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: 5 |
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:0005737 | cytoplasm | 2 | 12 |
GO:0005856 | cytoskeleton | 5 | 2 |
GO:0005874 | microtubule | 6 | 12 |
GO:0015630 | microtubule cytoskeleton | 6 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043228 | non-membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 2 |
GO:0051286 | cell tip | 3 | 2 |
GO:0060187 | cell pole | 2 | 2 |
GO:0099080 | supramolecular complex | 2 | 12 |
GO:0099081 | supramolecular polymer | 3 | 12 |
GO:0099512 | supramolecular fiber | 4 | 12 |
GO:0099513 | polymeric cytoskeletal fiber | 5 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
Related structures:
AlphaFold database: Q4Q8N0
Term | Name | Level | Count |
---|---|---|---|
GO:0000226 | microtubule cytoskeleton organization | 3 | 12 |
GO:0006996 | organelle organization | 4 | 12 |
GO:0007010 | cytoskeleton organization | 5 | 12 |
GO:0007017 | microtubule-based process | 2 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016043 | cellular component organization | 3 | 12 |
GO:0051013 | microtubule severing | 4 | 12 |
GO:0071840 | cellular component organization or biogenesis | 2 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005515 | protein binding | 2 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0008017 | microtubule binding | 5 | 12 |
GO:0008092 | cytoskeletal protein binding | 3 | 12 |
GO:0008568 | microtubule severing ATPase activity | 2 | 12 |
GO:0015631 | tubulin binding | 4 | 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:0016853 | isomerase activity | 2 | 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:0140096 | catalytic activity, acting on a protein | 2 | 12 |
GO:0140657 | ATP-dependent activity | 1 | 12 |
GO:0140776 | protein-containing complex destabilizing activity | 1 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 362 | 366 | PF00656 | 0.251 |
CLV_MEL_PAP_1 | 182 | 188 | PF00089 | 0.483 |
CLV_NRD_NRD_1 | 293 | 295 | PF00675 | 0.346 |
CLV_NRD_NRD_1 | 381 | 383 | PF00675 | 0.225 |
CLV_NRD_NRD_1 | 420 | 422 | PF00675 | 0.236 |
CLV_NRD_NRD_1 | 485 | 487 | PF00675 | 0.236 |
CLV_NRD_NRD_1 | 86 | 88 | PF00675 | 0.608 |
CLV_PCSK_KEX2_1 | 272 | 274 | PF00082 | 0.465 |
CLV_PCSK_KEX2_1 | 293 | 295 | PF00082 | 0.346 |
CLV_PCSK_KEX2_1 | 381 | 383 | PF00082 | 0.225 |
CLV_PCSK_KEX2_1 | 419 | 421 | PF00082 | 0.236 |
CLV_PCSK_KEX2_1 | 424 | 426 | PF00082 | 0.236 |
CLV_PCSK_KEX2_1 | 485 | 487 | PF00082 | 0.256 |
CLV_PCSK_KEX2_1 | 85 | 87 | PF00082 | 0.592 |
CLV_PCSK_PC1ET2_1 | 272 | 274 | PF00082 | 0.465 |
CLV_PCSK_PC1ET2_1 | 424 | 426 | PF00082 | 0.236 |
CLV_PCSK_PC1ET2_1 | 85 | 87 | PF00082 | 0.561 |
CLV_PCSK_PC7_1 | 420 | 426 | PF00082 | 0.236 |
CLV_PCSK_SKI1_1 | 26 | 30 | PF00082 | 0.495 |
CLV_PCSK_SKI1_1 | 272 | 276 | PF00082 | 0.307 |
CLV_PCSK_SKI1_1 | 297 | 301 | PF00082 | 0.236 |
CLV_PCSK_SKI1_1 | 309 | 313 | PF00082 | 0.236 |
CLV_PCSK_SKI1_1 | 345 | 349 | PF00082 | 0.236 |
CLV_PCSK_SKI1_1 | 381 | 385 | PF00082 | 0.236 |
CLV_PCSK_SKI1_1 | 445 | 449 | PF00082 | 0.395 |
CLV_PCSK_SKI1_1 | 486 | 490 | PF00082 | 0.332 |
DEG_APCC_DBOX_1 | 435 | 443 | PF00400 | 0.307 |
DEG_APCC_KENBOX_2 | 496 | 500 | PF00400 | 0.381 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.425 |
DOC_CYCLIN_RxL_1 | 342 | 349 | PF00134 | 0.236 |
DOC_MAPK_gen_1 | 419 | 430 | PF00069 | 0.251 |
DOC_MAPK_gen_1 | 445 | 455 | PF00069 | 0.359 |
DOC_MAPK_gen_1 | 540 | 547 | PF00069 | 0.454 |
DOC_MAPK_MEF2A_6 | 421 | 430 | PF00069 | 0.236 |
DOC_PP1_RVXF_1 | 343 | 349 | PF00149 | 0.236 |
DOC_PP4_FxxP_1 | 78 | 81 | PF00568 | 0.523 |
DOC_USP7_MATH_1 | 162 | 166 | PF00917 | 0.571 |
DOC_USP7_MATH_1 | 172 | 176 | PF00917 | 0.430 |
DOC_USP7_MATH_1 | 184 | 188 | PF00917 | 0.721 |
DOC_USP7_MATH_1 | 213 | 217 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 315 | 319 | PF00917 | 0.251 |
DOC_USP7_UBL2_3 | 11 | 15 | PF12436 | 0.346 |
DOC_USP7_UBL2_3 | 441 | 445 | PF12436 | 0.377 |
DOC_USP7_UBL2_3 | 489 | 493 | PF12436 | 0.255 |
DOC_WW_Pin1_4 | 167 | 172 | PF00397 | 0.540 |
DOC_WW_Pin1_4 | 325 | 330 | PF00397 | 0.236 |
LIG_14-3-3_CanoR_1 | 116 | 122 | PF00244 | 0.728 |
LIG_14-3-3_CanoR_1 | 160 | 169 | PF00244 | 0.636 |
LIG_14-3-3_CanoR_1 | 185 | 195 | PF00244 | 0.607 |
LIG_14-3-3_CanoR_1 | 96 | 106 | PF00244 | 0.723 |
LIG_APCC_ABBA_1 | 75 | 80 | PF00400 | 0.468 |
LIG_BRCT_BRCA1_1 | 169 | 173 | PF00533 | 0.550 |
LIG_BRCT_BRCA1_1 | 356 | 360 | PF00533 | 0.236 |
LIG_CtBP_PxDLS_1 | 511 | 515 | PF00389 | 0.257 |
LIG_deltaCOP1_diTrp_1 | 537 | 543 | PF00928 | 0.236 |
LIG_FHA_1 | 187 | 193 | PF00498 | 0.586 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.363 |
LIG_FHA_1 | 356 | 362 | PF00498 | 0.236 |
LIG_FHA_1 | 396 | 402 | PF00498 | 0.336 |
LIG_FHA_1 | 41 | 47 | PF00498 | 0.399 |
LIG_FHA_1 | 442 | 448 | PF00498 | 0.318 |
LIG_FHA_1 | 471 | 477 | PF00498 | 0.251 |
LIG_FHA_2 | 259 | 265 | PF00498 | 0.485 |
LIG_FHA_2 | 493 | 499 | PF00498 | 0.343 |
LIG_FHA_2 | 69 | 75 | PF00498 | 0.434 |
LIG_GBD_Chelix_1 | 245 | 253 | PF00786 | 0.325 |
LIG_Integrin_RGD_1 | 337 | 339 | PF01839 | 0.251 |
LIG_LIR_Gen_1 | 164 | 173 | PF02991 | 0.539 |
LIG_LIR_Gen_1 | 261 | 268 | PF02991 | 0.325 |
LIG_LIR_Gen_1 | 452 | 462 | PF02991 | 0.273 |
LIG_LIR_Gen_1 | 52 | 61 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 164 | 169 | PF02991 | 0.553 |
LIG_LIR_Nem_3 | 261 | 265 | PF02991 | 0.336 |
LIG_LIR_Nem_3 | 287 | 292 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 322 | 327 | PF02991 | 0.237 |
LIG_LIR_Nem_3 | 452 | 458 | PF02991 | 0.257 |
LIG_LIR_Nem_3 | 52 | 57 | PF02991 | 0.512 |
LIG_LYPXL_S_1 | 280 | 284 | PF13949 | 0.316 |
LIG_LYPXL_yS_3 | 281 | 284 | PF13949 | 0.321 |
LIG_MYND_1 | 282 | 286 | PF01753 | 0.330 |
LIG_NRBOX | 457 | 463 | PF00104 | 0.301 |
LIG_PDZ_Class_2 | 542 | 547 | PF00595 | 0.514 |
LIG_Pex14_1 | 539 | 543 | PF04695 | 0.284 |
LIG_SH2_CRK | 166 | 170 | PF00017 | 0.681 |
LIG_SH2_CRK | 289 | 293 | PF00017 | 0.387 |
LIG_SH2_CRK | 302 | 306 | PF00017 | 0.190 |
LIG_SH2_CRK | 32 | 36 | PF00017 | 0.467 |
LIG_SH2_NCK_1 | 166 | 170 | PF00017 | 0.552 |
LIG_SH2_PTP2 | 427 | 430 | PF00017 | 0.236 |
LIG_SH2_SRC | 354 | 357 | PF00017 | 0.251 |
LIG_SH2_STAT5 | 22 | 25 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 427 | 430 | PF00017 | 0.236 |
LIG_SH3_3 | 166 | 172 | PF00018 | 0.620 |
LIG_SH3_3 | 194 | 200 | PF00018 | 0.612 |
LIG_SH3_3 | 276 | 282 | PF00018 | 0.301 |
LIG_TRAF2_1 | 240 | 243 | PF00917 | 0.379 |
LIG_TYR_ITIM | 279 | 284 | PF00017 | 0.311 |
LIG_UBA3_1 | 439 | 445 | PF00899 | 0.343 |
LIG_UBA3_1 | 481 | 489 | PF00899 | 0.314 |
LIG_WW_3 | 182 | 186 | PF00397 | 0.638 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.569 |
MOD_CK1_1 | 174 | 180 | PF00069 | 0.551 |
MOD_CK1_1 | 187 | 193 | PF00069 | 0.446 |
MOD_CK1_1 | 216 | 222 | PF00069 | 0.658 |
MOD_CK1_1 | 231 | 237 | PF00069 | 0.526 |
MOD_CK1_1 | 328 | 334 | PF00069 | 0.251 |
MOD_CK1_1 | 97 | 103 | PF00069 | 0.685 |
MOD_CK2_1 | 492 | 498 | PF00069 | 0.391 |
MOD_CK2_1 | 68 | 74 | PF00069 | 0.498 |
MOD_CK2_1 | 96 | 102 | PF00069 | 0.720 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.691 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.543 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.613 |
MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.623 |
MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.643 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.591 |
MOD_GlcNHglycan | 467 | 470 | PF01048 | 0.330 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.683 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.582 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.531 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.453 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.251 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.508 |
MOD_GSK3_1 | 519 | 526 | PF00069 | 0.169 |
MOD_N-GLC_1 | 127 | 132 | PF02516 | 0.531 |
MOD_N-GLC_1 | 320 | 325 | PF02516 | 0.247 |
MOD_N-GLC_1 | 512 | 517 | PF02516 | 0.257 |
MOD_N-GLC_1 | 94 | 99 | PF02516 | 0.608 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.505 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.678 |
MOD_NEK2_1 | 405 | 410 | PF00069 | 0.249 |
MOD_NEK2_2 | 31 | 36 | PF00069 | 0.406 |
MOD_NEK2_2 | 320 | 325 | PF00069 | 0.236 |
MOD_NEK2_2 | 480 | 485 | PF00069 | 0.236 |
MOD_PIKK_1 | 456 | 462 | PF00454 | 0.363 |
MOD_PIKK_1 | 49 | 55 | PF00454 | 0.503 |
MOD_PIKK_1 | 68 | 74 | PF00454 | 0.412 |
MOD_PK_1 | 188 | 194 | PF00069 | 0.464 |
MOD_PKA_2 | 184 | 190 | PF00069 | 0.636 |
MOD_PKA_2 | 68 | 74 | PF00069 | 0.412 |
MOD_PKA_2 | 95 | 101 | PF00069 | 0.696 |
MOD_Plk_1 | 127 | 133 | PF00069 | 0.540 |
MOD_Plk_1 | 320 | 326 | PF00069 | 0.295 |
MOD_Plk_1 | 491 | 497 | PF00069 | 0.372 |
MOD_Plk_2-3 | 492 | 498 | PF00069 | 0.454 |
MOD_Plk_4 | 307 | 313 | PF00069 | 0.236 |
MOD_Plk_4 | 320 | 326 | PF00069 | 0.236 |
MOD_Plk_4 | 355 | 361 | PF00069 | 0.236 |
MOD_Plk_4 | 383 | 389 | PF00069 | 0.251 |
MOD_Plk_4 | 53 | 59 | PF00069 | 0.405 |
MOD_ProDKin_1 | 167 | 173 | PF00069 | 0.524 |
MOD_ProDKin_1 | 325 | 331 | PF00069 | 0.236 |
MOD_SUMO_rev_2 | 264 | 274 | PF00179 | 0.335 |
TRG_DiLeu_BaEn_1 | 244 | 249 | PF01217 | 0.342 |
TRG_DiLeu_BaEn_1 | 270 | 275 | PF01217 | 0.344 |
TRG_DiLeu_BaEn_2 | 73 | 79 | PF01217 | 0.534 |
TRG_DiLeu_LyEn_5 | 270 | 275 | PF01217 | 0.455 |
TRG_ENDOCYTIC_2 | 166 | 169 | PF00928 | 0.556 |
TRG_ENDOCYTIC_2 | 281 | 284 | PF00928 | 0.321 |
TRG_ENDOCYTIC_2 | 289 | 292 | PF00928 | 0.355 |
TRG_ENDOCYTIC_2 | 32 | 35 | PF00928 | 0.340 |
TRG_ENDOCYTIC_2 | 427 | 430 | PF00928 | 0.236 |
TRG_ER_diArg_1 | 224 | 227 | PF00400 | 0.654 |
TRG_ER_diArg_1 | 292 | 294 | PF00400 | 0.368 |
TRG_ER_diArg_1 | 418 | 421 | PF00400 | 0.236 |
TRG_ER_diArg_1 | 484 | 486 | PF00400 | 0.236 |
TRG_NLS_MonoCore_2 | 112 | 117 | PF00514 | 0.675 |
TRG_NLS_MonoExtC_3 | 111 | 116 | PF00514 | 0.612 |
TRG_NLS_MonoExtN_4 | 112 | 117 | PF00514 | 0.613 |
TRG_Pf-PMV_PEXEL_1 | 272 | 276 | PF00026 | 0.355 |
TRG_Pf-PMV_PEXEL_1 | 345 | 349 | PF00026 | 0.236 |
TRG_Pf-PMV_PEXEL_1 | 44 | 48 | PF00026 | 0.421 |
TRG_Pf-PMV_PEXEL_1 | 59 | 64 | PF00026 | 0.353 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HRH8 | Leptomonas seymouri | 68% | 100% |
A0A0S4IR32 | Bodo saltans | 41% | 100% |
A0A0S4IUM1 | Bodo saltans | 51% | 92% |
A0A1X0NYV7 | Trypanosomatidae | 57% | 97% |
A0A3Q8IJS0 | Leishmania donovani | 33% | 100% |
A0A3S7X163 | Leishmania donovani | 95% | 100% |
A0A3S7X2R4 | Leishmania donovani | 42% | 100% |
A0A422P1K0 | Trypanosoma rangeli | 57% | 98% |
A4HG81 | Leishmania braziliensis | 85% | 100% |
A4HPV3 | Leishmania braziliensis | 33% | 100% |
A4I3C0 | Leishmania infantum | 95% | 91% |
A4I4W4 | Leishmania infantum | 42% | 100% |
A4IE38 | Leishmania infantum | 33% | 100% |
A9RA82 | Papio anubis | 50% | 100% |
B2RYN7 | Rattus norvegicus | 37% | 94% |
B3EX35 | Sorex araneus | 49% | 100% |
B3M301 | Drosophila ananassae | 41% | 71% |
B3P8A3 | Drosophila erecta | 40% | 72% |
B4G437 | Drosophila persimilis | 41% | 69% |
B4HGG6 | Drosophila sechellia | 40% | 72% |
B4NBP4 | Drosophila willistoni | 42% | 70% |
B4PL32 | Drosophila yakuba | 40% | 72% |
B4QSF0 | Drosophila simulans | 40% | 72% |
B4USW8 | Otolemur garnettii | 49% | 100% |
B7NZ88 | Oryctolagus cuniculus | 50% | 100% |
D0A833 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 56% | 99% |
E9AEB2 | Leishmania major | 42% | 100% |
E9ATM0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
E9AZK1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
O75449 | Homo sapiens | 49% | 100% |
Q05AS3 | Xenopus tropicalis | 38% | 91% |
Q0IIR9 | Xenopus tropicalis | 41% | 100% |
Q1HGK7 | Gallus gallus | 42% | 100% |
Q4Q0X8 | Leishmania major | 33% | 100% |
Q5ZK92 | Gallus gallus | 38% | 89% |
Q6AZT2 | Xenopus laevis | 38% | 91% |
Q8I0P1 | Drosophila melanogaster | 40% | 72% |
Q9BW62 | Homo sapiens | 50% | 100% |
Q9ERZ6 | Mus musculus | 30% | 72% |
Q9QYY8 | Mus musculus | 37% | 89% |
Q9SEX2 | Arabidopsis thaliana | 41% | 100% |
V5B0U7 | Trypanosoma cruzi | 54% | 98% |