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: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4I2M3
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 13 |
GO:0003824 | catalytic activity | 1 | 13 |
GO:0005488 | binding | 1 | 13 |
GO:0005524 | ATP binding | 5 | 13 |
GO:0016462 | pyrophosphatase activity | 5 | 13 |
GO:0016787 | hydrolase activity | 2 | 13 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 13 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 13 |
GO:0016887 | ATP hydrolysis activity | 7 | 13 |
GO:0017076 | purine nucleotide binding | 4 | 13 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 13 |
GO:0030554 | adenyl nucleotide binding | 5 | 13 |
GO:0032553 | ribonucleotide binding | 3 | 13 |
GO:0032555 | purine ribonucleotide binding | 4 | 13 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 13 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 13 |
GO:0036094 | small molecule binding | 2 | 13 |
GO:0043167 | ion binding | 2 | 13 |
GO:0043168 | anion binding | 3 | 13 |
GO:0097159 | organic cyclic compound binding | 2 | 13 |
GO:0097367 | carbohydrate derivative binding | 2 | 13 |
GO:1901265 | nucleoside phosphate binding | 3 | 13 |
GO:1901363 | heterocyclic compound binding | 2 | 13 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 520 | 524 | PF00656 | 0.308 |
CLV_NRD_NRD_1 | 112 | 114 | PF00675 | 0.595 |
CLV_NRD_NRD_1 | 173 | 175 | PF00675 | 0.502 |
CLV_NRD_NRD_1 | 286 | 288 | PF00675 | 0.479 |
CLV_NRD_NRD_1 | 377 | 379 | PF00675 | 0.546 |
CLV_NRD_NRD_1 | 483 | 485 | PF00675 | 0.355 |
CLV_NRD_NRD_1 | 501 | 503 | PF00675 | 0.259 |
CLV_NRD_NRD_1 | 53 | 55 | PF00675 | 0.583 |
CLV_PCSK_FUR_1 | 481 | 485 | PF00082 | 0.425 |
CLV_PCSK_KEX2_1 | 112 | 114 | PF00082 | 0.595 |
CLV_PCSK_KEX2_1 | 173 | 175 | PF00082 | 0.667 |
CLV_PCSK_KEX2_1 | 377 | 379 | PF00082 | 0.546 |
CLV_PCSK_KEX2_1 | 483 | 485 | PF00082 | 0.411 |
CLV_PCSK_KEX2_1 | 501 | 503 | PF00082 | 0.170 |
CLV_PCSK_KEX2_1 | 53 | 55 | PF00082 | 0.582 |
CLV_PCSK_KEX2_1 | 637 | 639 | PF00082 | 0.365 |
CLV_PCSK_PC1ET2_1 | 637 | 639 | PF00082 | 0.365 |
CLV_PCSK_SKI1_1 | 104 | 108 | PF00082 | 0.437 |
CLV_PCSK_SKI1_1 | 147 | 151 | PF00082 | 0.507 |
CLV_PCSK_SKI1_1 | 230 | 234 | PF00082 | 0.499 |
CLV_PCSK_SKI1_1 | 342 | 346 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 428 | 432 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 476 | 480 | PF00082 | 0.311 |
DEG_APCC_DBOX_1 | 229 | 237 | PF00400 | 0.524 |
DEG_MDM2_SWIB_1 | 255 | 263 | PF02201 | 0.507 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.493 |
DEG_SPOP_SBC_1 | 175 | 179 | PF00917 | 0.700 |
DOC_ANK_TNKS_1 | 79 | 86 | PF00023 | 0.381 |
DOC_CYCLIN_yCln2_LP_2 | 542 | 548 | PF00134 | 0.425 |
DOC_MAPK_FxFP_2 | 334 | 337 | PF00069 | 0.434 |
DOC_MAPK_gen_1 | 481 | 491 | PF00069 | 0.347 |
DOC_MAPK_gen_1 | 549 | 559 | PF00069 | 0.298 |
DOC_MAPK_gen_1 | 87 | 94 | PF00069 | 0.538 |
DOC_MAPK_MEF2A_6 | 305 | 312 | PF00069 | 0.386 |
DOC_MAPK_MEF2A_6 | 483 | 491 | PF00069 | 0.329 |
DOC_MAPK_MEF2A_6 | 552 | 561 | PF00069 | 0.306 |
DOC_MAPK_MEF2A_6 | 567 | 575 | PF00069 | 0.354 |
DOC_PP1_RVXF_1 | 386 | 393 | PF00149 | 0.442 |
DOC_PP1_RVXF_1 | 405 | 412 | PF00149 | 0.416 |
DOC_PP2B_LxvP_1 | 318 | 321 | PF13499 | 0.553 |
DOC_PP4_FxxP_1 | 334 | 337 | PF00568 | 0.434 |
DOC_SPAK_OSR1_1 | 421 | 425 | PF12202 | 0.473 |
DOC_USP7_MATH_1 | 159 | 163 | PF00917 | 0.448 |
DOC_USP7_MATH_1 | 175 | 179 | PF00917 | 0.504 |
DOC_USP7_MATH_1 | 205 | 209 | PF00917 | 0.541 |
DOC_USP7_MATH_1 | 232 | 236 | PF00917 | 0.464 |
DOC_USP7_MATH_1 | 303 | 307 | PF00917 | 0.550 |
DOC_USP7_MATH_1 | 446 | 450 | PF00917 | 0.350 |
DOC_USP7_MATH_1 | 71 | 75 | PF00917 | 0.630 |
DOC_WW_Pin1_4 | 10 | 15 | PF00397 | 0.449 |
DOC_WW_Pin1_4 | 247 | 252 | PF00397 | 0.467 |
DOC_WW_Pin1_4 | 422 | 427 | PF00397 | 0.482 |
LIG_14-3-3_CanoR_1 | 147 | 152 | PF00244 | 0.452 |
LIG_14-3-3_CanoR_1 | 391 | 398 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 513 | 519 | PF00244 | 0.298 |
LIG_14-3-3_CanoR_1 | 53 | 62 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 622 | 630 | PF00244 | 0.458 |
LIG_Actin_WH2_2 | 282 | 299 | PF00022 | 0.434 |
LIG_Actin_WH2_2 | 461 | 478 | PF00022 | 0.311 |
LIG_APCC_ABBA_1 | 606 | 611 | PF00400 | 0.511 |
LIG_BRCT_BRCA1_1 | 245 | 249 | PF00533 | 0.536 |
LIG_BRCT_BRCA1_1 | 251 | 255 | PF00533 | 0.556 |
LIG_BRCT_BRCA1_1 | 56 | 60 | PF00533 | 0.538 |
LIG_Clathr_ClatBox_1 | 455 | 459 | PF01394 | 0.425 |
LIG_eIF4E_1 | 155 | 161 | PF01652 | 0.435 |
LIG_FHA_1 | 193 | 199 | PF00498 | 0.445 |
LIG_FHA_1 | 237 | 243 | PF00498 | 0.552 |
LIG_FHA_1 | 260 | 266 | PF00498 | 0.470 |
LIG_FHA_1 | 32 | 38 | PF00498 | 0.612 |
LIG_FHA_1 | 439 | 445 | PF00498 | 0.311 |
LIG_FHA_1 | 580 | 586 | PF00498 | 0.490 |
LIG_FHA_1 | 624 | 630 | PF00498 | 0.435 |
LIG_FHA_1 | 63 | 69 | PF00498 | 0.420 |
LIG_FHA_2 | 100 | 106 | PF00498 | 0.518 |
LIG_FHA_2 | 266 | 272 | PF00498 | 0.514 |
LIG_FHA_2 | 366 | 372 | PF00498 | 0.498 |
LIG_FHA_2 | 518 | 524 | PF00498 | 0.311 |
LIG_FHA_2 | 561 | 567 | PF00498 | 0.452 |
LIG_FHA_2 | 576 | 582 | PF00498 | 0.284 |
LIG_FHA_2 | 637 | 643 | PF00498 | 0.474 |
LIG_LIR_Gen_1 | 450 | 461 | PF02991 | 0.314 |
LIG_LIR_Gen_1 | 523 | 533 | PF02991 | 0.446 |
LIG_LIR_LC3C_4 | 262 | 267 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 141 | 146 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 450 | 456 | PF02991 | 0.316 |
LIG_LIR_Nem_3 | 523 | 528 | PF02991 | 0.446 |
LIG_NBox_RRM_1 | 336 | 346 | PF00076 | 0.298 |
LIG_NRBOX | 197 | 203 | PF00104 | 0.526 |
LIG_NRBOX | 514 | 520 | PF00104 | 0.311 |
LIG_NRBOX | 570 | 576 | PF00104 | 0.491 |
LIG_Pex14_1 | 245 | 249 | PF04695 | 0.536 |
LIG_Pex14_2 | 255 | 259 | PF04695 | 0.535 |
LIG_Pex14_2 | 330 | 334 | PF04695 | 0.435 |
LIG_SH2_CRK | 155 | 159 | PF00017 | 0.465 |
LIG_SH2_CRK | 433 | 437 | PF00017 | 0.298 |
LIG_SH2_PTP2 | 130 | 133 | PF00017 | 0.413 |
LIG_SH2_SRC | 457 | 460 | PF00017 | 0.326 |
LIG_SH2_STAP1 | 641 | 645 | PF00017 | 0.467 |
LIG_SH2_STAT3 | 628 | 631 | PF00017 | 0.522 |
LIG_SH2_STAT5 | 101 | 104 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 130 | 133 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 144 | 147 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 25 | 28 | PF00017 | 0.524 |
LIG_SH2_STAT5 | 335 | 338 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 457 | 460 | PF00017 | 0.318 |
LIG_SH2_STAT5 | 467 | 470 | PF00017 | 0.326 |
LIG_SH2_STAT5 | 474 | 477 | PF00017 | 0.311 |
LIG_SH2_STAT5 | 628 | 631 | PF00017 | 0.501 |
LIG_SH3_3 | 105 | 111 | PF00018 | 0.532 |
LIG_SH3_3 | 554 | 560 | PF00018 | 0.303 |
LIG_SH3_3 | 78 | 84 | PF00018 | 0.453 |
LIG_SUMO_SIM_anti_2 | 262 | 269 | PF11976 | 0.429 |
LIG_SUMO_SIM_anti_2 | 306 | 311 | PF11976 | 0.363 |
LIG_SUMO_SIM_anti_2 | 493 | 499 | PF11976 | 0.326 |
LIG_SUMO_SIM_par_1 | 262 | 269 | PF11976 | 0.505 |
LIG_TRAF2_1 | 254 | 257 | PF00917 | 0.429 |
LIG_UBA3_1 | 198 | 207 | PF00899 | 0.502 |
LIG_UBA3_1 | 605 | 610 | PF00899 | 0.511 |
LIG_WW_3 | 425 | 429 | PF00397 | 0.429 |
MOD_CDK_SPxK_1 | 422 | 428 | PF00069 | 0.478 |
MOD_CK1_1 | 247 | 253 | PF00069 | 0.495 |
MOD_CK1_1 | 72 | 78 | PF00069 | 0.503 |
MOD_CK2_1 | 247 | 253 | PF00069 | 0.548 |
MOD_CK2_1 | 265 | 271 | PF00069 | 0.481 |
MOD_CK2_1 | 365 | 371 | PF00069 | 0.479 |
MOD_CK2_1 | 72 | 78 | PF00069 | 0.605 |
MOD_CK2_1 | 99 | 105 | PF00069 | 0.491 |
MOD_Cter_Amidation | 499 | 502 | PF01082 | 0.326 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.486 |
MOD_GlcNHglycan | 352 | 355 | PF01048 | 0.544 |
MOD_GlcNHglycan | 358 | 361 | PF01048 | 0.434 |
MOD_GlcNHglycan | 459 | 462 | PF01048 | 0.318 |
MOD_GlcNHglycan | 464 | 467 | PF01048 | 0.302 |
MOD_GlcNHglycan | 503 | 506 | PF01048 | 0.420 |
MOD_GlcNHglycan | 592 | 595 | PF01048 | 0.411 |
MOD_GlcNHglycan | 611 | 614 | PF01048 | 0.461 |
MOD_GlcNHglycan | 633 | 636 | PF01048 | 0.505 |
MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.584 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.501 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.473 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.578 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.448 |
MOD_GSK3_1 | 513 | 520 | PF00069 | 0.311 |
MOD_GSK3_1 | 575 | 582 | PF00069 | 0.425 |
MOD_GSK3_1 | 586 | 593 | PF00069 | 0.295 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.548 |
MOD_GSK3_1 | 636 | 643 | PF00069 | 0.483 |
MOD_LATS_1 | 511 | 517 | PF00433 | 0.393 |
MOD_N-GLC_1 | 451 | 456 | PF02516 | 0.370 |
MOD_N-GLC_1 | 6 | 11 | PF02516 | 0.465 |
MOD_NEK2_1 | 243 | 248 | PF00069 | 0.497 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.312 |
MOD_NEK2_1 | 33 | 38 | PF00069 | 0.612 |
MOD_NEK2_1 | 345 | 350 | PF00069 | 0.457 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.496 |
MOD_NEK2_1 | 514 | 519 | PF00069 | 0.311 |
MOD_NEK2_1 | 575 | 580 | PF00069 | 0.392 |
MOD_NEK2_1 | 609 | 614 | PF00069 | 0.521 |
MOD_NEK2_1 | 62 | 67 | PF00069 | 0.524 |
MOD_NEK2_1 | 636 | 641 | PF00069 | 0.465 |
MOD_NEK2_1 | 99 | 104 | PF00069 | 0.497 |
MOD_NEK2_2 | 142 | 147 | PF00069 | 0.515 |
MOD_NEK2_2 | 244 | 249 | PF00069 | 0.385 |
MOD_PIKK_1 | 54 | 60 | PF00454 | 0.571 |
MOD_PKA_1 | 501 | 507 | PF00069 | 0.408 |
MOD_PKA_2 | 390 | 396 | PF00069 | 0.465 |
MOD_PKA_2 | 501 | 507 | PF00069 | 0.345 |
MOD_PKA_2 | 566 | 572 | PF00069 | 0.493 |
MOD_PKA_2 | 621 | 627 | PF00069 | 0.528 |
MOD_Plk_1 | 104 | 110 | PF00069 | 0.502 |
MOD_Plk_1 | 205 | 211 | PF00069 | 0.533 |
MOD_Plk_1 | 41 | 47 | PF00069 | 0.547 |
MOD_Plk_1 | 451 | 457 | PF00069 | 0.393 |
MOD_Plk_1 | 641 | 647 | PF00069 | 0.519 |
MOD_Plk_4 | 238 | 244 | PF00069 | 0.500 |
MOD_Plk_4 | 259 | 265 | PF00069 | 0.506 |
MOD_Plk_4 | 380 | 386 | PF00069 | 0.621 |
MOD_Plk_4 | 439 | 445 | PF00069 | 0.298 |
MOD_Plk_4 | 459 | 465 | PF00069 | 0.116 |
MOD_Plk_4 | 514 | 520 | PF00069 | 0.310 |
MOD_Plk_4 | 566 | 572 | PF00069 | 0.452 |
MOD_ProDKin_1 | 10 | 16 | PF00069 | 0.443 |
MOD_ProDKin_1 | 247 | 253 | PF00069 | 0.474 |
MOD_ProDKin_1 | 422 | 428 | PF00069 | 0.478 |
MOD_SUMO_rev_2 | 590 | 600 | PF00179 | 0.508 |
TRG_DiLeu_BaEn_1 | 194 | 199 | PF01217 | 0.514 |
TRG_DiLeu_BaEn_1 | 510 | 515 | PF01217 | 0.425 |
TRG_DiLeu_LyEn_5 | 510 | 515 | PF01217 | 0.425 |
TRG_ENDOCYTIC_2 | 130 | 133 | PF00928 | 0.395 |
TRG_ENDOCYTIC_2 | 155 | 158 | PF00928 | 0.480 |
TRG_ER_diArg_1 | 111 | 113 | PF00400 | 0.604 |
TRG_ER_diArg_1 | 166 | 169 | PF00400 | 0.533 |
TRG_ER_diArg_1 | 377 | 379 | PF00400 | 0.596 |
TRG_ER_diArg_1 | 481 | 484 | PF00400 | 0.425 |
TRG_ER_diArg_1 | 501 | 503 | PF00400 | 0.116 |
TRG_ER_diArg_1 | 53 | 55 | PF00400 | 0.589 |
TRG_Pf-PMV_PEXEL_1 | 287 | 292 | PF00026 | 0.434 |
TRG_Pf-PMV_PEXEL_1 | 473 | 477 | PF00026 | 0.326 |
TRG_Pf-PMV_PEXEL_1 | 583 | 587 | PF00026 | 0.527 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HYP0 | Leptomonas seymouri | 67% | 97% |
A0A0S4JUV1 | Bodo saltans | 40% | 100% |
A0A0S4KLG9 | Bodo saltans | 30% | 100% |
A0A1X0P3W8 | Trypanosomatidae | 44% | 100% |
A0A3R7L6R6 | Trypanosoma rangeli | 44% | 98% |
A0A3S7X0E5 | Leishmania donovani | 100% | 100% |
A4HFG1 | Leishmania braziliensis | 86% | 100% |
D0A5N6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
E9AD13 | Leishmania major | 92% | 100% |
E9AYT8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
O74941 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 25% | 70% |
V5BSQ8 | Trypanosoma cruzi | 42% | 79% |