Transporters, ABC transporter-like
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: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
Related structures:
AlphaFold database: A4I828
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0055085 | transmembrane transport | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 9 |
GO:0005215 | transporter activity | 1 | 9 |
GO:0005488 | binding | 1 | 9 |
GO:0005524 | ATP binding | 5 | 9 |
GO:0015399 | primary active transmembrane transporter activity | 4 | 9 |
GO:0017076 | purine nucleotide binding | 4 | 9 |
GO:0022804 | active transmembrane transporter activity | 3 | 9 |
GO:0022857 | transmembrane transporter activity | 2 | 9 |
GO:0030554 | adenyl nucleotide binding | 5 | 9 |
GO:0032553 | ribonucleotide binding | 3 | 9 |
GO:0032555 | purine ribonucleotide binding | 4 | 9 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 9 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 9 |
GO:0036094 | small molecule binding | 2 | 9 |
GO:0042626 | ATPase-coupled transmembrane transporter activity | 2 | 9 |
GO:0043167 | ion binding | 2 | 9 |
GO:0043168 | anion binding | 3 | 9 |
GO:0097159 | organic cyclic compound binding | 2 | 9 |
GO:0097367 | carbohydrate derivative binding | 2 | 9 |
GO:0140359 | ABC-type transporter activity | 3 | 9 |
GO:0140657 | ATP-dependent activity | 1 | 9 |
GO:1901265 | nucleoside phosphate binding | 3 | 9 |
GO:1901363 | heterocyclic compound binding | 2 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 212 | 214 | PF00675 | 0.190 |
CLV_NRD_NRD_1 | 562 | 564 | PF00675 | 0.360 |
CLV_NRD_NRD_1 | 624 | 626 | PF00675 | 0.303 |
CLV_NRD_NRD_1 | 717 | 719 | PF00675 | 0.389 |
CLV_PCSK_KEX2_1 | 212 | 214 | PF00082 | 0.190 |
CLV_PCSK_KEX2_1 | 562 | 564 | PF00082 | 0.360 |
CLV_PCSK_KEX2_1 | 624 | 626 | PF00082 | 0.291 |
CLV_PCSK_KEX2_1 | 717 | 719 | PF00082 | 0.389 |
CLV_PCSK_SKI1_1 | 122 | 126 | PF00082 | 0.721 |
CLV_PCSK_SKI1_1 | 134 | 138 | PF00082 | 0.533 |
CLV_PCSK_SKI1_1 | 173 | 177 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 212 | 216 | PF00082 | 0.243 |
CLV_PCSK_SKI1_1 | 367 | 371 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 47 | 51 | PF00082 | 0.490 |
CLV_PCSK_SKI1_1 | 563 | 567 | PF00082 | 0.300 |
CLV_PCSK_SKI1_1 | 624 | 628 | PF00082 | 0.398 |
CLV_PCSK_SKI1_1 | 662 | 666 | PF00082 | 0.398 |
CLV_PCSK_SKI1_1 | 708 | 712 | PF00082 | 0.404 |
DEG_APCC_DBOX_1 | 172 | 180 | PF00400 | 0.438 |
DEG_APCC_DBOX_1 | 415 | 423 | PF00400 | 0.667 |
DEG_APCC_DBOX_1 | 661 | 669 | PF00400 | 0.560 |
DEG_SCF_FBW7_2 | 214 | 221 | PF00400 | 0.542 |
DEG_SPOP_SBC_1 | 92 | 96 | PF00917 | 0.538 |
DOC_CKS1_1 | 215 | 220 | PF01111 | 0.548 |
DOC_MAPK_FxFP_2 | 476 | 479 | PF00069 | 0.608 |
DOC_MAPK_gen_1 | 134 | 144 | PF00069 | 0.398 |
DOC_MAPK_gen_1 | 559 | 567 | PF00069 | 0.542 |
DOC_MAPK_MEF2A_6 | 134 | 142 | PF00069 | 0.398 |
DOC_MAPK_MEF2A_6 | 173 | 181 | PF00069 | 0.369 |
DOC_MAPK_MEF2A_6 | 367 | 376 | PF00069 | 0.433 |
DOC_MAPK_MEF2A_6 | 689 | 696 | PF00069 | 0.630 |
DOC_PP1_RVXF_1 | 120 | 126 | PF00149 | 0.462 |
DOC_PP2B_LxvP_1 | 109 | 112 | PF13499 | 0.536 |
DOC_PP4_FxxP_1 | 476 | 479 | PF00568 | 0.608 |
DOC_USP7_MATH_1 | 159 | 163 | PF00917 | 0.341 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.730 |
DOC_USP7_MATH_1 | 338 | 342 | PF00917 | 0.556 |
DOC_USP7_MATH_1 | 359 | 363 | PF00917 | 0.424 |
DOC_USP7_MATH_1 | 497 | 501 | PF00917 | 0.707 |
DOC_USP7_MATH_1 | 508 | 512 | PF00917 | 0.717 |
DOC_USP7_MATH_1 | 595 | 599 | PF00917 | 0.568 |
DOC_USP7_MATH_1 | 630 | 634 | PF00917 | 0.560 |
DOC_WW_Pin1_4 | 16 | 21 | PF00397 | 0.761 |
DOC_WW_Pin1_4 | 161 | 166 | PF00397 | 0.328 |
DOC_WW_Pin1_4 | 214 | 219 | PF00397 | 0.548 |
DOC_WW_Pin1_4 | 461 | 466 | PF00397 | 0.606 |
DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.797 |
LIG_14-3-3_CanoR_1 | 15 | 20 | PF00244 | 0.674 |
LIG_14-3-3_CanoR_1 | 240 | 249 | PF00244 | 0.604 |
LIG_14-3-3_CanoR_1 | 302 | 310 | PF00244 | 0.556 |
LIG_14-3-3_CanoR_1 | 320 | 325 | PF00244 | 0.426 |
LIG_14-3-3_CanoR_1 | 36 | 42 | PF00244 | 0.587 |
LIG_14-3-3_CanoR_1 | 416 | 420 | PF00244 | 0.594 |
LIG_14-3-3_CanoR_1 | 421 | 426 | PF00244 | 0.567 |
LIG_14-3-3_CanoR_1 | 430 | 435 | PF00244 | 0.540 |
LIG_14-3-3_CanoR_1 | 624 | 631 | PF00244 | 0.522 |
LIG_14-3-3_CanoR_1 | 79 | 85 | PF00244 | 0.368 |
LIG_Actin_WH2_2 | 401 | 418 | PF00022 | 0.492 |
LIG_Actin_WH2_2 | 688 | 705 | PF00022 | 0.627 |
LIG_APCC_ABBA_1 | 163 | 168 | PF00400 | 0.342 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.799 |
LIG_BIR_III_2 | 156 | 160 | PF00653 | 0.245 |
LIG_BRCT_BRCA1_1 | 51 | 55 | PF00533 | 0.438 |
LIG_BRCT_BRCA1_1 | 639 | 643 | PF00533 | 0.548 |
LIG_Clathr_ClatBox_1 | 677 | 681 | PF01394 | 0.525 |
LIG_EH_1 | 640 | 644 | PF12763 | 0.548 |
LIG_eIF4E_1 | 184 | 190 | PF01652 | 0.438 |
LIG_FHA_1 | 185 | 191 | PF00498 | 0.417 |
LIG_FHA_1 | 244 | 250 | PF00498 | 0.531 |
LIG_FHA_1 | 273 | 279 | PF00498 | 0.395 |
LIG_FHA_1 | 29 | 35 | PF00498 | 0.645 |
LIG_FHA_1 | 321 | 327 | PF00498 | 0.510 |
LIG_FHA_1 | 346 | 352 | PF00498 | 0.556 |
LIG_FHA_1 | 364 | 370 | PF00498 | 0.251 |
LIG_FHA_1 | 41 | 47 | PF00498 | 0.567 |
LIG_FHA_1 | 449 | 455 | PF00498 | 0.747 |
LIG_FHA_1 | 464 | 470 | PF00498 | 0.599 |
LIG_FHA_1 | 521 | 527 | PF00498 | 0.525 |
LIG_FHA_1 | 553 | 559 | PF00498 | 0.562 |
LIG_FHA_1 | 682 | 688 | PF00498 | 0.582 |
LIG_FHA_1 | 707 | 713 | PF00498 | 0.555 |
LIG_FHA_1 | 80 | 86 | PF00498 | 0.490 |
LIG_FHA_2 | 20 | 26 | PF00498 | 0.721 |
LIG_FHA_2 | 243 | 249 | PF00498 | 0.531 |
LIG_FHA_2 | 302 | 308 | PF00498 | 0.560 |
LIG_FHA_2 | 437 | 443 | PF00498 | 0.749 |
LIG_FHA_2 | 575 | 581 | PF00498 | 0.483 |
LIG_FHA_2 | 616 | 622 | PF00498 | 0.542 |
LIG_FHA_2 | 643 | 649 | PF00498 | 0.525 |
LIG_FHA_2 | 683 | 689 | PF00498 | 0.615 |
LIG_FHA_2 | 696 | 702 | PF00498 | 0.528 |
LIG_FHA_2 | 96 | 102 | PF00498 | 0.603 |
LIG_LIR_Apic_2 | 475 | 479 | PF02991 | 0.572 |
LIG_LIR_Gen_1 | 618 | 626 | PF02991 | 0.542 |
LIG_LIR_Gen_1 | 640 | 650 | PF02991 | 0.595 |
LIG_LIR_Gen_1 | 672 | 683 | PF02991 | 0.544 |
LIG_LIR_Nem_3 | 133 | 139 | PF02991 | 0.348 |
LIG_LIR_Nem_3 | 475 | 481 | PF02991 | 0.585 |
LIG_LIR_Nem_3 | 618 | 622 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 640 | 646 | PF02991 | 0.526 |
LIG_LIR_Nem_3 | 672 | 678 | PF02991 | 0.544 |
LIG_LYPXL_yS_3 | 478 | 481 | PF13949 | 0.598 |
LIG_PCNA_yPIPBox_3 | 512 | 526 | PF02747 | 0.390 |
LIG_SH2_CRK | 358 | 362 | PF00017 | 0.438 |
LIG_SH2_CRK | 675 | 679 | PF00017 | 0.544 |
LIG_SH2_NCK_1 | 358 | 362 | PF00017 | 0.438 |
LIG_SH2_SRC | 166 | 169 | PF00017 | 0.360 |
LIG_SH2_STAP1 | 675 | 679 | PF00017 | 0.544 |
LIG_SH2_STAT3 | 379 | 382 | PF00017 | 0.324 |
LIG_SH2_STAT5 | 166 | 169 | PF00017 | 0.354 |
LIG_SH2_STAT5 | 259 | 262 | PF00017 | 0.412 |
LIG_SH2_STAT5 | 313 | 316 | PF00017 | 0.598 |
LIG_SH2_STAT5 | 394 | 397 | PF00017 | 0.358 |
LIG_SH3_3 | 135 | 141 | PF00018 | 0.360 |
LIG_SH3_3 | 476 | 482 | PF00018 | 0.589 |
LIG_SH3_3 | 599 | 605 | PF00018 | 0.598 |
LIG_SH3_3 | 607 | 613 | PF00018 | 0.504 |
LIG_SH3_3 | 647 | 653 | PF00018 | 0.598 |
LIG_SUMO_SIM_anti_2 | 221 | 227 | PF11976 | 0.560 |
LIG_SUMO_SIM_anti_2 | 275 | 281 | PF11976 | 0.438 |
LIG_SUMO_SIM_anti_2 | 366 | 372 | PF11976 | 0.438 |
LIG_SUMO_SIM_anti_2 | 455 | 460 | PF11976 | 0.612 |
LIG_SUMO_SIM_anti_2 | 676 | 682 | PF11976 | 0.525 |
LIG_SUMO_SIM_anti_2 | 690 | 698 | PF11976 | 0.591 |
LIG_SUMO_SIM_par_1 | 450 | 455 | PF11976 | 0.735 |
LIG_SUMO_SIM_par_1 | 457 | 464 | PF11976 | 0.639 |
LIG_SUMO_SIM_par_1 | 47 | 52 | PF11976 | 0.428 |
LIG_SUMO_SIM_par_1 | 60 | 65 | PF11976 | 0.337 |
LIG_SUMO_SIM_par_1 | 676 | 682 | PF11976 | 0.560 |
LIG_SUMO_SIM_par_1 | 708 | 714 | PF11976 | 0.569 |
LIG_SUMO_SIM_par_1 | 724 | 730 | PF11976 | 0.599 |
LIG_TRAF2_1 | 304 | 307 | PF00917 | 0.560 |
LIG_UBA3_1 | 695 | 700 | PF00899 | 0.568 |
LIG_WRC_WIRS_1 | 398 | 403 | PF05994 | 0.395 |
LIG_WRC_WIRS_1 | 587 | 592 | PF05994 | 0.542 |
LIG_WRC_WIRS_1 | 643 | 648 | PF05994 | 0.598 |
MOD_CDK_SPxxK_3 | 8 | 15 | PF00069 | 0.696 |
MOD_CK1_1 | 18 | 24 | PF00069 | 0.809 |
MOD_CK1_1 | 243 | 249 | PF00069 | 0.568 |
MOD_CK1_1 | 301 | 307 | PF00069 | 0.555 |
MOD_CK1_1 | 363 | 369 | PF00069 | 0.357 |
MOD_CK1_1 | 40 | 46 | PF00069 | 0.588 |
MOD_CK1_1 | 407 | 413 | PF00069 | 0.387 |
MOD_CK1_1 | 586 | 592 | PF00069 | 0.528 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.592 |
MOD_CK2_1 | 19 | 25 | PF00069 | 0.727 |
MOD_CK2_1 | 242 | 248 | PF00069 | 0.560 |
MOD_CK2_1 | 301 | 307 | PF00069 | 0.560 |
MOD_CK2_1 | 436 | 442 | PF00069 | 0.746 |
MOD_CK2_1 | 574 | 580 | PF00069 | 0.497 |
MOD_CK2_1 | 615 | 621 | PF00069 | 0.542 |
MOD_CK2_1 | 642 | 648 | PF00069 | 0.560 |
MOD_CK2_1 | 687 | 693 | PF00069 | 0.653 |
MOD_CK2_1 | 695 | 701 | PF00069 | 0.601 |
MOD_CK2_1 | 729 | 735 | PF00069 | 0.723 |
MOD_CK2_1 | 95 | 101 | PF00069 | 0.536 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.544 |
MOD_GlcNHglycan | 199 | 202 | PF01048 | 0.388 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.629 |
MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.341 |
MOD_GlcNHglycan | 339 | 343 | PF01048 | 0.377 |
MOD_GlcNHglycan | 362 | 365 | PF01048 | 0.427 |
MOD_GlcNHglycan | 409 | 412 | PF01048 | 0.415 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.346 |
MOD_GlcNHglycan | 535 | 538 | PF01048 | 0.301 |
MOD_GlcNHglycan | 591 | 594 | PF01048 | 0.318 |
MOD_GlcNHglycan | 597 | 600 | PF01048 | 0.312 |
MOD_GlcNHglycan | 606 | 609 | PF01048 | 0.231 |
MOD_GlcNHglycan | 632 | 635 | PF01048 | 0.360 |
MOD_GlcNHglycan | 655 | 658 | PF01048 | 0.283 |
MOD_GlcNHglycan | 688 | 692 | PF01048 | 0.412 |
MOD_GlcNHglycan | 728 | 732 | PF01048 | 0.484 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.586 |
MOD_GlcNHglycan | 95 | 98 | PF01048 | 0.769 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.823 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.548 |
MOD_GSK3_1 | 268 | 275 | PF00069 | 0.162 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.400 |
MOD_GSK3_1 | 397 | 404 | PF00069 | 0.448 |
MOD_GSK3_1 | 406 | 413 | PF00069 | 0.423 |
MOD_GSK3_1 | 504 | 511 | PF00069 | 0.751 |
MOD_GSK3_1 | 582 | 589 | PF00069 | 0.536 |
MOD_GSK3_1 | 591 | 598 | PF00069 | 0.552 |
MOD_GSK3_1 | 600 | 607 | PF00069 | 0.571 |
MOD_GSK3_1 | 611 | 618 | PF00069 | 0.439 |
MOD_GSK3_1 | 637 | 644 | PF00069 | 0.544 |
MOD_GSK3_1 | 669 | 676 | PF00069 | 0.556 |
MOD_GSK3_1 | 702 | 709 | PF00069 | 0.590 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.529 |
MOD_N-GLC_1 | 351 | 356 | PF02516 | 0.339 |
MOD_NEK2_1 | 146 | 151 | PF00069 | 0.267 |
MOD_NEK2_1 | 242 | 247 | PF00069 | 0.538 |
MOD_NEK2_1 | 268 | 273 | PF00069 | 0.381 |
MOD_NEK2_1 | 318 | 323 | PF00069 | 0.556 |
MOD_NEK2_1 | 351 | 356 | PF00069 | 0.558 |
MOD_NEK2_1 | 37 | 42 | PF00069 | 0.619 |
MOD_NEK2_1 | 374 | 379 | PF00069 | 0.376 |
MOD_NEK2_1 | 388 | 393 | PF00069 | 0.269 |
MOD_NEK2_1 | 401 | 406 | PF00069 | 0.423 |
MOD_NEK2_1 | 415 | 420 | PF00069 | 0.593 |
MOD_NEK2_1 | 436 | 441 | PF00069 | 0.759 |
MOD_NEK2_1 | 518 | 523 | PF00069 | 0.390 |
MOD_NEK2_1 | 574 | 579 | PF00069 | 0.525 |
MOD_NEK2_1 | 583 | 588 | PF00069 | 0.525 |
MOD_NEK2_1 | 62 | 67 | PF00069 | 0.447 |
MOD_NEK2_1 | 687 | 692 | PF00069 | 0.590 |
MOD_NEK2_1 | 695 | 700 | PF00069 | 0.546 |
MOD_NEK2_1 | 702 | 707 | PF00069 | 0.548 |
MOD_NEK2_1 | 729 | 734 | PF00069 | 0.676 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.417 |
MOD_OFUCOSY | 538 | 543 | PF10250 | 0.398 |
MOD_PIKK_1 | 252 | 258 | PF00454 | 0.492 |
MOD_PIKK_1 | 318 | 324 | PF00454 | 0.598 |
MOD_PIKK_1 | 410 | 416 | PF00454 | 0.560 |
MOD_PIKK_1 | 557 | 563 | PF00454 | 0.560 |
MOD_PKA_1 | 624 | 630 | PF00069 | 0.560 |
MOD_PKA_2 | 301 | 307 | PF00069 | 0.536 |
MOD_PKA_2 | 345 | 351 | PF00069 | 0.560 |
MOD_PKA_2 | 388 | 394 | PF00069 | 0.308 |
MOD_PKA_2 | 415 | 421 | PF00069 | 0.632 |
MOD_PKA_2 | 624 | 630 | PF00069 | 0.560 |
MOD_PKA_2 | 702 | 708 | PF00069 | 0.666 |
MOD_PKA_2 | 78 | 84 | PF00069 | 0.361 |
MOD_Plk_1 | 306 | 312 | PF00069 | 0.544 |
MOD_Plk_1 | 351 | 357 | PF00069 | 0.528 |
MOD_Plk_1 | 673 | 679 | PF00069 | 0.550 |
MOD_Plk_1 | 687 | 693 | PF00069 | 0.634 |
MOD_Plk_4 | 185 | 191 | PF00069 | 0.412 |
MOD_Plk_4 | 272 | 278 | PF00069 | 0.387 |
MOD_Plk_4 | 320 | 326 | PF00069 | 0.534 |
MOD_Plk_4 | 37 | 43 | PF00069 | 0.610 |
MOD_Plk_4 | 388 | 394 | PF00069 | 0.331 |
MOD_Plk_4 | 397 | 403 | PF00069 | 0.394 |
MOD_Plk_4 | 57 | 63 | PF00069 | 0.380 |
MOD_Plk_4 | 642 | 648 | PF00069 | 0.528 |
MOD_Plk_4 | 673 | 679 | PF00069 | 0.524 |
MOD_Plk_4 | 706 | 712 | PF00069 | 0.576 |
MOD_ProDKin_1 | 16 | 22 | PF00069 | 0.759 |
MOD_ProDKin_1 | 161 | 167 | PF00069 | 0.328 |
MOD_ProDKin_1 | 214 | 220 | PF00069 | 0.548 |
MOD_ProDKin_1 | 461 | 467 | PF00069 | 0.600 |
MOD_ProDKin_1 | 8 | 14 | PF00069 | 0.797 |
TRG_DiLeu_BaLyEn_6 | 135 | 140 | PF01217 | 0.398 |
TRG_DiLeu_BaLyEn_6 | 364 | 369 | PF01217 | 0.438 |
TRG_DiLeu_BaLyEn_6 | 542 | 547 | PF01217 | 0.560 |
TRG_ENDOCYTIC_2 | 358 | 361 | PF00928 | 0.438 |
TRG_ENDOCYTIC_2 | 39 | 42 | PF00928 | 0.641 |
TRG_ENDOCYTIC_2 | 478 | 481 | PF00928 | 0.598 |
TRG_ENDOCYTIC_2 | 675 | 678 | PF00928 | 0.544 |
TRG_ER_diArg_1 | 211 | 213 | PF00400 | 0.390 |
TRG_ER_diArg_1 | 624 | 626 | PF00400 | 0.527 |
TRG_ER_diArg_1 | 717 | 719 | PF00400 | 0.585 |
TRG_Pf-PMV_PEXEL_1 | 240 | 244 | PF00026 | 0.398 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I7P4 | Leptomonas seymouri | 64% | 100% |
A0A0S4J6G3 | Bodo saltans | 28% | 100% |
A0A1X0NU80 | Trypanosomatidae | 35% | 100% |
A0A3S5H7S2 | Leishmania donovani | 99% | 100% |
A4HKJ6 | Leishmania braziliensis | 78% | 99% |
E9B2Y6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 99% |
Q4Q570 | Leishmania major | 92% | 99% |