| Source | Evidence on protein | Close homologs |
|---|---|---|
| Cuervo et al. | no | yes: 0 |
| Hassani et al. | no | yes: 0 |
| Forrest at al. (metacyclic) | no | yes: 4 |
| Forrest at al. (procyclic) | no | yes: 4 |
| Silverman et al. | no | yes: 0 |
| Pissara et al. | no | yes: 9 |
| 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: 6 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| DeepLoc | ||
| SignalP6 | no | yes: 0, no: 19 |
| NetGPI | no | yes: 0, no: 19 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005886 | plasma membrane | 3 | 20 |
| GO:0016020 | membrane | 2 | 20 |
| GO:0110165 | cellular anatomical entity | 1 | 20 |
| GO:0005737 | cytoplasm | 2 | 2 |
| GO:0043226 | organelle | 2 | 2 |
| GO:0043227 | membrane-bounded organelle | 3 | 2 |
| GO:0043229 | intracellular organelle | 3 | 2 |
| GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
Related structures:
AlphaFold database: E9ARX9
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006810 | transport | 3 | 2 |
| GO:0006897 | endocytosis | 5 | 2 |
| GO:0009987 | cellular process | 1 | 2 |
| GO:0016192 | vesicle-mediated transport | 4 | 2 |
| GO:0016197 | endosomal transport | 4 | 2 |
| GO:0046907 | intracellular transport | 3 | 2 |
| GO:0051179 | localization | 1 | 2 |
| GO:0051234 | establishment of localization | 2 | 2 |
| GO:0051641 | cellular localization | 2 | 2 |
| GO:0051649 | establishment of localization in cell | 3 | 2 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0000166 | nucleotide binding | 3 | 20 |
| GO:0005488 | binding | 1 | 20 |
| GO:0005525 | GTP binding | 5 | 20 |
| GO:0017076 | purine nucleotide binding | 4 | 20 |
| GO:0019001 | guanyl nucleotide binding | 5 | 20 |
| GO:0032553 | ribonucleotide binding | 3 | 20 |
| GO:0032555 | purine ribonucleotide binding | 4 | 20 |
| GO:0032561 | guanyl ribonucleotide binding | 5 | 20 |
| GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 20 |
| GO:0036094 | small molecule binding | 2 | 20 |
| GO:0043167 | ion binding | 2 | 20 |
| GO:0043168 | anion binding | 3 | 20 |
| GO:0097159 | organic cyclic compound binding | 2 | 20 |
| GO:0097367 | carbohydrate derivative binding | 2 | 20 |
| GO:1901265 | nucleoside phosphate binding | 3 | 20 |
| GO:1901363 | heterocyclic compound binding | 2 | 20 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 197 | 201 | PF00656 | 0.369 |
| CLV_NRD_NRD_1 | 171 | 173 | PF00675 | 0.288 |
| CLV_NRD_NRD_1 | 344 | 346 | PF00675 | 0.317 |
| CLV_NRD_NRD_1 | 552 | 554 | PF00675 | 0.492 |
| CLV_PCSK_KEX2_1 | 344 | 346 | PF00082 | 0.317 |
| CLV_PCSK_KEX2_1 | 552 | 554 | PF00082 | 0.488 |
| CLV_PCSK_SKI1_1 | 128 | 132 | PF00082 | 0.274 |
| CLV_PCSK_SKI1_1 | 206 | 210 | PF00082 | 0.366 |
| CLV_PCSK_SKI1_1 | 221 | 225 | PF00082 | 0.317 |
| CLV_PCSK_SKI1_1 | 309 | 313 | PF00082 | 0.270 |
| CLV_PCSK_SKI1_1 | 367 | 371 | PF00082 | 0.295 |
| CLV_Separin_Metazoa | 234 | 238 | PF03568 | 0.333 |
| CLV_Separin_Metazoa | 254 | 258 | PF03568 | 0.345 |
| DEG_APCC_DBOX_1 | 185 | 193 | PF00400 | 0.255 |
| DEG_APCC_DBOX_1 | 321 | 329 | PF00400 | 0.296 |
| DEG_SCF_FBW7_1 | 583 | 590 | PF00400 | 0.709 |
| DEG_SPOP_SBC_1 | 506 | 510 | PF00917 | 0.571 |
| DEG_SPOP_SBC_1 | 522 | 526 | PF00917 | 0.452 |
| DOC_CKS1_1 | 157 | 162 | PF01111 | 0.254 |
| DOC_CKS1_1 | 584 | 589 | PF01111 | 0.651 |
| DOC_CYCLIN_RxL_1 | 123 | 135 | PF00134 | 0.385 |
| DOC_CYCLIN_RxL_1 | 27 | 37 | PF00134 | 0.132 |
| DOC_CYCLIN_yCln2_LP_2 | 70 | 76 | PF00134 | 0.244 |
| DOC_MAPK_gen_1 | 172 | 179 | PF00069 | 0.303 |
| DOC_MAPK_MEF2A_6 | 186 | 194 | PF00069 | 0.228 |
| DOC_MAPK_MEF2A_6 | 322 | 329 | PF00069 | 0.336 |
| DOC_PP4_FxxP_1 | 144 | 147 | PF00568 | 0.334 |
| DOC_PP4_FxxP_1 | 193 | 196 | PF00568 | 0.244 |
| DOC_USP7_MATH_1 | 184 | 188 | PF00917 | 0.255 |
| DOC_USP7_MATH_1 | 365 | 369 | PF00917 | 0.369 |
| DOC_USP7_MATH_1 | 466 | 470 | PF00917 | 0.624 |
| DOC_USP7_MATH_1 | 476 | 480 | PF00917 | 0.622 |
| DOC_USP7_MATH_1 | 489 | 493 | PF00917 | 0.637 |
| DOC_USP7_MATH_1 | 506 | 510 | PF00917 | 0.751 |
| DOC_USP7_MATH_1 | 517 | 521 | PF00917 | 0.530 |
| DOC_USP7_MATH_1 | 522 | 526 | PF00917 | 0.436 |
| DOC_USP7_MATH_1 | 572 | 576 | PF00917 | 0.750 |
| DOC_USP7_MATH_1 | 578 | 582 | PF00917 | 0.713 |
| DOC_USP7_MATH_1 | 587 | 591 | PF00917 | 0.715 |
| DOC_USP7_UBL2_3 | 331 | 335 | PF12436 | 0.275 |
| DOC_WW_Pin1_4 | 156 | 161 | PF00397 | 0.264 |
| DOC_WW_Pin1_4 | 470 | 475 | PF00397 | 0.677 |
| DOC_WW_Pin1_4 | 491 | 496 | PF00397 | 0.716 |
| DOC_WW_Pin1_4 | 497 | 502 | PF00397 | 0.686 |
| DOC_WW_Pin1_4 | 5 | 10 | PF00397 | 0.452 |
| DOC_WW_Pin1_4 | 511 | 516 | PF00397 | 0.493 |
| DOC_WW_Pin1_4 | 523 | 528 | PF00397 | 0.652 |
| DOC_WW_Pin1_4 | 567 | 572 | PF00397 | 0.737 |
| DOC_WW_Pin1_4 | 583 | 588 | PF00397 | 0.569 |
| LIG_14-3-3_CanoR_1 | 153 | 157 | PF00244 | 0.333 |
| LIG_14-3-3_CanoR_1 | 552 | 558 | PF00244 | 0.527 |
| LIG_14-3-3_CanoR_1 | 567 | 571 | PF00244 | 0.502 |
| LIG_14-3-3_CanoR_1 | 65 | 71 | PF00244 | 0.351 |
| LIG_Actin_WH2_2 | 209 | 227 | PF00022 | 0.280 |
| LIG_Actin_WH2_2 | 390 | 408 | PF00022 | 0.339 |
| LIG_APCC_ABBA_1 | 190 | 195 | PF00400 | 0.244 |
| LIG_APCC_ABBA_1 | 426 | 431 | PF00400 | 0.503 |
| LIG_BIR_III_4 | 200 | 204 | PF00653 | 0.312 |
| LIG_BRCT_BRCA1_1 | 273 | 277 | PF00533 | 0.322 |
| LIG_BRCT_BRCA1_1 | 493 | 497 | PF00533 | 0.529 |
| LIG_EH_1 | 414 | 418 | PF12763 | 0.592 |
| LIG_eIF4E_1 | 429 | 435 | PF01652 | 0.284 |
| LIG_FHA_1 | 157 | 163 | PF00498 | 0.254 |
| LIG_FHA_1 | 230 | 236 | PF00498 | 0.335 |
| LIG_FHA_1 | 35 | 41 | PF00498 | 0.403 |
| LIG_FHA_1 | 421 | 427 | PF00498 | 0.566 |
| LIG_FHA_1 | 445 | 451 | PF00498 | 0.551 |
| LIG_FHA_1 | 77 | 83 | PF00498 | 0.408 |
| LIG_FHA_2 | 153 | 159 | PF00498 | 0.247 |
| LIG_FHA_2 | 584 | 590 | PF00498 | 0.539 |
| LIG_FHA_2 | 617 | 623 | PF00498 | 0.510 |
| LIG_FHA_2 | 96 | 102 | PF00498 | 0.240 |
| LIG_FXI_DFP_1 | 357 | 361 | PF00024 | 0.255 |
| LIG_GBD_Chelix_1 | 317 | 325 | PF00786 | 0.214 |
| LIG_LIR_Apic_2 | 262 | 267 | PF02991 | 0.342 |
| LIG_LIR_Gen_1 | 175 | 184 | PF02991 | 0.285 |
| LIG_LIR_Gen_1 | 188 | 199 | PF02991 | 0.258 |
| LIG_LIR_Gen_1 | 272 | 278 | PF02991 | 0.382 |
| LIG_LIR_Gen_1 | 48 | 57 | PF02991 | 0.415 |
| LIG_LIR_Gen_1 | 64 | 73 | PF02991 | 0.430 |
| LIG_LIR_Gen_1 | 99 | 107 | PF02991 | 0.264 |
| LIG_LIR_Nem_3 | 175 | 179 | PF02991 | 0.276 |
| LIG_LIR_Nem_3 | 188 | 194 | PF02991 | 0.220 |
| LIG_LIR_Nem_3 | 211 | 216 | PF02991 | 0.450 |
| LIG_LIR_Nem_3 | 241 | 246 | PF02991 | 0.360 |
| LIG_LIR_Nem_3 | 272 | 276 | PF02991 | 0.380 |
| LIG_LIR_Nem_3 | 359 | 363 | PF02991 | 0.291 |
| LIG_LIR_Nem_3 | 419 | 425 | PF02991 | 0.409 |
| LIG_LIR_Nem_3 | 48 | 52 | PF02991 | 0.433 |
| LIG_LIR_Nem_3 | 64 | 70 | PF02991 | 0.316 |
| LIG_LIR_Nem_3 | 79 | 84 | PF02991 | 0.272 |
| LIG_LIR_Nem_3 | 99 | 105 | PF02991 | 0.254 |
| LIG_NRBOX | 284 | 290 | PF00104 | 0.422 |
| LIG_Pex14_1 | 264 | 268 | PF04695 | 0.345 |
| LIG_Pex14_2 | 133 | 137 | PF04695 | 0.264 |
| LIG_Pex14_2 | 209 | 213 | PF04695 | 0.296 |
| LIG_Pex14_2 | 273 | 277 | PF04695 | 0.356 |
| LIG_Pex14_2 | 52 | 56 | PF04695 | 0.283 |
| LIG_Pex14_2 | 67 | 71 | PF04695 | 0.229 |
| LIG_SH2_CRK | 174 | 178 | PF00017 | 0.274 |
| LIG_SH2_CRK | 239 | 243 | PF00017 | 0.326 |
| LIG_SH2_NCK_1 | 346 | 350 | PF00017 | 0.327 |
| LIG_SH2_PTP2 | 176 | 179 | PF00017 | 0.299 |
| LIG_SH2_SRC | 174 | 177 | PF00017 | 0.336 |
| LIG_SH2_STAP1 | 36 | 40 | PF00017 | 0.403 |
| LIG_SH2_STAP1 | 57 | 61 | PF00017 | 0.345 |
| LIG_SH2_STAT3 | 543 | 546 | PF00017 | 0.452 |
| LIG_SH2_STAT3 | 84 | 87 | PF00017 | 0.299 |
| LIG_SH2_STAT5 | 132 | 135 | PF00017 | 0.150 |
| LIG_SH2_STAT5 | 176 | 179 | PF00017 | 0.286 |
| LIG_SH2_STAT5 | 259 | 262 | PF00017 | 0.310 |
| LIG_SH2_STAT5 | 36 | 39 | PF00017 | 0.290 |
| LIG_SH2_STAT5 | 84 | 87 | PF00017 | 0.273 |
| LIG_SH3_3 | 143 | 149 | PF00018 | 0.322 |
| LIG_SH3_3 | 264 | 270 | PF00018 | 0.369 |
| LIG_SH3_3 | 513 | 519 | PF00018 | 0.717 |
| LIG_SH3_3 | 581 | 587 | PF00018 | 0.661 |
| LIG_SH3_3 | 602 | 608 | PF00018 | 0.635 |
| LIG_SUMO_SIM_anti_2 | 152 | 159 | PF11976 | 0.278 |
| LIG_SUMO_SIM_anti_2 | 279 | 287 | PF11976 | 0.406 |
| LIG_TRAF2_1 | 231 | 234 | PF00917 | 0.482 |
| LIG_TRAF2_1 | 416 | 419 | PF00917 | 0.414 |
| LIG_TRAF2_1 | 42 | 45 | PF00917 | 0.385 |
| LIG_TRAF2_1 | 586 | 589 | PF00917 | 0.569 |
| LIG_TRAF2_2 | 293 | 298 | PF00917 | 0.340 |
| LIG_WRC_WIRS_1 | 260 | 265 | PF05994 | 0.323 |
| LIG_WRC_WIRS_1 | 366 | 371 | PF05994 | 0.220 |
| LIG_WRC_WIRS_1 | 46 | 51 | PF05994 | 0.214 |
| LIG_WW_2 | 516 | 519 | PF00397 | 0.458 |
| LIG_WW_3 | 254 | 258 | PF00397 | 0.345 |
| MOD_CK1_1 | 24 | 30 | PF00069 | 0.400 |
| MOD_CK1_1 | 48 | 54 | PF00069 | 0.197 |
| MOD_CK1_1 | 491 | 497 | PF00069 | 0.614 |
| MOD_CK1_1 | 521 | 527 | PF00069 | 0.559 |
| MOD_CK1_1 | 563 | 569 | PF00069 | 0.578 |
| MOD_CK2_1 | 228 | 234 | PF00069 | 0.459 |
| MOD_CK2_1 | 365 | 371 | PF00069 | 0.262 |
| MOD_CK2_1 | 52 | 58 | PF00069 | 0.267 |
| MOD_CK2_1 | 583 | 589 | PF00069 | 0.718 |
| MOD_CK2_1 | 95 | 101 | PF00069 | 0.240 |
| MOD_DYRK1A_RPxSP_1 | 567 | 571 | PF00069 | 0.479 |
| MOD_GlcNHglycan | 164 | 167 | PF01048 | 0.361 |
| MOD_GlcNHglycan | 460 | 463 | PF01048 | 0.593 |
| MOD_GlcNHglycan | 491 | 494 | PF01048 | 0.672 |
| MOD_GlcNHglycan | 520 | 523 | PF01048 | 0.702 |
| MOD_GlcNHglycan | 555 | 558 | PF01048 | 0.714 |
| MOD_GlcNHglycan | 574 | 577 | PF01048 | 0.708 |
| MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.264 |
| MOD_GSK3_1 | 152 | 159 | PF00069 | 0.303 |
| MOD_GSK3_1 | 17 | 24 | PF00069 | 0.541 |
| MOD_GSK3_1 | 396 | 403 | PF00069 | 0.398 |
| MOD_GSK3_1 | 420 | 427 | PF00069 | 0.466 |
| MOD_GSK3_1 | 460 | 467 | PF00069 | 0.628 |
| MOD_GSK3_1 | 48 | 55 | PF00069 | 0.157 |
| MOD_GSK3_1 | 489 | 496 | PF00069 | 0.534 |
| MOD_GSK3_1 | 507 | 514 | PF00069 | 0.703 |
| MOD_GSK3_1 | 517 | 524 | PF00069 | 0.668 |
| MOD_GSK3_1 | 553 | 560 | PF00069 | 0.736 |
| MOD_GSK3_1 | 563 | 570 | PF00069 | 0.695 |
| MOD_GSK3_1 | 579 | 586 | PF00069 | 0.590 |
| MOD_GSK3_1 | 587 | 594 | PF00069 | 0.603 |
| MOD_GSK3_1 | 72 | 79 | PF00069 | 0.278 |
| MOD_GSK3_1 | 96 | 103 | PF00069 | 0.278 |
| MOD_N-GLC_1 | 244 | 249 | PF02516 | 0.345 |
| MOD_N-GLC_1 | 250 | 255 | PF02516 | 0.370 |
| MOD_NEK2_1 | 119 | 124 | PF00069 | 0.344 |
| MOD_NEK2_1 | 133 | 138 | PF00069 | 0.279 |
| MOD_NEK2_1 | 208 | 213 | PF00069 | 0.355 |
| MOD_NEK2_1 | 329 | 334 | PF00069 | 0.405 |
| MOD_NEK2_1 | 34 | 39 | PF00069 | 0.225 |
| MOD_NEK2_1 | 396 | 401 | PF00069 | 0.422 |
| MOD_NEK2_1 | 505 | 510 | PF00069 | 0.755 |
| MOD_NEK2_1 | 85 | 90 | PF00069 | 0.392 |
| MOD_NEK2_2 | 424 | 429 | PF00069 | 0.411 |
| MOD_NEK2_2 | 66 | 71 | PF00069 | 0.255 |
| MOD_PIKK_1 | 229 | 235 | PF00454 | 0.338 |
| MOD_PIKK_1 | 34 | 40 | PF00454 | 0.244 |
| MOD_PIKK_1 | 495 | 501 | PF00454 | 0.568 |
| MOD_PIKK_1 | 610 | 616 | PF00454 | 0.536 |
| MOD_PKA_1 | 552 | 558 | PF00069 | 0.440 |
| MOD_PKA_2 | 14 | 20 | PF00069 | 0.706 |
| MOD_PKA_2 | 152 | 158 | PF00069 | 0.299 |
| MOD_PKA_2 | 52 | 58 | PF00069 | 0.274 |
| MOD_PKA_2 | 551 | 557 | PF00069 | 0.516 |
| MOD_PKA_2 | 566 | 572 | PF00069 | 0.472 |
| MOD_Plk_1 | 100 | 106 | PF00069 | 0.241 |
| MOD_Plk_1 | 57 | 63 | PF00069 | 0.353 |
| MOD_Plk_1 | 579 | 585 | PF00069 | 0.704 |
| MOD_Plk_2-3 | 152 | 158 | PF00069 | 0.356 |
| MOD_Plk_2-3 | 45 | 51 | PF00069 | 0.367 |
| MOD_Plk_4 | 133 | 139 | PF00069 | 0.274 |
| MOD_Plk_4 | 152 | 158 | PF00069 | 0.296 |
| MOD_Plk_4 | 238 | 244 | PF00069 | 0.362 |
| MOD_Plk_4 | 24 | 30 | PF00069 | 0.414 |
| MOD_Plk_4 | 259 | 265 | PF00069 | 0.335 |
| MOD_Plk_4 | 300 | 306 | PF00069 | 0.274 |
| MOD_Plk_4 | 396 | 402 | PF00069 | 0.306 |
| MOD_Plk_4 | 424 | 430 | PF00069 | 0.479 |
| MOD_Plk_4 | 477 | 483 | PF00069 | 0.555 |
| MOD_Plk_4 | 52 | 58 | PF00069 | 0.281 |
| MOD_Plk_4 | 77 | 83 | PF00069 | 0.276 |
| MOD_ProDKin_1 | 156 | 162 | PF00069 | 0.264 |
| MOD_ProDKin_1 | 470 | 476 | PF00069 | 0.672 |
| MOD_ProDKin_1 | 491 | 497 | PF00069 | 0.692 |
| MOD_ProDKin_1 | 5 | 11 | PF00069 | 0.450 |
| MOD_ProDKin_1 | 511 | 517 | PF00069 | 0.517 |
| MOD_ProDKin_1 | 523 | 529 | PF00069 | 0.647 |
| MOD_ProDKin_1 | 567 | 573 | PF00069 | 0.737 |
| MOD_ProDKin_1 | 583 | 589 | PF00069 | 0.570 |
| MOD_SUMO_rev_2 | 274 | 282 | PF00179 | 0.404 |
| MOD_SUMO_rev_2 | 418 | 423 | PF00179 | 0.513 |
| TRG_DiLeu_BaEn_1 | 152 | 157 | PF01217 | 0.397 |
| TRG_DiLeu_BaEn_1 | 185 | 190 | PF01217 | 0.274 |
| TRG_DiLeu_BaEn_1 | 280 | 285 | PF01217 | 0.307 |
| TRG_DiLeu_BaEn_1 | 385 | 390 | PF01217 | 0.447 |
| TRG_DiLeu_BaLyEn_6 | 146 | 151 | PF01217 | 0.245 |
| TRG_ENDOCYTIC_2 | 174 | 177 | PF00928 | 0.269 |
| TRG_ENDOCYTIC_2 | 239 | 242 | PF00928 | 0.327 |
| TRG_ENDOCYTIC_2 | 346 | 349 | PF00928 | 0.272 |
| TRG_ENDOCYTIC_2 | 366 | 369 | PF00928 | 0.117 |
| TRG_ER_diArg_1 | 219 | 222 | PF00400 | 0.421 |
| TRG_ER_diArg_1 | 343 | 345 | PF00400 | 0.433 |
| TRG_ER_diArg_1 | 39 | 42 | PF00400 | 0.267 |
| TRG_NES_CRM1_1 | 280 | 295 | PF08389 | 0.452 |
| TRG_NLS_MonoExtC_3 | 334 | 340 | PF00514 | 0.274 |
| TRG_NLS_MonoExtN_4 | 333 | 339 | PF00514 | 0.255 |
| TRG_Pf-PMV_PEXEL_1 | 206 | 210 | PF00026 | 0.324 |
| TRG_Pf-PMV_PEXEL_1 | 391 | 395 | PF00026 | 0.244 |
| TRG_Pf-PMV_PEXEL_1 | 41 | 45 | PF00026 | 0.379 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P8K7 | Leptomonas seymouri | 79% | 100% |
| A0A0N0P9A4 | Leptomonas seymouri | 44% | 100% |
| A0A0S4KGM0 | Bodo saltans | 64% | 100% |
| A0A1X0P6D7 | Trypanosomatidae | 65% | 100% |
| A0A1X0P9Q8 | Trypanosomatidae | 47% | 100% |
| A0A3R7LDF3 | Trypanosoma rangeli | 62% | 100% |
| A0A3S7WV81 | Leishmania donovani | 87% | 100% |
| A0A3S7X801 | Leishmania donovani | 41% | 100% |
| A0A422P0G8 | Trypanosoma rangeli | 44% | 100% |
| A4H9Y5 | Leishmania braziliensis | 75% | 100% |
| A4HAT9 | Leishmania braziliensis | 45% | 100% |
| A4HY50 | Leishmania infantum | 87% | 100% |
| A4IA07 | Leishmania infantum | 41% | 100% |
| D0A0F1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 100% |
| E9B513 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 44% | 100% |
| Q4Q2X3 | Leishmania major | 43% | 100% |
| Q4QDJ3 | Leishmania major | 86% | 100% |
| Q4V8H8 | Rattus norvegicus | 35% | 100% |
| V5BSA9 | Trypanosoma cruzi | 60% | 100% |