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 | 11 |
GO:0043226 | organelle | 2 | 11 |
GO:0043227 | membrane-bounded organelle | 3 | 11 |
GO:0043229 | intracellular organelle | 3 | 11 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0031974 | membrane-enclosed lumen | 2 | 1 |
GO:0031981 | nuclear lumen | 5 | 1 |
GO:0043233 | organelle lumen | 3 | 1 |
GO:0070013 | intracellular organelle lumen | 4 | 1 |
Related structures:
AlphaFold database: A0A3Q8IHR3
Term | Name | Level | Count |
---|---|---|---|
GO:0006950 | response to stress | 2 | 12 |
GO:0006974 | DNA damage response | 4 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0033554 | cellular response to stress | 3 | 12 |
GO:0050896 | response to stimulus | 1 | 12 |
GO:0051716 | cellular response to stimulus | 2 | 12 |
GO:0000723 | telomere maintenance | 5 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006259 | DNA metabolic process | 4 | 1 |
GO:0006281 | DNA repair | 5 | 1 |
GO:0006302 | double-strand break repair | 6 | 1 |
GO:0006303 | double-strand break repair via nonhomologous end joining | 7 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0031848 | protection from non-homologous end joining at telomere | 6 | 1 |
GO:0032200 | telomere organization | 6 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0036297 | interstrand cross-link repair | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043247 | telomere maintenance in response to DNA damage | 5 | 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:0051276 | chromosome organization | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003677 | DNA binding | 4 | 1 |
GO:0003684 | damaged DNA binding | 5 | 1 |
GO:0003824 | catalytic activity | 1 | 1 |
GO:0004518 | nuclease activity | 4 | 1 |
GO:0004527 | exonuclease activity | 5 | 1 |
GO:0004529 | DNA exonuclease activity | 5 | 1 |
GO:0004536 | DNA nuclease activity | 4 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0008409 | 5'-3' exonuclease activity | 6 | 1 |
GO:0016787 | hydrolase activity | 2 | 1 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 1 |
GO:0016796 | exonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 5'-phosphomonoesters | 6 | 1 |
GO:0016895 | DNA exonuclease activity, producing 5'-phosphomonoesters | 6 | 1 |
GO:0035312 | 5'-3' DNA exonuclease activity | 7 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 1 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 298 | 302 | PF00656 | 0.609 |
CLV_C14_Caspase3-7 | 369 | 373 | PF00656 | 0.696 |
CLV_C14_Caspase3-7 | 550 | 554 | PF00656 | 0.723 |
CLV_MEL_PAP_1 | 506 | 512 | PF00089 | 0.662 |
CLV_NRD_NRD_1 | 337 | 339 | PF00675 | 0.756 |
CLV_NRD_NRD_1 | 535 | 537 | PF00675 | 0.734 |
CLV_NRD_NRD_1 | 583 | 585 | PF00675 | 0.729 |
CLV_PCSK_KEX2_1 | 116 | 118 | PF00082 | 0.733 |
CLV_PCSK_KEX2_1 | 339 | 341 | PF00082 | 0.558 |
CLV_PCSK_KEX2_1 | 444 | 446 | PF00082 | 0.332 |
CLV_PCSK_KEX2_1 | 535 | 537 | PF00082 | 0.728 |
CLV_PCSK_KEX2_1 | 585 | 587 | PF00082 | 0.776 |
CLV_PCSK_KEX2_1 | 624 | 626 | PF00082 | 0.673 |
CLV_PCSK_PC1ET2_1 | 116 | 118 | PF00082 | 0.665 |
CLV_PCSK_PC1ET2_1 | 339 | 341 | PF00082 | 0.558 |
CLV_PCSK_PC1ET2_1 | 444 | 446 | PF00082 | 0.344 |
CLV_PCSK_PC1ET2_1 | 585 | 587 | PF00082 | 0.776 |
CLV_PCSK_PC1ET2_1 | 624 | 626 | PF00082 | 0.702 |
CLV_PCSK_SKI1_1 | 149 | 153 | PF00082 | 0.522 |
CLV_PCSK_SKI1_1 | 183 | 187 | PF00082 | 0.458 |
CLV_PCSK_SKI1_1 | 223 | 227 | PF00082 | 0.387 |
CLV_PCSK_SKI1_1 | 229 | 233 | PF00082 | 0.431 |
CLV_PCSK_SKI1_1 | 270 | 274 | PF00082 | 0.500 |
CLV_PCSK_SKI1_1 | 549 | 553 | PF00082 | 0.624 |
CLV_Separin_Metazoa | 180 | 184 | PF03568 | 0.502 |
DEG_APCC_DBOX_1 | 148 | 156 | PF00400 | 0.527 |
DEG_APCC_DBOX_1 | 633 | 641 | PF00400 | 0.767 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.432 |
DEG_SCF_FBW7_1 | 606 | 613 | PF00400 | 0.541 |
DEG_SPOP_SBC_1 | 598 | 602 | PF00917 | 0.683 |
DOC_CKS1_1 | 21 | 26 | PF01111 | 0.482 |
DOC_CYCLIN_RxL_1 | 144 | 153 | PF00134 | 0.528 |
DOC_MAPK_gen_1 | 206 | 214 | PF00069 | 0.435 |
DOC_MAPK_gen_1 | 221 | 228 | PF00069 | 0.281 |
DOC_MAPK_gen_1 | 588 | 596 | PF00069 | 0.693 |
DOC_MAPK_MEF2A_6 | 149 | 156 | PF00069 | 0.473 |
DOC_MAPK_MEF2A_6 | 221 | 228 | PF00069 | 0.399 |
DOC_MAPK_MEF2A_6 | 361 | 370 | PF00069 | 0.688 |
DOC_PP2B_LxvP_1 | 33 | 36 | PF13499 | 0.665 |
DOC_PP2B_LxvP_1 | 458 | 461 | PF13499 | 0.487 |
DOC_PP4_FxxP_1 | 161 | 164 | PF00568 | 0.399 |
DOC_PP4_FxxP_1 | 394 | 397 | PF00568 | 0.398 |
DOC_PP4_FxxP_1 | 477 | 480 | PF00568 | 0.487 |
DOC_PP4_FxxP_1 | 71 | 74 | PF00568 | 0.382 |
DOC_USP7_MATH_1 | 196 | 200 | PF00917 | 0.627 |
DOC_USP7_MATH_1 | 243 | 247 | PF00917 | 0.671 |
DOC_USP7_MATH_1 | 289 | 293 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 36 | 40 | PF00917 | 0.705 |
DOC_USP7_MATH_1 | 397 | 401 | PF00917 | 0.431 |
DOC_USP7_MATH_1 | 485 | 489 | PF00917 | 0.476 |
DOC_USP7_MATH_1 | 608 | 612 | PF00917 | 0.731 |
DOC_USP7_MATH_2 | 564 | 570 | PF00917 | 0.501 |
DOC_WW_Pin1_4 | 20 | 25 | PF00397 | 0.524 |
DOC_WW_Pin1_4 | 264 | 269 | PF00397 | 0.406 |
DOC_WW_Pin1_4 | 31 | 36 | PF00397 | 0.627 |
DOC_WW_Pin1_4 | 411 | 416 | PF00397 | 0.584 |
DOC_WW_Pin1_4 | 606 | 611 | PF00397 | 0.612 |
DOC_WW_Pin1_4 | 628 | 633 | PF00397 | 0.794 |
DOC_WW_Pin1_4 | 70 | 75 | PF00397 | 0.407 |
LIG_14-3-3_CanoR_1 | 104 | 108 | PF00244 | 0.546 |
LIG_14-3-3_CanoR_1 | 291 | 297 | PF00244 | 0.587 |
LIG_14-3-3_CanoR_1 | 353 | 360 | PF00244 | 0.697 |
LIG_14-3-3_CanoR_1 | 459 | 468 | PF00244 | 0.513 |
LIG_14-3-3_CanoR_1 | 518 | 523 | PF00244 | 0.599 |
LIG_14-3-3_CanoR_1 | 591 | 597 | PF00244 | 0.526 |
LIG_BIR_III_2 | 230 | 234 | PF00653 | 0.525 |
LIG_BRCT_BRCA1_1 | 275 | 279 | PF00533 | 0.528 |
LIG_BRCT_BRCA1_1 | 72 | 76 | PF00533 | 0.411 |
LIG_deltaCOP1_diTrp_1 | 92 | 97 | PF00928 | 0.511 |
LIG_FHA_1 | 173 | 179 | PF00498 | 0.421 |
LIG_FHA_1 | 312 | 318 | PF00498 | 0.610 |
LIG_FHA_1 | 382 | 388 | PF00498 | 0.509 |
LIG_FHA_1 | 607 | 613 | PF00498 | 0.713 |
LIG_FHA_2 | 296 | 302 | PF00498 | 0.780 |
LIG_FHA_2 | 484 | 490 | PF00498 | 0.562 |
LIG_FHA_2 | 548 | 554 | PF00498 | 0.612 |
LIG_Integrin_isoDGR_2 | 102 | 104 | PF01839 | 0.489 |
LIG_LIR_Apic_2 | 106 | 110 | PF02991 | 0.517 |
LIG_LIR_Apic_2 | 158 | 164 | PF02991 | 0.383 |
LIG_LIR_Apic_2 | 392 | 397 | PF02991 | 0.424 |
LIG_LIR_Apic_2 | 476 | 480 | PF02991 | 0.497 |
LIG_LIR_Gen_1 | 269 | 279 | PF02991 | 0.426 |
LIG_LIR_Gen_1 | 400 | 410 | PF02991 | 0.503 |
LIG_LIR_Gen_1 | 429 | 439 | PF02991 | 0.556 |
LIG_LIR_Gen_1 | 473 | 481 | PF02991 | 0.515 |
LIG_LIR_Gen_1 | 494 | 503 | PF02991 | 0.427 |
LIG_LIR_Gen_1 | 517 | 528 | PF02991 | 0.655 |
LIG_LIR_Gen_1 | 617 | 628 | PF02991 | 0.718 |
LIG_LIR_Gen_1 | 92 | 98 | PF02991 | 0.534 |
LIG_LIR_Nem_3 | 230 | 235 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 269 | 274 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 281 | 287 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 400 | 406 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 429 | 434 | PF02991 | 0.572 |
LIG_LIR_Nem_3 | 473 | 477 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 489 | 495 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 517 | 523 | PF02991 | 0.635 |
LIG_LIR_Nem_3 | 617 | 623 | PF02991 | 0.706 |
LIG_LIR_Nem_3 | 73 | 79 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 92 | 97 | PF02991 | 0.458 |
LIG_MYND_1 | 321 | 325 | PF01753 | 0.562 |
LIG_NRBOX | 151 | 157 | PF00104 | 0.430 |
LIG_PCNA_yPIPBox_3 | 144 | 155 | PF02747 | 0.493 |
LIG_Pex14_2 | 168 | 172 | PF04695 | 0.500 |
LIG_Pex14_2 | 280 | 284 | PF04695 | 0.478 |
LIG_SH2_CRK | 166 | 170 | PF00017 | 0.498 |
LIG_SH2_CRK | 271 | 275 | PF00017 | 0.491 |
LIG_SH2_CRK | 403 | 407 | PF00017 | 0.537 |
LIG_SH2_CRK | 431 | 435 | PF00017 | 0.562 |
LIG_SH2_PTP2 | 107 | 110 | PF00017 | 0.556 |
LIG_SH2_SRC | 107 | 110 | PF00017 | 0.580 |
LIG_SH2_STAP1 | 133 | 137 | PF00017 | 0.518 |
LIG_SH2_STAP1 | 431 | 435 | PF00017 | 0.562 |
LIG_SH2_STAP1 | 495 | 499 | PF00017 | 0.477 |
LIG_SH2_STAT5 | 107 | 110 | PF00017 | 0.556 |
LIG_SH2_STAT5 | 217 | 220 | PF00017 | 0.410 |
LIG_SH2_STAT5 | 7 | 10 | PF00017 | 0.377 |
LIG_SH3_3 | 106 | 112 | PF00018 | 0.556 |
LIG_SH3_3 | 125 | 131 | PF00018 | 0.509 |
LIG_SH3_3 | 18 | 24 | PF00018 | 0.530 |
LIG_SH3_3 | 319 | 325 | PF00018 | 0.451 |
LIG_SH3_3 | 562 | 568 | PF00018 | 0.676 |
LIG_SH3_3 | 593 | 599 | PF00018 | 0.699 |
LIG_SUMO_SIM_anti_2 | 153 | 158 | PF11976 | 0.426 |
LIG_SUMO_SIM_anti_2 | 432 | 438 | PF11976 | 0.551 |
LIG_SUMO_SIM_par_1 | 153 | 158 | PF11976 | 0.503 |
LIG_SUMO_SIM_par_1 | 324 | 330 | PF11976 | 0.541 |
LIG_SUMO_SIM_par_1 | 416 | 422 | PF11976 | 0.550 |
LIG_SUMO_SIM_par_1 | 432 | 438 | PF11976 | 0.529 |
LIG_SUMO_SIM_par_1 | 656 | 664 | PF11976 | 0.659 |
LIG_TRAF2_1 | 636 | 639 | PF00917 | 0.691 |
LIG_TYR_ITIM | 401 | 406 | PF00017 | 0.377 |
LIG_WW_2 | 109 | 112 | PF00397 | 0.508 |
MOD_CDC14_SPxK_1 | 267 | 270 | PF00782 | 0.427 |
MOD_CDC14_SPxK_1 | 631 | 634 | PF00782 | 0.683 |
MOD_CDK_SPxK_1 | 264 | 270 | PF00069 | 0.402 |
MOD_CDK_SPxK_1 | 628 | 634 | PF00069 | 0.675 |
MOD_CK1_1 | 10 | 16 | PF00069 | 0.537 |
MOD_CK1_1 | 238 | 244 | PF00069 | 0.667 |
MOD_CK1_1 | 290 | 296 | PF00069 | 0.720 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.566 |
MOD_CK1_1 | 508 | 514 | PF00069 | 0.679 |
MOD_CK1_1 | 555 | 561 | PF00069 | 0.681 |
MOD_CK1_1 | 577 | 583 | PF00069 | 0.611 |
MOD_CK1_1 | 601 | 607 | PF00069 | 0.715 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.493 |
MOD_CK2_1 | 167 | 173 | PF00069 | 0.426 |
MOD_CK2_1 | 375 | 381 | PF00069 | 0.718 |
MOD_CK2_1 | 483 | 489 | PF00069 | 0.441 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.671 |
MOD_GlcNHglycan | 342 | 345 | PF01048 | 0.704 |
MOD_GlcNHglycan | 354 | 357 | PF01048 | 0.778 |
MOD_GlcNHglycan | 377 | 380 | PF01048 | 0.754 |
MOD_GlcNHglycan | 545 | 548 | PF01048 | 0.738 |
MOD_GlcNHglycan | 579 | 582 | PF01048 | 0.716 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.593 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.701 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.397 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.710 |
MOD_GSK3_1 | 449 | 456 | PF00069 | 0.393 |
MOD_GSK3_1 | 514 | 521 | PF00069 | 0.596 |
MOD_GSK3_1 | 539 | 546 | PF00069 | 0.694 |
MOD_GSK3_1 | 597 | 604 | PF00069 | 0.742 |
MOD_GSK3_1 | 606 | 613 | PF00069 | 0.710 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.374 |
MOD_N-GLC_1 | 375 | 380 | PF02516 | 0.710 |
MOD_N-GLC_1 | 87 | 92 | PF02516 | 0.449 |
MOD_N-GLC_2 | 61 | 63 | PF02516 | 0.393 |
MOD_NEK2_1 | 157 | 162 | PF00069 | 0.351 |
MOD_NEK2_1 | 247 | 252 | PF00069 | 0.655 |
MOD_NEK2_1 | 273 | 278 | PF00069 | 0.554 |
MOD_NEK2_1 | 287 | 292 | PF00069 | 0.540 |
MOD_NEK2_1 | 3 | 8 | PF00069 | 0.398 |
MOD_NEK2_1 | 552 | 557 | PF00069 | 0.673 |
MOD_NEK2_1 | 9 | 14 | PF00069 | 0.417 |
MOD_NEK2_1 | 97 | 102 | PF00069 | 0.525 |
MOD_NEK2_2 | 243 | 248 | PF00069 | 0.712 |
MOD_PIKK_1 | 167 | 173 | PF00454 | 0.493 |
MOD_PIKK_1 | 247 | 253 | PF00454 | 0.786 |
MOD_PK_1 | 518 | 524 | PF00069 | 0.689 |
MOD_PKA_2 | 235 | 241 | PF00069 | 0.630 |
MOD_PKA_2 | 243 | 249 | PF00069 | 0.724 |
MOD_PKA_2 | 290 | 296 | PF00069 | 0.658 |
MOD_PKA_2 | 352 | 358 | PF00069 | 0.707 |
MOD_PKA_2 | 360 | 366 | PF00069 | 0.739 |
MOD_PKA_2 | 508 | 514 | PF00069 | 0.609 |
MOD_PKA_2 | 90 | 96 | PF00069 | 0.516 |
MOD_PKA_2 | 98 | 104 | PF00069 | 0.533 |
MOD_PKB_1 | 338 | 346 | PF00069 | 0.559 |
MOD_Plk_1 | 157 | 163 | PF00069 | 0.354 |
MOD_Plk_1 | 45 | 51 | PF00069 | 0.468 |
MOD_Plk_2-3 | 381 | 387 | PF00069 | 0.581 |
MOD_Plk_2-3 | 566 | 572 | PF00069 | 0.645 |
MOD_Plk_4 | 103 | 109 | PF00069 | 0.585 |
MOD_Plk_4 | 28 | 34 | PF00069 | 0.321 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.402 |
MOD_Plk_4 | 389 | 395 | PF00069 | 0.398 |
MOD_Plk_4 | 453 | 459 | PF00069 | 0.334 |
MOD_Plk_4 | 75 | 81 | PF00069 | 0.386 |
MOD_ProDKin_1 | 20 | 26 | PF00069 | 0.530 |
MOD_ProDKin_1 | 264 | 270 | PF00069 | 0.402 |
MOD_ProDKin_1 | 31 | 37 | PF00069 | 0.638 |
MOD_ProDKin_1 | 411 | 417 | PF00069 | 0.480 |
MOD_ProDKin_1 | 606 | 612 | PF00069 | 0.610 |
MOD_ProDKin_1 | 628 | 634 | PF00069 | 0.797 |
MOD_ProDKin_1 | 70 | 76 | PF00069 | 0.411 |
TRG_DiLeu_BaEn_1 | 386 | 391 | PF01217 | 0.541 |
TRG_DiLeu_BaEn_1 | 453 | 458 | PF01217 | 0.444 |
TRG_DiLeu_BaEn_2 | 469 | 475 | PF01217 | 0.328 |
TRG_DiLeu_BaLyEn_6 | 53 | 58 | PF01217 | 0.452 |
TRG_ENDOCYTIC_2 | 133 | 136 | PF00928 | 0.525 |
TRG_ENDOCYTIC_2 | 271 | 274 | PF00928 | 0.437 |
TRG_ENDOCYTIC_2 | 403 | 406 | PF00928 | 0.369 |
TRG_ENDOCYTIC_2 | 431 | 434 | PF00928 | 0.418 |
TRG_ENDOCYTIC_2 | 495 | 498 | PF00928 | 0.473 |
TRG_ER_diArg_1 | 338 | 341 | PF00400 | 0.553 |
TRG_ER_diArg_1 | 504 | 507 | PF00400 | 0.452 |
TRG_ER_diArg_1 | 583 | 586 | PF00400 | 0.765 |
TRG_NES_CRM1_1 | 514 | 529 | PF08389 | 0.595 |
TRG_NLS_MonoExtC_3 | 583 | 588 | PF00514 | 0.779 |
TRG_NLS_MonoExtN_4 | 584 | 589 | PF00514 | 0.786 |
TRG_Pf-PMV_PEXEL_1 | 149 | 153 | PF00026 | 0.538 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PB91 | Leptomonas seymouri | 43% | 76% |
A0A0S4INP1 | Bodo saltans | 27% | 87% |
A0A1X0P9Y1 | Trypanosomatidae | 30% | 90% |
A0A3R7MJM0 | Trypanosoma rangeli | 30% | 94% |
A4HB44 | Leishmania braziliensis | 66% | 98% |
A4IA93 | Leishmania infantum | 99% | 100% |
C9ZM02 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 92% |
E9B5B5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
Q4Q2L8 | Leishmania major | 90% | 100% |
V5BQH0 | Trypanosoma cruzi | 32% | 93% |