| 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: E9ANE5
| 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 | 651 | 655 | PF00656 | 0.644 |
| CLV_NRD_NRD_1 | 260 | 262 | PF00675 | 0.321 |
| CLV_NRD_NRD_1 | 298 | 300 | PF00675 | 0.313 |
| CLV_PCSK_KEX2_1 | 134 | 136 | PF00082 | 0.292 |
| CLV_PCSK_KEX2_1 | 192 | 194 | PF00082 | 0.250 |
| CLV_PCSK_KEX2_1 | 298 | 300 | PF00082 | 0.374 |
| CLV_PCSK_PC1ET2_1 | 134 | 136 | PF00082 | 0.292 |
| CLV_PCSK_PC1ET2_1 | 192 | 194 | PF00082 | 0.207 |
| CLV_PCSK_PC1ET2_1 | 298 | 300 | PF00082 | 0.374 |
| CLV_PCSK_SKI1_1 | 117 | 121 | PF00082 | 0.353 |
| CLV_PCSK_SKI1_1 | 189 | 193 | PF00082 | 0.207 |
| CLV_PCSK_SKI1_1 | 588 | 592 | PF00082 | 0.483 |
| CLV_PCSK_SKI1_1 | 81 | 85 | PF00082 | 0.347 |
| DEG_SCF_FBW7_2 | 17 | 24 | PF00400 | 0.621 |
| DEG_SCF_TRCP1_1 | 225 | 230 | PF00400 | 0.202 |
| DEG_SIAH_1 | 640 | 648 | PF03145 | 0.578 |
| DEG_SPOP_SBC_1 | 559 | 563 | PF00917 | 0.460 |
| DEG_SPOP_SBC_1 | 575 | 579 | PF00917 | 0.246 |
| DOC_ANK_TNKS_1 | 104 | 111 | PF00023 | 0.542 |
| DOC_CKS1_1 | 18 | 23 | PF01111 | 0.607 |
| DOC_CKS1_1 | 596 | 601 | PF01111 | 0.432 |
| DOC_CYCLIN_RxL_1 | 77 | 87 | PF00134 | 0.602 |
| DOC_CYCLIN_yCln2_LP_2 | 398 | 404 | PF00134 | 0.442 |
| DOC_MAPK_gen_1 | 134 | 140 | PF00069 | 0.500 |
| DOC_MAPK_gen_1 | 261 | 268 | PF00069 | 0.553 |
| DOC_MAPK_MEF2A_6 | 228 | 235 | PF00069 | 0.328 |
| DOC_MAPK_MEF2A_6 | 499 | 506 | PF00069 | 0.356 |
| DOC_MAPK_MEF2A_6 | 64 | 71 | PF00069 | 0.534 |
| DOC_MAPK_NFAT4_5 | 64 | 72 | PF00069 | 0.605 |
| DOC_PP2B_LxvP_1 | 398 | 401 | PF13499 | 0.442 |
| DOC_PP2B_PxIxI_1 | 228 | 234 | PF00149 | 0.280 |
| DOC_PP4_FxxP_1 | 596 | 599 | PF00568 | 0.253 |
| DOC_USP7_MATH_1 | 277 | 281 | PF00917 | 0.601 |
| DOC_USP7_MATH_1 | 310 | 314 | PF00917 | 0.473 |
| DOC_USP7_MATH_1 | 333 | 337 | PF00917 | 0.412 |
| DOC_USP7_MATH_1 | 559 | 563 | PF00917 | 0.438 |
| DOC_USP7_MATH_1 | 575 | 579 | PF00917 | 0.270 |
| DOC_USP7_UBL2_3 | 296 | 300 | PF12436 | 0.408 |
| DOC_USP7_UBL2_3 | 632 | 636 | PF12436 | 0.552 |
| DOC_USP7_UBL2_3 | 646 | 650 | PF12436 | 0.614 |
| DOC_WW_Pin1_4 | 17 | 22 | PF00397 | 0.794 |
| DOC_WW_Pin1_4 | 306 | 311 | PF00397 | 0.562 |
| DOC_WW_Pin1_4 | 42 | 47 | PF00397 | 0.479 |
| DOC_WW_Pin1_4 | 576 | 581 | PF00397 | 0.348 |
| DOC_WW_Pin1_4 | 595 | 600 | PF00397 | 0.414 |
| DOC_WW_Pin1_4 | 637 | 642 | PF00397 | 0.560 |
| LIG_14-3-3_CanoR_1 | 299 | 304 | PF00244 | 0.527 |
| LIG_14-3-3_CanoR_1 | 351 | 356 | PF00244 | 0.500 |
| LIG_14-3-3_CanoR_1 | 476 | 480 | PF00244 | 0.490 |
| LIG_APCC_ABBAyCdc20_2 | 31 | 37 | PF00400 | 0.533 |
| LIG_BIR_III_2 | 43 | 47 | PF00653 | 0.614 |
| LIG_BRCT_BRCA1_1 | 110 | 114 | PF00533 | 0.407 |
| LIG_BRCT_BRCA1_1 | 123 | 127 | PF00533 | 0.426 |
| LIG_BRCT_BRCA1_1 | 442 | 446 | PF00533 | 0.317 |
| LIG_BRCT_BRCA1_1 | 544 | 548 | PF00533 | 0.492 |
| LIG_EVH1_2 | 580 | 584 | PF00568 | 0.360 |
| LIG_FHA_1 | 118 | 124 | PF00498 | 0.597 |
| LIG_FHA_1 | 228 | 234 | PF00498 | 0.355 |
| LIG_FHA_1 | 36 | 42 | PF00498 | 0.578 |
| LIG_FHA_1 | 361 | 367 | PF00498 | 0.348 |
| LIG_FHA_1 | 376 | 382 | PF00498 | 0.256 |
| LIG_FHA_1 | 393 | 399 | PF00498 | 0.356 |
| LIG_FHA_1 | 480 | 486 | PF00498 | 0.325 |
| LIG_FHA_1 | 5 | 11 | PF00498 | 0.725 |
| LIG_FHA_1 | 54 | 60 | PF00498 | 0.564 |
| LIG_FHA_1 | 596 | 602 | PF00498 | 0.417 |
| LIG_FHA_1 | 97 | 103 | PF00498 | 0.412 |
| LIG_FHA_2 | 18 | 24 | PF00498 | 0.689 |
| LIG_GBD_Chelix_1 | 71 | 79 | PF00786 | 0.230 |
| LIG_LIR_Apic_2 | 15 | 21 | PF02991 | 0.759 |
| LIG_LIR_Apic_2 | 30 | 36 | PF02991 | 0.640 |
| LIG_LIR_Gen_1 | 100 | 109 | PF02991 | 0.516 |
| LIG_LIR_Gen_1 | 124 | 132 | PF02991 | 0.521 |
| LIG_LIR_Gen_1 | 184 | 195 | PF02991 | 0.520 |
| LIG_LIR_Gen_1 | 203 | 214 | PF02991 | 0.499 |
| LIG_LIR_Gen_1 | 263 | 273 | PF02991 | 0.547 |
| LIG_LIR_Gen_1 | 377 | 386 | PF02991 | 0.294 |
| LIG_LIR_Gen_1 | 395 | 405 | PF02991 | 0.273 |
| LIG_LIR_Gen_1 | 445 | 454 | PF02991 | 0.325 |
| LIG_LIR_Gen_1 | 490 | 497 | PF02991 | 0.333 |
| LIG_LIR_Gen_1 | 545 | 554 | PF02991 | 0.510 |
| LIG_LIR_Gen_1 | 583 | 592 | PF02991 | 0.264 |
| LIG_LIR_Gen_1 | 86 | 96 | PF02991 | 0.547 |
| LIG_LIR_Nem_3 | 100 | 106 | PF02991 | 0.498 |
| LIG_LIR_Nem_3 | 124 | 130 | PF02991 | 0.496 |
| LIG_LIR_Nem_3 | 184 | 190 | PF02991 | 0.526 |
| LIG_LIR_Nem_3 | 203 | 209 | PF02991 | 0.310 |
| LIG_LIR_Nem_3 | 263 | 268 | PF02991 | 0.532 |
| LIG_LIR_Nem_3 | 377 | 382 | PF02991 | 0.289 |
| LIG_LIR_Nem_3 | 395 | 400 | PF02991 | 0.368 |
| LIG_LIR_Nem_3 | 417 | 421 | PF02991 | 0.383 |
| LIG_LIR_Nem_3 | 445 | 450 | PF02991 | 0.299 |
| LIG_LIR_Nem_3 | 490 | 495 | PF02991 | 0.336 |
| LIG_LIR_Nem_3 | 498 | 503 | PF02991 | 0.289 |
| LIG_LIR_Nem_3 | 545 | 551 | PF02991 | 0.472 |
| LIG_LIR_Nem_3 | 583 | 587 | PF02991 | 0.259 |
| LIG_LIR_Nem_3 | 86 | 92 | PF02991 | 0.438 |
| LIG_NRBOX | 586 | 592 | PF00104 | 0.223 |
| LIG_Pex14_1 | 633 | 637 | PF04695 | 0.479 |
| LIG_Pex14_2 | 170 | 174 | PF04695 | 0.365 |
| LIG_Pex14_2 | 242 | 246 | PF04695 | 0.299 |
| LIG_Pex14_2 | 247 | 251 | PF04695 | 0.285 |
| LIG_Pex14_2 | 409 | 413 | PF04695 | 0.360 |
| LIG_Pex14_2 | 442 | 446 | PF04695 | 0.305 |
| LIG_Pex14_2 | 466 | 470 | PF04695 | 0.364 |
| LIG_REV1ctd_RIR_1 | 265 | 274 | PF16727 | 0.382 |
| LIG_SH2_CRK | 103 | 107 | PF00017 | 0.508 |
| LIG_SH2_CRK | 137 | 141 | PF00017 | 0.377 |
| LIG_SH2_CRK | 152 | 156 | PF00017 | 0.377 |
| LIG_SH2_CRK | 18 | 22 | PF00017 | 0.618 |
| LIG_SH2_CRK | 187 | 191 | PF00017 | 0.514 |
| LIG_SH2_CRK | 358 | 362 | PF00017 | 0.345 |
| LIG_SH2_CRK | 379 | 383 | PF00017 | 0.309 |
| LIG_SH2_CRK | 447 | 451 | PF00017 | 0.299 |
| LIG_SH2_NCK_1 | 18 | 22 | PF00017 | 0.613 |
| LIG_SH2_NCK_1 | 447 | 451 | PF00017 | 0.300 |
| LIG_SH2_PTP2 | 33 | 36 | PF00017 | 0.630 |
| LIG_SH2_PTP2 | 418 | 421 | PF00017 | 0.349 |
| LIG_SH2_PTP2 | 503 | 506 | PF00017 | 0.399 |
| LIG_SH2_SRC | 33 | 36 | PF00017 | 0.636 |
| LIG_SH2_STAP1 | 132 | 136 | PF00017 | 0.500 |
| LIG_SH2_STAP1 | 187 | 191 | PF00017 | 0.486 |
| LIG_SH2_STAP1 | 520 | 524 | PF00017 | 0.405 |
| LIG_SH2_STAP1 | 89 | 93 | PF00017 | 0.536 |
| LIG_SH2_STAT5 | 132 | 135 | PF00017 | 0.502 |
| LIG_SH2_STAT5 | 265 | 268 | PF00017 | 0.468 |
| LIG_SH2_STAT5 | 33 | 36 | PF00017 | 0.627 |
| LIG_SH2_STAT5 | 418 | 421 | PF00017 | 0.340 |
| LIG_SH2_STAT5 | 464 | 467 | PF00017 | 0.289 |
| LIG_SH2_STAT5 | 503 | 506 | PF00017 | 0.302 |
| LIG_SH2_STAT5 | 512 | 515 | PF00017 | 0.293 |
| LIG_SH2_STAT5 | 73 | 76 | PF00017 | 0.518 |
| LIG_SH3_3 | 153 | 159 | PF00018 | 0.299 |
| LIG_SH3_3 | 434 | 440 | PF00018 | 0.286 |
| LIG_SH3_3 | 57 | 63 | PF00018 | 0.519 |
| LIG_SH3_3 | 605 | 611 | PF00018 | 0.390 |
| LIG_SH3_3 | 615 | 621 | PF00018 | 0.493 |
| LIG_SH3_4 | 646 | 653 | PF00018 | 0.634 |
| LIG_SUMO_SIM_anti_2 | 493 | 498 | PF11976 | 0.315 |
| LIG_SUMO_SIM_par_1 | 365 | 370 | PF11976 | 0.297 |
| LIG_SUMO_SIM_par_1 | 493 | 498 | PF11976 | 0.347 |
| LIG_TRAF2_1 | 21 | 24 | PF00917 | 0.653 |
| LIG_TYR_ITIM | 150 | 155 | PF00017 | 0.379 |
| LIG_TYR_ITIM | 381 | 386 | PF00017 | 0.374 |
| LIG_TYR_ITIM | 416 | 421 | PF00017 | 0.333 |
| LIG_TYR_ITSM | 443 | 450 | PF00017 | 0.404 |
| LIG_UBA3_1 | 266 | 270 | PF00899 | 0.522 |
| LIG_UBA3_1 | 534 | 541 | PF00899 | 0.222 |
| LIG_Vh1_VBS_1 | 367 | 385 | PF01044 | 0.447 |
| LIG_WRC_WIRS_1 | 551 | 556 | PF05994 | 0.225 |
| MOD_CDK_SPxxK_3 | 42 | 49 | PF00069 | 0.311 |
| MOD_CK1_1 | 422 | 428 | PF00069 | 0.380 |
| MOD_CK1_1 | 431 | 437 | PF00069 | 0.406 |
| MOD_CK1_1 | 471 | 477 | PF00069 | 0.351 |
| MOD_CK1_1 | 560 | 566 | PF00069 | 0.357 |
| MOD_CK2_1 | 17 | 23 | PF00069 | 0.583 |
| MOD_CK2_1 | 310 | 316 | PF00069 | 0.298 |
| MOD_GlcNHglycan | 106 | 109 | PF01048 | 0.322 |
| MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.630 |
| MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.361 |
| MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.362 |
| MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.374 |
| MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.371 |
| MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.434 |
| MOD_GSK3_1 | 104 | 111 | PF00069 | 0.410 |
| MOD_GSK3_1 | 117 | 124 | PF00069 | 0.352 |
| MOD_GSK3_1 | 223 | 230 | PF00069 | 0.392 |
| MOD_GSK3_1 | 290 | 297 | PF00069 | 0.437 |
| MOD_GSK3_1 | 306 | 313 | PF00069 | 0.392 |
| MOD_GSK3_1 | 347 | 354 | PF00069 | 0.459 |
| MOD_GSK3_1 | 442 | 449 | PF00069 | 0.372 |
| MOD_GSK3_1 | 471 | 478 | PF00069 | 0.363 |
| MOD_GSK3_1 | 557 | 564 | PF00069 | 0.374 |
| MOD_GSK3_1 | 648 | 655 | PF00069 | 0.812 |
| MOD_GSK3_1 | 79 | 86 | PF00069 | 0.383 |
| MOD_N-GLC_1 | 351 | 356 | PF02516 | 0.519 |
| MOD_N-GLC_1 | 84 | 89 | PF02516 | 0.399 |
| MOD_NEK2_1 | 112 | 117 | PF00069 | 0.377 |
| MOD_NEK2_1 | 130 | 135 | PF00069 | 0.346 |
| MOD_NEK2_1 | 138 | 143 | PF00069 | 0.347 |
| MOD_NEK2_1 | 223 | 228 | PF00069 | 0.360 |
| MOD_NEK2_1 | 332 | 337 | PF00069 | 0.511 |
| MOD_NEK2_1 | 375 | 380 | PF00069 | 0.296 |
| MOD_NEK2_1 | 392 | 397 | PF00069 | 0.289 |
| MOD_NEK2_1 | 442 | 447 | PF00069 | 0.355 |
| MOD_NEK2_1 | 479 | 484 | PF00069 | 0.362 |
| MOD_NEK2_1 | 533 | 538 | PF00069 | 0.302 |
| MOD_NEK2_1 | 557 | 562 | PF00069 | 0.353 |
| MOD_NEK2_1 | 569 | 574 | PF00069 | 0.351 |
| MOD_NEK2_1 | 79 | 84 | PF00069 | 0.363 |
| MOD_NEK2_2 | 543 | 548 | PF00069 | 0.222 |
| MOD_PIKK_1 | 440 | 446 | PF00454 | 0.222 |
| MOD_PK_1 | 351 | 357 | PF00069 | 0.222 |
| MOD_PKA_1 | 298 | 304 | PF00069 | 0.188 |
| MOD_PKA_2 | 104 | 110 | PF00069 | 0.325 |
| MOD_PKA_2 | 227 | 233 | PF00069 | 0.224 |
| MOD_PKA_2 | 298 | 304 | PF00069 | 0.189 |
| MOD_PKA_2 | 475 | 481 | PF00069 | 0.349 |
| MOD_Plk_1 | 333 | 339 | PF00069 | 0.321 |
| MOD_Plk_1 | 351 | 357 | PF00069 | 0.443 |
| MOD_Plk_1 | 431 | 437 | PF00069 | 0.391 |
| MOD_Plk_1 | 543 | 549 | PF00069 | 0.296 |
| MOD_Plk_1 | 84 | 90 | PF00069 | 0.423 |
| MOD_Plk_4 | 367 | 373 | PF00069 | 0.314 |
| MOD_Plk_4 | 400 | 406 | PF00069 | 0.421 |
| MOD_Plk_4 | 414 | 420 | PF00069 | 0.370 |
| MOD_Plk_4 | 442 | 448 | PF00069 | 0.451 |
| MOD_Plk_4 | 475 | 481 | PF00069 | 0.337 |
| MOD_Plk_4 | 487 | 493 | PF00069 | 0.321 |
| MOD_Plk_4 | 543 | 549 | PF00069 | 0.372 |
| MOD_Plk_4 | 569 | 575 | PF00069 | 0.347 |
| MOD_Plk_4 | 625 | 631 | PF00069 | 0.571 |
| MOD_ProDKin_1 | 17 | 23 | PF00069 | 0.762 |
| MOD_ProDKin_1 | 306 | 312 | PF00069 | 0.436 |
| MOD_ProDKin_1 | 42 | 48 | PF00069 | 0.317 |
| MOD_ProDKin_1 | 576 | 582 | PF00069 | 0.417 |
| MOD_ProDKin_1 | 595 | 601 | PF00069 | 0.414 |
| MOD_ProDKin_1 | 637 | 643 | PF00069 | 0.443 |
| MOD_SUMO_for_1 | 269 | 272 | PF00179 | 0.418 |
| MOD_SUMO_rev_2 | 617 | 624 | PF00179 | 0.408 |
| TRG_DiLeu_BaEn_1 | 254 | 259 | PF01217 | 0.453 |
| TRG_DiLeu_BaLyEn_6 | 186 | 191 | PF01217 | 0.276 |
| TRG_DiLeu_BaLyEn_6 | 596 | 601 | PF01217 | 0.320 |
| TRG_ENDOCYTIC_2 | 103 | 106 | PF00928 | 0.345 |
| TRG_ENDOCYTIC_2 | 137 | 140 | PF00928 | 0.346 |
| TRG_ENDOCYTIC_2 | 152 | 155 | PF00928 | 0.377 |
| TRG_ENDOCYTIC_2 | 187 | 190 | PF00928 | 0.337 |
| TRG_ENDOCYTIC_2 | 265 | 268 | PF00928 | 0.444 |
| TRG_ENDOCYTIC_2 | 358 | 361 | PF00928 | 0.346 |
| TRG_ENDOCYTIC_2 | 379 | 382 | PF00928 | 0.359 |
| TRG_ENDOCYTIC_2 | 383 | 386 | PF00928 | 0.358 |
| TRG_ENDOCYTIC_2 | 418 | 421 | PF00928 | 0.355 |
| TRG_ENDOCYTIC_2 | 447 | 450 | PF00928 | 0.352 |
| TRG_ENDOCYTIC_2 | 503 | 506 | PF00928 | 0.482 |
| TRG_ENDOCYTIC_2 | 89 | 92 | PF00928 | 0.369 |
| TRG_NLS_MonoExtN_4 | 296 | 302 | PF00514 | 0.186 |
| TRG_Pf-PMV_PEXEL_1 | 256 | 260 | PF00026 | 0.502 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P2U2 | Leptomonas seymouri | 44% | 94% |
| A0A0N1HY49 | Leptomonas seymouri | 46% | 98% |
| A0A0N1HZ06 | Leptomonas seymouri | 38% | 100% |
| A0A0N1IHL1 | Leptomonas seymouri | 40% | 92% |
| A0A0N1PAY4 | Leptomonas seymouri | 41% | 75% |
| A0A0N1PB77 | Leptomonas seymouri | 40% | 100% |
| A0A0N1PBZ2 | Leptomonas seymouri | 45% | 98% |
| A0A0N1PCC1 | Leptomonas seymouri | 42% | 99% |
| A0A0S4INN8 | Bodo saltans | 30% | 100% |
| A0A381MBI0 | Leishmania infantum | 94% | 100% |
| A0A3Q8I8X7 | Leishmania donovani | 94% | 100% |
| A0A3Q8IAZ0 | Leishmania donovani | 45% | 94% |
| A0A3Q8IH50 | Leishmania donovani | 48% | 91% |
| A0A3Q8IVN0 | Leishmania donovani | 39% | 100% |
| A0A3R7M4J1 | Trypanosoma rangeli | 41% | 100% |
| A0A3S5H5P4 | Leishmania donovani | 46% | 97% |
| A0A3S5H5V2 | Leishmania donovani | 45% | 100% |
| A0A3S5H6F6 | Leishmania donovani | 44% | 94% |
| A0A3S5H763 | Leishmania donovani | 48% | 98% |
| A0A3S7WR10 | Leishmania donovani | 41% | 88% |
| A0A3S7WR14 | Leishmania donovani | 47% | 96% |
| A0A3S7WR15 | Leishmania donovani | 44% | 78% |
| A0A3S7WR24 | Leishmania donovani | 44% | 94% |
| A4H4T8 | Leishmania braziliensis | 44% | 100% |
| A4H5Y4 | Leishmania braziliensis | 84% | 100% |
| A4H617 | Leishmania braziliensis | 45% | 100% |
| A4H618 | Leishmania braziliensis | 45% | 100% |
| A4H619 | Leishmania braziliensis | 46% | 100% |
| A4H620 | Leishmania braziliensis | 51% | 100% |
| A4H6C3 | Leishmania braziliensis | 84% | 100% |
| A4HNH7 | Leishmania braziliensis | 38% | 97% |
| A4HSS2 | Leishmania infantum | 46% | 97% |
| A4HUE4 | Leishmania infantum | 41% | 88% |
| A4HUE5 | Leishmania infantum | 44% | 95% |
| A4HUE6 | Leishmania infantum | 47% | 96% |
| A4HUE7 | Leishmania infantum | 45% | 94% |
| A4HUE8 | Leishmania infantum | 45% | 94% |
| A4HUF4 | Leishmania infantum | 44% | 94% |
| A4HUF5 | Leishmania infantum | 49% | 100% |
| A4HYA9 | Leishmania infantum | 47% | 98% |
| A4IC33 | Leishmania infantum | 38% | 100% |
| C9ZIK0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
| C9ZIK3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
| C9ZVE8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
| C9ZVE9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
| C9ZVF1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
| D0A423 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
| E8NHQ5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 44% | 100% |
| E9AG72 | Leishmania infantum | 45% | 100% |
| E9AI40 | Leishmania braziliensis | 46% | 100% |
| E9AJY4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 98% | 100% |
| E9AKQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 44% | 100% |
| E9AL06 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 44% | 100% |
| E9AN44 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 43% | 100% |
| E9AN45 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 45% | 100% |
| E9AN46 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 46% | 100% |
| E9AN47 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 49% | 100% |
| E9AS42 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 45% | 98% |
| E9B741 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 39% | 100% |
| Q4QDC4 | Leishmania major | 47% | 100% |
| Q4QH81 | Leishmania major | 94% | 100% |
| Q4QHH7 | Leishmania major | 48% | 100% |
| Q4QHH8 | Leishmania major | 43% | 100% |
| Q4QHH9 | Leishmania major | 43% | 100% |
| Q4QHI0 | Leishmania major | 44% | 100% |
| Q4QHI1 | Leishmania major | 46% | 100% |
| Q4QHI2 | Leishmania major | 43% | 100% |
| Q4QIU9 | Leishmania major | 44% | 100% |
| Q4QJ48 | Leishmania major | 46% | 100% |
| Q7KIP2 | Leishmania major | 39% | 100% |