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: 15 |
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: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 13 |
GO:0110165 | cellular anatomical entity | 1 | 13 |
GO:0005634 | nucleus | 5 | 1 |
GO:0005657 | replication fork | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: A0A3Q8IBY0
Term | Name | Level | Count |
---|---|---|---|
GO:0000723 | telomere maintenance | 5 | 13 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 13 |
GO:0006259 | DNA metabolic process | 4 | 13 |
GO:0006281 | DNA repair | 5 | 13 |
GO:0006310 | DNA recombination | 5 | 13 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 13 |
GO:0006807 | nitrogen compound metabolic process | 2 | 13 |
GO:0006950 | response to stress | 2 | 13 |
GO:0006974 | DNA damage response | 4 | 13 |
GO:0006996 | organelle organization | 4 | 13 |
GO:0008152 | metabolic process | 1 | 13 |
GO:0009987 | cellular process | 1 | 13 |
GO:0016043 | cellular component organization | 3 | 13 |
GO:0032200 | telomere organization | 6 | 13 |
GO:0033554 | cellular response to stress | 3 | 13 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 13 |
GO:0043170 | macromolecule metabolic process | 3 | 13 |
GO:0044237 | cellular metabolic process | 2 | 13 |
GO:0044238 | primary metabolic process | 2 | 13 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 13 |
GO:0046483 | heterocycle metabolic process | 3 | 13 |
GO:0050896 | response to stimulus | 1 | 13 |
GO:0051276 | chromosome organization | 5 | 13 |
GO:0051716 | cellular response to stimulus | 2 | 13 |
GO:0071704 | organic substance metabolic process | 2 | 13 |
GO:0071840 | cellular component organization or biogenesis | 2 | 13 |
GO:0090304 | nucleic acid metabolic process | 4 | 13 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 13 |
GO:0006260 | DNA replication | 5 | 1 |
GO:0032392 | DNA geometric change | 7 | 1 |
GO:0032508 | DNA duplex unwinding | 8 | 1 |
GO:0071103 | DNA conformation change | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 13 |
GO:0003678 | DNA helicase activity | 3 | 13 |
GO:0003824 | catalytic activity | 1 | 13 |
GO:0004386 | helicase activity | 2 | 13 |
GO:0005488 | binding | 1 | 13 |
GO:0005524 | ATP binding | 5 | 13 |
GO:0008094 | ATP-dependent activity, acting on DNA | 2 | 13 |
GO:0016462 | pyrophosphatase activity | 5 | 13 |
GO:0016787 | hydrolase activity | 2 | 13 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 13 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 13 |
GO:0016887 | ATP hydrolysis activity | 7 | 13 |
GO:0017076 | purine nucleotide binding | 4 | 13 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 13 |
GO:0030554 | adenyl nucleotide binding | 5 | 13 |
GO:0032553 | ribonucleotide binding | 3 | 13 |
GO:0032555 | purine ribonucleotide binding | 4 | 13 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 13 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 13 |
GO:0036094 | small molecule binding | 2 | 13 |
GO:0043167 | ion binding | 2 | 13 |
GO:0043168 | anion binding | 3 | 13 |
GO:0097159 | organic cyclic compound binding | 2 | 13 |
GO:0097367 | carbohydrate derivative binding | 2 | 13 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 13 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 13 |
GO:0140657 | ATP-dependent activity | 1 | 13 |
GO:1901265 | nucleoside phosphate binding | 3 | 13 |
GO:1901363 | heterocyclic compound binding | 2 | 13 |
GO:0000287 | magnesium ion binding | 5 | 1 |
GO:0043169 | cation binding | 3 | 1 |
GO:0046872 | metal ion binding | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 164 | 168 | PF00656 | 0.631 |
CLV_C14_Caspase3-7 | 553 | 557 | PF00656 | 0.397 |
CLV_MEL_PAP_1 | 505 | 511 | PF00089 | 0.485 |
CLV_NRD_NRD_1 | 133 | 135 | PF00675 | 0.523 |
CLV_NRD_NRD_1 | 410 | 412 | PF00675 | 0.357 |
CLV_NRD_NRD_1 | 485 | 487 | PF00675 | 0.422 |
CLV_NRD_NRD_1 | 502 | 504 | PF00675 | 0.315 |
CLV_NRD_NRD_1 | 519 | 521 | PF00675 | 0.391 |
CLV_NRD_NRD_1 | 636 | 638 | PF00675 | 0.329 |
CLV_NRD_NRD_1 | 681 | 683 | PF00675 | 0.385 |
CLV_NRD_NRD_1 | 777 | 779 | PF00675 | 0.536 |
CLV_PCSK_KEX2_1 | 410 | 412 | PF00082 | 0.390 |
CLV_PCSK_KEX2_1 | 485 | 487 | PF00082 | 0.386 |
CLV_PCSK_KEX2_1 | 519 | 521 | PF00082 | 0.412 |
CLV_PCSK_KEX2_1 | 636 | 638 | PF00082 | 0.329 |
CLV_PCSK_KEX2_1 | 779 | 781 | PF00082 | 0.547 |
CLV_PCSK_KEX2_1 | 93 | 95 | PF00082 | 0.507 |
CLV_PCSK_PC1ET2_1 | 779 | 781 | PF00082 | 0.547 |
CLV_PCSK_PC1ET2_1 | 93 | 95 | PF00082 | 0.548 |
CLV_PCSK_SKI1_1 | 296 | 300 | PF00082 | 0.723 |
CLV_PCSK_SKI1_1 | 494 | 498 | PF00082 | 0.433 |
CLV_PCSK_SKI1_1 | 661 | 665 | PF00082 | 0.348 |
CLV_PCSK_SKI1_1 | 666 | 670 | PF00082 | 0.355 |
CLV_PCSK_SKI1_1 | 779 | 783 | PF00082 | 0.754 |
DEG_SCF_FBW7_1 | 208 | 213 | PF00400 | 0.517 |
DEG_SPOP_SBC_1 | 210 | 214 | PF00917 | 0.530 |
DEG_SPOP_SBC_1 | 404 | 408 | PF00917 | 0.228 |
DOC_CYCLIN_yCln2_LP_2 | 397 | 403 | PF00134 | 0.228 |
DOC_MAPK_gen_1 | 485 | 493 | PF00069 | 0.429 |
DOC_MAPK_gen_1 | 636 | 643 | PF00069 | 0.311 |
DOC_MAPK_gen_1 | 680 | 689 | PF00069 | 0.341 |
DOC_MAPK_gen_1 | 93 | 100 | PF00069 | 0.472 |
DOC_MAPK_MEF2A_6 | 636 | 643 | PF00069 | 0.277 |
DOC_MAPK_MEF2A_6 | 651 | 659 | PF00069 | 0.299 |
DOC_PP1_RVXF_1 | 245 | 251 | PF00149 | 0.485 |
DOC_PP2B_LxvP_1 | 397 | 400 | PF13499 | 0.228 |
DOC_PP2B_LxvP_1 | 401 | 404 | PF13499 | 0.205 |
DOC_PP2B_LxvP_1 | 433 | 436 | PF13499 | 0.229 |
DOC_SPAK_OSR1_1 | 508 | 512 | PF12202 | 0.478 |
DOC_USP7_MATH_1 | 130 | 134 | PF00917 | 0.690 |
DOC_USP7_MATH_1 | 189 | 193 | PF00917 | 0.632 |
DOC_USP7_MATH_1 | 200 | 204 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 210 | 214 | PF00917 | 0.661 |
DOC_USP7_MATH_1 | 219 | 223 | PF00917 | 0.567 |
DOC_USP7_MATH_1 | 226 | 230 | PF00917 | 0.508 |
DOC_USP7_MATH_1 | 236 | 240 | PF00917 | 0.697 |
DOC_USP7_MATH_1 | 404 | 408 | PF00917 | 0.262 |
DOC_USP7_MATH_1 | 557 | 561 | PF00917 | 0.440 |
DOC_USP7_MATH_1 | 699 | 703 | PF00917 | 0.362 |
DOC_USP7_MATH_1 | 732 | 736 | PF00917 | 0.662 |
DOC_USP7_MATH_1 | 746 | 750 | PF00917 | 0.695 |
DOC_USP7_UBL2_3 | 119 | 123 | PF12436 | 0.497 |
DOC_WW_Pin1_4 | 204 | 209 | PF00397 | 0.634 |
DOC_WW_Pin1_4 | 727 | 732 | PF00397 | 0.707 |
LIG_14-3-3_CanoR_1 | 21 | 25 | PF00244 | 0.481 |
LIG_14-3-3_CanoR_1 | 221 | 225 | PF00244 | 0.777 |
LIG_14-3-3_CanoR_1 | 319 | 328 | PF00244 | 0.375 |
LIG_14-3-3_CanoR_1 | 410 | 420 | PF00244 | 0.242 |
LIG_14-3-3_CanoR_1 | 541 | 550 | PF00244 | 0.433 |
LIG_14-3-3_CanoR_1 | 609 | 617 | PF00244 | 0.432 |
LIG_14-3-3_CanoR_1 | 631 | 635 | PF00244 | 0.499 |
LIG_14-3-3_CanoR_1 | 84 | 88 | PF00244 | 0.464 |
LIG_14-3-3_CanoR_1 | 94 | 99 | PF00244 | 0.374 |
LIG_Actin_WH2_2 | 552 | 570 | PF00022 | 0.383 |
LIG_AP2alpha_2 | 197 | 199 | PF02296 | 0.479 |
LIG_APCC_ABBA_1 | 22 | 27 | PF00400 | 0.386 |
LIG_APCC_ABBAyCdc20_2 | 21 | 27 | PF00400 | 0.393 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.584 |
LIG_BRCT_BRCA1_1 | 383 | 387 | PF00533 | 0.264 |
LIG_BRCT_BRCA1_1 | 535 | 539 | PF00533 | 0.389 |
LIG_CaM_IQ_9 | 113 | 129 | PF13499 | 0.540 |
LIG_FHA_1 | 101 | 107 | PF00498 | 0.344 |
LIG_FHA_1 | 186 | 192 | PF00498 | 0.679 |
LIG_FHA_1 | 235 | 241 | PF00498 | 0.567 |
LIG_FHA_1 | 276 | 282 | PF00498 | 0.343 |
LIG_FHA_1 | 315 | 321 | PF00498 | 0.522 |
LIG_FHA_1 | 384 | 390 | PF00498 | 0.330 |
LIG_FHA_1 | 488 | 494 | PF00498 | 0.320 |
LIG_FHA_1 | 512 | 518 | PF00498 | 0.315 |
LIG_FHA_1 | 564 | 570 | PF00498 | 0.430 |
LIG_FHA_1 | 620 | 626 | PF00498 | 0.533 |
LIG_FHA_1 | 750 | 756 | PF00498 | 0.488 |
LIG_FHA_1 | 84 | 90 | PF00498 | 0.399 |
LIG_FHA_2 | 100 | 106 | PF00498 | 0.394 |
LIG_FHA_2 | 172 | 178 | PF00498 | 0.625 |
LIG_FHA_2 | 551 | 557 | PF00498 | 0.549 |
LIG_FHA_2 | 610 | 616 | PF00498 | 0.346 |
LIG_FHA_2 | 688 | 694 | PF00498 | 0.352 |
LIG_LIR_Gen_1 | 384 | 394 | PF02991 | 0.369 |
LIG_LIR_Gen_1 | 431 | 438 | PF02991 | 0.229 |
LIG_LIR_Gen_1 | 544 | 555 | PF02991 | 0.422 |
LIG_LIR_Gen_1 | 65 | 75 | PF02991 | 0.551 |
LIG_LIR_Nem_3 | 384 | 390 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 431 | 435 | PF02991 | 0.282 |
LIG_LIR_Nem_3 | 536 | 542 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 544 | 550 | PF02991 | 0.320 |
LIG_LIR_Nem_3 | 63 | 69 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 707 | 711 | PF02991 | 0.374 |
LIG_MAD2 | 395 | 403 | PF02301 | 0.264 |
LIG_SH2_CRK | 547 | 551 | PF00017 | 0.466 |
LIG_SH2_NCK_1 | 547 | 551 | PF00017 | 0.442 |
LIG_SH2_PTP2 | 675 | 678 | PF00017 | 0.278 |
LIG_SH2_STAT3 | 526 | 529 | PF00017 | 0.307 |
LIG_SH2_STAT5 | 675 | 678 | PF00017 | 0.278 |
LIG_SH3_3 | 202 | 208 | PF00018 | 0.633 |
LIG_SH3_3 | 397 | 403 | PF00018 | 0.245 |
LIG_SH3_3 | 556 | 562 | PF00018 | 0.380 |
LIG_SH3_3 | 577 | 583 | PF00018 | 0.363 |
LIG_SH3_3 | 600 | 606 | PF00018 | 0.364 |
LIG_SH3_3 | 84 | 90 | PF00018 | 0.400 |
LIG_SUMO_SIM_anti_2 | 372 | 378 | PF11976 | 0.264 |
LIG_SUMO_SIM_anti_2 | 693 | 698 | PF11976 | 0.347 |
LIG_SUMO_SIM_par_1 | 372 | 378 | PF11976 | 0.218 |
LIG_SUMO_SIM_par_1 | 425 | 431 | PF11976 | 0.244 |
LIG_SUMO_SIM_par_1 | 572 | 578 | PF11976 | 0.316 |
LIG_TRAF2_1 | 175 | 178 | PF00917 | 0.516 |
LIG_TRAF2_1 | 193 | 196 | PF00917 | 0.445 |
LIG_TRAF2_1 | 442 | 445 | PF00917 | 0.382 |
MOD_CK1_1 | 213 | 219 | PF00069 | 0.617 |
MOD_CK1_1 | 230 | 236 | PF00069 | 0.700 |
MOD_CK1_1 | 380 | 386 | PF00069 | 0.377 |
MOD_CK1_1 | 43 | 49 | PF00069 | 0.376 |
MOD_CK1_1 | 560 | 566 | PF00069 | 0.457 |
MOD_CK1_1 | 716 | 722 | PF00069 | 0.707 |
MOD_CK1_1 | 735 | 741 | PF00069 | 0.515 |
MOD_CK1_1 | 749 | 755 | PF00069 | 0.655 |
MOD_CK1_1 | 772 | 778 | PF00069 | 0.565 |
MOD_CK2_1 | 171 | 177 | PF00069 | 0.677 |
MOD_CK2_1 | 200 | 206 | PF00069 | 0.729 |
MOD_CK2_1 | 609 | 615 | PF00069 | 0.381 |
MOD_CK2_1 | 664 | 670 | PF00069 | 0.468 |
MOD_Cter_Amidation | 501 | 504 | PF01082 | 0.458 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.401 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.711 |
MOD_GlcNHglycan | 173 | 177 | PF01048 | 0.656 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.610 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.651 |
MOD_GlcNHglycan | 269 | 272 | PF01048 | 0.331 |
MOD_GlcNHglycan | 341 | 344 | PF01048 | 0.302 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.458 |
MOD_GlcNHglycan | 701 | 704 | PF01048 | 0.472 |
MOD_GlcNHglycan | 715 | 718 | PF01048 | 0.689 |
MOD_GlcNHglycan | 734 | 737 | PF01048 | 0.530 |
MOD_GlcNHglycan | 757 | 760 | PF01048 | 0.597 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.609 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.625 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.595 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.558 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.670 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.521 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.404 |
MOD_GSK3_1 | 712 | 719 | PF00069 | 0.604 |
MOD_GSK3_1 | 722 | 729 | PF00069 | 0.444 |
MOD_N-GLC_1 | 185 | 190 | PF02516 | 0.728 |
MOD_N-GLC_1 | 248 | 253 | PF02516 | 0.454 |
MOD_NEK2_1 | 13 | 18 | PF00069 | 0.419 |
MOD_NEK2_1 | 161 | 166 | PF00069 | 0.537 |
MOD_NEK2_1 | 211 | 216 | PF00069 | 0.706 |
MOD_NEK2_1 | 381 | 386 | PF00069 | 0.404 |
MOD_NEK2_1 | 575 | 580 | PF00069 | 0.352 |
MOD_NEK2_1 | 632 | 637 | PF00069 | 0.458 |
MOD_NEK2_1 | 664 | 669 | PF00069 | 0.477 |
MOD_NEK2_1 | 687 | 692 | PF00069 | 0.431 |
MOD_NEK2_2 | 20 | 25 | PF00069 | 0.355 |
MOD_NEK2_2 | 334 | 339 | PF00069 | 0.229 |
MOD_NEK2_2 | 645 | 650 | PF00069 | 0.288 |
MOD_PIKK_1 | 211 | 217 | PF00454 | 0.735 |
MOD_PIKK_1 | 405 | 411 | PF00454 | 0.262 |
MOD_PIKK_1 | 717 | 723 | PF00454 | 0.711 |
MOD_PK_1 | 94 | 100 | PF00069 | 0.512 |
MOD_PKA_2 | 147 | 153 | PF00069 | 0.739 |
MOD_PKA_2 | 20 | 26 | PF00069 | 0.286 |
MOD_PKA_2 | 220 | 226 | PF00069 | 0.759 |
MOD_PKA_2 | 231 | 237 | PF00069 | 0.787 |
MOD_PKA_2 | 412 | 418 | PF00069 | 0.430 |
MOD_PKA_2 | 43 | 49 | PF00069 | 0.398 |
MOD_PKA_2 | 54 | 60 | PF00069 | 0.445 |
MOD_PKA_2 | 608 | 614 | PF00069 | 0.501 |
MOD_PKA_2 | 630 | 636 | PF00069 | 0.509 |
MOD_PKA_2 | 740 | 746 | PF00069 | 0.593 |
MOD_PKA_2 | 772 | 778 | PF00069 | 0.533 |
MOD_PKA_2 | 83 | 89 | PF00069 | 0.398 |
MOD_PKB_1 | 778 | 786 | PF00069 | 0.524 |
MOD_Plk_1 | 377 | 383 | PF00069 | 0.288 |
MOD_Plk_1 | 487 | 493 | PF00069 | 0.465 |
MOD_Plk_1 | 511 | 517 | PF00069 | 0.456 |
MOD_Plk_1 | 557 | 563 | PF00069 | 0.378 |
MOD_Plk_1 | 664 | 670 | PF00069 | 0.455 |
MOD_Plk_1 | 685 | 691 | PF00069 | 0.322 |
MOD_Plk_4 | 200 | 206 | PF00069 | 0.611 |
MOD_Plk_4 | 220 | 226 | PF00069 | 0.716 |
MOD_Plk_4 | 487 | 493 | PF00069 | 0.382 |
MOD_Plk_4 | 512 | 518 | PF00069 | 0.353 |
MOD_Plk_4 | 560 | 566 | PF00069 | 0.388 |
MOD_Plk_4 | 62 | 68 | PF00069 | 0.440 |
MOD_Plk_4 | 664 | 670 | PF00069 | 0.504 |
MOD_Plk_4 | 746 | 752 | PF00069 | 0.563 |
MOD_Plk_4 | 83 | 89 | PF00069 | 0.386 |
MOD_Plk_4 | 94 | 100 | PF00069 | 0.382 |
MOD_ProDKin_1 | 204 | 210 | PF00069 | 0.629 |
MOD_ProDKin_1 | 727 | 733 | PF00069 | 0.707 |
MOD_SUMO_for_1 | 781 | 784 | PF00179 | 0.569 |
TRG_DiLeu_BaEn_1 | 488 | 493 | PF01217 | 0.233 |
TRG_DiLeu_BaEn_1 | 512 | 517 | PF01217 | 0.490 |
TRG_DiLeu_BaLyEn_6 | 328 | 333 | PF01217 | 0.375 |
TRG_ENDOCYTIC_2 | 547 | 550 | PF00928 | 0.403 |
TRG_ENDOCYTIC_2 | 675 | 678 | PF00928 | 0.291 |
TRG_ER_diArg_1 | 290 | 293 | PF00400 | 0.505 |
TRG_ER_diArg_1 | 410 | 413 | PF00400 | 0.343 |
TRG_ER_diArg_1 | 484 | 486 | PF00400 | 0.383 |
TRG_NES_CRM1_1 | 653 | 665 | PF08389 | 0.498 |
TRG_NLS_MonoExtC_3 | 777 | 782 | PF00514 | 0.542 |
TRG_NLS_MonoExtN_4 | 778 | 783 | PF00514 | 0.525 |
TRG_Pf-PMV_PEXEL_1 | 151 | 155 | PF00026 | 0.670 |
TRG_Pf-PMV_PEXEL_1 | 503 | 507 | PF00026 | 0.372 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4IK87 | Bodo saltans | 31% | 85% |
A0A0S4JCS0 | Bodo saltans | 40% | 100% |
A0A1X0NZA2 | Trypanosomatidae | 39% | 92% |
A0A3R7MKN4 | Trypanosoma rangeli | 31% | 82% |
A0A422NAK1 | Trypanosoma rangeli | 48% | 100% |
A4HBX5 | Leishmania braziliensis | 80% | 100% |
A4HZ95 | Leishmania infantum | 100% | 100% |
C9ZUJ0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 79% |
D0A177 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 99% |
E9AVA3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 98% |
Q38CE9 | Trypanosoma brucei brucei (strain 927/4 GUTat10.1) | 45% | 99% |
Q4QC77 | Leishmania major | 94% | 100% |
Q57YG0 | Trypanosoma brucei brucei (strain 927/4 GUTat10.1) | 29% | 79% |
Q9UUA2 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 30% | 98% |
V5B8C2 | Trypanosoma cruzi | 29% | 81% |
V5BE68 | Trypanosoma cruzi | 48% | 100% |