| 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: 18 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| DeepLoc | ||
| SignalP6 | no | yes: 0, no: 10 |
| NetGPI | no | yes: 0, no: 10 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005737 | cytoplasm | 2 | 10 |
| GO:0110165 | cellular anatomical entity | 1 | 10 |
| GO:0005634 | nucleus | 5 | 1 |
| GO:0005829 | cytosol | 2 | 1 |
| GO:0010494 | cytoplasmic stress granule | 5 | 1 |
| GO:0032991 | protein-containing complex | 1 | 1 |
| GO:0035770 | ribonucleoprotein granule | 3 | 1 |
| GO:0036464 | cytoplasmic ribonucleoprotein granule | 4 | 1 |
| GO:0043226 | organelle | 2 | 1 |
| GO:0043227 | membrane-bounded organelle | 3 | 1 |
| GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
| GO:0043229 | intracellular organelle | 3 | 1 |
| GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
| GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
| GO:0099080 | supramolecular complex | 2 | 1 |
| GO:1990904 | ribonucleoprotein complex | 2 | 1 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
| GO:0006378 | mRNA polyadenylation | 7 | 1 |
| GO:0006396 | RNA processing | 6 | 1 |
| GO:0006397 | mRNA processing | 7 | 1 |
| GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
| GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
| GO:0008152 | metabolic process | 1 | 1 |
| GO:0009987 | cellular process | 1 | 1 |
| GO:0016070 | RNA metabolic process | 5 | 1 |
| GO:0016071 | mRNA metabolic process | 6 | 1 |
| GO:0031123 | RNA 3'-end processing | 7 | 1 |
| GO:0031124 | mRNA 3'-end processing | 8 | 1 |
| GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
| GO:0043170 | macromolecule metabolic process | 3 | 1 |
| GO:0043631 | RNA polyadenylation | 6 | 1 |
| GO:0044237 | cellular metabolic process | 2 | 1 |
| GO:0044238 | primary metabolic process | 2 | 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:0003676 | nucleic acid binding | 3 | 11 |
| GO:0003723 | RNA binding | 4 | 11 |
| GO:0005488 | binding | 1 | 11 |
| GO:0097159 | organic cyclic compound binding | 2 | 11 |
| GO:1901363 | heterocyclic compound binding | 2 | 11 |
| GO:0003727 | single-stranded RNA binding | 5 | 1 |
| GO:0003729 | mRNA binding | 5 | 1 |
| GO:0003730 | mRNA 3'-UTR binding | 6 | 1 |
| GO:0005515 | protein binding | 2 | 1 |
| GO:0008143 | poly(A) binding | 7 | 1 |
| GO:0008187 | poly-pyrimidine tract binding | 6 | 1 |
| GO:0008190 | eukaryotic initiation factor 4E binding | 4 | 1 |
| GO:0008266 | poly(U) RNA binding | 7 | 1 |
| GO:0031369 | translation initiation factor binding | 3 | 1 |
| GO:0031370 | eukaryotic initiation factor 4G binding | 4 | 1 |
| GO:0070717 | poly-purine tract binding | 6 | 1 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 165 | 169 | PF00656 | 0.570 |
| CLV_NRD_NRD_1 | 194 | 196 | PF00675 | 0.449 |
| CLV_NRD_NRD_1 | 384 | 386 | PF00675 | 0.495 |
| CLV_NRD_NRD_1 | 89 | 91 | PF00675 | 0.184 |
| CLV_PCSK_KEX2_1 | 194 | 196 | PF00082 | 0.449 |
| CLV_PCSK_KEX2_1 | 384 | 386 | PF00082 | 0.495 |
| CLV_PCSK_KEX2_1 | 535 | 537 | PF00082 | 0.341 |
| CLV_PCSK_KEX2_1 | 89 | 91 | PF00082 | 0.273 |
| CLV_PCSK_PC1ET2_1 | 535 | 537 | PF00082 | 0.341 |
| CLV_PCSK_SKI1_1 | 184 | 188 | PF00082 | 0.489 |
| CLV_PCSK_SKI1_1 | 212 | 216 | PF00082 | 0.281 |
| CLV_PCSK_SKI1_1 | 493 | 497 | PF00082 | 0.281 |
| CLV_PCSK_SKI1_1 | 499 | 503 | PF00082 | 0.284 |
| DEG_ODPH_VHL_1 | 507 | 520 | PF01847 | 0.478 |
| DEG_SCF_FBW7_1 | 459 | 466 | PF00400 | 0.681 |
| DOC_CDC14_PxL_1 | 505 | 513 | PF14671 | 0.541 |
| DOC_CKS1_1 | 450 | 455 | PF01111 | 0.656 |
| DOC_CKS1_1 | 460 | 465 | PF01111 | 0.634 |
| DOC_CKS1_1 | 471 | 476 | PF01111 | 0.635 |
| DOC_CKS1_1 | 478 | 483 | PF01111 | 0.369 |
| DOC_MAPK_gen_1 | 151 | 160 | PF00069 | 0.461 |
| DOC_MAPK_gen_1 | 384 | 394 | PF00069 | 0.521 |
| DOC_MAPK_MEF2A_6 | 388 | 396 | PF00069 | 0.531 |
| DOC_MAPK_MEF2A_6 | 514 | 522 | PF00069 | 0.475 |
| DOC_PP1_RVXF_1 | 391 | 397 | PF00149 | 0.546 |
| DOC_PP1_RVXF_1 | 95 | 101 | PF00149 | 0.502 |
| DOC_PP4_FxxP_1 | 450 | 453 | PF00568 | 0.642 |
| DOC_USP7_MATH_1 | 16 | 20 | PF00917 | 0.462 |
| DOC_USP7_MATH_1 | 444 | 448 | PF00917 | 0.657 |
| DOC_USP7_MATH_1 | 451 | 455 | PF00917 | 0.656 |
| DOC_USP7_MATH_1 | 82 | 86 | PF00917 | 0.541 |
| DOC_USP7_MATH_2 | 481 | 487 | PF00917 | 0.426 |
| DOC_USP7_UBL2_3 | 118 | 122 | PF12436 | 0.564 |
| DOC_WW_Pin1_4 | 440 | 445 | PF00397 | 0.742 |
| DOC_WW_Pin1_4 | 449 | 454 | PF00397 | 0.672 |
| DOC_WW_Pin1_4 | 459 | 464 | PF00397 | 0.635 |
| DOC_WW_Pin1_4 | 470 | 475 | PF00397 | 0.664 |
| DOC_WW_Pin1_4 | 477 | 482 | PF00397 | 0.376 |
| DOC_WW_Pin1_4 | 485 | 490 | PF00397 | 0.475 |
| LIG_14-3-3_CanoR_1 | 388 | 392 | PF00244 | 0.546 |
| LIG_14-3-3_CanoR_1 | 540 | 548 | PF00244 | 0.541 |
| LIG_Actin_WH2_2 | 92 | 110 | PF00022 | 0.545 |
| LIG_APCC_ABBA_1 | 324 | 329 | PF00400 | 0.541 |
| LIG_BRCT_BRCA1_1 | 345 | 349 | PF00533 | 0.461 |
| LIG_BRCT_BRCA1_1 | 446 | 450 | PF00533 | 0.619 |
| LIG_BRCT_BRCA1_1 | 84 | 88 | PF00533 | 0.541 |
| LIG_CaM_IQ_9 | 391 | 407 | PF13499 | 0.541 |
| LIG_FHA_1 | 471 | 477 | PF00498 | 0.651 |
| LIG_FHA_1 | 540 | 546 | PF00498 | 0.492 |
| LIG_FHA_2 | 2 | 8 | PF00498 | 0.505 |
| LIG_FHA_2 | 317 | 323 | PF00498 | 0.502 |
| LIG_FHA_2 | 478 | 484 | PF00498 | 0.588 |
| LIG_Integrin_isoDGR_2 | 368 | 370 | PF01839 | 0.261 |
| LIG_LIR_Apic_2 | 447 | 453 | PF02991 | 0.553 |
| LIG_LIR_Gen_1 | 131 | 140 | PF02991 | 0.521 |
| LIG_LIR_Gen_1 | 224 | 233 | PF02991 | 0.453 |
| LIG_LIR_Gen_1 | 386 | 396 | PF02991 | 0.523 |
| LIG_LIR_Gen_1 | 498 | 509 | PF02991 | 0.475 |
| LIG_LIR_Gen_1 | 516 | 527 | PF02991 | 0.475 |
| LIG_LIR_Nem_3 | 131 | 136 | PF02991 | 0.455 |
| LIG_LIR_Nem_3 | 152 | 158 | PF02991 | 0.461 |
| LIG_LIR_Nem_3 | 224 | 230 | PF02991 | 0.453 |
| LIG_LIR_Nem_3 | 325 | 330 | PF02991 | 0.461 |
| LIG_LIR_Nem_3 | 346 | 352 | PF02991 | 0.461 |
| LIG_LIR_Nem_3 | 386 | 392 | PF02991 | 0.525 |
| LIG_LIR_Nem_3 | 43 | 48 | PF02991 | 0.455 |
| LIG_LIR_Nem_3 | 498 | 504 | PF02991 | 0.475 |
| LIG_LIR_Nem_3 | 526 | 531 | PF02991 | 0.492 |
| LIG_LIR_Nem_3 | 65 | 71 | PF02991 | 0.457 |
| LIG_LIR_Nem_3 | 85 | 91 | PF02991 | 0.513 |
| LIG_MYND_1 | 474 | 478 | PF01753 | 0.633 |
| LIG_MYND_1 | 509 | 513 | PF01753 | 0.541 |
| LIG_PCNA_TLS_4 | 220 | 227 | PF02747 | 0.461 |
| LIG_PCNA_yPIPBox_3 | 194 | 203 | PF02747 | 0.445 |
| LIG_Pex14_2 | 226 | 230 | PF04695 | 0.461 |
| LIG_Pex14_2 | 314 | 318 | PF04695 | 0.461 |
| LIG_PTB_Apo_2 | 304 | 311 | PF02174 | 0.416 |
| LIG_PTB_Phospho_1 | 304 | 310 | PF10480 | 0.424 |
| LIG_REV1ctd_RIR_1 | 224 | 233 | PF16727 | 0.461 |
| LIG_SH2_CRK | 155 | 159 | PF00017 | 0.461 |
| LIG_SH2_CRK | 389 | 393 | PF00017 | 0.577 |
| LIG_SH2_CRK | 68 | 72 | PF00017 | 0.492 |
| LIG_SH2_GRB2like | 70 | 73 | PF00017 | 0.461 |
| LIG_SH2_NCK_1 | 505 | 509 | PF00017 | 0.541 |
| LIG_SH2_SRC | 505 | 508 | PF00017 | 0.541 |
| LIG_SH2_STAT3 | 210 | 213 | PF00017 | 0.461 |
| LIG_SH2_STAT5 | 188 | 191 | PF00017 | 0.406 |
| LIG_SH2_STAT5 | 210 | 213 | PF00017 | 0.455 |
| LIG_SH2_STAT5 | 28 | 31 | PF00017 | 0.461 |
| LIG_SH2_STAT5 | 281 | 284 | PF00017 | 0.405 |
| LIG_SH2_STAT5 | 310 | 313 | PF00017 | 0.461 |
| LIG_SH2_STAT5 | 389 | 392 | PF00017 | 0.583 |
| LIG_SH2_STAT5 | 70 | 73 | PF00017 | 0.461 |
| LIG_SH3_3 | 15 | 21 | PF00018 | 0.526 |
| LIG_SH3_3 | 468 | 474 | PF00018 | 0.679 |
| LIG_SH3_3 | 475 | 481 | PF00018 | 0.614 |
| LIG_TRAF2_1 | 4 | 7 | PF00917 | 0.594 |
| LIG_TRAF2_1 | 480 | 483 | PF00917 | 0.668 |
| LIG_TRAF2_1 | 488 | 491 | PF00917 | 0.541 |
| LIG_TYR_ITIM | 66 | 71 | PF00017 | 0.314 |
| LIG_UBA3_1 | 292 | 298 | PF00899 | 0.510 |
| LIG_UBA3_1 | 323 | 328 | PF00899 | 0.426 |
| LIG_UBA3_1 | 518 | 525 | PF00899 | 0.334 |
| LIG_WRC_WIRS_1 | 351 | 356 | PF05994 | 0.314 |
| LIG_WRPW_2 | 45 | 48 | PF00400 | 0.334 |
| LIG_WW_2 | 474 | 477 | PF00397 | 0.637 |
| MOD_CDK_SPK_2 | 459 | 464 | PF00069 | 0.750 |
| MOD_CK1_1 | 138 | 144 | PF00069 | 0.407 |
| MOD_CK1_1 | 343 | 349 | PF00069 | 0.459 |
| MOD_CK2_1 | 1 | 7 | PF00069 | 0.506 |
| MOD_CK2_1 | 477 | 483 | PF00069 | 0.608 |
| MOD_CK2_1 | 485 | 491 | PF00069 | 0.298 |
| MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.454 |
| MOD_GlcNHglycan | 162 | 167 | PF01048 | 0.442 |
| MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.317 |
| MOD_GlcNHglycan | 241 | 245 | PF01048 | 0.310 |
| MOD_GlcNHglycan | 342 | 345 | PF01048 | 0.459 |
| MOD_GlcNHglycan | 453 | 456 | PF01048 | 0.703 |
| MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.334 |
| MOD_GSK3_1 | 1 | 8 | PF00069 | 0.538 |
| MOD_GSK3_1 | 103 | 110 | PF00069 | 0.552 |
| MOD_GSK3_1 | 131 | 138 | PF00069 | 0.352 |
| MOD_GSK3_1 | 440 | 447 | PF00069 | 0.655 |
| MOD_GSK3_1 | 459 | 466 | PF00069 | 0.705 |
| MOD_N-GLC_1 | 204 | 209 | PF02516 | 0.386 |
| MOD_NEK2_1 | 1 | 6 | PF00069 | 0.614 |
| MOD_NEK2_1 | 107 | 112 | PF00069 | 0.462 |
| MOD_NEK2_1 | 340 | 345 | PF00069 | 0.206 |
| MOD_PIKK_1 | 444 | 450 | PF00454 | 0.684 |
| MOD_PIKK_1 | 59 | 65 | PF00454 | 0.314 |
| MOD_PK_1 | 135 | 141 | PF00069 | 0.401 |
| MOD_PKA_2 | 107 | 113 | PF00069 | 0.455 |
| MOD_PKA_2 | 387 | 393 | PF00069 | 0.547 |
| MOD_PKA_2 | 539 | 545 | PF00069 | 0.426 |
| MOD_Plk_2-3 | 125 | 131 | PF00069 | 0.426 |
| MOD_Plk_2-3 | 178 | 184 | PF00069 | 0.650 |
| MOD_Plk_4 | 135 | 141 | PF00069 | 0.347 |
| MOD_Plk_4 | 23 | 29 | PF00069 | 0.397 |
| MOD_Plk_4 | 387 | 393 | PF00069 | 0.547 |
| MOD_Plk_4 | 47 | 53 | PF00069 | 0.314 |
| MOD_ProDKin_1 | 440 | 446 | PF00069 | 0.744 |
| MOD_ProDKin_1 | 449 | 455 | PF00069 | 0.671 |
| MOD_ProDKin_1 | 459 | 465 | PF00069 | 0.634 |
| MOD_ProDKin_1 | 470 | 476 | PF00069 | 0.659 |
| MOD_ProDKin_1 | 477 | 483 | PF00069 | 0.374 |
| MOD_ProDKin_1 | 485 | 491 | PF00069 | 0.334 |
| MOD_SUMO_for_1 | 160 | 163 | PF00179 | 0.426 |
| MOD_SUMO_rev_2 | 121 | 129 | PF00179 | 0.426 |
| MOD_SUMO_rev_2 | 146 | 152 | PF00179 | 0.384 |
| MOD_SUMO_rev_2 | 178 | 187 | PF00179 | 0.530 |
| MOD_SUMO_rev_2 | 329 | 335 | PF00179 | 0.459 |
| MOD_SUMO_rev_2 | 529 | 537 | PF00179 | 0.380 |
| TRG_DiLeu_BaEn_1 | 526 | 531 | PF01217 | 0.357 |
| TRG_DiLeu_BaLyEn_6 | 288 | 293 | PF01217 | 0.477 |
| TRG_DiLeu_BaLyEn_6 | 373 | 378 | PF01217 | 0.334 |
| TRG_ENDOCYTIC_2 | 155 | 158 | PF00928 | 0.314 |
| TRG_ENDOCYTIC_2 | 330 | 333 | PF00928 | 0.314 |
| TRG_ENDOCYTIC_2 | 389 | 392 | PF00928 | 0.583 |
| TRG_ENDOCYTIC_2 | 528 | 531 | PF00928 | 0.426 |
| TRG_ENDOCYTIC_2 | 68 | 71 | PF00928 | 0.357 |
| TRG_ER_diArg_1 | 193 | 195 | PF00400 | 0.440 |
| TRG_ER_diArg_1 | 421 | 424 | PF00400 | 0.762 |
| TRG_ER_diArg_1 | 88 | 90 | PF00400 | 0.206 |
| TRG_NES_CRM1_1 | 510 | 521 | PF08389 | 0.426 |
| TRG_Pf-PMV_PEXEL_1 | 535 | 539 | PF00026 | 0.378 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P3Y8 | Leptomonas seymouri | 87% | 98% |
| A0A0N0P5A9 | Leptomonas seymouri | 37% | 98% |
| A0A0N1I0F0 | Leptomonas seymouri | 35% | 100% |
| A0A0R4IEW8 | Danio rerio | 23% | 100% |
| A0A0S4IKZ4 | Bodo saltans | 36% | 97% |
| A0A0S4JPT3 | Bodo saltans | 40% | 98% |
| A0A1X0P4T3 | Trypanosomatidae | 72% | 99% |
| A0A1X0P4V5 | Trypanosomatidae | 40% | 97% |
| A0A1X0P525 | Trypanosomatidae | 33% | 100% |
| A0A3Q8IF40 | Leishmania donovani | 34% | 100% |
| A0A3Q8IGR8 | Leishmania donovani | 95% | 99% |
| A0A3Q8IMW2 | Leishmania donovani | 37% | 95% |
| A0A3R7NAH9 | Trypanosoma rangeli | 75% | 100% |
| A0A422NK82 | Trypanosoma rangeli | 34% | 100% |
| A0JM51 | Xenopus tropicalis | 21% | 100% |
| A1CRM1 | Aspergillus clavatus (strain ATCC 1007 / CBS 513.65 / DSM 816 / NCTC 3887 / NRRL 1 / QM 1276 / 107) | 35% | 73% |
| A1D4K4 | Neosartorya fischeri (strain ATCC 1020 / DSM 3700 / CBS 544.65 / FGSC A1164 / JCM 1740 / NRRL 181 / WB 181) | 39% | 74% |
| A3LXL0 | Scheffersomyces stipitis (strain ATCC 58785 / CBS 6054 / NBRC 10063 / NRRL Y-11545) | 36% | 88% |
| A4HDV5 | Leishmania braziliensis | 39% | 100% |
| A4HN85 | Leishmania braziliensis | 38% | 96% |
| A4I150 | Leishmania infantum | 34% | 100% |
| A4IBV3 | Leishmania infantum | 37% | 95% |
| A4IC57 | Leishmania infantum | 95% | 99% |
| A4QNI8 | Xenopus tropicalis | 21% | 100% |
| A4QUF0 | Magnaporthe oryzae (strain 70-15 / ATCC MYA-4617 / FGSC 8958) | 36% | 73% |
| A5DM21 | Meyerozyma guilliermondii (strain ATCC 6260 / CBS 566 / DSM 6381 / JCM 1539 / NBRC 10279 / NRRL Y-324) | 38% | 88% |
| A5DW14 | Lodderomyces elongisporus (strain ATCC 11503 / CBS 2605 / JCM 1781 / NBRC 1676 / NRRL YB-4239) | 37% | 84% |
| C9ZYE6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 69% | 98% |
| C9ZYQ8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
| E9AFP0 | Leishmania major | 37% | 93% |
| E9AFX7 | Leishmania major | 94% | 100% |
| E9AX84 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
| E9B6U3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 93% |
| E9B730 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 98% |
| F1QB54 | Danio rerio | 45% | 87% |
| F4HT49 | Arabidopsis thaliana | 39% | 100% |
| O04319 | Arabidopsis thaliana | 36% | 100% |
| O09032 | Rattus norvegicus | 24% | 100% |
| O22173 | Arabidopsis thaliana | 38% | 84% |
| O64380 | Arabidopsis thaliana | 42% | 84% |
| P04147 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 40% | 96% |
| P08199 | Mesocricetus auratus | 23% | 78% |
| P09405 | Mus musculus | 24% | 78% |
| P0CB38 | Homo sapiens | 41% | 100% |
| P0CP46 | Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) | 39% | 82% |
| P0CP47 | Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) | 39% | 82% |
| P11940 | Homo sapiens | 46% | 87% |
| P13383 | Rattus norvegicus | 22% | 78% |
| P15771 | Gallus gallus | 22% | 80% |
| P19338 | Homo sapiens | 23% | 78% |
| P20397 | Xenopus laevis | 22% | 85% |
| P20965 | Xenopus laevis | 41% | 88% |
| P21187 | Drosophila melanogaster | 43% | 87% |
| P26378 | Homo sapiens | 23% | 100% |
| P29341 | Mus musculus | 47% | 87% |
| P31209 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 39% | 85% |
| P39684 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 26% | 91% |
| P42731 | Arabidopsis thaliana | 37% | 88% |
| P52912 | Mus musculus | 23% | 100% |
| P61286 | Bos taurus | 46% | 87% |
| Q05196 | Arabidopsis thaliana | 38% | 81% |
| Q0CR95 | Aspergillus terreus (strain NIH 2624 / FGSC A1156) | 34% | 74% |
| Q13310 | Homo sapiens | 44% | 86% |
| Q1DXH0 | Coccidioides immitis (strain RS) | 34% | 72% |
| Q1ZXC2 | Dictyostelium discoideum | 35% | 68% |
| Q2GSX8 | Chaetomium globosum (strain ATCC 6205 / CBS 148.51 / DSM 1962 / NBRC 6347 / NRRL 1970) | 37% | 71% |
| Q4P8R9 | Ustilago maydis (strain 521 / FGSC 9021) | 39% | 85% |
| Q4QA88 | Leishmania major | 34% | 99% |
| Q4R4J7 | Macaca fascicularis | 22% | 78% |
| Q4VXU2 | Homo sapiens | 45% | 90% |
| Q4WK03 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 39% | 74% |
| Q54BM2 | Dictyostelium discoideum | 35% | 98% |
| Q5AI15 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 37% | 88% |
| Q5B630 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 35% | 76% |
| Q5R8F7 | Pongo abelii | 46% | 87% |
| Q5RF26 | Pongo abelii | 23% | 78% |
| Q61701 | Mus musculus | 24% | 100% |
| Q6BI95 | Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / BCRC 21394 / JCM 1990 / NBRC 0083 / IGC 2968) | 37% | 88% |
| Q6CDH3 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 34% | 88% |
| Q6CSV3 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 39% | 94% |
| Q6DEY7 | Xenopus tropicalis | 40% | 88% |
| Q6FKG4 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 39% | 96% |
| Q6GR16 | Xenopus laevis | 41% | 88% |
| Q6IP09 | Xenopus laevis | 46% | 88% |
| Q74ZS6 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 39% | 95% |
| Q7S6N6 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 37% | 73% |
| Q7SZT7 | Xenopus laevis | 21% | 100% |
| Q8SR30 | Encephalitozoon cuniculi (strain GB-M1) | 29% | 100% |
| Q91903 | Xenopus laevis | 24% | 100% |
| Q98SP8 | Xenopus laevis | 40% | 88% |
| Q9EPH8 | Rattus norvegicus | 46% | 87% |
| Q9FXA2 | Arabidopsis thaliana | 42% | 83% |
| Q9H361 | Homo sapiens | 43% | 88% |
| Q9ZQA8 | Arabidopsis thaliana | 34% | 91% |
| V5BYR2 | Trypanosoma cruzi | 71% | 98% |
| V5DUJ1 | Trypanosoma cruzi | 34% | 100% |