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: 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: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0010008 | endosome membrane | 5 | 11 |
GO:0012506 | vesicle membrane | 4 | 11 |
GO:0016020 | membrane | 2 | 11 |
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 | 12 |
GO:0005737 | cytoplasm | 2 | 2 |
GO:0000502 | proteasome complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0140535 | intracellular protein-containing complex | 2 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1905368 | peptidase complex | 3 | 1 |
GO:1905369 | endopeptidase complex | 4 | 1 |
Related structures:
AlphaFold database: A4HB54
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009057 | macromolecule catabolic process | 4 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0030163 | protein catabolic process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0016462 | pyrophosphatase activity | 5 | 12 |
GO:0016787 | hydrolase activity | 2 | 12 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 12 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 12 |
GO:0016887 | ATP hydrolysis activity | 7 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 12 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0036402 | proteasome-activating activity | 2 | 1 |
GO:0140657 | ATP-dependent activity | 1 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 250 | 254 | PF00656 | 0.274 |
CLV_C14_Caspase3-7 | 391 | 395 | PF00656 | 0.531 |
CLV_C14_Caspase3-7 | 82 | 86 | PF00656 | 0.451 |
CLV_NRD_NRD_1 | 184 | 186 | PF00675 | 0.415 |
CLV_NRD_NRD_1 | 269 | 271 | PF00675 | 0.289 |
CLV_NRD_NRD_1 | 304 | 306 | PF00675 | 0.312 |
CLV_NRD_NRD_1 | 321 | 323 | PF00675 | 0.448 |
CLV_NRD_NRD_1 | 356 | 358 | PF00675 | 0.475 |
CLV_NRD_NRD_1 | 37 | 39 | PF00675 | 0.388 |
CLV_PCSK_KEX2_1 | 184 | 186 | PF00082 | 0.398 |
CLV_PCSK_KEX2_1 | 269 | 271 | PF00082 | 0.289 |
CLV_PCSK_KEX2_1 | 304 | 306 | PF00082 | 0.319 |
CLV_PCSK_KEX2_1 | 320 | 322 | PF00082 | 0.433 |
CLV_PCSK_KEX2_1 | 356 | 358 | PF00082 | 0.496 |
CLV_PCSK_KEX2_1 | 36 | 38 | PF00082 | 0.526 |
CLV_PCSK_PC1ET2_1 | 320 | 322 | PF00082 | 0.454 |
CLV_PCSK_PC1ET2_1 | 36 | 38 | PF00082 | 0.620 |
CLV_PCSK_PC7_1 | 180 | 186 | PF00082 | 0.425 |
CLV_PCSK_SKI1_1 | 163 | 167 | PF00082 | 0.360 |
CLV_PCSK_SKI1_1 | 17 | 21 | PF00082 | 0.420 |
CLV_PCSK_SKI1_1 | 184 | 188 | PF00082 | 0.274 |
CLV_PCSK_SKI1_1 | 232 | 236 | PF00082 | 0.303 |
CLV_PCSK_SKI1_1 | 244 | 248 | PF00082 | 0.353 |
CLV_PCSK_SKI1_1 | 269 | 273 | PF00082 | 0.274 |
CLV_PCSK_SKI1_1 | 321 | 325 | PF00082 | 0.422 |
CLV_PCSK_SKI1_1 | 329 | 333 | PF00082 | 0.437 |
CLV_PCSK_SKI1_1 | 356 | 360 | PF00082 | 0.535 |
CLV_PCSK_SKI1_1 | 75 | 79 | PF00082 | 0.469 |
DEG_APCC_DBOX_1 | 40 | 48 | PF00400 | 0.513 |
DEG_APCC_DBOX_1 | 74 | 82 | PF00400 | 0.360 |
DEG_Kelch_Keap1_1 | 382 | 387 | PF01344 | 0.511 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.547 |
DEG_SCF_TRCP1_1 | 384 | 389 | PF00400 | 0.500 |
DOC_CDC14_PxL_1 | 425 | 433 | PF14671 | 0.488 |
DOC_CYCLIN_RxL_1 | 318 | 327 | PF00134 | 0.455 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 289 | 298 | PF00134 | 0.368 |
DOC_CYCLIN_yCln2_LP_2 | 170 | 176 | PF00134 | 0.417 |
DOC_MAPK_gen_1 | 269 | 279 | PF00069 | 0.289 |
DOC_MAPK_gen_1 | 304 | 314 | PF00069 | 0.288 |
DOC_MAPK_HePTP_8 | 267 | 279 | PF00069 | 0.350 |
DOC_MAPK_MEF2A_6 | 270 | 279 | PF00069 | 0.308 |
DOC_MAPK_MEF2A_6 | 305 | 314 | PF00069 | 0.289 |
DOC_MAPK_MEF2A_6 | 75 | 83 | PF00069 | 0.439 |
DOC_MAPK_NFAT4_5 | 272 | 280 | PF00069 | 0.308 |
DOC_PP1_RVXF_1 | 242 | 249 | PF00149 | 0.304 |
DOC_PP4_FxxP_1 | 176 | 179 | PF00568 | 0.474 |
DOC_SPAK_OSR1_1 | 349 | 353 | PF12202 | 0.424 |
DOC_USP7_MATH_1 | 238 | 242 | PF00917 | 0.366 |
DOC_USP7_MATH_1 | 254 | 258 | PF00917 | 0.376 |
DOC_USP7_MATH_1 | 28 | 32 | PF00917 | 0.588 |
DOC_USP7_MATH_1 | 458 | 462 | PF00917 | 0.743 |
DOC_USP7_MATH_1 | 512 | 516 | PF00917 | 0.518 |
DOC_WW_Pin1_4 | 412 | 417 | PF00397 | 0.761 |
DOC_WW_Pin1_4 | 454 | 459 | PF00397 | 0.767 |
DOC_WW_Pin1_4 | 473 | 478 | PF00397 | 0.489 |
LIG_14-3-3_CanoR_1 | 10 | 20 | PF00244 | 0.467 |
LIG_14-3-3_CanoR_1 | 139 | 145 | PF00244 | 0.448 |
LIG_14-3-3_CanoR_1 | 150 | 154 | PF00244 | 0.490 |
LIG_14-3-3_CanoR_1 | 163 | 169 | PF00244 | 0.415 |
LIG_14-3-3_CanoR_1 | 269 | 279 | PF00244 | 0.328 |
LIG_14-3-3_CanoR_1 | 349 | 353 | PF00244 | 0.424 |
LIG_14-3-3_CanoR_1 | 356 | 362 | PF00244 | 0.477 |
LIG_14-3-3_CanoR_1 | 41 | 45 | PF00244 | 0.387 |
LIG_14-3-3_CanoR_1 | 469 | 477 | PF00244 | 0.515 |
LIG_14-3-3_CanoR_1 | 521 | 526 | PF00244 | 0.573 |
LIG_Actin_WH2_2 | 316 | 331 | PF00022 | 0.448 |
LIG_APCC_ABBAyCdc20_2 | 244 | 250 | PF00400 | 0.289 |
LIG_BRCT_BRCA1_1 | 460 | 464 | PF00533 | 0.704 |
LIG_Clathr_ClatBox_1 | 78 | 82 | PF01394 | 0.294 |
LIG_FHA_1 | 119 | 125 | PF00498 | 0.600 |
LIG_FHA_1 | 165 | 171 | PF00498 | 0.380 |
LIG_FHA_1 | 271 | 277 | PF00498 | 0.289 |
LIG_FHA_1 | 283 | 289 | PF00498 | 0.256 |
LIG_FHA_1 | 330 | 336 | PF00498 | 0.374 |
LIG_FHA_1 | 366 | 372 | PF00498 | 0.526 |
LIG_FHA_1 | 432 | 438 | PF00498 | 0.711 |
LIG_FHA_1 | 449 | 455 | PF00498 | 0.516 |
LIG_FHA_1 | 490 | 496 | PF00498 | 0.540 |
LIG_FHA_1 | 64 | 70 | PF00498 | 0.497 |
LIG_FHA_1 | 7 | 13 | PF00498 | 0.523 |
LIG_FHA_2 | 124 | 130 | PF00498 | 0.638 |
LIG_FHA_2 | 201 | 207 | PF00498 | 0.334 |
LIG_FHA_2 | 375 | 381 | PF00498 | 0.608 |
LIG_FHA_2 | 512 | 518 | PF00498 | 0.558 |
LIG_GBD_Chelix_1 | 267 | 275 | PF00786 | 0.350 |
LIG_LIR_Gen_1 | 307 | 315 | PF02991 | 0.438 |
LIG_LIR_Gen_1 | 347 | 358 | PF02991 | 0.439 |
LIG_LIR_Gen_1 | 360 | 367 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 205 | 210 | PF02991 | 0.266 |
LIG_LIR_Nem_3 | 307 | 312 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 347 | 353 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 422 | 428 | PF02991 | 0.531 |
LIG_MYND_1 | 409 | 413 | PF01753 | 0.523 |
LIG_PDZ_Class_2 | 527 | 532 | PF00595 | 0.388 |
LIG_Pex14_1 | 149 | 153 | PF04695 | 0.511 |
LIG_Pex14_2 | 302 | 306 | PF04695 | 0.334 |
LIG_PTAP_UEV_1 | 119 | 124 | PF05743 | 0.556 |
LIG_PTB_Apo_2 | 94 | 101 | PF02174 | 0.423 |
LIG_PTB_Phospho_1 | 94 | 100 | PF10480 | 0.417 |
LIG_RPA_C_Fungi | 317 | 329 | PF08784 | 0.285 |
LIG_SH2_CRK | 189 | 193 | PF00017 | 0.289 |
LIG_SH2_CRK | 207 | 211 | PF00017 | 0.289 |
LIG_SH2_CRK | 425 | 429 | PF00017 | 0.492 |
LIG_SH2_STAP1 | 361 | 365 | PF00017 | 0.266 |
LIG_SH2_STAP1 | 67 | 71 | PF00017 | 0.512 |
LIG_SH2_STAT3 | 57 | 60 | PF00017 | 0.351 |
LIG_SH2_STAT5 | 522 | 525 | PF00017 | 0.332 |
LIG_SH2_STAT5 | 63 | 66 | PF00017 | 0.469 |
LIG_SH3_2 | 120 | 125 | PF14604 | 0.474 |
LIG_SH3_2 | 179 | 184 | PF14604 | 0.474 |
LIG_SH3_2 | 413 | 418 | PF14604 | 0.483 |
LIG_SH3_3 | 117 | 123 | PF00018 | 0.630 |
LIG_SH3_3 | 176 | 182 | PF00018 | 0.432 |
LIG_SH3_3 | 309 | 315 | PF00018 | 0.308 |
LIG_SH3_3 | 360 | 366 | PF00018 | 0.381 |
LIG_SH3_3 | 410 | 416 | PF00018 | 0.758 |
LIG_SUMO_SIM_anti_2 | 285 | 290 | PF11976 | 0.208 |
LIG_SUMO_SIM_anti_2 | 393 | 400 | PF11976 | 0.640 |
LIG_SUMO_SIM_par_1 | 77 | 82 | PF11976 | 0.409 |
LIG_TYR_ITSM | 203 | 210 | PF00017 | 0.193 |
MOD_CDC14_SPxK_1 | 415 | 418 | PF00782 | 0.616 |
MOD_CDK_SPxK_1 | 412 | 418 | PF00069 | 0.616 |
MOD_CK1_1 | 382 | 388 | PF00069 | 0.748 |
MOD_CK1_1 | 414 | 420 | PF00069 | 0.692 |
MOD_CK1_1 | 443 | 449 | PF00069 | 0.738 |
MOD_CK1_1 | 450 | 456 | PF00069 | 0.764 |
MOD_CK1_1 | 471 | 477 | PF00069 | 0.743 |
MOD_CK2_1 | 123 | 129 | PF00069 | 0.590 |
MOD_CK2_1 | 200 | 206 | PF00069 | 0.323 |
MOD_CK2_1 | 385 | 391 | PF00069 | 0.670 |
MOD_CK2_1 | 443 | 449 | PF00069 | 0.659 |
MOD_CK2_1 | 475 | 481 | PF00069 | 0.506 |
MOD_CK2_1 | 512 | 518 | PF00069 | 0.494 |
MOD_CK2_1 | 62 | 68 | PF00069 | 0.533 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.285 |
MOD_GlcNHglycan | 256 | 259 | PF01048 | 0.417 |
MOD_GlcNHglycan | 384 | 387 | PF01048 | 0.760 |
MOD_GlcNHglycan | 442 | 445 | PF01048 | 0.785 |
MOD_GlcNHglycan | 514 | 517 | PF01048 | 0.584 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.545 |
MOD_GSK3_1 | 329 | 336 | PF00069 | 0.435 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.413 |
MOD_GSK3_1 | 382 | 389 | PF00069 | 0.770 |
MOD_GSK3_1 | 443 | 450 | PF00069 | 0.734 |
MOD_GSK3_1 | 454 | 461 | PF00069 | 0.761 |
MOD_GSK3_1 | 468 | 475 | PF00069 | 0.669 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.501 |
MOD_GSK3_1 | 508 | 515 | PF00069 | 0.619 |
MOD_GSK3_1 | 520 | 527 | PF00069 | 0.510 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.541 |
MOD_NEK2_1 | 174 | 179 | PF00069 | 0.499 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.283 |
MOD_NEK2_1 | 289 | 294 | PF00069 | 0.374 |
MOD_NEK2_1 | 371 | 376 | PF00069 | 0.570 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.342 |
MOD_PIKK_1 | 371 | 377 | PF00454 | 0.509 |
MOD_PK_1 | 424 | 430 | PF00069 | 0.649 |
MOD_PKA_2 | 149 | 155 | PF00069 | 0.501 |
MOD_PKA_2 | 348 | 354 | PF00069 | 0.431 |
MOD_PKA_2 | 380 | 386 | PF00069 | 0.725 |
MOD_PKA_2 | 40 | 46 | PF00069 | 0.468 |
MOD_PKA_2 | 468 | 474 | PF00069 | 0.581 |
MOD_PKA_2 | 520 | 526 | PF00069 | 0.462 |
MOD_PKB_1 | 485 | 493 | PF00069 | 0.469 |
MOD_Plk_1 | 448 | 454 | PF00069 | 0.679 |
MOD_Plk_1 | 6 | 12 | PF00069 | 0.488 |
MOD_Plk_1 | 67 | 73 | PF00069 | 0.392 |
MOD_Plk_2-3 | 348 | 354 | PF00069 | 0.498 |
MOD_Plk_4 | 284 | 290 | PF00069 | 0.378 |
MOD_Plk_4 | 49 | 55 | PF00069 | 0.439 |
MOD_Plk_4 | 59 | 65 | PF00069 | 0.531 |
MOD_ProDKin_1 | 412 | 418 | PF00069 | 0.761 |
MOD_ProDKin_1 | 454 | 460 | PF00069 | 0.766 |
MOD_ProDKin_1 | 473 | 479 | PF00069 | 0.514 |
MOD_SUMO_for_1 | 271 | 274 | PF00179 | 0.289 |
TRG_DiLeu_BaEn_1 | 8 | 13 | PF01217 | 0.399 |
TRG_DiLeu_BaLyEn_6 | 182 | 187 | PF01217 | 0.427 |
TRG_DiLeu_BaLyEn_6 | 319 | 324 | PF01217 | 0.489 |
TRG_DiLeu_BaLyEn_6 | 354 | 359 | PF01217 | 0.474 |
TRG_DiLeu_BaLyEn_6 | 406 | 411 | PF01217 | 0.719 |
TRG_DiLeu_BaLyEn_6 | 484 | 489 | PF01217 | 0.607 |
TRG_ENDOCYTIC_2 | 207 | 210 | PF00928 | 0.350 |
TRG_ENDOCYTIC_2 | 361 | 364 | PF00928 | 0.268 |
TRG_ENDOCYTIC_2 | 425 | 428 | PF00928 | 0.494 |
TRG_ER_diArg_1 | 183 | 185 | PF00400 | 0.424 |
TRG_ER_diArg_1 | 269 | 271 | PF00400 | 0.289 |
TRG_ER_diArg_1 | 303 | 305 | PF00400 | 0.296 |
TRG_ER_diArg_1 | 321 | 323 | PF00400 | 0.444 |
TRG_ER_diArg_1 | 355 | 357 | PF00400 | 0.544 |
TRG_ER_diArg_1 | 485 | 488 | PF00400 | 0.494 |
TRG_NES_CRM1_1 | 266 | 280 | PF08389 | 0.417 |
TRG_NLS_Bipartite_1 | 304 | 324 | PF00514 | 0.421 |
TRG_Pf-PMV_PEXEL_1 | 269 | 274 | PF00026 | 0.417 |
TRG_Pf-PMV_PEXEL_1 | 322 | 327 | PF00026 | 0.511 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P643 | Leptomonas seymouri | 49% | 99% |
A0A1X0P9Z1 | Trypanosomatidae | 41% | 100% |
A0A3Q8IIF1 | Leishmania donovani | 74% | 99% |
A0A422NNS9 | Trypanosoma rangeli | 44% | 100% |
A4IAA1 | Leishmania infantum | 74% | 99% |
C9ZLZ3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
E9B5C4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 99% |
Q4Q2K9 | Leishmania major | 75% | 100% |
V5B5D2 | Trypanosoma cruzi | 44% | 100% |
V5BKL6 | Trypanosoma cruzi | 28% | 100% |