A large and likely artifical grouping of protease domain carrying proteins related to proteasomal proteases. Only a tiny subgroup (the AFG3-related mitochondrail proteins) seem to have a TM segment.. Localization: Cytoplasmic (by homology) / Mitochondrial (by homology)
| 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: 18 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| Pires et al. | no | yes: 0 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| Silverman et al. | no | yes: 5 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| Jamdhade et al. | no | yes: 10 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| DeepLoc | ||
| SignalP6 | no | yes: 0, no: 18 |
| NetGPI | no | yes: 0, no: 18 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0010008 | endosome membrane | 5 | 11 |
| GO:0012506 | vesicle membrane | 4 | 11 |
| GO:0016020 | membrane | 2 | 12 |
| GO:0030659 | cytoplasmic vesicle membrane | 5 | 11 |
| GO:0031090 | organelle membrane | 3 | 11 |
| GO:0031902 | late endosome membrane | 6 | 11 |
| GO:0098588 | bounding membrane of organelle | 4 | 11 |
| GO:0110165 | cellular anatomical entity | 1 | 16 |
| GO:0000502 | proteasome complex | 3 | 5 |
| GO:0005737 | cytoplasm | 2 | 5 |
| GO:0032991 | protein-containing complex | 1 | 5 |
| GO:0140535 | intracellular protein-containing complex | 2 | 5 |
| GO:1902494 | catalytic complex | 2 | 5 |
| GO:1905368 | peptidase complex | 3 | 5 |
| GO:1905369 | endopeptidase complex | 4 | 5 |
| GO:0008540 | proteasome regulatory particle, base subcomplex | 2 | 1 |
| GO:0031597 | cytosolic proteasome complex | 4 | 1 |
Related structures:
AlphaFold database: A4IAA1
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006508 | proteolysis | 4 | 5 |
| GO:0006807 | nitrogen compound metabolic process | 2 | 5 |
| GO:0008152 | metabolic process | 1 | 5 |
| GO:0009056 | catabolic process | 2 | 5 |
| GO:0009057 | macromolecule catabolic process | 4 | 5 |
| GO:0019538 | protein metabolic process | 3 | 5 |
| GO:0030163 | protein catabolic process | 4 | 5 |
| GO:0043170 | macromolecule metabolic process | 3 | 5 |
| GO:0044238 | primary metabolic process | 2 | 5 |
| GO:0071704 | organic substance metabolic process | 2 | 5 |
| GO:1901564 | organonitrogen compound metabolic process | 3 | 5 |
| GO:1901565 | organonitrogen compound catabolic process | 4 | 5 |
| GO:1901575 | organic substance catabolic process | 3 | 5 |
| GO:0006355 | regulation of DNA-templated transcription | 6 | 1 |
| GO:0006357 | regulation of transcription by RNA polymerase II | 7 | 1 |
| GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 1 |
| GO:0006950 | response to stress | 2 | 1 |
| GO:0009889 | regulation of biosynthetic process | 4 | 1 |
| GO:0009891 | positive regulation of biosynthetic process | 5 | 1 |
| GO:0009893 | positive regulation of metabolic process | 4 | 1 |
| GO:0009987 | cellular process | 1 | 1 |
| GO:0010033 | response to organic substance | 3 | 1 |
| GO:0010243 | response to organonitrogen compound | 4 | 1 |
| GO:0010468 | regulation of gene expression | 5 | 1 |
| GO:0010498 | proteasomal protein catabolic process | 5 | 1 |
| GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 1 |
| GO:0010557 | positive regulation of macromolecule biosynthetic process | 6 | 1 |
| GO:0010604 | positive regulation of macromolecule metabolic process | 5 | 1 |
| GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 1 |
| GO:0019222 | regulation of metabolic process | 3 | 1 |
| GO:0019941 | modification-dependent protein catabolic process | 6 | 1 |
| GO:0030433 | ubiquitin-dependent ERAD pathway | 6 | 1 |
| GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
| GO:0031325 | positive regulation of cellular metabolic process | 5 | 1 |
| GO:0031326 | regulation of cellular biosynthetic process | 5 | 1 |
| GO:0031328 | positive regulation of cellular biosynthetic process | 6 | 1 |
| GO:0031334 | positive regulation of protein-containing complex assembly | 6 | 1 |
| GO:0033554 | cellular response to stress | 3 | 1 |
| GO:0034976 | response to endoplasmic reticulum stress | 4 | 1 |
| GO:0036503 | ERAD pathway | 5 | 1 |
| GO:0042221 | response to chemical | 2 | 1 |
| GO:0043161 | proteasome-mediated ubiquitin-dependent protein catabolic process | 6 | 1 |
| GO:0043254 | regulation of protein-containing complex assembly | 5 | 1 |
| GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 1 |
| GO:0044087 | regulation of cellular component biogenesis | 4 | 1 |
| GO:0044089 | positive regulation of cellular component biogenesis | 5 | 1 |
| GO:0044237 | cellular metabolic process | 2 | 1 |
| GO:0044248 | cellular catabolic process | 3 | 1 |
| GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
| GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 1 |
| GO:0045893 | positive regulation of DNA-templated transcription | 7 | 1 |
| GO:0045898 | regulation of RNA polymerase II transcription preinitiation complex assembly | 6 | 1 |
| GO:0045899 | positive regulation of RNA polymerase II transcription preinitiation complex assembly | 7 | 1 |
| GO:0045935 | positive regulation of nucleobase-containing compound metabolic process | 6 | 1 |
| GO:0045944 | positive regulation of transcription by RNA polymerase II | 8 | 1 |
| GO:0048518 | positive regulation of biological process | 3 | 1 |
| GO:0048522 | positive regulation of cellular process | 4 | 1 |
| GO:0050789 | regulation of biological process | 2 | 1 |
| GO:0050794 | regulation of cellular process | 3 | 1 |
| GO:0050896 | response to stimulus | 1 | 1 |
| GO:0051128 | regulation of cellular component organization | 4 | 1 |
| GO:0051130 | positive regulation of cellular component organization | 5 | 1 |
| GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
| GO:0051173 | positive regulation of nitrogen compound metabolic process | 5 | 1 |
| GO:0051252 | regulation of RNA metabolic process | 5 | 1 |
| GO:0051254 | positive regulation of RNA metabolic process | 6 | 1 |
| GO:0051603 | proteolysis involved in protein catabolic process | 5 | 1 |
| GO:0051716 | cellular response to stimulus | 2 | 1 |
| GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
| GO:0060260 | regulation of transcription initiation by RNA polymerase II | 8 | 1 |
| GO:0060261 | positive regulation of transcription initiation by RNA polymerase II | 9 | 1 |
| GO:0065007 | biological regulation | 1 | 1 |
| GO:0080090 | regulation of primary metabolic process | 4 | 1 |
| GO:1901698 | response to nitrogen compound | 3 | 1 |
| GO:1902680 | positive regulation of RNA biosynthetic process | 7 | 1 |
| GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 1 |
| GO:1903508 | positive regulation of nucleic acid-templated transcription | 8 | 1 |
| GO:2000142 | regulation of DNA-templated transcription initiation | 7 | 1 |
| GO:2000144 | positive regulation of DNA-templated transcription initiation | 8 | 1 |
| GO:2001141 | regulation of RNA biosynthetic process | 6 | 1 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0000166 | nucleotide binding | 3 | 19 |
| GO:0003824 | catalytic activity | 1 | 19 |
| GO:0005488 | binding | 1 | 19 |
| GO:0005524 | ATP binding | 5 | 19 |
| GO:0016462 | pyrophosphatase activity | 5 | 19 |
| GO:0016787 | hydrolase activity | 2 | 19 |
| GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 19 |
| GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 19 |
| GO:0016887 | ATP hydrolysis activity | 7 | 19 |
| GO:0017076 | purine nucleotide binding | 4 | 19 |
| GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 19 |
| GO:0030554 | adenyl nucleotide binding | 5 | 19 |
| GO:0032553 | ribonucleotide binding | 3 | 19 |
| GO:0032555 | purine ribonucleotide binding | 4 | 19 |
| GO:0032559 | adenyl ribonucleotide binding | 5 | 19 |
| GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 19 |
| GO:0036094 | small molecule binding | 2 | 19 |
| GO:0043167 | ion binding | 2 | 19 |
| GO:0043168 | anion binding | 3 | 19 |
| GO:0097159 | organic cyclic compound binding | 2 | 19 |
| GO:0097367 | carbohydrate derivative binding | 2 | 19 |
| GO:1901265 | nucleoside phosphate binding | 3 | 19 |
| GO:1901363 | heterocyclic compound binding | 2 | 19 |
| GO:0008233 | peptidase activity | 3 | 5 |
| GO:0036402 | proteasome-activating activity | 2 | 5 |
| GO:0140096 | catalytic activity, acting on a protein | 2 | 5 |
| GO:0140657 | ATP-dependent activity | 1 | 5 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 258 | 262 | PF00656 | 0.281 |
| CLV_NRD_NRD_1 | 114 | 116 | PF00675 | 0.733 |
| CLV_NRD_NRD_1 | 192 | 194 | PF00675 | 0.337 |
| CLV_NRD_NRD_1 | 277 | 279 | PF00675 | 0.216 |
| CLV_NRD_NRD_1 | 312 | 314 | PF00675 | 0.272 |
| CLV_NRD_NRD_1 | 329 | 331 | PF00675 | 0.465 |
| CLV_NRD_NRD_1 | 364 | 366 | PF00675 | 0.412 |
| CLV_PCSK_KEX2_1 | 192 | 194 | PF00082 | 0.330 |
| CLV_PCSK_KEX2_1 | 277 | 279 | PF00082 | 0.216 |
| CLV_PCSK_KEX2_1 | 312 | 314 | PF00082 | 0.240 |
| CLV_PCSK_KEX2_1 | 328 | 330 | PF00082 | 0.352 |
| CLV_PCSK_KEX2_1 | 364 | 366 | PF00082 | 0.412 |
| CLV_PCSK_PC1ET2_1 | 328 | 330 | PF00082 | 0.308 |
| CLV_PCSK_PC7_1 | 188 | 194 | PF00082 | 0.372 |
| CLV_PCSK_SKI1_1 | 171 | 175 | PF00082 | 0.377 |
| CLV_PCSK_SKI1_1 | 192 | 196 | PF00082 | 0.299 |
| CLV_PCSK_SKI1_1 | 240 | 244 | PF00082 | 0.254 |
| CLV_PCSK_SKI1_1 | 252 | 256 | PF00082 | 0.254 |
| CLV_PCSK_SKI1_1 | 26 | 30 | PF00082 | 0.396 |
| CLV_PCSK_SKI1_1 | 277 | 281 | PF00082 | 0.283 |
| CLV_PCSK_SKI1_1 | 329 | 333 | PF00082 | 0.341 |
| CLV_PCSK_SKI1_1 | 364 | 368 | PF00082 | 0.509 |
| CLV_PCSK_SKI1_1 | 450 | 454 | PF00082 | 0.666 |
| CLV_PCSK_SKI1_1 | 50 | 54 | PF00082 | 0.331 |
| CLV_PCSK_SKI1_1 | 529 | 533 | PF00082 | 0.389 |
| DEG_APCC_DBOX_1 | 49 | 57 | PF00400 | 0.507 |
| DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.451 |
| DOC_CKS1_1 | 126 | 131 | PF01111 | 0.490 |
| DOC_CYCLIN_RxL_1 | 326 | 335 | PF00134 | 0.384 |
| DOC_CYCLIN_yClb5_NLxxxL_5 | 297 | 306 | PF00134 | 0.301 |
| DOC_CYCLIN_yCln2_LP_2 | 126 | 132 | PF00134 | 0.447 |
| DOC_MAPK_gen_1 | 277 | 287 | PF00069 | 0.228 |
| DOC_MAPK_gen_1 | 312 | 322 | PF00069 | 0.282 |
| DOC_MAPK_HePTP_8 | 275 | 287 | PF00069 | 0.226 |
| DOC_MAPK_MEF2A_6 | 278 | 287 | PF00069 | 0.267 |
| DOC_MAPK_MEF2A_6 | 313 | 322 | PF00069 | 0.276 |
| DOC_MAPK_NFAT4_5 | 280 | 288 | PF00069 | 0.247 |
| DOC_PP1_RVXF_1 | 250 | 257 | PF00149 | 0.240 |
| DOC_PP4_FxxP_1 | 184 | 187 | PF00568 | 0.424 |
| DOC_SPAK_OSR1_1 | 357 | 361 | PF12202 | 0.287 |
| DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.660 |
| DOC_USP7_MATH_1 | 150 | 154 | PF00917 | 0.507 |
| DOC_USP7_MATH_1 | 246 | 250 | PF00917 | 0.226 |
| DOC_USP7_MATH_1 | 262 | 266 | PF00917 | 0.277 |
| DOC_USP7_MATH_1 | 466 | 470 | PF00917 | 0.700 |
| DOC_USP7_MATH_1 | 520 | 524 | PF00917 | 0.363 |
| DOC_WW_Pin1_4 | 125 | 130 | PF00397 | 0.609 |
| DOC_WW_Pin1_4 | 420 | 425 | PF00397 | 0.745 |
| DOC_WW_Pin1_4 | 456 | 461 | PF00397 | 0.687 |
| DOC_WW_Pin1_4 | 462 | 467 | PF00397 | 0.721 |
| LIG_14-3-3_CanoR_1 | 171 | 177 | PF00244 | 0.361 |
| LIG_14-3-3_CanoR_1 | 2 | 10 | PF00244 | 0.534 |
| LIG_14-3-3_CanoR_1 | 277 | 287 | PF00244 | 0.217 |
| LIG_14-3-3_CanoR_1 | 357 | 361 | PF00244 | 0.539 |
| LIG_14-3-3_CanoR_1 | 364 | 374 | PF00244 | 0.464 |
| LIG_14-3-3_CanoR_1 | 380 | 386 | PF00244 | 0.380 |
| LIG_14-3-3_CanoR_1 | 529 | 534 | PF00244 | 0.461 |
| LIG_Actin_WH2_2 | 324 | 339 | PF00022 | 0.511 |
| LIG_APCC_ABBAyCdc20_2 | 252 | 258 | PF00400 | 0.228 |
| LIG_FHA_1 | 16 | 22 | PF00498 | 0.419 |
| LIG_FHA_1 | 173 | 179 | PF00498 | 0.353 |
| LIG_FHA_1 | 279 | 285 | PF00498 | 0.234 |
| LIG_FHA_1 | 374 | 380 | PF00498 | 0.475 |
| LIG_FHA_1 | 4 | 10 | PF00498 | 0.595 |
| LIG_FHA_1 | 440 | 446 | PF00498 | 0.499 |
| LIG_FHA_1 | 73 | 79 | PF00498 | 0.348 |
| LIG_FHA_2 | 209 | 215 | PF00498 | 0.246 |
| LIG_FHA_2 | 340 | 346 | PF00498 | 0.360 |
| LIG_FHA_2 | 383 | 389 | PF00498 | 0.528 |
| LIG_FHA_2 | 425 | 431 | PF00498 | 0.675 |
| LIG_FHA_2 | 520 | 526 | PF00498 | 0.397 |
| LIG_GBD_Chelix_1 | 275 | 283 | PF00786 | 0.440 |
| LIG_LIR_Apic_2 | 182 | 187 | PF02991 | 0.341 |
| LIG_LIR_Gen_1 | 315 | 323 | PF02991 | 0.384 |
| LIG_LIR_Gen_1 | 355 | 366 | PF02991 | 0.400 |
| LIG_LIR_Gen_1 | 376 | 386 | PF02991 | 0.366 |
| LIG_LIR_Gen_1 | 67 | 78 | PF02991 | 0.338 |
| LIG_LIR_Nem_3 | 315 | 320 | PF02991 | 0.384 |
| LIG_LIR_Nem_3 | 355 | 361 | PF02991 | 0.384 |
| LIG_LIR_Nem_3 | 376 | 381 | PF02991 | 0.499 |
| LIG_LIR_Nem_3 | 502 | 508 | PF02991 | 0.348 |
| LIG_LIR_Nem_3 | 67 | 73 | PF02991 | 0.435 |
| LIG_Pex14_1 | 157 | 161 | PF04695 | 0.452 |
| LIG_Pex14_2 | 310 | 314 | PF04695 | 0.267 |
| LIG_SH2_CRK | 197 | 201 | PF00017 | 0.294 |
| LIG_SH2_CRK | 31 | 35 | PF00017 | 0.441 |
| LIG_SH2_CRK | 70 | 74 | PF00017 | 0.344 |
| LIG_SH2_STAP1 | 66 | 70 | PF00017 | 0.497 |
| LIG_SH2_STAP1 | 76 | 80 | PF00017 | 0.484 |
| LIG_SH2_STAT5 | 437 | 440 | PF00017 | 0.468 |
| LIG_SH2_STAT5 | 70 | 73 | PF00017 | 0.584 |
| LIG_SH3_2 | 187 | 192 | PF14604 | 0.423 |
| LIG_SH3_2 | 471 | 476 | PF14604 | 0.511 |
| LIG_SH3_3 | 126 | 132 | PF00018 | 0.507 |
| LIG_SH3_3 | 184 | 190 | PF00018 | 0.415 |
| LIG_SH3_3 | 317 | 323 | PF00018 | 0.272 |
| LIG_SH3_3 | 368 | 374 | PF00018 | 0.315 |
| LIG_SH3_3 | 419 | 425 | PF00018 | 0.510 |
| LIG_SH3_3 | 465 | 471 | PF00018 | 0.510 |
| LIG_SUMO_SIM_anti_2 | 401 | 409 | PF11976 | 0.507 |
| LIG_SUMO_SIM_par_1 | 218 | 223 | PF11976 | 0.221 |
| LIG_TRAF2_1 | 523 | 526 | PF00917 | 0.368 |
| LIG_TYR_ITIM | 29 | 34 | PF00017 | 0.357 |
| LIG_WW_3 | 423 | 427 | PF00397 | 0.479 |
| MOD_CDC14_SPxK_1 | 423 | 426 | PF00782 | 0.531 |
| MOD_CDK_SPK_2 | 462 | 467 | PF00069 | 0.519 |
| MOD_CDK_SPxK_1 | 420 | 426 | PF00069 | 0.538 |
| MOD_CK1_1 | 153 | 159 | PF00069 | 0.368 |
| MOD_CK1_1 | 182 | 188 | PF00069 | 0.401 |
| MOD_CK1_1 | 321 | 327 | PF00069 | 0.531 |
| MOD_CK1_1 | 390 | 396 | PF00069 | 0.631 |
| MOD_CK1_1 | 451 | 457 | PF00069 | 0.623 |
| MOD_CK1_1 | 458 | 464 | PF00069 | 0.615 |
| MOD_CK1_1 | 479 | 485 | PF00069 | 0.653 |
| MOD_CK2_1 | 208 | 214 | PF00069 | 0.267 |
| MOD_CK2_1 | 424 | 430 | PF00069 | 0.675 |
| MOD_CK2_1 | 451 | 457 | PF00069 | 0.536 |
| MOD_CK2_1 | 519 | 525 | PF00069 | 0.358 |
| MOD_CK2_1 | 71 | 77 | PF00069 | 0.344 |
| MOD_DYRK1A_RPxSP_1 | 467 | 471 | PF00069 | 0.493 |
| MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.576 |
| MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.245 |
| MOD_GlcNHglycan | 248 | 251 | PF01048 | 0.365 |
| MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.351 |
| MOD_GlcNHglycan | 395 | 398 | PF01048 | 0.689 |
| MOD_GlcNHglycan | 453 | 456 | PF01048 | 0.533 |
| MOD_GlcNHglycan | 512 | 515 | PF01048 | 0.490 |
| MOD_GlcNHglycan | 522 | 525 | PF01048 | 0.434 |
| MOD_GlcNHglycan | 536 | 539 | PF01048 | 0.398 |
| MOD_GSK3_1 | 120 | 127 | PF00069 | 0.569 |
| MOD_GSK3_1 | 153 | 160 | PF00069 | 0.349 |
| MOD_GSK3_1 | 352 | 359 | PF00069 | 0.344 |
| MOD_GSK3_1 | 406 | 413 | PF00069 | 0.525 |
| MOD_GSK3_1 | 420 | 427 | PF00069 | 0.770 |
| MOD_GSK3_1 | 451 | 458 | PF00069 | 0.692 |
| MOD_GSK3_1 | 462 | 469 | PF00069 | 0.649 |
| MOD_GSK3_1 | 476 | 483 | PF00069 | 0.571 |
| MOD_GSK3_1 | 516 | 523 | PF00069 | 0.494 |
| MOD_GSK3_1 | 58 | 65 | PF00069 | 0.391 |
| MOD_GSK3_1 | 68 | 75 | PF00069 | 0.372 |
| MOD_NEK2_1 | 1 | 6 | PF00069 | 0.451 |
| MOD_NEK2_1 | 218 | 223 | PF00069 | 0.256 |
| MOD_NEK2_1 | 297 | 302 | PF00069 | 0.328 |
| MOD_NEK2_1 | 379 | 384 | PF00069 | 0.374 |
| MOD_PIKK_1 | 379 | 385 | PF00454 | 0.499 |
| MOD_PK_1 | 432 | 438 | PF00069 | 0.511 |
| MOD_PKA_2 | 1 | 7 | PF00069 | 0.403 |
| MOD_PKA_2 | 356 | 362 | PF00069 | 0.462 |
| MOD_PKA_2 | 379 | 385 | PF00069 | 0.414 |
| MOD_PKA_2 | 388 | 394 | PF00069 | 0.523 |
| MOD_PKA_2 | 466 | 472 | PF00069 | 0.745 |
| MOD_Plk_1 | 68 | 74 | PF00069 | 0.355 |
| MOD_Plk_1 | 93 | 99 | PF00069 | 0.598 |
| MOD_Plk_2-3 | 356 | 362 | PF00069 | 0.424 |
| MOD_Plk_4 | 179 | 185 | PF00069 | 0.516 |
| MOD_Plk_4 | 292 | 298 | PF00069 | 0.322 |
| MOD_Plk_4 | 58 | 64 | PF00069 | 0.332 |
| MOD_Plk_4 | 68 | 74 | PF00069 | 0.386 |
| MOD_ProDKin_1 | 125 | 131 | PF00069 | 0.603 |
| MOD_ProDKin_1 | 420 | 426 | PF00069 | 0.745 |
| MOD_ProDKin_1 | 456 | 462 | PF00069 | 0.687 |
| MOD_ProDKin_1 | 467 | 473 | PF00069 | 0.717 |
| MOD_SUMO_for_1 | 279 | 282 | PF00179 | 0.256 |
| MOD_SUMO_rev_2 | 8 | 15 | PF00179 | 0.554 |
| TRG_DiLeu_BaEn_1 | 100 | 105 | PF01217 | 0.438 |
| TRG_DiLeu_BaEn_4 | 16 | 22 | PF01217 | 0.282 |
| TRG_DiLeu_BaLyEn_6 | 190 | 195 | PF01217 | 0.314 |
| TRG_DiLeu_BaLyEn_6 | 327 | 332 | PF01217 | 0.427 |
| TRG_DiLeu_BaLyEn_6 | 362 | 367 | PF01217 | 0.420 |
| TRG_DiLeu_BaLyEn_6 | 414 | 419 | PF01217 | 0.520 |
| TRG_ENDOCYTIC_2 | 215 | 218 | PF00928 | 0.226 |
| TRG_ENDOCYTIC_2 | 31 | 34 | PF00928 | 0.562 |
| TRG_ENDOCYTIC_2 | 508 | 511 | PF00928 | 0.289 |
| TRG_ENDOCYTIC_2 | 70 | 73 | PF00928 | 0.424 |
| TRG_ER_diArg_1 | 191 | 193 | PF00400 | 0.375 |
| TRG_ER_diArg_1 | 277 | 279 | PF00400 | 0.216 |
| TRG_ER_diArg_1 | 311 | 313 | PF00400 | 0.242 |
| TRG_ER_diArg_1 | 329 | 331 | PF00400 | 0.218 |
| TRG_ER_diArg_1 | 363 | 365 | PF00400 | 0.536 |
| TRG_ER_diArg_1 | 533 | 536 | PF00400 | 0.390 |
| TRG_NES_CRM1_1 | 274 | 288 | PF08389 | 0.301 |
| TRG_NLS_Bipartite_1 | 312 | 332 | PF00514 | 0.290 |
| TRG_Pf-PMV_PEXEL_1 | 277 | 282 | PF00026 | 0.425 |
| TRG_Pf-PMV_PEXEL_1 | 330 | 335 | PF00026 | 0.444 |
| TRG_Pf-PMV_PEXEL_1 | 39 | 44 | PF00026 | 0.354 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P3G0 | Leptomonas seymouri | 30% | 68% |
| A0A0N0P643 | Leptomonas seymouri | 47% | 100% |
| A0A0S4JAU3 | Bodo saltans | 30% | 81% |
| A0A1X0P433 | Trypanosomatidae | 31% | 82% |
| A0A1X0P8T7 | Trypanosomatidae | 29% | 100% |
| A0A1X0P9Z1 | Trypanosomatidae | 40% | 100% |
| A0A3Q8IIF1 | Leishmania donovani | 100% | 100% |
| A0A3R7KPY1 | Trypanosoma rangeli | 32% | 100% |
| A0A3S5H547 | Leishmania donovani | 33% | 100% |
| A0A422NNS9 | Trypanosoma rangeli | 45% | 100% |
| A0A7N9VSG0 | Mus musculus | 30% | 72% |
| A4H3L6 | Leishmania braziliensis | 32% | 100% |
| A4HB54 | Leishmania braziliensis | 74% | 99% |
| A4HME8 | Leishmania braziliensis | 35% | 100% |
| C9ZLZ3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
| D2NT89 | Rothia mucilaginosa (strain DY-18) | 28% | 89% |
| E9ACJ9 | Leishmania major | 33% | 100% |
| E9AG43 | Leishmania infantum | 33% | 100% |
| E9AJT7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
| E9B5C4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 99% |
| P54774 | Glycine max | 29% | 67% |
| P54812 | Caenorhabditis elegans | 29% | 67% |
| Q4Q2K9 | Leishmania major | 94% | 99% |
| Q8SSJ5 | Encephalitozoon cuniculi (strain GB-M1) | 30% | 69% |
| V5B5D2 | Trypanosoma cruzi | 42% | 100% |
| V5BSS5 | Trypanosoma cruzi | 30% | 100% |