 0.419 |
MOD_GSK3_1 | 538 | 545 | PF00069 | 0.431 |
MOD_GSK3_1 | 629 | 636 | PF00069 | 0.724 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.462 |
MOD_N-GLC_1 | 425 | 430 | PF02516 | 0.410 |
MOD_N-GLC_1 | 640 | 645 | PF02516 | 0.779 |
MOD_N-GLC_2 | 584 | 586 | PF02516 | 0.540 |
MOD_NEK2_1 | 130 | 135 | PF00069 | 0.400 |
MOD_NEK2_1 | 229 | 234 | PF00069 | 0.465 |
MOD_NEK2_1 | 29 | 34 | PF00069 | 0.484 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.421 |
MOD_NEK2_1 | 360 | 365 | PF00069 | 0.352 |
MOD_NEK2_1 | 371 | 376 | PF00069 | 0.369 |
MOD_NEK2_1 | 427 | 432 | PF00069 | 0.411 |
MOD_NEK2_1 | 464 | 469 | PF00069 | 0.418 |
MOD_NEK2_1 | 542 | 547 | PF00069 | 0.409 |
MOD_NEK2_1 | 72 | 77 | PF00069 | 0.432 |
MOD_NEK2_1 | 90 | 95 | PF00069 | 0.338 |
MOD_NEK2_1 | 98 | 103 | PF00069 | 0.394 |
MOD_NEK2_2 | 189 | 194 | PF00069 | 0.522 |
MOD_NEK2_2 | 409 | 414 | PF00069 | 0.393 |
MOD_PK_1 | 65 | 71 | PF00069 | 0.506 |
MOD_PKA_2 | 460 | 466 | PF00069 | 0.405 |
MOD_PKA_2 | 525 | 531 | PF00069 | 0.390 |
MOD_PKA_2 | 543 | 549 | PF00069 | 0.390 |
MOD_PKA_2 | 64 | 70 | PF00069 | 0.432 |
MOD_Plk_1 | 425 | 431 | PF00069 | 0.429 |
MOD_Plk_4 | 160 | 166 | PF00069 | 0.394 |
MOD_Plk_4 | 174 | 180 | PF00069 | 0.381 |
MOD_Plk_4 | 341 | 347 | PF00069 | 0.407 |
MOD_Plk_4 | 378 | 384 | PF00069 | 0.446 |
MOD_Plk_4 | 409 | 415 | PF00069 | 0.394 |
MOD_Plk_4 | 427 | 433 | PF00069 | 0.492 |
MOD_Plk_4 | 527 | 533 | PF00069 | 0.426 |
MOD_Plk_4 | 592 | 598 | PF00069 | 0.424 |
MOD_ProDKin_1 | 260 | 266 | PF00069 | 0.527 |
MOD_ProDKin_1 | 405 | 411 | PF00069 | 0.387 |
MOD_ProDKin_1 | 584 | 590 | PF00069 | 0.469 |
MOD_ProDKin_1 | 630 | 636 | PF00069 | 0.603 |
MOD_SUMO_for_1 | 650 | 653 | PF00179 | 0.518 |
MOD_SUMO_rev_2 | 605 | 614 | PF00179 | 0.463 |
TRG_DiLeu_BaEn_2 | 222 | 228 | PF01217 | 0.365 |
TRG_ENDOCYTIC_2 | 112 | 115 | PF00928 | 0.392 |
TRG_ENDOCYTIC_2 | 147 | 150 | PF00928 | 0.393 |
TRG_ENDOCYTIC_2 | 343 | 346 | PF00928 | 0.403 |
TRG_ENDOCYTIC_2 | 403 | 406 | PF00928 | 0.407 |
TRG_ENDOCYTIC_2 | 432 | 435 | PF00928 | 0.407 |
TRG_ENDOCYTIC_2 | 488 | 491 | PF00928 | 0.534 |
TRG_ENDOCYTIC_2 | 49 | 52 | PF00928 | 0.406 |
TRG_ENDOCYTIC_2 | 513 | 516 | PF00928 | 0.360 |
TRG_ENDOCYTIC_2 | 533 | 536 | PF00928 | 0.396 |
TRG_ENDOCYTIC_2 | 63 | 66 | PF00928 | 0.376 |
TRG_ENDOCYTIC_2 | 97 | 100 | PF00928 | 0.401 |
TRG_ER_diArg_1 | 239 | 241 | PF00400 | 0.375 |
TRG_ER_diArg_1 | 8 | 10 | PF00400 | 0.670 |
TRG_Pf-PMV_PEXEL_1 | 218 | 223 | PF00026 | 0.541 |
TRG_Pf-PMV_PEXEL_1 | 42 | 47 | PF00026 | 0.255 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2U2 | Leptomonas seymouri | 47% | 93% |
A0A0N1HY49 | Leptomonas seymouri | 47% | 97% |
A0A0N1HZ06 | Leptomonas seymouri | 35% | 100% |
A0A0N1IHL1 | Leptomonas seymouri | 40% | 92% |
A0A0N1PAY4 | Leptomonas seymouri | 47% | 74% |
A0A0N1PB77 | Leptomonas seymouri | 35% | 100% |
A0A0N1PBZ2 | Leptomonas seymouri | 67% | 97% |
A0A0N1PCC1 | Leptomonas seymouri | 42% | 98% |
A0A0S4INN8 | Bodo saltans | 28% | 100% |
A0A381MBI0 | Leishmania infantum | 44% | 99% |
A0A3Q8I8X7 | Leishmania donovani | 44% | 99% |
A0A3Q8IAZ0 | Leishmania donovani | 73% | 94% |
A0A3Q8IH50 | Leishmania donovani | 58% | 91% |
A0A3Q8IVN0 | Leishmania donovani | 37% | 100% |
A0A3R7M4J1 | Trypanosoma rangeli | 40% | 100% |
A0A3S5H5P4 | Leishmania donovani | 43% | 97% |
A0A3S5H5V2 | Leishmania donovani | 42% | 100% |
A0A3S5H6F6 | Leishmania donovani | 74% | 94% |
A0A3S5H763 | Leishmania donovani | 52% | 97% |
A0A3S7WR10 | Leishmania donovani | 44% | 88% |
A0A3S7WR14 | Leishmania donovani | 75% | 95% |
A0A3S7WR15 | Leishmania donovani | 91% | 77% |
A0A3S7WR24 | Leishmania donovani | 73% | 93% |
A4H4T8 | Leishmania braziliensis | 41% | 100% |
A4H5Y4 | Leishmania braziliensis | 45% | 100% |
A4H617 | Leishmania braziliensis | 70% | 100% |
A4H618 | Leishmania braziliensis | 69% | 100% |
A4H619 | Leishmania braziliensis | 70% | 100% |
A4H620 | Leishmania braziliensis | 61% | 100% |
A4H6C3 | Leishmania braziliensis | 45% | 100% |
A4HNH7 | Leishmania braziliensis | 35% | 99% |
A4HSS2 | Leishmania infantum | 44% | 97% |
A4HUE4 | Leishmania infantum | 43% | 88% |
A4HUE5 | Leishmania infantum | 91% | 95% |
A4HUE6 | Leishmania infantum | 74% | 95% |
A4HUE7 | Leishmania infantum | 74% | 94% |
A4HUE8 | Leishmania infantum | 74% | 93% |
A4HUF4 | Leishmania infantum | 74% | 94% |
A4HUF5 | Leishmania infantum | 58% | 100% |
A4HYA9 | Leishmania infantum | 52% | 97% |
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) | 38% | 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) | 39% | 100% |
D0A423 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
E8NHQ5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 73% | 100% |
E9AG72 | Leishmania infantum | 41% | 100% |
E9AI40 | Leishmania braziliensis | 78% | 100% |
E9AJY4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 46% | 100% |
E9AKQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 41% | 100% |
E9AL06 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 99% |
E9AN44 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 43% | 100% |
E9AN46 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 74% | 100% |
E9AN47 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 58% | 92% |
E9ANE5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 45% | 99% |
E9AS42 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 51% | 97% |
E9B741 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 100% |
Q4QDC4 | Leishmania major | 51% | 100% |
Q4QH81 | Leishmania major | 44% | 100% |
Q4QHH7 | Leishmania major | 58% | 100% |
Q4QHH8 | Leishmania major | 72% | 100% |
Q4QHH9 | Leishmania major | 72% | 100% |
Q4QHI0 | Leishmania major | 72% | 100% |
Q4QHI1 | Leishmania major | 73% | 99% |
Q4QHI2 | Leishmania major | 84% | 100% |
Q4QIU9 | Leishmania major | 41% | 100% |
Q4QJ48 | Leishmania major | 42% | 100% |
Q7KIP2 | Leishmania major | 36% | 100% |