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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 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 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9APB8
Term | Name | Level | Count |
---|---|---|---|
GO:0001510 | RNA methylation | 4 | 1 |
GO:0002940 | tRNA N2-guanine methylation | 6 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0006399 | tRNA metabolic process | 7 | 1 |
GO:0006400 | tRNA modification | 6 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008033 | tRNA processing | 8 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009451 | RNA modification | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0030488 | tRNA methylation | 5 | 1 |
GO:0032259 | methylation | 2 | 1 |
GO:0034470 | ncRNA processing | 7 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0034660 | ncRNA metabolic process | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0043414 | macromolecule methylation | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000049 | tRNA binding | 5 | 12 |
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003723 | RNA binding | 4 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004809 | tRNA (guanine-N2-)-methyltransferase activity | 6 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0008168 | methyltransferase activity | 4 | 12 |
GO:0008170 | N-methyltransferase activity | 5 | 12 |
GO:0008173 | RNA methyltransferase activity | 4 | 12 |
GO:0008175 | tRNA methyltransferase activity | 5 | 12 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 12 |
GO:0016423 | tRNA (guanine) methyltransferase activity | 6 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 12 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 280 | 284 | PF00656 | 0.266 |
CLV_C14_Caspase3-7 | 640 | 644 | PF00656 | 0.583 |
CLV_NRD_NRD_1 | 395 | 397 | PF00675 | 0.510 |
CLV_NRD_NRD_1 | 406 | 408 | PF00675 | 0.520 |
CLV_NRD_NRD_1 | 463 | 465 | PF00675 | 0.682 |
CLV_NRD_NRD_1 | 698 | 700 | PF00675 | 0.564 |
CLV_NRD_NRD_1 | 97 | 99 | PF00675 | 0.286 |
CLV_PCSK_FUR_1 | 396 | 400 | PF00082 | 0.574 |
CLV_PCSK_FUR_1 | 404 | 408 | PF00082 | 0.567 |
CLV_PCSK_KEX2_1 | 223 | 225 | PF00082 | 0.568 |
CLV_PCSK_KEX2_1 | 394 | 396 | PF00082 | 0.276 |
CLV_PCSK_KEX2_1 | 398 | 400 | PF00082 | 0.512 |
CLV_PCSK_KEX2_1 | 406 | 408 | PF00082 | 0.512 |
CLV_PCSK_KEX2_1 | 444 | 446 | PF00082 | 0.833 |
CLV_PCSK_KEX2_1 | 697 | 699 | PF00082 | 0.549 |
CLV_PCSK_KEX2_1 | 96 | 98 | PF00082 | 0.302 |
CLV_PCSK_PC1ET2_1 | 223 | 225 | PF00082 | 0.539 |
CLV_PCSK_PC1ET2_1 | 398 | 400 | PF00082 | 0.412 |
CLV_PCSK_PC1ET2_1 | 444 | 446 | PF00082 | 0.834 |
CLV_PCSK_PC7_1 | 391 | 397 | PF00082 | 0.421 |
CLV_PCSK_PC7_1 | 440 | 446 | PF00082 | 0.676 |
CLV_PCSK_SKI1_1 | 120 | 124 | PF00082 | 0.348 |
CLV_PCSK_SKI1_1 | 241 | 245 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 269 | 273 | PF00082 | 0.300 |
CLV_PCSK_SKI1_1 | 315 | 319 | PF00082 | 0.266 |
CLV_PCSK_SKI1_1 | 345 | 349 | PF00082 | 0.337 |
CLV_PCSK_SKI1_1 | 554 | 558 | PF00082 | 0.358 |
CLV_PCSK_SKI1_1 | 618 | 622 | PF00082 | 0.300 |
CLV_PCSK_SKI1_1 | 657 | 661 | PF00082 | 0.564 |
DEG_APCC_DBOX_1 | 314 | 322 | PF00400 | 0.281 |
DEG_APCC_DBOX_1 | 553 | 561 | PF00400 | 0.411 |
DEG_SCF_FBW7_2 | 659 | 666 | PF00400 | 0.500 |
DOC_CKS1_1 | 581 | 586 | PF01111 | 0.360 |
DOC_CKS1_1 | 660 | 665 | PF01111 | 0.497 |
DOC_CYCLIN_RxL_1 | 310 | 322 | PF00134 | 0.266 |
DOC_CYCLIN_RxL_1 | 654 | 662 | PF00134 | 0.539 |
DOC_CYCLIN_yCln2_LP_2 | 512 | 518 | PF00134 | 0.325 |
DOC_MAPK_DCC_7 | 330 | 338 | PF00069 | 0.269 |
DOC_MAPK_DCC_7 | 608 | 617 | PF00069 | 0.277 |
DOC_MAPK_gen_1 | 269 | 279 | PF00069 | 0.281 |
DOC_MAPK_gen_1 | 327 | 335 | PF00069 | 0.266 |
DOC_MAPK_gen_1 | 349 | 359 | PF00069 | 0.210 |
DOC_MAPK_MEF2A_6 | 330 | 338 | PF00069 | 0.269 |
DOC_MAPK_MEF2A_6 | 548 | 557 | PF00069 | 0.277 |
DOC_MAPK_MEF2A_6 | 608 | 617 | PF00069 | 0.277 |
DOC_PP2B_LxvP_1 | 32 | 35 | PF13499 | 0.428 |
DOC_PP4_FxxP_1 | 331 | 334 | PF00568 | 0.393 |
DOC_PP4_FxxP_1 | 68 | 71 | PF00568 | 0.266 |
DOC_USP7_MATH_1 | 187 | 191 | PF00917 | 0.492 |
DOC_USP7_MATH_1 | 214 | 218 | PF00917 | 0.578 |
DOC_USP7_MATH_1 | 232 | 236 | PF00917 | 0.681 |
DOC_USP7_MATH_1 | 256 | 260 | PF00917 | 0.316 |
DOC_USP7_MATH_1 | 387 | 391 | PF00917 | 0.331 |
DOC_USP7_MATH_1 | 413 | 417 | PF00917 | 0.559 |
DOC_USP7_MATH_1 | 430 | 434 | PF00917 | 0.775 |
DOC_USP7_MATH_1 | 470 | 474 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 642 | 646 | PF00917 | 0.684 |
DOC_USP7_MATH_1 | 650 | 654 | PF00917 | 0.604 |
DOC_WW_Pin1_4 | 14 | 19 | PF00397 | 0.515 |
DOC_WW_Pin1_4 | 185 | 190 | PF00397 | 0.689 |
DOC_WW_Pin1_4 | 234 | 239 | PF00397 | 0.620 |
DOC_WW_Pin1_4 | 258 | 263 | PF00397 | 0.314 |
DOC_WW_Pin1_4 | 468 | 473 | PF00397 | 0.571 |
DOC_WW_Pin1_4 | 478 | 483 | PF00397 | 0.480 |
DOC_WW_Pin1_4 | 580 | 585 | PF00397 | 0.360 |
DOC_WW_Pin1_4 | 659 | 664 | PF00397 | 0.442 |
LIG_14-3-3_CanoR_1 | 379 | 389 | PF00244 | 0.411 |
LIG_14-3-3_CanoR_1 | 537 | 543 | PF00244 | 0.397 |
LIG_14-3-3_CanoR_1 | 89 | 95 | PF00244 | 0.393 |
LIG_Actin_WH2_2 | 101 | 119 | PF00022 | 0.281 |
LIG_Actin_WH2_2 | 76 | 93 | PF00022 | 0.331 |
LIG_APCC_ABBA_1 | 336 | 341 | PF00400 | 0.266 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.596 |
LIG_BRCT_BRCA1_1 | 4 | 8 | PF00533 | 0.473 |
LIG_FAT_LD_1 | 527 | 535 | PF03623 | 0.355 |
LIG_FHA_1 | 235 | 241 | PF00498 | 0.565 |
LIG_FHA_1 | 26 | 32 | PF00498 | 0.412 |
LIG_FHA_1 | 548 | 554 | PF00498 | 0.369 |
LIG_FHA_1 | 581 | 587 | PF00498 | 0.325 |
LIG_FHA_2 | 104 | 110 | PF00498 | 0.266 |
LIG_FHA_2 | 157 | 163 | PF00498 | 0.416 |
LIG_FHA_2 | 278 | 284 | PF00498 | 0.266 |
LIG_FHA_2 | 623 | 629 | PF00498 | 0.313 |
LIG_LIR_Apic_2 | 374 | 380 | PF02991 | 0.331 |
LIG_LIR_Gen_1 | 521 | 532 | PF02991 | 0.167 |
LIG_LIR_Gen_1 | 574 | 581 | PF02991 | 0.267 |
LIG_LIR_Gen_1 | 85 | 95 | PF02991 | 0.325 |
LIG_LIR_Nem_3 | 265 | 271 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 521 | 527 | PF02991 | 0.167 |
LIG_LIR_Nem_3 | 574 | 578 | PF02991 | 0.306 |
LIG_LIR_Nem_3 | 85 | 90 | PF02991 | 0.325 |
LIG_LYPXL_yS_3 | 157 | 160 | PF13949 | 0.544 |
LIG_MYND_1 | 238 | 242 | PF01753 | 0.456 |
LIG_NRBOX | 526 | 532 | PF00104 | 0.266 |
LIG_PCNA_yPIPBox_3 | 241 | 252 | PF02747 | 0.329 |
LIG_PTB_Apo_2 | 124 | 131 | PF02174 | 0.411 |
LIG_PTB_Apo_2 | 144 | 151 | PF02174 | 0.411 |
LIG_PTB_Phospho_1 | 124 | 130 | PF10480 | 0.411 |
LIG_PTB_Phospho_1 | 144 | 150 | PF10480 | 0.411 |
LIG_REV1ctd_RIR_1 | 345 | 353 | PF16727 | 0.325 |
LIG_SH2_CRK | 10 | 14 | PF00017 | 0.553 |
LIG_SH2_CRK | 150 | 154 | PF00017 | 0.411 |
LIG_SH2_CRK | 351 | 355 | PF00017 | 0.281 |
LIG_SH2_CRK | 517 | 521 | PF00017 | 0.281 |
LIG_SH2_NCK_1 | 10 | 14 | PF00017 | 0.514 |
LIG_SH2_NCK_1 | 517 | 521 | PF00017 | 0.266 |
LIG_SH2_NCK_1 | 69 | 73 | PF00017 | 0.266 |
LIG_SH2_PTP2 | 575 | 578 | PF00017 | 0.411 |
LIG_SH2_SRC | 130 | 133 | PF00017 | 0.325 |
LIG_SH2_STAT3 | 366 | 369 | PF00017 | 0.296 |
LIG_SH2_STAT5 | 121 | 124 | PF00017 | 0.285 |
LIG_SH2_STAT5 | 130 | 133 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 343 | 346 | PF00017 | 0.266 |
LIG_SH2_STAT5 | 567 | 570 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 575 | 578 | PF00017 | 0.386 |
LIG_SH3_1 | 686 | 692 | PF00018 | 0.440 |
LIG_SH3_2 | 469 | 474 | PF14604 | 0.514 |
LIG_SH3_3 | 152 | 158 | PF00018 | 0.505 |
LIG_SH3_3 | 225 | 231 | PF00018 | 0.584 |
LIG_SH3_3 | 28 | 34 | PF00018 | 0.389 |
LIG_SH3_3 | 466 | 472 | PF00018 | 0.512 |
LIG_SH3_3 | 558 | 564 | PF00018 | 0.294 |
LIG_SH3_3 | 575 | 581 | PF00018 | 0.199 |
LIG_SH3_3 | 686 | 692 | PF00018 | 0.440 |
LIG_SUMO_SIM_anti_2 | 103 | 109 | PF11976 | 0.360 |
LIG_SUMO_SIM_par_1 | 250 | 255 | PF11976 | 0.272 |
LIG_SUMO_SIM_par_1 | 657 | 662 | PF11976 | 0.288 |
LIG_SUMO_SIM_par_1 | 82 | 88 | PF11976 | 0.331 |
LIG_TRAF2_1 | 390 | 393 | PF00917 | 0.287 |
LIG_TRAF2_1 | 408 | 411 | PF00917 | 0.384 |
LIG_TRAF2_1 | 54 | 57 | PF00917 | 0.592 |
LIG_TRAF2_1 | 556 | 559 | PF00917 | 0.281 |
LIG_TRFH_1 | 566 | 570 | PF08558 | 0.331 |
LIG_TYR_ITIM | 155 | 160 | PF00017 | 0.451 |
LIG_UBA3_1 | 616 | 624 | PF00899 | 0.337 |
MOD_CDC14_SPxK_1 | 471 | 474 | PF00782 | 0.657 |
MOD_CDK_SPxK_1 | 468 | 474 | PF00069 | 0.602 |
MOD_CDK_SPxxK_3 | 234 | 241 | PF00069 | 0.455 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.624 |
MOD_CK1_1 | 281 | 287 | PF00069 | 0.280 |
MOD_CK1_1 | 371 | 377 | PF00069 | 0.474 |
MOD_CK1_1 | 423 | 429 | PF00069 | 0.752 |
MOD_CK1_1 | 473 | 479 | PF00069 | 0.582 |
MOD_CK1_1 | 490 | 496 | PF00069 | 0.533 |
MOD_CK1_1 | 51 | 57 | PF00069 | 0.677 |
MOD_CK2_1 | 103 | 109 | PF00069 | 0.266 |
MOD_CK2_1 | 156 | 162 | PF00069 | 0.409 |
MOD_CK2_1 | 387 | 393 | PF00069 | 0.364 |
MOD_CK2_1 | 413 | 419 | PF00069 | 0.495 |
MOD_CK2_1 | 51 | 57 | PF00069 | 0.684 |
MOD_CK2_1 | 522 | 528 | PF00069 | 0.167 |
MOD_Cter_Amidation | 221 | 224 | PF01082 | 0.583 |
MOD_GlcNHglycan | 111 | 114 | PF01048 | 0.266 |
MOD_GlcNHglycan | 233 | 237 | PF01048 | 0.722 |
MOD_GlcNHglycan | 258 | 261 | PF01048 | 0.298 |
MOD_GlcNHglycan | 283 | 286 | PF01048 | 0.322 |
MOD_GlcNHglycan | 359 | 362 | PF01048 | 0.421 |
MOD_GlcNHglycan | 373 | 376 | PF01048 | 0.423 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.476 |
MOD_GlcNHglycan | 415 | 418 | PF01048 | 0.574 |
MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.638 |
MOD_GlcNHglycan | 489 | 492 | PF01048 | 0.596 |
MOD_GlcNHglycan | 512 | 515 | PF01048 | 0.273 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.526 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.571 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.314 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.581 |
MOD_GSK3_1 | 490 | 497 | PF00069 | 0.559 |
MOD_GSK3_1 | 506 | 513 | PF00069 | 0.299 |
MOD_GSK3_1 | 518 | 525 | PF00069 | 0.227 |
MOD_GSK3_1 | 622 | 629 | PF00069 | 0.550 |
MOD_LATS_1 | 296 | 302 | PF00433 | 0.266 |
MOD_N-GLC_1 | 413 | 418 | PF02516 | 0.483 |
MOD_N-GLC_1 | 51 | 56 | PF02516 | 0.707 |
MOD_N-GLC_1 | 522 | 527 | PF02516 | 0.240 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.280 |
MOD_NEK2_1 | 277 | 282 | PF00069 | 0.279 |
MOD_NEK2_1 | 291 | 296 | PF00069 | 0.266 |
MOD_NEK2_1 | 368 | 373 | PF00069 | 0.333 |
MOD_NEK2_2 | 334 | 339 | PF00069 | 0.266 |
MOD_OGLYCOS | 580 | 585 | PF02709 | 0.167 |
MOD_PIKK_1 | 518 | 524 | PF00454 | 0.281 |
MOD_PIKK_1 | 595 | 601 | PF00454 | 0.266 |
MOD_PK_1 | 77 | 83 | PF00069 | 0.266 |
MOD_PKA_1 | 398 | 404 | PF00069 | 0.395 |
MOD_PKA_2 | 387 | 393 | PF00069 | 0.373 |
MOD_PKA_2 | 398 | 404 | PF00069 | 0.620 |
MOD_PKA_2 | 473 | 479 | PF00069 | 0.615 |
MOD_PKA_2 | 536 | 542 | PF00069 | 0.353 |
MOD_PKA_2 | 547 | 553 | PF00069 | 0.295 |
MOD_PKA_2 | 595 | 601 | PF00069 | 0.281 |
MOD_PKA_2 | 679 | 685 | PF00069 | 0.556 |
MOD_PKA_2 | 90 | 96 | PF00069 | 0.337 |
MOD_PKB_1 | 577 | 585 | PF00069 | 0.167 |
MOD_PKB_1 | 96 | 104 | PF00069 | 0.411 |
MOD_Plk_1 | 522 | 528 | PF00069 | 0.240 |
MOD_Plk_1 | 667 | 673 | PF00069 | 0.372 |
MOD_Plk_1 | 77 | 83 | PF00069 | 0.276 |
MOD_Plk_2-3 | 103 | 109 | PF00069 | 0.360 |
MOD_Plk_4 | 156 | 162 | PF00069 | 0.445 |
MOD_Plk_4 | 506 | 512 | PF00069 | 0.356 |
MOD_Plk_4 | 571 | 577 | PF00069 | 0.266 |
MOD_ProDKin_1 | 14 | 20 | PF00069 | 0.516 |
MOD_ProDKin_1 | 185 | 191 | PF00069 | 0.675 |
MOD_ProDKin_1 | 234 | 240 | PF00069 | 0.613 |
MOD_ProDKin_1 | 258 | 264 | PF00069 | 0.314 |
MOD_ProDKin_1 | 468 | 474 | PF00069 | 0.575 |
MOD_ProDKin_1 | 478 | 484 | PF00069 | 0.483 |
MOD_ProDKin_1 | 580 | 586 | PF00069 | 0.360 |
MOD_ProDKin_1 | 659 | 665 | PF00069 | 0.448 |
MOD_SUMO_rev_2 | 415 | 423 | PF00179 | 0.708 |
TRG_DiLeu_BaLyEn_6 | 239 | 244 | PF01217 | 0.436 |
TRG_DiLeu_BaLyEn_6 | 331 | 336 | PF01217 | 0.302 |
TRG_DiLeu_BaLyEn_6 | 655 | 660 | PF01217 | 0.359 |
TRG_ENDOCYTIC_2 | 10 | 13 | PF00928 | 0.551 |
TRG_ENDOCYTIC_2 | 150 | 153 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 157 | 160 | PF00928 | 0.544 |
TRG_ENDOCYTIC_2 | 299 | 302 | PF00928 | 0.266 |
TRG_ENDOCYTIC_2 | 575 | 578 | PF00928 | 0.411 |
TRG_ER_diArg_1 | 394 | 396 | PF00400 | 0.360 |
TRG_ER_diArg_1 | 404 | 407 | PF00400 | 0.583 |
TRG_ER_diArg_1 | 576 | 579 | PF00400 | 0.264 |
TRG_ER_diArg_1 | 677 | 680 | PF00400 | 0.537 |
TRG_ER_diArg_1 | 696 | 699 | PF00400 | 0.685 |
TRG_ER_diArg_1 | 89 | 92 | PF00400 | 0.283 |
TRG_ER_diArg_1 | 95 | 98 | PF00400 | 0.279 |
TRG_NLS_MonoExtC_3 | 645 | 650 | PF00514 | 0.642 |
TRG_Pf-PMV_PEXEL_1 | 241 | 245 | PF00026 | 0.435 |
TRG_Pf-PMV_PEXEL_1 | 269 | 273 | PF00026 | 0.300 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PF43 | Leptomonas seymouri | 71% | 99% |
A0A0S4IT52 | Bodo saltans | 47% | 100% |
A0A1X0NNC1 | Trypanosomatidae | 49% | 96% |
A0A3R7KAT5 | Trypanosoma rangeli | 52% | 100% |
A0A3S7WSL8 | Leishmania donovani | 91% | 100% |
A4H782 | Leishmania braziliensis | 81% | 100% |
A4HVM2 | Leishmania infantum | 91% | 100% |
D0A6N2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 100% |
Q4QG60 | Leishmania major | 90% | 100% |
V5BB27 | Trypanosoma cruzi | 52% | 100% |