Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 2 |
Forrest at al. (procyclic) | no | yes: 2 |
Silverman et al. | yes | yes: 2 |
Pissara et al. | yes | yes: 8 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | yes | yes: 4 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 4 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005856 | cytoskeleton | 5 | 2 |
GO:0005871 | kinesin complex | 3 | 2 |
GO:0005874 | microtubule | 6 | 2 |
GO:0005875 | microtubule associated complex | 2 | 2 |
GO:0015630 | microtubule cytoskeleton | 6 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043228 | non-membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 2 |
GO:0051286 | cell tip | 3 | 2 |
GO:0060187 | cell pole | 2 | 2 |
GO:0099080 | supramolecular complex | 2 | 2 |
GO:0099081 | supramolecular polymer | 3 | 2 |
GO:0099512 | supramolecular fiber | 4 | 2 |
GO:0099513 | polymeric cytoskeletal fiber | 5 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4Q0P7
Term | Name | Level | Count |
---|---|---|---|
GO:0000226 | microtubule cytoskeleton organization | 3 | 2 |
GO:0000902 | cell morphogenesis | 3 | 2 |
GO:0006996 | organelle organization | 4 | 2 |
GO:0007010 | cytoskeleton organization | 5 | 2 |
GO:0007017 | microtubule-based process | 2 | 13 |
GO:0007018 | microtubule-based movement | 3 | 13 |
GO:0009653 | anatomical structure morphogenesis | 2 | 2 |
GO:0009987 | cellular process | 1 | 13 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0030865 | cortical cytoskeleton organization | 6 | 2 |
GO:0031122 | cytoplasmic microtubule organization | 4 | 2 |
GO:0032502 | developmental process | 1 | 2 |
GO:0043622 | cortical microtubule organization | 5 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
GO:0097435 | supramolecular fiber organization | 4 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 13 |
GO:0003774 | cytoskeletal motor activity | 1 | 13 |
GO:0003777 | microtubule motor activity | 2 | 13 |
GO:0003824 | catalytic activity | 1 | 2 |
GO:0005488 | binding | 1 | 13 |
GO:0005515 | protein binding | 2 | 13 |
GO:0005524 | ATP binding | 5 | 13 |
GO:0008017 | microtubule binding | 5 | 13 |
GO:0008092 | cytoskeletal protein binding | 3 | 13 |
GO:0015631 | tubulin binding | 4 | 13 |
GO:0016462 | pyrophosphatase activity | 5 | 2 |
GO:0016787 | hydrolase activity | 2 | 2 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 2 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 2 |
GO:0016887 | ATP hydrolysis activity | 7 | 2 |
GO:0017076 | purine nucleotide binding | 4 | 13 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 2 |
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:0140657 | ATP-dependent activity | 1 | 13 |
GO:1901265 | nucleoside phosphate binding | 3 | 13 |
GO:1901363 | heterocyclic compound binding | 2 | 13 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 191 | 195 | PF00656 | 0.433 |
CLV_NRD_NRD_1 | 265 | 267 | PF00675 | 0.466 |
CLV_NRD_NRD_1 | 367 | 369 | PF00675 | 0.618 |
CLV_NRD_NRD_1 | 380 | 382 | PF00675 | 0.597 |
CLV_NRD_NRD_1 | 439 | 441 | PF00675 | 0.683 |
CLV_NRD_NRD_1 | 528 | 530 | PF00675 | 0.791 |
CLV_NRD_NRD_1 | 58 | 60 | PF00675 | 0.553 |
CLV_NRD_NRD_1 | 607 | 609 | PF00675 | 0.620 |
CLV_PCSK_KEX2_1 | 234 | 236 | PF00082 | 0.554 |
CLV_PCSK_KEX2_1 | 265 | 267 | PF00082 | 0.466 |
CLV_PCSK_KEX2_1 | 367 | 369 | PF00082 | 0.650 |
CLV_PCSK_KEX2_1 | 450 | 452 | PF00082 | 0.628 |
CLV_PCSK_KEX2_1 | 469 | 471 | PF00082 | 0.598 |
CLV_PCSK_KEX2_1 | 528 | 530 | PF00082 | 0.759 |
CLV_PCSK_KEX2_1 | 539 | 541 | PF00082 | 0.748 |
CLV_PCSK_KEX2_1 | 58 | 60 | PF00082 | 0.641 |
CLV_PCSK_KEX2_1 | 607 | 609 | PF00082 | 0.656 |
CLV_PCSK_PC1ET2_1 | 234 | 236 | PF00082 | 0.569 |
CLV_PCSK_PC1ET2_1 | 450 | 452 | PF00082 | 0.674 |
CLV_PCSK_PC1ET2_1 | 469 | 471 | PF00082 | 0.567 |
CLV_PCSK_PC1ET2_1 | 539 | 541 | PF00082 | 0.800 |
CLV_PCSK_PC7_1 | 230 | 236 | PF00082 | 0.531 |
CLV_PCSK_SKI1_1 | 138 | 142 | PF00082 | 0.420 |
CLV_PCSK_SKI1_1 | 17 | 21 | PF00082 | 0.551 |
CLV_PCSK_SKI1_1 | 349 | 353 | PF00082 | 0.556 |
CLV_PCSK_SKI1_1 | 35 | 39 | PF00082 | 0.421 |
CLV_PCSK_SKI1_1 | 423 | 427 | PF00082 | 0.624 |
CLV_PCSK_SKI1_1 | 528 | 532 | PF00082 | 0.755 |
CLV_PCSK_SKI1_1 | 87 | 91 | PF00082 | 0.466 |
DOC_CKS1_1 | 18 | 23 | PF01111 | 0.622 |
DOC_CKS1_1 | 199 | 204 | PF01111 | 0.517 |
DOC_MAPK_gen_1 | 263 | 272 | PF00069 | 0.483 |
DOC_MAPK_gen_1 | 381 | 389 | PF00069 | 0.681 |
DOC_MAPK_MEF2A_6 | 263 | 271 | PF00069 | 0.498 |
DOC_MAPK_RevD_3 | 219 | 235 | PF00069 | 0.479 |
DOC_PP4_FxxP_1 | 251 | 254 | PF00568 | 0.568 |
DOC_PP4_FxxP_1 | 72 | 75 | PF00568 | 0.677 |
DOC_PP4_FxxP_1 | 98 | 101 | PF00568 | 0.316 |
DOC_USP7_MATH_1 | 117 | 121 | PF00917 | 0.466 |
DOC_USP7_MATH_1 | 214 | 218 | PF00917 | 0.453 |
DOC_USP7_MATH_1 | 28 | 32 | PF00917 | 0.700 |
DOC_USP7_MATH_1 | 579 | 583 | PF00917 | 0.771 |
DOC_USP7_UBL2_3 | 81 | 85 | PF12436 | 0.834 |
DOC_WW_Pin1_4 | 17 | 22 | PF00397 | 0.547 |
DOC_WW_Pin1_4 | 198 | 203 | PF00397 | 0.502 |
DOC_WW_Pin1_4 | 215 | 220 | PF00397 | 0.462 |
DOC_WW_Pin1_4 | 326 | 331 | PF00397 | 0.444 |
DOC_WW_Pin1_4 | 520 | 525 | PF00397 | 0.723 |
LIG_14-3-3_CanoR_1 | 124 | 129 | PF00244 | 0.411 |
LIG_14-3-3_CanoR_1 | 235 | 243 | PF00244 | 0.533 |
LIG_14-3-3_CanoR_1 | 244 | 251 | PF00244 | 0.561 |
LIG_14-3-3_CanoR_1 | 381 | 389 | PF00244 | 0.653 |
LIG_14-3-3_CanoR_1 | 552 | 558 | PF00244 | 0.828 |
LIG_14-3-3_CanoR_1 | 87 | 95 | PF00244 | 0.512 |
LIG_APCC_ABBA_1 | 328 | 333 | PF00400 | 0.485 |
LIG_BRCT_BRCA1_1 | 241 | 245 | PF00533 | 0.557 |
LIG_CaM_IQ_9 | 222 | 237 | PF13499 | 0.573 |
LIG_CaM_IQ_9 | 339 | 354 | PF13499 | 0.623 |
LIG_deltaCOP1_diTrp_1 | 67 | 72 | PF00928 | 0.624 |
LIG_FHA_1 | 216 | 222 | PF00498 | 0.526 |
LIG_FHA_1 | 236 | 242 | PF00498 | 0.401 |
LIG_FHA_1 | 511 | 517 | PF00498 | 0.819 |
LIG_FHA_2 | 173 | 179 | PF00498 | 0.448 |
LIG_FHA_2 | 18 | 24 | PF00498 | 0.543 |
LIG_FHA_2 | 189 | 195 | PF00498 | 0.469 |
LIG_FHA_2 | 409 | 415 | PF00498 | 0.646 |
LIG_FHA_2 | 552 | 558 | PF00498 | 0.733 |
LIG_FHA_2 | 600 | 606 | PF00498 | 0.634 |
LIG_FHA_2 | 88 | 94 | PF00498 | 0.432 |
LIG_KLC1_Yacidic_2 | 174 | 178 | PF13176 | 0.469 |
LIG_LIR_Apic_2 | 248 | 254 | PF02991 | 0.547 |
LIG_LIR_Apic_2 | 71 | 75 | PF02991 | 0.664 |
LIG_LIR_Gen_1 | 12 | 21 | PF02991 | 0.550 |
LIG_LIR_Gen_1 | 174 | 181 | PF02991 | 0.405 |
LIG_LIR_Gen_1 | 305 | 316 | PF02991 | 0.483 |
LIG_LIR_Gen_1 | 329 | 339 | PF02991 | 0.564 |
LIG_LIR_Gen_1 | 360 | 370 | PF02991 | 0.696 |
LIG_LIR_Gen_1 | 456 | 464 | PF02991 | 0.655 |
LIG_LIR_Gen_1 | 93 | 103 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 12 | 16 | PF02991 | 0.534 |
LIG_LIR_Nem_3 | 174 | 179 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 305 | 311 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 93 | 98 | PF02991 | 0.436 |
LIG_NRBOX | 269 | 275 | PF00104 | 0.465 |
LIG_Pex14_2 | 245 | 249 | PF04695 | 0.516 |
LIG_Pex14_2 | 308 | 312 | PF04695 | 0.544 |
LIG_SH2_NCK_1 | 110 | 114 | PF00017 | 0.429 |
LIG_SH2_NCK_1 | 572 | 576 | PF00017 | 0.672 |
LIG_SH2_PTP2 | 176 | 179 | PF00017 | 0.448 |
LIG_SH2_SRC | 572 | 575 | PF00017 | 0.653 |
LIG_SH2_STAP1 | 499 | 503 | PF00017 | 0.757 |
LIG_SH2_STAP1 | 572 | 576 | PF00017 | 0.693 |
LIG_SH2_STAP1 | 595 | 599 | PF00017 | 0.719 |
LIG_SH2_STAT5 | 126 | 129 | PF00017 | 0.478 |
LIG_SH2_STAT5 | 176 | 179 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 54 | 57 | PF00017 | 0.597 |
LIG_SH3_1 | 15 | 21 | PF00018 | 0.599 |
LIG_SH3_3 | 15 | 21 | PF00018 | 0.599 |
LIG_SH3_3 | 199 | 205 | PF00018 | 0.471 |
LIG_SH3_3 | 45 | 51 | PF00018 | 0.590 |
LIG_SH3_3 | 518 | 524 | PF00018 | 0.752 |
LIG_SH3_3 | 98 | 104 | PF00018 | 0.432 |
LIG_SUMO_SIM_anti_2 | 174 | 182 | PF11976 | 0.438 |
LIG_SUMO_SIM_anti_2 | 385 | 391 | PF11976 | 0.689 |
LIG_SUMO_SIM_anti_2 | 398 | 403 | PF11976 | 0.429 |
LIG_SUMO_SIM_par_1 | 44 | 50 | PF11976 | 0.495 |
LIG_TRAF2_1 | 71 | 74 | PF00917 | 0.641 |
LIG_TRAF2_1 | 75 | 78 | PF00917 | 0.734 |
LIG_WRC_WIRS_1 | 149 | 154 | PF05994 | 0.472 |
LIG_WRC_WIRS_1 | 69 | 74 | PF05994 | 0.519 |
MOD_CK1_1 | 151 | 157 | PF00069 | 0.517 |
MOD_CK1_1 | 160 | 166 | PF00069 | 0.447 |
MOD_CK1_1 | 172 | 178 | PF00069 | 0.462 |
MOD_CK1_1 | 188 | 194 | PF00069 | 0.471 |
MOD_CK1_1 | 200 | 206 | PF00069 | 0.504 |
MOD_CK1_1 | 237 | 243 | PF00069 | 0.516 |
MOD_CK1_1 | 306 | 312 | PF00069 | 0.528 |
MOD_CK1_1 | 326 | 332 | PF00069 | 0.492 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.688 |
MOD_CK2_1 | 128 | 134 | PF00069 | 0.529 |
MOD_CK2_1 | 17 | 23 | PF00069 | 0.524 |
MOD_CK2_1 | 214 | 220 | PF00069 | 0.499 |
MOD_CK2_1 | 359 | 365 | PF00069 | 0.649 |
MOD_CK2_1 | 408 | 414 | PF00069 | 0.625 |
MOD_CK2_1 | 520 | 526 | PF00069 | 0.691 |
MOD_CK2_1 | 551 | 557 | PF00069 | 0.730 |
MOD_CK2_1 | 599 | 605 | PF00069 | 0.705 |
MOD_CK2_1 | 68 | 74 | PF00069 | 0.587 |
MOD_DYRK1A_RPxSP_1 | 17 | 21 | PF00069 | 0.614 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.431 |
MOD_GlcNHglycan | 170 | 174 | PF01048 | 0.550 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.559 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.518 |
MOD_GlcNHglycan | 278 | 281 | PF01048 | 0.578 |
MOD_GlcNHglycan | 29 | 33 | PF01048 | 0.704 |
MOD_GlcNHglycan | 292 | 295 | PF01048 | 0.413 |
MOD_GlcNHglycan | 305 | 308 | PF01048 | 0.487 |
MOD_GlcNHglycan | 532 | 535 | PF01048 | 0.834 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.760 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.443 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.469 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.495 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.512 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.640 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.588 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.775 |
MOD_N-GLC_1 | 158 | 163 | PF02516 | 0.444 |
MOD_N-GLC_1 | 235 | 240 | PF02516 | 0.614 |
MOD_N-GLC_1 | 257 | 262 | PF02516 | 0.687 |
MOD_N-GLC_1 | 408 | 413 | PF02516 | 0.650 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.754 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.529 |
MOD_NEK2_1 | 342 | 347 | PF00069 | 0.582 |
MOD_NEK2_1 | 530 | 535 | PF00069 | 0.827 |
MOD_NEK2_2 | 76 | 81 | PF00069 | 0.685 |
MOD_PIKK_1 | 558 | 564 | PF00454 | 0.577 |
MOD_PIKK_1 | 599 | 605 | PF00454 | 0.713 |
MOD_PIKK_1 | 615 | 621 | PF00454 | 0.691 |
MOD_PIKK_1 | 87 | 93 | PF00454 | 0.446 |
MOD_PKA_1 | 234 | 240 | PF00069 | 0.531 |
MOD_PKA_1 | 615 | 621 | PF00069 | 0.720 |
MOD_PKA_2 | 234 | 240 | PF00069 | 0.539 |
MOD_PKA_2 | 243 | 249 | PF00069 | 0.529 |
MOD_PKA_2 | 303 | 309 | PF00069 | 0.470 |
MOD_PKA_2 | 380 | 386 | PF00069 | 0.665 |
MOD_PKA_2 | 551 | 557 | PF00069 | 0.823 |
MOD_Plk_1 | 158 | 164 | PF00069 | 0.423 |
MOD_Plk_1 | 257 | 263 | PF00069 | 0.677 |
MOD_Plk_1 | 28 | 34 | PF00069 | 0.685 |
MOD_Plk_1 | 359 | 365 | PF00069 | 0.666 |
MOD_Plk_1 | 408 | 414 | PF00069 | 0.641 |
MOD_Plk_1 | 76 | 82 | PF00069 | 0.773 |
MOD_Plk_4 | 124 | 130 | PF00069 | 0.405 |
MOD_Plk_4 | 172 | 178 | PF00069 | 0.422 |
MOD_Plk_4 | 311 | 317 | PF00069 | 0.547 |
MOD_Plk_4 | 359 | 365 | PF00069 | 0.666 |
MOD_Plk_4 | 385 | 391 | PF00069 | 0.623 |
MOD_ProDKin_1 | 17 | 23 | PF00069 | 0.543 |
MOD_ProDKin_1 | 198 | 204 | PF00069 | 0.502 |
MOD_ProDKin_1 | 215 | 221 | PF00069 | 0.462 |
MOD_ProDKin_1 | 326 | 332 | PF00069 | 0.453 |
MOD_ProDKin_1 | 520 | 526 | PF00069 | 0.722 |
MOD_SUMO_for_1 | 402 | 405 | PF00179 | 0.605 |
MOD_SUMO_for_1 | 511 | 514 | PF00179 | 0.637 |
MOD_SUMO_for_1 | 593 | 596 | PF00179 | 0.655 |
MOD_SUMO_rev_2 | 371 | 376 | PF00179 | 0.576 |
MOD_SUMO_rev_2 | 379 | 383 | PF00179 | 0.566 |
MOD_SUMO_rev_2 | 474 | 480 | PF00179 | 0.657 |
MOD_SUMO_rev_2 | 508 | 513 | PF00179 | 0.763 |
MOD_SUMO_rev_2 | 533 | 541 | PF00179 | 0.830 |
MOD_SUMO_rev_2 | 611 | 618 | PF00179 | 0.662 |
TRG_DiLeu_BaEn_1 | 526 | 531 | PF01217 | 0.736 |
TRG_DiLeu_LyEn_5 | 526 | 531 | PF01217 | 0.736 |
TRG_ENDOCYTIC_2 | 176 | 179 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 332 | 335 | PF00928 | 0.622 |
TRG_ENDOCYTIC_2 | 54 | 57 | PF00928 | 0.597 |
TRG_ENDOCYTIC_2 | 95 | 98 | PF00928 | 0.411 |
TRG_ER_diArg_1 | 14 | 17 | PF00400 | 0.458 |
TRG_ER_diArg_1 | 265 | 267 | PF00400 | 0.466 |
TRG_ER_diArg_1 | 366 | 368 | PF00400 | 0.651 |
TRG_ER_diArg_1 | 528 | 530 | PF00400 | 0.736 |
TRG_ER_diArg_1 | 57 | 59 | PF00400 | 0.648 |
TRG_ER_diArg_1 | 606 | 608 | PF00400 | 0.662 |
TRG_NLS_MonoExtC_3 | 83 | 88 | PF00514 | 0.550 |
TRG_NLS_MonoExtN_4 | 347 | 353 | PF00514 | 0.629 |
TRG_NLS_MonoExtN_4 | 81 | 88 | PF00514 | 0.565 |
TRG_Pf-PMV_PEXEL_1 | 35 | 39 | PF00026 | 0.589 |
TRG_Pf-PMV_PEXEL_1 | 367 | 371 | PF00026 | 0.573 |
TRG_Pf-PMV_PEXEL_1 | 607 | 611 | PF00026 | 0.603 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1K9 | Leptomonas seymouri | 69% | 100% |
A0A0S4J0Q2 | Bodo saltans | 21% | 75% |
A0A0S4JFN9 | Bodo saltans | 25% | 73% |
A0A0S4JPE8 | Bodo saltans | 34% | 69% |
A0A1X0NP27 | Trypanosomatidae | 21% | 84% |
A0A1X0NPH9 | Trypanosomatidae | 21% | 68% |
A0A1X0P435 | Trypanosomatidae | 43% | 100% |
A0A3R7KHX7 | Trypanosoma rangeli | 22% | 85% |
A0A3S7WU64 | Leishmania donovani | 22% | 72% |
A0A3S7XBW9 | Leishmania donovani | 94% | 100% |
A0A422NMD1 | Trypanosoma rangeli | 45% | 100% |
A4HQ31 | Leishmania braziliensis | 74% | 100% |
A4HX45 | Leishmania infantum | 22% | 79% |
A4IDT7 | Leishmania infantum | 94% | 100% |
C9ZV26 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 22% | 83% |
D0A8T5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
E9ATU9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
P46873 | Caenorhabditis elegans | 22% | 89% |
Q1MTQ1 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 24% | 100% |
Q4QEL8 | Leishmania major | 22% | 77% |
V5B325 | Trypanosoma cruzi | 22% | 75% |
V5B6Q5 | Trypanosoma cruzi | 45% | 100% |
V5D733 | Trypanosoma cruzi | 23% | 83% |