A complex and fast-evolving family of glycosyltransferases. Their structural innovations and expansion is in accordance with a role in interactions with the environment. Despite the short hydrophobic segment, the N-terminal signal-like stretch is likely to be a signal-anchor as wil all Golgi-resident glycosyltransferases, not a secretory signal. Localization: Golgi (by homology)
GPI anchor biosynthesis, Mannosyltransferase-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: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 1, no: 13 |
NetGPI | no | yes: 0, no: 14 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 5 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
Related structures:
AlphaFold database: A4I6X8
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 15 |
GO:0016740 | transferase activity | 2 | 15 |
GO:0016757 | glycosyltransferase activity | 3 | 15 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 278 | 282 | PF00656 | 0.418 |
CLV_NRD_NRD_1 | 262 | 264 | PF00675 | 0.441 |
CLV_NRD_NRD_1 | 292 | 294 | PF00675 | 0.484 |
CLV_NRD_NRD_1 | 395 | 397 | PF00675 | 0.438 |
CLV_NRD_NRD_1 | 524 | 526 | PF00675 | 0.587 |
CLV_NRD_NRD_1 | 571 | 573 | PF00675 | 0.530 |
CLV_NRD_NRD_1 | 637 | 639 | PF00675 | 0.426 |
CLV_NRD_NRD_1 | 674 | 676 | PF00675 | 0.435 |
CLV_NRD_NRD_1 | 820 | 822 | PF00675 | 0.369 |
CLV_NRD_NRD_1 | 824 | 826 | PF00675 | 0.345 |
CLV_PCSK_KEX2_1 | 262 | 264 | PF00082 | 0.474 |
CLV_PCSK_KEX2_1 | 292 | 294 | PF00082 | 0.484 |
CLV_PCSK_KEX2_1 | 394 | 396 | PF00082 | 0.440 |
CLV_PCSK_KEX2_1 | 523 | 525 | PF00082 | 0.526 |
CLV_PCSK_KEX2_1 | 571 | 573 | PF00082 | 0.486 |
CLV_PCSK_KEX2_1 | 674 | 676 | PF00082 | 0.435 |
CLV_PCSK_KEX2_1 | 820 | 822 | PF00082 | 0.343 |
CLV_PCSK_KEX2_1 | 824 | 826 | PF00082 | 0.315 |
CLV_PCSK_PC1ET2_1 | 523 | 525 | PF00082 | 0.591 |
CLV_PCSK_PC7_1 | 820 | 826 | PF00082 | 0.383 |
CLV_PCSK_SKI1_1 | 109 | 113 | PF00082 | 0.604 |
CLV_PCSK_SKI1_1 | 196 | 200 | PF00082 | 0.532 |
CLV_PCSK_SKI1_1 | 372 | 376 | PF00082 | 0.557 |
CLV_PCSK_SKI1_1 | 483 | 487 | PF00082 | 0.600 |
CLV_PCSK_SKI1_1 | 505 | 509 | PF00082 | 0.460 |
CLV_PCSK_SKI1_1 | 626 | 630 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 69 | 73 | PF00082 | 0.629 |
CLV_Separin_Metazoa | 807 | 811 | PF03568 | 0.374 |
DEG_SCF_FBW7_1 | 92 | 97 | PF00400 | 0.643 |
DOC_ANK_TNKS_1 | 773 | 780 | PF00023 | 0.450 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 18 | 27 | PF00134 | 0.521 |
DOC_CYCLIN_yCln2_LP_2 | 129 | 135 | PF00134 | 0.550 |
DOC_MAPK_gen_1 | 501 | 510 | PF00069 | 0.535 |
DOC_MAPK_gen_1 | 638 | 645 | PF00069 | 0.428 |
DOC_MAPK_gen_1 | 661 | 668 | PF00069 | 0.547 |
DOC_MAPK_MEF2A_6 | 327 | 336 | PF00069 | 0.544 |
DOC_MAPK_MEF2A_6 | 525 | 534 | PF00069 | 0.578 |
DOC_PP1_RVXF_1 | 624 | 631 | PF00149 | 0.517 |
DOC_PP2B_LxvP_1 | 129 | 132 | PF13499 | 0.567 |
DOC_PP2B_PxIxI_1 | 707 | 713 | PF00149 | 0.436 |
DOC_PP4_FxxP_1 | 432 | 435 | PF00568 | 0.496 |
DOC_PP4_FxxP_1 | 519 | 522 | PF00568 | 0.518 |
DOC_PP4_FxxP_1 | 732 | 735 | PF00568 | 0.327 |
DOC_PP4_FxxP_1 | 773 | 776 | PF00568 | 0.402 |
DOC_USP7_MATH_1 | 366 | 370 | PF00917 | 0.526 |
DOC_USP7_MATH_1 | 493 | 497 | PF00917 | 0.616 |
DOC_USP7_MATH_1 | 58 | 62 | PF00917 | 0.667 |
DOC_USP7_MATH_1 | 601 | 605 | PF00917 | 0.557 |
DOC_USP7_MATH_1 | 798 | 802 | PF00917 | 0.337 |
DOC_USP7_MATH_1 | 94 | 98 | PF00917 | 0.656 |
DOC_WW_Pin1_4 | 488 | 493 | PF00397 | 0.643 |
DOC_WW_Pin1_4 | 573 | 578 | PF00397 | 0.520 |
DOC_WW_Pin1_4 | 674 | 679 | PF00397 | 0.565 |
DOC_WW_Pin1_4 | 781 | 786 | PF00397 | 0.442 |
DOC_WW_Pin1_4 | 90 | 95 | PF00397 | 0.723 |
LIG_14-3-3_CanoR_1 | 126 | 130 | PF00244 | 0.571 |
LIG_14-3-3_CanoR_1 | 171 | 177 | PF00244 | 0.690 |
LIG_14-3-3_CanoR_1 | 229 | 235 | PF00244 | 0.637 |
LIG_14-3-3_CanoR_1 | 273 | 277 | PF00244 | 0.482 |
LIG_14-3-3_CanoR_1 | 37 | 47 | PF00244 | 0.539 |
LIG_14-3-3_CanoR_1 | 372 | 378 | PF00244 | 0.597 |
LIG_14-3-3_CanoR_1 | 380 | 389 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 427 | 435 | PF00244 | 0.575 |
LIG_14-3-3_CanoR_1 | 464 | 468 | PF00244 | 0.536 |
LIG_14-3-3_CanoR_1 | 615 | 624 | PF00244 | 0.557 |
LIG_14-3-3_CanoR_1 | 663 | 667 | PF00244 | 0.535 |
LIG_14-3-3_CanoR_1 | 69 | 77 | PF00244 | 0.623 |
LIG_BIR_III_4 | 296 | 300 | PF00653 | 0.553 |
LIG_deltaCOP1_diTrp_1 | 557 | 566 | PF00928 | 0.364 |
LIG_deltaCOP1_diTrp_1 | 759 | 766 | PF00928 | 0.418 |
LIG_FHA_1 | 13 | 19 | PF00498 | 0.618 |
LIG_FHA_1 | 138 | 144 | PF00498 | 0.559 |
LIG_FHA_1 | 186 | 192 | PF00498 | 0.605 |
LIG_FHA_1 | 259 | 265 | PF00498 | 0.529 |
LIG_FHA_1 | 413 | 419 | PF00498 | 0.646 |
LIG_FHA_1 | 662 | 668 | PF00498 | 0.507 |
LIG_FHA_1 | 712 | 718 | PF00498 | 0.421 |
LIG_FHA_1 | 803 | 809 | PF00498 | 0.365 |
LIG_FHA_2 | 137 | 143 | PF00498 | 0.661 |
LIG_FHA_2 | 181 | 187 | PF00498 | 0.686 |
LIG_FHA_2 | 229 | 235 | PF00498 | 0.639 |
LIG_FHA_2 | 552 | 558 | PF00498 | 0.514 |
LIG_FHA_2 | 559 | 565 | PF00498 | 0.485 |
LIG_FHA_2 | 617 | 623 | PF00498 | 0.583 |
LIG_FHA_2 | 734 | 740 | PF00498 | 0.327 |
LIG_LIR_Apic_2 | 220 | 226 | PF02991 | 0.675 |
LIG_LIR_Apic_2 | 430 | 435 | PF02991 | 0.564 |
LIG_LIR_Apic_2 | 730 | 735 | PF02991 | 0.328 |
LIG_LIR_Apic_2 | 739 | 744 | PF02991 | 0.329 |
LIG_LIR_Apic_2 | 758 | 763 | PF02991 | 0.327 |
LIG_LIR_Apic_2 | 770 | 776 | PF02991 | 0.402 |
LIG_LIR_Gen_1 | 14 | 24 | PF02991 | 0.662 |
LIG_LIR_Gen_1 | 158 | 167 | PF02991 | 0.413 |
LIG_LIR_Gen_1 | 275 | 283 | PF02991 | 0.462 |
LIG_LIR_Gen_1 | 384 | 392 | PF02991 | 0.527 |
LIG_LIR_Gen_1 | 484 | 493 | PF02991 | 0.609 |
LIG_LIR_Gen_1 | 564 | 570 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 14 | 20 | PF02991 | 0.618 |
LIG_LIR_Nem_3 | 158 | 163 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 275 | 279 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 384 | 389 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 484 | 489 | PF02991 | 0.600 |
LIG_LIR_Nem_3 | 564 | 569 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 706 | 710 | PF02991 | 0.374 |
LIG_LYPXL_yS_3 | 707 | 710 | PF13949 | 0.451 |
LIG_NRBOX | 19 | 25 | PF00104 | 0.573 |
LIG_PCNA_yPIPBox_3 | 371 | 383 | PF02747 | 0.586 |
LIG_Pex14_2 | 629 | 633 | PF04695 | 0.424 |
LIG_Pex14_2 | 688 | 692 | PF04695 | 0.549 |
LIG_PTAP_UEV_1 | 653 | 658 | PF05743 | 0.506 |
LIG_REV1ctd_RIR_1 | 495 | 505 | PF16727 | 0.598 |
LIG_SH2_CRK | 295 | 299 | PF00017 | 0.548 |
LIG_SH2_CRK | 386 | 390 | PF00017 | 0.566 |
LIG_SH2_CRK | 479 | 483 | PF00017 | 0.617 |
LIG_SH2_GRB2like | 726 | 729 | PF00017 | 0.471 |
LIG_SH2_NCK_1 | 174 | 178 | PF00017 | 0.694 |
LIG_SH2_NCK_1 | 267 | 271 | PF00017 | 0.557 |
LIG_SH2_NCK_1 | 295 | 299 | PF00017 | 0.548 |
LIG_SH2_NCK_1 | 386 | 390 | PF00017 | 0.503 |
LIG_SH2_NCK_1 | 592 | 596 | PF00017 | 0.573 |
LIG_SH2_NCK_1 | 726 | 730 | PF00017 | 0.471 |
LIG_SH2_PTP2 | 17 | 20 | PF00017 | 0.510 |
LIG_SH2_PTP2 | 446 | 449 | PF00017 | 0.497 |
LIG_SH2_SRC | 592 | 595 | PF00017 | 0.565 |
LIG_SH2_SRC | 726 | 729 | PF00017 | 0.471 |
LIG_SH2_SRC | 791 | 794 | PF00017 | 0.445 |
LIG_SH2_STAT3 | 597 | 600 | PF00017 | 0.593 |
LIG_SH2_STAT5 | 17 | 20 | PF00017 | 0.510 |
LIG_SH2_STAT5 | 174 | 177 | PF00017 | 0.677 |
LIG_SH2_STAT5 | 259 | 262 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 446 | 449 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 533 | 536 | PF00017 | 0.410 |
LIG_SH2_STAT5 | 627 | 630 | PF00017 | 0.496 |
LIG_SH2_STAT5 | 811 | 814 | PF00017 | 0.321 |
LIG_SH3_3 | 129 | 135 | PF00018 | 0.550 |
LIG_SH3_3 | 252 | 258 | PF00018 | 0.669 |
LIG_SH3_3 | 394 | 400 | PF00018 | 0.551 |
LIG_SH3_3 | 486 | 492 | PF00018 | 0.577 |
LIG_SH3_3 | 651 | 657 | PF00018 | 0.377 |
LIG_SH3_3 | 782 | 788 | PF00018 | 0.407 |
LIG_SH3_3 | 810 | 816 | PF00018 | 0.365 |
LIG_SUMO_SIM_anti_2 | 125 | 131 | PF11976 | 0.578 |
LIG_SUMO_SIM_anti_2 | 138 | 146 | PF11976 | 0.321 |
LIG_SUMO_SIM_par_1 | 664 | 670 | PF11976 | 0.521 |
LIG_SUMO_SIM_par_1 | 709 | 714 | PF11976 | 0.404 |
LIG_SUMO_SIM_par_1 | 753 | 759 | PF11976 | 0.372 |
LIG_TRAF2_1 | 275 | 278 | PF00917 | 0.554 |
LIG_TRAF2_1 | 619 | 622 | PF00917 | 0.528 |
LIG_TYR_ITIM | 477 | 482 | PF00017 | 0.586 |
LIG_TYR_ITSM | 382 | 389 | PF00017 | 0.452 |
LIG_WRC_WIRS_1 | 163 | 168 | PF05994 | 0.542 |
LIG_WRC_WIRS_1 | 630 | 635 | PF05994 | 0.449 |
LIG_WW_3 | 226 | 230 | PF00397 | 0.541 |
MOD_CDC14_SPxK_1 | 576 | 579 | PF00782 | 0.532 |
MOD_CDK_SPxK_1 | 573 | 579 | PF00069 | 0.517 |
MOD_CK1_1 | 11 | 17 | PF00069 | 0.603 |
MOD_CK1_1 | 265 | 271 | PF00069 | 0.569 |
MOD_CK1_1 | 387 | 393 | PF00069 | 0.584 |
MOD_CK1_1 | 408 | 414 | PF00069 | 0.628 |
MOD_CK1_1 | 487 | 493 | PF00069 | 0.597 |
MOD_CK1_1 | 539 | 545 | PF00069 | 0.392 |
MOD_CK1_1 | 608 | 614 | PF00069 | 0.451 |
MOD_CK1_1 | 655 | 661 | PF00069 | 0.370 |
MOD_CK1_1 | 681 | 687 | PF00069 | 0.493 |
MOD_CK1_1 | 784 | 790 | PF00069 | 0.419 |
MOD_CK2_1 | 136 | 142 | PF00069 | 0.619 |
MOD_CK2_1 | 180 | 186 | PF00069 | 0.771 |
MOD_CK2_1 | 228 | 234 | PF00069 | 0.653 |
MOD_CK2_1 | 272 | 278 | PF00069 | 0.526 |
MOD_CK2_1 | 534 | 540 | PF00069 | 0.407 |
MOD_CK2_1 | 614 | 620 | PF00069 | 0.522 |
MOD_CK2_1 | 715 | 721 | PF00069 | 0.478 |
MOD_CK2_1 | 733 | 739 | PF00069 | 0.192 |
MOD_CMANNOS | 343 | 346 | PF00535 | 0.434 |
MOD_CMANNOS | 98 | 101 | PF00535 | 0.461 |
MOD_Cter_Amidation | 822 | 825 | PF01082 | 0.326 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.624 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.638 |
MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.562 |
MOD_GlcNHglycan | 40 | 43 | PF01048 | 0.658 |
MOD_GlcNHglycan | 410 | 413 | PF01048 | 0.646 |
MOD_GlcNHglycan | 431 | 435 | PF01048 | 0.569 |
MOD_GlcNHglycan | 469 | 472 | PF01048 | 0.553 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.634 |
MOD_GlcNHglycan | 654 | 657 | PF01048 | 0.566 |
MOD_GlcNHglycan | 716 | 720 | PF01048 | 0.478 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.620 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.558 |
MOD_GSK3_1 | 408 | 415 | PF00069 | 0.697 |
MOD_GSK3_1 | 463 | 470 | PF00069 | 0.547 |
MOD_GSK3_1 | 484 | 491 | PF00069 | 0.613 |
MOD_GSK3_1 | 601 | 608 | PF00069 | 0.464 |
MOD_GSK3_1 | 674 | 681 | PF00069 | 0.496 |
MOD_GSK3_1 | 711 | 718 | PF00069 | 0.428 |
MOD_GSK3_1 | 798 | 805 | PF00069 | 0.361 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.661 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.620 |
MOD_N-GLC_1 | 12 | 17 | PF02516 | 0.569 |
MOD_NEK2_1 | 167 | 172 | PF00069 | 0.577 |
MOD_NEK2_1 | 194 | 199 | PF00069 | 0.549 |
MOD_NEK2_1 | 485 | 490 | PF00069 | 0.595 |
MOD_NEK2_1 | 565 | 570 | PF00069 | 0.412 |
MOD_NEK2_1 | 629 | 634 | PF00069 | 0.448 |
MOD_NEK2_1 | 688 | 693 | PF00069 | 0.516 |
MOD_NEK2_1 | 847 | 852 | PF00069 | 0.553 |
MOD_NEK2_2 | 330 | 335 | PF00069 | 0.394 |
MOD_NEK2_2 | 493 | 498 | PF00069 | 0.563 |
MOD_OFUCOSY | 606 | 612 | PF10250 | 0.472 |
MOD_PIKK_1 | 196 | 202 | PF00454 | 0.575 |
MOD_PIKK_1 | 655 | 661 | PF00454 | 0.387 |
MOD_PK_1 | 605 | 611 | PF00069 | 0.437 |
MOD_PKA_1 | 262 | 268 | PF00069 | 0.552 |
MOD_PKA_2 | 125 | 131 | PF00069 | 0.580 |
MOD_PKA_2 | 228 | 234 | PF00069 | 0.651 |
MOD_PKA_2 | 262 | 268 | PF00069 | 0.537 |
MOD_PKA_2 | 272 | 278 | PF00069 | 0.436 |
MOD_PKA_2 | 463 | 469 | PF00069 | 0.575 |
MOD_PKA_2 | 614 | 620 | PF00069 | 0.590 |
MOD_PKA_2 | 662 | 668 | PF00069 | 0.541 |
MOD_PKA_2 | 681 | 687 | PF00069 | 0.266 |
MOD_PKA_2 | 768 | 774 | PF00069 | 0.474 |
MOD_Plk_1 | 137 | 143 | PF00069 | 0.604 |
MOD_Plk_1 | 412 | 418 | PF00069 | 0.588 |
MOD_Plk_1 | 661 | 667 | PF00069 | 0.490 |
MOD_Plk_2-3 | 312 | 318 | PF00069 | 0.711 |
MOD_Plk_4 | 125 | 131 | PF00069 | 0.617 |
MOD_Plk_4 | 162 | 168 | PF00069 | 0.537 |
MOD_Plk_4 | 209 | 215 | PF00069 | 0.417 |
MOD_Plk_4 | 384 | 390 | PF00069 | 0.556 |
MOD_Plk_4 | 493 | 499 | PF00069 | 0.564 |
MOD_Plk_4 | 565 | 571 | PF00069 | 0.473 |
MOD_Plk_4 | 59 | 65 | PF00069 | 0.644 |
MOD_Plk_4 | 662 | 668 | PF00069 | 0.423 |
MOD_Plk_4 | 681 | 687 | PF00069 | 0.300 |
MOD_Plk_4 | 847 | 853 | PF00069 | 0.495 |
MOD_ProDKin_1 | 488 | 494 | PF00069 | 0.637 |
MOD_ProDKin_1 | 573 | 579 | PF00069 | 0.517 |
MOD_ProDKin_1 | 674 | 680 | PF00069 | 0.556 |
MOD_ProDKin_1 | 781 | 787 | PF00069 | 0.442 |
MOD_ProDKin_1 | 90 | 96 | PF00069 | 0.725 |
MOD_SUMO_for_1 | 633 | 636 | PF00179 | 0.364 |
TRG_DiLeu_BaEn_1 | 186 | 191 | PF01217 | 0.611 |
TRG_DiLeu_BaEn_1 | 662 | 667 | PF01217 | 0.546 |
TRG_ENDOCYTIC_2 | 17 | 20 | PF00928 | 0.610 |
TRG_ENDOCYTIC_2 | 295 | 298 | PF00928 | 0.539 |
TRG_ENDOCYTIC_2 | 386 | 389 | PF00928 | 0.569 |
TRG_ENDOCYTIC_2 | 479 | 482 | PF00928 | 0.596 |
TRG_ENDOCYTIC_2 | 627 | 630 | PF00928 | 0.496 |
TRG_ENDOCYTIC_2 | 707 | 710 | PF00928 | 0.459 |
TRG_ER_diArg_1 | 149 | 152 | PF00400 | 0.584 |
TRG_ER_diArg_1 | 262 | 264 | PF00400 | 0.421 |
TRG_ER_diArg_1 | 292 | 294 | PF00400 | 0.532 |
TRG_ER_diArg_1 | 394 | 396 | PF00400 | 0.448 |
TRG_ER_diArg_1 | 401 | 404 | PF00400 | 0.493 |
TRG_ER_diArg_1 | 502 | 505 | PF00400 | 0.507 |
TRG_ER_diArg_1 | 524 | 526 | PF00400 | 0.608 |
TRG_ER_diArg_1 | 552 | 555 | PF00400 | 0.525 |
TRG_ER_diArg_1 | 570 | 572 | PF00400 | 0.401 |
TRG_ER_diArg_1 | 674 | 676 | PF00400 | 0.414 |
TRG_ER_diArg_1 | 820 | 822 | PF00400 | 0.339 |
TRG_ER_diArg_1 | 824 | 827 | PF00400 | 0.312 |
TRG_NLS_MonoExtC_3 | 522 | 528 | PF00514 | 0.487 |
TRG_NLS_MonoExtN_4 | 520 | 527 | PF00514 | 0.472 |
TRG_Pf-PMV_PEXEL_1 | 121 | 125 | PF00026 | 0.661 |
TRG_Pf-PMV_PEXEL_1 | 448 | 452 | PF00026 | 0.426 |
TRG_Pf-PMV_PEXEL_1 | 832 | 836 | PF00026 | 0.494 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A1X0NJI2 | Trypanosomatidae | 36% | 96% |
A0A1X0NR25 | Trypanosomatidae | 31% | 83% |
A0A3R7NS98 | Trypanosoma rangeli | 31% | 85% |
A0A3R7RH60 | Trypanosoma rangeli | 40% | 100% |
A0A3S7X4M2 | Leishmania donovani | 100% | 89% |
A0A3S7X4P3 | Leishmania donovani | 100% | 89% |
A4HJG8 | Leishmania braziliensis | 77% | 100% |
E9B1Y5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
E9B1Y6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
E9B1Y7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
Q4Q674 | Leishmania major | 94% | 100% |
Q4Q675 | Leishmania major | 94% | 100% |
V5BEQ4 | Trypanosoma cruzi | 38% | 100% |