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. | no | 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: E9AN47
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 | 58 | 60 | PF00675 | 0.422 |
CLV_PCSK_KEX2_1 | 143 | 145 | PF00082 | 0.296 |
CLV_PCSK_KEX2_1 | 543 | 545 | PF00082 | 0.525 |
CLV_PCSK_KEX2_1 | 58 | 60 | PF00082 | 0.455 |
CLV_PCSK_PC1ET2_1 | 143 | 145 | PF00082 | 0.296 |
CLV_PCSK_PC1ET2_1 | 543 | 545 | PF00082 | 0.525 |
CLV_PCSK_SKI1_1 | 11 | 15 | PF00082 | 0.404 |
CLV_PCSK_SKI1_1 | 126 | 130 | PF00082 | 0.357 |
CLV_PCSK_SKI1_1 | 25 | 29 | PF00082 | 0.557 |
CLV_PCSK_SKI1_1 | 285 | 289 | PF00082 | 0.269 |
CLV_PCSK_SKI1_1 | 345 | 349 | PF00082 | 0.359 |
CLV_PCSK_SKI1_1 | 668 | 672 | PF00082 | 0.252 |
DEG_APCC_DBOX_1 | 284 | 292 | PF00400 | 0.425 |
DEG_COP1_1 | 332 | 340 | PF00400 | 0.390 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.603 |
DOC_CDC14_PxL_1 | 629 | 637 | PF14671 | 0.335 |
DOC_CYCLIN_yCln2_LP_2 | 646 | 652 | PF00134 | 0.375 |
DOC_MAPK_gen_1 | 143 | 149 | PF00069 | 0.504 |
DOC_MAPK_gen_1 | 283 | 290 | PF00069 | 0.542 |
DOC_MAPK_gen_1 | 543 | 551 | PF00069 | 0.327 |
DOC_MAPK_gen_1 | 656 | 665 | PF00069 | 0.589 |
DOC_MAPK_HePTP_8 | 232 | 244 | PF00069 | 0.222 |
DOC_MAPK_MEF2A_6 | 235 | 244 | PF00069 | 0.324 |
DOC_MAPK_MEF2A_6 | 283 | 290 | PF00069 | 0.404 |
DOC_MAPK_MEF2A_6 | 543 | 551 | PF00069 | 0.360 |
DOC_MAPK_MEF2A_6 | 73 | 80 | PF00069 | 0.537 |
DOC_MAPK_NFAT4_5 | 73 | 81 | PF00069 | 0.607 |
DOC_PP1_RVXF_1 | 519 | 525 | PF00149 | 0.509 |
DOC_PP2B_LxvP_1 | 464 | 467 | PF13499 | 0.380 |
DOC_PP2B_LxvP_1 | 646 | 649 | PF13499 | 0.361 |
DOC_PP2B_LxvP_1 | 652 | 655 | PF13499 | 0.330 |
DOC_PP4_FxxP_1 | 42 | 45 | PF00568 | 0.574 |
DOC_SPAK_OSR1_1 | 104 | 108 | PF12202 | 0.415 |
DOC_USP7_MATH_1 | 209 | 213 | PF00917 | 0.328 |
DOC_USP7_MATH_1 | 293 | 297 | PF00917 | 0.525 |
DOC_USP7_MATH_1 | 469 | 473 | PF00917 | 0.331 |
DOC_USP7_MATH_1 | 585 | 589 | PF00917 | 0.489 |
DOC_USP7_MATH_1 | 669 | 673 | PF00917 | 0.555 |
DOC_USP7_MATH_1 | 685 | 689 | PF00917 | 0.807 |
DOC_WW_Pin1_4 | 18 | 23 | PF00397 | 0.772 |
DOC_WW_Pin1_4 | 31 | 36 | PF00397 | 0.779 |
DOC_WW_Pin1_4 | 6 | 11 | PF00397 | 0.659 |
DOC_WW_Pin1_4 | 621 | 626 | PF00397 | 0.352 |
LIG_14-3-3_CanoR_1 | 297 | 307 | PF00244 | 0.437 |
LIG_14-3-3_CanoR_1 | 521 | 525 | PF00244 | 0.495 |
LIG_APCC_ABBAyCdc20_2 | 322 | 328 | PF00400 | 0.387 |
LIG_BRCT_BRCA1_1 | 487 | 491 | PF00533 | 0.321 |
LIG_CSL_BTD_1 | 572 | 575 | PF09270 | 0.403 |
LIG_EH1_1 | 523 | 531 | PF00400 | 0.346 |
LIG_EVH1_2 | 625 | 629 | PF00568 | 0.363 |
LIG_FHA_1 | 127 | 133 | PF00498 | 0.572 |
LIG_FHA_1 | 406 | 412 | PF00498 | 0.355 |
LIG_FHA_1 | 421 | 427 | PF00498 | 0.258 |
LIG_FHA_1 | 459 | 465 | PF00498 | 0.427 |
LIG_FHA_1 | 521 | 527 | PF00498 | 0.490 |
LIG_FHA_1 | 649 | 655 | PF00498 | 0.421 |
LIG_FHA_1 | 690 | 696 | PF00498 | 0.595 |
LIG_FHA_1 | 700 | 706 | PF00498 | 0.545 |
LIG_LIR_Apic_2 | 440 | 446 | PF02991 | 0.406 |
LIG_LIR_Gen_1 | 110 | 118 | PF02991 | 0.505 |
LIG_LIR_Gen_1 | 134 | 141 | PF02991 | 0.524 |
LIG_LIR_Gen_1 | 193 | 204 | PF02991 | 0.522 |
LIG_LIR_Gen_1 | 212 | 223 | PF02991 | 0.501 |
LIG_LIR_Gen_1 | 408 | 414 | PF02991 | 0.295 |
LIG_LIR_Gen_1 | 461 | 470 | PF02991 | 0.350 |
LIG_LIR_Gen_1 | 490 | 499 | PF02991 | 0.327 |
LIG_LIR_Gen_1 | 509 | 515 | PF02991 | 0.386 |
LIG_LIR_Gen_1 | 535 | 542 | PF02991 | 0.340 |
LIG_LIR_Gen_1 | 590 | 599 | PF02991 | 0.515 |
LIG_LIR_Gen_1 | 628 | 637 | PF02991 | 0.268 |
LIG_LIR_Nem_3 | 110 | 115 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 134 | 139 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 142 | 148 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 193 | 199 | PF02991 | 0.528 |
LIG_LIR_Nem_3 | 212 | 218 | PF02991 | 0.297 |
LIG_LIR_Nem_3 | 252 | 258 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 369 | 374 | PF02991 | 0.562 |
LIG_LIR_Nem_3 | 408 | 412 | PF02991 | 0.323 |
LIG_LIR_Nem_3 | 440 | 445 | PF02991 | 0.372 |
LIG_LIR_Nem_3 | 461 | 466 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 488 | 492 | PF02991 | 0.300 |
LIG_LIR_Nem_3 | 49 | 54 | PF02991 | 0.610 |
LIG_LIR_Nem_3 | 509 | 514 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 535 | 540 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 628 | 632 | PF02991 | 0.263 |
LIG_LYPXL_yS_3 | 54 | 57 | PF13949 | 0.450 |
LIG_Pex14_1 | 213 | 217 | PF04695 | 0.380 |
LIG_Pex14_2 | 101 | 105 | PF04695 | 0.408 |
LIG_Pex14_2 | 487 | 491 | PF04695 | 0.310 |
LIG_Pex14_2 | 511 | 515 | PF04695 | 0.370 |
LIG_Rb_pABgroove_1 | 531 | 539 | PF01858 | 0.339 |
LIG_SH2_CRK | 112 | 116 | PF00017 | 0.516 |
LIG_SH2_CRK | 146 | 150 | PF00017 | 0.373 |
LIG_SH2_CRK | 161 | 165 | PF00017 | 0.327 |
LIG_SH2_CRK | 196 | 200 | PF00017 | 0.518 |
LIG_SH2_CRK | 403 | 407 | PF00017 | 0.351 |
LIG_SH2_CRK | 492 | 496 | PF00017 | 0.302 |
LIG_SH2_NCK_1 | 278 | 282 | PF00017 | 0.380 |
LIG_SH2_NCK_1 | 492 | 496 | PF00017 | 0.304 |
LIG_SH2_SRC | 278 | 281 | PF00017 | 0.406 |
LIG_SH2_STAP1 | 141 | 145 | PF00017 | 0.505 |
LIG_SH2_STAP1 | 196 | 200 | PF00017 | 0.490 |
LIG_SH2_STAP1 | 403 | 407 | PF00017 | 0.399 |
LIG_SH2_STAP1 | 593 | 597 | PF00017 | 0.345 |
LIG_SH2_STAT3 | 95 | 98 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 141 | 144 | PF00017 | 0.502 |
LIG_SH2_STAT5 | 256 | 259 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 371 | 374 | PF00017 | 0.583 |
LIG_SH2_STAT5 | 457 | 460 | PF00017 | 0.356 |
LIG_SH2_STAT5 | 463 | 466 | PF00017 | 0.345 |
LIG_SH2_STAT5 | 474 | 477 | PF00017 | 0.283 |
LIG_SH2_STAT5 | 489 | 492 | PF00017 | 0.265 |
LIG_SH2_STAT5 | 513 | 516 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 557 | 560 | PF00017 | 0.298 |
LIG_SH2_STAT5 | 82 | 85 | PF00017 | 0.521 |
LIG_SH3_3 | 162 | 168 | PF00018 | 0.305 |
LIG_SH3_3 | 373 | 379 | PF00018 | 0.599 |
LIG_SH3_3 | 479 | 485 | PF00018 | 0.284 |
LIG_SH3_3 | 49 | 55 | PF00018 | 0.551 |
LIG_SUMO_SIM_anti_2 | 301 | 311 | PF11976 | 0.389 |
LIG_SUMO_SIM_par_1 | 575 | 581 | PF11976 | 0.334 |
LIG_TRAF2_1 | 332 | 335 | PF00917 | 0.390 |
LIG_TRFH_1 | 161 | 165 | PF08558 | 0.367 |
LIG_TYR_ITIM | 159 | 164 | PF00017 | 0.383 |
LIG_TYR_ITIM | 276 | 281 | PF00017 | 0.196 |
LIG_TYR_ITIM | 52 | 57 | PF00017 | 0.484 |
LIG_TYR_ITSM | 488 | 495 | PF00017 | 0.409 |
LIG_UBA3_1 | 159 | 167 | PF00899 | 0.359 |
LIG_UBA3_1 | 383 | 391 | PF00899 | 0.391 |
LIG_UBA3_1 | 536 | 543 | PF00899 | 0.329 |
LIG_Vh1_VBS_1 | 412 | 430 | PF01044 | 0.451 |
LIG_Vh1_VBS_1 | 491 | 509 | PF01044 | 0.392 |
LIG_WRC_WIRS_1 | 406 | 411 | PF05994 | 0.252 |
LIG_WRC_WIRS_1 | 470 | 475 | PF05994 | 0.341 |
MOD_CDK_SPK_2 | 6 | 11 | PF00069 | 0.500 |
MOD_CDK_SPxxK_3 | 18 | 25 | PF00069 | 0.757 |
MOD_CK1_1 | 516 | 522 | PF00069 | 0.357 |
MOD_CK1_1 | 620 | 626 | PF00069 | 0.303 |
MOD_CK1_1 | 672 | 678 | PF00069 | 0.533 |
MOD_CK2_1 | 329 | 335 | PF00069 | 0.323 |
MOD_CK2_1 | 690 | 696 | PF00069 | 0.493 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.354 |
MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.377 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.262 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.704 |
MOD_GlcNHglycan | 671 | 674 | PF01048 | 0.448 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.402 |
MOD_GSK3_1 | 329 | 336 | PF00069 | 0.416 |
MOD_GSK3_1 | 401 | 408 | PF00069 | 0.365 |
MOD_GSK3_1 | 487 | 494 | PF00069 | 0.375 |
MOD_GSK3_1 | 516 | 523 | PF00069 | 0.369 |
MOD_GSK3_1 | 602 | 609 | PF00069 | 0.380 |
MOD_GSK3_1 | 617 | 624 | PF00069 | 0.350 |
MOD_GSK3_1 | 685 | 692 | PF00069 | 0.662 |
MOD_N-GLC_1 | 690 | 695 | PF02516 | 0.486 |
MOD_NEK2_1 | 100 | 105 | PF00069 | 0.297 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.382 |
MOD_NEK2_1 | 139 | 144 | PF00069 | 0.288 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.344 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.350 |
MOD_NEK2_1 | 401 | 406 | PF00069 | 0.371 |
MOD_NEK2_1 | 420 | 425 | PF00069 | 0.302 |
MOD_NEK2_1 | 458 | 463 | PF00069 | 0.473 |
MOD_NEK2_1 | 487 | 492 | PF00069 | 0.361 |
MOD_NEK2_1 | 524 | 529 | PF00069 | 0.368 |
MOD_NEK2_1 | 602 | 607 | PF00069 | 0.359 |
MOD_NEK2_2 | 469 | 474 | PF00069 | 0.343 |
MOD_PKA_2 | 520 | 526 | PF00069 | 0.355 |
MOD_PKA_2 | 585 | 591 | PF00069 | 0.340 |
MOD_Plk_1 | 333 | 339 | PF00069 | 0.256 |
MOD_Plk_1 | 690 | 696 | PF00069 | 0.659 |
MOD_Plk_2-3 | 333 | 339 | PF00069 | 0.181 |
MOD_Plk_4 | 209 | 215 | PF00069 | 0.344 |
MOD_Plk_4 | 305 | 311 | PF00069 | 0.470 |
MOD_Plk_4 | 401 | 407 | PF00069 | 0.357 |
MOD_Plk_4 | 415 | 421 | PF00069 | 0.309 |
MOD_Plk_4 | 438 | 444 | PF00069 | 0.396 |
MOD_Plk_4 | 458 | 464 | PF00069 | 0.359 |
MOD_Plk_4 | 46 | 52 | PF00069 | 0.516 |
MOD_Plk_4 | 469 | 475 | PF00069 | 0.344 |
MOD_Plk_4 | 487 | 493 | PF00069 | 0.442 |
MOD_Plk_4 | 525 | 531 | PF00069 | 0.316 |
MOD_Plk_4 | 532 | 538 | PF00069 | 0.326 |
MOD_Plk_4 | 587 | 593 | PF00069 | 0.376 |
MOD_Plk_4 | 648 | 654 | PF00069 | 0.374 |
MOD_ProDKin_1 | 18 | 24 | PF00069 | 0.731 |
MOD_ProDKin_1 | 31 | 37 | PF00069 | 0.739 |
MOD_ProDKin_1 | 6 | 12 | PF00069 | 0.572 |
MOD_ProDKin_1 | 621 | 627 | PF00069 | 0.422 |
MOD_SUMO_rev_2 | 3 | 7 | PF00179 | 0.485 |
MOD_SUMO_rev_2 | 34 | 40 | PF00179 | 0.551 |
MOD_SUMO_rev_2 | 661 | 670 | PF00179 | 0.413 |
MOD_SUMO_rev_2 | 704 | 712 | PF00179 | 0.437 |
TRG_DiLeu_BaEn_2 | 37 | 43 | PF01217 | 0.414 |
TRG_DiLeu_BaEn_4 | 362 | 368 | PF01217 | 0.202 |
TRG_DiLeu_BaLyEn_6 | 641 | 646 | PF01217 | 0.326 |
TRG_ENDOCYTIC_2 | 112 | 115 | PF00928 | 0.326 |
TRG_ENDOCYTIC_2 | 146 | 149 | PF00928 | 0.351 |
TRG_ENDOCYTIC_2 | 161 | 164 | PF00928 | 0.342 |
TRG_ENDOCYTIC_2 | 196 | 199 | PF00928 | 0.343 |
TRG_ENDOCYTIC_2 | 278 | 281 | PF00928 | 0.452 |
TRG_ENDOCYTIC_2 | 403 | 406 | PF00928 | 0.353 |
TRG_ENDOCYTIC_2 | 457 | 460 | PF00928 | 0.358 |
TRG_ENDOCYTIC_2 | 463 | 466 | PF00928 | 0.357 |
TRG_ENDOCYTIC_2 | 492 | 495 | PF00928 | 0.357 |
TRG_ENDOCYTIC_2 | 54 | 57 | PF00928 | 0.490 |
TRG_ENDOCYTIC_2 | 593 | 596 | PF00928 | 0.346 |
TRG_ER_diArg_1 | 57 | 59 | PF00400 | 0.582 |
TRG_ER_diLys_1 | 709 | 712 | PF00400 | 0.431 |
TRG_NES_CRM1_1 | 465 | 479 | PF08389 | 0.306 |
TRG_Pf-PMV_PEXEL_1 | 11 | 15 | PF00026 | 0.520 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2U2 | Leptomonas seymouri | 50% | 100% |
A0A0N1HY49 | Leptomonas seymouri | 52% | 100% |
A0A0N1HZ06 | Leptomonas seymouri | 40% | 100% |
A0A0N1IHL1 | Leptomonas seymouri | 44% | 100% |
A0A0N1PAY4 | Leptomonas seymouri | 51% | 81% |
A0A0N1PB77 | Leptomonas seymouri | 39% | 100% |
A0A0N1PBZ2 | Leptomonas seymouri | 60% | 100% |
A0A0N1PCC1 | Leptomonas seymouri | 45% | 100% |
A0A0S4INN8 | Bodo saltans | 32% | 100% |
A0A381MBI0 | Leishmania infantum | 48% | 100% |
A0A3Q8I8X7 | Leishmania donovani | 47% | 100% |
A0A3Q8IAZ0 | Leishmania donovani | 60% | 100% |
A0A3Q8IH50 | Leishmania donovani | 88% | 99% |
A0A3Q8IVN0 | Leishmania donovani | 39% | 100% |
A0A3R7M4J1 | Trypanosoma rangeli | 46% | 100% |
A0A3S5H5P4 | Leishmania donovani | 51% | 100% |
A0A3S5H5V2 | Leishmania donovani | 43% | 100% |
A0A3S5H6F6 | Leishmania donovani | 58% | 100% |
A0A3S5H763 | Leishmania donovani | 60% | 100% |
A0A3S7WR10 | Leishmania donovani | 50% | 96% |
A0A3S7WR14 | Leishmania donovani | 61% | 100% |
A0A3S7WR15 | Leishmania donovani | 58% | 84% |
A0A3S7WR24 | Leishmania donovani | 59% | 100% |
A4H4T8 | Leishmania braziliensis | 43% | 98% |
A4H5Y4 | Leishmania braziliensis | 48% | 99% |
A4H617 | Leishmania braziliensis | 56% | 100% |
A4H618 | Leishmania braziliensis | 56% | 100% |
A4H619 | Leishmania braziliensis | 56% | 100% |
A4H620 | Leishmania braziliensis | 81% | 100% |
A4H6C3 | Leishmania braziliensis | 48% | 99% |
A4HNH7 | Leishmania braziliensis | 38% | 95% |
A4HSS2 | Leishmania infantum | 51% | 100% |
A4HUE4 | Leishmania infantum | 51% | 96% |
A4HUE5 | Leishmania infantum | 58% | 100% |
A4HUE6 | Leishmania infantum | 61% | 100% |
A4HUE7 | Leishmania infantum | 60% | 100% |
A4HUE8 | Leishmania infantum | 59% | 100% |
A4HUF4 | Leishmania infantum | 58% | 100% |
A4HUF5 | Leishmania infantum | 90% | 100% |
A4HYA9 | Leishmania infantum | 60% | 100% |
A4IC33 | Leishmania infantum | 39% | 100% |
C9ZIK0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
C9ZIK3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
C9ZVE8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
C9ZVE9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
C9ZVF1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
D0A423 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
E8NHQ5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 57% | 100% |
E9AG72 | Leishmania infantum | 43% | 100% |
E9AI40 | Leishmania braziliensis | 57% | 100% |
E9AJY4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 49% | 98% |
E9AKQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 49% | 100% |
E9AL06 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 44% | 100% |
E9AN44 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 51% | 100% |
E9AN45 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 58% | 96% |
E9AN46 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 58% | 97% |
E9ANE5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 49% | 100% |
E9AS42 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 60% | 100% |
E9B741 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 39% | 100% |
Q4QDC4 | Leishmania major | 58% | 100% |
Q4QH81 | Leishmania major | 49% | 100% |
Q4QHH7 | Leishmania major | 87% | 100% |
Q4QHH8 | Leishmania major | 57% | 100% |
Q4QHH9 | Leishmania major | 56% | 100% |
Q4QHI0 | Leishmania major | 60% | 100% |
Q4QHI1 | Leishmania major | 60% | 97% |
Q4QHI2 | Leishmania major | 60% | 99% |
Q4QIU9 | Leishmania major | 46% | 100% |
Q4QJ48 | Leishmania major | 49% | 100% |
Q7KIP2 | Leishmania major | 39% | 96% |