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: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: A4I3C0
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 | 417 | 421 | PF00656 | 0.244 |
CLV_NRD_NRD_1 | 158 | 160 | PF00675 | 0.609 |
CLV_NRD_NRD_1 | 20 | 22 | PF00675 | 0.541 |
CLV_NRD_NRD_1 | 23 | 25 | PF00675 | 0.527 |
CLV_NRD_NRD_1 | 348 | 350 | PF00675 | 0.342 |
CLV_NRD_NRD_1 | 436 | 438 | PF00675 | 0.218 |
CLV_NRD_NRD_1 | 475 | 477 | PF00675 | 0.228 |
CLV_NRD_NRD_1 | 540 | 542 | PF00675 | 0.228 |
CLV_PCSK_FUR_1 | 21 | 25 | PF00082 | 0.461 |
CLV_PCSK_KEX2_1 | 157 | 159 | PF00082 | 0.609 |
CLV_PCSK_KEX2_1 | 20 | 22 | PF00082 | 0.458 |
CLV_PCSK_KEX2_1 | 23 | 25 | PF00082 | 0.458 |
CLV_PCSK_KEX2_1 | 327 | 329 | PF00082 | 0.449 |
CLV_PCSK_KEX2_1 | 348 | 350 | PF00082 | 0.342 |
CLV_PCSK_KEX2_1 | 436 | 438 | PF00082 | 0.218 |
CLV_PCSK_KEX2_1 | 474 | 476 | PF00082 | 0.228 |
CLV_PCSK_KEX2_1 | 479 | 481 | PF00082 | 0.228 |
CLV_PCSK_KEX2_1 | 540 | 542 | PF00082 | 0.228 |
CLV_PCSK_PC1ET2_1 | 157 | 159 | PF00082 | 0.557 |
CLV_PCSK_PC1ET2_1 | 327 | 329 | PF00082 | 0.449 |
CLV_PCSK_PC1ET2_1 | 479 | 481 | PF00082 | 0.228 |
CLV_PCSK_PC7_1 | 475 | 481 | PF00082 | 0.228 |
CLV_PCSK_SKI1_1 | 327 | 331 | PF00082 | 0.297 |
CLV_PCSK_SKI1_1 | 352 | 356 | PF00082 | 0.228 |
CLV_PCSK_SKI1_1 | 364 | 368 | PF00082 | 0.228 |
CLV_PCSK_SKI1_1 | 400 | 404 | PF00082 | 0.228 |
CLV_PCSK_SKI1_1 | 436 | 440 | PF00082 | 0.228 |
CLV_PCSK_SKI1_1 | 44 | 48 | PF00082 | 0.347 |
CLV_PCSK_SKI1_1 | 500 | 504 | PF00082 | 0.386 |
CLV_PCSK_SKI1_1 | 541 | 545 | PF00082 | 0.324 |
CLV_PCSK_SKI1_1 | 64 | 68 | PF00082 | 0.311 |
CLV_PCSK_SKI1_1 | 98 | 102 | PF00082 | 0.424 |
DEG_APCC_DBOX_1 | 490 | 498 | PF00400 | 0.295 |
DEG_APCC_KENBOX_2 | 551 | 555 | PF00400 | 0.374 |
DEG_SPOP_SBC_1 | 244 | 248 | PF00917 | 0.579 |
DEG_SPOP_SBC_1 | 4 | 8 | PF00917 | 0.395 |
DOC_CYCLIN_RxL_1 | 397 | 404 | PF00134 | 0.228 |
DOC_MAPK_gen_1 | 474 | 485 | PF00069 | 0.244 |
DOC_MAPK_gen_1 | 500 | 510 | PF00069 | 0.350 |
DOC_MAPK_gen_1 | 595 | 602 | PF00069 | 0.441 |
DOC_MAPK_gen_1 | 62 | 69 | PF00069 | 0.340 |
DOC_MAPK_MEF2A_6 | 476 | 485 | PF00069 | 0.228 |
DOC_PP1_RVXF_1 | 398 | 404 | PF00149 | 0.228 |
DOC_PP4_FxxP_1 | 15 | 18 | PF00568 | 0.434 |
DOC_PP4_FxxP_1 | 150 | 153 | PF00568 | 0.514 |
DOC_USP7_MATH_1 | 230 | 234 | PF00917 | 0.590 |
DOC_USP7_MATH_1 | 244 | 248 | PF00917 | 0.408 |
DOC_USP7_MATH_1 | 268 | 272 | PF00917 | 0.636 |
DOC_USP7_MATH_1 | 370 | 374 | PF00917 | 0.244 |
DOC_USP7_UBL2_3 | 496 | 500 | PF12436 | 0.366 |
DOC_USP7_UBL2_3 | 544 | 548 | PF12436 | 0.248 |
DOC_USP7_UBL2_3 | 83 | 87 | PF12436 | 0.342 |
DOC_WW_Pin1_4 | 239 | 244 | PF00397 | 0.525 |
DOC_WW_Pin1_4 | 34 | 39 | PF00397 | 0.412 |
DOC_WW_Pin1_4 | 380 | 385 | PF00397 | 0.228 |
DOC_WW_Pin1_4 | 56 | 61 | PF00397 | 0.348 |
DOC_WW_Pin1_4 | 6 | 11 | PF00397 | 0.400 |
LIG_14-3-3_CanoR_1 | 168 | 178 | PF00244 | 0.697 |
LIG_14-3-3_CanoR_1 | 188 | 194 | PF00244 | 0.714 |
LIG_14-3-3_CanoR_1 | 232 | 241 | PF00244 | 0.618 |
LIG_14-3-3_CanoR_1 | 44 | 54 | PF00244 | 0.340 |
LIG_APCC_ABBA_1 | 147 | 152 | PF00400 | 0.461 |
LIG_BRCT_BRCA1_1 | 241 | 245 | PF00533 | 0.535 |
LIG_BRCT_BRCA1_1 | 411 | 415 | PF00533 | 0.228 |
LIG_CtBP_PxDLS_1 | 566 | 570 | PF00389 | 0.249 |
LIG_deltaCOP1_diTrp_1 | 592 | 598 | PF00928 | 0.228 |
LIG_FHA_1 | 113 | 119 | PF00498 | 0.392 |
LIG_FHA_1 | 27 | 33 | PF00498 | 0.465 |
LIG_FHA_1 | 411 | 417 | PF00498 | 0.255 |
LIG_FHA_1 | 451 | 457 | PF00498 | 0.329 |
LIG_FHA_1 | 497 | 503 | PF00498 | 0.308 |
LIG_FHA_1 | 526 | 532 | PF00498 | 0.244 |
LIG_FHA_2 | 141 | 147 | PF00498 | 0.413 |
LIG_FHA_2 | 314 | 320 | PF00498 | 0.478 |
LIG_FHA_2 | 548 | 554 | PF00498 | 0.336 |
LIG_GBD_Chelix_1 | 300 | 308 | PF00786 | 0.323 |
LIG_Integrin_RGD_1 | 392 | 394 | PF01839 | 0.244 |
LIG_LIR_Apic_2 | 14 | 18 | PF02991 | 0.431 |
LIG_LIR_Gen_1 | 124 | 133 | PF02991 | 0.457 |
LIG_LIR_Gen_1 | 236 | 245 | PF02991 | 0.519 |
LIG_LIR_Gen_1 | 316 | 323 | PF02991 | 0.315 |
LIG_LIR_Gen_1 | 507 | 517 | PF02991 | 0.245 |
LIG_LIR_Nem_3 | 124 | 129 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 236 | 241 | PF02991 | 0.528 |
LIG_LIR_Nem_3 | 316 | 320 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 342 | 347 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 377 | 382 | PF02991 | 0.230 |
LIG_LIR_Nem_3 | 507 | 513 | PF02991 | 0.230 |
LIG_LYPXL_S_1 | 335 | 339 | PF13949 | 0.308 |
LIG_LYPXL_yS_3 | 336 | 339 | PF13949 | 0.313 |
LIG_MYND_1 | 337 | 341 | PF01753 | 0.323 |
LIG_NRBOX | 512 | 518 | PF00104 | 0.293 |
LIG_PDZ_Class_2 | 597 | 602 | PF00595 | 0.504 |
LIG_Pex14_1 | 594 | 598 | PF04695 | 0.228 |
LIG_Pex14_2 | 42 | 46 | PF04695 | 0.353 |
LIG_SH2_CRK | 104 | 108 | PF00017 | 0.460 |
LIG_SH2_CRK | 238 | 242 | PF00017 | 0.655 |
LIG_SH2_CRK | 344 | 348 | PF00017 | 0.440 |
LIG_SH2_CRK | 357 | 361 | PF00017 | 0.228 |
LIG_SH2_NCK_1 | 238 | 242 | PF00017 | 0.526 |
LIG_SH2_PTP2 | 482 | 485 | PF00017 | 0.228 |
LIG_SH2_SRC | 409 | 412 | PF00017 | 0.244 |
LIG_SH2_STAT5 | 482 | 485 | PF00017 | 0.228 |
LIG_SH2_STAT5 | 94 | 97 | PF00017 | 0.399 |
LIG_SH3_3 | 218 | 224 | PF00018 | 0.554 |
LIG_SH3_3 | 238 | 244 | PF00018 | 0.603 |
LIG_SH3_3 | 249 | 255 | PF00018 | 0.569 |
LIG_SH3_3 | 331 | 337 | PF00018 | 0.295 |
LIG_SH3_3 | 50 | 56 | PF00018 | 0.349 |
LIG_SH3_3 | 7 | 13 | PF00018 | 0.401 |
LIG_TRAF2_1 | 295 | 298 | PF00917 | 0.379 |
LIG_TYR_ITIM | 334 | 339 | PF00017 | 0.303 |
LIG_UBA3_1 | 494 | 500 | PF00899 | 0.332 |
LIG_UBA3_1 | 536 | 544 | PF00899 | 0.307 |
LIG_WW_3 | 59 | 63 | PF00397 | 0.328 |
MOD_CDC14_SPxK_1 | 59 | 62 | PF00782 | 0.338 |
MOD_CDK_SPxK_1 | 56 | 62 | PF00069 | 0.351 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.654 |
MOD_CK1_1 | 196 | 202 | PF00069 | 0.576 |
MOD_CK1_1 | 233 | 239 | PF00069 | 0.664 |
MOD_CK1_1 | 271 | 277 | PF00069 | 0.694 |
MOD_CK1_1 | 286 | 292 | PF00069 | 0.560 |
MOD_CK1_1 | 383 | 389 | PF00069 | 0.269 |
MOD_CK1_1 | 76 | 82 | PF00069 | 0.445 |
MOD_CK2_1 | 140 | 146 | PF00069 | 0.477 |
MOD_CK2_1 | 168 | 174 | PF00069 | 0.682 |
MOD_CK2_1 | 547 | 553 | PF00069 | 0.384 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.694 |
MOD_GlcNHglycan | 195 | 198 | PF01048 | 0.676 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.677 |
MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.553 |
MOD_GlcNHglycan | 271 | 274 | PF01048 | 0.669 |
MOD_GlcNHglycan | 285 | 288 | PF01048 | 0.599 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.482 |
MOD_GlcNHglycan | 522 | 525 | PF01048 | 0.322 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.498 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.619 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.495 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.600 |
MOD_GSK3_1 | 239 | 246 | PF00069 | 0.513 |
MOD_GSK3_1 | 370 | 377 | PF00069 | 0.293 |
MOD_GSK3_1 | 69 | 76 | PF00069 | 0.472 |
MOD_N-GLC_1 | 166 | 171 | PF02516 | 0.561 |
MOD_N-GLC_1 | 199 | 204 | PF02516 | 0.500 |
MOD_N-GLC_1 | 375 | 380 | PF02516 | 0.239 |
MOD_N-GLC_1 | 567 | 572 | PF02516 | 0.249 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.639 |
MOD_NEK2_1 | 245 | 250 | PF00069 | 0.463 |
MOD_NEK2_1 | 460 | 465 | PF00069 | 0.228 |
MOD_NEK2_1 | 73 | 78 | PF00069 | 0.488 |
MOD_NEK2_2 | 103 | 108 | PF00069 | 0.399 |
MOD_NEK2_2 | 375 | 380 | PF00069 | 0.228 |
MOD_NEK2_2 | 535 | 540 | PF00069 | 0.228 |
MOD_PIKK_1 | 121 | 127 | PF00454 | 0.475 |
MOD_PIKK_1 | 140 | 146 | PF00454 | 0.406 |
MOD_PIKK_1 | 511 | 517 | PF00454 | 0.356 |
MOD_PKA_2 | 140 | 146 | PF00069 | 0.406 |
MOD_PKA_2 | 167 | 173 | PF00069 | 0.678 |
MOD_PKA_2 | 22 | 28 | PF00069 | 0.466 |
MOD_PKA_2 | 69 | 75 | PF00069 | 0.340 |
MOD_PKB_1 | 24 | 32 | PF00069 | 0.470 |
MOD_Plk_1 | 199 | 205 | PF00069 | 0.498 |
MOD_Plk_1 | 375 | 381 | PF00069 | 0.299 |
MOD_Plk_1 | 546 | 552 | PF00069 | 0.293 |
MOD_Plk_2-3 | 547 | 553 | PF00069 | 0.447 |
MOD_Plk_4 | 125 | 131 | PF00069 | 0.471 |
MOD_Plk_4 | 362 | 368 | PF00069 | 0.247 |
MOD_Plk_4 | 375 | 381 | PF00069 | 0.149 |
MOD_Plk_4 | 410 | 416 | PF00069 | 0.228 |
MOD_Plk_4 | 438 | 444 | PF00069 | 0.244 |
MOD_ProDKin_1 | 239 | 245 | PF00069 | 0.507 |
MOD_ProDKin_1 | 34 | 40 | PF00069 | 0.407 |
MOD_ProDKin_1 | 380 | 386 | PF00069 | 0.228 |
MOD_ProDKin_1 | 56 | 62 | PF00069 | 0.351 |
MOD_ProDKin_1 | 6 | 12 | PF00069 | 0.401 |
MOD_SUMO_rev_2 | 319 | 329 | PF00179 | 0.322 |
TRG_DiLeu_BaEn_1 | 299 | 304 | PF01217 | 0.340 |
TRG_DiLeu_BaEn_1 | 325 | 330 | PF01217 | 0.334 |
TRG_DiLeu_BaEn_2 | 145 | 151 | PF01217 | 0.529 |
TRG_DiLeu_BaLyEn_6 | 50 | 55 | PF01217 | 0.347 |
TRG_DiLeu_LyEn_5 | 325 | 330 | PF01217 | 0.445 |
TRG_ENDOCYTIC_2 | 104 | 107 | PF00928 | 0.306 |
TRG_ENDOCYTIC_2 | 238 | 241 | PF00928 | 0.529 |
TRG_ENDOCYTIC_2 | 336 | 339 | PF00928 | 0.361 |
TRG_ENDOCYTIC_2 | 344 | 347 | PF00928 | 0.399 |
TRG_ENDOCYTIC_2 | 482 | 485 | PF00928 | 0.228 |
TRG_ER_diArg_1 | 20 | 23 | PF00400 | 0.458 |
TRG_ER_diArg_1 | 279 | 282 | PF00400 | 0.645 |
TRG_ER_diArg_1 | 347 | 349 | PF00400 | 0.361 |
TRG_ER_diArg_1 | 473 | 476 | PF00400 | 0.228 |
TRG_ER_diArg_1 | 539 | 541 | PF00400 | 0.228 |
TRG_ER_diArg_1 | 67 | 70 | PF00400 | 0.364 |
TRG_NLS_MonoCore_2 | 184 | 189 | PF00514 | 0.669 |
TRG_NLS_MonoExtC_3 | 183 | 188 | PF00514 | 0.602 |
TRG_NLS_MonoExtN_4 | 184 | 189 | PF00514 | 0.607 |
TRG_Pf-PMV_PEXEL_1 | 116 | 120 | PF00026 | 0.411 |
TRG_Pf-PMV_PEXEL_1 | 327 | 331 | PF00026 | 0.297 |
TRG_Pf-PMV_PEXEL_1 | 400 | 404 | PF00026 | 0.228 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HRH8 | Leptomonas seymouri | 70% | 100% |
A0A0S4IUM1 | Bodo saltans | 51% | 100% |
A0A1X0NYV7 | Trypanosomatidae | 57% | 100% |
A0A3Q8IJS0 | Leishmania donovani | 35% | 100% |
A0A3S7X163 | Leishmania donovani | 100% | 100% |
A0A3S7X2R4 | Leishmania donovani | 42% | 100% |
A0A422P1K0 | Trypanosoma rangeli | 57% | 100% |
A4HG81 | Leishmania braziliensis | 88% | 98% |
A4HPV3 | Leishmania braziliensis | 35% | 100% |
A4I4W4 | Leishmania infantum | 42% | 100% |
A4IE38 | Leishmania infantum | 35% | 100% |
B2RYN7 | Rattus norvegicus | 38% | 100% |
D0A833 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 58% | 100% |
E9AEB2 | Leishmania major | 42% | 100% |
E9ATM0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E9AZK1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 99% |
O75449 | Homo sapiens | 41% | 100% |
Q0IIR9 | Xenopus tropicalis | 42% | 100% |
Q1HGK7 | Gallus gallus | 43% | 100% |
Q4Q0X8 | Leishmania major | 35% | 100% |
Q4Q8N0 | Leishmania major | 95% | 100% |
Q4R407 | Macaca fascicularis | 42% | 100% |
Q5U3S1 | Danio rerio | 42% | 100% |
Q9PUL2 | Xenopus laevis | 42% | 100% |
Q9SEX2 | Arabidopsis thaliana | 42% | 100% |
V5B0U7 | Trypanosoma cruzi | 56% | 100% |