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: 6 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 16 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 12 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 16 |
NetGPI | no | yes: 0, no: 16 |
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 | 15 |
GO:0005654 | nucleoplasm | 2 | 1 |
GO:0005737 | cytoplasm | 2 | 4 |
GO:0005838 | proteasome regulatory particle | 2 | 1 |
GO:0008540 | proteasome regulatory particle, base subcomplex | 2 | 1 |
GO:0032991 | protein-containing complex | 1 | 3 |
GO:0000502 | proteasome complex | 3 | 2 |
GO:0140535 | intracellular protein-containing complex | 2 | 2 |
GO:1902494 | catalytic complex | 2 | 2 |
GO:1905368 | peptidase complex | 3 | 2 |
GO:1905369 | endopeptidase complex | 4 | 2 |
Related structures:
AlphaFold database: E9B5C4
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 1 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 3 |
GO:0008152 | metabolic process | 1 | 3 |
GO:0009056 | catabolic process | 2 | 3 |
GO:0009057 | macromolecule catabolic process | 4 | 3 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010498 | proteasomal protein catabolic process | 5 | 1 |
GO:0019538 | protein metabolic process | 3 | 3 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 1 |
GO:0030163 | protein catabolic process | 4 | 3 |
GO:0043161 | proteasome-mediated ubiquitin-dependent protein catabolic process | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 3 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 3 |
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:0051603 | proteolysis involved in protein catabolic process | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 3 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 3 |
GO:1901565 | organonitrogen compound catabolic process | 4 | 3 |
GO:1901575 | organic substance catabolic process | 3 | 3 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 17 |
GO:0003824 | catalytic activity | 1 | 17 |
GO:0005488 | binding | 1 | 17 |
GO:0005524 | ATP binding | 5 | 17 |
GO:0016462 | pyrophosphatase activity | 5 | 17 |
GO:0016787 | hydrolase activity | 2 | 17 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 17 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 17 |
GO:0016887 | ATP hydrolysis activity | 7 | 17 |
GO:0017076 | purine nucleotide binding | 4 | 17 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 17 |
GO:0030554 | adenyl nucleotide binding | 5 | 17 |
GO:0032553 | ribonucleotide binding | 3 | 17 |
GO:0032555 | purine ribonucleotide binding | 4 | 17 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 17 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 17 |
GO:0036094 | small molecule binding | 2 | 17 |
GO:0043167 | ion binding | 2 | 17 |
GO:0043168 | anion binding | 3 | 17 |
GO:0097159 | organic cyclic compound binding | 2 | 17 |
GO:0097367 | carbohydrate derivative binding | 2 | 17 |
GO:1901265 | nucleoside phosphate binding | 3 | 17 |
GO:1901363 | heterocyclic compound binding | 2 | 17 |
GO:0036402 | proteasome-activating activity | 2 | 3 |
GO:0140657 | ATP-dependent activity | 1 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 115 | 119 | PF00656 | 0.484 |
CLV_C14_Caspase3-7 | 260 | 264 | PF00656 | 0.307 |
CLV_C14_Caspase3-7 | 95 | 99 | PF00656 | 0.523 |
CLV_NRD_NRD_1 | 194 | 196 | PF00675 | 0.359 |
CLV_NRD_NRD_1 | 279 | 281 | PF00675 | 0.240 |
CLV_NRD_NRD_1 | 314 | 316 | PF00675 | 0.280 |
CLV_NRD_NRD_1 | 331 | 333 | PF00675 | 0.428 |
CLV_NRD_NRD_1 | 366 | 368 | PF00675 | 0.379 |
CLV_PCSK_KEX2_1 | 194 | 196 | PF00082 | 0.360 |
CLV_PCSK_KEX2_1 | 279 | 281 | PF00082 | 0.240 |
CLV_PCSK_KEX2_1 | 314 | 316 | PF00082 | 0.258 |
CLV_PCSK_KEX2_1 | 330 | 332 | PF00082 | 0.399 |
CLV_PCSK_KEX2_1 | 366 | 368 | PF00082 | 0.379 |
CLV_PCSK_PC1ET2_1 | 330 | 332 | PF00082 | 0.534 |
CLV_PCSK_PC7_1 | 190 | 196 | PF00082 | 0.402 |
CLV_PCSK_SKI1_1 | 173 | 177 | PF00082 | 0.402 |
CLV_PCSK_SKI1_1 | 194 | 198 | PF00082 | 0.307 |
CLV_PCSK_SKI1_1 | 242 | 246 | PF00082 | 0.296 |
CLV_PCSK_SKI1_1 | 254 | 258 | PF00082 | 0.171 |
CLV_PCSK_SKI1_1 | 26 | 30 | PF00082 | 0.460 |
CLV_PCSK_SKI1_1 | 279 | 283 | PF00082 | 0.310 |
CLV_PCSK_SKI1_1 | 331 | 335 | PF00082 | 0.384 |
CLV_PCSK_SKI1_1 | 366 | 370 | PF00082 | 0.347 |
CLV_PCSK_SKI1_1 | 452 | 456 | PF00082 | 0.700 |
CLV_PCSK_SKI1_1 | 50 | 54 | PF00082 | 0.395 |
CLV_PCSK_SKI1_1 | 526 | 530 | PF00082 | 0.607 |
DEG_APCC_DBOX_1 | 49 | 57 | PF00400 | 0.542 |
DEG_Kelch_Keap1_1 | 392 | 397 | PF01344 | 0.466 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.505 |
DOC_CKS1_1 | 126 | 131 | PF01111 | 0.525 |
DOC_CYCLIN_RxL_1 | 328 | 337 | PF00134 | 0.383 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 299 | 308 | PF00134 | 0.331 |
DOC_CYCLIN_yCln2_LP_2 | 133 | 139 | PF00134 | 0.449 |
DOC_MAPK_gen_1 | 279 | 289 | PF00069 | 0.251 |
DOC_MAPK_gen_1 | 314 | 324 | PF00069 | 0.309 |
DOC_MAPK_HePTP_8 | 277 | 289 | PF00069 | 0.257 |
DOC_MAPK_MEF2A_6 | 280 | 289 | PF00069 | 0.273 |
DOC_MAPK_MEF2A_6 | 315 | 324 | PF00069 | 0.261 |
DOC_MAPK_NFAT4_5 | 282 | 290 | PF00069 | 0.273 |
DOC_PP1_RVXF_1 | 252 | 259 | PF00149 | 0.273 |
DOC_PP2B_LxvP_1 | 133 | 136 | PF13499 | 0.505 |
DOC_PP2B_PxIxI_1 | 57 | 63 | PF00149 | 0.314 |
DOC_PP4_FxxP_1 | 186 | 189 | PF00568 | 0.451 |
DOC_SPAK_OSR1_1 | 359 | 363 | PF12202 | 0.336 |
DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.700 |
DOC_USP7_MATH_1 | 152 | 156 | PF00917 | 0.556 |
DOC_USP7_MATH_1 | 248 | 252 | PF00917 | 0.260 |
DOC_USP7_MATH_1 | 264 | 268 | PF00917 | 0.323 |
DOC_USP7_MATH_1 | 424 | 428 | PF00917 | 0.542 |
DOC_USP7_MATH_1 | 468 | 472 | PF00917 | 0.737 |
DOC_USP7_MATH_1 | 517 | 521 | PF00917 | 0.542 |
DOC_WW_Pin1_4 | 125 | 130 | PF00397 | 0.653 |
DOC_WW_Pin1_4 | 458 | 463 | PF00397 | 0.747 |
DOC_WW_Pin1_4 | 464 | 469 | PF00397 | 0.786 |
LIG_14-3-3_CanoR_1 | 160 | 164 | PF00244 | 0.477 |
LIG_14-3-3_CanoR_1 | 173 | 179 | PF00244 | 0.391 |
LIG_14-3-3_CanoR_1 | 2 | 10 | PF00244 | 0.558 |
LIG_14-3-3_CanoR_1 | 279 | 289 | PF00244 | 0.273 |
LIG_14-3-3_CanoR_1 | 359 | 363 | PF00244 | 0.336 |
LIG_14-3-3_CanoR_1 | 366 | 376 | PF00244 | 0.317 |
LIG_14-3-3_CanoR_1 | 382 | 388 | PF00244 | 0.484 |
LIG_14-3-3_CanoR_1 | 526 | 531 | PF00244 | 0.630 |
LIG_Actin_WH2_2 | 326 | 341 | PF00022 | 0.544 |
LIG_APCC_ABBAyCdc20_2 | 254 | 260 | PF00400 | 0.256 |
LIG_FHA_1 | 128 | 134 | PF00498 | 0.644 |
LIG_FHA_1 | 175 | 181 | PF00498 | 0.400 |
LIG_FHA_1 | 281 | 287 | PF00498 | 0.234 |
LIG_FHA_1 | 376 | 382 | PF00498 | 0.470 |
LIG_FHA_1 | 4 | 10 | PF00498 | 0.645 |
LIG_FHA_1 | 442 | 448 | PF00498 | 0.589 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.485 |
LIG_FHA_2 | 113 | 119 | PF00498 | 0.542 |
LIG_FHA_2 | 211 | 217 | PF00498 | 0.275 |
LIG_FHA_2 | 342 | 348 | PF00498 | 0.493 |
LIG_FHA_2 | 385 | 391 | PF00498 | 0.603 |
LIG_FHA_2 | 427 | 433 | PF00498 | 0.703 |
LIG_FHA_2 | 517 | 523 | PF00498 | 0.575 |
LIG_FHA_2 | 93 | 99 | PF00498 | 0.437 |
LIG_GBD_Chelix_1 | 277 | 285 | PF00786 | 0.257 |
LIG_LIR_Apic_2 | 184 | 189 | PF02991 | 0.375 |
LIG_LIR_Gen_1 | 317 | 325 | PF02991 | 0.390 |
LIG_LIR_Gen_1 | 357 | 368 | PF02991 | 0.412 |
LIG_LIR_Gen_1 | 378 | 388 | PF02991 | 0.393 |
LIG_LIR_Gen_1 | 67 | 78 | PF02991 | 0.550 |
LIG_LIR_Nem_3 | 317 | 322 | PF02991 | 0.390 |
LIG_LIR_Nem_3 | 357 | 363 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 378 | 383 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 499 | 505 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 67 | 73 | PF02991 | 0.533 |
LIG_Pex14_1 | 159 | 163 | PF04695 | 0.481 |
LIG_Pex14_2 | 312 | 316 | PF04695 | 0.296 |
LIG_PTAP_UEV_1 | 128 | 133 | PF05743 | 0.503 |
LIG_RPA_C_Fungi | 14 | 26 | PF08784 | 0.334 |
LIG_SH2_CRK | 199 | 203 | PF00017 | 0.336 |
LIG_SH2_CRK | 31 | 35 | PF00017 | 0.422 |
LIG_SH2_CRK | 70 | 74 | PF00017 | 0.693 |
LIG_SH2_STAP1 | 66 | 70 | PF00017 | 0.527 |
LIG_SH2_STAP1 | 76 | 80 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 70 | 73 | PF00017 | 0.524 |
LIG_SH3_2 | 189 | 194 | PF14604 | 0.454 |
LIG_SH3_2 | 473 | 478 | PF14604 | 0.547 |
LIG_SH3_3 | 126 | 132 | PF00018 | 0.546 |
LIG_SH3_3 | 186 | 192 | PF00018 | 0.432 |
LIG_SH3_3 | 31 | 37 | PF00018 | 0.518 |
LIG_SH3_3 | 319 | 325 | PF00018 | 0.320 |
LIG_SH3_3 | 370 | 376 | PF00018 | 0.373 |
LIG_SH3_3 | 467 | 473 | PF00018 | 0.547 |
LIG_Sin3_3 | 18 | 25 | PF02671 | 0.320 |
LIG_SUMO_SIM_anti_2 | 403 | 410 | PF11976 | 0.530 |
LIG_TRAF2_1 | 520 | 523 | PF00917 | 0.510 |
LIG_TYR_ITIM | 29 | 34 | PF00017 | 0.418 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.647 |
MOD_CK1_1 | 155 | 161 | PF00069 | 0.366 |
MOD_CK1_1 | 184 | 190 | PF00069 | 0.440 |
MOD_CK1_1 | 392 | 398 | PF00069 | 0.682 |
MOD_CK1_1 | 412 | 418 | PF00069 | 0.487 |
MOD_CK1_1 | 453 | 459 | PF00069 | 0.673 |
MOD_CK1_1 | 460 | 466 | PF00069 | 0.663 |
MOD_CK1_1 | 481 | 487 | PF00069 | 0.718 |
MOD_CK2_1 | 210 | 216 | PF00069 | 0.300 |
MOD_CK2_1 | 426 | 432 | PF00069 | 0.699 |
MOD_CK2_1 | 453 | 459 | PF00069 | 0.571 |
MOD_CK2_1 | 516 | 522 | PF00069 | 0.506 |
MOD_CK2_1 | 71 | 77 | PF00069 | 0.639 |
MOD_GlcNHglycan | 121 | 125 | PF01048 | 0.641 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.299 |
MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.263 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.451 |
MOD_GlcNHglycan | 394 | 397 | PF01048 | 0.742 |
MOD_GlcNHglycan | 411 | 414 | PF01048 | 0.491 |
MOD_GlcNHglycan | 455 | 458 | PF01048 | 0.571 |
MOD_GlcNHglycan | 519 | 522 | PF01048 | 0.599 |
MOD_GlcNHglycan | 533 | 536 | PF01048 | 0.622 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.668 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.595 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.410 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.408 |
MOD_GSK3_1 | 424 | 431 | PF00069 | 0.711 |
MOD_GSK3_1 | 453 | 460 | PF00069 | 0.728 |
MOD_GSK3_1 | 464 | 471 | PF00069 | 0.748 |
MOD_GSK3_1 | 478 | 485 | PF00069 | 0.651 |
MOD_GSK3_1 | 513 | 520 | PF00069 | 0.613 |
MOD_GSK3_1 | 58 | 65 | PF00069 | 0.486 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.546 |
MOD_NEK2_1 | 220 | 225 | PF00069 | 0.275 |
MOD_NEK2_1 | 299 | 304 | PF00069 | 0.360 |
MOD_NEK2_1 | 381 | 386 | PF00069 | 0.562 |
MOD_NEK2_1 | 409 | 414 | PF00069 | 0.494 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.587 |
MOD_PIKK_1 | 3 | 9 | PF00454 | 0.487 |
MOD_PIKK_1 | 381 | 387 | PF00454 | 0.524 |
MOD_PK_1 | 434 | 440 | PF00069 | 0.544 |
MOD_PKA_2 | 159 | 165 | PF00069 | 0.473 |
MOD_PKA_2 | 358 | 364 | PF00069 | 0.546 |
MOD_PKA_2 | 381 | 387 | PF00069 | 0.468 |
MOD_PKA_2 | 390 | 396 | PF00069 | 0.603 |
MOD_Plk_1 | 120 | 126 | PF00069 | 0.583 |
MOD_Plk_1 | 68 | 74 | PF00069 | 0.483 |
MOD_Plk_1 | 76 | 82 | PF00069 | 0.415 |
MOD_Plk_1 | 93 | 99 | PF00069 | 0.686 |
MOD_Plk_2-3 | 358 | 364 | PF00069 | 0.475 |
MOD_Plk_4 | 181 | 187 | PF00069 | 0.624 |
MOD_Plk_4 | 294 | 300 | PF00069 | 0.356 |
MOD_Plk_4 | 68 | 74 | PF00069 | 0.560 |
MOD_Plk_4 | 86 | 92 | PF00069 | 0.517 |
MOD_ProDKin_1 | 125 | 131 | PF00069 | 0.649 |
MOD_ProDKin_1 | 458 | 464 | PF00069 | 0.743 |
MOD_ProDKin_1 | 469 | 475 | PF00069 | 0.808 |
MOD_SUMO_for_1 | 281 | 284 | PF00179 | 0.234 |
MOD_SUMO_rev_2 | 8 | 15 | PF00179 | 0.432 |
TRG_DiLeu_BaEn_1 | 17 | 22 | PF01217 | 0.446 |
TRG_DiLeu_BaEn_2 | 99 | 105 | PF01217 | 0.454 |
TRG_DiLeu_BaLyEn_6 | 192 | 197 | PF01217 | 0.344 |
TRG_DiLeu_BaLyEn_6 | 329 | 334 | PF01217 | 0.460 |
TRG_DiLeu_BaLyEn_6 | 364 | 369 | PF01217 | 0.468 |
TRG_DiLeu_BaLyEn_6 | 416 | 421 | PF01217 | 0.589 |
TRG_ENDOCYTIC_2 | 217 | 220 | PF00928 | 0.257 |
TRG_ENDOCYTIC_2 | 31 | 34 | PF00928 | 0.560 |
TRG_ENDOCYTIC_2 | 505 | 508 | PF00928 | 0.489 |
TRG_ENDOCYTIC_2 | 70 | 73 | PF00928 | 0.516 |
TRG_ER_diArg_1 | 193 | 195 | PF00400 | 0.387 |
TRG_ER_diArg_1 | 279 | 281 | PF00400 | 0.241 |
TRG_ER_diArg_1 | 313 | 315 | PF00400 | 0.259 |
TRG_ER_diArg_1 | 331 | 333 | PF00400 | 0.542 |
TRG_ER_diArg_1 | 365 | 367 | PF00400 | 0.338 |
TRG_ER_diArg_1 | 530 | 533 | PF00400 | 0.540 |
TRG_NES_CRM1_1 | 276 | 290 | PF08389 | 0.331 |
TRG_NLS_Bipartite_1 | 314 | 334 | PF00514 | 0.328 |
TRG_Pf-PMV_PEXEL_1 | 279 | 284 | PF00026 | 0.390 |
TRG_Pf-PMV_PEXEL_1 | 332 | 337 | PF00026 | 0.477 |
TRG_Pf-PMV_PEXEL_1 | 39 | 44 | PF00026 | 0.520 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P643 | Leptomonas seymouri | 47% | 100% |
A0A0S4JUG1 | Bodo saltans | 32% | 67% |
A0A1X0P9Z1 | Trypanosomatidae | 41% | 100% |
A0A3Q8IIF1 | Leishmania donovani | 91% | 99% |
A0A3Q8IJS0 | Leishmania donovani | 31% | 100% |
A0A3R7KPY1 | Trypanosoma rangeli | 31% | 100% |
A0A422NNS9 | Trypanosoma rangeli | 45% | 100% |
A4HB54 | Leishmania braziliensis | 76% | 100% |
A4HME8 | Leishmania braziliensis | 35% | 100% |
A4IAA1 | Leishmania infantum | 91% | 99% |
A4IE38 | Leishmania infantum | 31% | 100% |
C9ZLZ3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
Q4Q0X8 | Leishmania major | 31% | 100% |
Q4Q2K9 | Leishmania major | 92% | 100% |
V5B5D2 | Trypanosoma cruzi | 43% | 100% |