| Source | Evidence on protein | Close homologs |
|---|---|---|
| Cuervo et al. | no | yes: 1 |
| 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: 10 |
| 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: 5 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| DeepLoc | ||
| SignalP6 | no | yes: 0, no: 11 |
| NetGPI | no | yes: 0, no: 11 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005737 | cytoplasm | 2 | 2 |
| GO:0005852 | eukaryotic translation initiation factor 3 complex | 2 | 12 |
| GO:0016282 | eukaryotic 43S preinitiation complex | 4 | 12 |
| GO:0032991 | protein-containing complex | 1 | 12 |
| GO:0033290 | eukaryotic 48S preinitiation complex | 4 | 12 |
| GO:0070993 | translation preinitiation complex | 3 | 12 |
| GO:0071541 | eukaryotic translation initiation factor 3 complex, eIF3m | 3 | 2 |
| GO:0110165 | cellular anatomical entity | 1 | 2 |
| GO:1990904 | ribonucleoprotein complex | 2 | 12 |
Related structures:
AlphaFold database: Q4Q127
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0001732 | formation of cytoplasmic translation initiation complex | 7 | 12 |
| GO:0002183 | cytoplasmic translational initiation | 4 | 2 |
| GO:0006413 | translational initiation | 3 | 2 |
| GO:0006417 | regulation of translation | 6 | 2 |
| GO:0006446 | regulation of translational initiation | 7 | 2 |
| GO:0008152 | metabolic process | 1 | 2 |
| GO:0009889 | regulation of biosynthetic process | 4 | 2 |
| GO:0009987 | cellular process | 1 | 12 |
| GO:0010468 | regulation of gene expression | 5 | 2 |
| GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 2 |
| GO:0010608 | post-transcriptional regulation of gene expression | 6 | 2 |
| GO:0016043 | cellular component organization | 3 | 12 |
| GO:0019222 | regulation of metabolic process | 3 | 2 |
| GO:0022607 | cellular component assembly | 4 | 12 |
| GO:0022618 | ribonucleoprotein complex assembly | 6 | 12 |
| GO:0031323 | regulation of cellular metabolic process | 4 | 2 |
| GO:0031326 | regulation of cellular biosynthetic process | 5 | 2 |
| GO:0034248 | regulation of amide metabolic process | 5 | 2 |
| GO:0043933 | protein-containing complex organization | 4 | 12 |
| GO:0044237 | cellular metabolic process | 2 | 2 |
| GO:0050789 | regulation of biological process | 2 | 2 |
| GO:0050794 | regulation of cellular process | 3 | 2 |
| GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 2 |
| GO:0051246 | regulation of protein metabolic process | 5 | 2 |
| GO:0060255 | regulation of macromolecule metabolic process | 4 | 2 |
| GO:0065003 | protein-containing complex assembly | 5 | 12 |
| GO:0065007 | biological regulation | 1 | 2 |
| GO:0071826 | ribonucleoprotein complex subunit organization | 5 | 12 |
| GO:0071840 | cellular component organization or biogenesis | 2 | 12 |
| GO:0080090 | regulation of primary metabolic process | 4 | 2 |
| GO:2000112 | obsolete regulation of cellular macromolecule biosynthetic process | 6 | 2 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0003676 | nucleic acid binding | 3 | 12 |
| GO:0003723 | RNA binding | 4 | 2 |
| GO:0003743 | translation initiation factor activity | 4 | 12 |
| GO:0005488 | binding | 1 | 12 |
| GO:0008135 | translation factor activity, RNA binding | 3 | 12 |
| GO:0045182 | translation regulator activity | 1 | 12 |
| GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 12 |
| GO:0097159 | organic cyclic compound binding | 2 | 12 |
| GO:1901363 | heterocyclic compound binding | 2 | 12 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_MEL_PAP_1 | 280 | 286 | PF00089 | 0.562 |
| CLV_PCSK_SKI1_1 | 80 | 84 | PF00082 | 0.316 |
| DEG_SCF_FBW7_1 | 220 | 227 | PF00400 | 0.676 |
| DEG_SIAH_1 | 11 | 19 | PF03145 | 0.504 |
| DOC_CKS1_1 | 20 | 25 | PF01111 | 0.442 |
| DOC_CKS1_1 | 221 | 226 | PF01111 | 0.678 |
| DOC_CKS1_1 | 231 | 236 | PF01111 | 0.310 |
| DOC_MAPK_gen_1 | 48 | 57 | PF00069 | 0.388 |
| DOC_MAPK_gen_1 | 86 | 95 | PF00069 | 0.531 |
| DOC_PP4_FxxP_1 | 209 | 212 | PF00568 | 0.509 |
| DOC_PP4_FxxP_1 | 231 | 234 | PF00568 | 0.578 |
| DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.514 |
| DOC_USP7_MATH_1 | 147 | 151 | PF00917 | 0.553 |
| DOC_USP7_MATH_1 | 294 | 298 | PF00917 | 0.502 |
| DOC_USP7_MATH_1 | 390 | 394 | PF00917 | 0.604 |
| DOC_USP7_UBL2_3 | 357 | 361 | PF12436 | 0.424 |
| DOC_WW_Pin1_4 | 14 | 19 | PF00397 | 0.499 |
| DOC_WW_Pin1_4 | 21 | 26 | PF00397 | 0.423 |
| DOC_WW_Pin1_4 | 220 | 225 | PF00397 | 0.681 |
| DOC_WW_Pin1_4 | 230 | 235 | PF00397 | 0.307 |
| DOC_WW_Pin1_4 | 325 | 330 | PF00397 | 0.442 |
| DOC_WW_Pin1_4 | 407 | 412 | PF00397 | 0.541 |
| LIG_14-3-3_CanoR_1 | 171 | 179 | PF00244 | 0.573 |
| LIG_14-3-3_CanoR_1 | 195 | 202 | PF00244 | 0.608 |
| LIG_14-3-3_CanoR_1 | 283 | 287 | PF00244 | 0.478 |
| LIG_14-3-3_CanoR_1 | 387 | 397 | PF00244 | 0.597 |
| LIG_14-3-3_CanoR_1 | 59 | 65 | PF00244 | 0.430 |
| LIG_BRCT_BRCA1_1 | 177 | 181 | PF00533 | 0.508 |
| LIG_BRCT_BRCA1_1 | 23 | 27 | PF00533 | 0.427 |
| LIG_FHA_1 | 110 | 116 | PF00498 | 0.567 |
| LIG_FHA_1 | 299 | 305 | PF00498 | 0.424 |
| LIG_FHA_1 | 310 | 316 | PF00498 | 0.436 |
| LIG_FHA_1 | 50 | 56 | PF00498 | 0.374 |
| LIG_FHA_1 | 63 | 69 | PF00498 | 0.350 |
| LIG_GBD_Chelix_1 | 36 | 44 | PF00786 | 0.440 |
| LIG_LIR_Apic_2 | 229 | 234 | PF02991 | 0.614 |
| LIG_LIR_Gen_1 | 118 | 125 | PF02991 | 0.594 |
| LIG_LIR_Gen_1 | 223 | 231 | PF02991 | 0.608 |
| LIG_LIR_Gen_1 | 253 | 264 | PF02991 | 0.560 |
| LIG_LIR_Gen_1 | 287 | 296 | PF02991 | 0.501 |
| LIG_LIR_Nem_3 | 118 | 122 | PF02991 | 0.572 |
| LIG_LIR_Nem_3 | 223 | 228 | PF02991 | 0.597 |
| LIG_LIR_Nem_3 | 253 | 259 | PF02991 | 0.518 |
| LIG_LIR_Nem_3 | 287 | 293 | PF02991 | 0.443 |
| LIG_LIR_Nem_3 | 306 | 310 | PF02991 | 0.451 |
| LIG_LIR_Nem_3 | 391 | 397 | PF02991 | 0.522 |
| LIG_MLH1_MIPbox_1 | 23 | 27 | PF16413 | 0.427 |
| LIG_NRBOX | 35 | 41 | PF00104 | 0.429 |
| LIG_Pex14_1 | 286 | 290 | PF04695 | 0.577 |
| LIG_Pex14_2 | 354 | 358 | PF04695 | 0.443 |
| LIG_PTB_Apo_2 | 203 | 210 | PF02174 | 0.490 |
| LIG_REV1ctd_RIR_1 | 356 | 365 | PF16727 | 0.587 |
| LIG_SH2_CRK | 119 | 123 | PF00017 | 0.586 |
| LIG_SH2_CRK | 205 | 209 | PF00017 | 0.487 |
| LIG_SH2_CRK | 256 | 260 | PF00017 | 0.546 |
| LIG_SH2_CRK | 394 | 398 | PF00017 | 0.606 |
| LIG_SH2_GRB2like | 256 | 259 | PF00017 | 0.549 |
| LIG_SH2_NCK_1 | 119 | 123 | PF00017 | 0.586 |
| LIG_SH2_NCK_1 | 205 | 209 | PF00017 | 0.487 |
| LIG_SH2_STAP1 | 130 | 134 | PF00017 | 0.520 |
| LIG_SH2_STAT5 | 119 | 122 | PF00017 | 0.567 |
| LIG_SH2_STAT5 | 290 | 293 | PF00017 | 0.434 |
| LIG_SH3_3 | 218 | 224 | PF00018 | 0.664 |
| LIG_SUMO_SIM_par_1 | 133 | 138 | PF11976 | 0.496 |
| LIG_SUMO_SIM_par_1 | 258 | 263 | PF11976 | 0.449 |
| LIG_TRAF2_1 | 151 | 154 | PF00917 | 0.624 |
| LIG_WRC_WIRS_1 | 225 | 230 | PF05994 | 0.600 |
| MOD_CK1_1 | 118 | 124 | PF00069 | 0.592 |
| MOD_CK1_1 | 159 | 165 | PF00069 | 0.589 |
| MOD_CK1_1 | 172 | 178 | PF00069 | 0.470 |
| MOD_CK1_1 | 197 | 203 | PF00069 | 0.623 |
| MOD_CK1_1 | 344 | 350 | PF00069 | 0.640 |
| MOD_CK1_1 | 406 | 412 | PF00069 | 0.561 |
| MOD_CK1_1 | 58 | 64 | PF00069 | 0.437 |
| MOD_CK2_1 | 147 | 153 | PF00069 | 0.506 |
| MOD_CK2_1 | 226 | 232 | PF00069 | 0.595 |
| MOD_CK2_1 | 349 | 355 | PF00069 | 0.512 |
| MOD_CMANNOS | 239 | 242 | PF00535 | 0.553 |
| MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.570 |
| MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.514 |
| MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.559 |
| MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.427 |
| MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.385 |
| MOD_GlcNHglycan | 199 | 202 | PF01048 | 0.481 |
| MOD_GlcNHglycan | 390 | 393 | PF01048 | 0.313 |
| MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.652 |
| MOD_GlcNHglycan | 96 | 99 | PF01048 | 0.425 |
| MOD_GSK3_1 | 10 | 17 | PF00069 | 0.654 |
| MOD_GSK3_1 | 141 | 148 | PF00069 | 0.437 |
| MOD_GSK3_1 | 165 | 172 | PF00069 | 0.555 |
| MOD_GSK3_1 | 175 | 182 | PF00069 | 0.472 |
| MOD_GSK3_1 | 189 | 196 | PF00069 | 0.499 |
| MOD_GSK3_1 | 220 | 227 | PF00069 | 0.629 |
| MOD_GSK3_1 | 245 | 252 | PF00069 | 0.448 |
| MOD_GSK3_1 | 294 | 301 | PF00069 | 0.425 |
| MOD_GSK3_1 | 31 | 38 | PF00069 | 0.418 |
| MOD_GSK3_1 | 403 | 410 | PF00069 | 0.594 |
| MOD_GSK3_1 | 58 | 65 | PF00069 | 0.428 |
| MOD_GSK3_1 | 94 | 101 | PF00069 | 0.606 |
| MOD_LATS_1 | 78 | 84 | PF00433 | 0.520 |
| MOD_N-GLC_1 | 101 | 106 | PF02516 | 0.383 |
| MOD_N-GLC_1 | 245 | 250 | PF02516 | 0.478 |
| MOD_NEK2_1 | 115 | 120 | PF00069 | 0.572 |
| MOD_NEK2_1 | 145 | 150 | PF00069 | 0.422 |
| MOD_NEK2_1 | 165 | 170 | PF00069 | 0.576 |
| MOD_NEK2_1 | 189 | 194 | PF00069 | 0.462 |
| MOD_NEK2_1 | 31 | 36 | PF00069 | 0.532 |
| MOD_NEK2_1 | 44 | 49 | PF00069 | 0.537 |
| MOD_NEK2_1 | 93 | 98 | PF00069 | 0.510 |
| MOD_NEK2_2 | 349 | 354 | PF00069 | 0.645 |
| MOD_PIKK_1 | 344 | 350 | PF00454 | 0.587 |
| MOD_PIKK_1 | 49 | 55 | PF00454 | 0.383 |
| MOD_PKA_2 | 140 | 146 | PF00069 | 0.565 |
| MOD_PKA_2 | 194 | 200 | PF00069 | 0.622 |
| MOD_PKA_2 | 282 | 288 | PF00069 | 0.499 |
| MOD_PKA_2 | 58 | 64 | PF00069 | 0.437 |
| MOD_Plk_1 | 141 | 147 | PF00069 | 0.464 |
| MOD_Plk_1 | 183 | 189 | PF00069 | 0.532 |
| MOD_Plk_1 | 245 | 251 | PF00069 | 0.455 |
| MOD_Plk_1 | 323 | 329 | PF00069 | 0.490 |
| MOD_Plk_2-3 | 126 | 132 | PF00069 | 0.656 |
| MOD_Plk_4 | 141 | 147 | PF00069 | 0.432 |
| MOD_Plk_4 | 183 | 189 | PF00069 | 0.572 |
| MOD_Plk_4 | 245 | 251 | PF00069 | 0.467 |
| MOD_Plk_4 | 349 | 355 | PF00069 | 0.631 |
| MOD_Plk_4 | 35 | 41 | PF00069 | 0.562 |
| MOD_Plk_4 | 80 | 86 | PF00069 | 0.531 |
| MOD_ProDKin_1 | 14 | 20 | PF00069 | 0.496 |
| MOD_ProDKin_1 | 21 | 27 | PF00069 | 0.421 |
| MOD_ProDKin_1 | 220 | 226 | PF00069 | 0.679 |
| MOD_ProDKin_1 | 230 | 236 | PF00069 | 0.309 |
| MOD_ProDKin_1 | 325 | 331 | PF00069 | 0.445 |
| MOD_ProDKin_1 | 407 | 413 | PF00069 | 0.540 |
| MOD_SUMO_rev_2 | 352 | 359 | PF00179 | 0.531 |
| TRG_DiLeu_BaEn_1 | 161 | 166 | PF01217 | 0.576 |
| TRG_DiLeu_BaLyEn_6 | 15 | 20 | PF01217 | 0.492 |
| TRG_ENDOCYTIC_2 | 119 | 122 | PF00928 | 0.567 |
| TRG_ENDOCYTIC_2 | 256 | 259 | PF00928 | 0.469 |
| TRG_ENDOCYTIC_2 | 290 | 293 | PF00928 | 0.434 |
| TRG_ENDOCYTIC_2 | 394 | 397 | PF00928 | 0.606 |
| TRG_ER_diArg_1 | 268 | 271 | PF00400 | 0.619 |
| TRG_ER_diArg_1 | 4 | 7 | PF00400 | 0.523 |
| TRG_Pf-PMV_PEXEL_1 | 271 | 275 | PF00026 | 0.590 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P675 | Leptomonas seymouri | 83% | 100% |
| A0A0S4JEJ1 | Bodo saltans | 48% | 100% |
| A0A1X0P3N7 | Trypanosomatidae | 54% | 100% |
| A0A3S7XBB2 | Leishmania donovani | 99% | 100% |
| A0A422NKQ7 | Trypanosoma rangeli | 54% | 100% |
| A1CJY4 | Aspergillus clavatus (strain ATCC 1007 / CBS 513.65 / DSM 816 / NCTC 3887 / NRRL 1 / QM 1276 / 107) | 33% | 100% |
| A1D7I5 | Neosartorya fischeri (strain ATCC 1020 / DSM 3700 / CBS 544.65 / FGSC A1164 / JCM 1740 / NRRL 181 / WB 181) | 33% | 100% |
| A2QEV8 | Aspergillus niger (strain CBS 513.88 / FGSC A1513) | 31% | 100% |
| A3LX18 | Scheffersomyces stipitis (strain ATCC 58785 / CBS 6054 / NBRC 10063 / NRRL Y-11545) | 32% | 100% |
| A4HPQ5 | Leishmania braziliensis | 97% | 100% |
| A4ID08 | Leishmania infantum | 100% | 100% |
| A4RDD7 | Magnaporthe oryzae (strain 70-15 / ATCC MYA-4617 / FGSC 8958) | 32% | 100% |
| A5DGL8 | Meyerozyma guilliermondii (strain ATCC 6260 / CBS 566 / DSM 6381 / JCM 1539 / NBRC 10279 / NRRL Y-324) | 32% | 100% |
| A5DVY3 | Lodderomyces elongisporus (strain ATCC 11503 / CBS 2605 / JCM 1781 / NBRC 1676 / NRRL YB-4239) | 31% | 100% |
| A6RUL1 | Botryotinia fuckeliana (strain B05.10) | 31% | 100% |
| A6ZMK5 | Saccharomyces cerevisiae (strain YJM789) | 28% | 100% |
| A7EF03 | Sclerotinia sclerotiorum (strain ATCC 18683 / 1980 / Ss-1) | 31% | 100% |
| A7RM20 | Nematostella vectensis | 31% | 100% |
| A7TH19 | Vanderwaltozyma polyspora (strain ATCC 22028 / DSM 70294 / BCRC 21397 / CBS 2163 / NBRC 10782 / NRRL Y-8283 / UCD 57-17) | 26% | 100% |
| A8QBF3 | Brugia malayi | 29% | 100% |
| A8WVX8 | Caenorhabditis briggsae | 31% | 100% |
| B0BNA7 | Rattus norvegicus | 30% | 100% |
| B0XFT7 | Culex quinquefasciatus | 32% | 100% |
| B0XYC8 | Neosartorya fumigata (strain CEA10 / CBS 144.89 / FGSC A1163) | 33% | 100% |
| B3MVL6 | Drosophila ananassae | 32% | 100% |
| B3N4C7 | Drosophila erecta | 32% | 100% |
| B4GSH1 | Drosophila persimilis | 32% | 100% |
| B4I195 | Drosophila sechellia | 32% | 100% |
| B4JB43 | Drosophila grimshawi | 31% | 100% |
| B4KGX9 | Drosophila mojavensis | 31% | 100% |
| B4LUA5 | Drosophila virilis | 32% | 100% |
| B4N0L0 | Drosophila willistoni | 34% | 100% |
| B4NW98 | Drosophila yakuba | 32% | 100% |
| B4Q354 | Drosophila simulans | 32% | 100% |
| B5FZ19 | Taeniopygia guttata | 30% | 100% |
| D0A8F9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 55% | 100% |
| E3LB80 | Puccinia graminis f. sp. tritici (strain CRL 75-36-700-3 / race SCCL) | 26% | 100% |
| E9ATH0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 98% | 100% |
| O02195 | Drosophila melanogaster | 32% | 100% |
| P0CS32 | Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) | 31% | 100% |
| P0CS33 | Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) | 31% | 100% |
| P40217 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 28% | 100% |
| P79083 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 32% | 100% |
| Q0CXH9 | Aspergillus terreus (strain NIH 2624 / FGSC A1156) | 33% | 100% |
| Q0V320 | Phaeosphaeria nodorum (strain SN15 / ATCC MYA-4574 / FGSC 10173) | 30% | 100% |
| Q13347 | Homo sapiens | 30% | 100% |
| Q16K15 | Aedes aegypti | 31% | 100% |
| Q1DPU4 | Coccidioides immitis (strain RS) | 31% | 100% |
| Q1HPW4 | Bombyx mori | 31% | 100% |
| Q29L19 | Drosophila pseudoobscura pseudoobscura | 32% | 100% |
| Q2GTM8 | Chaetomium globosum (strain ATCC 6205 / CBS 148.51 / DSM 1962 / NBRC 6347 / NRRL 1970) | 32% | 100% |
| Q2UQ34 | Aspergillus oryzae (strain ATCC 42149 / RIB 40) | 33% | 100% |
| Q38884 | Arabidopsis thaliana | 34% | 100% |
| Q4P6E2 | Ustilago maydis (strain 521 / FGSC 9021) | 32% | 100% |
| Q4WX90 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 33% | 100% |
| Q54MT0 | Dictyostelium discoideum | 34% | 100% |
| Q5AI86 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 32% | 100% |
| Q5B8Y3 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 32% | 100% |
| Q5E966 | Bos taurus | 30% | 100% |
| Q5EBE8 | Xenopus tropicalis | 31% | 100% |
| Q5IH81 | Oryctolagus cuniculus | 29% | 100% |
| Q5R7R2 | Pongo abelii | 30% | 100% |
| Q66J51 | Xenopus laevis | 31% | 100% |
| Q6BSL7 | Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / BCRC 21394 / JCM 1990 / NBRC 0083 / IGC 2968) | 32% | 100% |
| Q6CI08 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 31% | 100% |
| Q6CKX3 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 29% | 100% |
| Q6FL15 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 28% | 100% |
| Q759L2 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 28% | 100% |
| Q7PP77 | Anopheles gambiae | 31% | 100% |
| Q7RXH4 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 31% | 100% |
| Q7ZV55 | Danio rerio | 31% | 100% |
| Q7ZVF0 | Danio rerio | 23% | 100% |
| Q965S8 | Caenorhabditis elegans | 31% | 100% |
| Q9QZD9 | Mus musculus | 30% | 100% |
| V5BE86 | Trypanosoma cruzi | 54% | 100% |