Proteasome, proteasome regulatory non-ATP-ase subunit 5
| Source | Evidence on protein | Close homologs | 
|---|---|---|
| Cuervo et al. | no | yes: 0 | 
| Hassani et al. | no | yes: 0 | 
| Forrest at al. (metacyclic) | yes | yes: 2 | 
| Forrest at al. (procyclic) | yes | yes: 2 | 
| Silverman et al. | no | yes: 2 | 
| Pissara et al. | yes | yes: 8 | 
| Source | Evidence on protein | Close homologs | 
|---|---|---|
| Pires et al. | no | yes: 0 | 
| Source | Evidence on protein | Close homologs | 
|---|---|---|
| Silverman et al. | no | yes: 4 | 
| Source | Evidence on protein | Close homologs | 
|---|---|---|
| Jamdhade et al. | no | yes: 4 | 
| Source | Evidence on protein | Close homologs | 
|---|---|---|
| DeepLoc | ||
| SignalP6 | no | yes: 0, no: 11 | 
| NetGPI | no | yes: 0, no: 11 | 
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0005838 | proteasome regulatory particle | 2 | 12 | 
| GO:0032991 | protein-containing complex | 1 | 12 | 
| GO:0000502 | proteasome complex | 3 | 1 | 
| GO:0005654 | nucleoplasm | 2 | 1 | 
| GO:0005737 | cytoplasm | 2 | 1 | 
| GO:0008541 | proteasome regulatory particle, lid subcomplex | 2 | 1 | 
| GO:0031595 | nuclear proteasome complex | 3 | 1 | 
| GO:0110165 | cellular anatomical entity | 1 | 1 | 
| GO:0140513 | nuclear protein-containing complex | 2 | 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 | 
| 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: A4HZ77
| 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 | 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 | 1 | 
| GO:0019538 | protein metabolic process | 3 | 1 | 
| GO:0019941 | modification-dependent protein catabolic process | 6 | 1 | 
| GO:0043170 | macromolecule metabolic process | 3 | 1 | 
| GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 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:0051603 | proteolysis involved in protein catabolic process | 5 | 1 | 
| GO:0071704 | organic substance metabolic process | 2 | 1 | 
| GO:1901564 | organonitrogen compound metabolic process | 3 | 1 | 
| GO:1901575 | organic substance catabolic process | 3 | 1 | 
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0003824 | catalytic activity | 1 | 1 | 
| GO:0004175 | endopeptidase activity | 4 | 1 | 
| GO:0008233 | peptidase activity | 3 | 1 | 
| GO:0016787 | hydrolase activity | 2 | 1 | 
| GO:0140096 | catalytic activity, acting on a protein | 2 | 1 | 
| Leishmania | From | To | Domain/Motif | Score | 
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 440 | 444 | PF00656 | 0.389 | 
| CLV_MEL_PAP_1 | 339 | 345 | PF00089 | 0.519 | 
| CLV_NRD_NRD_1 | 162 | 164 | PF00675 | 0.454 | 
| CLV_NRD_NRD_1 | 211 | 213 | PF00675 | 0.351 | 
| CLV_NRD_NRD_1 | 430 | 432 | PF00675 | 0.536 | 
| CLV_NRD_NRD_1 | 470 | 472 | PF00675 | 0.458 | 
| CLV_PCSK_KEX2_1 | 164 | 166 | PF00082 | 0.352 | 
| CLV_PCSK_KEX2_1 | 389 | 391 | PF00082 | 0.266 | 
| CLV_PCSK_KEX2_1 | 97 | 99 | PF00082 | 0.416 | 
| CLV_PCSK_PC1ET2_1 | 164 | 166 | PF00082 | 0.352 | 
| CLV_PCSK_PC1ET2_1 | 389 | 391 | PF00082 | 0.229 | 
| CLV_PCSK_PC1ET2_1 | 97 | 99 | PF00082 | 0.416 | 
| CLV_PCSK_PC7_1 | 385 | 391 | PF00082 | 0.316 | 
| CLV_Separin_Metazoa | 233 | 237 | PF03568 | 0.330 | 
| CLV_Separin_Metazoa | 73 | 77 | PF03568 | 0.463 | 
| DEG_APCC_DBOX_1 | 316 | 324 | PF00400 | 0.374 | 
| DEG_APCC_DBOX_1 | 384 | 392 | PF00400 | 0.413 | 
| DOC_CDC14_PxL_1 | 320 | 328 | PF14671 | 0.371 | 
| DOC_MAPK_gen_1 | 389 | 397 | PF00069 | 0.432 | 
| DOC_MAPK_gen_1 | 418 | 428 | PF00069 | 0.413 | 
| DOC_SPAK_OSR1_1 | 149 | 153 | PF12202 | 0.335 | 
| DOC_USP7_MATH_1 | 208 | 212 | PF00917 | 0.368 | 
| DOC_WW_Pin1_4 | 395 | 400 | PF00397 | 0.413 | 
| LIG_14-3-3_CanoR_1 | 163 | 171 | PF00244 | 0.479 | 
| LIG_14-3-3_CanoR_1 | 27 | 37 | PF00244 | 0.495 | 
| LIG_14-3-3_CanoR_1 | 342 | 350 | PF00244 | 0.433 | 
| LIG_14-3-3_CanoR_1 | 370 | 378 | PF00244 | 0.433 | 
| LIG_14-3-3_CanoR_1 | 431 | 441 | PF00244 | 0.554 | 
| LIG_14-3-3_CanoR_1 | 447 | 452 | PF00244 | 0.543 | 
| LIG_14-3-3_CanoR_1 | 76 | 84 | PF00244 | 0.462 | 
| LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.569 | 
| LIG_Clathr_ClatBox_1 | 425 | 429 | PF01394 | 0.423 | 
| LIG_Clathr_ClatBox_1 | 51 | 55 | PF01394 | 0.365 | 
| LIG_Clathr_ClatBox_1 | 69 | 73 | PF01394 | 0.406 | 
| LIG_deltaCOP1_diTrp_1 | 3 | 11 | PF00928 | 0.573 | 
| LIG_eIF4E_1 | 204 | 210 | PF01652 | 0.360 | 
| LIG_FAT_LD_1 | 84 | 92 | PF03623 | 0.490 | 
| LIG_FHA_1 | 149 | 155 | PF00498 | 0.460 | 
| LIG_FHA_1 | 171 | 177 | PF00498 | 0.429 | 
| LIG_FHA_1 | 19 | 25 | PF00498 | 0.448 | 
| LIG_FHA_1 | 30 | 36 | PF00498 | 0.465 | 
| LIG_FHA_1 | 432 | 438 | PF00498 | 0.446 | 
| LIG_FHA_1 | 65 | 71 | PF00498 | 0.346 | 
| LIG_FHA_2 | 154 | 160 | PF00498 | 0.470 | 
| LIG_FHA_2 | 281 | 287 | PF00498 | 0.498 | 
| LIG_FHA_2 | 309 | 315 | PF00498 | 0.416 | 
| LIG_FHA_2 | 351 | 357 | PF00498 | 0.473 | 
| LIG_FHA_2 | 78 | 84 | PF00498 | 0.450 | 
| LIG_LIR_Gen_1 | 202 | 210 | PF02991 | 0.471 | 
| LIG_LIR_Gen_1 | 254 | 263 | PF02991 | 0.482 | 
| LIG_LIR_Gen_1 | 414 | 422 | PF02991 | 0.413 | 
| LIG_LIR_LC3C_4 | 423 | 427 | PF02991 | 0.423 | 
| LIG_LIR_Nem_3 | 202 | 207 | PF02991 | 0.496 | 
| LIG_LIR_Nem_3 | 243 | 248 | PF02991 | 0.369 | 
| LIG_LIR_Nem_3 | 254 | 259 | PF02991 | 0.450 | 
| LIG_MYND_1 | 355 | 359 | PF01753 | 0.515 | 
| LIG_MYND_3 | 182 | 186 | PF01753 | 0.451 | 
| LIG_NRBOX | 325 | 331 | PF00104 | 0.378 | 
| LIG_PCNA_yPIPBox_3 | 76 | 88 | PF02747 | 0.356 | 
| LIG_Pex14_1 | 252 | 256 | PF04695 | 0.306 | 
| LIG_SH2_CRK | 256 | 260 | PF00017 | 0.475 | 
| LIG_SH2_CRK | 327 | 331 | PF00017 | 0.380 | 
| LIG_SH2_CRK | 383 | 387 | PF00017 | 0.423 | 
| LIG_SH2_NCK_1 | 204 | 208 | PF00017 | 0.478 | 
| LIG_SH2_NCK_1 | 383 | 387 | PF00017 | 0.505 | 
| LIG_SH2_SRC | 204 | 207 | PF00017 | 0.491 | 
| LIG_SH2_SRC | 276 | 279 | PF00017 | 0.304 | 
| LIG_SH2_STAT3 | 78 | 81 | PF00017 | 0.433 | 
| LIG_SH2_STAT5 | 135 | 138 | PF00017 | 0.483 | 
| LIG_SH2_STAT5 | 231 | 234 | PF00017 | 0.299 | 
| LIG_SH2_STAT5 | 276 | 279 | PF00017 | 0.304 | 
| LIG_SH2_STAT5 | 383 | 386 | PF00017 | 0.455 | 
| LIG_SUMO_SIM_anti_2 | 335 | 341 | PF11976 | 0.370 | 
| LIG_SUMO_SIM_anti_2 | 344 | 351 | PF11976 | 0.390 | 
| LIG_SUMO_SIM_anti_2 | 375 | 380 | PF11976 | 0.413 | 
| LIG_SUMO_SIM_anti_2 | 448 | 453 | PF11976 | 0.391 | 
| LIG_SUMO_SIM_par_1 | 150 | 156 | PF11976 | 0.420 | 
| LIG_SUMO_SIM_par_1 | 31 | 40 | PF11976 | 0.507 | 
| LIG_SUMO_SIM_par_1 | 50 | 55 | PF11976 | 0.255 | 
| LIG_SUMO_SIM_par_1 | 66 | 73 | PF11976 | 0.337 | 
| LIG_SxIP_EBH_1 | 27 | 39 | PF03271 | 0.464 | 
| LIG_SxIP_EBH_1 | 379 | 390 | PF03271 | 0.516 | 
| LIG_TRAF2_1 | 362 | 365 | PF00917 | 0.316 | 
| LIG_TYR_ITIM | 229 | 234 | PF00017 | 0.341 | 
| LIG_UBA3_1 | 406 | 413 | PF00899 | 0.437 | 
| LIG_UBA3_1 | 464 | 472 | PF00899 | 0.538 | 
| LIG_UBA3_1 | 51 | 56 | PF00899 | 0.339 | 
| LIG_UBA3_1 | 87 | 96 | PF00899 | 0.449 | 
| MOD_CK1_1 | 18 | 24 | PF00069 | 0.497 | 
| MOD_CK1_1 | 267 | 273 | PF00069 | 0.398 | 
| MOD_CK1_1 | 310 | 316 | PF00069 | 0.493 | 
| MOD_CK2_1 | 153 | 159 | PF00069 | 0.466 | 
| MOD_CK2_1 | 280 | 286 | PF00069 | 0.420 | 
| MOD_CK2_1 | 308 | 314 | PF00069 | 0.505 | 
| MOD_CK2_1 | 315 | 321 | PF00069 | 0.468 | 
| MOD_CK2_1 | 342 | 348 | PF00069 | 0.439 | 
| MOD_CK2_1 | 350 | 356 | PF00069 | 0.426 | 
| MOD_CK2_1 | 77 | 83 | PF00069 | 0.499 | 
| MOD_Cter_Amidation | 161 | 164 | PF01082 | 0.454 | 
| MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.358 | 
| MOD_GlcNHglycan | 14 | 20 | PF01048 | 0.569 | 
| MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.406 | 
| MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.459 | 
| MOD_GSK3_1 | 255 | 262 | PF00069 | 0.522 | 
| MOD_GSK3_1 | 365 | 372 | PF00069 | 0.516 | 
| MOD_GSK3_1 | 395 | 402 | PF00069 | 0.399 | 
| MOD_GSK3_1 | 437 | 444 | PF00069 | 0.548 | 
| MOD_GSK3_1 | 453 | 460 | PF00069 | 0.454 | 
| MOD_N-GLC_1 | 28 | 33 | PF02516 | 0.428 | 
| MOD_N-GLC_1 | 280 | 285 | PF02516 | 0.503 | 
| MOD_N-GLC_1 | 411 | 416 | PF02516 | 0.316 | 
| MOD_N-GLC_1 | 432 | 437 | PF02516 | 0.433 | 
| MOD_N-GLC_1 | 441 | 446 | PF02516 | 0.437 | 
| MOD_N-GLC_2 | 369 | 371 | PF02516 | 0.316 | 
| MOD_NEK2_1 | 170 | 175 | PF00069 | 0.426 | 
| MOD_NEK2_1 | 255 | 260 | PF00069 | 0.314 | 
| MOD_NEK2_1 | 350 | 355 | PF00069 | 0.447 | 
| MOD_NEK2_1 | 36 | 41 | PF00069 | 0.471 | 
| MOD_NEK2_1 | 405 | 410 | PF00069 | 0.439 | 
| MOD_PIKK_1 | 77 | 83 | PF00454 | 0.447 | 
| MOD_PK_1 | 332 | 338 | PF00069 | 0.366 | 
| MOD_PKA_1 | 163 | 169 | PF00069 | 0.483 | 
| MOD_PKA_1 | 431 | 437 | PF00069 | 0.533 | 
| MOD_PKA_2 | 148 | 154 | PF00069 | 0.458 | 
| MOD_PKA_2 | 341 | 347 | PF00069 | 0.477 | 
| MOD_PKA_2 | 369 | 375 | PF00069 | 0.450 | 
| MOD_PKA_2 | 37 | 43 | PF00069 | 0.443 | 
| MOD_Plk_1 | 117 | 123 | PF00069 | 0.513 | 
| MOD_Plk_1 | 28 | 34 | PF00069 | 0.431 | 
| MOD_Plk_1 | 291 | 297 | PF00069 | 0.376 | 
| MOD_Plk_1 | 411 | 417 | PF00069 | 0.479 | 
| MOD_Plk_1 | 441 | 447 | PF00069 | 0.430 | 
| MOD_Plk_2-3 | 153 | 159 | PF00069 | 0.466 | 
| MOD_Plk_4 | 241 | 247 | PF00069 | 0.415 | 
| MOD_Plk_4 | 405 | 411 | PF00069 | 0.435 | 
| MOD_Plk_4 | 447 | 453 | PF00069 | 0.256 | 
| MOD_ProDKin_1 | 395 | 401 | PF00069 | 0.413 | 
| MOD_SUMO_rev_2 | 261 | 267 | PF00179 | 0.486 | 
| MOD_SUMO_rev_2 | 3 | 9 | PF00179 | 0.612 | 
| TRG_DiLeu_BaEn_1 | 20 | 25 | PF01217 | 0.567 | 
| TRG_ENDOCYTIC_2 | 204 | 207 | PF00928 | 0.491 | 
| TRG_ENDOCYTIC_2 | 231 | 234 | PF00928 | 0.323 | 
| TRG_ENDOCYTIC_2 | 256 | 259 | PF00928 | 0.441 | 
| TRG_ENDOCYTIC_2 | 327 | 330 | PF00928 | 0.371 | 
| TRG_ENDOCYTIC_2 | 383 | 386 | PF00928 | 0.413 | 
| TRG_ENDOCYTIC_2 | 416 | 419 | PF00928 | 0.413 | 
| TRG_NES_CRM1_1 | 189 | 205 | PF08389 | 0.322 | 
| TRG_NES_CRM1_1 | 337 | 352 | PF08389 | 0.436 | 
| TRG_Pf-PMV_PEXEL_1 | 172 | 177 | PF00026 | 0.448 | 
| TRG_Pf-PMV_PEXEL_1 | 217 | 222 | PF00026 | 0.550 | 
| TRG_Pf-PMV_PEXEL_1 | 389 | 393 | PF00026 | 0.287 | 
| Protein | Taxonomy | Sequence identity | Coverage | 
|---|---|---|---|
| A0A0N1IAV3 | Leptomonas seymouri | 90% | 100% | 
| A0A0S4IPZ2 | Bodo saltans | 51% | 96% | 
| A0A1X0NY92 | Trypanosomatidae | 67% | 99% | 
| A0A3S7WWF6 | Leishmania donovani | 100% | 100% | 
| A0A422NHB9 | Trypanosoma rangeli | 66% | 99% | 
| A4HBS3 | Leishmania braziliensis | 95% | 100% | 
| D0A1G0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 62% | 98% | 
| E9AV44 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 98% | 100% | 
| O00232 | Homo sapiens | 31% | 100% | 
| P0CU17 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 27% | 100% | 
| P0CU18 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 27% | 100% | 
| Q12250 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 29% | 100% | 
| Q2KJ25 | Bos taurus | 31% | 100% | 
| Q4QCD7 | Leishmania major | 99% | 100% | 
| Q54UJ0 | Dictyostelium discoideum | 30% | 100% | 
| Q5RBI3 | Pongo abelii | 31% | 100% | 
| Q8VWK0 | Arabidopsis thaliana | 29% | 100% | 
| Q9D8W5 | Mus musculus | 31% | 100% | 
| Q9FIB6 | Arabidopsis thaliana | 29% | 100% | 
| V5BDS8 | Trypanosoma cruzi | 65% | 66% |