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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 11 |
GO:0005874 | microtubule | 6 | 11 |
GO:0099080 | supramolecular complex | 2 | 11 |
GO:0099081 | supramolecular polymer | 3 | 11 |
GO:0099512 | supramolecular fiber | 4 | 11 |
GO:0099513 | polymeric cytoskeletal fiber | 5 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:0005856 | cytoskeleton | 5 | 1 |
GO:0015630 | microtubule cytoskeleton | 6 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0051286 | cell tip | 3 | 1 |
GO:0060187 | cell pole | 2 | 1 |
Related structures:
AlphaFold database: A0A3S7X163
Term | Name | Level | Count |
---|---|---|---|
GO:0000226 | microtubule cytoskeleton organization | 3 | 11 |
GO:0006996 | organelle organization | 4 | 11 |
GO:0007010 | cytoskeleton organization | 5 | 11 |
GO:0007017 | microtubule-based process | 2 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016043 | cellular component organization | 3 | 11 |
GO:0051013 | microtubule severing | 4 | 11 |
GO:0071840 | cellular component organization or biogenesis | 2 | 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0005515 | protein binding | 2 | 11 |
GO:0005524 | ATP binding | 5 | 11 |
GO:0008017 | microtubule binding | 5 | 11 |
GO:0008092 | cytoskeletal protein binding | 3 | 11 |
GO:0008568 | microtubule severing ATPase activity | 2 | 11 |
GO:0015631 | tubulin binding | 4 | 11 |
GO:0016462 | pyrophosphatase activity | 5 | 11 |
GO:0016787 | hydrolase activity | 2 | 11 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 11 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 11 |
GO:0016853 | isomerase activity | 2 | 11 |
GO:0016887 | ATP hydrolysis activity | 7 | 11 |
GO:0017076 | purine nucleotide binding | 4 | 11 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 11 |
GO:0030554 | adenyl nucleotide binding | 5 | 11 |
GO:0032553 | ribonucleotide binding | 3 | 11 |
GO:0032555 | purine ribonucleotide binding | 4 | 11 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 11 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 11 |
GO:0036094 | small molecule binding | 2 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043168 | anion binding | 3 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0097367 | carbohydrate derivative binding | 2 | 11 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 11 |
GO:0140657 | ATP-dependent activity | 1 | 11 |
GO:0140776 | protein-containing complex destabilizing activity | 1 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 345 | 349 | PF00656 | 0.266 |
CLV_NRD_NRD_1 | 276 | 278 | PF00675 | 0.350 |
CLV_NRD_NRD_1 | 364 | 366 | PF00675 | 0.232 |
CLV_NRD_NRD_1 | 403 | 405 | PF00675 | 0.285 |
CLV_NRD_NRD_1 | 468 | 470 | PF00675 | 0.241 |
CLV_NRD_NRD_1 | 86 | 88 | PF00675 | 0.607 |
CLV_PCSK_KEX2_1 | 255 | 257 | PF00082 | 0.453 |
CLV_PCSK_KEX2_1 | 276 | 278 | PF00082 | 0.350 |
CLV_PCSK_KEX2_1 | 364 | 366 | PF00082 | 0.232 |
CLV_PCSK_KEX2_1 | 402 | 404 | PF00082 | 0.283 |
CLV_PCSK_KEX2_1 | 407 | 409 | PF00082 | 0.296 |
CLV_PCSK_KEX2_1 | 468 | 470 | PF00082 | 0.241 |
CLV_PCSK_KEX2_1 | 85 | 87 | PF00082 | 0.632 |
CLV_PCSK_PC1ET2_1 | 255 | 257 | PF00082 | 0.453 |
CLV_PCSK_PC1ET2_1 | 407 | 409 | PF00082 | 0.289 |
CLV_PCSK_PC1ET2_1 | 85 | 87 | PF00082 | 0.564 |
CLV_PCSK_PC7_1 | 403 | 409 | PF00082 | 0.285 |
CLV_PCSK_SKI1_1 | 255 | 259 | PF00082 | 0.312 |
CLV_PCSK_SKI1_1 | 26 | 30 | PF00082 | 0.461 |
CLV_PCSK_SKI1_1 | 280 | 284 | PF00082 | 0.241 |
CLV_PCSK_SKI1_1 | 292 | 296 | PF00082 | 0.255 |
CLV_PCSK_SKI1_1 | 328 | 332 | PF00082 | 0.241 |
CLV_PCSK_SKI1_1 | 364 | 368 | PF00082 | 0.241 |
CLV_PCSK_SKI1_1 | 428 | 432 | PF00082 | 0.397 |
CLV_PCSK_SKI1_1 | 469 | 473 | PF00082 | 0.374 |
DEG_APCC_DBOX_1 | 418 | 426 | PF00400 | 0.311 |
DEG_APCC_KENBOX_2 | 479 | 483 | PF00400 | 0.374 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.435 |
DEG_SPOP_SBC_1 | 172 | 176 | PF00917 | 0.613 |
DOC_CYCLIN_RxL_1 | 325 | 332 | PF00134 | 0.241 |
DOC_MAPK_gen_1 | 402 | 413 | PF00069 | 0.259 |
DOC_MAPK_gen_1 | 428 | 438 | PF00069 | 0.373 |
DOC_MAPK_gen_1 | 523 | 530 | PF00069 | 0.477 |
DOC_MAPK_MEF2A_6 | 404 | 413 | PF00069 | 0.241 |
DOC_PP1_RVXF_1 | 326 | 332 | PF00149 | 0.241 |
DOC_PP4_FxxP_1 | 78 | 81 | PF00568 | 0.509 |
DOC_USP7_MATH_1 | 158 | 162 | PF00917 | 0.607 |
DOC_USP7_MATH_1 | 172 | 176 | PF00917 | 0.655 |
DOC_USP7_MATH_1 | 196 | 200 | PF00917 | 0.603 |
DOC_USP7_MATH_1 | 298 | 302 | PF00917 | 0.274 |
DOC_USP7_UBL2_3 | 11 | 15 | PF12436 | 0.348 |
DOC_USP7_UBL2_3 | 424 | 428 | PF12436 | 0.438 |
DOC_USP7_UBL2_3 | 472 | 476 | PF12436 | 0.255 |
DOC_WW_Pin1_4 | 167 | 172 | PF00397 | 0.543 |
DOC_WW_Pin1_4 | 308 | 313 | PF00397 | 0.247 |
LIG_14-3-3_CanoR_1 | 116 | 122 | PF00244 | 0.720 |
LIG_14-3-3_CanoR_1 | 160 | 169 | PF00244 | 0.630 |
LIG_14-3-3_CanoR_1 | 96 | 106 | PF00244 | 0.707 |
LIG_APCC_ABBA_1 | 75 | 80 | PF00400 | 0.469 |
LIG_BRCT_BRCA1_1 | 169 | 173 | PF00533 | 0.537 |
LIG_BRCT_BRCA1_1 | 339 | 343 | PF00533 | 0.241 |
LIG_CtBP_PxDLS_1 | 494 | 498 | PF00389 | 0.262 |
LIG_deltaCOP1_diTrp_1 | 520 | 526 | PF00928 | 0.241 |
LIG_FHA_1 | 339 | 345 | PF00498 | 0.241 |
LIG_FHA_1 | 379 | 385 | PF00498 | 0.326 |
LIG_FHA_1 | 41 | 47 | PF00498 | 0.404 |
LIG_FHA_1 | 425 | 431 | PF00498 | 0.356 |
LIG_FHA_1 | 454 | 460 | PF00498 | 0.241 |
LIG_FHA_2 | 242 | 248 | PF00498 | 0.483 |
LIG_FHA_2 | 476 | 482 | PF00498 | 0.385 |
LIG_FHA_2 | 69 | 75 | PF00498 | 0.425 |
LIG_GBD_Chelix_1 | 228 | 236 | PF00786 | 0.333 |
LIG_Integrin_RGD_1 | 320 | 322 | PF01839 | 0.241 |
LIG_LIR_Gen_1 | 164 | 173 | PF02991 | 0.547 |
LIG_LIR_Gen_1 | 244 | 251 | PF02991 | 0.334 |
LIG_LIR_Gen_1 | 435 | 445 | PF02991 | 0.259 |
LIG_LIR_Gen_1 | 52 | 61 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 164 | 169 | PF02991 | 0.558 |
LIG_LIR_Nem_3 | 244 | 248 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 270 | 275 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 305 | 310 | PF02991 | 0.243 |
LIG_LIR_Nem_3 | 435 | 441 | PF02991 | 0.241 |
LIG_LIR_Nem_3 | 52 | 57 | PF02991 | 0.477 |
LIG_LYPXL_S_1 | 263 | 267 | PF13949 | 0.318 |
LIG_LYPXL_yS_3 | 264 | 267 | PF13949 | 0.322 |
LIG_MYND_1 | 265 | 269 | PF01753 | 0.333 |
LIG_NRBOX | 440 | 446 | PF00104 | 0.306 |
LIG_PDZ_Class_2 | 525 | 530 | PF00595 | 0.505 |
LIG_Pex14_1 | 522 | 526 | PF04695 | 0.241 |
LIG_SH2_CRK | 166 | 170 | PF00017 | 0.675 |
LIG_SH2_CRK | 272 | 276 | PF00017 | 0.382 |
LIG_SH2_CRK | 285 | 289 | PF00017 | 0.201 |
LIG_SH2_CRK | 32 | 36 | PF00017 | 0.455 |
LIG_SH2_NCK_1 | 166 | 170 | PF00017 | 0.557 |
LIG_SH2_PTP2 | 410 | 413 | PF00017 | 0.241 |
LIG_SH2_SRC | 337 | 340 | PF00017 | 0.259 |
LIG_SH2_STAT5 | 22 | 25 | PF00017 | 0.467 |
LIG_SH2_STAT5 | 410 | 413 | PF00017 | 0.241 |
LIG_SH3_3 | 146 | 152 | PF00018 | 0.546 |
LIG_SH3_3 | 166 | 172 | PF00018 | 0.705 |
LIG_SH3_3 | 177 | 183 | PF00018 | 0.593 |
LIG_SH3_3 | 259 | 265 | PF00018 | 0.305 |
LIG_TRAF2_1 | 223 | 226 | PF00917 | 0.390 |
LIG_TYR_ITIM | 262 | 267 | PF00017 | 0.314 |
LIG_UBA3_1 | 422 | 428 | PF00899 | 0.350 |
LIG_UBA3_1 | 464 | 472 | PF00899 | 0.303 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.574 |
MOD_CK1_1 | 161 | 167 | PF00069 | 0.509 |
MOD_CK1_1 | 199 | 205 | PF00069 | 0.658 |
MOD_CK1_1 | 214 | 220 | PF00069 | 0.531 |
MOD_CK1_1 | 311 | 317 | PF00069 | 0.259 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.433 |
MOD_CK1_1 | 97 | 103 | PF00069 | 0.642 |
MOD_CK2_1 | 475 | 481 | PF00069 | 0.306 |
MOD_CK2_1 | 68 | 74 | PF00069 | 0.473 |
MOD_CK2_1 | 96 | 102 | PF00069 | 0.707 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.585 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.565 |
MOD_GlcNHglycan | 175 | 178 | PF01048 | 0.636 |
MOD_GlcNHglycan | 199 | 202 | PF01048 | 0.642 |
MOD_GlcNHglycan | 213 | 216 | PF01048 | 0.616 |
MOD_GlcNHglycan | 450 | 453 | PF01048 | 0.402 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.640 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.587 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.681 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.485 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.259 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.499 |
MOD_N-GLC_1 | 127 | 132 | PF02516 | 0.672 |
MOD_N-GLC_1 | 303 | 308 | PF02516 | 0.250 |
MOD_N-GLC_1 | 495 | 500 | PF02516 | 0.262 |
MOD_N-GLC_1 | 94 | 99 | PF02516 | 0.634 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.497 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.639 |
MOD_NEK2_1 | 173 | 178 | PF00069 | 0.495 |
MOD_NEK2_1 | 388 | 393 | PF00069 | 0.241 |
MOD_NEK2_1 | 500 | 505 | PF00069 | 0.131 |
MOD_NEK2_2 | 303 | 308 | PF00069 | 0.241 |
MOD_NEK2_2 | 31 | 36 | PF00069 | 0.448 |
MOD_NEK2_2 | 463 | 468 | PF00069 | 0.241 |
MOD_PIKK_1 | 439 | 445 | PF00454 | 0.354 |
MOD_PIKK_1 | 49 | 55 | PF00454 | 0.481 |
MOD_PIKK_1 | 68 | 74 | PF00454 | 0.415 |
MOD_PKA_2 | 68 | 74 | PF00069 | 0.415 |
MOD_PKA_2 | 95 | 101 | PF00069 | 0.676 |
MOD_Plk_1 | 127 | 133 | PF00069 | 0.671 |
MOD_Plk_1 | 303 | 309 | PF00069 | 0.284 |
MOD_Plk_1 | 474 | 480 | PF00069 | 0.306 |
MOD_Plk_2-3 | 475 | 481 | PF00069 | 0.306 |
MOD_Plk_4 | 290 | 296 | PF00069 | 0.268 |
MOD_Plk_4 | 303 | 309 | PF00069 | 0.241 |
MOD_Plk_4 | 338 | 344 | PF00069 | 0.241 |
MOD_Plk_4 | 366 | 372 | PF00069 | 0.241 |
MOD_Plk_4 | 53 | 59 | PF00069 | 0.481 |
MOD_ProDKin_1 | 167 | 173 | PF00069 | 0.547 |
MOD_ProDKin_1 | 308 | 314 | PF00069 | 0.247 |
MOD_SUMO_rev_2 | 247 | 257 | PF00179 | 0.344 |
TRG_DiLeu_BaEn_1 | 227 | 232 | PF01217 | 0.381 |
TRG_DiLeu_BaEn_1 | 253 | 258 | PF01217 | 0.359 |
TRG_DiLeu_BaEn_2 | 73 | 79 | PF01217 | 0.524 |
TRG_DiLeu_LyEn_5 | 253 | 258 | PF01217 | 0.449 |
TRG_ENDOCYTIC_2 | 166 | 169 | PF00928 | 0.559 |
TRG_ENDOCYTIC_2 | 264 | 267 | PF00928 | 0.322 |
TRG_ENDOCYTIC_2 | 272 | 275 | PF00928 | 0.358 |
TRG_ENDOCYTIC_2 | 32 | 35 | PF00928 | 0.313 |
TRG_ENDOCYTIC_2 | 410 | 413 | PF00928 | 0.241 |
TRG_ER_diArg_1 | 207 | 210 | PF00400 | 0.648 |
TRG_ER_diArg_1 | 275 | 277 | PF00400 | 0.371 |
TRG_ER_diArg_1 | 401 | 404 | PF00400 | 0.281 |
TRG_ER_diArg_1 | 467 | 469 | PF00400 | 0.241 |
TRG_NLS_MonoCore_2 | 112 | 117 | PF00514 | 0.666 |
TRG_NLS_MonoExtC_3 | 111 | 116 | PF00514 | 0.615 |
TRG_NLS_MonoExtN_4 | 112 | 117 | PF00514 | 0.617 |
TRG_Pf-PMV_PEXEL_1 | 255 | 259 | PF00026 | 0.325 |
TRG_Pf-PMV_PEXEL_1 | 328 | 332 | PF00026 | 0.241 |
TRG_Pf-PMV_PEXEL_1 | 44 | 48 | PF00026 | 0.424 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HRH8 | Leptomonas seymouri | 70% | 97% |
A0A0S4IR32 | Bodo saltans | 40% | 99% |
A0A0S4IUM1 | Bodo saltans | 51% | 89% |
A0A1X0NYV7 | Trypanosomatidae | 56% | 94% |
A0A3Q8IHU1 | Leishmania donovani | 33% | 100% |
A0A3Q8IJS0 | Leishmania donovani | 34% | 100% |
A0A3S7X2R4 | Leishmania donovani | 42% | 100% |
A0A422P1K0 | Trypanosoma rangeli | 57% | 95% |
A4H6T6 | Leishmania braziliensis | 36% | 100% |
A4HG81 | Leishmania braziliensis | 88% | 98% |
A4HME8 | Leishmania braziliensis | 35% | 100% |
A4I3C0 | Leishmania infantum | 100% | 100% |
A4I4W4 | Leishmania infantum | 42% | 100% |
A4IB20 | Leishmania infantum | 33% | 100% |
A4IE38 | Leishmania infantum | 34% | 100% |
A9RA82 | Papio anubis | 50% | 100% |
B2RYN7 | Rattus norvegicus | 38% | 91% |
B3EX35 | Sorex araneus | 49% | 100% |
B3M301 | Drosophila ananassae | 41% | 69% |
B4NBP4 | Drosophila willistoni | 42% | 68% |
B4PL32 | Drosophila yakuba | 39% | 70% |
B4USW8 | Otolemur garnettii | 51% | 100% |
B7NZ88 | Oryctolagus cuniculus | 50% | 100% |
B7PXE3 | Ixodes scapularis | 39% | 82% |
C9ZKZ7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
D0A833 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 58% | 96% |
E9AEB2 | Leishmania major | 42% | 100% |
E9AEU9 | Leishmania major | 33% | 100% |
E9AZK1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 99% |
E9B605 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
O75449 | Homo sapiens | 41% | 100% |
P51327 | Porphyra purpurea | 34% | 84% |
Q05AS3 | Xenopus tropicalis | 39% | 88% |
Q09803 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 42% | 100% |
Q0IIR9 | Xenopus tropicalis | 42% | 100% |
Q1HGK7 | Gallus gallus | 43% | 100% |
Q4Q8N0 | Leishmania major | 95% | 100% |
Q4R407 | Macaca fascicularis | 41% | 100% |
Q5RII9 | Danio rerio | 43% | 100% |
Q5U3S1 | Danio rerio | 42% | 100% |
Q5XIK7 | Rattus norvegicus | 49% | 100% |
Q5ZK92 | Gallus gallus | 40% | 86% |
Q6AZT2 | Xenopus laevis | 39% | 88% |
Q6E0V2 | Rattus norvegicus | 41% | 100% |
Q6PIW4 | Homo sapiens | 38% | 79% |
Q8K0T4 | Mus musculus | 50% | 100% |
Q9BW62 | Homo sapiens | 50% | 100% |
Q9ERZ6 | Mus musculus | 30% | 70% |
Q9PUL2 | Xenopus laevis | 42% | 100% |
Q9SEX2 | Arabidopsis thaliana | 42% | 100% |
V5B0U7 | Trypanosoma cruzi | 56% | 95% |