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: 0 |
| Forrest at al. (procyclic) | no | yes: 3 |
| Silverman et al. | no | yes: 3 |
| Pissara et al. | yes | yes: 15 |
| 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. | yes | yes: 5 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| DeepLoc | ||
| SignalP6 | no | yes: 0, no: 9 |
| NetGPI | no | yes: 0, no: 9 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005634 | nucleus | 5 | 1 |
| GO:0005654 | nucleoplasm | 2 | 1 |
| GO:0005737 | cytoplasm | 2 | 1 |
| GO:0005829 | cytosol | 2 | 1 |
| GO:0016020 | membrane | 2 | 1 |
| GO:0032991 | protein-containing complex | 1 | 1 |
| GO:0034098 | VCP-NPL4-UFD1 AAA ATPase complex | 3 | 1 |
| GO:0043226 | organelle | 2 | 1 |
| GO:0043227 | membrane-bounded organelle | 3 | 1 |
| GO:0043229 | intracellular organelle | 3 | 1 |
| GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
| GO:0098552 | side of membrane | 2 | 1 |
| GO:0098554 | cytoplasmic side of endoplasmic reticulum membrane | 4 | 1 |
| GO:0098562 | cytoplasmic side of membrane | 3 | 1 |
| GO:0098796 | membrane protein complex | 2 | 1 |
| GO:0110165 | cellular anatomical entity | 1 | 1 |
| GO:0140534 | endoplasmic reticulum protein-containing complex | 2 | 1 |
Related structures:
AlphaFold database: A0A3Q8IQP5
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0000226 | microtubule cytoskeleton organization | 3 | 1 |
| GO:0006508 | proteolysis | 4 | 1 |
| GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 1 |
| GO:0006515 | protein quality control for misfolded or incompletely synthesized proteins | 6 | 1 |
| GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
| GO:0006810 | transport | 3 | 1 |
| GO:0006886 | intracellular protein transport | 4 | 1 |
| GO:0006950 | response to stress | 2 | 1 |
| GO:0006996 | organelle organization | 4 | 1 |
| GO:0007010 | cytoskeleton organization | 5 | 1 |
| GO:0007017 | microtubule-based process | 2 | 1 |
| GO:0007051 | spindle organization | 3 | 1 |
| GO:0007052 | mitotic spindle organization | 4 | 1 |
| GO:0008104 | protein localization | 4 | 1 |
| GO:0008152 | metabolic process | 1 | 1 |
| GO:0009056 | catabolic process | 2 | 1 |
| GO:0009057 | macromolecule catabolic process | 4 | 1 |
| GO:0009987 | cellular process | 1 | 2 |
| GO:0010033 | response to organic substance | 3 | 1 |
| GO:0010243 | response to organonitrogen compound | 4 | 1 |
| GO:0010498 | proteasomal protein catabolic process | 5 | 1 |
| GO:0015031 | protein transport | 4 | 1 |
| GO:0016043 | cellular component organization | 3 | 1 |
| GO:0019538 | protein metabolic process | 3 | 1 |
| GO:0019941 | modification-dependent protein catabolic process | 6 | 1 |
| GO:0022402 | cell cycle process | 2 | 1 |
| GO:0022411 | cellular component disassembly | 4 | 1 |
| GO:0030163 | protein catabolic process | 4 | 1 |
| GO:0030433 | ubiquitin-dependent ERAD pathway | 6 | 1 |
| GO:0030970 | retrograde protein transport, ER to cytosol | 5 | 1 |
| GO:0032527 | protein exit from endoplasmic reticulum | 5 | 1 |
| GO:0032984 | protein-containing complex disassembly | 5 | 1 |
| GO:0033036 | macromolecule localization | 2 | 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:0043170 | macromolecule metabolic process | 3 | 1 |
| GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 1 |
| GO:0043933 | protein-containing complex organization | 4 | 1 |
| GO:0044237 | cellular metabolic process | 2 | 1 |
| GO:0044238 | primary 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:0045184 | establishment of protein localization | 3 | 1 |
| GO:0046907 | intracellular transport | 3 | 1 |
| GO:0050896 | response to stimulus | 1 | 1 |
| GO:0051179 | localization | 1 | 1 |
| GO:0051228 | mitotic spindle disassembly | 5 | 1 |
| GO:0051230 | spindle disassembly | 4 | 1 |
| GO:0051234 | establishment of localization | 2 | 1 |
| GO:0051603 | proteolysis involved in protein catabolic process | 5 | 1 |
| GO:0051641 | cellular localization | 2 | 1 |
| GO:0051649 | establishment of localization in cell | 3 | 1 |
| GO:0051716 | cellular response to stimulus | 2 | 1 |
| GO:0070727 | cellular macromolecule localization | 3 | 1 |
| GO:0071702 | organic substance transport | 4 | 1 |
| GO:0071704 | organic substance metabolic process | 2 | 1 |
| GO:0071705 | nitrogen compound transport | 4 | 1 |
| GO:0071712 | ER-associated misfolded protein catabolic process | 6 | 1 |
| GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
| GO:0097352 | autophagosome maturation | 6 | 1 |
| GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
| GO:1901565 | organonitrogen compound catabolic process | 4 | 1 |
| GO:1901575 | organic substance catabolic process | 3 | 1 |
| GO:1901698 | response to nitrogen compound | 3 | 1 |
| GO:1902850 | microtubule cytoskeleton organization involved in mitosis | 4 | 1 |
| GO:1903008 | organelle disassembly | 5 | 1 |
| GO:1903047 | mitotic cell cycle process | 3 | 1 |
| GO:1903513 | endoplasmic reticulum to cytosol transport | 4 | 1 |
| GO:0051301 | cell division | 2 | 1 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0000166 | nucleotide binding | 3 | 10 |
| GO:0003824 | catalytic activity | 1 | 10 |
| GO:0005488 | binding | 1 | 10 |
| GO:0005524 | ATP binding | 5 | 10 |
| GO:0016462 | pyrophosphatase activity | 5 | 10 |
| GO:0016787 | hydrolase activity | 2 | 10 |
| GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 10 |
| GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 10 |
| GO:0016887 | ATP hydrolysis activity | 7 | 10 |
| GO:0017076 | purine nucleotide binding | 4 | 10 |
| GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 10 |
| GO:0030554 | adenyl nucleotide binding | 5 | 10 |
| GO:0032553 | ribonucleotide binding | 3 | 10 |
| GO:0032555 | purine ribonucleotide binding | 4 | 10 |
| GO:0032559 | adenyl ribonucleotide binding | 5 | 10 |
| GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 10 |
| GO:0036094 | small molecule binding | 2 | 10 |
| GO:0043167 | ion binding | 2 | 10 |
| GO:0043168 | anion binding | 3 | 10 |
| GO:0097159 | organic cyclic compound binding | 2 | 10 |
| GO:0097367 | carbohydrate derivative binding | 2 | 10 |
| GO:1901265 | nucleoside phosphate binding | 3 | 10 |
| GO:1901363 | heterocyclic compound binding | 2 | 10 |
| GO:0005515 | protein binding | 2 | 1 |
| GO:0031593 | polyubiquitin modification-dependent protein binding | 4 | 1 |
| GO:0042802 | identical protein binding | 3 | 1 |
| GO:0140030 | modification-dependent protein binding | 3 | 1 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 186 | 190 | PF00656 | 0.655 |
| CLV_C14_Caspase3-7 | 294 | 298 | PF00656 | 0.344 |
| CLV_C14_Caspase3-7 | 320 | 324 | PF00656 | 0.349 |
| CLV_C14_Caspase3-7 | 567 | 571 | PF00656 | 0.349 |
| CLV_C14_Caspase3-7 | 594 | 598 | PF00656 | 0.349 |
| CLV_C14_Caspase3-7 | 733 | 737 | PF00656 | 0.454 |
| CLV_NRD_NRD_1 | 199 | 201 | PF00675 | 0.571 |
| CLV_NRD_NRD_1 | 276 | 278 | PF00675 | 0.368 |
| CLV_NRD_NRD_1 | 348 | 350 | PF00675 | 0.349 |
| CLV_NRD_NRD_1 | 649 | 651 | PF00675 | 0.455 |
| CLV_NRD_NRD_1 | 731 | 733 | PF00675 | 0.506 |
| CLV_NRD_NRD_1 | 740 | 742 | PF00675 | 0.485 |
| CLV_NRD_NRD_1 | 80 | 82 | PF00675 | 0.388 |
| CLV_PCSK_KEX2_1 | 302 | 304 | PF00082 | 0.344 |
| CLV_PCSK_KEX2_1 | 312 | 314 | PF00082 | 0.344 |
| CLV_PCSK_KEX2_1 | 348 | 350 | PF00082 | 0.349 |
| CLV_PCSK_KEX2_1 | 35 | 37 | PF00082 | 0.349 |
| CLV_PCSK_KEX2_1 | 476 | 478 | PF00082 | 0.430 |
| CLV_PCSK_KEX2_1 | 731 | 733 | PF00082 | 0.506 |
| CLV_PCSK_KEX2_1 | 740 | 742 | PF00082 | 0.485 |
| CLV_PCSK_KEX2_1 | 80 | 82 | PF00082 | 0.349 |
| CLV_PCSK_PC1ET2_1 | 302 | 304 | PF00082 | 0.344 |
| CLV_PCSK_PC1ET2_1 | 312 | 314 | PF00082 | 0.344 |
| CLV_PCSK_PC1ET2_1 | 35 | 37 | PF00082 | 0.349 |
| CLV_PCSK_PC1ET2_1 | 476 | 478 | PF00082 | 0.430 |
| CLV_PCSK_SKI1_1 | 135 | 139 | PF00082 | 0.408 |
| CLV_PCSK_SKI1_1 | 229 | 233 | PF00082 | 0.344 |
| CLV_PCSK_SKI1_1 | 277 | 281 | PF00082 | 0.344 |
| CLV_PCSK_SKI1_1 | 376 | 380 | PF00082 | 0.449 |
| CLV_PCSK_SKI1_1 | 388 | 392 | PF00082 | 0.349 |
| CLV_PCSK_SKI1_1 | 502 | 506 | PF00082 | 0.349 |
| CLV_PCSK_SKI1_1 | 514 | 518 | PF00082 | 0.349 |
| CLV_PCSK_SKI1_1 | 550 | 554 | PF00082 | 0.349 |
| CLV_PCSK_SKI1_1 | 603 | 607 | PF00082 | 0.349 |
| DEG_APCC_DBOX_1 | 103 | 111 | PF00400 | 0.424 |
| DEG_APCC_DBOX_1 | 199 | 207 | PF00400 | 0.453 |
| DEG_APCC_DBOX_1 | 413 | 421 | PF00400 | 0.466 |
| DEG_COP1_1 | 707 | 718 | PF00400 | 0.548 |
| DOC_CKS1_1 | 459 | 464 | PF01111 | 0.499 |
| DOC_MAPK_gen_1 | 11 | 19 | PF00069 | 0.563 |
| DOC_MAPK_gen_1 | 326 | 333 | PF00069 | 0.349 |
| DOC_MAPK_gen_1 | 348 | 359 | PF00069 | 0.349 |
| DOC_MAPK_gen_1 | 35 | 42 | PF00069 | 0.349 |
| DOC_MAPK_gen_1 | 376 | 386 | PF00069 | 0.456 |
| DOC_MAPK_gen_1 | 51 | 61 | PF00069 | 0.349 |
| DOC_MAPK_gen_1 | 623 | 633 | PF00069 | 0.349 |
| DOC_MAPK_gen_1 | 77 | 87 | PF00069 | 0.414 |
| DOC_MAPK_MEF2A_6 | 207 | 214 | PF00069 | 0.440 |
| DOC_MAPK_MEF2A_6 | 285 | 292 | PF00069 | 0.344 |
| DOC_MAPK_MEF2A_6 | 352 | 361 | PF00069 | 0.349 |
| DOC_MAPK_MEF2A_6 | 54 | 63 | PF00069 | 0.349 |
| DOC_MAPK_MEF2A_6 | 557 | 565 | PF00069 | 0.349 |
| DOC_MAPK_MEF2A_6 | 626 | 635 | PF00069 | 0.349 |
| DOC_MAPK_MEF2A_6 | 80 | 87 | PF00069 | 0.373 |
| DOC_MAPK_RevD_3 | 288 | 303 | PF00069 | 0.344 |
| DOC_PP1_RVXF_1 | 148 | 155 | PF00149 | 0.349 |
| DOC_PP1_RVXF_1 | 500 | 507 | PF00149 | 0.416 |
| DOC_PP4_FxxP_1 | 125 | 128 | PF00568 | 0.349 |
| DOC_PP4_FxxP_1 | 506 | 509 | PF00568 | 0.349 |
| DOC_PP4_MxPP_1 | 498 | 501 | PF00568 | 0.525 |
| DOC_USP7_MATH_1 | 148 | 152 | PF00917 | 0.349 |
| DOC_USP7_MATH_1 | 269 | 273 | PF00917 | 0.344 |
| DOC_USP7_MATH_1 | 390 | 394 | PF00917 | 0.349 |
| DOC_USP7_MATH_1 | 653 | 657 | PF00917 | 0.520 |
| DOC_USP7_MATH_1 | 730 | 734 | PF00917 | 0.485 |
| DOC_USP7_MATH_1 | 768 | 772 | PF00917 | 0.866 |
| DOC_WW_Pin1_4 | 165 | 170 | PF00397 | 0.373 |
| DOC_WW_Pin1_4 | 458 | 463 | PF00397 | 0.525 |
| DOC_WW_Pin1_4 | 496 | 501 | PF00397 | 0.493 |
| DOC_WW_Pin1_4 | 649 | 654 | PF00397 | 0.451 |
| LIG_14-3-3_CanoR_1 | 313 | 322 | PF00244 | 0.344 |
| LIG_14-3-3_CanoR_1 | 56 | 60 | PF00244 | 0.478 |
| LIG_14-3-3_CanoR_1 | 731 | 739 | PF00244 | 0.479 |
| LIG_Actin_WH2_2 | 261 | 279 | PF00022 | 0.344 |
| LIG_Actin_WH2_2 | 439 | 457 | PF00022 | 0.486 |
| LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.662 |
| LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.731 |
| LIG_BIR_III_4 | 3 | 7 | PF00653 | 0.648 |
| LIG_BRCT_BRCA1_1 | 150 | 154 | PF00533 | 0.349 |
| LIG_BRCT_BRCA1_1 | 392 | 396 | PF00533 | 0.414 |
| LIG_BRCT_BRCA1_1 | 751 | 755 | PF00533 | 0.588 |
| LIG_CaM_IQ_9 | 435 | 450 | PF13499 | 0.466 |
| LIG_Clathr_ClatBox_1 | 107 | 111 | PF01394 | 0.416 |
| LIG_deltaCOP1_diTrp_1 | 488 | 493 | PF00928 | 0.458 |
| LIG_FHA_1 | 116 | 122 | PF00498 | 0.351 |
| LIG_FHA_1 | 363 | 369 | PF00498 | 0.482 |
| LIG_FHA_1 | 424 | 430 | PF00498 | 0.315 |
| LIG_FHA_1 | 45 | 51 | PF00498 | 0.365 |
| LIG_FHA_1 | 459 | 465 | PF00498 | 0.493 |
| LIG_FHA_1 | 56 | 62 | PF00498 | 0.420 |
| LIG_FHA_1 | 88 | 94 | PF00498 | 0.396 |
| LIG_FHA_2 | 318 | 324 | PF00498 | 0.349 |
| LIG_FHA_2 | 455 | 461 | PF00498 | 0.552 |
| LIG_FHA_2 | 592 | 598 | PF00498 | 0.349 |
| LIG_GBD_Chelix_1 | 314 | 322 | PF00786 | 0.344 |
| LIG_Integrin_RGD_1 | 44 | 46 | PF01839 | 0.349 |
| LIG_LIR_Apic_2 | 123 | 128 | PF02991 | 0.349 |
| LIG_LIR_Gen_1 | 120 | 130 | PF02991 | 0.349 |
| LIG_LIR_Gen_1 | 163 | 172 | PF02991 | 0.373 |
| LIG_LIR_Nem_3 | 120 | 125 | PF02991 | 0.349 |
| LIG_LIR_Nem_3 | 132 | 137 | PF02991 | 0.402 |
| LIG_LIR_Nem_3 | 151 | 157 | PF02991 | 0.355 |
| LIG_LIR_Nem_3 | 163 | 167 | PF02991 | 0.349 |
| LIG_LIR_Nem_3 | 218 | 223 | PF02991 | 0.486 |
| LIG_LIR_Nem_3 | 252 | 258 | PF02991 | 0.344 |
| LIG_SH2_CRK | 134 | 138 | PF00017 | 0.349 |
| LIG_SH2_CRK | 164 | 168 | PF00017 | 0.408 |
| LIG_SH2_CRK | 234 | 238 | PF00017 | 0.344 |
| LIG_SH2_CRK | 507 | 511 | PF00017 | 0.349 |
| LIG_SH2_NCK_1 | 193 | 197 | PF00017 | 0.431 |
| LIG_SH2_PTP2 | 632 | 635 | PF00017 | 0.349 |
| LIG_SH2_SRC | 193 | 196 | PF00017 | 0.440 |
| LIG_SH2_STAT5 | 129 | 132 | PF00017 | 0.349 |
| LIG_SH2_STAT5 | 164 | 167 | PF00017 | 0.408 |
| LIG_SH2_STAT5 | 632 | 635 | PF00017 | 0.349 |
| LIG_SH3_3 | 16 | 22 | PF00018 | 0.466 |
| LIG_SH3_3 | 207 | 213 | PF00018 | 0.442 |
| LIG_SH3_3 | 456 | 462 | PF00018 | 0.536 |
| LIG_SH3_3 | 480 | 486 | PF00018 | 0.428 |
| LIG_SH3_3 | 613 | 619 | PF00018 | 0.373 |
| LIG_SUMO_SIM_anti_2 | 329 | 335 | PF11976 | 0.373 |
| LIG_SUMO_SIM_anti_2 | 415 | 421 | PF11976 | 0.466 |
| LIG_SUMO_SIM_anti_2 | 428 | 433 | PF11976 | 0.465 |
| LIG_SUMO_SIM_anti_2 | 640 | 646 | PF11976 | 0.413 |
| LIG_SUMO_SIM_par_1 | 155 | 160 | PF11976 | 0.349 |
| LIG_SUMO_SIM_par_1 | 316 | 323 | PF11976 | 0.349 |
| LIG_SUMO_SIM_par_1 | 423 | 430 | PF11976 | 0.315 |
| LIG_TRAF2_1 | 279 | 282 | PF00917 | 0.368 |
| LIG_TYR_ITIM | 191 | 196 | PF00017 | 0.444 |
| LIG_TYR_ITIM | 630 | 635 | PF00017 | 0.349 |
| LIG_UBA3_1 | 219 | 226 | PF00899 | 0.485 |
| LIG_UBA3_1 | 318 | 326 | PF00899 | 0.373 |
| LIG_UBA3_1 | 370 | 376 | PF00899 | 0.436 |
| LIG_UBA3_1 | 630 | 638 | PF00899 | 0.365 |
| LIG_WW_3 | 226 | 230 | PF00397 | 0.442 |
| MOD_CDC14_SPxK_1 | 499 | 502 | PF00782 | 0.484 |
| MOD_CDK_SPxK_1 | 496 | 502 | PF00069 | 0.491 |
| MOD_CK1_1 | 168 | 174 | PF00069 | 0.373 |
| MOD_CK1_1 | 239 | 245 | PF00069 | 0.344 |
| MOD_CK1_1 | 28 | 34 | PF00069 | 0.491 |
| MOD_CK2_1 | 454 | 460 | PF00069 | 0.546 |
| MOD_Cter_Amidation | 51 | 54 | PF01082 | 0.349 |
| MOD_GlcNHglycan | 238 | 241 | PF01048 | 0.344 |
| MOD_GlcNHglycan | 451 | 454 | PF01048 | 0.507 |
| MOD_GlcNHglycan | 670 | 673 | PF01048 | 0.349 |
| MOD_GlcNHglycan | 674 | 678 | PF01048 | 0.349 |
| MOD_GlcNHglycan | 770 | 773 | PF01048 | 0.751 |
| MOD_GSK3_1 | 168 | 175 | PF00069 | 0.466 |
| MOD_GSK3_1 | 313 | 320 | PF00069 | 0.344 |
| MOD_GSK3_1 | 454 | 461 | PF00069 | 0.546 |
| MOD_GSK3_1 | 568 | 575 | PF00069 | 0.408 |
| MOD_GSK3_1 | 645 | 652 | PF00069 | 0.477 |
| MOD_GSK3_1 | 664 | 671 | PF00069 | 0.250 |
| MOD_GSK3_1 | 745 | 752 | PF00069 | 0.524 |
| MOD_N-GLC_1 | 115 | 120 | PF02516 | 0.349 |
| MOD_N-GLC_1 | 249 | 254 | PF02516 | 0.344 |
| MOD_NEK2_1 | 130 | 135 | PF00069 | 0.384 |
| MOD_NEK2_1 | 334 | 339 | PF00069 | 0.349 |
| MOD_NEK2_1 | 446 | 451 | PF00069 | 0.504 |
| MOD_NEK2_1 | 454 | 459 | PF00069 | 0.571 |
| MOD_NEK2_1 | 744 | 749 | PF00069 | 0.485 |
| MOD_NEK2_1 | 755 | 760 | PF00069 | 0.652 |
| MOD_NEK2_1 | 87 | 92 | PF00069 | 0.373 |
| MOD_PIKK_1 | 313 | 319 | PF00454 | 0.346 |
| MOD_PIKK_1 | 326 | 332 | PF00454 | 0.357 |
| MOD_PIKK_1 | 435 | 441 | PF00454 | 0.462 |
| MOD_PIKK_1 | 454 | 460 | PF00454 | 0.456 |
| MOD_PKA_2 | 454 | 460 | PF00069 | 0.546 |
| MOD_PKA_2 | 55 | 61 | PF00069 | 0.362 |
| MOD_PKA_2 | 687 | 693 | PF00069 | 0.349 |
| MOD_PKA_2 | 730 | 736 | PF00069 | 0.483 |
| MOD_Plk_1 | 110 | 116 | PF00069 | 0.462 |
| MOD_Plk_1 | 25 | 31 | PF00069 | 0.349 |
| MOD_Plk_1 | 423 | 429 | PF00069 | 0.349 |
| MOD_Plk_2-3 | 415 | 421 | PF00069 | 0.358 |
| MOD_Plk_2-3 | 423 | 429 | PF00069 | 0.337 |
| MOD_Plk_4 | 139 | 145 | PF00069 | 0.534 |
| MOD_Plk_4 | 168 | 174 | PF00069 | 0.349 |
| MOD_Plk_4 | 239 | 245 | PF00069 | 0.344 |
| MOD_Plk_4 | 25 | 31 | PF00069 | 0.368 |
| MOD_Plk_4 | 317 | 323 | PF00069 | 0.349 |
| MOD_Plk_4 | 415 | 421 | PF00069 | 0.373 |
| MOD_Plk_4 | 44 | 50 | PF00069 | 0.386 |
| MOD_Plk_4 | 512 | 518 | PF00069 | 0.349 |
| MOD_Plk_4 | 536 | 542 | PF00069 | 0.349 |
| MOD_ProDKin_1 | 165 | 171 | PF00069 | 0.373 |
| MOD_ProDKin_1 | 458 | 464 | PF00069 | 0.511 |
| MOD_ProDKin_1 | 496 | 502 | PF00069 | 0.491 |
| MOD_ProDKin_1 | 649 | 655 | PF00069 | 0.445 |
| MOD_SUMO_for_1 | 301 | 304 | PF00179 | 0.344 |
| MOD_SUMO_for_1 | 475 | 478 | PF00179 | 0.422 |
| MOD_SUMO_rev_2 | 151 | 157 | PF00179 | 0.349 |
| MOD_SUMO_rev_2 | 694 | 703 | PF00179 | 0.466 |
| TRG_DiLeu_BaEn_1 | 478 | 483 | PF01217 | 0.420 |
| TRG_ENDOCYTIC_2 | 134 | 137 | PF00928 | 0.349 |
| TRG_ENDOCYTIC_2 | 164 | 167 | PF00928 | 0.408 |
| TRG_ENDOCYTIC_2 | 193 | 196 | PF00928 | 0.440 |
| TRG_ENDOCYTIC_2 | 632 | 635 | PF00928 | 0.349 |
| TRG_ENDOCYTIC_2 | 742 | 745 | PF00928 | 0.472 |
| TRG_ER_diArg_1 | 347 | 349 | PF00400 | 0.349 |
| TRG_ER_diArg_1 | 739 | 741 | PF00400 | 0.607 |
| TRG_NES_CRM1_1 | 205 | 218 | PF08389 | 0.453 |
| TRG_NES_CRM1_1 | 425 | 440 | PF08389 | 0.373 |
| TRG_NLS_Bipartite_1 | 35 | 57 | PF00514 | 0.349 |
| TRG_NLS_MonoExtN_4 | 51 | 57 | PF00514 | 0.349 |
| TRG_Pf-PMV_PEXEL_1 | 477 | 481 | PF00026 | 0.431 |
| TRG_Pf-PMV_PEXEL_1 | 587 | 591 | PF00026 | 0.349 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P3G0 | Leptomonas seymouri | 92% | 99% |
| A0A0N0P6J4 | Leptomonas seymouri | 45% | 100% |
| A0A0S4IKL1 | Bodo saltans | 30% | 100% |
| A0A0S4IMC7 | Bodo saltans | 53% | 100% |
| A0A0S4JAU3 | Bodo saltans | 44% | 100% |
| A0A0S4JI00 | Bodo saltans | 73% | 100% |
| A0A1X0P433 | Trypanosomatidae | 45% | 100% |
| A0A1X0P870 | Trypanosomatidae | 85% | 100% |
| A0A1X0PA10 | Trypanosomatidae | 29% | 86% |
| A0A3R7M308 | Trypanosoma rangeli | 33% | 100% |
| A0A3R7M9L0 | Trypanosoma rangeli | 84% | 100% |
| A0A3S7X0L3 | Leishmania donovani | 45% | 100% |
| A0A422MWE3 | Trypanosoma rangeli | 44% | 100% |
| A4HFM9 | Leishmania braziliensis | 45% | 100% |
| A4HNZ5 | Leishmania braziliensis | 96% | 100% |
| A4I2Q7 | Leishmania infantum | 45% | 100% |
| A4ICJ9 | Leishmania infantum | 97% | 100% |
| A7YSY2 | Bos taurus | 39% | 100% |
| C9ZR48 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 99% |
| D0A2X0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 83% | 100% |
| D0A5V8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
| D4A2B7 | Rattus norvegicus | 37% | 100% |
| E9AD83 | Leishmania major | 46% | 100% |
| E9ASQ6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 99% | 100% |
| E9AZ07 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 45% | 100% |
| G1X4S3 | Arthrobotrys oligospora (strain ATCC 24927 / CBS 115.81 / DSM 1491) | 36% | 66% |
| O05209 | Thermoplasma acidophilum (strain ATCC 25905 / DSM 1728 / JCM 9062 / NBRC 15155 / AMRC-C165) | 50% | 100% |
| O13764 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 33% | 83% |
| O14325 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 41% | 100% |
| O15381 | Homo sapiens | 42% | 92% |
| O28972 | Archaeoglobus fulgidus (strain ATCC 49558 / DSM 4304 / JCM 9628 / NBRC 100126 / VC-16) | 48% | 100% |
| O60058 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 45% | 97% |
| P03974 | Sus scrofa | 74% | 97% |
| P23787 | Xenopus laevis | 74% | 97% |
| P25694 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 63% | 94% |
| P32794 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 43% | 100% |
| P46462 | Rattus norvegicus | 74% | 97% |
| P46463 | Komagataella pastoris | 31% | 68% |
| P54609 | Arabidopsis thaliana | 71% | 97% |
| P54774 | Glycine max | 71% | 97% |
| P54777 | Rattus norvegicus | 35% | 80% |
| P54811 | Caenorhabditis elegans | 69% | 97% |
| P54812 | Caenorhabditis elegans | 71% | 97% |
| P55072 | Homo sapiens | 74% | 97% |
| Q01853 | Mus musculus | 74% | 97% |
| Q07590 | Sulfolobus acidocaldarius (strain ATCC 33909 / DSM 639 / JCM 8929 / NBRC 15157 / NCIMB 11770) | 44% | 100% |
| Q07844 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 40% | 94% |
| Q13608 | Homo sapiens | 35% | 80% |
| Q3UMC0 | Mus musculus | 48% | 88% |
| Q3ZBT1 | Bos taurus | 74% | 97% |
| Q4Q1T9 | Leishmania major | 99% | 100% |
| Q54SY2 | Dictyostelium discoideum | 39% | 90% |
| Q58556 | Methanocaldococcus jannaschii (strain ATCC 43067 / DSM 2661 / JAL-1 / JCM 10045 / NBRC 100440) | 49% | 87% |
| Q5AWS6 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 66% | 95% |
| Q6CPV1 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 34% | 78% |
| Q6GL04 | Xenopus tropicalis | 74% | 97% |
| Q74Z13 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 32% | 77% |
| Q7KN62 | Drosophila melanogaster | 71% | 98% |
| Q7ZU99 | Danio rerio | 73% | 97% |
| Q8NB90 | Homo sapiens | 49% | 88% |
| Q8RY16 | Arabidopsis thaliana | 33% | 83% |
| Q8SSJ5 | Encephalitozoon cuniculi (strain GB-M1) | 59% | 100% |
| Q96372 | Capsicum annuum | 71% | 97% |
| Q99LC9 | Mus musculus | 36% | 80% |
| Q9DBY8 | Mus musculus | 41% | 92% |
| Q9HPF0 | Halobacterium salinarum (strain ATCC 700922 / JCM 11081 / NRC-1) | 42% | 100% |
| Q9LZF6 | Arabidopsis thaliana | 71% | 97% |
| Q9M0Y8 | Arabidopsis thaliana | 27% | 100% |
| Q9NAG4 | Caenorhabditis elegans | 36% | 96% |
| Q9P3A7 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 64% | 96% |
| Q9SCN8 | Arabidopsis thaliana | 69% | 96% |
| Q9SS94 | Arabidopsis thaliana | 43% | 96% |
| V5BD45 | Trypanosoma cruzi | 44% | 100% |
| V5BKY8 | Trypanosoma cruzi | 27% | 100% |