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)
Metal Binding, Transitional endoplasmic reticulum ATPase
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) | yes | yes: 3 |
Silverman et al. | no | yes: 3 |
Pissara et al. | yes | yes: 12 |
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: 5 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 8 |
NetGPI | no | yes: 0, no: 8 |
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 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pescher et al. (upgregulation) | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Lahav et al. - mRNA
- Protein
|
Related structures:
AlphaFold database: A4ICJ9
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 | 3 |
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 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 9 |
GO:0003824 | catalytic activity | 1 | 9 |
GO:0005488 | binding | 1 | 9 |
GO:0005524 | ATP binding | 5 | 9 |
GO:0016462 | pyrophosphatase activity | 5 | 9 |
GO:0016787 | hydrolase activity | 2 | 9 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 9 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 9 |
GO:0016887 | ATP hydrolysis activity | 7 | 9 |
GO:0017076 | purine nucleotide binding | 4 | 9 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 9 |
GO:0030554 | adenyl nucleotide binding | 5 | 9 |
GO:0032553 | ribonucleotide binding | 3 | 9 |
GO:0032555 | purine ribonucleotide binding | 4 | 9 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 9 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 9 |
GO:0036094 | small molecule binding | 2 | 9 |
GO:0043167 | ion binding | 2 | 9 |
GO:0043168 | anion binding | 3 | 9 |
GO:0097159 | organic cyclic compound binding | 2 | 9 |
GO:0097367 | carbohydrate derivative binding | 2 | 9 |
GO:1901265 | nucleoside phosphate binding | 3 | 9 |
GO:1901363 | heterocyclic compound binding | 2 | 9 |
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 | 0.567 |
CLV_C14_Caspase3-7 | 226 | 230 | PF00656 | 0.292 |
CLV_C14_Caspase3-7 | 473 | 477 | PF00656 | 0.292 |
CLV_C14_Caspase3-7 | 500 | 504 | PF00656 | 0.292 |
CLV_C14_Caspase3-7 | 639 | 643 | PF00656 | 0.391 |
CLV_NRD_NRD_1 | 254 | 256 | PF00675 | 0.292 |
CLV_NRD_NRD_1 | 555 | 557 | PF00675 | 0.390 |
CLV_NRD_NRD_1 | 637 | 639 | PF00675 | 0.441 |
CLV_NRD_NRD_1 | 646 | 648 | PF00675 | 0.425 |
CLV_NRD_NRD_1 | 80 | 82 | PF00675 | 0.293 |
CLV_PCSK_KEX2_1 | 254 | 256 | PF00082 | 0.292 |
CLV_PCSK_KEX2_1 | 35 | 37 | PF00082 | 0.316 |
CLV_PCSK_KEX2_1 | 382 | 384 | PF00082 | 0.364 |
CLV_PCSK_KEX2_1 | 637 | 639 | PF00082 | 0.441 |
CLV_PCSK_KEX2_1 | 646 | 648 | PF00082 | 0.425 |
CLV_PCSK_KEX2_1 | 80 | 82 | PF00082 | 0.316 |
CLV_PCSK_PC1ET2_1 | 35 | 37 | PF00082 | 0.316 |
CLV_PCSK_PC1ET2_1 | 382 | 384 | PF00082 | 0.364 |
CLV_PCSK_SKI1_1 | 135 | 139 | PF00082 | 0.316 |
CLV_PCSK_SKI1_1 | 282 | 286 | PF00082 | 0.388 |
CLV_PCSK_SKI1_1 | 294 | 298 | PF00082 | 0.272 |
CLV_PCSK_SKI1_1 | 408 | 412 | PF00082 | 0.292 |
CLV_PCSK_SKI1_1 | 420 | 424 | PF00082 | 0.292 |
CLV_PCSK_SKI1_1 | 456 | 460 | PF00082 | 0.292 |
CLV_PCSK_SKI1_1 | 509 | 513 | PF00082 | 0.292 |
DEG_APCC_DBOX_1 | 103 | 111 | PF00400 | 0.402 |
DEG_APCC_DBOX_1 | 319 | 327 | PF00400 | 0.391 |
DEG_COP1_1 | 613 | 624 | PF00400 | 0.428 |
DOC_CKS1_1 | 365 | 370 | PF01111 | 0.422 |
DOC_MAPK_gen_1 | 11 | 19 | PF00069 | 0.544 |
DOC_MAPK_gen_1 | 232 | 239 | PF00069 | 0.316 |
DOC_MAPK_gen_1 | 254 | 265 | PF00069 | 0.292 |
DOC_MAPK_gen_1 | 282 | 292 | PF00069 | 0.404 |
DOC_MAPK_gen_1 | 35 | 42 | PF00069 | 0.311 |
DOC_MAPK_gen_1 | 51 | 61 | PF00069 | 0.232 |
DOC_MAPK_gen_1 | 529 | 539 | PF00069 | 0.292 |
DOC_MAPK_gen_1 | 77 | 87 | PF00069 | 0.316 |
DOC_MAPK_MEF2A_6 | 258 | 267 | PF00069 | 0.292 |
DOC_MAPK_MEF2A_6 | 463 | 471 | PF00069 | 0.273 |
DOC_MAPK_MEF2A_6 | 532 | 541 | PF00069 | 0.292 |
DOC_MAPK_MEF2A_6 | 54 | 63 | PF00069 | 0.292 |
DOC_MAPK_MEF2A_6 | 80 | 87 | PF00069 | 0.316 |
DOC_PP1_RVXF_1 | 148 | 155 | PF00149 | 0.292 |
DOC_PP1_RVXF_1 | 406 | 413 | PF00149 | 0.352 |
DOC_PP4_FxxP_1 | 125 | 128 | PF00568 | 0.292 |
DOC_PP4_FxxP_1 | 412 | 415 | PF00568 | 0.292 |
DOC_PP4_MxPP_1 | 404 | 407 | PF00568 | 0.455 |
DOC_USP7_MATH_1 | 148 | 152 | PF00917 | 0.316 |
DOC_USP7_MATH_1 | 296 | 300 | PF00917 | 0.316 |
DOC_USP7_MATH_1 | 559 | 563 | PF00917 | 0.445 |
DOC_USP7_MATH_1 | 636 | 640 | PF00917 | 0.443 |
DOC_USP7_MATH_1 | 674 | 678 | PF00917 | 0.766 |
DOC_WW_Pin1_4 | 165 | 170 | PF00397 | 0.303 |
DOC_WW_Pin1_4 | 212 | 217 | PF00397 | 0.123 |
DOC_WW_Pin1_4 | 364 | 369 | PF00397 | 0.437 |
DOC_WW_Pin1_4 | 402 | 407 | PF00397 | 0.404 |
DOC_WW_Pin1_4 | 555 | 560 | PF00397 | 0.382 |
LIG_14-3-3_CanoR_1 | 56 | 60 | PF00244 | 0.348 |
LIG_14-3-3_CanoR_1 | 637 | 645 | PF00244 | 0.420 |
LIG_Actin_WH2_2 | 345 | 363 | PF00022 | 0.463 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.609 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.618 |
LIG_BIR_III_4 | 3 | 7 | PF00653 | 0.630 |
LIG_BRCT_BRCA1_1 | 150 | 154 | PF00533 | 0.316 |
LIG_BRCT_BRCA1_1 | 298 | 302 | PF00533 | 0.432 |
LIG_BRCT_BRCA1_1 | 657 | 661 | PF00533 | 0.558 |
LIG_CaM_IQ_9 | 341 | 356 | PF13499 | 0.391 |
LIG_Clathr_ClatBox_1 | 107 | 111 | PF01394 | 0.391 |
LIG_CSL_BTD_1 | 197 | 200 | PF09270 | 0.369 |
LIG_deltaCOP1_diTrp_1 | 394 | 399 | PF00928 | 0.391 |
LIG_FHA_1 | 116 | 122 | PF00498 | 0.309 |
LIG_FHA_1 | 269 | 275 | PF00498 | 0.470 |
LIG_FHA_1 | 330 | 336 | PF00498 | 0.246 |
LIG_FHA_1 | 365 | 371 | PF00498 | 0.405 |
LIG_FHA_1 | 45 | 51 | PF00498 | 0.292 |
LIG_FHA_1 | 56 | 62 | PF00498 | 0.274 |
LIG_FHA_1 | 88 | 94 | PF00498 | 0.292 |
LIG_FHA_2 | 224 | 230 | PF00498 | 0.292 |
LIG_FHA_2 | 361 | 367 | PF00498 | 0.453 |
LIG_FHA_2 | 498 | 504 | PF00498 | 0.292 |
LIG_Integrin_RGD_1 | 44 | 46 | PF01839 | 0.292 |
LIG_LIR_Apic_2 | 123 | 128 | PF02991 | 0.292 |
LIG_LIR_Apic_2 | 194 | 200 | PF02991 | 0.351 |
LIG_LIR_Gen_1 | 120 | 130 | PF02991 | 0.292 |
LIG_LIR_Gen_1 | 163 | 172 | PF02991 | 0.272 |
LIG_LIR_Nem_3 | 120 | 125 | PF02991 | 0.292 |
LIG_LIR_Nem_3 | 132 | 137 | PF02991 | 0.292 |
LIG_LIR_Nem_3 | 151 | 157 | PF02991 | 0.175 |
LIG_LIR_Nem_3 | 163 | 167 | PF02991 | 0.256 |
LIG_MAD2 | 92 | 100 | PF02301 | 0.205 |
LIG_PCNA_yPIPBox_3 | 218 | 228 | PF02747 | 0.123 |
LIG_SH2_CRK | 134 | 138 | PF00017 | 0.292 |
LIG_SH2_CRK | 164 | 168 | PF00017 | 0.292 |
LIG_SH2_CRK | 413 | 417 | PF00017 | 0.292 |
LIG_SH2_PTP2 | 538 | 541 | PF00017 | 0.292 |
LIG_SH2_SRC | 193 | 196 | PF00017 | 0.490 |
LIG_SH2_STAP1 | 193 | 197 | PF00017 | 0.333 |
LIG_SH2_STAT5 | 129 | 132 | PF00017 | 0.292 |
LIG_SH2_STAT5 | 164 | 167 | PF00017 | 0.292 |
LIG_SH2_STAT5 | 538 | 541 | PF00017 | 0.292 |
LIG_SH3_3 | 16 | 22 | PF00018 | 0.364 |
LIG_SH3_3 | 362 | 368 | PF00018 | 0.446 |
LIG_SH3_3 | 386 | 392 | PF00018 | 0.359 |
LIG_SH3_3 | 519 | 525 | PF00018 | 0.323 |
LIG_SUMO_SIM_anti_2 | 235 | 241 | PF11976 | 0.334 |
LIG_SUMO_SIM_anti_2 | 321 | 327 | PF11976 | 0.391 |
LIG_SUMO_SIM_anti_2 | 334 | 339 | PF11976 | 0.391 |
LIG_SUMO_SIM_anti_2 | 546 | 552 | PF11976 | 0.348 |
LIG_SUMO_SIM_par_1 | 155 | 160 | PF11976 | 0.292 |
LIG_SUMO_SIM_par_1 | 222 | 229 | PF11976 | 0.316 |
LIG_SUMO_SIM_par_1 | 329 | 336 | PF11976 | 0.246 |
LIG_TRAF2_1 | 219 | 222 | PF00917 | 0.123 |
LIG_TYR_ITIM | 191 | 196 | PF00017 | 0.492 |
LIG_TYR_ITIM | 536 | 541 | PF00017 | 0.292 |
LIG_UBA3_1 | 224 | 232 | PF00899 | 0.320 |
LIG_UBA3_1 | 276 | 282 | PF00899 | 0.377 |
LIG_UBA3_1 | 536 | 544 | PF00899 | 0.308 |
LIG_WW_3 | 215 | 219 | PF00397 | 0.123 |
MOD_CDC14_SPxK_1 | 215 | 218 | PF00782 | 0.123 |
MOD_CDC14_SPxK_1 | 405 | 408 | PF00782 | 0.392 |
MOD_CDK_SPxK_1 | 212 | 218 | PF00069 | 0.123 |
MOD_CDK_SPxK_1 | 402 | 408 | PF00069 | 0.401 |
MOD_CK1_1 | 168 | 174 | PF00069 | 0.316 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.388 |
MOD_CK2_1 | 360 | 366 | PF00069 | 0.474 |
MOD_Cter_Amidation | 51 | 54 | PF01082 | 0.292 |
MOD_GlcNHglycan | 357 | 360 | PF01048 | 0.488 |
MOD_GlcNHglycan | 576 | 579 | PF01048 | 0.292 |
MOD_GlcNHglycan | 580 | 584 | PF01048 | 0.292 |
MOD_GlcNHglycan | 676 | 679 | PF01048 | 0.686 |
MOD_GSK3_1 | 168 | 175 | PF00069 | 0.391 |
MOD_GSK3_1 | 360 | 367 | PF00069 | 0.478 |
MOD_GSK3_1 | 474 | 481 | PF00069 | 0.364 |
MOD_GSK3_1 | 551 | 558 | PF00069 | 0.444 |
MOD_GSK3_1 | 570 | 577 | PF00069 | 0.133 |
MOD_GSK3_1 | 651 | 658 | PF00069 | 0.498 |
MOD_N-GLC_1 | 115 | 120 | PF02516 | 0.292 |
MOD_NEK2_1 | 130 | 135 | PF00069 | 0.325 |
MOD_NEK2_1 | 240 | 245 | PF00069 | 0.301 |
MOD_NEK2_1 | 352 | 357 | PF00069 | 0.455 |
MOD_NEK2_1 | 360 | 365 | PF00069 | 0.476 |
MOD_NEK2_1 | 650 | 655 | PF00069 | 0.430 |
MOD_NEK2_1 | 661 | 666 | PF00069 | 0.594 |
MOD_NEK2_1 | 87 | 92 | PF00069 | 0.285 |
MOD_PIKK_1 | 232 | 238 | PF00454 | 0.325 |
MOD_PIKK_1 | 341 | 347 | PF00454 | 0.388 |
MOD_PIKK_1 | 360 | 366 | PF00454 | 0.355 |
MOD_PKA_2 | 360 | 366 | PF00069 | 0.480 |
MOD_PKA_2 | 55 | 61 | PF00069 | 0.292 |
MOD_PKA_2 | 593 | 599 | PF00069 | 0.292 |
MOD_PKA_2 | 636 | 642 | PF00069 | 0.420 |
MOD_Plk_1 | 110 | 116 | PF00069 | 0.395 |
MOD_Plk_1 | 25 | 31 | PF00069 | 0.298 |
MOD_Plk_1 | 329 | 335 | PF00069 | 0.278 |
MOD_Plk_2-3 | 321 | 327 | PF00069 | 0.292 |
MOD_Plk_2-3 | 329 | 335 | PF00069 | 0.292 |
MOD_Plk_4 | 139 | 145 | PF00069 | 0.432 |
MOD_Plk_4 | 168 | 174 | PF00069 | 0.292 |
MOD_Plk_4 | 223 | 229 | PF00069 | 0.292 |
MOD_Plk_4 | 25 | 31 | PF00069 | 0.315 |
MOD_Plk_4 | 321 | 327 | PF00069 | 0.274 |
MOD_Plk_4 | 418 | 424 | PF00069 | 0.287 |
MOD_Plk_4 | 44 | 50 | PF00069 | 0.162 |
MOD_Plk_4 | 442 | 448 | PF00069 | 0.292 |
MOD_ProDKin_1 | 165 | 171 | PF00069 | 0.303 |
MOD_ProDKin_1 | 212 | 218 | PF00069 | 0.123 |
MOD_ProDKin_1 | 364 | 370 | PF00069 | 0.426 |
MOD_ProDKin_1 | 402 | 408 | PF00069 | 0.401 |
MOD_ProDKin_1 | 555 | 561 | PF00069 | 0.377 |
MOD_SUMO_for_1 | 381 | 384 | PF00179 | 0.356 |
MOD_SUMO_rev_2 | 151 | 157 | PF00179 | 0.316 |
MOD_SUMO_rev_2 | 600 | 609 | PF00179 | 0.348 |
TRG_DiLeu_BaEn_1 | 384 | 389 | PF01217 | 0.355 |
TRG_ENDOCYTIC_2 | 134 | 137 | PF00928 | 0.292 |
TRG_ENDOCYTIC_2 | 164 | 167 | PF00928 | 0.292 |
TRG_ENDOCYTIC_2 | 193 | 196 | PF00928 | 0.490 |
TRG_ENDOCYTIC_2 | 538 | 541 | PF00928 | 0.276 |
TRG_ENDOCYTIC_2 | 648 | 651 | PF00928 | 0.415 |
TRG_ER_diArg_1 | 253 | 255 | PF00400 | 0.292 |
TRG_ER_diArg_1 | 645 | 647 | PF00400 | 0.530 |
TRG_NES_CRM1_1 | 331 | 346 | PF08389 | 0.292 |
TRG_NLS_Bipartite_1 | 35 | 57 | PF00514 | 0.316 |
TRG_NLS_MonoExtN_4 | 51 | 57 | PF00514 | 0.292 |
TRG_Pf-PMV_PEXEL_1 | 383 | 387 | PF00026 | 0.365 |
TRG_Pf-PMV_PEXEL_1 | 493 | 497 | PF00026 | 0.292 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3G0 | Leptomonas seymouri | 88% | 87% |
A0A0S4JI00 | Bodo saltans | 71% | 94% |
A0A1X0P870 | Trypanosomatidae | 82% | 88% |
A0A3Q8IQP5 | Leishmania donovani | 97% | 88% |
A0A3R7M9L0 | Trypanosoma rangeli | 82% | 88% |
A0A3S7X0L3 | Leishmania donovani | 44% | 100% |
A4HFM9 | Leishmania braziliensis | 44% | 100% |
A4HNZ5 | Leishmania braziliensis | 93% | 88% |
A4I2Q7 | Leishmania infantum | 44% | 100% |
C9ZR48 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 87% |
D4A2B7 | Rattus norvegicus | 37% | 92% |
E9AD83 | Leishmania major | 44% | 100% |
E9AZ07 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 44% | 100% |
O14325 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 38% | 89% |
O15381 | Homo sapiens | 39% | 81% |
O60058 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 38% | 85% |
P25694 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 59% | 83% |
P54609 | Arabidopsis thaliana | 63% | 85% |
P54774 | Glycine max | 64% | 86% |
P54811 | Caenorhabditis elegans | 70% | 85% |
P54812 | Caenorhabditis elegans | 70% | 85% |
Q07844 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 38% | 82% |
Q4Q1T9 | Leishmania major | 96% | 88% |
Q5AWS6 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 65% | 84% |
Q7KN62 | Drosophila melanogaster | 70% | 86% |
Q8SSJ5 | Encephalitozoon cuniculi (strain GB-M1) | 62% | 88% |
Q96372 | Capsicum annuum | 69% | 86% |
Q9DBY8 | Mus musculus | 39% | 81% |
Q9LZF6 | Arabidopsis thaliana | 64% | 85% |
Q9P3A7 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 62% | 85% |
Q9SCN8 | Arabidopsis thaliana | 62% | 85% |