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. | yes | 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:0005874 | microtubule | 6 | 12 |
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 |
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: A4HG81
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 | 338 | 342 | PF00656 | 0.305 |
CLV_NRD_NRD_1 | 269 | 271 | PF00675 | 0.391 |
CLV_NRD_NRD_1 | 346 | 348 | PF00675 | 0.402 |
CLV_NRD_NRD_1 | 357 | 359 | PF00675 | 0.275 |
CLV_NRD_NRD_1 | 396 | 398 | PF00675 | 0.328 |
CLV_NRD_NRD_1 | 461 | 463 | PF00675 | 0.313 |
CLV_NRD_NRD_1 | 86 | 88 | PF00675 | 0.608 |
CLV_PCSK_KEX2_1 | 248 | 250 | PF00082 | 0.509 |
CLV_PCSK_KEX2_1 | 269 | 271 | PF00082 | 0.391 |
CLV_PCSK_KEX2_1 | 346 | 348 | PF00082 | 0.402 |
CLV_PCSK_KEX2_1 | 357 | 359 | PF00082 | 0.275 |
CLV_PCSK_KEX2_1 | 395 | 397 | PF00082 | 0.326 |
CLV_PCSK_KEX2_1 | 400 | 402 | PF00082 | 0.339 |
CLV_PCSK_KEX2_1 | 461 | 463 | PF00082 | 0.313 |
CLV_PCSK_KEX2_1 | 85 | 87 | PF00082 | 0.624 |
CLV_PCSK_PC1ET2_1 | 248 | 250 | PF00082 | 0.509 |
CLV_PCSK_PC1ET2_1 | 400 | 402 | PF00082 | 0.332 |
CLV_PCSK_PC1ET2_1 | 85 | 87 | PF00082 | 0.593 |
CLV_PCSK_PC7_1 | 396 | 402 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 248 | 252 | PF00082 | 0.356 |
CLV_PCSK_SKI1_1 | 26 | 30 | PF00082 | 0.503 |
CLV_PCSK_SKI1_1 | 273 | 277 | PF00082 | 0.284 |
CLV_PCSK_SKI1_1 | 285 | 289 | PF00082 | 0.298 |
CLV_PCSK_SKI1_1 | 321 | 325 | PF00082 | 0.284 |
CLV_PCSK_SKI1_1 | 357 | 361 | PF00082 | 0.284 |
CLV_PCSK_SKI1_1 | 421 | 425 | PF00082 | 0.457 |
CLV_PCSK_SKI1_1 | 462 | 466 | PF00082 | 0.407 |
DEG_APCC_DBOX_1 | 411 | 419 | PF00400 | 0.356 |
DEG_APCC_KENBOX_2 | 472 | 476 | PF00400 | 0.429 |
DOC_CYCLIN_RxL_1 | 318 | 325 | PF00134 | 0.284 |
DOC_MAPK_gen_1 | 269 | 277 | PF00069 | 0.298 |
DOC_MAPK_gen_1 | 395 | 406 | PF00069 | 0.299 |
DOC_MAPK_gen_1 | 421 | 431 | PF00069 | 0.406 |
DOC_MAPK_gen_1 | 516 | 523 | PF00069 | 0.508 |
DOC_MAPK_MEF2A_6 | 397 | 406 | PF00069 | 0.284 |
DOC_PP1_RVXF_1 | 319 | 325 | PF00149 | 0.284 |
DOC_PP2B_LxvP_1 | 50 | 53 | PF13499 | 0.333 |
DOC_PP4_FxxP_1 | 78 | 81 | PF00568 | 0.566 |
DOC_USP7_MATH_1 | 158 | 162 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 163 | 167 | PF00917 | 0.616 |
DOC_USP7_MATH_1 | 291 | 295 | PF00917 | 0.313 |
DOC_USP7_MATH_1 | 53 | 57 | PF00917 | 0.600 |
DOC_USP7_UBL2_3 | 417 | 421 | PF12436 | 0.483 |
DOC_USP7_UBL2_3 | 465 | 469 | PF12436 | 0.303 |
DOC_WW_Pin1_4 | 149 | 154 | PF00397 | 0.586 |
DOC_WW_Pin1_4 | 301 | 306 | PF00397 | 0.290 |
LIG_14-3-3_CanoR_1 | 116 | 122 | PF00244 | 0.751 |
LIG_14-3-3_CanoR_1 | 51 | 61 | PF00244 | 0.453 |
LIG_APCC_ABBA_1 | 75 | 80 | PF00400 | 0.509 |
LIG_BRCT_BRCA1_1 | 160 | 164 | PF00533 | 0.601 |
LIG_BRCT_BRCA1_1 | 332 | 336 | PF00533 | 0.284 |
LIG_deltaCOP1_diTrp_1 | 513 | 519 | PF00928 | 0.284 |
LIG_FHA_1 | 332 | 338 | PF00498 | 0.284 |
LIG_FHA_1 | 372 | 378 | PF00498 | 0.384 |
LIG_FHA_1 | 408 | 414 | PF00498 | 0.449 |
LIG_FHA_1 | 418 | 424 | PF00498 | 0.400 |
LIG_FHA_1 | 447 | 453 | PF00498 | 0.305 |
LIG_FHA_1 | 53 | 59 | PF00498 | 0.324 |
LIG_FHA_2 | 235 | 241 | PF00498 | 0.531 |
LIG_FHA_2 | 469 | 475 | PF00498 | 0.391 |
LIG_FHA_2 | 69 | 75 | PF00498 | 0.467 |
LIG_GBD_Chelix_1 | 221 | 229 | PF00786 | 0.376 |
LIG_Integrin_RGD_1 | 313 | 315 | PF01839 | 0.299 |
LIG_LIR_Gen_1 | 237 | 244 | PF02991 | 0.379 |
LIG_LIR_Gen_1 | 428 | 438 | PF02991 | 0.300 |
LIG_LIR_Nem_3 | 237 | 241 | PF02991 | 0.390 |
LIG_LIR_Nem_3 | 263 | 268 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 298 | 303 | PF02991 | 0.285 |
LIG_LIR_Nem_3 | 428 | 434 | PF02991 | 0.285 |
LIG_LYPXL_S_1 | 256 | 260 | PF13949 | 0.363 |
LIG_LYPXL_yS_3 | 257 | 260 | PF13949 | 0.368 |
LIG_MYND_1 | 258 | 262 | PF01753 | 0.377 |
LIG_NRBOX | 433 | 439 | PF00104 | 0.348 |
LIG_PDZ_Class_2 | 518 | 523 | PF00595 | 0.567 |
LIG_Pex14_1 | 515 | 519 | PF04695 | 0.284 |
LIG_SH2_CRK | 265 | 269 | PF00017 | 0.433 |
LIG_SH2_CRK | 278 | 282 | PF00017 | 0.238 |
LIG_SH2_CRK | 32 | 36 | PF00017 | 0.501 |
LIG_SH2_PTP2 | 403 | 406 | PF00017 | 0.284 |
LIG_SH2_SRC | 330 | 333 | PF00017 | 0.299 |
LIG_SH2_STAT5 | 128 | 131 | PF00017 | 0.586 |
LIG_SH2_STAT5 | 22 | 25 | PF00017 | 0.518 |
LIG_SH2_STAT5 | 403 | 406 | PF00017 | 0.284 |
LIG_SH3_3 | 252 | 258 | PF00018 | 0.351 |
LIG_TRAF2_1 | 216 | 219 | PF00917 | 0.438 |
LIG_TYR_ITIM | 255 | 260 | PF00017 | 0.359 |
LIG_UBA3_1 | 415 | 421 | PF00899 | 0.411 |
LIG_UBA3_1 | 457 | 465 | PF00899 | 0.411 |
LIG_WW_1 | 89 | 92 | PF00397 | 0.507 |
MOD_CDK_SPxxK_3 | 149 | 156 | PF00069 | 0.594 |
MOD_CK1_1 | 120 | 126 | PF00069 | 0.593 |
MOD_CK1_1 | 207 | 213 | PF00069 | 0.604 |
MOD_CK1_1 | 304 | 310 | PF00069 | 0.299 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.492 |
MOD_CK2_1 | 468 | 474 | PF00069 | 0.439 |
MOD_CK2_1 | 53 | 59 | PF00069 | 0.559 |
MOD_CK2_1 | 68 | 74 | PF00069 | 0.528 |
MOD_Cter_Amidation | 344 | 347 | PF01082 | 0.206 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.707 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.742 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.650 |
MOD_GlcNHglycan | 443 | 446 | PF01048 | 0.412 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.725 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.604 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.672 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.299 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.540 |
MOD_N-GLC_1 | 192 | 197 | PF02516 | 0.633 |
MOD_N-GLC_1 | 296 | 301 | PF02516 | 0.294 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.696 |
MOD_NEK2_1 | 381 | 386 | PF00069 | 0.284 |
MOD_NEK2_2 | 296 | 301 | PF00069 | 0.284 |
MOD_NEK2_2 | 31 | 36 | PF00069 | 0.456 |
MOD_NEK2_2 | 456 | 461 | PF00069 | 0.284 |
MOD_PIKK_1 | 68 | 74 | PF00454 | 0.457 |
MOD_PKA_2 | 68 | 74 | PF00069 | 0.457 |
MOD_Plk_1 | 296 | 302 | PF00069 | 0.343 |
MOD_Plk_1 | 467 | 473 | PF00069 | 0.433 |
MOD_Plk_2-3 | 468 | 474 | PF00069 | 0.502 |
MOD_Plk_4 | 283 | 289 | PF00069 | 0.311 |
MOD_Plk_4 | 296 | 302 | PF00069 | 0.284 |
MOD_Plk_4 | 331 | 337 | PF00069 | 0.284 |
MOD_Plk_4 | 359 | 365 | PF00069 | 0.299 |
MOD_Plk_4 | 53 | 59 | PF00069 | 0.538 |
MOD_ProDKin_1 | 149 | 155 | PF00069 | 0.588 |
MOD_ProDKin_1 | 301 | 307 | PF00069 | 0.290 |
MOD_SUMO_rev_2 | 240 | 250 | PF00179 | 0.383 |
TRG_DiLeu_BaEn_1 | 220 | 225 | PF01217 | 0.397 |
TRG_DiLeu_BaEn_1 | 246 | 251 | PF01217 | 0.393 |
TRG_DiLeu_BaEn_2 | 73 | 79 | PF01217 | 0.578 |
TRG_DiLeu_LyEn_5 | 246 | 251 | PF01217 | 0.504 |
TRG_ENDOCYTIC_2 | 257 | 260 | PF00928 | 0.368 |
TRG_ENDOCYTIC_2 | 265 | 268 | PF00928 | 0.401 |
TRG_ENDOCYTIC_2 | 32 | 35 | PF00928 | 0.349 |
TRG_ENDOCYTIC_2 | 403 | 406 | PF00928 | 0.284 |
TRG_ER_diArg_1 | 200 | 203 | PF00400 | 0.711 |
TRG_ER_diArg_1 | 268 | 270 | PF00400 | 0.412 |
TRG_ER_diArg_1 | 394 | 397 | PF00400 | 0.324 |
TRG_ER_diArg_1 | 460 | 462 | PF00400 | 0.317 |
TRG_NLS_MonoExtC_3 | 111 | 116 | PF00514 | 0.719 |
TRG_NLS_MonoExtN_4 | 112 | 117 | PF00514 | 0.776 |
TRG_Pf-PMV_PEXEL_1 | 248 | 252 | PF00026 | 0.370 |
TRG_Pf-PMV_PEXEL_1 | 321 | 325 | PF00026 | 0.284 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HRH8 | Leptomonas seymouri | 68% | 96% |
A0A0S4IUM1 | Bodo saltans | 51% | 88% |
A0A1X0NYV7 | Trypanosomatidae | 56% | 93% |
A0A3Q8IHU1 | Leishmania donovani | 34% | 100% |
A0A3Q8IJS0 | Leishmania donovani | 35% | 100% |
A0A3S7X163 | Leishmania donovani | 88% | 99% |
A0A3S7X2R4 | Leishmania donovani | 40% | 100% |
A0A422P1K0 | Trypanosoma rangeli | 58% | 94% |
A2VDN5 | Bos taurus | 39% | 85% |
A4H6T6 | Leishmania braziliensis | 37% | 100% |
A4HHP9 | Leishmania braziliensis | 41% | 100% |
A4HME8 | Leishmania braziliensis | 35% | 100% |
A4HPV3 | Leishmania braziliensis | 35% | 100% |
A4I3C0 | Leishmania infantum | 88% | 87% |
A4I4W4 | Leishmania infantum | 40% | 100% |
A4IB20 | Leishmania infantum | 34% | 100% |
A4IE38 | Leishmania infantum | 35% | 100% |
A9RA82 | Papio anubis | 42% | 100% |
B2RYN7 | Rattus norvegicus | 40% | 90% |
B3EX35 | Sorex araneus | 42% | 100% |
B4F6J6 | Xenopus tropicalis | 34% | 100% |
B4USW8 | Otolemur garnettii | 42% | 100% |
B5X3X5 | Salmo salar | 42% | 100% |
B7NZ88 | Oryctolagus cuniculus | 42% | 100% |
D0A833 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 58% | 94% |
E9AEB2 | Leishmania major | 40% | 100% |
E9AEU9 | Leishmania major | 34% | 100% |
E9ALH4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 42% | 100% |
E9ATM0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E9AZK1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 97% |
E9B605 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
F6QV99 | Bos taurus | 33% | 100% |
O61577 | Strongylocentrotus purpuratus | 43% | 100% |
O75449 | Homo sapiens | 42% | 100% |
Q05AS3 | Xenopus tropicalis | 41% | 87% |
Q0IIR9 | Xenopus tropicalis | 43% | 100% |
Q1HGK7 | Gallus gallus | 44% | 100% |
Q4Q0X8 | Leishmania major | 35% | 100% |
Q4Q8N0 | Leishmania major | 85% | 100% |
Q4R407 | Macaca fascicularis | 42% | 100% |
Q505J9 | Rattus norvegicus | 33% | 100% |
Q5RII9 | Danio rerio | 44% | 100% |
Q5U3S1 | Danio rerio | 42% | 100% |
Q5XIK7 | Rattus norvegicus | 42% | 100% |
Q6E0V2 | Rattus norvegicus | 42% | 100% |
Q6NW58 | Danio rerio | 40% | 92% |
Q719N1 | Sus scrofa | 37% | 85% |
Q793F9 | Rattus norvegicus | 40% | 100% |
Q7ZZ25 | Danio rerio | 32% | 100% |
Q8K0T4 | Mus musculus | 43% | 100% |
Q8NBU5 | Homo sapiens | 33% | 100% |
Q8VEJ9 | Mus musculus | 40% | 100% |
Q9BW62 | Homo sapiens | 42% | 100% |
Q9D5T0 | Mus musculus | 33% | 100% |
Q9PUL2 | Xenopus laevis | 43% | 100% |
Q9QYY8 | Mus musculus | 40% | 85% |
Q9SEX2 | Arabidopsis thaliana | 42% | 100% |
Q9UBP0 | Homo sapiens | 40% | 85% |
Q9UN37 | Homo sapiens | 40% | 100% |
Q9WV86 | Mus musculus | 42% | 100% |
V5B0U7 | Trypanosoma cruzi | 57% | 94% |