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: 0, no: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000159 | protein phosphatase type 2A complex | 5 | 2 |
GO:0005737 | cytoplasm | 2 | 2 |
GO:0008287 | protein serine/threonine phosphatase complex | 4 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:1902494 | catalytic complex | 2 | 2 |
GO:1903293 | phosphatase complex | 3 | 2 |
Related structures:
AlphaFold database: Q4QF92
Term | Name | Level | Count |
---|---|---|---|
GO:0006470 | protein dephosphorylation | 5 | 2 |
GO:0006793 | phosphorus metabolic process | 3 | 2 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016311 | dephosphorylation | 5 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0036211 | protein modification process | 4 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043412 | macromolecule modification | 4 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0019208 | phosphatase regulator activity | 3 | 2 |
GO:0019888 | protein phosphatase regulator activity | 4 | 2 |
GO:0030234 | enzyme regulator activity | 2 | 2 |
GO:0098772 | molecular function regulator activity | 1 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 270 | 276 | PF00089 | 0.444 |
CLV_NRD_NRD_1 | 103 | 105 | PF00675 | 0.639 |
CLV_NRD_NRD_1 | 156 | 158 | PF00675 | 0.442 |
CLV_NRD_NRD_1 | 480 | 482 | PF00675 | 0.477 |
CLV_NRD_NRD_1 | 567 | 569 | PF00675 | 0.701 |
CLV_NRD_NRD_1 | 614 | 616 | PF00675 | 0.555 |
CLV_NRD_NRD_1 | 745 | 747 | PF00675 | 0.473 |
CLV_PCSK_KEX2_1 | 103 | 105 | PF00082 | 0.639 |
CLV_PCSK_KEX2_1 | 156 | 158 | PF00082 | 0.419 |
CLV_PCSK_KEX2_1 | 480 | 482 | PF00082 | 0.477 |
CLV_PCSK_KEX2_1 | 567 | 569 | PF00082 | 0.701 |
CLV_PCSK_KEX2_1 | 616 | 618 | PF00082 | 0.481 |
CLV_PCSK_KEX2_1 | 745 | 747 | PF00082 | 0.474 |
CLV_PCSK_PC1ET2_1 | 616 | 618 | PF00082 | 0.522 |
CLV_PCSK_SKI1_1 | 243 | 247 | PF00082 | 0.481 |
CLV_PCSK_SKI1_1 | 366 | 370 | PF00082 | 0.395 |
CLV_PCSK_SKI1_1 | 387 | 391 | PF00082 | 0.345 |
CLV_PCSK_SKI1_1 | 661 | 665 | PF00082 | 0.471 |
CLV_PCSK_SKI1_1 | 684 | 688 | PF00082 | 0.505 |
CLV_Separin_Metazoa | 496 | 500 | PF03568 | 0.486 |
DEG_APCC_DBOX_1 | 341 | 349 | PF00400 | 0.453 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.774 |
DEG_SPOP_SBC_1 | 244 | 248 | PF00917 | 0.491 |
DEG_SPOP_SBC_1 | 382 | 386 | PF00917 | 0.522 |
DOC_CYCLIN_RxL_1 | 363 | 372 | PF00134 | 0.413 |
DOC_CYCLIN_RxL_1 | 383 | 392 | PF00134 | 0.191 |
DOC_CYCLIN_yCln2_LP_2 | 264 | 270 | PF00134 | 0.404 |
DOC_MAPK_gen_1 | 639 | 647 | PF00069 | 0.404 |
DOC_MAPK_MEF2A_6 | 115 | 124 | PF00069 | 0.748 |
DOC_MAPK_MEF2A_6 | 764 | 772 | PF00069 | 0.529 |
DOC_PP1_RVXF_1 | 271 | 277 | PF00149 | 0.488 |
DOC_PP2B_LxvP_1 | 264 | 267 | PF13499 | 0.375 |
DOC_USP7_MATH_1 | 102 | 106 | PF00917 | 0.616 |
DOC_USP7_MATH_1 | 313 | 317 | PF00917 | 0.462 |
DOC_USP7_MATH_1 | 520 | 524 | PF00917 | 0.466 |
DOC_USP7_MATH_1 | 543 | 547 | PF00917 | 0.656 |
DOC_USP7_MATH_1 | 571 | 575 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 598 | 602 | PF00917 | 0.653 |
DOC_USP7_MATH_1 | 734 | 738 | PF00917 | 0.434 |
DOC_USP7_MATH_1 | 816 | 820 | PF00917 | 0.397 |
DOC_USP7_MATH_1 | 96 | 100 | PF00917 | 0.750 |
DOC_USP7_UBL2_3 | 383 | 387 | PF12436 | 0.486 |
DOC_WW_Pin1_4 | 110 | 115 | PF00397 | 0.620 |
DOC_WW_Pin1_4 | 33 | 38 | PF00397 | 0.721 |
DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.742 |
DOC_WW_Pin1_4 | 583 | 588 | PF00397 | 0.692 |
DOC_WW_Pin1_4 | 653 | 658 | PF00397 | 0.481 |
DOC_WW_Pin1_4 | 737 | 742 | PF00397 | 0.466 |
DOC_WW_Pin1_4 | 85 | 90 | PF00397 | 0.718 |
LIG_14-3-3_CanoR_1 | 103 | 107 | PF00244 | 0.596 |
LIG_14-3-3_CanoR_1 | 156 | 160 | PF00244 | 0.447 |
LIG_14-3-3_CanoR_1 | 218 | 226 | PF00244 | 0.515 |
LIG_14-3-3_CanoR_1 | 273 | 277 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 342 | 346 | PF00244 | 0.502 |
LIG_14-3-3_CanoR_1 | 403 | 412 | PF00244 | 0.398 |
LIG_14-3-3_CanoR_1 | 480 | 487 | PF00244 | 0.476 |
LIG_14-3-3_CanoR_1 | 59 | 64 | PF00244 | 0.691 |
LIG_14-3-3_CanoR_1 | 623 | 632 | PF00244 | 0.487 |
LIG_14-3-3_CanoR_1 | 715 | 720 | PF00244 | 0.512 |
LIG_Actin_WH2_2 | 671 | 689 | PF00022 | 0.466 |
LIG_BIR_III_2 | 474 | 478 | PF00653 | 0.549 |
LIG_BRCT_BRCA1_1 | 131 | 135 | PF00533 | 0.585 |
LIG_EH1_1 | 224 | 232 | PF00400 | 0.427 |
LIG_FHA_1 | 171 | 177 | PF00498 | 0.420 |
LIG_FHA_1 | 218 | 224 | PF00498 | 0.466 |
LIG_FHA_1 | 244 | 250 | PF00498 | 0.489 |
LIG_FHA_1 | 269 | 275 | PF00498 | 0.466 |
LIG_FHA_1 | 356 | 362 | PF00498 | 0.482 |
LIG_FHA_1 | 625 | 631 | PF00498 | 0.513 |
LIG_FHA_1 | 662 | 668 | PF00498 | 0.434 |
LIG_FHA_1 | 701 | 707 | PF00498 | 0.417 |
LIG_FHA_1 | 712 | 718 | PF00498 | 0.397 |
LIG_FHA_1 | 751 | 757 | PF00498 | 0.459 |
LIG_FHA_1 | 760 | 766 | PF00498 | 0.434 |
LIG_FHA_2 | 114 | 120 | PF00498 | 0.703 |
LIG_FHA_2 | 184 | 190 | PF00498 | 0.466 |
LIG_FHA_2 | 342 | 348 | PF00498 | 0.537 |
LIG_FHA_2 | 5 | 11 | PF00498 | 0.707 |
LIG_FHA_2 | 683 | 689 | PF00498 | 0.531 |
LIG_FHA_2 | 699 | 705 | PF00498 | 0.363 |
LIG_FHA_2 | 784 | 790 | PF00498 | 0.531 |
LIG_GBD_Chelix_1 | 241 | 249 | PF00786 | 0.453 |
LIG_GBD_Chelix_1 | 283 | 291 | PF00786 | 0.430 |
LIG_LIR_Apic_2 | 275 | 280 | PF02991 | 0.376 |
LIG_LIR_Apic_2 | 46 | 51 | PF02991 | 0.697 |
LIG_LIR_Apic_2 | 582 | 587 | PF02991 | 0.515 |
LIG_LIR_Gen_1 | 333 | 340 | PF02991 | 0.458 |
LIG_LIR_Gen_1 | 364 | 374 | PF02991 | 0.448 |
LIG_LIR_Gen_1 | 42 | 51 | PF02991 | 0.540 |
LIG_LIR_Nem_3 | 224 | 229 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 263 | 268 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 275 | 279 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 28 | 33 | PF02991 | 0.559 |
LIG_LIR_Nem_3 | 306 | 312 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 333 | 337 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 364 | 370 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 42 | 47 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 658 | 663 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 718 | 724 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 781 | 785 | PF02991 | 0.411 |
LIG_LYPXL_SIV_4 | 792 | 800 | PF13949 | 0.495 |
LIG_MYND_3 | 528 | 532 | PF01753 | 0.437 |
LIG_Pex14_1 | 402 | 406 | PF04695 | 0.322 |
LIG_Pex14_1 | 779 | 783 | PF04695 | 0.466 |
LIG_Pex3_1 | 177 | 188 | PF04882 | 0.525 |
LIG_SH2_CRK | 584 | 588 | PF00017 | 0.514 |
LIG_SH2_NCK_1 | 406 | 410 | PF00017 | 0.421 |
LIG_SH2_STAP1 | 126 | 130 | PF00017 | 0.471 |
LIG_SH2_STAT5 | 225 | 228 | PF00017 | 0.398 |
LIG_SH2_STAT5 | 290 | 293 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 367 | 370 | PF00017 | 0.373 |
LIG_SH2_STAT5 | 388 | 391 | PF00017 | 0.373 |
LIG_SH2_STAT5 | 406 | 409 | PF00017 | 0.212 |
LIG_SH2_STAT5 | 760 | 763 | PF00017 | 0.469 |
LIG_SH3_3 | 651 | 657 | PF00018 | 0.486 |
LIG_SH3_3 | 728 | 734 | PF00018 | 0.449 |
LIG_SUMO_SIM_anti_2 | 423 | 431 | PF11976 | 0.481 |
LIG_SUMO_SIM_anti_2 | 805 | 810 | PF11976 | 0.467 |
LIG_SUMO_SIM_par_1 | 31 | 36 | PF11976 | 0.707 |
LIG_TRAF2_1 | 152 | 155 | PF00917 | 0.535 |
LIG_TRAF2_1 | 515 | 518 | PF00917 | 0.482 |
LIG_TRFH_1 | 110 | 114 | PF08558 | 0.641 |
LIG_TYR_ITIM | 288 | 293 | PF00017 | 0.284 |
LIG_TYR_ITIM | 365 | 370 | PF00017 | 0.369 |
LIG_WRC_WIRS_1 | 390 | 395 | PF05994 | 0.463 |
LIG_WRC_WIRS_1 | 622 | 627 | PF05994 | 0.545 |
MOD_CDK_SPK_2 | 110 | 115 | PF00069 | 0.613 |
MOD_CDK_SPK_2 | 737 | 742 | PF00069 | 0.493 |
MOD_CK1_1 | 113 | 119 | PF00069 | 0.699 |
MOD_CK1_1 | 16 | 22 | PF00069 | 0.580 |
MOD_CK1_1 | 275 | 281 | PF00069 | 0.372 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.727 |
MOD_CK1_1 | 301 | 307 | PF00069 | 0.415 |
MOD_CK1_1 | 317 | 323 | PF00069 | 0.410 |
MOD_CK1_1 | 355 | 361 | PF00069 | 0.512 |
MOD_CK1_1 | 36 | 42 | PF00069 | 0.654 |
MOD_CK1_1 | 557 | 563 | PF00069 | 0.781 |
MOD_CK1_1 | 576 | 582 | PF00069 | 0.655 |
MOD_CK1_1 | 624 | 630 | PF00069 | 0.515 |
MOD_CK1_1 | 737 | 743 | PF00069 | 0.432 |
MOD_CK1_1 | 819 | 825 | PF00069 | 0.689 |
MOD_CK1_1 | 83 | 89 | PF00069 | 0.723 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.678 |
MOD_CK2_1 | 115 | 121 | PF00069 | 0.712 |
MOD_CK2_1 | 149 | 155 | PF00069 | 0.539 |
MOD_CK2_1 | 183 | 189 | PF00069 | 0.453 |
MOD_CK2_1 | 20 | 26 | PF00069 | 0.735 |
MOD_CK2_1 | 341 | 347 | PF00069 | 0.446 |
MOD_CK2_1 | 4 | 10 | PF00069 | 0.699 |
MOD_CK2_1 | 512 | 518 | PF00069 | 0.415 |
MOD_CK2_1 | 682 | 688 | PF00069 | 0.486 |
MOD_CK2_1 | 698 | 704 | PF00069 | 0.359 |
MOD_CK2_1 | 737 | 743 | PF00069 | 0.522 |
MOD_CK2_1 | 783 | 789 | PF00069 | 0.441 |
MOD_CMANNOS | 779 | 782 | PF00535 | 0.427 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.695 |
MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.464 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.414 |
MOD_GlcNHglycan | 318 | 322 | PF01048 | 0.427 |
MOD_GlcNHglycan | 481 | 484 | PF01048 | 0.468 |
MOD_GlcNHglycan | 52 | 56 | PF01048 | 0.789 |
MOD_GlcNHglycan | 545 | 548 | PF01048 | 0.608 |
MOD_GlcNHglycan | 550 | 553 | PF01048 | 0.627 |
MOD_GlcNHglycan | 563 | 566 | PF01048 | 0.664 |
MOD_GlcNHglycan | 573 | 576 | PF01048 | 0.590 |
MOD_GlcNHglycan | 594 | 597 | PF01048 | 0.736 |
MOD_GlcNHglycan | 600 | 603 | PF01048 | 0.621 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.700 |
MOD_GlcNHglycan | 818 | 821 | PF01048 | 0.583 |
MOD_GlcNHglycan | 82 | 85 | PF01048 | 0.742 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.635 |
MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.625 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.791 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.637 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.461 |
MOD_GSK3_1 | 268 | 275 | PF00069 | 0.364 |
MOD_GSK3_1 | 313 | 320 | PF00069 | 0.479 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.679 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.408 |
MOD_GSK3_1 | 554 | 561 | PF00069 | 0.696 |
MOD_GSK3_1 | 569 | 576 | PF00069 | 0.610 |
MOD_GSK3_1 | 579 | 586 | PF00069 | 0.660 |
MOD_GSK3_1 | 588 | 595 | PF00069 | 0.493 |
MOD_GSK3_1 | 673 | 680 | PF00069 | 0.456 |
MOD_GSK3_1 | 707 | 714 | PF00069 | 0.545 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.688 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.682 |
MOD_N-GLC_1 | 221 | 226 | PF02516 | 0.470 |
MOD_N-GLC_1 | 558 | 563 | PF02516 | 0.700 |
MOD_N-GLC_1 | 71 | 76 | PF02516 | 0.769 |
MOD_N-GLC_1 | 809 | 814 | PF02516 | 0.535 |
MOD_NEK2_1 | 20 | 25 | PF00069 | 0.719 |
MOD_NEK2_1 | 268 | 273 | PF00069 | 0.356 |
MOD_NEK2_1 | 298 | 303 | PF00069 | 0.486 |
MOD_NEK2_1 | 352 | 357 | PF00069 | 0.492 |
MOD_NEK2_1 | 361 | 366 | PF00069 | 0.437 |
MOD_NEK2_1 | 389 | 394 | PF00069 | 0.351 |
MOD_NEK2_1 | 531 | 536 | PF00069 | 0.503 |
MOD_NEK2_1 | 58 | 63 | PF00069 | 0.705 |
MOD_NEK2_1 | 632 | 637 | PF00069 | 0.470 |
MOD_NEK2_1 | 749 | 754 | PF00069 | 0.483 |
MOD_NEK2_1 | 809 | 814 | PF00069 | 0.493 |
MOD_NEK2_2 | 674 | 679 | PF00069 | 0.516 |
MOD_NEK2_2 | 682 | 687 | PF00069 | 0.452 |
MOD_PIKK_1 | 170 | 176 | PF00454 | 0.442 |
MOD_PIKK_1 | 469 | 475 | PF00454 | 0.548 |
MOD_PIKK_1 | 677 | 683 | PF00454 | 0.476 |
MOD_PKA_2 | 102 | 108 | PF00069 | 0.627 |
MOD_PKA_2 | 155 | 161 | PF00069 | 0.489 |
MOD_PKA_2 | 217 | 223 | PF00069 | 0.520 |
MOD_PKA_2 | 272 | 278 | PF00069 | 0.482 |
MOD_PKA_2 | 341 | 347 | PF00069 | 0.485 |
MOD_PKA_2 | 404 | 410 | PF00069 | 0.373 |
MOD_PKA_2 | 479 | 485 | PF00069 | 0.433 |
MOD_PKA_2 | 561 | 567 | PF00069 | 0.644 |
MOD_PKA_2 | 579 | 585 | PF00069 | 0.644 |
MOD_PKA_2 | 58 | 64 | PF00069 | 0.657 |
MOD_Plk_1 | 128 | 134 | PF00069 | 0.636 |
MOD_Plk_1 | 16 | 22 | PF00069 | 0.780 |
MOD_Plk_1 | 221 | 227 | PF00069 | 0.398 |
MOD_Plk_1 | 317 | 323 | PF00069 | 0.475 |
MOD_Plk_1 | 71 | 77 | PF00069 | 0.769 |
MOD_Plk_4 | 221 | 227 | PF00069 | 0.424 |
MOD_Plk_4 | 272 | 278 | PF00069 | 0.400 |
MOD_Plk_4 | 389 | 395 | PF00069 | 0.349 |
MOD_Plk_4 | 43 | 49 | PF00069 | 0.560 |
MOD_Plk_4 | 715 | 721 | PF00069 | 0.505 |
MOD_Plk_4 | 778 | 784 | PF00069 | 0.453 |
MOD_ProDKin_1 | 110 | 116 | PF00069 | 0.621 |
MOD_ProDKin_1 | 33 | 39 | PF00069 | 0.718 |
MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.743 |
MOD_ProDKin_1 | 583 | 589 | PF00069 | 0.689 |
MOD_ProDKin_1 | 653 | 659 | PF00069 | 0.481 |
MOD_ProDKin_1 | 737 | 743 | PF00069 | 0.464 |
MOD_ProDKin_1 | 85 | 91 | PF00069 | 0.719 |
TRG_DiLeu_BaEn_1 | 257 | 262 | PF01217 | 0.430 |
TRG_DiLeu_BaEn_3 | 154 | 160 | PF01217 | 0.517 |
TRG_DiLeu_BaEn_4 | 371 | 377 | PF01217 | 0.451 |
TRG_DiLeu_BaLyEn_6 | 29 | 34 | PF01217 | 0.692 |
TRG_DiLeu_BaLyEn_6 | 348 | 353 | PF01217 | 0.471 |
TRG_DiLeu_BaLyEn_6 | 752 | 757 | PF01217 | 0.487 |
TRG_ENDOCYTIC_2 | 290 | 293 | PF00928 | 0.482 |
TRG_ENDOCYTIC_2 | 367 | 370 | PF00928 | 0.390 |
TRG_ENDOCYTIC_2 | 487 | 490 | PF00928 | 0.435 |
TRG_ENDOCYTIC_2 | 780 | 783 | PF00928 | 0.513 |
TRG_ER_diArg_1 | 102 | 104 | PF00400 | 0.654 |
TRG_ER_diArg_1 | 402 | 405 | PF00400 | 0.315 |
TRG_ER_diArg_1 | 479 | 481 | PF00400 | 0.473 |
TRG_ER_diArg_1 | 638 | 641 | PF00400 | 0.386 |
TRG_ER_diArg_1 | 744 | 746 | PF00400 | 0.473 |
TRG_NES_CRM1_1 | 250 | 263 | PF08389 | 0.442 |
TRG_NES_CRM1_1 | 359 | 372 | PF08389 | 0.472 |
TRG_Pf-PMV_PEXEL_1 | 206 | 210 | PF00026 | 0.443 |
TRG_Pf-PMV_PEXEL_1 | 366 | 371 | PF00026 | 0.485 |
TRG_Pf-PMV_PEXEL_1 | 684 | 688 | PF00026 | 0.516 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PA72 | Leptomonas seymouri | 66% | 84% |
A0A3Q8IDF8 | Leishmania donovani | 96% | 100% |
A0A3R7N5C8 | Trypanosoma rangeli | 37% | 100% |
A4H865 | Leishmania braziliensis | 84% | 94% |
A4HWJ0 | Leishmania infantum | 96% | 100% |
C9ZXV3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
E9AQ91 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 88% |
Q9UT08 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 22% | 100% |
V5DL61 | Trypanosoma cruzi | 38% | 100% |