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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000922 | spindle pole | 2 | 11 |
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:0005815 | microtubule organizing center | 2 | 1 |
GO:0036064 | ciliary basal body | 3 | 1 |
Related structures:
AlphaFold database: A0A3Q8I9I1
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 | 112 | 116 | PF00656 | 0.661 |
CLV_C14_Caspase3-7 | 378 | 382 | PF00656 | 0.235 |
CLV_C14_Caspase3-7 | 405 | 409 | PF00656 | 0.368 |
CLV_C14_Caspase3-7 | 75 | 79 | PF00656 | 0.470 |
CLV_NRD_NRD_1 | 132 | 134 | PF00675 | 0.584 |
CLV_NRD_NRD_1 | 220 | 222 | PF00675 | 0.650 |
CLV_NRD_NRD_1 | 244 | 246 | PF00675 | 0.543 |
CLV_NRD_NRD_1 | 38 | 40 | PF00675 | 0.462 |
CLV_NRD_NRD_1 | 397 | 399 | PF00675 | 0.235 |
CLV_NRD_NRD_1 | 413 | 415 | PF00675 | 0.235 |
CLV_NRD_NRD_1 | 437 | 439 | PF00675 | 0.235 |
CLV_NRD_NRD_1 | 458 | 460 | PF00675 | 0.460 |
CLV_NRD_NRD_1 | 498 | 500 | PF00675 | 0.368 |
CLV_PCSK_FUR_1 | 36 | 40 | PF00082 | 0.387 |
CLV_PCSK_KEX2_1 | 220 | 222 | PF00082 | 0.650 |
CLV_PCSK_KEX2_1 | 244 | 246 | PF00082 | 0.503 |
CLV_PCSK_KEX2_1 | 38 | 40 | PF00082 | 0.383 |
CLV_PCSK_KEX2_1 | 397 | 399 | PF00082 | 0.235 |
CLV_PCSK_KEX2_1 | 412 | 414 | PF00082 | 0.235 |
CLV_PCSK_KEX2_1 | 437 | 439 | PF00082 | 0.235 |
CLV_PCSK_KEX2_1 | 441 | 443 | PF00082 | 0.235 |
CLV_PCSK_KEX2_1 | 458 | 460 | PF00082 | 0.355 |
CLV_PCSK_PC1ET2_1 | 412 | 414 | PF00082 | 0.254 |
CLV_PCSK_PC1ET2_1 | 441 | 443 | PF00082 | 0.235 |
CLV_PCSK_PC7_1 | 437 | 443 | PF00082 | 0.235 |
CLV_PCSK_SKI1_1 | 140 | 144 | PF00082 | 0.729 |
CLV_PCSK_SKI1_1 | 244 | 248 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 267 | 271 | PF00082 | 0.326 |
CLV_PCSK_SKI1_1 | 288 | 292 | PF00082 | 0.309 |
CLV_PCSK_SKI1_1 | 313 | 317 | PF00082 | 0.246 |
CLV_PCSK_SKI1_1 | 325 | 329 | PF00082 | 0.215 |
CLV_PCSK_SKI1_1 | 361 | 365 | PF00082 | 0.235 |
CLV_PCSK_SKI1_1 | 38 | 42 | PF00082 | 0.393 |
CLV_PCSK_SKI1_1 | 397 | 401 | PF00082 | 0.235 |
CLV_PCSK_SKI1_1 | 441 | 445 | PF00082 | 0.254 |
CLV_PCSK_SKI1_1 | 458 | 462 | PF00082 | 0.394 |
DEG_APCC_DBOX_1 | 243 | 251 | PF00400 | 0.465 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.586 |
DEG_SPOP_SBC_1 | 141 | 145 | PF00917 | 0.622 |
DEG_SPOP_SBC_1 | 6 | 10 | PF00917 | 0.458 |
DOC_CYCLIN_RxL_1 | 358 | 365 | PF00134 | 0.235 |
DOC_CYCLIN_RxL_1 | 453 | 464 | PF00134 | 0.418 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 161 | 170 | PF00134 | 0.669 |
DOC_MAPK_gen_1 | 310 | 318 | PF00069 | 0.299 |
DOC_MAPK_gen_1 | 358 | 368 | PF00069 | 0.254 |
DOC_MAPK_gen_1 | 36 | 46 | PF00069 | 0.355 |
DOC_MAPK_gen_1 | 412 | 421 | PF00069 | 0.314 |
DOC_MAPK_gen_1 | 437 | 447 | PF00069 | 0.235 |
DOC_MAPK_HePTP_8 | 35 | 47 | PF00069 | 0.434 |
DOC_MAPK_MEF2A_6 | 38 | 47 | PF00069 | 0.365 |
DOC_MAPK_MEF2A_6 | 438 | 447 | PF00069 | 0.235 |
DOC_MAPK_RevD_3 | 443 | 459 | PF00069 | 0.442 |
DOC_PP1_RVXF_1 | 451 | 458 | PF00149 | 0.387 |
DOC_PP1_SILK_1 | 306 | 311 | PF00149 | 0.436 |
DOC_PP2B_LxvP_1 | 523 | 526 | PF13499 | 0.335 |
DOC_PP4_FxxP_1 | 318 | 321 | PF00568 | 0.235 |
DOC_USP7_MATH_1 | 141 | 145 | PF00917 | 0.728 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.456 |
DOC_USP7_MATH_1 | 209 | 213 | PF00917 | 0.700 |
DOC_USP7_MATH_1 | 227 | 231 | PF00917 | 0.656 |
DOC_USP7_MATH_1 | 240 | 244 | PF00917 | 0.599 |
DOC_USP7_MATH_1 | 344 | 348 | PF00917 | 0.258 |
DOC_USP7_MATH_1 | 386 | 390 | PF00917 | 0.303 |
DOC_USP7_MATH_1 | 6 | 10 | PF00917 | 0.533 |
DOC_WW_Pin1_4 | 144 | 149 | PF00397 | 0.697 |
LIG_14-3-3_CanoR_1 | 107 | 117 | PF00244 | 0.543 |
LIG_14-3-3_CanoR_1 | 140 | 148 | PF00244 | 0.708 |
LIG_14-3-3_CanoR_1 | 337 | 341 | PF00244 | 0.254 |
LIG_14-3-3_CanoR_1 | 397 | 407 | PF00244 | 0.235 |
LIG_14-3-3_CanoR_1 | 442 | 448 | PF00244 | 0.295 |
LIG_14-3-3_CanoR_1 | 541 | 545 | PF00244 | 0.300 |
LIG_14-3-3_CanoR_1 | 68 | 72 | PF00244 | 0.488 |
LIG_Actin_WH2_2 | 147 | 164 | PF00022 | 0.623 |
LIG_Actin_WH2_2 | 254 | 269 | PF00022 | 0.491 |
LIG_BIR_III_4 | 113 | 117 | PF00653 | 0.608 |
LIG_BIR_III_4 | 226 | 230 | PF00653 | 0.467 |
LIG_BRCT_BRCA1_1 | 372 | 376 | PF00533 | 0.235 |
LIG_CaM_IQ_9 | 60 | 75 | PF13499 | 0.469 |
LIG_EVH1_1 | 250 | 254 | PF00568 | 0.423 |
LIG_FHA_1 | 193 | 199 | PF00498 | 0.667 |
LIG_FHA_1 | 253 | 259 | PF00498 | 0.457 |
LIG_FHA_1 | 372 | 378 | PF00498 | 0.235 |
LIG_FHA_1 | 399 | 405 | PF00498 | 0.271 |
LIG_FHA_1 | 431 | 437 | PF00498 | 0.278 |
LIG_FHA_2 | 403 | 409 | PF00498 | 0.450 |
LIG_FHA_2 | 527 | 533 | PF00498 | 0.262 |
LIG_Integrin_RGD_1 | 353 | 355 | PF01839 | 0.235 |
LIG_LIR_Nem_3 | 275 | 281 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 303 | 308 | PF02991 | 0.348 |
LIG_LIR_Nem_3 | 338 | 343 | PF02991 | 0.235 |
LIG_LIR_Nem_3 | 88 | 92 | PF02991 | 0.372 |
LIG_LYPXL_yS_3 | 301 | 304 | PF13949 | 0.359 |
LIG_MYND_1 | 159 | 163 | PF01753 | 0.660 |
LIG_Rb_pABgroove_1 | 358 | 366 | PF01858 | 0.278 |
LIG_SH2_SRC | 370 | 373 | PF00017 | 0.254 |
LIG_SH2_STAP1 | 471 | 475 | PF00017 | 0.368 |
LIG_SH2_STAP1 | 89 | 93 | PF00017 | 0.380 |
LIG_SH3_1 | 248 | 254 | PF00018 | 0.426 |
LIG_SH3_2 | 519 | 524 | PF14604 | 0.394 |
LIG_SH3_3 | 151 | 157 | PF00018 | 0.599 |
LIG_SH3_3 | 234 | 240 | PF00018 | 0.551 |
LIG_SH3_3 | 246 | 252 | PF00018 | 0.401 |
LIG_SH3_3 | 292 | 298 | PF00018 | 0.344 |
LIG_SH3_3 | 442 | 448 | PF00018 | 0.235 |
LIG_SH3_3 | 513 | 519 | PF00018 | 0.616 |
LIG_SUMO_SIM_anti_2 | 485 | 490 | PF11976 | 0.235 |
LIG_SUMO_SIM_anti_2 | 78 | 84 | PF11976 | 0.394 |
LIG_SUMO_SIM_par_1 | 42 | 48 | PF11976 | 0.401 |
LIG_SUMO_SIM_par_1 | 443 | 449 | PF11976 | 0.368 |
LIG_TRAF2_1 | 28 | 31 | PF00917 | 0.442 |
LIG_TYR_ITIM | 299 | 304 | PF00017 | 0.355 |
LIG_UBA3_1 | 304 | 313 | PF00899 | 0.347 |
LIG_UBA3_1 | 403 | 412 | PF00899 | 0.254 |
LIG_UBA3_1 | 435 | 441 | PF00899 | 0.270 |
MOD_CK1_1 | 144 | 150 | PF00069 | 0.623 |
MOD_CK1_1 | 347 | 353 | PF00069 | 0.246 |
MOD_CK1_1 | 382 | 388 | PF00069 | 0.245 |
MOD_CK1_1 | 446 | 452 | PF00069 | 0.522 |
MOD_CK1_1 | 464 | 470 | PF00069 | 0.415 |
MOD_CK1_1 | 67 | 73 | PF00069 | 0.403 |
MOD_CK2_1 | 209 | 215 | PF00069 | 0.636 |
MOD_CK2_1 | 386 | 392 | PF00069 | 0.334 |
MOD_CK2_1 | 500 | 506 | PF00069 | 0.379 |
MOD_Cter_Amidation | 218 | 221 | PF01082 | 0.648 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.597 |
MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.645 |
MOD_GlcNHglycan | 195 | 198 | PF01048 | 0.641 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.759 |
MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.574 |
MOD_GlcNHglycan | 285 | 288 | PF01048 | 0.430 |
MOD_GlcNHglycan | 384 | 387 | PF01048 | 0.260 |
MOD_GlcNHglycan | 481 | 484 | PF01048 | 0.303 |
MOD_GlcNHglycan | 560 | 563 | PF01048 | 0.407 |
MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.582 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.662 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.235 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.235 |
MOD_GSK3_1 | 382 | 389 | PF00069 | 0.249 |
MOD_GSK3_1 | 398 | 405 | PF00069 | 0.247 |
MOD_GSK3_1 | 475 | 482 | PF00069 | 0.250 |
MOD_GSK3_1 | 533 | 540 | PF00069 | 0.227 |
MOD_GSK3_1 | 558 | 565 | PF00069 | 0.462 |
MOD_LATS_1 | 515 | 521 | PF00433 | 0.383 |
MOD_NEK2_1 | 129 | 134 | PF00069 | 0.501 |
MOD_NEK2_1 | 198 | 203 | PF00069 | 0.761 |
MOD_NEK2_1 | 261 | 266 | PF00069 | 0.330 |
MOD_NEK2_1 | 422 | 427 | PF00069 | 0.236 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.644 |
MOD_NEK2_2 | 336 | 341 | PF00069 | 0.235 |
MOD_PIKK_1 | 402 | 408 | PF00454 | 0.368 |
MOD_PIKK_1 | 500 | 506 | PF00454 | 0.258 |
MOD_PIKK_1 | 69 | 75 | PF00454 | 0.554 |
MOD_PKA_2 | 161 | 167 | PF00069 | 0.687 |
MOD_PKA_2 | 336 | 342 | PF00069 | 0.254 |
MOD_PKA_2 | 386 | 392 | PF00069 | 0.314 |
MOD_PKA_2 | 540 | 546 | PF00069 | 0.334 |
MOD_PKA_2 | 67 | 73 | PF00069 | 0.486 |
MOD_PKB_1 | 105 | 113 | PF00069 | 0.517 |
MOD_Plk_4 | 261 | 267 | PF00069 | 0.435 |
MOD_Plk_4 | 323 | 329 | PF00069 | 0.245 |
MOD_Plk_4 | 336 | 342 | PF00069 | 0.235 |
MOD_Plk_4 | 344 | 350 | PF00069 | 0.235 |
MOD_Plk_4 | 371 | 377 | PF00069 | 0.235 |
MOD_Plk_4 | 379 | 385 | PF00069 | 0.235 |
MOD_Plk_4 | 81 | 87 | PF00069 | 0.350 |
MOD_ProDKin_1 | 144 | 150 | PF00069 | 0.698 |
MOD_SUMO_for_1 | 399 | 402 | PF00179 | 0.235 |
MOD_SUMO_rev_2 | 30 | 35 | PF00179 | 0.478 |
TRG_DiLeu_BaEn_1 | 379 | 384 | PF01217 | 0.235 |
TRG_DiLeu_BaEn_1 | 440 | 445 | PF01217 | 0.235 |
TRG_DiLeu_BaEn_4 | 30 | 36 | PF01217 | 0.484 |
TRG_DiLeu_BaLyEn_6 | 456 | 461 | PF01217 | 0.402 |
TRG_ENDOCYTIC_2 | 301 | 304 | PF00928 | 0.359 |
TRG_ENDOCYTIC_2 | 92 | 95 | PF00928 | 0.374 |
TRG_ER_diArg_1 | 104 | 107 | PF00400 | 0.487 |
TRG_ER_diArg_1 | 244 | 246 | PF00400 | 0.503 |
TRG_ER_diArg_1 | 35 | 38 | PF00400 | 0.414 |
TRG_ER_diArg_1 | 397 | 399 | PF00400 | 0.235 |
TRG_ER_diArg_1 | 436 | 438 | PF00400 | 0.235 |
TRG_ER_diArg_1 | 457 | 459 | PF00400 | 0.467 |
TRG_NLS_Bipartite_1 | 397 | 416 | PF00514 | 0.254 |
TRG_NLS_MonoExtC_3 | 411 | 417 | PF00514 | 0.254 |
TRG_Pf-PMV_PEXEL_1 | 267 | 271 | PF00026 | 0.346 |
TRG_Pf-PMV_PEXEL_1 | 279 | 283 | PF00026 | 0.334 |
TRG_Pf-PMV_PEXEL_1 | 361 | 365 | PF00026 | 0.235 |
TRG_Pf-PMV_PEXEL_1 | 499 | 504 | PF00026 | 0.319 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P897 | Leptomonas seymouri | 69% | 98% |
A0A0S4IR32 | Bodo saltans | 53% | 100% |
A0A1X0NPJ1 | Trypanosomatidae | 58% | 98% |
A0JMA9 | Xenopus tropicalis | 45% | 100% |
A2VDN5 | Bos taurus | 38% | 92% |
A4H784 | Leishmania braziliensis | 82% | 100% |
A4HVM4 | Leishmania infantum | 100% | 100% |
D0A6N0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 57% | 100% |
E9APC0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 99% |
Q05AS3 | Xenopus tropicalis | 38% | 94% |
Q3B8D5 | Xenopus laevis | 39% | 100% |
Q4QG58 | Leishmania major | 95% | 100% |
Q8IYT4 | Homo sapiens | 42% | 100% |
Q9D3R6 | Mus musculus | 41% | 100% |
V5DBR1 | Trypanosoma cruzi | 58% | 95% |